Spawning: Difference between revisions
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{{Short description|Eggs and sperm released into water}} |
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{{other uses|Spawn (disambiguation)}} |
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{{Redirect|Spawn (biology)||Spawn (disambiguation){{!}}Spawn}} |
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[[File:Anemone Fish Eggs.jpg|thumb|300px|right|The spawn (eggs) of a [[clownfish]]. The black spots are the eyes developing.]] |
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[[File:Anemone Fish Eggs.jpg|thumb|300px|right|The spawn (eggs) of a [[clownfish]]. The black spots are the developing eyes.]] |
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'''Spawn''' is the [[ |
'''Spawn''' is the [[Egg cell|eggs]] and [[Spermatozoa|sperm]] released or deposited into water by [[aquatic animal]]s. As a verb, ''to spawn'' refers to the process of freely releasing eggs and sperm into a body of water (fresh or marine); the physical act is known as '''spawning'''. The vast majority of aquatic and amphibious animals reproduce through spawning. These include the following groups: |
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*[[Bony fishes]] |
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Spawn consists of the reproductive cells ([[gamete]]s) of aquatic animals, some of which will become [[fertilize]]d and produce offspring. The process of spawning typically involves females releasing [[Ovum|ova]] (unfertilized eggs) into the water, often in large quantities, while males simultaneously or sequentially release [[spermatozoa]] ([[milt]]) to fertilize the eggs.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=spawn&sc=is Spawn] Fishbase Glossary. Retrieved 3 February 2011.</ref><ref>[http://www.fishbase.org/Glossary/Glossary.php?q=spawning&language=english&sc=is Spawning] Fishbase Glossary. Retrieved 3 February 2011.</ref><ref>[http://www.fishbase.org/Glossary/Glossary.php?q=gametes&sc=is Gametes] Fishbase Glossary. Retrieved 3 February 2011.</ref> |
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*[[Crustacean]]s (such as [[crab]]s, [[shrimp]]s, etc.) |
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*[[Mollusk]]s (such as [[oysters]], [[octopus]], [[squid]]) |
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*[[Echinoderm]]s (such as [[sea urchins]], [[sea stars]], [[sea cucumbers]], etc.) |
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*[[Amphibia]]ns (such as [[frogs]], [[toads]], [[salamanders]], [[newts]]) |
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*[[Aquatic insect]]s (such as [[dragonflies]], [[mayflies]], [[mosquitoes]]) |
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*[[Coral]], which are living colonies of tiny, aquatic organisms—not plants, as they are sometimes perceived to be. Corals, while appearing sedentary or botanical by nature, actually spawn by releasing clouds of sperm and egg cells into the water column, where the two mix. |
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As a general rule, aquatic or semiaquatic [[reptile]]s, [[bird]]s, and [[mammal]]s do not reproduce through spawning, but rather through [[copulation (zoology)|copulation]] like their terrestrial counterparts. This is also true of [[cartilaginous fish]]es (such as [[sharks]], [[Ray (fish)|rays]] and [[Skate (fish)|skates]]). |
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Most fish reproduce by spawning, and so do most other aquatic animals, including [[crustacean]]s such as crabs and shrimps, [[mollusc]]s such as oysters and squid, [[echinoderm]]s such as sea urchins and sea cucumbers, [[amphibian]]s such as frogs and newts, other [[wikt:amphibious|amphibious]] animals such as turtles, [[aquatic insect]]s such as mayflies and mosquitoes, and [[coral]]s (which are small aquatic animals and not plants). [[Fungi]], such as mushrooms, are also said to "spawn" a white fibrous matter that forms the matrix from which they grow. |
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Spawn consists of the reproductive cells ([[gamete]]s) of many aquatic animals, some of which will become [[fertilize]]d and produce offspring. The process of spawning typically involves females releasing [[Ovum|ova]] (unfertilized eggs) into the water, often in large quantities, while males simultaneously or sequentially release [[spermatozoa]] ([[milt]]) to fertilize the eggs.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=spawn&sc=is Spawn] {{webarchive|url=https://web.archive.org/web/20141129110357/http://www.fishbase.org/Glossary/Glossary.php?q=spawn&sc=is |date=2014-11-29 }} Fishbase Glossary. Retrieved 3 February 2011.</ref><ref>[http://www.fishbase.org/Glossary/Glossary.php?q=spawning&language=english&sc=is Spawning] {{webarchive|url=https://web.archive.org/web/20130621170810/http://fishbase.org/Glossary/Glossary.php?q=spawning&language=english&sc=is |date=2013-06-21 }} Fishbase Glossary. Retrieved 3 February 2011.</ref><ref>[http://www.fishbase.org/Glossary/Glossary.php?q=gametes&sc=is Gametes] {{webarchive|url=https://web.archive.org/web/20130915235345/http://fishbase.org/Glossary/Glossary.php?q=gametes&sc=is |date=2013-09-15 }} Fishbase Glossary. Retrieved 3 February 2011.</ref> |
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There are many variations in the way spawning occurs, depending on sexual differences in anatomy, on how the sexes relate to each other, on where and how the spawn is released, and on whether or how the spawn is subsequently guarded. |
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The [[fungi]] ([[mushrooms]]), are also said to "spawn" when they release a white, ‘fibrous’ matter, forming the matrix from-which they grow.{{citation needed|reason=Some of the statements above need accurate sources. Reptiles (e.g., turtles) actually reproduce sexually|date=January 2016}} |
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There are many variations in the way spawning occurs, depending on sexual differences in anatomy, how the sexes relate to each other, where and how the spawn is released and whether or how the spawn is subsequently guarded. |
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{{TOC limit|limit=3}} |
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==Overview== |
==Overview== |
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[[File: |
[[File:Oncorhynchus nerka 2.jpg|thumb|[[Oncorhynchus|Pacific salmon]] are [[semelparous]] or "big bang" spawners, which means they die shortly after spawning]] |
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[[File:Mullet roe by comicpie in Taiwan.jpg|thumb|right|The pickled and dehydrated [[roe]] of [[mullet (fish)|mullet]]]] |
[[File:Mullet roe by comicpie in Taiwan.jpg|thumb|right|The pickled and dehydrated [[roe]] of [[mullet (fish)|mullet]]]] |
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Marine animals, and particularly [[bony fish]], commonly reproduce by ''broadcast spawning''. This is an external method of reproduction where the female releases many unfertilised eggs into the water. At the same time, a male or many males release a |
Marine animals, and particularly [[bony fish]], commonly reproduce by ''broadcast spawning''. This is an external method of reproduction where the female releases many unfertilised eggs into the water. At the same time, a male or many males release a large amount of sperm into the water which fertilises some of these eggs. The eggs contain a drop of nutrient oil to sustain the embryo as it develops inside the egg case. The oil also provides buoyancy, so the eggs float and drift with the current. The strategy for survival of broadcast spawning is to disperse the fertilised eggs, preferably away from the coast into the relative safety of the open ocean. There the [[larvae]] develop as they consume their fat stores, and eventually hatch from the egg capsule into miniature versions of their parents. |
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To survive, they must then become miniature predators themselves, feeding on plankton. Fish eventually encounter others of their own kind ([[conspecific]]s), where they form aggregations and learn to school. |
To survive, they must then become miniature predators themselves, feeding on plankton. Fish eventually encounter others of their own kind ([[conspecific]]s), where they form aggregations and learn to school. |
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Internally, the sexes of most marine animals can be determined by looking at the [[gonad]]s. For example, male [[ |
Internally, the sexes of most marine animals can be determined by looking at the [[gonad]]s. For example, male [[testes]] of spawning fish are smooth and white and account for up to 12% of the mass of the fish, while female [[ovary|ovaries]] are granular and orange or yellow, accounting for up to 70% of the fish's mass. Male lampreys, hagfish and salmon discharge their sperm into the body cavity where it is expelled through pores in the abdomen. Male [[shark]]s and [[Batoidea|rays]] can pass sperm along a duct into a [[seminal vesicle]], where they store it for a while before it is expelled, while [[teleost]]s usually employ separate sperm ducts.<ref name="Moyle&Cech">Moyle PB and Cech JJ (2004) ''Fishes, An Introduction to Ichthyology.'' 5th Ed, Benjamin Cummings. {{ISBN|978-0-13-100847-2}}</ref>{{Rp|141}} |
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Externally, many marine animals, even when spawning, show little [[sexual dimorphism]] (difference in body shape or size) or little difference in [[Animal colouration|colouration]]. Where species are dimorphic, such as sharks or [[guppy|guppies]], the males often have penis-like [[intromittent organ]]s in the form of a modified fin.<ref name="Moyle&Cech" />{{Rp|141}} |
Externally, many marine animals, even when spawning, show little [[sexual dimorphism]] (difference in body shape or size) or little difference in [[Animal colouration|colouration]]. Where species are dimorphic, such as sharks or [[guppy|guppies]], the males often have penis-like [[intromittent organ]]s in the form of a modified fin.<ref name="Moyle&Cech" />{{Rp|141}} |
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A species is [[semelparous]] if its individuals spawn only once in their lifetime, and [[iteroparous]] if its individuals spawn more than once. The term semelparity comes from the [[Latin]] ''semel'', once, and ''pario'', to beget, while iteroparity comes from ''itero'', to repeat, and ''pario'', to beget. |
A species is [[semelparous]] if its individuals spawn only once in their lifetime, and [[iteroparous]] if its individuals spawn more than once. The term semelparity comes from the [[Latin]] ''semel'', once, and ''pario'', to beget, while iteroparity comes from ''itero'', to repeat, and ''pario'', to beget. |
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Semelparity is sometimes called "big bang" reproduction, since the single reproductive event of semelparous organisms is usually large and fatal to the spawners.<ref>Robert E. Ricklefs and Gary Leon Miller (1999). ''Ecology.'' Macmillan ISBN |
Semelparity is sometimes called "big bang" reproduction, since the single reproductive event of semelparous organisms is usually large and fatal to the spawners.<ref>Robert E. Ricklefs and Gary Leon Miller (1999). ''Ecology.'' Macmillan {{ISBN|0-7167-2829-X}}</ref> The classic example of a semelparous animal is the [[Pacific salmon]], which lives for many years in the ocean before swimming to the freshwater stream of its birth, spawning, and then dying. Other spawning animals which are semelparous include [[mayfly|mayflies]], [[squid]], [[octopus]], [[smelts|smelt]], [[capelin]] and some amphibians.<ref name="Leiner">{{Cite journal |
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| last = Leiner | first = NO | |
| last = Leiner | first = NO |author2=Setz EZF |author3=Silva WR |
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| title = Semelparity and Factors Affecting the Reproductive Activity of the Brazilian Slender Opossum (''Marmosps paulensis'') in Southeastern Brazil |
| title = Semelparity and Factors Affecting the Reproductive Activity of the Brazilian Slender Opossum (''Marmosps paulensis'') in Southeastern Brazil |
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| journal = Journal of Mammalogy | volume = 89 | issue = 1 | pages = 153–158 |
| journal = Journal of Mammalogy | volume = 89 | issue = 1 | pages = 153–158 |
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| year = 2008 |
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| doi = 10.1644/07-MAMM-A-083.1 | doi-access = free}}</ref> Semelparity is often associated with [[r/K selection theory|r-strategists]]. However, most fish and other spawning animals are iteroparous. |
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| url = http://www.bioone.org/doi/abs/10.1644/07-MAMM-A-083.1 | issn = |
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| doi = 10.1644/07-MAMM-A-083.1 | id = }}</ref> Semelparity is often associated with [[r/K selection theory|r-strategists]]. However, most fish and other spawning animals are iteroparous. |
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When the internal [[Ovary|ovaries]] or egg masses of fish and certain marine animals are ripe for spawning they are called [[roe]]. Roe from certain species, such as [[shrimp]], [[scallop]], [[crab]] and [[sea urchin]]s, are sought as human delicacies in many parts of the world. ''[[Caviar]]'' is a name for the processed, salted roe of non-fertilized [[sturgeon]]. The term ''soft roe'' or ''white roe'' denotes [[milt|fish milt]]. Lobster roe is called ''coral'' because it turns bright red when cooked. Roe (reproductive organs) are usually eaten either raw or briefly cooked. |
When the internal [[Ovary|ovaries]] or egg masses of fish and certain marine animals are ripe for spawning they are called [[roe]]. Roe from certain species, such as [[shrimp]], [[scallop]], [[crab]] and [[sea urchin]]s, are sought as human delicacies in many parts of the world. ''[[Caviar]]'' is a name for the processed, salted roe of non-fertilized [[sturgeon]]. The term ''soft roe'' or ''white roe'' denotes [[milt|fish milt]]. Lobster roe is called ''coral'' because it turns bright red when cooked. Roe (reproductive organs) are usually eaten either raw or briefly cooked. |
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"The reproductive behaviour of fishes is remarkably diversified: they may be oviparous (lay eggs), |
"The reproductive behaviour of fishes is remarkably diversified: they may be oviparous (lay eggs), ovoviviparous (retain the eggs in the body until they hatch), or viviparous (have a direct tissue connection with the developing embryos and give birth to live young). All cartilaginous fishes—the elasmobranches (e.g., sharks, rays, and skates)—employ internal fertilization and usually lay large, heavy-shelled eggs or give birth to live young. The most characteristic features of the more primitive bony fishes is the assemblage of polyandrous (many males) breeding aggregations in open water and the absence of parental care..."<ref>"spawning." Encyclopædia Britannica. Encyclopædia Britannica Online. Encyclopædia Britannica, 2011. Web. 03 Feb. 2011. <{{cite web |url=http://www.britannica.com/EBchecked/topic/558450/spawning |title=Spawning | biology | Britannica |access-date=2011-02-05 |url-status=live |archive-url=https://web.archive.org/web/20121102183243/http://www.britannica.com/EBchecked/topic/558450/spawning |archive-date=2012-11-02 }}></ref> |
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There are two main reproduction methods in fish. The first method is by laying eggs and the second by ''live-bearing'' (producing their young alive). |
There are two main reproduction methods in fish. The first method is by laying eggs and the second by ''live-bearing'' (producing their young alive). |
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==Sexual strategies== |
==Sexual strategies== |
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{{ |
{{See also|Animal sexual behaviour}} |
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===Basic strategies=== |
===Basic strategies=== |
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{| class="wikitable" |
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|+ The four basic mating systems<ref name="Moyle&Cech" />{{Rp|160–161}}<ref name="Berglund1997">Berglund A (1997) [https://books.google.com/books?id=cF2Uw8HPA60C&pg=PA237 "Mating systems and sex allocation"] Pages 237–265 in JJ Godon, ed. ''Behavioural ecology of teleost fishes''. Oxford University Press. {{ISBN|0-19-850503-5}}.</ref> |
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! colspan=3 align="center" width="400px"| The four basic mating systems<ref name="Moyle&Cech" />{{Rp|160–161}}<ref name="Berglund1997">Berglund A (1997) [http://books.google.co.nz/books?id=cF2Uw8HPA60C&pg=PA237&dq=%22Mating+systems+and+sex+allocation%22+%22Behavioural+ecology+of+teleost+fishes%22&hl=en&ei=rKdUTeuzM8yPcenaxaYF&sa=X&oi=book_result&ct=result&resnum=1&ved=0CDgQ6AEwAA#v=onepage&q&f=false "Mating systems and sex allocation"] Pages 237–265 in JJ Godon, ed. ''Behavioural ecology of teleost fishes''. Oxford University Press. ISBN 0-19-850503-5.</ref> |
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! Single male |
! Single male |
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| align="center" | [[ |
| align="center" | [[Monogamy in animals|Monogamy]] |
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| align="center" | [[Polygyny |
| align="center" | [[Polygyny in animals|Polygyny]] |
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! Multiple males |
! Multiple males |
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| align="center" | [[Polyandry |
| align="center" | [[Polyandry in animals|Polyandry]] |
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| align="center" | [[Polygynandry]] |
| align="center" | [[Polygynandry]] |
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[[File:Hamol u0.gif|thumb|right|The anglerfish ''[[Haplophryne mollis]]'' is polyandrous. This female is trailing the atrophied remains of males she has encountered]] |
[[File:Hamol u0.gif|thumb|right|The anglerfish ''[[Haplophryne mollis]]'' is polyandrous. This female is trailing the atrophied remains of males she has encountered]] |
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[[Monogamous pairing in animals|Monogamy]] occurs when one male mates with one female exclusively. This is also called ''pair spawning''.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=pair+spawning&language=english&sc=is Pair spawning] Fishbase Glossary. Retrieved 3 February 2011.</ref> Most fish are not monogamous, and when they are, they often alternate with non-monogamous behaviours. Monogamy can occur when feeding and breeding grounds are small, when it is difficult for fish to find partners, or when both sexes look after the young.<ref name="Berglund1997" /> Many tropical [[cichlid]]s, which rear their young together in locations where they must fiercely defend against competitors and predators are monogamous.<ref name="Barlow2000">Barlow GW (2000) [ |
[[Monogamous pairing in animals|Monogamy]] occurs when one male mates with one female exclusively. This is also called ''pair spawning''.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=pair+spawning&language=english&sc=is Pair spawning] {{webarchive|url=https://web.archive.org/web/20130621181023/http://fishbase.org/Glossary/Glossary.php?q=pair+spawning&language=english&sc=is |date=2013-06-21 }} Fishbase Glossary. Retrieved 3 February 2011.</ref> Most fish are not monogamous, and when they are, they often alternate with non-monogamous behaviours. Monogamy can occur when feeding and breeding grounds are small, when it is difficult for fish to find partners, or when both sexes look after the young.<ref name="Berglund1997" /> Many tropical [[cichlid]]s, which rear their young together in locations where they must fiercely defend against competitors and predators are monogamous.<ref name="Barlow2000">Barlow GW (2000) [https://books.google.com/books?id=pVQWAQAAIAAJ&q=Barlow+2000+%27%27The+cichlid+fishes%22+monogamous ''The cichlid fishes: Nature's grand experiment in evolution''] {{webarchive|url=https://web.archive.org/web/20180502161516/https://books.google.com/books?id=pVQWAQAAIAAJ&q=Barlow+2000+%27%27The+cichlid+fishes%22+monogamous&dq=Barlow+2000+%27%27The+cichlid+fishes%22+monogamous&hl=en&ei=-KlUTcKEIsKdcd_MhKcF&sa=X&oi=book_result&ct=result&resnum=1&ved=0CCgQ6AEwAA |date=2018-05-02 }} Perseus Publishing, {{ISBN|0-7382-0528-1}}.</ref> "In some [[pipefish]]es and [[seahorse]]s, development of eggs takes a long time before the female can place them in the brood pouch of a male, where they are fertilized. While the male is pregnant, the female starts a new batch of eggs, which are ready at about the same time that the male gives birth to the young from the previous mating. This close timing of development promotes monogamy, especially if the likelihood of encountering another potential mate is low."<ref name="Berglund1997" /> |
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[[Polygyny |
[[Polygyny in animals|Polygyny]] occurs when one male gets exclusive mating rights with multiple females. In polygyny, a large conspicuous male usually defends females from other males or defends a breeding site.<ref name="Berglund1997" /> The females choose large males that are successfully defending prime breeding sites which the females find attractive. For example, [[sculpin]] males defend "caves" underneath rocks which are suitable for the incubation of embryos. |
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Another way males get to mate with several females is through the use of leks. [[Lek (biology)|Leks]] are places where many fish come together, and the males display to each |
Another way males get to mate with several females is through the use of leks. [[Lek (biology)|Leks]] are places where many fish come together, and the males display to each other. Based on these displays, each female then selects the male they want to be their mate. For example, among the cichlid ''Cyrtocara eucinostomus'' in [[Lake Malawi]], up to 50,000 large and colourful males display together on a lek four kilometres long. The females, which are mouth brooders, choose which male they want to fertilize their eggs.<ref>{{cite journal | author = McKaye | year = 1983 | title = Ecology and breeding behavior of a cichilid fish, ''Cyrtocara eucinostomus'', on a large lek in Lake Malawi, Africa | journal = Environ. Biol. Fish. | volume = 8 | issue = 2| pages = 81–96 | doi = 10.1007/BF00005175 | bibcode = 1983EnvBF...8...81M | s2cid = 27001657 }}</ref> |
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[[Polyandry |
[[Polyandry in animals|Polyandry]] occurs when one female gets exclusive mating rights with multiple males. This happens among fish like [[clownfish]] that change their sex. It can also happen when males do the brooding but cannot handle all the eggs the female produce, such as with some [[pipefish]].<ref name="Moyle&Cech" />{{Rp|161}} |
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The males in some deep sea [[anglerfish]]es are much smaller than the females. When they find a female they bite into her skin, releasing an [[enzyme]] that digests the skin of their mouth and her body and fusing the pair down to the blood-vessel level. The male then slowly [[atrophy|atrophies]], losing first his digestive organs, then his brain, heart, and eyes, ending as nothing more than a pair of [[gonads]], which release [[Spermatozoon|sperm]] in response to [[hormones]] in the female's bloodstream indicating [[ovum|egg]] release. This |
The males in some deep sea [[anglerfish]]es are much smaller than the females. When they find a female they bite into her skin, releasing an [[enzyme]] that digests the skin of their mouth and her body and fusing the pair down to the blood-vessel level. The male then slowly [[atrophy|atrophies]], losing first his digestive organs, then his brain, heart, and eyes, ending as nothing more than a pair of [[gonads]], which release [[Spermatozoon|sperm]] in response to [[hormones]] in the female's bloodstream indicating [[ovum|egg]] release. This ensures that, when the female is ready to spawn, she has a mate immediately available.<ref name="doran">{{cite journal | author = Theodore W. Pietsch | title = Precocious sexual parasitism in the deep sea ceratioid anglerfish, Cryptopsaras couesi Gill | volume = 256 | issue = 5512 | doi = 10.1038/256038a0 | journal = Nature | pages = 38–40 | bibcode = 1975Natur.256...38P | year = 1975 | s2cid = 4226567 }}</ref> A single anglerfish female can "mate" with many males in this manner. |
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[[Polygynandry]] occurs when multiple males mate indiscriminately with multiple females. This mutual promiscuity is the approach most commonly used by spawning animals, and is perhaps the "original fish mating system."<ref name="Moyle&Cech" />{{Rp|161}} Common examples are [[forage fish]], such as [[herring]]s, which form huge mating [[Shoaling and schooling|shoals]] in shallow water. The water becomes milky with sperm and the bottom is draped with millions of fertilized eggs.<ref name="Moyle&Cech" />{{Rp|161}} |
[[Polygynandry]] occurs when multiple males mate indiscriminately with multiple females. This mutual promiscuity is the approach most commonly used by spawning animals, and is perhaps the "original fish mating system."<ref name="Moyle&Cech" />{{Rp|161}} Common examples are [[forage fish]], such as [[herring]]s, which form huge mating [[Shoaling and schooling|shoals]] in shallow water. The water becomes milky with sperm and the bottom is draped with millions of fertilized eggs.<ref name="Moyle&Cech" />{{Rp|161}} |
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[[File:Anemone purple anemonefish.jpg|thumb|right|An [[anemone fish]] couple guarding their [[sea anemone|anemone]]. If the female dies, a juvenile male moves in, and the resident male changes sex.]] |
[[File:Anemone purple anemonefish.jpg|thumb|right|An [[anemone fish]] couple guarding their [[sea anemone|anemone]]. If the female dies, a juvenile male moves in, and the resident male changes sex.]] |
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Alternate male strategies which allow small males to engage in [[cuckoldry]] can develop in species where spawning is dominated by large and aggressive males. Cuckoldry is a variant of polyandry, and can occur with ''sneak spawners'' (sometimes called ''streak spawners''). A sneak spawner is a male that rushes in to join the spawning rush of a spawning pair.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=streak+spawning&language=english&sc=is Streak spawning] Fishbase Glossary. Retrieved 11 February 2011.</ref> A spawning rush occurs when a fish makes a burst of speed, usually on a near vertical incline, releasing gametes at the apex, followed by a rapid return to the lake or sea floor or fish aggregation.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=spawning+rush&language=english&sc=is Spawning rush] Fishbase Glossary. Retrieved 11 February 2011.</ref> Sneaking males do not take part in courtship. In salmon and trout, for example, ''jack males'' are common. These are small silvery males that migrate upstream along with the standard, large, hook-nosed males and that spawn by sneaking into |
Alternate male strategies which allow small males to engage in [[cuckoldry]] can develop in species where spawning is dominated by large and aggressive males. Cuckoldry is a variant of polyandry, and can occur with ''sneak spawners'' (sometimes called ''streak spawners''). A sneak spawner is a male that rushes in to join the spawning rush of a spawning pair.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=streak+spawning&language=english&sc=is Streak spawning] {{webarchive|url=https://web.archive.org/web/20150210190505/http://www.fishbase.org/Glossary/Glossary.php?q=streak+spawning&language=english&sc=is |date=2015-02-10 }} Fishbase Glossary. Retrieved 11 February 2011.</ref> A spawning rush occurs when a fish makes a burst of speed, usually on a near vertical incline, releasing gametes at the apex, followed by a rapid return to the lake or sea floor or fish aggregation.<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=spawning+rush&language=english&sc=is Spawning rush] {{webarchive|url=https://web.archive.org/web/20150210190502/http://www.fishbase.org/Glossary/Glossary.php?q=spawning+rush&language=english&sc=is |date=2015-02-10 }} Fishbase Glossary. Retrieved 11 February 2011.</ref> Sneaking males do not take part in courtship. In salmon and trout, for example, ''jack males'' are common. These are small silvery males that migrate upstream along with the standard, large, hook-nosed males and that spawn by sneaking into a [[Salmon run#Spawning|redd]] (spawning nest) to release sperm simultaneously with a mated pair. This behaviour is an [[evolutionarily stable strategy]] for reproduction, because it is favoured by natural selection just like the "standard" strategy of large males.<ref>Gross MR (1984) "[http://labs.eeb.utoronto.ca/gross/Gross1984a.pdf Sunfish, salmon, and the evolution of alternative reproductive strategies and tactics in fishes] {{Webarchive|url=https://web.archive.org/web/20190524025026/http://labs.eeb.utoronto.ca/gross/Gross1984a.pdf |date=2019-05-24 }}". Pages 55–75 in GW Potts and RJ Wottoon, eds. ''Fish reproduction: Strategies and tactics''. Academic Press.</ref> |
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Cuckoldry occurs in many fish species, including [[parrotfish]]es and [[ |
Cuckoldry occurs in many fish species, including [[dragonets]], [[parrotfish]]es and [[wrasse]]s on tropical reefs and the [[bluegill]] sunfish in fresh water. Sneaker males that become too large to hide effectively become ''satellite males''. With bluegill sunfish, satellite males mimic the behaviour and colouration of the females. They hover over a nest containing a pair of courting sunfish, and gradually descend to reach the pair just as they spawn. Males may need to be 6 or 7 years old to function capably as parental males, but may be able to function as sneaker or satellite males when they are as young as 2 or 3 years old. The smaller satellite and sneaker males may get mauled by the more powerful parental males, but they spawn when they are younger and they do not put energy into parental care.<ref name="Moyle&Cech" />{{Rp|161–2}}<ref>{{cite journal | author = Gross MR | year = 1982 | title = Sneakers, satellites and parentals: Polymorphic mating strategies in North American sunfishes | journal = Zeitschrift für Tierpsychologie | volume = 60 | pages = 1–26 | doi=10.1111/j.1439-0310.1982.tb01073.x}}</ref> |
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===Hermaphroditism=== |
===Hermaphroditism=== |
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[[Hermaphroditism]] occurs when a given individual in a species possesses both male and female reproductive organs, or can alternate between possessing first one, and then the other. Hermaphroditism is common in invertebrates but rare in vertebrates. It can contrasted with [[gonochorism]], where each individual in a species is either male or female, and remains that way throughout their lives. Most fish are gonochorists, but hermaphroditism is known to occur in 14 families of [[teleost]] fishes.<ref name="Shapiro1984">Shapiro DY (1984) "Sex reversal and sociodemographics processes in coral reef fishes" Pages 103–116 in GW Potts and RK Wootoon, eds., ''Fish reproduction: Strategies and tactics'', Academic Press.</ref> |
[[Hermaphroditism]] occurs when a given individual in a species possesses both male and female reproductive organs, or can alternate between possessing first one, and then the other. Hermaphroditism is common in invertebrates but rare in vertebrates. It can be contrasted with [[gonochorism]], where each individual in a species is either male or female, and remains that way throughout their lives. Most fish are gonochorists, but hermaphroditism is known to occur in 14 families of [[teleost]] fishes.<ref name="Shapiro1984">Shapiro DY (1984) "Sex reversal and sociodemographics processes in coral reef fishes" Pages 103–116 in GW Potts and RK Wootoon, eds., ''Fish reproduction: Strategies and tactics'', Academic Press.</ref> |
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Usually hermaphrodites are ''[[Sequential hermaphroditism|sequential]]'', meaning they can switch sex, usually from female to male ([[protogyny]]). This can happen if a dominant male is removed from a group of females. The largest female in the harem can switch sex over a few days and replace the dominant male.<ref name="Shapiro1984" /> This is found amongst [[coral reef fish]]es such as [[grouper]]s, [[parrotfish]]es and [[wrasse]]s. It is less common for a male to switch to a female ([[protandry]]).<ref name="Moyle&Cech" />{{Rp|162}} As an example, most [[wrasse]]s are [[protogynous]] hermaphrodites within a haremic mating system.<ref name="Robertson1978">{{Cite journal |
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* Example: Most [[wrasse]]s are [[protogynous]] hermaphrodites within a haremic mating system.<ref name=Robertson1978>{{Cite journal |
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| last = Robertson |
| last = Robertson |
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| first = D.R. |
| first = D.R. |
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| |
|author2=R.R. Warner |
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| title = Sexual patterns in the labroid fishes of the Western Caribbean II: the parrotfishes (Scaridae) |
| title = Sexual patterns in the labroid fishes of the Western Caribbean II: the parrotfishes (Scaridae) |
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| journal = Smithsonian Contributions to Zoology |
| journal = Smithsonian Contributions to Zoology |
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| volume = 255 |
| volume = 255 |
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| issue = |
| issue = 255 |
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| pages = 1–26 |
| pages = 1–26 |
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| doi = 10.5479/si.00810282.255 |
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| publisher = |
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| |
| year = 1978 |
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}}</ref><ref name="Kazancioglu2010">{{Cite journal |
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| date = |
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| url = |
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| issn = |
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| doi = |
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| id = |
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| accessdate = }}</ref><ref name=Kazancioglu2010> |
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{{Cite journal |
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| last = Kazancioglu |
| last = Kazancioglu |
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| first = E. |
| first = E. |
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| |
|author2=S.H. Alonzo |
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| title = A comparative analysis of sex change in Labridae supports the size advantage hypothesis |
| title = A comparative analysis of sex change in Labridae supports the size advantage hypothesis |
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| journal = Evolution |
| journal = Evolution |
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| volume = 64 |
| volume = 64 |
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| issue = 8 |
| issue = 8 |
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| pages = 2254–2264 |
| pages = 2254–2264 |
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| publisher = |
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| location = |
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| date = |
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| url = |
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| issn = |
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| doi = 10.1111/j.1558-5646.2010.01016.x |
| doi = 10.1111/j.1558-5646.2010.01016.x |
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| |
| pmid = 20394662 |
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| date=August 2010| doi-access = free |
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| accessdate = |
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}}</ref> Hermaphroditism allows for complex mating systems. Wrasses exhibit three different mating systems: polygynous, [[Lek (biology)|lek-like]], and promiscuous mating systems.<ref name="Colin1992">{{Cite journal |
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{{Cite journal |
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| last = Colin |
| last = Colin |
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| first = P.L. |
| first = P.L. |
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| |
|author2=L. J. Bell |
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| title = Aspects of the spawning of labrid and scarid fishes (Pisces, Labroidei) at Enewetak Atoll, Marshall Islands with notes on other families (corrected reprint.) |
| title = Aspects of the spawning of labrid and scarid fishes (Pisces, Labroidei) at Enewetak Atoll, Marshall Islands with notes on other families (corrected reprint.) |
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| journal = Environmental Biology of Fishes |
| journal = Environmental Biology of Fishes |
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| volume = 33 |
| volume = 33 |
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| issue = 3 |
| issue = 3 |
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| pages = 330–345 |
| pages = 330–345 |
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| publisher = |
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| location = |
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| date = |
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| url = |
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| issn = |
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| doi = 10.1007/BF00005881 |
| doi = 10.1007/BF00005881 |
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| |
| year = 1992 |
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| doi-access = free |
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| accessdate = }}</ref> Group spawning and pair spawning occur within mating systems. The type of spawning that occurs depends on male body size.<ref name="Kazancioglu2010"/> Labroids typically exhibit broadcast spawning, releasing high amounts of planktonic eggs, which are broadcast by tidal currents; adult wrasses have no interaction with offspring.<ref name=Hanel2002> |
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}}</ref> Group spawning and pair spawning occur within mating systems. The type of spawning that occurs depends on male body size.<ref name="Kazancioglu2010" /> Labroids typically exhibit broadcast spawning, releasing high amounts of planktonic eggs, which are broadcast by tidal currents; adult wrasses have no interaction with offspring.<ref name="Hanel2002">{{Cite journal |
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{{Cite journal |
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| last = Hanel |
| last = Hanel |
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| first = R. |
| first = R. |author2=M. W. Westneat |author3=C. Sturmbauer |
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| coauthors = M. W. Westneat and C. Sturmbauer |
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| title = Phylogenetic relationships, evolution of broodcare behavior, and geographic speciation in the Wrasse tribe Labrini |
| title = Phylogenetic relationships, evolution of broodcare behavior, and geographic speciation in the Wrasse tribe Labrini |
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| journal = Journal of Molecular Evolution |
| journal = Journal of Molecular Evolution |
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| issue = 6 |
| issue = 6 |
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| pages = 776–789 |
| pages = 776–789 |
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| doi = 10.1007/s00239-002-2373-6 |
| doi = 10.1007/s00239-002-2373-6 |
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| |
| pmid = 12486536 |
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| date=December 2002| bibcode =2002JMolE..55..776H| s2cid = 3002410 }}</ref> Wrasse of a particular subgroup of the family [[Labridae]], Labrini, do not exhibit broadcast spawning. |
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| accessdate = |
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| pmid = 12486536 }}</ref> Wrasse of a particular subgroup of the Labridae family Labrini do not exhibit broadcast spawning. |
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* [[homogamy (biology)|homogamy]] versus [[dichogamy]]: Dichogamy, also known as sequential hermaphrodism, is the separation in time of gender expression in a [[Hermaphrodite|hermaphroditic]] organism, a characteristic of some fishes, gastropods, crustaceans. This is the opposite of simultaneous hermaphrodites, or homogamy. |
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* "Hermaphrodites have both male and female sex organs, either throughout their lives (homgamy) or that develop and mature at different points in their life cycle (dichogamy). Homogamy is the maturation in hermaphroditic animals of the ova and sperm at different times so as to preclude self-fertilization. It is the condition in which an organism changes sex during its lifetime."<ref>[http://www.wordnik.com/words/dichogamy Dichogamy] - ''[[Wordnik]]''</ref> |
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Less commonly hermaphrodites can be ''synchronous'', meaning they simultaneously possess both ovaries and testicles and can function as either sex at any one time. [[Hypoplectrus nigricans|Black hamlet]]s "take turns releasing sperm and eggs during spawning. Because such egg trading is advantageous to both individuals, hamlets are typically monogamous for short periods of time–an unusual situation in fishes."<ref>{{cite journal |vauthors=Fischer EA, Peterson CW | year = 1987 | title = The evolution of sexuality in the seabasses | journal = BioScience | volume = 37 | issue = 7| pages = 482–489 | doi = 10.2307/1310420 | jstor = 1310420 }}</ref> The sex of many fishes is not fixed, but can change with physical and social changes to the environment where the fish lives.<ref>Chan STH and Yeung WSB (1983) "Sex control and sex reversal in fish under natural conditions". Pages 171–222 in WS Hoar, DJ Randall and EM Donaldson, eds., ''Fish physiology 9B: Reproduction, behavior and fertility control''. Academic Press.</ref> |
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The sex of many fishes is not fixed, but can change with physical and social changes to the environment where the fish lives.<ref>Chan STH and Yeung WSB (1983) "Sex control and sex reversal in fish under natural conditions". Pages 171–222 in WS Hoar, DJ Randall and EM Donaldson, eds., ''Fish physiology 9B: Reproduction, behavior and fertility control''. Academic Press.</ref> "[[Sex change]] occurs mainly in fishes in which one sex had higher survival and reproductive rates, usually as the result of larger size. In such situations it may pay for an individual of the smaller sex to change to the larger sex when the opportunity arises.<ref name="Kuwamura">{{cite journal | doi= 10.1023/A:1007389519702 | year= 1998 | last1= Kuwamura | first1= Tetsuo | last2= Nakashima | first2= Yasuhiro | journal= Environmental Biology of Fishes | volume= 52 | pages= 125–135 }}</ref> For example [[anemone fish]]es live as monogamous pairs in single [[sea anemone | anemone]]s, protected from predators by the stings of the anemone. Female anemone fish are typically larger than males, because a male does not have to vigorously compete for mates once he has paired with a female. If the female dies, however, a juvenile anemone fish quickly moves in; such fish are always male. The resident male then turns into a female and reproductive advantages of the large female–small male combination continue.<ref>{{cite journal | doi= 10.1038/266830a0 | title= Monogamy and sex change by aggressive dominance in coral reef fish | year= 1977 | last1= Fricke | first1= Hans | last2= Fricke | first2= Simone | journal= Nature | volume= 266 | issue= 5605 | pages= 830–832 | pmid= 865603 |bibcode = 1977Natur.266..830F }}</ref> In some fishes, sex change is reversible, depending on the social situation. Thus some [[Goby|gobies]] will switch sex when kept in what initially were single sex groups of either sex."<ref name="Moyle&Cech" />{{Rp|164}}<ref name="Kuwamura" /> |
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Particularly among fishes, hermaphroditism can pay off in situations where one sex is more likely to survive and reproduce, perhaps because it is larger.<ref name="Kuwamura">{{cite journal | title = New aspects of sex change among reef fishes: recent studies in Japan | doi= 10.1023/A:1007389519702 | year= 1998 | last1= Kuwamura | first1= Tetsuo | last2= Nakashima | first2= Yasuhiro | journal= Environmental Biology of Fishes | volume= 52 | issue= 1–3 | pages= 125–135 | bibcode= 1998EnvBF..52..125K | s2cid= 30244987 }}</ref> [[Anemone fish]]es are sequential hermaphrodites which are born as males, and become females only when they are mature. Anemone fishes live together monogamously in an [[sea anemone|anemone]], protected by the anemone stings. The males do not have to compete with other males, and female anemone fish are typically larger. When a female dies a juvenile (male) anemone fish moves in, and "the resident male then turns into a female and reproductive advantages of the large female–small male combination continue".<ref>{{cite journal | doi= 10.1038/266830a0 | title= Monogamy and sex change by aggressive dominance in coral reef fish | year= 1977 | last1= Fricke | first1= Hans | last2= Fricke | first2= Simone | journal= Nature | volume= 266 | issue= 5605 | pages= 830–832 | pmid= 865603 |bibcode = 1977Natur.266..830F | s2cid= 4177265 }}</ref> In other fishes sex changes are reversible. For example, if some [[Goby|gobies]] are grouped by sex (male or female), some will switch sex.<ref name="Moyle&Cech" />{{Rp|164}}<ref name="Kuwamura" /> |
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===Unisexuality=== |
===Unisexuality=== |
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[[Unisexuality]] occurs when a species is all-male or all-female. Unisexuality occurs in some fish species, and can take complex forms. ''[[Squalius alburnoides]]'', a minnow found in several river basins in Portugal and Spain, appears to be an all-male species. The existence of this species illustrates the potential complexity of mating systems in fish. The species originated as a hybrid between two species, and is [[diploid]], but not hermaphroditic. It can have [[triploid]] and [[tetraploid]] forms, including all-female forms that reproduce mainly through [[hybridogenesis]].<ref>{{cite journal | |
[[Unisexuality]] occurs when a species is all-male or all-female. Unisexuality occurs in some fish species, and can take complex forms. ''[[Squalius alburnoides]]'', a minnow found in several river basins in Portugal and Spain, appears to be an all-male species. The existence of this species illustrates the potential complexity of mating systems in fish. The species originated as a hybrid between two species, and is [[diploid]], but not hermaphroditic. It can have [[triploid]] and [[tetraploid]] forms, including all-female forms that reproduce mainly through [[hybridogenesis]].<ref>{{cite journal |vauthors=Alves MJ, Collarea-Pereira MJ, Dowling TE, Coelho MM | year = 2002 | title = The genetics of maintenance of an all-male lineage in the ''Squalius alburnoides'' complex | journal = J. Fish Biol. | volume = 60 | issue = 3| pages = 649–662 | doi=10.1111/j.1095-8649.2002.tb01691.x| bibcode = 2002JFBio..60..649A }}</ref> |
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It is rare to find true [[parthenogenesis]] in fishes, where females produce female offspring with no input from males. All-female species include the Texas [[silverside (fish)|silverside]], ''Menidia clarkhubbsi''<ref>{{cite journal | |
It is rare to find true [[parthenogenesis]] in fishes, where females produce female offspring with no input from males. All-female species include the Texas [[silverside (fish)|silverside]], ''Menidia clarkhubbsi''<ref>{{cite journal |vauthors=Echelle AA, Echelle AF, Crozier CD | year = 1983 | title = Evolution of an all-female fish, ''Menidia clarkhubbsi'' (Atherinidae) | journal = Evolution | volume = 37 | issue = 4| pages = 772–784 | doi = 10.2307/2407918 | jstor = 2407918 | pmid = 28568119 }}</ref> as well as the [[Amazon molly]].<ref name="Moyle&Cech" />{{Rp|162}} Parthenogenesis has been recently observed in [[hammerhead shark]]s<ref>{{Cite news|url=http://news.bbc.co.uk/2/hi/science/nature/6681793.stm|title=Captive shark had 'virgin birth'|access-date=23 December 2008|work=BBC News|date=2007-05-23|url-status=live|archive-url=https://web.archive.org/web/20081217051435/http://news.bbc.co.uk/2/hi/science/nature/6681793.stm|archive-date=17 December 2008}}</ref> and [[blacktip shark]]s.<ref name="metro">{{Cite news| title='Virgin birth' for aquarium shark| url=http://www.metro.co.uk/weird/article.html?Virgin_birth_for_aquarium_shark&in_article_id=351241&in_page_id=2| publisher=[[Metro.co.uk]]| date=2008-10-10| access-date=2008-10-10| url-status=live| archive-url=https://web.archive.org/web/20081011190939/http://www.metro.co.uk/weird/article.html?Virgin_birth_for_aquarium_shark&in_article_id=351241&in_page_id=2| archive-date=2008-10-11}}</ref> It is also known to occur in crayfish<ref>{{cite journal |last1=Scholtz |first1=Gerhard |last2=Braband |first2=Anke |last3=Tolley |first3=Laura |last4=Reimann |first4=André |last5=Mittmann |first5=Beate |last6=Lukhaup |first6=Chris |last7=Steuerwald |first7=Frank |last8=Vogt |first8=GüNter |title=Ecology: Parthenogenesis in an outsider crayfish |journal=Nature |volume=421 |issue=6925 |pages=806 |year=2003 |pmid=12594502 |doi=10.1038/421806a|bibcode = 2003Natur.421..806S |s2cid=84740187 |doi-access=free }}</ref><ref>{{cite journal |last1=Martin |first1=Peer |last2=Kohlmann |first2=Klaus |last3=Scholtz |first3=Gerhard |title=The parthenogenetic Marmorkrebs (marbled crayfish) produces genetically uniform offspring |journal=Naturwissenschaften |volume=94 |issue=10 |pages=843–6 |year=2007 |pmid=17541537 |doi=10.1007/s00114-007-0260-0|bibcode = 2007NW.....94..843M |s2cid=21568188 }}</ref> and amphibians.<ref>{{Cite book |
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|editor-last = Halliday |
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|editor-first = Tim R. |
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|editor2=Kraig Adler |
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| title = Reptiles & Amphibians |
| title = Reptiles & Amphibians |
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| publisher = Torstar Books |
| publisher = Torstar Books |
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| year= 1986 |
| year= 1986 |
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| page = 101 |
| page = 101 |
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| isbn = 0-920269-81- |
| isbn = 978-0-920269-81-7 }}</ref><ref>{{cite news |
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|title = Scientists discover unknown lizard species at lunch buffet |
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|first = Brian |
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|last = Walker |
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|url = http://www.cnn.com/2010/LIVING/11/10/lizard.lunch.discovery/ |
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|newspaper = CNN |
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|access-date = 2010-11-11 |
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|date = 2010-11-11 |
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|archive-url = https://web.archive.org/web/20121108222100/http://www.cnn.com/2010/LIVING/11/10/lizard.lunch.discovery/ |
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|archive-date = 2012-11-08 |
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==Spawning strategies== |
==Spawning strategies== |
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This section is patterned after a classification of the spawning behaviours of fish by Balon (1975, 1984) into reproductive [[Guild (ecology)|guilds]]. This classification is based on how the eggs are fertilized (internal or external spawners), where the eggs are deposited ([[pelagic]] or [[benthic]] spawners), and whether and how the parents look after the eggs after spawning (bearers, guarders and nonguarders).<ref name |
This section is patterned after a classification of the spawning behaviours of fish by Balon (1975, 1984) into reproductive [[Guild (ecology)|guilds]]. This classification is based on how the eggs are fertilized (internal or external spawners), where the eggs are deposited ([[pelagic]] or [[benthic]] spawners), and whether and how the parents look after the eggs after spawning (bearers, guarders and nonguarders).<ref name="Balon">Adapted from |
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* {{cite journal | author = Balon EK | year = 1975 | title = Reproductive guilds in fishes: A proposal and definition |
* {{cite journal | author = Balon EK | year = 1975 | title = Reproductive guilds in fishes: A proposal and definition | journal =J. Fish. Res. Board Can. | volume = 32 | issue = 6| pages = 821–864 | doi = 10.1139/f75-110 }} |
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* Balon EK (1984) "Patterns in the evolution of reproductive styles in fishes". Pages 35–53 in GW Potts and RJ Wootton, eds., ''Fish reproduction: Strategies and tactics''. London: Academic Press.</ref |
* Balon EK (1984) "Patterns in the evolution of reproductive styles in fishes". Pages 35–53 in GW Potts and RJ Wootton, eds., ''Fish reproduction: Strategies and tactics''. London: Academic Press.</ref> |
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===Nonguarders=== |
===Nonguarders=== |
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| quote = |
| quote = {{center|'''Nonguarders: Open substrate spawners'''<ref name ="Balon" />}} |
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* Pelagic spawners |
* Pelagic spawners |
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* Benthic spawners |
* Benthic spawners |
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** Spawners on fine substrates |
** Spawners on fine substrates |
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* Terrestrial spawners |
* Terrestrial spawners |
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[[File:Hecht.jpg|thumb|center|[[ |
[[File:Hecht.jpg|thumb|center|[[Esox|Pike]] usually spawn on vegetation flooded by high water. Their eggs adhere to the stems of plants.]] |
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}} |
}} |
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{{quote box |
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| quote = |
| quote = {{center|'''Nonguarders: Brood hiders'''<ref name ="Balon" />}} |
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* Benthic spawners |
* Benthic spawners |
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* Crevice spawners |
* Crevice spawners |
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Open substrate spawners scatter their eggs in the environment. They usually spawn in [[Shoaling and schooling|shoals]] without complex courtship rituals, and males outnumber females. |
Open substrate spawners scatter their eggs in the environment. They usually spawn in [[Shoaling and schooling|shoals]] without complex courtship rituals, and males outnumber females. |
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'''Broadcast spawners''': release their gametes (sperm and eggs) into open water for external fertilisation. There is no subsequent parental care.<ref>[http://www.fishbase.org/glossary/Glossary.php?q=broadcast%20spawners Broadcast spawners] Fishbase Glossary. Retrieved 3 February 2011.</ref> About 75% of coral species are broadcasters, the majority of which are hermatypic, or reef-building corals.<ref name=Veron /> |
'''Broadcast spawners''': release their gametes (sperm and eggs) into open water for external fertilisation. There is no subsequent parental care.<ref>[http://www.fishbase.org/glossary/Glossary.php?q=broadcast%20spawners Broadcast spawners] {{webarchive|url=https://web.archive.org/web/20150925084237/http://www.fishbase.org/glossary/Glossary.php?q=broadcast%20spawners |date=2015-09-25 }} Fishbase Glossary. Retrieved 3 February 2011.</ref> About 75% of coral species are broadcasters, the majority of which are hermatypic, or reef-building corals.<ref name="Veron" /> |
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* '''Pelagic spawners''': a type of broadcast spawners, spawn in the open sea, mostly near the surface. They are usually [[pelagic fish]] such as [[tuna]] and [[sardine]]s. Some [[demersal fish]] leave the bottom to spawn pelagically, particularly [[coral reef fish]] such as [[parrotfish]] and [[ |
* '''Pelagic spawners''': a type of broadcast spawners, spawn in the open sea, mostly near the surface. They are usually [[pelagic fish]] such as [[tuna]] and [[sardine]]s. Some [[demersal fish]] leave the bottom to spawn pelagically, particularly [[coral reef fish]] such as [[parrotfish]] and [[wrasse]]s. Pelagic spawning means water currents widely disperse the young. The eggs, embryos and larvae of pelagic spawners contain oil globules or have a high water content. As a result, they are buoyant and are widely dispersed by currents. The downside is that [[Fish mortality|mortality]] is high, because they can be eaten so easily by pelagic predators or they can drift into unsuitable areas. Females compensate by spawning large numbers of eggs and extending their spawning periods. Pelagic spawners that live in or around [[coral reef]]s can spawn a small number of eggs almost daily over a period of months. These fishes have complex breeding behaviours including [[Sequential hermaphroditism|sex change]]s, [[Harem (zoology)|harems]], [[Lek (biology)|leks]] and [[territoriality]].<ref name="Moyle&Cech" />{{rp|143}} |
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* '''Benthic spawners''': deposit their spawn on or near the bottom of the sea (or lake). They are usually [[demersal fish]] such as [[cod]] and [[flatfish]]. These species typically spawn without ceremony; they do not engage in elaborate courtship rituals. Each female is usually followed by several males who fertilize the eggs as they are released. Various strategies ensure the eggs and embryos remain in place, and do not drift with the current. The eggs can adhere to other eggs or to whatever they are deposited on, or the eggs can be laid in long strings which are wrapped around plants or rocks. Some eggs take on water after they are released, so they can be dropped into cracks where they swell and wedge themselves in place. |
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* '''Benthic spawners''': deposit their spawn on or near the bottom of the sea (or lake). They are usually [[demersal fish]] such as [[cod]] and [[flatfish]]. These species typically spawn without ceremony; they do not engage in elaborate courtship rituals. Each female is usually followed by several males who fertilize the eggs as they are released. Various strategies ensure the eggs and embryos remain in place, and do not drift with the current. The eggs can adhere to other eggs or to whatever they are deposited on, or the eggs can be laid in long strings which are wrapped around plants or rocks. Some eggs take on water after they are released, so they can be dropped into cracks where they swell and wedge themselves in place. "The free embryos and larvae of these fishes may be either pelagic or benthic. Those that are pelagic (e.g., those of [[Smelt (fish)|smelt]]) become active or buoyant immediately after "hatching", whereas those that are benthic stay close to the spawning area until they can swim freely. In lakes or shallow ocean waters, plants are often important substrates for the adhesive embryos of benthic spawners. Some fishes always spawn on such plants. For example, [[common carp]]s and [[Esox|pikes]] generally spawn only on vegetation that is flooded by high water in the spring. If such material is not available, spawning either does not take place or is much less successful. Once the embryos hatch, the young remain among the plants; some of them have adhesive organs on their heads, with which they can stick to the stems of the plants."<ref name="Moyle&Cech" />{{rp|143–5}} |
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** Egg scatterers: scatter adhesive or non-adhesive eggs to fall to the substrate, into plants, or float to the surface. These species do not look after their brood and even eat their own eggs. These are often [[Shoaling and schooling|schooling fish]] which spawn in groups or pairs, often laying a large number of small eggs. The fry hatch quickly. |
** Egg scatterers: scatter adhesive or non-adhesive eggs to fall to the substrate, into plants, or float to the surface. These species do not look after their brood and even eat their own eggs. These are often [[Shoaling and schooling|schooling fish]] which spawn in groups or pairs, often laying a large number of small eggs. The fry hatch quickly. |
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** Egg |
** Egg depositors: deposit eggs on a substrate (tank glass, wood, rocks, plants). Egg depositors usually lay fewer eggs than egg-scatterers, although the eggs are larger. Egg depositors fall into two groups: those that care for their eggs, and those that do not. Among egg depositors that care for their eggs are [[cichlid]]s and some catfish. Egg depositors that care for their young can be divided into two groups: cavity spawners and open spawners. |
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** Cavity spawners: lay eggs in a cave or cavity. These fish form pairs and have advanced brood care where the eggs are defended and cleaned. The eggs take a few days to hatch, and the fry are often guarded by the parents. Various [[catfish]], [[Cyprinidae]], and [[killifish]] make up the majority. Cavity spawners can be contrasted with open (shelter) spawners, which lay their eggs on an open surface. |
** Cavity spawners: lay eggs in a cave or cavity. These fish form pairs and have advanced brood care where the eggs are defended and cleaned. The eggs take a few days to hatch, and the fry are often guarded by the parents. Various [[catfish]], [[Cyprinidae]], and [[killifish]] make up the majority. Cavity spawners can be contrasted with open (shelter) spawners, which lay their eggs on an open surface. |
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* Rock tenders |
* Rock tenders |
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* Plant tenders |
* Plant tenders |
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* Rock and gravel nesters |
* Rock and gravel nesters |
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* Sand nesters |
* Sand nesters |
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Guarders protect their eggs and offspring after spawning by practicing ''parental care'' (also called ''brood care''). Parental care is an "investment by parents in offspring that increases the |
Guarders protect their eggs and offspring after spawning by practicing ''parental care'' (also called ''brood care''). Parental care is an "investment by parents in offspring that increases the offspring's chances of surviving (and hence reproducing). In fish, parental care can take a variety of forms including guarding, nest building, fanning, splashing, removal of dead eggs, retrieval of straying fry, external egg carrying, egg burying, moving eggs or young, ectodermal feeding, oral brooding, internal gestation, brood-pouch egg carrying, etc."<ref>[http://www.fishbase.org/Glossary/Glossary.php?q=parental+care&sc=is Parental care] {{webarchive|url=https://web.archive.org/web/20160125142508/http://www.fishbase.org/Glossary/Glossary.php?q=parental+care&sc=is |date=2016-01-25 }} Fishbase Glossary. Retrieved 3 February 2011.</ref> |
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[[Territoriality|Territorial behaviour]] is generally necessary for guarders, and the embryos are almost always guarded by males (apart from cichlids). There is a need to be territorial because looking after embryos usually includes defending the site where they are being looked after. It also often means there is competition for the best egg-laying sites. Elaborate courtship behaviour is usual among guarders.<ref name="Moyle&Cech" />{{Rp|145}} |
[[Territoriality|Territorial behaviour]] is generally necessary for guarders, and the embryos are almost always guarded by males (apart from cichlids). There is a need to be territorial because looking after embryos usually includes defending the site where they are being looked after. It also often means there is competition for the best egg-laying sites. Elaborate courtship behaviour is usual among guarders.<ref name="Moyle&Cech" />{{Rp|145}} |
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====Substrate spawners==== |
====Substrate spawners==== |
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Some guarders build nests (''nest spawners'') and some do not (''substrate spawners''), though the difference between the two groups can be small.<ref name="Moyle&Cech" />{{Rp|142}} Substrate spawners clean off a suitable area of surface suitable for egg laying, and look after the area, but they do not actively build a nest. |
Some guarders build nests (''nest spawners'') and some do not (''substrate spawners''), though the difference between the two groups can be small.<ref name="Moyle&Cech" />{{Rp|142}} Substrate spawners clean off a suitable area of surface suitable for egg laying, and look after the area, but they do not actively build a nest. |
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====Nest spawners==== |
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Nest spawners construct "some sort of structure, cavity, or pit in which the eggs are laid and fertilized and the embryos are defended. The young are often defended in a nest as well, and in some species, the parents even herd schools of young around for a period of time. Pit nests can be made of a wide variety of material, but the most common are nests of gravel and rocks. Such nests are typically shallow depressions that are carefully constructed and tended by territorial males. Most sunfishes and [[black bass]]es ([[Centrarchidae]]) construct nests of this sort, often in colonies. The males defend the embryos and the young until the young become too active to be kept in the nest. In some cichlids eggs are laid and incubated in one nest depression, but the young are tended (by both parents) in one or more additional depressions that are constructed nearby."<ref name="Moyle&Cech" />{{Rp|146}} |
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"A few species construct nests on sandy bottoms. Either the eggs and embryos in such nests have special adaptations (e.g., semibuoyancy) to reduce the possibility of being smothered, or the parent fish must spend considerable time handling them."<ref name="Moyle&Cech" />{{Rp|146}} |
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"In areas where bottoms are muddy, nest-building fish commonly build nests of plant material. Usually plant-nesting fishes construct loose aggregations of material in which the eggs are laid. One special type of plant-nest builder uses a kidney secretion to glue the pieces of plant together to form a tight nest. The main examples of this type of nesting are the [[stickleback]]s in which the male builds a tube which is usually attached to rooted plants or is placed in a small pit. By means of a complicated courtship ritual, a female is enticed into a nest, where she deposits some eggs after being nudged by the male. After the eggs are laid, he chases the female out and fertilizes them. This process is repeated several times, until enough embryos are in the nest and the male begins to incubate them by fanning currents of water across them. After the embryos hatch, the male guards the young for several days, first in the nest, and then in a shoal outside the nest."<ref name="Moyle&Cech" />{{Rp|146}} |
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"Perhaps the most common type of nests among fishes are those in caves, cavities, or burrows. These nests are characteristic of fish that live in active habitats, such as rocky intertidal zone or streams. For stream-dwelling fishes, the typical cave nest is the underside of a flat rock in midstream, which has plenty of current to keep the water well oxygenated. [[Sculpin]]s and many [[darter]]s deposit their eggs in clusters on the roofs of such shelters and then guard the embryos until they hatch. In quieter water, minnows, such as the [[fathead minnow]], lay their eggs on the underside of a log or a board in an area that has been cleaned off by the male. Spawning males develop a thick horny pad on their head, which is used for rubbing algae and other materials of the spawning surface. Many large [[catfish]]es lay their eggs in cavities ranging from hollow logs to old muskrat burrows to oil drums, where the embryoes are guarded by the males. These catfish also guard schools of young for one or more weeks after they emerge from the nest."<ref name="Moyle&Cech" />{{Rp|146}} |
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<gallery> |
<gallery> |
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File:Spawn hatched fish 1.JPG|Baby [[paradise fish]] just hatched, gathered under the surface of a [[bubble nest]] |
File:Spawn hatched fish 1.JPG|Baby [[paradise fish]] just hatched, gathered under the surface of a [[bubble nest]] |
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File:Anemone Fish protecting |
File:Anemone Fish protecting its spawn.jpg|[[Anemone fish]] nest in an [[anemone]]. Here a male is protecting spawn produced by his partner. |
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</gallery> |
</gallery> |
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* Transfer brooders |
* Transfer brooders |
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* Auxiliary brooders |
* Auxiliary brooders |
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* Gill-chamber brooders |
* Gill-chamber brooders |
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* Pouch brooders |
* Pouch brooders |
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[[File:Hippocampus.jpg|thumb|center|Male [[seahorse]] |
[[File:Hippocampus.jpg|thumb|center|Male [[seahorse]]s are pouch brooders]] |
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[[File:Cyphotilapia frontosa mouthbrooding.jpg|thumb|center |
[[File:Cyphotilapia frontosa mouthbrooding.jpg|thumb|center|A female cichlid mouthbrooding fry which can be seen looking out her mouth{{external media |
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|video1=[ |
|video1=[https://www.youtube.com/watch?v=9KsWGj_0k7s Mouthbrooding tilapia] — ''YouTube'' |
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|video2=[ |
|video2=[https://www.youtube.com/watch?v=X9z5tXl0SCk Mouthbrooding cichlid] — ''YouTube'' |
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====External bearers==== |
====External bearers==== |
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[[Mouthbrooder|Mouth brooders]] - carry eggs or larvae in their mouth. Mouth brooders can be [[ovophile]]s or larvophiles. Ovophile or egg-loving mouth-brooders lay their eggs in a pit, which are sucked up into the mouth of the female. The small number of large eggs hatch in the mother's mouth, and the fry remain there for a period of time. Fertilization often occurs with the help of egg-spots, which are colorful spots on the anal fin of the male. When the female sees these spots, she tries to pick up the egg-spots, but instead gets sperm that fertilizes the eggs in her mouth. Many cichlids and some labyrinth fish are ovophile mouthbrooders. Larvophile or larvae-loving mouth-brooders lay their eggs on a substrate and guard them until the eggs hatch. After hatching, the female picks up the fry and keeps them in her mouth. When the fry can fend for themselves, they are released. Some [[eartheater]]s are larvophile mouthbrooders. |
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"Fishes that carry their embryos externally have developed a wide variety of ways for doing so, ranging from the short-term attachment of embryos to the adult until a suitable place is found to put them (''transfer brooders'') to the carrying of embryos and young in special pouches. Good examples of various kinds of bearers can be found amongst [[pipefish]]es and [[seahorse]]s. In this family, only the males do the brooding. After the eggs are fertilized, the female places the embryos on the male. Herald (1950) notes a continuum of forms in the [[Syngnathidae]], starting with skin-brooding pipefishes and ending with seahorses, which have closed pouches with only one opening. In seahorses, after an extended courtship period, the female deposits eggs in the pouch ([[Brood pouch (Syngnathidae)|marsupium]]) of the male by means of a penis-like [[oviduct]]. The eggs are fertilized as they enter the marsupium, and 25 to 100 embryos are provided with nutrients, oxygen and protection (Jones and Avise 1997). After hatching, the free embryos are carried in the pouch until they are capable of fairly active swimming, at which time they are expelled by the brooding male."<ref name="Moyle&Cech" />{{Rp|146–147}} |
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"Another method of internally carrying young that are spawned externally occurs in ''mouth brooders''. This method is found in families as diverse as [[Ariidae|sea catfishes]], [[cichlid]]s, [[cardinal fish]]es and [[bonytongue]]s. Mouthbrooders carry the large, yolky embryos until they hatch, and these brooders typically carry the free embryos about as well. Even after the young become active, they are usually closely associated with the parent fish for a period of time and may flee back into the mouth cavity when threatened. In cichlids, both sexes may participate in some species, but the female usually carries the embryos, which she picks up quickly after spawning."<ref name="Moyle&Cech" />{{Rp|147}} |
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[[Mouthbrooder|Mouth brooders]] - carry eggs or larvae in their mouth. Mouth brooders can be [[ovophile]]s or larvophiles. Ovophile or egg-loving mouth-brooders lay their eggs in a pit, which are sucked up into the mouth of the female. The small number of large eggs hatch in the mother's mouth, and the fry remain there for a period of time. Fertilization often occurs with the help of egg-spots, which are colorful spots on the anal fin of the male. When the female sees these spots, she tries to pick up the egg-spots, but instead gets a mouthful of sperm, fertilizing the eggs in her mouth. Many cichlids and some labyrinth fish are ovophile mouthbrooders. Larvophile or larvae-loving mouth-brooders lay their eggs on a substrate and guard them until the eggs hatch. After hatching, the female picks up the fry and keeps them in her mouth. When the fry can fend for themselves, they are released. Some [[eartheater]]s are larvophile mouthbrooders. |
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====Internal bearers==== |
====Internal bearers==== |
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"Internal bearers may have similarities to pouch brooders, although fertilization is internal and females always carry the embryos and/or young. Internal bearers typically produce only a small number of large, active young, which is a strategy characteristic of all [[sharks]] and [[Batoidea|rays]] and a few [[bony fish]]. There seems to be no strong correlation between internal bearing families and the elaborateness of courtship behaviour. In guppies, [[mosquitofish]] and other livebearing [[poeciliid]]s. the most important trait of the courtship behaviour of males that successfully copulate with females seems to be persistence (although subtle interactions among competing males and other courtship-related behaviour do exist). In contrast, some [[surfperch]]es have fairly elaborate courtship behaviour, with males establishing breeding territories to attract passing females."<ref name="Moyle&Cech" />{{Rp|147}} |
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=====Facultative internal bearers===== |
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'''Facultative internal bearers''': The beginning of the evolutionary process of livebearing starts with ''[[facultative]]'' (optional) internal bearing. The process occurs in several species of [[oviparous]] (egg-laying) [[killifish]]es which spawn in the normal way on the substrate, but in the process accidentally fertilize eggs which the female retains and does not spawn. These eggs are spawned later, usually without allowing much time for embryonic development.<ref name="Moyle&Cech" />{{Rp|147}} |
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The beginning of the evolutionary process of livebearing starts with ''[[:Wiktionary:facultative|facultative]]'' (optional) internal bearing. The process occurs in several species of [[oviparous]] (egg-laying) [[killifish]]es which spawn in the normal way on the substrate, but in the process accidentally fertilize eggs that the female retains and does not spawn. These eggs are spawned later, usually without allowing much time for embryonic development.<ref name="Moyle&Cech" />{{Rp|147}} |
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* Facultative internal bearers |
* Facultative internal bearers |
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* Obligate internal bearers |
* Obligate internal bearers |
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* Livebearers |
* Livebearers |
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[[File:Pregnant guppy.JPG|thumb| |
[[File:Pregnant guppy.JPG|thumb|220px|[[Guppy|Guppies]] are [[livebearers]]. This one has been pregnant for about 26 days.]] |
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=====Obligate internal bearers===== |
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'''Obligate internal bearers''': The next step in the evolution of livebearing is ''[[obligate]]'' (by necessity) internal bearing, where the female retains all the embryos. "The only source of nutrition for these embryos, however, is the egg yolk, as in externally spawned eggs. This situation, also referred to as [[ovoviviparity]], is characteristic of [[Scorpaenidae|marine rock fishes]] and the Lake Baikal [[sculpin]]s. This strategy allows these fish to have fecundities approaching those of pelagic fish with external fertilization, but it also enables them to protect the young during their most vulnerable stage of development. By contrast, sharks and rays using this strategy produce a relatively small number of embryos and retain them for a few weeks to 16 months or longer. The shorter times spans are characteristic of species that eventually deposit their embryos in the environment, surrounded by a horny capsule; whereas the longer periods are characteristic of sharks that retain the embryos until they are ready to emerge as actively swimming young."<ref name="Moyle&Cech" />{{Rp|147}}<ref>{{cite journal | author = Wourms JP | year = 1981 | title = Viviparity: The Maternal-Fetal Relationship in Fishes | url = http://icb.oxfordjournals.org/content/21/2/473.abstract | journal = Integrative and Comparative Biology | volume = 21 | issue = 2| pages = 473–515 | doi = 10.1093/icb/21.2.473 }}</ref> |
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The next step in the evolution of livebearing is ''[[obligate]]'' (by necessity) internal bearing, where the female retains all the embryos. "The only source of nutrition for these embryos, however, is the egg yolk, as in externally spawned eggs. This situation, also referred to as [[ovoviviparity]], is characteristic of [[Scorpaenidae|marine rock fishes]] and the Lake Baikal [[sculpin]]s. This strategy allows these fish to have fecundities approaching those of pelagic fish with external fertilization, but it also enables them to protect the young during their most vulnerable stage of development. By contrast, sharks and rays using this strategy produce a relatively small number of embryos and retain them for a few weeks to 16 months or longer. The shorter times spans are characteristic of species that eventually deposit their embryos in the environment, surrounded by a horny capsule; whereas the longer periods are characteristic of sharks that retain the embryos until they are ready to emerge as actively swimming young."<ref name="Moyle&Cech" />{{Rp|147}}<ref>{{cite journal | author = Wourms JP | year = 1981 | title = Viviparity: The Maternal-Fetal Relationship in Fishes | journal = Integrative and Comparative Biology | volume = 21 | issue = 2 | pages = 473–515 | doi = 10.1093/icb/21.2.473 | doi-access = free }}</ref> |
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=====Viviparous fish===== |
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'''Viviparous fish''': "Given the advantages of retaining the embryos internally, it is not surprising that a number of fishes have developed means to provide additional nutrition for their young while the female is carrying them and then give birth to large, active young (''viviparity''). [[Viviparous]] fishes provide nutrition for their young in various ways. The greatest variety occurs in sharks, but the [[teleost]]s also show a considerable range of methods. In the superperches, the young develop in the mother's ovary and obtain nutrients through the close contact of the extra-large fins with the ovarian wall. Many [[poeciliid]] embryos have highly vascular pericardial tissue that loops around the neck and is in close contact with the ovarian wall of the mother, through which nutrients are exchanged."<ref name="Moyle&Cech" />{{Rp|148}} |
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However, some fish do not fit these categories. The livebearing largespring [[gambusia]] (''Gambusia geiseri'') was thought to be [[ovoviviparous]] until it was shown in 2001 that the embryos received nutrients from the mother.<ref>Marsh-Matthews E, Skierkowski P and DeMarais A (2001) [ |
However, some fish do not fit these categories. The livebearing largespring [[gambusia]] (''Gambusia geiseri'') was thought to be [[ovoviviparous]] until it was shown in 2001 that the embryos received nutrients from the mother.<ref>Marsh-Matthews E, Skierkowski P and DeMarais A (2001) [https://www.jstor.org/pss/1448091 "Direct Evidence for Mother-to-Embryo Transfer of Nutrients in the Livebearing Fish Gambusia geiseri"] ''Copeia'', '''2001''': 1(1-6).</ref> |
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==Spawning grounds== |
==Spawning grounds== |
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[[File:Mallotus villosus.gif||thumb|right|Capelin migrate huge distances to their spawning grounds]] |
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[[File:Capelin-iceland.svg|thumb|right|Migration of Icelandic [[capelin]]]] |
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{{see also|Spawning bed}} |
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| caption1 = Capelin migrate huge distances to their spawning grounds |
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| caption2 = Migration of [[capelin]] around Iceland. Capelin on the way to feeding grounds is green, capelin on the way back is blue, the breeding grounds are red. |
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{{See also|Spawning bed|Salmon run}} |
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Spawning grounds are the areas of water where aquatic animals spawn, or produce their eggs. After spawning, the spawn may or may not drift to new grounds which become their nursery grounds. Many species undertake [[Fish migration|migrations]] each year, and sometimes great migrations, to reach their spawning grounds. For example, lakes and river watersheds can be major spawning grounds for [[anadromous]] fish such as [[salmon]]. These days, it is often necessary to construct [[fish ladder]]s and other bypass systems so salmon can navigate their way past hydroelectric dams on their way to spawning grounds.<ref>Office Of Technology Assessment Washington DC (1995) [ |
Spawning grounds are the areas of water where aquatic animals spawn, or produce their eggs. After spawning, the spawn may or may not drift to new grounds which become their nursery grounds. Many species undertake [[Fish migration|migrations]] each year, and sometimes great migrations, to reach their spawning grounds. For example, lakes and river watersheds can be major spawning grounds for [[anadromous]] fish such as [[salmon]]. These days, it is often necessary to construct [[fish ladder]]s and other bypass systems so salmon can navigate their way past hydroelectric dams or other obstructions such as weirs on their way to spawning grounds.<ref>Office Of Technology Assessment Washington DC (1995) [https://books.google.com/books?id=ctBsJJ0oKHEC&dq=%22Fish+passage+technologies%22&pg=PA9 ''Fish passage technologies : protection at hydropower facilities''] Diana Publishing, {{ISBN|1-4289-2016-1}}.</ref><ref>[http://www.nwp.usace.army.mil/pa/docs/pubs/salmon.pdf ''To Save the Salmon''] {{webarchive|url=https://web.archive.org/web/20110518112904/https://www.nwp.usace.army.mil/pa/docs/pubs/salmon.pdf |date=2011-05-18 }} (1997) US Army Corps of Engineers.</ref> [[Coastal fish]] often use [[mangrove]]s and [[estuaries]] as spawning grounds, while [[reef fish]] can find adjacent [[seagrass meadow]]s that make good spawning grounds. [[Short-finned eel]]s can travel anything up to three or four thousand kilometres to their spawning ground in deep water somewhere in the [[Coral Sea]]. |
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[[Forage fish]] often make great migrations between their spawning, feeding and nursery grounds. Schools of a particular stock usually travel in a triangle between these grounds. For example, one stock of herrings have their spawning ground in southern [[Norway]], their feeding ground in [[Iceland]], and their nursery ground in northern Norway. Wide triangular journeys such as these may be important because forage fish, when feeding, cannot distinguish their own offspring.<ref>{{cite journal | |
[[Forage fish]] often make great migrations between their spawning, feeding and nursery grounds. Schools of a particular stock usually travel in a triangle between these grounds. For example, one stock of herrings have their spawning ground in southern [[Norway]], their feeding ground in [[Iceland]], and their nursery ground in northern Norway. Wide triangular journeys such as these may be important because forage fish, when feeding, cannot distinguish their own offspring.<ref>{{cite journal | vauthors = Dragesund O, Johannessen A, Ulltang Ø | year = 1997 | title = Variation in migration and abundance of Norwegian spring spawning herring ''(Clupea harengus L.)'' | url = http://www.vliz.be/imisdocs/publications/31859.pdf | journal = Sarsia | volume = 82 | issue = 2| pages = 97–105 | url-status = live | archive-url = https://web.archive.org/web/20110928101719/http://www.vliz.be/imisdocs/publications/31859.pdf | archive-date = 2011-09-28 | doi = 10.1080/00364827.1997.10413643 }}</ref> |
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[[Capelin]] are a forage fish of the [[Smelt (fish)|smelt]] family found in the [[Atlantic Ocean|Atlantic]] and [[Arctic Ocean|Arctic]] oceans. In summer, they graze on dense swarms of [[plankton]] at the edge of the ice shelf. Larger capelin also eat [[krill]] and other [[crustacean]]s. The capelin move inshore in large schools to spawn and migrate in spring and summer to feed in plankton rich areas between [[Iceland]], [[Greenland]], and [[Jan Mayen]]. The migration is affected by [[ocean current]]s. Around Iceland maturing capelin make large northward feeding migrations in spring and summer. The return migration takes place in September to November. The spawning migration starts north of Iceland in December or January.<ref name="Vilhjalmsson">Vilhjalmsson H |
[[Capelin]] are a forage fish of the [[Smelt (fish)|smelt]] family found in the [[Atlantic Ocean|Atlantic]] and [[Arctic Ocean|Arctic]] oceans. In summer, they graze on dense swarms of [[plankton]] at the edge of the ice shelf. Larger capelin also eat [[krill]] and other [[crustacean]]s. The capelin move inshore in large schools to spawn and migrate in spring and summer to feed in plankton rich areas between [[Iceland]], [[Greenland]], and [[Jan Mayen]]. The migration is affected by [[ocean current]]s. Around Iceland maturing capelin make large northward feeding migrations in spring and summer. The return migration takes place in September to November. The spawning migration starts north of Iceland in December or January.<ref name="Vilhjalmsson">{{cite journal | last1 = Vilhjalmsson | first1 = H | year = 2002 | title = Capelin ''(Mallotus villosus)'' in the Iceland–East Greenland–Jan Mayen ecosystem | journal = ICES Journal of Marine Science | volume = 59 | issue = 5| pages = 870–883 | doi = 10.1006/jmsc.2002.1233 | doi-access = | bibcode = 2002ICJMS..59..870V }}</ref> |
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The diagram on the right shows the main spawning grounds and [[larval]] drift routes. Capelin on the way to feeding grounds is coloured green, capelin on the way back is blue, and the breeding grounds are red.<ref name="Vilhjalmsson" /> In a paper published in 2009, researchers from Iceland recount their application of an interacting particle model to the capelin stock around Iceland, successfully predicting the spawning migration route for 2008.<ref> |
The diagram on the right shows the main spawning grounds and [[larval]] drift routes. Capelin on the way to feeding grounds is coloured green, capelin on the way back is blue, and the breeding grounds are red.<ref name="Vilhjalmsson" /> In a paper published in 2009, researchers from Iceland recount their application of an interacting particle model to the capelin stock around Iceland, successfully predicting the spawning migration route for 2008.<ref>Barbaro1 A, Einarsson B, Birnir1 B, Sigurðsson S, Valdimarsson S, Pálsson ÓK, Sveinbjörnsson S and Sigurðsson P (2009) [http://icesjms.oxfordjournals.org/cgi/content/short/66/5/826 "Modelling and simulations of the migration of pelagic fish"] {{webarchive|url=https://web.archive.org/web/20100625044642/http://icesjms.oxfordjournals.org/cgi/content/short/66/5/826 |date=2010-06-25 }} ''ICES Journal of Marine Science'', '''66'''(5):826-838.</ref> |
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Barbaro1 A, Einarsson B, Birnir1 B, Sigurðsson S, Valdimarsson S, Pálsson ÓK, Sveinbjörnsson S and Sigurðsson P (2009) [http://icesjms.oxfordjournals.org/cgi/content/short/66/5/826 "Modelling and simulations of the migration of pelagic fish"] ''Journal of Marine Science'', '''66'''(5):826-838.</ref> |
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Referred to as "the greatest [[Shoaling and schooling|shoal]] on earth", the [[sardine run]] occurs when millions of [[sardine]]s migrate from their spawning grounds south of the southern tip of Africa northward along the Eastern Cape coastline. [[Chinook salmon]] make the longest freshwater migration of any salmon, over {{convert|3000|km}} up the [[Yukon River]] to spawning grounds upstream of [[Whitehorse, Yukon|Whitehorse]], Yukon. Some [[green sea turtle]]s swim more than {{convert|2600|km}} to reach their spawning grounds. |
Referred to as "the greatest [[Shoaling and schooling|shoal]] on earth", the [[sardine run]] occurs when millions of [[sardine]]s migrate from their spawning grounds south of the southern tip of Africa northward along the Eastern Cape coastline. [[Chinook salmon]] make the longest freshwater migration of any salmon, over {{convert|3000|km}} up the [[Yukon River]] to spawning grounds upstream of [[Whitehorse, Yukon|Whitehorse]], Yukon. Some [[green sea turtle]]s swim more than {{convert|2600|km}} to reach their spawning grounds. |
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[[File:Goldfishfry.JPG|thumb|right|Within two or three days, the vulnerable goldfish eggs hatch into [[larva]]e, and rapidly develop into fry]] |
[[File:Goldfishfry.JPG|thumb|right|Within two or three days, the vulnerable goldfish eggs hatch into [[larva]]e, and rapidly develop into fry]] |
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====Goldfish==== |
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[[Goldfish]], like all [[cyprinid]]s, are egg-layers. They usually start breeding after a significant temperature change, often in spring. Males chase females, prompting them to release their eggs by bumping and nudging them. As the female goldfish spawns her eggs, the male goldfish stays close behind fertilizing them. Their eggs are adhesive and attach to aquatic vegetation. The eggs hatch within 48 to 72 hours. Within a week or so, the fry begins to assume its final shape, although a year may pass before they develop a mature goldfish colour; until then they are a metallic brown like their wild ancestors. In their first weeks of life, the fry grow quickly—an adaptation born of the high risk of getting devoured by the adult goldfish. |
[[Goldfish]], like all [[cyprinid]]s, are egg-layers. They usually start breeding after a significant temperature change, often in spring. Males chase females, prompting them to release their eggs by bumping and nudging them. As the female goldfish spawns her eggs, the male goldfish stays close behind fertilizing them. Their eggs are adhesive and attach to aquatic vegetation. The eggs hatch within 48 to 72 hours. Within a week or so, the fry begins to assume its final shape, although a year may pass before they develop a mature goldfish colour; until then they are a metallic brown like their wild ancestors. In their first weeks of life, the fry grow quickly—an adaptation born of the high risk of getting devoured by the adult goldfish. |
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====Carp==== |
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[[Carp]] typically spawn in the spring and summer, depending on the climate and conditions. Oxygen levels of the water, availability of food, size of each fish, age, number of times the fish has spawned before and water temperature are all factors known to effect when and how many eggs each carp will spawn at any one time.<ref>http://www.carp.me.uk {{webarchive|url=https://web.archive.org/web/20110321205019/http://www.carp.me.uk/ |date=2011-03-21 }} Carp Spawning Information</ref> |
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====Siamese fighting fish==== |
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Prior to spawning, male [[Siamese fighting fish]] build [[bubble nest]]s of varying sizes at the surface of the water. When a male becomes interested in a female, he will flare his gills, twist his body, and spread his fins. The female darkens in colour and curves her body back and forth. The act of spawning takes place in a "nuptial embrace" where the male wraps his body around the female, each embrace resulting in the release of |
Prior to spawning, male [[Siamese fighting fish]] build [[bubble nest]]s of varying sizes at the surface of the water. When a male becomes interested in a female, he will flare his gills, twist his body, and spread his fins. The female darkens in colour and curves her body back and forth. The act of spawning takes place in a "nuptial embrace" where the male wraps his body around the female, each embrace resulting in the release of 10–40 eggs until the female is out of eggs. The male, from his side, releases [[milt]] into the water and fertilization takes place externally. During and after spawning, the male uses his mouth to retrieve sinking eggs and deposit them in the bubble nest (during mating the female sometimes assists her partner, but more often she will simply devour all the eggs that she manages to catch). Once the female has released all of her eggs, she is chased away from the male's territory, as it is likely that she'll eat the eggs due to hunger.<ref>Leong, Paul (2004). {{cite web|url=http://www.cbsbettas.org/doc/articles/Tips_on_Spawning_Bettas.htm |title=Tips on Spawning Bettas |access-date=2009-03-13 |url-status=dead |archive-url=https://web.archive.org/web/20090302133251/http://www.cbsbettas.org/doc/articles/Tips_on_Spawning_Bettas.htm |archive-date=2009-03-02 }}. Retrieved on March 13, 2009.</ref> The eggs then remain in the male's care. He keeps them in the bubble nest, making sure none fall to the bottom and repairing the nest as needed. Incubation lasts for 24–36 hours, and the newly hatched larvae remain in the nest for the next 2–3 days, until their yolk sacs are fully absorbed. Afterwards the fry leave the nest and the free-swimming stage begins.<ref>Rainwate FL and Miller EJ (1967) [http://digital.library.okstate.edu/oas/oas_pdf/v47/p98_114.pdf "Courtship and reproductive behavior of the Siamese fighting fish, ''Betta splendens'' Regan"] {{webarchive|url=https://web.archive.org/web/20130513081057/http://digital.library.okstate.edu/oas/oas_pdf/v47/p98_114.pdf |date=2013-05-13 }} ''Proceedings of the Oklahoma Academy of Science'', Oklahoma State University.</ref> |
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File:Building-mah-bubblenest-19.jpg|[[Siamese fighting fish]] build [[bubble nest]]s of varying sizes. |
File:Building-mah-bubblenest-19.jpg|[[Siamese fighting fish]] build [[bubble nest]]s of varying sizes. |
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File:Betta spawning.jpg|A pair of Siamese fighting fish spawning under their bubble nest. |
File:Betta spawning.jpg|A pair of Siamese fighting fish spawning under their bubble nest. |
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File:Betta fry in bubble nest.jpg|One |
File:Betta fry in bubble nest.jpg|One-day-old Siamese fighting fish larvae in a bubble nest - their yolk sacs have not yet been absorbed |
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File:Betta fry.jpg|A 15-day |
File:Betta fry.jpg|A 15-day-old free-swimming fry of a Siamese fighting fish |
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===Crustaceans=== |
===Crustaceans=== |
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{{See also|Crustacean larvae}} |
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[[File:copepodkils.jpg|thumb|right| |
[[File:copepodkils.jpg|thumb|right|{{center|[[Copepod]]}}]] |
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[[File:California spiny lobster.JPG|thumb|right| |
[[File:California spiny lobster.JPG|thumb|right|{{center|[[California spiny lobster]]}} |
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|video1=[http://www.red3d.com/cwr/boids/ Lobster migration train]<br /><small>(from [[The Trials of Life]])</small> |
|video1=[http://www.red3d.com/cwr/boids/ Lobster migration train]<br /><small>(from [[The Trials of Life]])</small> |
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====Copepods==== |
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[[Copepod]]s are tiny [[crustacean]]s which usually reproduce either by ''broadcast spawning'' or by ''sac spawning''. Broadcasting copepods scatter their eggs into the water, but sac spawners lay their eggs into an ovigerous sac. Sac spawners spawn few but relatively large eggs that develop slowly. By contrast, broadcast spawners spawn numerous small eggs that develop rapidly.<ref>Miller CB (2004) [ |
[[Copepod]]s are tiny [[crustacean]]s which usually reproduce either by ''broadcast spawning'' or by ''sac spawning''. Broadcasting copepods scatter their eggs into the water, but sac spawners lay their eggs into an ovigerous sac. Sac spawners spawn few but relatively large eggs that develop slowly. By contrast, broadcast spawners spawn numerous small eggs that develop rapidly.<ref>Miller CB (2004) [https://books.google.com/books?id=7etkpSJuWoMC&pg=PA160&dq=%22sac+spawner%22|%22sac+spawners%22&hl=en&ei=0MNVTebJNYa3cOXGiIQN&sa=X&oi=book_result&ct=result&resnum=10&ved=0CFUQ6AEwCQ#v=onepage&q=%22sac%20spawner%22|%22sac%20spawners%22&f=false ''Biological oceanography''] Wiley-Blackwell, {{ISBN|0-632-05536-7}}.</ref> However, the shorter hatch times that result from broadcasting are not short enough to compensate for the higher mortality compared to sac spawners. To produce a given number of hatched eggs, broadcasters must spawn more eggs than sac spawners.<ref>{{cite journal |vauthors=Kiorboe T, Sabatini M | year = 1995 | title = Scaling of fecundity, growth and development in marine planktonic copepods | journal = Mar. Ecol. Prog. Ser. | volume = 120 | pages = 285–298 | doi = 10.3354/meps120285 | bibcode = 1995MEPS..120..285K | doi-access = free }}</ref> |
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====Spiny lobsters==== |
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After mating, the fertilized eggs of the [[California spiny lobster]] are carried on the female's [[pleopod]]s until they hatch, with between 120,000 and 680,000 carried by a single female.<ref name="Cascorbi">{{cite web |url=http://www.montereybayaquarium.org/cr/cr_seafoodwatch/content/media/MBA_SeafoodWatch_CaliforniaSpinyLobsterReport.pdf |
After mating, the fertilized eggs of the [[California spiny lobster]] are carried on the female's [[pleopod]]s until they hatch, with between 120,000 and 680,000 carried by a single female.<ref name="Cascorbi">{{cite web |url=http://www.montereybayaquarium.org/cr/cr_seafoodwatch/content/media/MBA_SeafoodWatch_CaliforniaSpinyLobsterReport.pdf |publisher=[[Monterey Bay Aquarium]] |date=February 10, 2004 |title=Seafood Watch Seafood Report. Spiny Lobsters, Vol. II. California Spiny Lobster ''Panulirus interruptus'' |author=Alice Cascorbi |url-status=dead |archive-url=https://web.archive.org/web/20100706013902/http://www.montereybayaquarium.org/cr/cr_seafoodwatch/content/media/MBA_SeafoodWatch_CaliforniaSpinyLobsterReport.pdf |archive-date=July 6, 2010 }}</ref> The eggs begin coral red, but darken as they develop to a deep maroon.<ref name="Shaw">{{Cite journal |author=William N. Shaw |year=1986 |title=Species profiles: life histories and environmental requirements of coastal fishes and invertebrates (Pacific Southwest) – spiny lobster |journal=U. S. Fish and Wildlife Service Biological Reports |volume=82 |issue=11.47 |publisher=[[U.S. Army Corps of Engineers]] |pages=TR EL–82–4. 10 pp |url=http://www.nwrc.usgs.gov/wdb/pub/species_profiles/82_11-047.pdf |url-status=live |archive-url=https://web.archive.org/web/20070713212545/http://www.nwrc.usgs.gov/wdb/pub/species_profiles/82_11-047.pdf |archive-date=2007-07-13 }}</ref> When she is carrying the eggs, the female is said to be "berried". The eggs are ready to hatch after 10 weeks,<ref name="Cascorbi" /> and spawning takes place from May to August.<ref name="MLW">{{cite book |chapter-url=http://nlbif.eti.uva.nl/bis/lobsters.php?menuentry=soorten&id=209 |chapter=''Panulirus interruptus'' |title=FAO Species Catalogue, Volume 13. Marine Lobsters of the World |author=Lipke B. Holthuis |publisher=[[Food and Agriculture Organization]] |year=1991 |isbn=978-92-5-103027-1 |series=FAO Fisheries Synopsis No. 125 |url-status=dead |archive-url=https://web.archive.org/web/20110607223948/http://nlbif.eti.uva.nl/bis/lobsters.php?menuentry=soorten&id=209 |archive-date=2011-06-07 |author-link=Lipke Holthuis }}</ref> The [[larva]]e that hatch (called ''[[phyllosoma]]'' larvae) do not resemble the adults. Instead, they are flat, [[transparency and translucency|transparent]] animals around {{cvt|14|mm}} long, but as thin as a sheet of paper.<ref name="Johnson">{{cite journal |author=Martin W. Johnson |title=The offshore drift of larvae of the California spiny lobster ''Panulirus interruptus'' |journal=California Co-operative Oceanic Fisheries Investigations |year=1960 |volume=7 |pages=147–161 |url=http://calcofi.ucsd.edu/newhome/publications/CalCOFI_Reports/v07/pdfs/Vol_07_Johnson.pdf |url-status=dead |archive-url=https://web.archive.org/web/20110720075314/http://calcofi.ucsd.edu/newhome/publications/CalCOFI_Reports/v07/pdfs/Vol_07_Johnson.pdf |archive-date=2011-07-20 |author-link=Martin W. Johnson }}</ref> The larvae feed on [[plankton]],<ref name="Shaw" /> and grow through ten [[ecdysis|molts]] into ten further larval stages, the last of which is around {{cvt|30|-|32|mm}} long.<ref name="Johnson" /> The full series of larval molts takes around 7 months, and when the last stage molts, it [[metamorphosis|metamorphoses]] into the ''puerulus'' state, which is a [[juvenile (organism)|juvenile]] form of the adult, though still transparent.<ref name="Johnson" /> The puerulus larvae settle to the sea floor when the water is near its maximum temperature, which in Baja California is in the fall.<ref>{{cite journal |doi=10.1163/156854096X00394 |title=The puerulus settlement of red spiny lobster (''Panulirus interruptus'') in Bahía Tortugas, Baja California, Mexico |author=Sergio A. Guzmán-Del Próo, Jorge Carrillo-Laguna, Jorge Belmar-Pérez, Sara de la Campa J., Alejandro Villa B. |journal=[[Crustaceana]] |volume=69 |issue=8 |year=1996 |pages=949–957 |jstor=20105816}}</ref> |
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Egg-bearing female [[lobster]]s migrate inshore from deeper waters to hatch their eggs, though they do not have specific spawning grounds.<ref>[http://www.nmfs.noaa.gov/fishwatch/species/amer_lobster.htm American Lobster ''(Homarus americanus)''] NMFS and NOAA. Updated 5 October 2010. Retrieved 3 February 2011.</ref><ref>Fogarty MJ (1998) [ |
Egg-bearing female [[lobster]]s migrate inshore from deeper waters to hatch their eggs, though they do not have specific spawning grounds.<ref>[http://www.nmfs.noaa.gov/fishwatch/species/amer_lobster.htm American Lobster ''(Homarus americanus)''] {{webarchive|url=https://web.archive.org/web/20110104171803/http://www.nmfs.noaa.gov/fishwatch/species/amer_lobster.htm |date=2011-01-04 }} NMFS and NOAA. Updated 5 October 2010. Retrieved 3 February 2011.</ref><ref>Fogarty MJ (1998) [https://books.google.com/books?id=WnNVQKNwRsQC&dq=fogarty+%22implications+of+migration+and+larval+interchange+in+american+lobster+stocks%22&pg=PA273 "Implications of migration and larval interchange in American lobster stocks: spatial structure and resilience"] {{webarchive|url=https://web.archive.org/web/20160105142523/https://books.google.com/books?hl=en |date=2016-01-05 }} pp. 273–282 in ''Proceedings of the North Pacific Symposium on Invertebrate Stock Assessment and Management'', Issue 125, A Campbell, Eds. GS Jamieson andA Campbell, NRC Research Press, {{ISBN|0-660-17221-6}}.</ref> These lobster migrations can occur in close single-file formation "lobster trains". |
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[[File:Crassostrea gigas p1040847.jpg|thumb|right|[[Pacific oyster]]]] |
[[File:Crassostrea gigas p1040847.jpg|thumb|right|[[Pacific oyster]]]] |
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====Pacific oysters==== |
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Oysters are ''broadcast spawners'', that is, eggs and sperm are released into open water where fertilisation occurs. They are [[protandric]]; during their first year they spawn as males by releasing [[sperm]] into the water. As they grow over the next two or three years and develop greater energy reserves, they spawn as females by releasing [[egg (biology)|eggs]]. Bay oysters usually spawn by the end of June. An increase in water temperature prompts a few oysters to spawn. This triggers spawning in the rest, clouding the water with millions of eggs and sperm. A single female oyster can produce up to 100 million eggs annually. The eggs become fertilized in the water and develop rapidly into [[planktonic]] [[larva]]e. which eventually find suitable sites, such as another oyster's shell, on which to settle. Attached oyster larvae are called '''spat'''. Spat are oysters less than {{convert|25|mm|in}} long. |
Oysters are ''broadcast spawners'', that is, eggs and sperm are released into open water where fertilisation occurs. They are [[protandric]]; during their first year they spawn as males by releasing [[sperm]] into the water. As they grow over the next two or three years and develop greater energy reserves, they spawn as females by releasing [[egg (biology)|eggs]]. Bay oysters usually spawn by the end of June. An increase in water temperature prompts a few oysters to spawn. This triggers spawning in the rest, clouding the water with millions of eggs and sperm. A single female oyster can produce up to 100 million eggs annually. The eggs become fertilized in the water and develop rapidly into [[planktonic]] [[larva]]e. which eventually find suitable sites, such as another oyster's shell, on which to settle. Attached oyster larvae are called '''spat'''. Spat are oysters less than {{convert|25|mm|in}} long. |
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The [[Pacific oyster]] usually has separate sexes. Their sex can be determined by examining the [[gonad]]s, and it can change from year to year, normally during the winter months. In certain environmental conditions, one sex is favoured over the other. [[Dichogamy|Protandry]] is favoured in areas of high food abundance and protogyny occurs in areas of low food abundance. In habitats with a high food supply, the [[sex ratio]] in the adult population tends to favour females, and areas with low food abundances tend to have a larger proportion of male adults. Spawning in the Pacific oyster occurs at {{convert|20|°C}}. This species is very [[Fecundity|fecund]], with females releasing about 50–200 million eggs in regular intervals (at a rate of 5–10 times a minute) in a single spawning. Once released from the |
The [[Pacific oyster]] usually has separate sexes. Their sex can be determined by examining the [[gonad]]s, and it can change from year to year, normally during the winter months. In certain environmental conditions, one sex is favoured over the other. [[Dichogamy|Protandry]] is favoured in areas of high food abundance and protogyny occurs in areas of low food abundance. In habitats with a high food supply, the [[sex ratio]] in the adult population tends to favour females, and areas with low food abundances tend to have a larger proportion of male adults. Spawning in the Pacific oyster occurs at {{convert|20|°C}}. This species is very [[Fecundity|fecund]], with females releasing about 50–200 million eggs in regular intervals (at a rate of 5–10 times a minute) in a single spawning. Once released from the gonads, the eggs move through the suprabranchial chambers ([[gill]]s), are then pushed through the gill ostia into the mantle chamber, and are finally released in the water, forming a small cloud. In males, the sperm is released at the opposite end of the oyster, along with the normal exhalent stream of water.<ref name="quayle">Quayle, D.B (1969). ''Pacific oyster culture in British Columbia'', p. 23. First Edition. Ottawa: The Queen’s Printer.</ref> A rise in water temperature is thought to be the main cue in the initiation of spawning, as the onset of higher water temperatures in the summer results in earlier spawning in the Pacific oyster.<ref name="grangere">{{cite journal | last1 = Grangeré | first1 = K. |display-authors=etal | year = 2009 | title = Modelling the influence of environmental factors on the physiological status of the Pacific oyster Crassostrea gigas in an estuarine embayment; The Baie des Veys (France) | url = https://archimer.ifremer.fr/doc/2009/publication-6809.pdf| journal = Journal of Sea Research | volume = 62 | issue = 2–3| pages = 147–158 | doi=10.1016/j.seares.2009.02.002| bibcode = 2009JSR....62..147G }}</ref> |
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The |
The larvae of the Pacific oyster are [[Marine larval ecology|planktotrophic]], and are about 70 μm at the [[Apex (mollusc)|prodissoconch]] 1 stage. The larvae move through the water column via the use of a larval foot to find suitable settlement locations. They can spend several weeks at this phase, which is dependent on water temperature, salinity and food supply. Over these weeks, larvae can disperse great distances by water currents before they [[Metamorphosis|metamorphose]] and settle as small spat. Similar to other oyster species, once the Pacific oyster larvae find a suitable habitat, they attach to it permanently using cement secreted from a gland in their foot. After settlement, the larvae metamorphose into juvenile spat. The growth rate is very rapid in optimum environmental conditions, and market size can be achieved in 18 to 30 months.<ref name="FAO">[http://www.fao.org/fishery/culturedspecies/Crassostrea_gigas/en Pacific Oyster factsheet] {{webarchive|url=https://web.archive.org/web/20120513033820/http://www.fao.org/fishery/culturedspecies/Crassostrea_gigas/en |date=2012-05-13 }}, Food and Agriculture Organization of the United Nations (FAO)</ref> |
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[[File:SquidEggCases-MontereryAquarium-April2-07.png|thumb|right|Egg cases laid by a female squid |
[[File:SquidEggCases-MontereryAquarium-April2-07.png|thumb|right|Egg cases laid by a female squid |
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[[File:Squidu.jpg|thumb|right|A juvenile squid]] |
[[File:Squidu.jpg|thumb|right|A juvenile squid]] |
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====Cephalopods==== |
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[[Cephalopod]]s, such as squid and octopuses, have prominent heads and a set of arms ([[tentacle]]s) modified from the primitive foot of molluscs. All cephalopods are [[sexual dimorphism|sexually dimorphic]]. However, they lack external sexual characteristics, so they use colour communication. A courting male approaches a likely looking mate flashing his brightest colours, often in rippling displays. If the other cephalopod is female and receptive, her skin will change colour to become pale, and mating will occur. If the other cephalopod remains brightly coloured, it is taken as a warning.<ref name=Branch1981>{{cite book|author=Branch George, Branch, Margo and Bannister, Anthony |year= |
[[Cephalopod]]s, such as squid and octopuses, have prominent heads and a set of arms ([[tentacle]]s) modified from the primitive foot of molluscs. All cephalopods are [[sexual dimorphism|sexually dimorphic]]. However, they lack external sexual characteristics, so they use colour communication. A courting male approaches a likely looking mate flashing his brightest colours, often in rippling displays. If the other cephalopod is female and receptive, her skin will change colour to become pale, and mating will occur. If the other cephalopod remains brightly coloured, it is taken as a warning.<ref name="Branch1981">{{cite book|author=Branch George, Branch, Margo and Bannister, Anthony |year=1981 |title=''The Living Shores of Southern Africa''|isbn=978-0-86977-115-0|publisher=C. Struik|location=Cape Town}}</ref> |
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All cephalopods reproduce by spawning [[egg (biology)|egg]]s. Most cephalopods use semi-internal fertilization where the male places his gametes inside the female's [[mantle cavity]] to fertilize the [[Ovum|ova]] in the female's single [[ovary]].<ref>[http://www.weichtiere.at/Mollusks/Kopffuesser/haupt.html Cephalopods.] The Living World of Molluscs. Robert Nordsieck.</ref> The "penis" in most male cephalopods is a long and muscular end of the gonoduct used to transfer spermatophores to a modified sperm-carrying arm called a [[hectocotylus]]. That in turn is used to transfer the spermatophores to the female. In species where the hectocotylus is missing, the "penis" is long and able to extend beyond the mantle cavity and transfers the spermatophores directly to the female. In many cephalopods, mating occurs head |
All cephalopods reproduce by spawning [[egg (biology)|egg]]s. Most cephalopods use semi-internal fertilization where the male places his gametes inside the female's [[mantle cavity]] to fertilize the [[Ovum|ova]] in the female's single [[ovary]].<ref>[http://www.weichtiere.at/Mollusks/Kopffuesser/haupt.html Cephalopods.] {{webarchive|url=https://web.archive.org/web/20071020065950/http://www.weichtiere.at/Mollusks/Kopffuesser/haupt.html |date=2007-10-20 }} The Living World of Molluscs. Robert Nordsieck.</ref> The "penis" in most male cephalopods is a long and muscular end of the gonoduct used to transfer spermatophores to a modified sperm-carrying arm called a [[hectocotylus]]. That in turn is used to transfer the spermatophores to the female. In species where the hectocotylus is missing, the "penis" is long and able to extend beyond the mantle cavity and transfers the spermatophores directly to the female. In many cephalopods, mating occurs head-to-head and the male may simply transfer sperm to the female. Others may detach the sperm-carrying arm and leave it attached to the female. Deep water squid have the greatest known penis length relative to body size of all mobile animals, second in the entire animal kingdom only to certain sessile [[barnacle]]s. Penis elongation in the [[greater hooked squid]] may result in a penis that is as long as the mantle, head and arms combined.<ref name="penis">{{cite journal | last1 = Arkhipkin | first1 = A.I. | last2 = Laptikhovsky | first2 = V.V. | year = 2010 | title = Observation of penis elongation in ''Onykia ingens'': implications for spermatophore transfer in deep-water squid | journal = Journal of Molluscan Studies | volume = 76| issue = 3| pages = 299–300| doi = 10.1093/mollus/eyq019 | doi-access = free }}</ref><ref name="supersquid">Walker, M. 2010. [http://news.bbc.co.uk/earth/hi/earth_news/newsid_8792000/8792008.stm Super squid sex organ discovered] {{webarchive|url=https://web.archive.org/web/20100707185137/http://news.bbc.co.uk/earth/hi/earth_news/newsid_8792000/8792008.stm |date=2010-07-07 }}. ''BBC Earth News'', July 7, 2010.</ref> |
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[[File:Onykia ingens with erect penis.jpg|thumb|left|A [[ |
[[File:Onykia ingens with erect penis.jpg|thumb|left|A [[greater hooked squid]] with an erect penis 67 cm long<ref name=penis /><ref name="supersquid" />]] |
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Some species brood their fertilized eggs: female [[paper nautilus]] construct shelters for the young, while Gonatiid squid carry a larva-laden membrane from the hooks on their arms.<ref name='Siebel2005'>{{ |
Some species brood their fertilized eggs: female [[paper nautilus]] construct shelters for the young, while Gonatiid squid carry a larva-laden membrane from the hooks on their arms.<ref name='Siebel2005'>{{Cite journal | first1=B. A.| last2= Robison| last3= Haddock | first2 = B. H. | first3 = S. H. |author3-link=Steven Haddock | journal = Nature | volume = 438| last1 = Seibel| title = Post-spawning egg care by a squid | issue = 7070 | pages = 929 | date=Dec 2005 | issn = 0028-0836 | pmid = 16355206 | doi = 10.1038/438929a|bibcode = 2005Natur.438..929S | doi-access = free }}</ref> Other cephalopods deposit their young under rocks and aerate them with their tentacles hatching. Mostly the eggs are left to their own devices; many squid lay sausage-like bunches of eggs in crevices or occasionally on the sea floor. [[Cuttlefish]] lay eggs separately in cases and attach them to coral or algal fronds.<ref name=Mapes2009>{{cite journal| first1 = R. H. | first2 = Alexander | last2 = Nützel | title = Late Palaeozoic mollusc reproduction: cephalopod egg-laying behavior and gastropod larval palaeobiology | last1 = Mapes | journal = Lethaia | volume = 42 | issue = 3 | pages = 341 | year = 2009 | doi = 10.1111/j.1502-3931.2008.00141.x | bibcode = 2009Letha..42..341M }}</ref> Like Pacific salmon, cephalopods are mostly [[semelparous]], spawning many small eggs in one batch and then dying. Cephalopods usually live fast and die young. Most of the energy extracted from their food is used for growing, and they mature rapidly to their adult size. Some gain as much as 12% of their body mass each day. Most live for one to two years, reproducing and then dying shortly thereafter.<ref name=Boyle>{{cite book |
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| isbn= 0-632-06048- |
| isbn= 978-0-632-06048-1 |
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| first1= Peter |last1=Boyle |
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| first2= Paul |last2=Rodhouse |
| first2= Paul |last2=Rodhouse |
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| year= 2004 |
| year= 2004 |
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| publisher= Blackwell |
| publisher= Blackwell |
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| location= Ames, Iowa |
| location= Ames, Iowa |
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| url= |
| url=https://books.google.com/books?id=4UtCi2B4VnoC |
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| doi = 10.1002/9780470995310.ch2 |
| doi = 10.1002/9780470995310.ch2 |
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| title= Cephalopods : ecology and fisheries }}</ref><ref name=Norman>Norman, M.D. (2000). ''Cephalopods: A World Guide''. ConchBooks.</ref> |
| title= Cephalopods : ecology and fisheries }}</ref><ref name=Norman>Norman, M.D. (2000). ''Cephalopods: A World Guide''. ConchBooks.</ref> |
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[[File:Sea urchin eggs.jpg|thumb|right|[[Sea urchin]]s have five [[gonad]]s. These gonads ([[roe]]) are a sought after as a delicacy. |
[[File:Sea urchin eggs.jpg|thumb|right|[[Sea urchin]]s have five [[gonad]]s. These gonads ([[roe]]) are a sought after as a delicacy. |
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[[Echinoderm]]s are marine animals, widespread in all oceans, but not found in fresh water. Just below their skin is an [[endoskeleton]] composed of [[calcareous]] plates or [[ossicle]]s. |
[[Echinoderm]]s are marine animals, widespread in all oceans, but not found in fresh water. Just below their skin is an [[endoskeleton]] composed of [[calcareous]] plates or [[ossicle]]s. |
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====Sea urchins==== |
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[[Sea urchin]]s are spiky echinoderms with spherical bodies which usually contain five [[gonad]]s. They move slowly, feed mostly on [[seaweed]], and are important for the diet of [[sea otter]]s. Sea urchins are [[dioecious]], having separate male and female sexes, although there is generally no easy way to distinguish the two. The gonads are lined with muscles underneath the [[peritoneum]], and these allow the animal to squeeze its [[gamete]]s through the duct and into the surrounding sea water, where fertilization takes place.<ref name=IZ>{{cite book |last=Barnes |first=Robert D. |year=1982 |title= Invertebrate Zoology |publisher= Holt-Saunders International |location= Philadelphia, PA|pages= 961–981|isbn= 0-03-056747- |
[[Sea urchin]]s are spiky echinoderms with spherical bodies which usually contain five [[gonad]]s. They move slowly, feed mostly on [[seaweed]], and are important for the diet of [[sea otter]]s. Sea urchins are [[dioecious]], having separate male and female sexes, although there is generally no easy way to distinguish the two. The gonads are lined with muscles underneath the [[peritoneum]], and these allow the animal to squeeze its [[gamete]]s through the duct and into the surrounding sea water, where fertilization takes place.<ref name=IZ>{{cite book |last=Barnes |first=Robert D. |year=1982 |title= Invertebrate Zoology |publisher= Holt-Saunders International |location= Philadelphia, PA|pages= 961–981|isbn= 978-0-03-056747-6}}</ref> Their [[roe]] (male and female gonads) is soft and melting, with a colour ranging from orange to pale yellow, and is sought after as a human delicacy in many parts of the world. |
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====Sea cucumbers==== |
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[[Sea cucumber]]s are leathery echinoderms with elongated bodies which contain a single, branched gonad. They are found on the sea floor worldwide, and occur in great numbers on the deep sea floor where they often make up the majority of the animal [[Biomass (ecology)|biomass]].<ref>{{cite web | url = http://jrscience.wcp.muohio.edu/fieldcourses05/PapersMarineEcologyArticles/SeaCucumbers.html | title = Sea Cucumbers | last = Miller | first = Nat | |
[[Sea cucumber]]s are leathery echinoderms with elongated bodies which contain a single, branched gonad. They are found on the sea floor worldwide, and occur in great numbers on the deep sea floor where they often make up the majority of the animal [[Biomass (ecology)|biomass]].<ref>{{cite web | url = http://jrscience.wcp.muohio.edu/fieldcourses05/PapersMarineEcologyArticles/SeaCucumbers.html | title = Sea Cucumbers | last = Miller | first = Nat | access-date = 2007-10-03 | url-status = live | archive-url = https://web.archive.org/web/20071014115420/http://jrscience.wcp.muohio.edu/fieldcourses05/PapersMarineEcologyArticles/SeaCucumbers.html | archive-date = 2007-10-14 }}</ref> They feed on [[plankton]] and decaying organic debris found at the sea bottom, catching food that flows by with their open tentacles or sifting through bottom [[sediment]]s. Like sea urchins, most sea cucumbers reproduce by releasing [[sperm]] and [[Ovum|ova]] into the ocean water. Depending on conditions, one organism can produce thousands of [[gamete]]s. |
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[[File:Espardenya (animal).jpg|thumb|left|[[Sea cucumber]]s have one gonad]] |
[[File:Espardenya (animal).jpg|thumb|left|[[Sea cucumber]]s have one gonad]] |
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Sea cucumbers are typically [[dioecious]], with separate male and female individuals. The reproductive system consists of a single [[gonad]], consisting of a cluster of tubules emptying into a single duct that opens on the upper surface of the animal, close to the tentacles.<ref name=IZ/> Many species fertilise their eggs internally. The fertilised egg develops in a pouch on the adult's body and eventually hatches as a juvenile sea cucumber.<ref>Branch GM, Griffiths CL, Branch ML and Beckley LE (2005) ''Two Oceans'' ISBN |
Sea cucumbers are typically [[dioecious]], with separate male and female individuals. The reproductive system consists of a single [[gonad]], consisting of a cluster of tubules emptying into a single duct that opens on the upper surface of the animal, close to the tentacles.<ref name=IZ/> Many species fertilise their eggs internally. The fertilised egg develops in a pouch on the adult's body and eventually hatches as a juvenile sea cucumber.<ref>Branch GM, Griffiths CL, Branch ML and Beckley LE (2005) ''Two Oceans'' {{ISBN|0-86486-672-0}}</ref> A few species brood their young inside the body cavity, giving birth through a small rupture in the body wall close to the anus. The remaining species develop their eggs into a free-swimming [[larva]], usually after about three days of development. This larva swims by means of a long band of [[cilia]] wrapped around its body. As the larva grows it transforms into a barrel-shaped body with three to five separate rings of cilia. The tentacles are usually the first adult features to appear, before the regular tube feet.<ref name=IZ/> |
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| quote = Amphibians have successfully solved most of the problems associated with exposure to air. But their reproductive system was and is linked to water, and it remains very fishlike. Almost all amphibians spawn in water and lay a great number of small eggs that hatch quickly into swimming larvae. The eggs do not need any complex protection against drying, because if the environment dries, the larvae are doomed as well as the eggs. Thus selection has acted to encourage the selection of suitable sites for laying eggs, rather than suitable devices for protecting eggs. Both fishes and amphibians may migrate long distances for spawning, and favoured sites are often disputed vigorously.| source = Richard Cowen<ref name="Cowen">Cowen, Richard (2005) [ |
| quote = Amphibians have successfully solved most of the problems associated with exposure to air. But their reproductive system was and is linked to water, and it remains very fishlike. Almost all amphibians spawn in water and lay a great number of small eggs that hatch quickly into swimming larvae. The eggs do not need any complex protection against drying, because if the environment dries, the larvae are doomed as well as the eggs. Thus selection has acted to encourage the selection of suitable sites for laying eggs, rather than suitable devices for protecting eggs. Both fishes and amphibians may migrate long distances for spawning, and favoured sites are often disputed vigorously.| source = Richard Cowen<ref name="Cowen">Cowen, Richard (2005) [https://books.google.com/books?id=Z-Tam4XuXLkC&dq=Amphibian+spawning&pg=PA117 ''History of life''] John Wiley and Sons, {{ISBN|1-4051-1756-7}}.</ref>{{Rp|117–8}} |
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[[File:RanaTemporariaAmplex.JPG|thumb|right|[[Common frog]]s sorting out their spawn]] |
[[File:RanaTemporariaAmplex.JPG|thumb|right|[[Common frog]]s sorting out their spawn]] |
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[[Amphibian]]s are found in and around fresh water lakes and ponds, but not in marine environments. Examples are frogs and toads, [[salamander]]s, [[newt]]s and [[caecilian]]s (which resemble snakes). They are cold-blooded animals that [[Metamorphosis|metamorphose]] from a juvenile water-breathing form, usually to an adult air-breathing form, though [[mudpuppies]] retain juvenile gills in adulthood. |
[[Amphibian]]s are found in and around fresh water lakes and ponds, but not in marine environments. Examples are frogs and toads, [[salamander]]s, [[newt]]s and [[caecilian]]s (which resemble snakes). They are cold-blooded animals that [[Metamorphosis|metamorphose]] from a juvenile water-breathing form, usually to an adult air-breathing form, though [[mudpuppies]] retain juvenile gills in adulthood. |
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====Frogs and toads==== |
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Female frogs and toads usually spawn gelatinous egg masses containing thousands of eggs in water. Different species lay eggs in distinctive and identifiable ways. For example, the [[American toad]] lays long strings of eggs. The eggs are highly vulnerable to [[predation]], so frogs have evolved many techniques to ensure the survival of the next generation. In colder areas the embryo is black to absorb more heat from the sun, which speeds up development. Most commonly, this involves [[synchronous reproduction]]. Many individuals will breed at the same time, overwhelming the actions of predators; the majority of the offspring will still die due to predation, but there is a greater chance some will survive. Another way in which some species avoid predators and the pathogens eggs are exposed to in ponds is to lay eggs on leaves above the pond, with a gelatinous coating designed to retain moisture. In these species the tadpoles drop into the water upon hatching. The eggs of some species laid out of water can detect vibrations of nearby predatory wasps or snakes, and will hatch early to avoid being eaten.<ref>{{cite journal| last=Warkentin| first=K.M.| year=1995| title=Adaptive plasticity in hatching age: a response to predation risk trade-offs| journal=Proceedings of the National Academy of Sciences| volume=92| pages=3507–3510| doi=10.1073/pnas.92.8.3507| pmid=| issue=8|bibcode = 1995PNAS...92.3507W }}</ref> |
Female frogs and toads usually spawn gelatinous egg masses containing thousands of eggs in water. Different species lay eggs in distinctive and identifiable ways. For example, the [[American toad]] lays long strings of eggs. The eggs are highly vulnerable to [[predation]], so frogs have evolved many techniques to ensure the survival of the next generation. In colder areas the embryo is black to absorb more heat from the sun, which speeds up development. Most commonly, this involves [[synchronous reproduction]]. Many individuals will breed at the same time, overwhelming the actions of predators; the majority of the offspring will still die due to predation, but there is a greater chance some will survive. Another way in which some species avoid predators and the pathogens eggs are exposed to in ponds is to lay eggs on leaves above the pond, with a gelatinous coating designed to retain moisture. In these species the tadpoles drop into the water upon hatching. The eggs of some species laid out of water can detect vibrations of nearby predatory wasps or snakes, and will hatch early to avoid being eaten.<ref>{{cite journal| last=Warkentin| first=K.M.| year=1995| title=Adaptive plasticity in hatching age: a response to predation risk trade-offs| journal=Proceedings of the National Academy of Sciences| volume=92| pages=3507–3510| doi=10.1073/pnas.92.8.3507| pmid=11607529| issue=8|bibcode = 1995PNAS...92.3507W | pmc=42196| doi-access=free}}</ref> |
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While the length of the egg stage depends on the species and environmental conditions, aquatic eggs generally hatch within one week. Unlike salamanders and newts, frogs and toads never become sexually mature while still in their larval stage. The hatched eggs continue life as [[tadpole]]s, which typically have oval bodies and long, vertically flattened tails. As a general rule, free living larvae are fully aquatic. They lack eyelids and have a cartilaginous skeleton, a [[lateral line system]], gills for respiration (external gills at first, internal gills later) and tails with dorsal and ventral folds of skin for swimming.<ref>{{cite web|url=http://www.britannica.com/eb/article-40603/Anura |title=Anura :: From tadpole to adult - Britannica Online Encyclopedia |publisher=Britannica.com |date= | |
While the length of the egg stage depends on the species and environmental conditions, aquatic eggs generally hatch within one week. Unlike salamanders and newts, frogs and toads never become sexually mature while still in their larval stage. The hatched eggs continue life as [[tadpole]]s, which typically have oval bodies and long, vertically flattened tails. As a general rule, free living larvae are fully aquatic. They lack eyelids and have a cartilaginous skeleton, a [[lateral line system]], gills for respiration (external gills at first, internal gills later) and tails with dorsal and ventral folds of skin for swimming.<ref>{{cite web |url=http://www.britannica.com/eb/article-40603/Anura |title=Anura :: From tadpole to adult - Britannica Online Encyclopedia |publisher=Britannica.com |access-date=2008-11-03 |url-status=live |archive-url=https://web.archive.org/web/20121102234820/http://www.britannica.com/EBchecked/topic/29023/Anura |archive-date=2012-11-02 }}</ref> They quickly develop a gill pouch that covers the gills and the front legs; the lungs are also developed at an early stage as an accessory breathing organ. Some species which go through the metamorphosis inside the egg and hatch to small frogs never develop gills; instead there are specialised areas of skin that take care of respiration. Tadpoles also lack true teeth, but the jaws in most species usually have two elongate, parallel rows of small [[keratin]]ized structures called keradonts in the upper jaw while the lower jaw has three rows of keradonts, surrounded by a [[keratin|horny]] beak, but the number of rows can be lower (sometimes zero), or much higher.<ref>{{cite web |url=http://www.answers.com/topic/larvae |title=Larvae: Information from |publisher=Answers.com |access-date=2010-03-18 |url-status=live |archive-url=https://web.archive.org/web/20100608224846/http://www.answers.com/topic/larvae |archive-date=2010-06-08 }}</ref> Tadpoles feed on [[alga]]e, including [[diatom]]s filtered from the water through the [[gill]]s. Some species are carnivorous at the tadpole stage, eating insects, smaller tadpoles, and fish. [[Cannibalism]] has been observed among tadpoles. Early developers who gain legs may be eaten by the others, so the late bloomers survive longer.<ref>[http://www.marinebiology.co.uk/frogs.htm Frogs Found in the U.K.]. Retrieved 18 July 2007. {{webarchive |url=https://web.archive.org/web/20090605043613/http://www.marinebiology.co.uk/frogs.htm |date=June 5, 2009 }}</ref> |
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====Sea turtles==== |
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[[File:Sea turtle eggs.jpg|thumb|right|[[Sea turtle]] laying eggs |
[[File:Sea turtle eggs.jpg|thumb|right|[[Sea turtle]] laying eggs |
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[[Sea turtle]]s are amphibious reptiles, but they are not [[amphibian]]s. Reptiles belong to the class [[Reptilia]] while amphibians belong to the class [[Amphibia]]. These are two distinct taxonomic groups. Reptiles have scales and leathery skins, while the skins of amphibians are smooth and porous. Unlike frogs, sea turtle eggs have tough, leathery shells which allow them to survive on land without drying out. |
[[Sea turtle]]s are amphibious reptiles, but they are not [[amphibian]]s. Reptiles belong to the class [[Reptilia]] while amphibians belong to the class [[Amphibia]]. These are two distinct taxonomic groups. Reptiles have scales and leathery skins, while the skins of amphibians are smooth and porous. Unlike frogs, sea turtle eggs have tough, leathery shells which allow them to survive on land without drying out. |
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Some sea turtles migrate long distances between feeding and spawning grounds. [[Green turtle]]s have feeding grounds along the Brazilian coast. Each year, thousands of these turtles migrate about {{convert|2300|km}} to their spawning ground, [[Ascension Island]] in the Atlantic, an island only {{convert|11|km}} across. Each year the returning turtles dig between 6,000 and 15,000 nests, often returning to the same beach from where they hatched. Females usually mate every two to four years. Males on the other hand visit the breeding areas every year, attempting to mate.<ref name="AuThreatenedSpecies">{{cite press release |
Some sea turtles migrate long distances between feeding and spawning grounds. [[Green turtle]]s have feeding grounds along the Brazilian coast. Each year, thousands of these turtles migrate about {{convert|2300|km}} to their spawning ground, [[Ascension Island]] in the Atlantic, an island only {{convert|11|km}} across. Each year the returning turtles dig between 6,000 and 15,000 nests, often returning to the same beach from where they hatched. Females usually mate every two to four years. Males on the other hand visit the breeding areas every year, attempting to mate.<ref name="AuThreatenedSpecies">{{cite press release|title=Australian Threatened Species: Green turtle (''Chelonia mydas'') |publisher=Government of Australia |year=2006 |url=http://www.environment.gov.au/biodiversity/threatened/publications/pubs/tsd06green-turtle.pdf |access-date=2007-08-15 |url-status=dead |archive-url=https://web.archive.org/web/20070911072001/http://www.environment.gov.au/biodiversity/threatened/publications/pubs/tsd06green-turtle.pdf |archive-date=2007-09-11 }}</ref> Green sea turtles' mating is similar to other marine turtles. Female turtles control the process. A few populations practice [[Polyandry in animals|polyandry]], although this does not seem to benefit hatchlings.<ref name="Lee2004">{{cite journal |last =Lee |first =Patricia L. M. |author-link =Patricia L. M. Lee |author2=Graeme C. Hays |title =Polyandry in a marine turtle: Females make the best of a bad job |journal =Proceedings of the National Academy of Sciences |volume =101 |issue =17 |pages =6530–6535 |date =2004-04-27 |doi =10.1073/pnas.0307982101 |pmid =15096623 |pmc =404079|bibcode = 2004PNAS..101.6530L |doi-access =free }}</ref> After mating in the water, the female moves above the beach's high tide line where she digs a hole with her hind flippers and deposits her eggs. Litter size depends on the age of the female and species, but green turtle clutches range between 100 and 200. She then covers the nest with sand and returns to the sea.<ref name="NGeo">{{cite web |title =Green Sea Turtle (''Chelonia mydas'') |work =National Geographic - Animals |publisher =National Geographic Society |date =2005-12-29 |url =http://www3.nationalgeographic.com/animals/reptiles/green-turtle.html |access-date =2007-02-21 |url-status =dead |archive-url =https://web.archive.org/web/20070205055313/http://www3.nationalgeographic.com/animals/reptiles/green-turtle.html |archive-date =2007-02-05 }}</ref> |
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[[File:Baby Chelonia mydas 20060319.jpg|thumb |
[[File:Baby Chelonia mydas 20060319.jpg|thumb|left|[[Green turtle]] hatchling|alt=Photo of newly hatched turtle held in a human hand]] |
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At around 45 to 75 days, the eggs hatch during the night and the hatchlings [[instinct]]ively head directly into the water. This is the most dangerous time in a turtle's life. As they walk, predators such as [[gull]]s and [[crab]]s grab them. A significant percentage never make it to the ocean. Little is known of the initial life history of newly hatched sea turtles.<ref name="FWS">{{cite web |title =Green sea turtle (''Chelonia mydas'') |work =North Florida Field Office |publisher =United States Fish and Wildlife Service |date =2005-12-29 |url=http://www.fws.gov/northflorida/SeaTurtles/Turtle%20Factsheets/Green-Sea-Turtle.htm | |
At around 45 to 75 days, the eggs hatch during the night and the hatchlings [[instinct]]ively head directly into the water. This is the most dangerous time in a turtle's life. As they walk, predators such as [[gull]]s and [[crab]]s grab them. A significant percentage never make it to the ocean. Little is known of the initial life history of newly hatched sea turtles.<ref name="FWS">{{cite web |title =Green sea turtle (''Chelonia mydas'') |work =North Florida Field Office |publisher =United States Fish and Wildlife Service |date =2005-12-29 |url =http://www.fws.gov/northflorida/SeaTurtles/Turtle%20Factsheets/Green-Sea-Turtle.htm |access-date =2007-02-21 |url-status =live |archive-url =https://web.archive.org/web/20070224123808/http://www.fws.gov/northflorida/SeaTurtles/Turtle%20Factsheets/green-sea-turtle.htm |archive-date =2007-02-24 }}</ref> Juveniles spend three to five years in the open ocean before they settle as still-immature juveniles into their permanent shallow-water lifestyle.<ref name="Reich2007">{{cite journal|last=Reich |first=Kimberly J. |author2=Karen A. Bjorndal |author3=Alan B. Bolten |title=The 'lost years' of green turtles: using stable isotopes to study cryptic lifestages |journal=Biology Letters |volume=3 |issue=6 |date=2007-09-18 |doi=10.1098/rsbl.2007.0394 |pmid=17878144 |pmc=2391226 |pages=712–4}}</ref><ref name="LS20070918">{{cite news |last =Brynner |first =Jeanna |title =Sea Turtles' Mystery Hideout Revealed |work =LiveScience |publisher =Imaginova Corp. |date =2007-09-19 |url = http://www.livescience.com/animals/070919_sea_turtle.html |access-date =2007-09-20}}</ref> It is speculated that they take twenty to fifty years to reach [[sexual maturity]]. Individuals live up to eighty years in the wild.<ref name="NGeo"/> They are among the larger sea turtles, many more than a meter long and weighing up to {{convert|300|kg|lb}}.<ref name="AscensionGT">{{cite web |last =Fowler |first =Stephen |title =About The Green Turtle on Ascension |work =Turtles |publisher =Ascension Island Heritage Society |date =2002-04-21 |url =http://www.heritage.org.ac/HS2right.htm |access-date =2007-09-16 |url-status =live |archive-url =https://web.archive.org/web/20071030074741/http://www.heritage.org.ac/HS2right.htm |archive-date =2007-10-30 }}</ref> |
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===Aquatic insects=== |
===Aquatic insects=== |
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[[Aquatic insect]]s also spawn. [[Mayfly|Mayflies]] "are famed for their short adult life. Some species have under an hour to mate and lay their eggs before they die. Their pre-adult stage, known as the subimago, may be even shorter - perhaps lasting just a few minutes before they moult into their adult form. Therefore a mayfly spends most of its life as a nymph, hidden from view under the water."<ref>[ |
[[Aquatic insect]]s also spawn. [[Mayfly|Mayflies]] "are famed for their short adult life. Some species have under an hour to mate and lay their eggs before they die. Their pre-adult stage, known as the subimago, may be even shorter - perhaps lasting just a few minutes before they moult into their adult form. Therefore a mayfly spends most of its life as a nymph, hidden from view under the water."<ref>[https://www.bbc.co.uk/nature/life/Mayfly Mayfly] {{webarchive|url=https://web.archive.org/web/20110206120308/http://www.bbc.co.uk/nature/life/Mayfly |date=2011-02-06 }} BBC. Retrieved 3 February 2011.</ref> |
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===Corals=== |
===Corals=== |
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[[File:Coral Life Cycles ZP.svg|thumb|400px|Life cycles of broadcasters and brooders |
[[File:Coral Life Cycles ZP.svg|thumb|400px|Life cycles of broadcasters and brooders]] |
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Corals can be both [[Gonochorism|gonochoristic]] (unisexual) and [[Hermaphroditism|hermaphroditic]], each of which can reproduce sexually and asexually. Reproduction also allows corals to settle new areas. |
Corals can be both [[Gonochorism|gonochoristic]] (unisexual) and [[Hermaphroditism|hermaphroditic]], each of which can reproduce sexually and asexually. Reproduction also allows corals to settle new areas. |
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Corals predominantly reproduce [[sexual reproduction|sexually]]. 25% of [[hermatypic coral]]s (stony corals) form single sex ([[gonochoristic]]) colonies, while the rest are [[hermaphroditic]].<ref name=Veron> |
Corals predominantly reproduce [[sexual reproduction|sexually]]. 25% of [[hermatypic coral]]s (stony corals) form single sex ([[gonochoristic]]) colonies, while the rest are [[hermaphroditic]].<ref name="Veron">{{cite book |
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{{cite book |
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| author = Veron, J.E.N. |
| author = Veron, J.E.N. |
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| year = 2000 |
| year = 2000 |
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| title = Corals of the World. Vol 3 |
| title = Corals of the World. Vol 3 |
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| edition = 3rd |
| edition = 3rd |
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| pages = |
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| publisher = Australian Institute of Marine Sciences and CRR Qld Pty Ltd. |
| publisher = Australian Institute of Marine Sciences and CRR Qld Pty Ltd. |
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| location = Australia |
| location = Australia |
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| isbn = 0-642-32236- |
| isbn = 978-0-642-32236-4 |
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}}</ref> About 75% of all hermatypic corals "broadcast spawn" by releasing [[gamete]]s—[[egg (biology)|eggs]] and [[sperm]]—into the water to spread offspring. The gametes fuse during fertilization to form a microscopic [[larva]] called a [[planula]], typically pink and elliptical in shape. A typical coral colony form several thousand larvae per year to overcome the odds against formation of a new colony.<ref name=Barnes99> |
}}</ref> About 75% of all hermatypic corals "broadcast spawn" by releasing [[gamete]]s—[[egg (biology)|eggs]] and [[sperm]]—into the water to spread offspring. The gametes fuse during fertilization to form a microscopic [[larva]] called a [[planula]], typically pink and elliptical in shape. A typical coral colony form several thousand larvae per year to overcome the odds against formation of a new colony.<ref name=Barnes99> |
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{{cite book |
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| publisher = Blackwell Science, Inc. |
| publisher = Blackwell Science, Inc. |
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| location = Malden, MA |
| location = Malden, MA |
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| isbn = 0-86542-834- |
| isbn = 978-0-86542-834-8 |
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Planulae exhibit positive ''[[phototaxis]]'', swimming towards light to reach surface waters where they drift and grow before descending to seek a hard surface to which they can attach and establish a new colony. They also exhibit positive ''sonotaxis'', moving towards sounds that emanate from the reef and away from open water.<ref>{{cite |
Planulae exhibit positive ''[[phototaxis]]'', swimming towards light to reach surface waters where they drift and grow before descending to seek a hard surface to which they can attach and establish a new colony. They also exhibit positive ''sonotaxis'', moving towards sounds that emanate from the reef and away from open water.<ref>{{cite journal |
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url= |
|url = https://www.sciencedaily.com/releases/2010/05/100514171908.htm |
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|journal=New Scientist |
|journal = New Scientist |
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|title=Baby Corals Dance Their Way Home |
|title = Baby Corals Dance Their Way Home |
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|date=May 16, 2010 |
|date = May 16, 2010 |
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|access-date = June 8, 2010 |
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|accessdate=June 2010}}</ref> High failure rates afflict many stages of this process, and even though millions of gametes are released by each colony very few new colonies form.<!--thousands of gametes or millions?--> The time from spawning to settling is usually 2–3 days, but can be up to 2 months.<ref name=Jones> |
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|url-status = live |
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{{cite book |
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|archive-url = https://web.archive.org/web/20100520060146/http://www.sciencedaily.com/releases/2010/05/100514171908.htm |
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| author = Jones, O.A. and R. Endean. |
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|archive-date = May 20, 2010 |
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| year = 1973 |
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}}</ref> High failure rates afflict many stages of this process, and even though millions of gametes are released by each colony very few new colonies form.<!--thousands of gametes or millions?--> The time from spawning to settling is usually 2–3 days, but can be up to 2 months.<ref name=Jones> |
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| title = Biology and Geology of Coral Reefs |
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{{cite book |author1 = Jones, O.A. |
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| pages = 205–245 |
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|author2 = R. Endean. |
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| publisher = Harcourt Brace Jovanovich |
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|name-list-style = amp |
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| location = New York, USA |
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|year = 1973 |
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| isbn = 0-12-389602-9 |
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|title = Biology and Geology of Coral Reefs |
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|pages = [https://archive.org/details/biologygeologyof0000jone/page/205 205–245] |
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|publisher = Harcourt Brace Jovanovich |
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|location = New York, USA |
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|isbn = 978-0-12-389602-5 |
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|url = https://archive.org/details/biologygeologyof0000jone/page/205 |
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}}</ref> The larva grows into a polyp and eventually becomes a coral head by asexual budding and growth. |
}}</ref> The larva grows into a polyp and eventually becomes a coral head by asexual budding and growth. |
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[[File:Stony coral spawning 2.jpg|thumb|right|A male [[Great star coral|star coral]], ''Montastraea cavernosa'', releases sperm into the water]] |
[[File:Stony coral spawning 2.jpg|thumb|right|A male [[Great star coral|star coral]], ''Montastraea cavernosa'', releases sperm into the water]] |
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[[Reproductive synchrony|Synchronous spawning]] is very typical on the coral reef and often, even when multiple [[species]] are present, all corals spawn on the same night. This synchrony is essential so that male and female gametes can meet. Corals must rely on environmental cues, varying from species to species, to determine the proper time to release gametes into the water. The cues involve lunar changes, sunset time, and possibly chemical signalling.<ref name=Veron /> Synchronous spawning may form hybrids and is perhaps involved in coral [[speciation]].<ref name=Hatta> |
[[Reproductive synchrony|Synchronous spawning]] is very typical on the coral reef and often, even when multiple [[species]] are present, all corals spawn on the same night. This synchrony is essential so that male and female gametes can meet. Corals must rely on environmental cues, varying from species to species, to determine the proper time to release gametes into the water. The cues involve lunar changes, sunset time, and possibly chemical signalling.<ref name="Veron" /> Synchronous spawning may form hybrids and is perhaps involved in coral [[speciation]].<ref name=Hatta> |
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{{cite journal |
{{cite journal |
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|author = Hatta, M., Fukami, H., Wang, W., Omori, M., Shimoike, K., Hayashibara, T., Ina, Y., Sugiyama, T. |
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|title = Reproductive and genetic evidence for a reticulate evolutionary theory of mass spawning corals |
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|journal = Molecular Biology and Evolution |
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|year = 1999 |
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|pages = 1607–1613 |
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|volume = 16 |
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|issue = 11 |
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|pmid = 10555292 |
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| url=http://mbe.oxfordjournals.org/content/16/11/1607.full.pdf |
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|doi = 10.1093/oxfordjournals.molbev.a026073 |
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| format=PDF |
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|doi-access= free |
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| pmid=10555292 |
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}}</ref> In some places the spawn can be visually dramatic, clouding the usually clear water with gametes, typically at night. |
}}</ref> In some places the spawn can be visually dramatic, clouding the usually clear water with gametes, typically at night. |
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Corals use two methods for sexual reproduction, which differ in whether the female gametes are released: |
Corals use two methods for sexual reproduction, which differ in whether the female gametes are released: |
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*'''Broadcasters''', the majority of which mass spawn, rely heavily on environmental cues, because they release both sperm and eggs into the water. The corals use long-term cues such as [[day length]], water temperature, and/or rate of temperature change. The short-term cue is most often the [[Lunar phase|lunar cycle]], with sunset cuing the release.<ref name=Veron /> About 75% of coral species are broadcasters, the majority of which are hermatypic, or reef-building corals.<ref name=Veron /> The positively buoyant gametes float towards the surface where fertilization produces [[planula]] larvae. The larvae swim towards the surface light to enter into currents, where they usually remain for two days, but sometimes up to three weeks, and in one known case two months,<ref name=Jones /> after which they settle and metamorphose into polyps and form colonies. |
*'''Broadcasters''', the majority of which mass spawn, rely heavily on environmental cues, because they release both sperm and eggs into the water. The corals use long-term cues such as [[day length]], water temperature, and/or rate of temperature change. The short-term cue is most often the [[Lunar phase|lunar cycle]], with sunset cuing the release.<ref name="Veron" /> About 75% of coral species are broadcasters, the majority of which are hermatypic, or reef-building corals.<ref name="Veron" /> The positively buoyant gametes float towards the surface where fertilization produces [[planula]] larvae. The larvae swim towards the surface light to enter into currents, where they usually remain for two days, but sometimes up to three weeks, and in one known case two months,<ref name=Jones /> after which they settle and metamorphose into polyps and form colonies. |
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*'''Brooders''' are most often ahermatypic (non-reef building) in areas of high current or wave action. Brooders release only sperm, which is negatively buoyant, and can harbor unfertilized eggs for weeks, lowering the need for mass synchronous spawning events, which do sometimes occur.<ref name=Veron /> After fertilization the corals release [[planula]] larvae which are ready to settle.<ref name=MilneBay> |
*'''Brooders''' are most often ahermatypic (non-reef building) in areas of high current or wave action. Brooders release only sperm, which is negatively buoyant, and can harbor unfertilized eggs for weeks, lowering the need for mass synchronous spawning events, which do sometimes occur.<ref name="Veron" /> After fertilization the corals release [[planula]] larvae which are ready to settle.<ref name=MilneBay> |
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{{cite web |
{{cite web |
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| |
|author1 = Madl, P. |
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|author2 = Yip, M. |
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| year = 2000 |
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|name-list-style = amp |
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| url = http://biophysics.sbg.ac.at/png/png3.htm |
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|year = 2000 |
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| title = Field Excursion to Milne Bay Province – Papua New Guinea |
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|url = http://biophysics.sbg.ac.at/png/png3.htm |
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| work = |
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|title = Field Excursion to Milne Bay Province – Papua New Guinea |
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| publisher = |
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|access-date = 2006-03-31 |
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|url-status = live |
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|archive-url = https://web.archive.org/web/20120128205517/http://biophysics.sbg.ac.at/png/png3.htm |
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|archive-date = 2012-01-28 |
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}}</ref> |
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[[Fungus|Fungi]] are not plants, and require different conditions for optimal growth. Plants develop through [[photosynthesis]], a process that converts atmospheric [[carbon dioxide]] into [[carbohydrate]]s, especially [[cellulose]]. While sunlight provides an energy source for plants, mushrooms derive all of their energy and growth materials from their [[growth medium]], through biochemical [[decomposition]] processes. This does not mean that light is an unnecessary requirement, since some fungi use light as a signal to induce fruiting. However, all the materials for growth must already be present in the growth medium. Instead of seeds, mushrooms reproduce sexually during underground growth, and asexually through [[spore]]s. Either of these can be contaminated with airborne microorganisms, which will interfere with mushroom growth and prevent a healthy crop. [[Mycelium]], or actively growing mushroom culture, is placed on growth substrate to seed or introduce mushrooms to grow on a [[substrate (biology)|substrate]]. This is also known as inoculation, spawning or adding spawn. Its main advantages are to reduce chances of contamination while giving mushrooms a firm beginning.<ref name="r10"> |
[[Fungus|Fungi]] are not plants, and require different conditions for optimal growth. Plants develop through [[photosynthesis]], a process that converts atmospheric [[carbon dioxide]] into [[carbohydrate]]s, especially [[cellulose]]. While sunlight provides an energy source for plants, mushrooms derive all of their energy and growth materials from their [[growth medium]], through biochemical [[decomposition]] processes. This does not mean that light is an unnecessary requirement, since some fungi use light as a signal to induce fruiting. However, all the materials for growth must already be present in the growth medium. Instead of seeds, mushrooms reproduce sexually during underground growth, and asexually through [[spore]]s. Either of these can be contaminated with airborne microorganisms, which will interfere with mushroom growth and prevent a healthy crop. [[Mycelium]], or actively growing mushroom culture, is placed on growth substrate to seed or introduce mushrooms to grow on a [[substrate (biology)|substrate]]. This is also known as inoculation, spawning or adding spawn. Its main advantages are to reduce chances of contamination while giving mushrooms a firm beginning.<ref name="r10"> |
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{{cite book |
{{cite book |
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|author2=Chang, S. |author3=Miles, P.G. |
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| last = |
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| first = |
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| authorlink = |
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| coauthors = Chang, S., and Miles, P.G. |
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| title = Mushrooms, Cultivation, Nutritional Value, Medicinal Effect, and Environmental Impact |
| title = Mushrooms, Cultivation, Nutritional Value, Medicinal Effect, and Environmental Impact |
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| publisher = CRC Press |
| publisher = CRC Press |
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| year = 2004 |
| year = 2004 |
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| location = |
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| pages = 15,17,69,73,139 |
| pages = 15,17,69,73,139 |
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| url = |
| url =https://books.google.com/books?id=XO4EGzpp1M0C |
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| |
| isbn = 978-0-8493-1043-0 |
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| id = |
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| isbn = 0-8493-1043-1 |
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| author1 =Chang, Shu-Ting }} |
| author1 =Chang, Shu-Ting }} |
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</ref><ref name="r17"> |
</ref><ref name="r17"> |
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{{cite web |
{{cite web |
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|last = Bratkovich |
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|first = Stephen M. |
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|title = Shiitake Mushroom Production: Fruiting, Harvesting and Crop Storage |
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| authorlink = |
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|url = http://ohioline.osu.edu/for-fact/0042.html |
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| coauthors = |
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|url-status = dead |
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| title = Shiitake Mushroom Production: Fruiting, Harvesting and Crop Storage |
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|archive-url = https://web.archive.org/web/20071206215811/http://ohioline.osu.edu/for-fact/0042.html |
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| work = |
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|archive-date = 2007-12-06 |
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| publisher = |
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}} |
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| date = |
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| url = http://ohioline.osu.edu/for-fact/0042.html |
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| accessdate = }} |
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File:Laichender Schlangenstern 72.jpg|Spawning [[brittle star]] |
File:Laichender Schlangenstern 72.jpg|Spawning [[brittle star]] |
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File:Nematoscelis difficilis female.jpg|Head of female krill with her brood sac |
File:Nematoscelis difficilis female.jpg|Head of female krill with her brood sac |
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File:Dead salmon in spawning season.jpg|Dead salmon in spawning season |
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File:SockeyeSpawn inAdams.JPG|Spawning [[sockeye salmon]] |
File:SockeyeSpawn inAdams.JPG|Spawning [[sockeye salmon]] |
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File:Dead salmon in spawning season.jpg|Dead salmon after spawning |
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File:Lagoons, Preston Park - geograph.org.uk - 281594.jpg|These lagoons, connected to the River Tees, provide a quiet backwater for fish to spawn and to take refuge in times of high water levels |
File:Lagoons, Preston Park - geograph.org.uk - 281594.jpg|These lagoons, connected to the River Tees, provide a quiet backwater for fish to spawn and to take refuge in times of high water levels |
||
File:Hornby Castle and the River Wenning - geograph.org.uk - 632943.jpg|In the middle of this [[weir]] is a [[fish ladder]], which allows trout and salmon to pass the weir to go upriver to spawn. |
File:Hornby Castle and the River Wenning - geograph.org.uk - 632943.jpg|In the middle of this [[weir]] is a [[fish ladder]], which allows trout and salmon to pass the weir to go upriver to spawn. |
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== See also == |
== See also == |
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{{ |
{{Commons category|Spawn}} |
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{{ |
{{Div col}} |
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* [[Anadromous]] |
* [[Anadromous]] |
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* [[Egg case (Chondrichthyes)|Egg case]] |
* [[Egg case (Chondrichthyes)|Egg case]] |
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==Notes== |
==Notes== |
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{{ |
{{Reflist|30em}} |
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==Further reading== |
==Further reading== |
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* Cole, Kathleen S (2010) [ |
* Cole, Kathleen S (2010) [https://books.google.com/books?id=_4xZ_QoYNSwC&q=%22Reproduction+and+Sexuality+in+Marine+Fishes%22 ''Reproduction and Sexuality in Marine Fishes: Patterns and Processes''] University of California Press. {{ISBN|978-0-520-26433-5}}. |
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==External links== |
==External links== |
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* [http://www.fishbase.org/fishonline/FOL_reproduction.htm Reproduction] [[FAO]], Rome. |
* [http://www.fishbase.org/fishonline/FOL_reproduction.htm Reproduction] [[FAO]], Rome. |
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{{ |
{{Diversity of fish|state=active}} |
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{{Eggs}} |
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{{Animal sexual behavior}} |
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{{aquatic ecosystem topics|expanded=none}} |
{{aquatic ecosystem topics|expanded=none}} |
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{{Authority control}} |
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{{DEFAULTSORT:Spawn (Biology)}} |
{{DEFAULTSORT:Spawn (Biology)}} |
Latest revision as of 03:31, 29 November 2024
Spawn is the eggs and sperm released or deposited into water by aquatic animals. As a verb, to spawn refers to the process of freely releasing eggs and sperm into a body of water (fresh or marine); the physical act is known as spawning. The vast majority of aquatic and amphibious animals reproduce through spawning. These include the following groups:
- Bony fishes
- Crustaceans (such as crabs, shrimps, etc.)
- Mollusks (such as oysters, octopus, squid)
- Echinoderms (such as sea urchins, sea stars, sea cucumbers, etc.)
- Amphibians (such as frogs, toads, salamanders, newts)
- Aquatic insects (such as dragonflies, mayflies, mosquitoes)
- Coral, which are living colonies of tiny, aquatic organisms—not plants, as they are sometimes perceived to be. Corals, while appearing sedentary or botanical by nature, actually spawn by releasing clouds of sperm and egg cells into the water column, where the two mix.
As a general rule, aquatic or semiaquatic reptiles, birds, and mammals do not reproduce through spawning, but rather through copulation like their terrestrial counterparts. This is also true of cartilaginous fishes (such as sharks, rays and skates).
Spawn consists of the reproductive cells (gametes) of many aquatic animals, some of which will become fertilized and produce offspring. The process of spawning typically involves females releasing ova (unfertilized eggs) into the water, often in large quantities, while males simultaneously or sequentially release spermatozoa (milt) to fertilize the eggs.[1][2][3]
The fungi (mushrooms), are also said to "spawn" when they release a white, ‘fibrous’ matter, forming the matrix from-which they grow.[citation needed]
There are many variations in the way spawning occurs, depending on sexual differences in anatomy, how the sexes relate to each other, where and how the spawn is released and whether or how the spawn is subsequently guarded.
Overview
[edit]Marine animals, and particularly bony fish, commonly reproduce by broadcast spawning. This is an external method of reproduction where the female releases many unfertilised eggs into the water. At the same time, a male or many males release a large amount of sperm into the water which fertilises some of these eggs. The eggs contain a drop of nutrient oil to sustain the embryo as it develops inside the egg case. The oil also provides buoyancy, so the eggs float and drift with the current. The strategy for survival of broadcast spawning is to disperse the fertilised eggs, preferably away from the coast into the relative safety of the open ocean. There the larvae develop as they consume their fat stores, and eventually hatch from the egg capsule into miniature versions of their parents. To survive, they must then become miniature predators themselves, feeding on plankton. Fish eventually encounter others of their own kind (conspecifics), where they form aggregations and learn to school.
Internally, the sexes of most marine animals can be determined by looking at the gonads. For example, male testes of spawning fish are smooth and white and account for up to 12% of the mass of the fish, while female ovaries are granular and orange or yellow, accounting for up to 70% of the fish's mass. Male lampreys, hagfish and salmon discharge their sperm into the body cavity where it is expelled through pores in the abdomen. Male sharks and rays can pass sperm along a duct into a seminal vesicle, where they store it for a while before it is expelled, while teleosts usually employ separate sperm ducts.[4]: 141
Externally, many marine animals, even when spawning, show little sexual dimorphism (difference in body shape or size) or little difference in colouration. Where species are dimorphic, such as sharks or guppies, the males often have penis-like intromittent organs in the form of a modified fin.[4]: 141
A species is semelparous if its individuals spawn only once in their lifetime, and iteroparous if its individuals spawn more than once. The term semelparity comes from the Latin semel, once, and pario, to beget, while iteroparity comes from itero, to repeat, and pario, to beget.
Semelparity is sometimes called "big bang" reproduction, since the single reproductive event of semelparous organisms is usually large and fatal to the spawners.[5] The classic example of a semelparous animal is the Pacific salmon, which lives for many years in the ocean before swimming to the freshwater stream of its birth, spawning, and then dying. Other spawning animals which are semelparous include mayflies, squid, octopus, smelt, capelin and some amphibians.[6] Semelparity is often associated with r-strategists. However, most fish and other spawning animals are iteroparous.
When the internal ovaries or egg masses of fish and certain marine animals are ripe for spawning they are called roe. Roe from certain species, such as shrimp, scallop, crab and sea urchins, are sought as human delicacies in many parts of the world. Caviar is a name for the processed, salted roe of non-fertilized sturgeon. The term soft roe or white roe denotes fish milt. Lobster roe is called coral because it turns bright red when cooked. Roe (reproductive organs) are usually eaten either raw or briefly cooked.
"The reproductive behaviour of fishes is remarkably diversified: they may be oviparous (lay eggs), ovoviviparous (retain the eggs in the body until they hatch), or viviparous (have a direct tissue connection with the developing embryos and give birth to live young). All cartilaginous fishes—the elasmobranches (e.g., sharks, rays, and skates)—employ internal fertilization and usually lay large, heavy-shelled eggs or give birth to live young. The most characteristic features of the more primitive bony fishes is the assemblage of polyandrous (many males) breeding aggregations in open water and the absence of parental care..."[7]
There are two main reproduction methods in fish. The first method is by laying eggs and the second by live-bearing (producing their young alive).
- In the first method, the female fish lays eggs either on the sea floor or on the leaves of an aquatic plant. A male fish fertilizes the eggs, and both then work together to protect the eggs/babies from danger until they can defend themselves.
- In the second method, the male fish uses its anal fin to transmit sperm into the female fish and fertilize the fish eggs. Later, the female gives live birth to her fry.
Sexual strategies
[edit]Basic strategies
[edit]Single female | Multiple females | |
---|---|---|
Single male | Monogamy | Polygyny |
Multiple males | Polyandry | Polygynandry |
Monogamy occurs when one male mates with one female exclusively. This is also called pair spawning.[9] Most fish are not monogamous, and when they are, they often alternate with non-monogamous behaviours. Monogamy can occur when feeding and breeding grounds are small, when it is difficult for fish to find partners, or when both sexes look after the young.[8] Many tropical cichlids, which rear their young together in locations where they must fiercely defend against competitors and predators are monogamous.[10] "In some pipefishes and seahorses, development of eggs takes a long time before the female can place them in the brood pouch of a male, where they are fertilized. While the male is pregnant, the female starts a new batch of eggs, which are ready at about the same time that the male gives birth to the young from the previous mating. This close timing of development promotes monogamy, especially if the likelihood of encountering another potential mate is low."[8]
Polygyny occurs when one male gets exclusive mating rights with multiple females. In polygyny, a large conspicuous male usually defends females from other males or defends a breeding site.[8] The females choose large males that are successfully defending prime breeding sites which the females find attractive. For example, sculpin males defend "caves" underneath rocks which are suitable for the incubation of embryos.
Another way males get to mate with several females is through the use of leks. Leks are places where many fish come together, and the males display to each other. Based on these displays, each female then selects the male they want to be their mate. For example, among the cichlid Cyrtocara eucinostomus in Lake Malawi, up to 50,000 large and colourful males display together on a lek four kilometres long. The females, which are mouth brooders, choose which male they want to fertilize their eggs.[11]
Polyandry occurs when one female gets exclusive mating rights with multiple males. This happens among fish like clownfish that change their sex. It can also happen when males do the brooding but cannot handle all the eggs the female produce, such as with some pipefish.[4]: 161
The males in some deep sea anglerfishes are much smaller than the females. When they find a female they bite into her skin, releasing an enzyme that digests the skin of their mouth and her body and fusing the pair down to the blood-vessel level. The male then slowly atrophies, losing first his digestive organs, then his brain, heart, and eyes, ending as nothing more than a pair of gonads, which release sperm in response to hormones in the female's bloodstream indicating egg release. This ensures that, when the female is ready to spawn, she has a mate immediately available.[12] A single anglerfish female can "mate" with many males in this manner.
Polygynandry occurs when multiple males mate indiscriminately with multiple females. This mutual promiscuity is the approach most commonly used by spawning animals, and is perhaps the "original fish mating system."[4]: 161 Common examples are forage fish, such as herrings, which form huge mating shoals in shallow water. The water becomes milky with sperm and the bottom is draped with millions of fertilized eggs.[4]: 161
Cuckoldry
[edit]Alternate male strategies which allow small males to engage in cuckoldry can develop in species where spawning is dominated by large and aggressive males. Cuckoldry is a variant of polyandry, and can occur with sneak spawners (sometimes called streak spawners). A sneak spawner is a male that rushes in to join the spawning rush of a spawning pair.[13] A spawning rush occurs when a fish makes a burst of speed, usually on a near vertical incline, releasing gametes at the apex, followed by a rapid return to the lake or sea floor or fish aggregation.[14] Sneaking males do not take part in courtship. In salmon and trout, for example, jack males are common. These are small silvery males that migrate upstream along with the standard, large, hook-nosed males and that spawn by sneaking into a redd (spawning nest) to release sperm simultaneously with a mated pair. This behaviour is an evolutionarily stable strategy for reproduction, because it is favoured by natural selection just like the "standard" strategy of large males.[15]
Cuckoldry occurs in many fish species, including dragonets, parrotfishes and wrasses on tropical reefs and the bluegill sunfish in fresh water. Sneaker males that become too large to hide effectively become satellite males. With bluegill sunfish, satellite males mimic the behaviour and colouration of the females. They hover over a nest containing a pair of courting sunfish, and gradually descend to reach the pair just as they spawn. Males may need to be 6 or 7 years old to function capably as parental males, but may be able to function as sneaker or satellite males when they are as young as 2 or 3 years old. The smaller satellite and sneaker males may get mauled by the more powerful parental males, but they spawn when they are younger and they do not put energy into parental care.[4]: 161–2 [16]
Hermaphroditism
[edit]Hermaphroditism occurs when a given individual in a species possesses both male and female reproductive organs, or can alternate between possessing first one, and then the other. Hermaphroditism is common in invertebrates but rare in vertebrates. It can be contrasted with gonochorism, where each individual in a species is either male or female, and remains that way throughout their lives. Most fish are gonochorists, but hermaphroditism is known to occur in 14 families of teleost fishes.[17]
Usually hermaphrodites are sequential, meaning they can switch sex, usually from female to male (protogyny). This can happen if a dominant male is removed from a group of females. The largest female in the harem can switch sex over a few days and replace the dominant male.[17] This is found amongst coral reef fishes such as groupers, parrotfishes and wrasses. It is less common for a male to switch to a female (protandry).[4]: 162 As an example, most wrasses are protogynous hermaphrodites within a haremic mating system.[18][19] Hermaphroditism allows for complex mating systems. Wrasses exhibit three different mating systems: polygynous, lek-like, and promiscuous mating systems.[20] Group spawning and pair spawning occur within mating systems. The type of spawning that occurs depends on male body size.[19] Labroids typically exhibit broadcast spawning, releasing high amounts of planktonic eggs, which are broadcast by tidal currents; adult wrasses have no interaction with offspring.[21] Wrasse of a particular subgroup of the family Labridae, Labrini, do not exhibit broadcast spawning.
Less commonly hermaphrodites can be synchronous, meaning they simultaneously possess both ovaries and testicles and can function as either sex at any one time. Black hamlets "take turns releasing sperm and eggs during spawning. Because such egg trading is advantageous to both individuals, hamlets are typically monogamous for short periods of time–an unusual situation in fishes."[22] The sex of many fishes is not fixed, but can change with physical and social changes to the environment where the fish lives.[23]
Particularly among fishes, hermaphroditism can pay off in situations where one sex is more likely to survive and reproduce, perhaps because it is larger.[24] Anemone fishes are sequential hermaphrodites which are born as males, and become females only when they are mature. Anemone fishes live together monogamously in an anemone, protected by the anemone stings. The males do not have to compete with other males, and female anemone fish are typically larger. When a female dies a juvenile (male) anemone fish moves in, and "the resident male then turns into a female and reproductive advantages of the large female–small male combination continue".[25] In other fishes sex changes are reversible. For example, if some gobies are grouped by sex (male or female), some will switch sex.[4]: 164 [24]
Unisexuality
[edit]Unisexuality occurs when a species is all-male or all-female. Unisexuality occurs in some fish species, and can take complex forms. Squalius alburnoides, a minnow found in several river basins in Portugal and Spain, appears to be an all-male species. The existence of this species illustrates the potential complexity of mating systems in fish. The species originated as a hybrid between two species, and is diploid, but not hermaphroditic. It can have triploid and tetraploid forms, including all-female forms that reproduce mainly through hybridogenesis.[26]
It is rare to find true parthenogenesis in fishes, where females produce female offspring with no input from males. All-female species include the Texas silverside, Menidia clarkhubbsi[27] as well as the Amazon molly.[4]: 162 Parthenogenesis has been recently observed in hammerhead sharks[28] and blacktip sharks.[29] It is also known to occur in crayfish[30][31] and amphibians.[32][33]
Spawning strategies
[edit]This section is patterned after a classification of the spawning behaviours of fish by Balon (1975, 1984) into reproductive guilds. This classification is based on how the eggs are fertilized (internal or external spawners), where the eggs are deposited (pelagic or benthic spawners), and whether and how the parents look after the eggs after spawning (bearers, guarders and nonguarders).[34]
Nonguarders
[edit]Nonguarders do not protect their eggs and offspring after spawning
Open substrate spawners
[edit]Nonguarders: Open substrate spawners[34]
- Pelagic spawners
- Benthic spawners
- Spawners on coarse bottoms
- Pelagic free embryo and larvae
- Benthic free embryo and larvae
- Spawners on plants
- Obligatory
- Nonobligatory
- Spawners on fine substrates
- Terrestrial spawners
Nonguarders: Brood hiders[34]
- Benthic spawners
- Crevice spawners
- Spawners on invertebrates
- Beach spawners
Open substrate spawners scatter their eggs in the environment. They usually spawn in shoals without complex courtship rituals, and males outnumber females.
Broadcast spawners: release their gametes (sperm and eggs) into open water for external fertilisation. There is no subsequent parental care.[35] About 75% of coral species are broadcasters, the majority of which are hermatypic, or reef-building corals.[36]
- Pelagic spawners: a type of broadcast spawners, spawn in the open sea, mostly near the surface. They are usually pelagic fish such as tuna and sardines. Some demersal fish leave the bottom to spawn pelagically, particularly coral reef fish such as parrotfish and wrasses. Pelagic spawning means water currents widely disperse the young. The eggs, embryos and larvae of pelagic spawners contain oil globules or have a high water content. As a result, they are buoyant and are widely dispersed by currents. The downside is that mortality is high, because they can be eaten so easily by pelagic predators or they can drift into unsuitable areas. Females compensate by spawning large numbers of eggs and extending their spawning periods. Pelagic spawners that live in or around coral reefs can spawn a small number of eggs almost daily over a period of months. These fishes have complex breeding behaviours including sex changes, harems, leks and territoriality.[4]: 143
- Benthic spawners: deposit their spawn on or near the bottom of the sea (or lake). They are usually demersal fish such as cod and flatfish. These species typically spawn without ceremony; they do not engage in elaborate courtship rituals. Each female is usually followed by several males who fertilize the eggs as they are released. Various strategies ensure the eggs and embryos remain in place, and do not drift with the current. The eggs can adhere to other eggs or to whatever they are deposited on, or the eggs can be laid in long strings which are wrapped around plants or rocks. Some eggs take on water after they are released, so they can be dropped into cracks where they swell and wedge themselves in place.
- Egg scatterers: scatter adhesive or non-adhesive eggs to fall to the substrate, into plants, or float to the surface. These species do not look after their brood and even eat their own eggs. These are often schooling fish which spawn in groups or pairs, often laying a large number of small eggs. The fry hatch quickly.
- Egg depositors: deposit eggs on a substrate (tank glass, wood, rocks, plants). Egg depositors usually lay fewer eggs than egg-scatterers, although the eggs are larger. Egg depositors fall into two groups: those that care for their eggs, and those that do not. Among egg depositors that care for their eggs are cichlids and some catfish. Egg depositors that care for their young can be divided into two groups: cavity spawners and open spawners.
- Cavity spawners: lay eggs in a cave or cavity. These fish form pairs and have advanced brood care where the eggs are defended and cleaned. The eggs take a few days to hatch, and the fry are often guarded by the parents. Various catfish, Cyprinidae, and killifish make up the majority. Cavity spawners can be contrasted with open (shelter) spawners, which lay their eggs on an open surface.
Brood hiders
[edit]Brood hiders hide their eggs but do not give parental care after they have hidden them. Brood hiders are mostly benthic spawners that bury the fertilized eggs. For example, among salmon and trout the female digs a nest with her tail in gravel. These nests are called redds. The female then lays her eggs while the male fertilizes them, while both fish defend the redd if necessary from other members of the same species. Then the female buries the nest, and the nest site is abandoned. In North America, some minnows build nests out of piles of stones rather than dig holes. The minnow males have tubercles on their head and body which they use to help them defend the nest site.[4]: 145
- Egg buriers - can inhabit waters that dry up at some time of the year. An example are annual killifish which lay their eggs in mud. The parents mature quickly and lay their eggs before dying when the water dries up. The eggs remain in a dormant stage until rains stimulate hatching.
Bitterlings have a remarkable reproduction strategy where parents transfer responsibility for the care of their young to mussels. The female extends her ovipositor into the mantle cavity of the mussel and deposits her eggs between the gill filaments. The male then ejects his sperm into the mussel's inhalant water current and fertilization takes place within the gills of the host. The same female may use a number of mussels, and she deposits only one or two yellow, oval eggs into each. Early developmental stages are protected from predation within the body of the mussel. After 3 to 4 weeks larvae swim away from the host to continue life on their own.
Guarders
[edit]Guarders: Substrate spawners[34]
- Rock tenders
- Plant tenders
- Terrestrial tenders
- Pelagic tenders
Guarders: Nest spawners[34]
- Rock and gravel nesters
- Sand nesters
- Plant-material nesters
- Gluemakers
- Nongluemakers
- Bubble nesters
- Hole nesters
- Misc-materials nesters
- Anemone nesters
Guarders protect their eggs and offspring after spawning by practicing parental care (also called brood care). Parental care is an "investment by parents in offspring that increases the offspring's chances of surviving (and hence reproducing). In fish, parental care can take a variety of forms including guarding, nest building, fanning, splashing, removal of dead eggs, retrieval of straying fry, external egg carrying, egg burying, moving eggs or young, ectodermal feeding, oral brooding, internal gestation, brood-pouch egg carrying, etc."[37]
Territorial behaviour is generally necessary for guarders, and the embryos are almost always guarded by males (apart from cichlids). There is a need to be territorial because looking after embryos usually includes defending the site where they are being looked after. It also often means there is competition for the best egg-laying sites. Elaborate courtship behaviour is usual among guarders.[4]: 145
Guarding males keep the embryos safe from predators, keep oxygen levels high by fanning water currents, and keep the area free from dead embryos and debris. They protect the embryos until they hatch, and often look after the larval stages as well. The time spent guarding can range from a few days to several months.[4]: 145
Substrate spawners
[edit]Some guarders build nests (nest spawners) and some do not (substrate spawners), though the difference between the two groups can be small.[4]: 142 Substrate spawners clean off a suitable area of surface suitable for egg laying, and look after the area, but they do not actively build a nest.
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Baby paradise fish just hatched, gathered under the surface of a bubble nest
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Anemone fish nest in an anemone. Here a male is protecting spawn produced by his partner.
Bearers
[edit]Bearers: External[34]
- Transfer brooders
- Auxiliary brooders
- Mouth brooders
- Gill-chamber brooders
- Pouch brooders
A female cichlid mouthbrooding fry which can be seen looking out her mouth
External videos Mouthbrooding tilapia — YouTube Mouthbrooding cichlid — YouTube
Bearers are fish that carry their embryos (and sometimes their young) around with them, either externally or internally.
External bearers
[edit]Mouth brooders - carry eggs or larvae in their mouth. Mouth brooders can be ovophiles or larvophiles. Ovophile or egg-loving mouth-brooders lay their eggs in a pit, which are sucked up into the mouth of the female. The small number of large eggs hatch in the mother's mouth, and the fry remain there for a period of time. Fertilization often occurs with the help of egg-spots, which are colorful spots on the anal fin of the male. When the female sees these spots, she tries to pick up the egg-spots, but instead gets sperm that fertilizes the eggs in her mouth. Many cichlids and some labyrinth fish are ovophile mouthbrooders. Larvophile or larvae-loving mouth-brooders lay their eggs on a substrate and guard them until the eggs hatch. After hatching, the female picks up the fry and keeps them in her mouth. When the fry can fend for themselves, they are released. Some eartheaters are larvophile mouthbrooders.
Internal bearers
[edit]Facultative internal bearers
[edit]The beginning of the evolutionary process of livebearing starts with facultative (optional) internal bearing. The process occurs in several species of oviparous (egg-laying) killifishes which spawn in the normal way on the substrate, but in the process accidentally fertilize eggs that the female retains and does not spawn. These eggs are spawned later, usually without allowing much time for embryonic development.[4]: 147
Bearers: Internal[34]
- Facultative internal bearers
- Obligate internal bearers
- Livebearers
Obligate internal bearers
[edit]The next step in the evolution of livebearing is obligate (by necessity) internal bearing, where the female retains all the embryos. "The only source of nutrition for these embryos, however, is the egg yolk, as in externally spawned eggs. This situation, also referred to as ovoviviparity, is characteristic of marine rock fishes and the Lake Baikal sculpins. This strategy allows these fish to have fecundities approaching those of pelagic fish with external fertilization, but it also enables them to protect the young during their most vulnerable stage of development. By contrast, sharks and rays using this strategy produce a relatively small number of embryos and retain them for a few weeks to 16 months or longer. The shorter times spans are characteristic of species that eventually deposit their embryos in the environment, surrounded by a horny capsule; whereas the longer periods are characteristic of sharks that retain the embryos until they are ready to emerge as actively swimming young."[4]: 147 [38]
Viviparous fish
[edit]However, some fish do not fit these categories. The livebearing largespring gambusia (Gambusia geiseri) was thought to be ovoviviparous until it was shown in 2001 that the embryos received nutrients from the mother.[39]
Spawning grounds
[edit]Spawning grounds are the areas of water where aquatic animals spawn, or produce their eggs. After spawning, the spawn may or may not drift to new grounds which become their nursery grounds. Many species undertake migrations each year, and sometimes great migrations, to reach their spawning grounds. For example, lakes and river watersheds can be major spawning grounds for anadromous fish such as salmon. These days, it is often necessary to construct fish ladders and other bypass systems so salmon can navigate their way past hydroelectric dams or other obstructions such as weirs on their way to spawning grounds.[40][41] Coastal fish often use mangroves and estuaries as spawning grounds, while reef fish can find adjacent seagrass meadows that make good spawning grounds. Short-finned eels can travel anything up to three or four thousand kilometres to their spawning ground in deep water somewhere in the Coral Sea.
Forage fish often make great migrations between their spawning, feeding and nursery grounds. Schools of a particular stock usually travel in a triangle between these grounds. For example, one stock of herrings have their spawning ground in southern Norway, their feeding ground in Iceland, and their nursery ground in northern Norway. Wide triangular journeys such as these may be important because forage fish, when feeding, cannot distinguish their own offspring.[42]
Capelin are a forage fish of the smelt family found in the Atlantic and Arctic oceans. In summer, they graze on dense swarms of plankton at the edge of the ice shelf. Larger capelin also eat krill and other crustaceans. The capelin move inshore in large schools to spawn and migrate in spring and summer to feed in plankton rich areas between Iceland, Greenland, and Jan Mayen. The migration is affected by ocean currents. Around Iceland maturing capelin make large northward feeding migrations in spring and summer. The return migration takes place in September to November. The spawning migration starts north of Iceland in December or January.[43]
The diagram on the right shows the main spawning grounds and larval drift routes. Capelin on the way to feeding grounds is coloured green, capelin on the way back is blue, and the breeding grounds are red.[43] In a paper published in 2009, researchers from Iceland recount their application of an interacting particle model to the capelin stock around Iceland, successfully predicting the spawning migration route for 2008.[44]
Referred to as "the greatest shoal on earth", the sardine run occurs when millions of sardines migrate from their spawning grounds south of the southern tip of Africa northward along the Eastern Cape coastline. Chinook salmon make the longest freshwater migration of any salmon, over 3,000 kilometres (1,900 mi) up the Yukon River to spawning grounds upstream of Whitehorse, Yukon. Some green sea turtles swim more than 2,600 kilometres (1,600 mi) to reach their spawning grounds.
Examples
[edit]Fish
[edit]Goldfish
[edit]Goldfish, like all cyprinids, are egg-layers. They usually start breeding after a significant temperature change, often in spring. Males chase females, prompting them to release their eggs by bumping and nudging them. As the female goldfish spawns her eggs, the male goldfish stays close behind fertilizing them. Their eggs are adhesive and attach to aquatic vegetation. The eggs hatch within 48 to 72 hours. Within a week or so, the fry begins to assume its final shape, although a year may pass before they develop a mature goldfish colour; until then they are a metallic brown like their wild ancestors. In their first weeks of life, the fry grow quickly—an adaptation born of the high risk of getting devoured by the adult goldfish.
Carp
[edit]Carp typically spawn in the spring and summer, depending on the climate and conditions. Oxygen levels of the water, availability of food, size of each fish, age, number of times the fish has spawned before and water temperature are all factors known to effect when and how many eggs each carp will spawn at any one time.[45]
Siamese fighting fish
[edit]Prior to spawning, male Siamese fighting fish build bubble nests of varying sizes at the surface of the water. When a male becomes interested in a female, he will flare his gills, twist his body, and spread his fins. The female darkens in colour and curves her body back and forth. The act of spawning takes place in a "nuptial embrace" where the male wraps his body around the female, each embrace resulting in the release of 10–40 eggs until the female is out of eggs. The male, from his side, releases milt into the water and fertilization takes place externally. During and after spawning, the male uses his mouth to retrieve sinking eggs and deposit them in the bubble nest (during mating the female sometimes assists her partner, but more often she will simply devour all the eggs that she manages to catch). Once the female has released all of her eggs, she is chased away from the male's territory, as it is likely that she'll eat the eggs due to hunger.[46] The eggs then remain in the male's care. He keeps them in the bubble nest, making sure none fall to the bottom and repairing the nest as needed. Incubation lasts for 24–36 hours, and the newly hatched larvae remain in the nest for the next 2–3 days, until their yolk sacs are fully absorbed. Afterwards the fry leave the nest and the free-swimming stage begins.[47]
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Siamese fighting fish build bubble nests of varying sizes.
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A pair of Siamese fighting fish spawning under their bubble nest.
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One-day-old Siamese fighting fish larvae in a bubble nest - their yolk sacs have not yet been absorbed
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A 15-day-old free-swimming fry of a Siamese fighting fish
Crustaceans
[edit]External videos | |
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Lobster migration train (from The Trials of Life) |
Copepods
[edit]Copepods are tiny crustaceans which usually reproduce either by broadcast spawning or by sac spawning. Broadcasting copepods scatter their eggs into the water, but sac spawners lay their eggs into an ovigerous sac. Sac spawners spawn few but relatively large eggs that develop slowly. By contrast, broadcast spawners spawn numerous small eggs that develop rapidly.[48] However, the shorter hatch times that result from broadcasting are not short enough to compensate for the higher mortality compared to sac spawners. To produce a given number of hatched eggs, broadcasters must spawn more eggs than sac spawners.[49]
Spiny lobsters
[edit]After mating, the fertilized eggs of the California spiny lobster are carried on the female's pleopods until they hatch, with between 120,000 and 680,000 carried by a single female.[50] The eggs begin coral red, but darken as they develop to a deep maroon.[51] When she is carrying the eggs, the female is said to be "berried". The eggs are ready to hatch after 10 weeks,[50] and spawning takes place from May to August.[52] The larvae that hatch (called phyllosoma larvae) do not resemble the adults. Instead, they are flat, transparent animals around 14 mm (0.55 in) long, but as thin as a sheet of paper.[53] The larvae feed on plankton,[51] and grow through ten molts into ten further larval stages, the last of which is around 30–32 mm (1.2–1.3 in) long.[53] The full series of larval molts takes around 7 months, and when the last stage molts, it metamorphoses into the puerulus state, which is a juvenile form of the adult, though still transparent.[53] The puerulus larvae settle to the sea floor when the water is near its maximum temperature, which in Baja California is in the fall.[54]
Egg-bearing female lobsters migrate inshore from deeper waters to hatch their eggs, though they do not have specific spawning grounds.[55][56] These lobster migrations can occur in close single-file formation "lobster trains".
Molluscs
[edit]Pacific oysters
[edit]Oysters are broadcast spawners, that is, eggs and sperm are released into open water where fertilisation occurs. They are protandric; during their first year they spawn as males by releasing sperm into the water. As they grow over the next two or three years and develop greater energy reserves, they spawn as females by releasing eggs. Bay oysters usually spawn by the end of June. An increase in water temperature prompts a few oysters to spawn. This triggers spawning in the rest, clouding the water with millions of eggs and sperm. A single female oyster can produce up to 100 million eggs annually. The eggs become fertilized in the water and develop rapidly into planktonic larvae. which eventually find suitable sites, such as another oyster's shell, on which to settle. Attached oyster larvae are called spat. Spat are oysters less than 25 millimetres (0.98 in) long.
The Pacific oyster usually has separate sexes. Their sex can be determined by examining the gonads, and it can change from year to year, normally during the winter months. In certain environmental conditions, one sex is favoured over the other. Protandry is favoured in areas of high food abundance and protogyny occurs in areas of low food abundance. In habitats with a high food supply, the sex ratio in the adult population tends to favour females, and areas with low food abundances tend to have a larger proportion of male adults. Spawning in the Pacific oyster occurs at 20 °C (68 °F). This species is very fecund, with females releasing about 50–200 million eggs in regular intervals (at a rate of 5–10 times a minute) in a single spawning. Once released from the gonads, the eggs move through the suprabranchial chambers (gills), are then pushed through the gill ostia into the mantle chamber, and are finally released in the water, forming a small cloud. In males, the sperm is released at the opposite end of the oyster, along with the normal exhalent stream of water.[57] A rise in water temperature is thought to be the main cue in the initiation of spawning, as the onset of higher water temperatures in the summer results in earlier spawning in the Pacific oyster.[58]
The larvae of the Pacific oyster are planktotrophic, and are about 70 μm at the prodissoconch 1 stage. The larvae move through the water column via the use of a larval foot to find suitable settlement locations. They can spend several weeks at this phase, which is dependent on water temperature, salinity and food supply. Over these weeks, larvae can disperse great distances by water currents before they metamorphose and settle as small spat. Similar to other oyster species, once the Pacific oyster larvae find a suitable habitat, they attach to it permanently using cement secreted from a gland in their foot. After settlement, the larvae metamorphose into juvenile spat. The growth rate is very rapid in optimum environmental conditions, and market size can be achieved in 18 to 30 months.[59]
External videos | |
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Squid spawning |
Cephalopods
[edit]Cephalopods, such as squid and octopuses, have prominent heads and a set of arms (tentacles) modified from the primitive foot of molluscs. All cephalopods are sexually dimorphic. However, they lack external sexual characteristics, so they use colour communication. A courting male approaches a likely looking mate flashing his brightest colours, often in rippling displays. If the other cephalopod is female and receptive, her skin will change colour to become pale, and mating will occur. If the other cephalopod remains brightly coloured, it is taken as a warning.[60]
All cephalopods reproduce by spawning eggs. Most cephalopods use semi-internal fertilization where the male places his gametes inside the female's mantle cavity to fertilize the ova in the female's single ovary.[61] The "penis" in most male cephalopods is a long and muscular end of the gonoduct used to transfer spermatophores to a modified sperm-carrying arm called a hectocotylus. That in turn is used to transfer the spermatophores to the female. In species where the hectocotylus is missing, the "penis" is long and able to extend beyond the mantle cavity and transfers the spermatophores directly to the female. In many cephalopods, mating occurs head-to-head and the male may simply transfer sperm to the female. Others may detach the sperm-carrying arm and leave it attached to the female. Deep water squid have the greatest known penis length relative to body size of all mobile animals, second in the entire animal kingdom only to certain sessile barnacles. Penis elongation in the greater hooked squid may result in a penis that is as long as the mantle, head and arms combined.[62][63]
Some species brood their fertilized eggs: female paper nautilus construct shelters for the young, while Gonatiid squid carry a larva-laden membrane from the hooks on their arms.[64] Other cephalopods deposit their young under rocks and aerate them with their tentacles hatching. Mostly the eggs are left to their own devices; many squid lay sausage-like bunches of eggs in crevices or occasionally on the sea floor. Cuttlefish lay eggs separately in cases and attach them to coral or algal fronds.[65] Like Pacific salmon, cephalopods are mostly semelparous, spawning many small eggs in one batch and then dying. Cephalopods usually live fast and die young. Most of the energy extracted from their food is used for growing, and they mature rapidly to their adult size. Some gain as much as 12% of their body mass each day. Most live for one to two years, reproducing and then dying shortly thereafter.[66][67]
Echinoderms
[edit]External videos | |
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Sea urchin spawning |
Echinoderms are marine animals, widespread in all oceans, but not found in fresh water. Just below their skin is an endoskeleton composed of calcareous plates or ossicles.
Sea urchins
[edit]Sea urchins are spiky echinoderms with spherical bodies which usually contain five gonads. They move slowly, feed mostly on seaweed, and are important for the diet of sea otters. Sea urchins are dioecious, having separate male and female sexes, although there is generally no easy way to distinguish the two. The gonads are lined with muscles underneath the peritoneum, and these allow the animal to squeeze its gametes through the duct and into the surrounding sea water, where fertilization takes place.[68] Their roe (male and female gonads) is soft and melting, with a colour ranging from orange to pale yellow, and is sought after as a human delicacy in many parts of the world.
Sea cucumbers
[edit]Sea cucumbers are leathery echinoderms with elongated bodies which contain a single, branched gonad. They are found on the sea floor worldwide, and occur in great numbers on the deep sea floor where they often make up the majority of the animal biomass.[69] They feed on plankton and decaying organic debris found at the sea bottom, catching food that flows by with their open tentacles or sifting through bottom sediments. Like sea urchins, most sea cucumbers reproduce by releasing sperm and ova into the ocean water. Depending on conditions, one organism can produce thousands of gametes.
Sea cucumbers are typically dioecious, with separate male and female individuals. The reproductive system consists of a single gonad, consisting of a cluster of tubules emptying into a single duct that opens on the upper surface of the animal, close to the tentacles.[68] Many species fertilise their eggs internally. The fertilised egg develops in a pouch on the adult's body and eventually hatches as a juvenile sea cucumber.[70] A few species brood their young inside the body cavity, giving birth through a small rupture in the body wall close to the anus. The remaining species develop their eggs into a free-swimming larva, usually after about three days of development. This larva swims by means of a long band of cilia wrapped around its body. As the larva grows it transforms into a barrel-shaped body with three to five separate rings of cilia. The tentacles are usually the first adult features to appear, before the regular tube feet.[68]
Amphibious animals
[edit]Amphibians have successfully solved most of the problems associated with exposure to air. But their reproductive system was and is linked to water, and it remains very fishlike. Almost all amphibians spawn in water and lay a great number of small eggs that hatch quickly into swimming larvae. The eggs do not need any complex protection against drying, because if the environment dries, the larvae are doomed as well as the eggs. Thus selection has acted to encourage the selection of suitable sites for laying eggs, rather than suitable devices for protecting eggs. Both fishes and amphibians may migrate long distances for spawning, and favoured sites are often disputed vigorously.
Amphibians are found in and around fresh water lakes and ponds, but not in marine environments. Examples are frogs and toads, salamanders, newts and caecilians (which resemble snakes). They are cold-blooded animals that metamorphose from a juvenile water-breathing form, usually to an adult air-breathing form, though mudpuppies retain juvenile gills in adulthood.
Frogs and toads
[edit]Female frogs and toads usually spawn gelatinous egg masses containing thousands of eggs in water. Different species lay eggs in distinctive and identifiable ways. For example, the American toad lays long strings of eggs. The eggs are highly vulnerable to predation, so frogs have evolved many techniques to ensure the survival of the next generation. In colder areas the embryo is black to absorb more heat from the sun, which speeds up development. Most commonly, this involves synchronous reproduction. Many individuals will breed at the same time, overwhelming the actions of predators; the majority of the offspring will still die due to predation, but there is a greater chance some will survive. Another way in which some species avoid predators and the pathogens eggs are exposed to in ponds is to lay eggs on leaves above the pond, with a gelatinous coating designed to retain moisture. In these species the tadpoles drop into the water upon hatching. The eggs of some species laid out of water can detect vibrations of nearby predatory wasps or snakes, and will hatch early to avoid being eaten.[72]
While the length of the egg stage depends on the species and environmental conditions, aquatic eggs generally hatch within one week. Unlike salamanders and newts, frogs and toads never become sexually mature while still in their larval stage. The hatched eggs continue life as tadpoles, which typically have oval bodies and long, vertically flattened tails. As a general rule, free living larvae are fully aquatic. They lack eyelids and have a cartilaginous skeleton, a lateral line system, gills for respiration (external gills at first, internal gills later) and tails with dorsal and ventral folds of skin for swimming.[73] They quickly develop a gill pouch that covers the gills and the front legs; the lungs are also developed at an early stage as an accessory breathing organ. Some species which go through the metamorphosis inside the egg and hatch to small frogs never develop gills; instead there are specialised areas of skin that take care of respiration. Tadpoles also lack true teeth, but the jaws in most species usually have two elongate, parallel rows of small keratinized structures called keradonts in the upper jaw while the lower jaw has three rows of keradonts, surrounded by a horny beak, but the number of rows can be lower (sometimes zero), or much higher.[74] Tadpoles feed on algae, including diatoms filtered from the water through the gills. Some species are carnivorous at the tadpole stage, eating insects, smaller tadpoles, and fish. Cannibalism has been observed among tadpoles. Early developers who gain legs may be eaten by the others, so the late bloomers survive longer.[75]
Sea turtles
[edit]External videos | |
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Spawning sea turtle |
Sea turtles are amphibious reptiles, but they are not amphibians. Reptiles belong to the class Reptilia while amphibians belong to the class Amphibia. These are two distinct taxonomic groups. Reptiles have scales and leathery skins, while the skins of amphibians are smooth and porous. Unlike frogs, sea turtle eggs have tough, leathery shells which allow them to survive on land without drying out.
Some sea turtles migrate long distances between feeding and spawning grounds. Green turtles have feeding grounds along the Brazilian coast. Each year, thousands of these turtles migrate about 2,300 kilometres (1,400 mi) to their spawning ground, Ascension Island in the Atlantic, an island only 11 kilometres (6.8 mi) across. Each year the returning turtles dig between 6,000 and 15,000 nests, often returning to the same beach from where they hatched. Females usually mate every two to four years. Males on the other hand visit the breeding areas every year, attempting to mate.[76] Green sea turtles' mating is similar to other marine turtles. Female turtles control the process. A few populations practice polyandry, although this does not seem to benefit hatchlings.[77] After mating in the water, the female moves above the beach's high tide line where she digs a hole with her hind flippers and deposits her eggs. Litter size depends on the age of the female and species, but green turtle clutches range between 100 and 200. She then covers the nest with sand and returns to the sea.[78]
At around 45 to 75 days, the eggs hatch during the night and the hatchlings instinctively head directly into the water. This is the most dangerous time in a turtle's life. As they walk, predators such as gulls and crabs grab them. A significant percentage never make it to the ocean. Little is known of the initial life history of newly hatched sea turtles.[79] Juveniles spend three to five years in the open ocean before they settle as still-immature juveniles into their permanent shallow-water lifestyle.[80][81] It is speculated that they take twenty to fifty years to reach sexual maturity. Individuals live up to eighty years in the wild.[78] They are among the larger sea turtles, many more than a meter long and weighing up to 300 kilograms (660 lb).[82]
Aquatic insects
[edit]Aquatic insects also spawn. Mayflies "are famed for their short adult life. Some species have under an hour to mate and lay their eggs before they die. Their pre-adult stage, known as the subimago, may be even shorter - perhaps lasting just a few minutes before they moult into their adult form. Therefore a mayfly spends most of its life as a nymph, hidden from view under the water."[83]
Corals
[edit]Corals can be both gonochoristic (unisexual) and hermaphroditic, each of which can reproduce sexually and asexually. Reproduction also allows corals to settle new areas.
Corals predominantly reproduce sexually. 25% of hermatypic corals (stony corals) form single sex (gonochoristic) colonies, while the rest are hermaphroditic.[36] About 75% of all hermatypic corals "broadcast spawn" by releasing gametes—eggs and sperm—into the water to spread offspring. The gametes fuse during fertilization to form a microscopic larva called a planula, typically pink and elliptical in shape. A typical coral colony form several thousand larvae per year to overcome the odds against formation of a new colony.[84]
Planulae exhibit positive phototaxis, swimming towards light to reach surface waters where they drift and grow before descending to seek a hard surface to which they can attach and establish a new colony. They also exhibit positive sonotaxis, moving towards sounds that emanate from the reef and away from open water.[85] High failure rates afflict many stages of this process, and even though millions of gametes are released by each colony very few new colonies form. The time from spawning to settling is usually 2–3 days, but can be up to 2 months.[86] The larva grows into a polyp and eventually becomes a coral head by asexual budding and growth.
Synchronous spawning is very typical on the coral reef and often, even when multiple species are present, all corals spawn on the same night. This synchrony is essential so that male and female gametes can meet. Corals must rely on environmental cues, varying from species to species, to determine the proper time to release gametes into the water. The cues involve lunar changes, sunset time, and possibly chemical signalling.[36] Synchronous spawning may form hybrids and is perhaps involved in coral speciation.[87] In some places the spawn can be visually dramatic, clouding the usually clear water with gametes, typically at night.
Corals use two methods for sexual reproduction, which differ in whether the female gametes are released:
- Broadcasters, the majority of which mass spawn, rely heavily on environmental cues, because they release both sperm and eggs into the water. The corals use long-term cues such as day length, water temperature, and/or rate of temperature change. The short-term cue is most often the lunar cycle, with sunset cuing the release.[36] About 75% of coral species are broadcasters, the majority of which are hermatypic, or reef-building corals.[36] The positively buoyant gametes float towards the surface where fertilization produces planula larvae. The larvae swim towards the surface light to enter into currents, where they usually remain for two days, but sometimes up to three weeks, and in one known case two months,[86] after which they settle and metamorphose into polyps and form colonies.
- Brooders are most often ahermatypic (non-reef building) in areas of high current or wave action. Brooders release only sperm, which is negatively buoyant, and can harbor unfertilized eggs for weeks, lowering the need for mass synchronous spawning events, which do sometimes occur.[36] After fertilization the corals release planula larvae which are ready to settle.[88]
Fungi
[edit]Fungi are not plants, and require different conditions for optimal growth. Plants develop through photosynthesis, a process that converts atmospheric carbon dioxide into carbohydrates, especially cellulose. While sunlight provides an energy source for plants, mushrooms derive all of their energy and growth materials from their growth medium, through biochemical decomposition processes. This does not mean that light is an unnecessary requirement, since some fungi use light as a signal to induce fruiting. However, all the materials for growth must already be present in the growth medium. Instead of seeds, mushrooms reproduce sexually during underground growth, and asexually through spores. Either of these can be contaminated with airborne microorganisms, which will interfere with mushroom growth and prevent a healthy crop. Mycelium, or actively growing mushroom culture, is placed on growth substrate to seed or introduce mushrooms to grow on a substrate. This is also known as inoculation, spawning or adding spawn. Its main advantages are to reduce chances of contamination while giving mushrooms a firm beginning.[89][90]
Gallery
[edit]-
Spawning brittle star
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Head of female krill with her brood sac
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Spawning sockeye salmon
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Dead salmon after spawning
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These lagoons, connected to the River Tees, provide a quiet backwater for fish to spawn and to take refuge in times of high water levels
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In the middle of this weir is a fish ladder, which allows trout and salmon to pass the weir to go upriver to spawn.
See also
[edit]Notes
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Further reading
[edit]- Cole, Kathleen S (2010) Reproduction and Sexuality in Marine Fishes: Patterns and Processes University of California Press. ISBN 978-0-520-26433-5.
External links
[edit]- Reproduction FAO, Rome.