Serpentinization: Difference between revisions
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'''Serpentinization''' is a geological [[metamorphic rock|metamorphic]] process involving heat and water in which low-[[silica]] [[mafic]] and [[ultramafic]] rocks are [[oxidation|oxidized]] and [[hydrolyzed]] with water into [[serpentinite]]. The [[peridotite]]s and [[dunite]]s of the seafloor are converted to [[serpentine]] and [[magnetite]]. In the process large amounts of water are absorbed into the rock increasing the volume and destroying the structure. The density changes from 3.3 to 2.7 g/cm<sup>3</sup> with a concurrent volume increase of about 40%. The reaction is exothermic and large amounts of heat energy are produced in the process. Rock temperatures can be raised by about 260 <sup>o</sup>C. The chemical reactions producing the magnetite produces hydrogen gas. [[Sulfate]]s and [[carbonate]]s are reduced and form [[methane]] and [[hydrogen sulfide]]. The hydrogen, methane, and hydrogen sulfide provide energy sources for deep sea microorganisms. |
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{{Short description|Formation of serpentinite by hydration and metamorphic transformation of olivine}} |
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{{Use dmy dates|date=May 2022}} |
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[[File:Mineraly.sk - chryzotil.jpg|right|thumb|[[Serpentinite]] partially made of [[chrysotile]], from Slovakia]] |
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'''Serpentinization''' is a hydration and [[Metamorphic rock|metamorphic]] transformation of ferromagnesian minerals, such as [[olivine]] and [[pyroxene]], in [[mafic]] and [[ultramafic]] rock to produce [[serpentinite]].<ref name=":0">{{Cite journal |last1=Holm |first1=N.G. |last2=Oze |first2=C. |last3=Mousis |first3=O. |last4=Waite |first4=J.H. |last5=Guilbert-Lepoutre |first5=A. |date=2015-07-01 |title=Serpentinization and the Formation of H2 and CH4 on Celestial Bodies (Planets, Moons, Comets) |journal=Astrobiology |volume=15 |issue=7 |pages=587–600 |doi=10.1089/ast.2014.1188 |issn=1531-1074 |pmc=4523005 |pmid=26154779|bibcode=2015AsBio..15..587H }}</ref> Minerals formed by serpentinization include the [[Serpentine subgroup|serpentine group]] minerals ([[antigorite]], [[lizardite]], [[chrysotile]]), [[brucite]], [[talc]], Ni-Fe alloys, and [[magnetite]].<ref name=":0" /><ref name="Moody1976" /> The [[mineral alteration]] is particularly important at the [[sea floor]] at [[plate tectonics|tectonic plate]] boundaries.<ref name="GeologyDictionary">{{cite web |url=https://www.theodora.com/geology/glossarys.html#serpentine |title=Serpentine definition |work=Dictionary of Geology |access-date=2018-10-23}}</ref><ref name=":2">{{Cite journal |last1=Holm |first1=N.g. |last2=Oze |first2=C. |last3=Mousis |first3=O. |last4=Waite |first4=J.h. |last5=Guilbert-Lepoutre |first5=A. |date=2015-07-01 |title=Serpentinization and the Formation of H2 and CH4 on Celestial Bodies (Planets, Moons, Comets) |journal=Astrobiology |volume=15 |issue=7 |pages=587–600 |doi=10.1089/ast.2014.1188 |issn=1531-1074 |pmc=4523005 |pmid=26154779|bibcode=2015AsBio..15..587H }}</ref> |
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== Formation and petrology == |
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Serpentinization is a form of low-temperature (0 to ~600 °C) <ref>{{Cite journal |last=Evans |first=Bernard W. |date=2004-06-01 |title=The Serpentinite Multisystem Revisited: Chrysotile Is Metastable |url=https://doi.org/10.2747/0020-6814.46.6.479 |journal=International Geology Review |volume=46 |issue=6 |pages=479–506 |doi=10.2747/0020-6814.46.6.479 |bibcode=2004IGRv...46..479E |s2cid=98271088 |issn=0020-6814}}</ref> [[metamorphism]] of ferromagnesian minerals in mafic and [[ultramafic]] rocks, such as [[dunite]], [[harzburgite]], or [[lherzolite]]. These are rocks low in [[silica]] and composed mostly of [[olivine]] ({{chem2|(Mg(2+), Fe(2+))2SiO4}}), [[pyroxene]] ({{chem2|XY(Si,Al)2O6}}), and [[chromite]] (approximately {{chem2|FeCr2O4}}). Serpentinization is driven largely by [[Mineral hydration|hydration]] and [[oxidation]] of olivine and pyroxene to [[serpentine subgroup|serpentine group]] minerals (antigorite, lizardite, and chrysotile), [[brucite]] ({{chem2|Mg(OH)2}}), [[talc]] ({{chem2|Mg3Si4O10(OH)2}}), and [[magnetite]] ({{chem2|Fe3O4}}).<ref name=Moody1976>{{cite journal |last1=Moody |first1=Judith B. |title=Serpentinization: a review |journal=Lithos |date=April 1976 |volume=9 |issue=2 |pages=125–138 |doi=10.1016/0024-4937(76)90030-X|bibcode=1976Litho...9..125M }}</ref> Under the unusual chemical conditions accompanying serpentinization, water is the oxidizing agent, and is itself reduced to hydrogen, {{chem|[[hydrogen|H]]|2}}. This leads to further reactions that produce rare [[iron group]] [[native element mineral]]s, such as [[awaruite]] ({{chem|Ni|3|Fe}}) and [[native iron]]; [[methane]] and other [[hydrocarbon]] compounds; and [[hydrogen sulfide]].<ref name=":0" /><ref name=BerndtEtal1996>{{cite journal |last1=Berndt |first1=Michael E. |last2=Allen |first2=Douglas E. |last3=Seyfried |first3=William E. |title=Reduction of {{CO2}} during serpentinization of olivine at 300 °C and 500 bar |journal=Geology |date=1 April 1996 |volume=24 |issue=4 |pages=351–354 |doi=10.1130/0091-7613(1996)024<0351:ROCDSO>2.3.CO;2|bibcode=1996Geo....24..351B }}</ref> |
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During serpentinization, large amounts of water are absorbed into the rock, increasing the volume, reducing the density and destroying the original structure.{{sfn|Moody|1976|p=128-129}} The density changes from {{convert|3.3|to|2.5|g/cm3|abbr=on}} with a concurrent volume increase on the order of 30-40%.<ref name=Mevel2003>{{cite journal |last1=Mével |first1=Catherine |title=Serpentinization of abyssal peridotites at mid-ocean ridges |journal=Comptes Rendus Geoscience |date=September 2003 |volume=335 |issue=10–11 |pages=825–852 |doi=10.1016/j.crte.2003.08.006|bibcode=2003CRGeo.335..825M }}</ref> The reaction is highly [[exothermic]], releasing up to {{convert|40|kJ|kcal|sp=us}} per mole of water reacting with the rock, and rock temperatures can be raised by about {{convert|260|Celsius}},<ref name="LC">[http://www.lostcity.washington.edu/science/chemistry/serpentinization.html Serpentinization: The heat engine at Lost City and sponge of the oceanic crust]</ref><ref name="FruhGreenEtal20042">{{cite journal |last1=Früh-Green |first1=Gretchen L. |last2=Connolly |first2=James A.D. |last3=Plas |first3=Alessio |last4=Kelley |first4=Deborah S. |last5=Grobéty |first5=Bernard |date=2004 |title=Serpentinization of oceanic peridotites: Implications for geochemical cycles and biological activity |journal=Geophysical Monograph Series |volume=144 |pages=119–136 |bibcode=2004GMS...144..119F |doi=10.1029/144GM08 |isbn=0-87590-409-2}}</ref> providing an energy source for formation of non-volcanic [[hydrothermal vent]]s.<ref name=Lowell2002>{{cite journal |last1=Lowell |first1=R. P. |title=Seafloor hydrothermal systems driven by the serpentinization of peridotite |journal=Geophysical Research Letters |date=2002 |volume=29 |issue=11 |pages=1531 |doi=10.1029/2001GL014411|bibcode=2002GeoRL..29.1531L |doi-access=free }}</ref> The hydrogen, methane, and hydrogen sulfide produced during serpentinization are released at these vents and provide energy sources for deep sea [[chemotroph]] [[microorganism]]s.<ref name=FruhGreenEtal2004>{{cite journal |last1=Früh-Green |first1=Gretchen L. |last2=Connolly |first2=James A.D. |last3=Plas |first3=Alessio |last4=Kelley |first4=Deborah S. |last5=Grobéty |first5=Bernard |title=Serpentinization of oceanic peridotites: Implications for geochemical cycles and biological activity |journal=Geophysical Monograph Series |date=2004 |volume=144 |pages=119–136 |doi=10.1029/144GM08|bibcode=2004GMS...144..119F |isbn=0-87590-409-2 }}</ref><ref name=LC/> |
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===Formation of serpentine minerals === |
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Olivine is a [[solid solution]] of [[forsterite]], the [[magnesium]] endmember of {{chem2|(Mg(2+), Fe(2+))2SiO4}}, and [[fayalite]], the [[iron]] endmember, with forsterite typically making up about 90% of the olivine in ultramafic rocks.<ref name=SnowDick1995>{{cite journal |last1=Snow |first1=Jonathan E. |last2=Dick |first2=Henry J.B. |title=Pervasive magnesium loss by marine weathering of peridotite |journal=Geochimica et Cosmochimica Acta |date=October 1995 |volume=59 |issue=20 |pages=4219–4235 |doi=10.1016/0016-7037(95)00239-V|bibcode=1995GeCoA..59.4219S }}</ref> [[Serpentine subgroup|Serpentine]] can form from [[olivine]] via several reactions: |
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{{NumBlk|: |
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|{{overset|[[Forsterite]]|3 {{chem|Mg|2|SiO|4}}}} + {{overset|silicon dioxide|{{chem|SiO|2}}}} + 4 {{chem|H|2|O}} → {{overset|serpentine|2 {{chem|Mg|3|Si|2|O|5|(OH)|4}}}} |
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|{{EquationRef|Reaction 1a}}}} |
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{{NumBlk|: |
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|{{overset|[[Forsterite]]|2 {{chem|Mg|2|SiO|4}}}} + {{overset|water|3 {{chem|H|2|O}}}} → {{overset|serpentine|{{chem|Mg|3|Si|2|O|5|(OH)|4}}}} + {{overset|[[brucite]]|{{chem|Mg|(OH)|2}}}} |
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|{{EquationRef|Reaction 1b}}}} |
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Reaction 1a tightly binds silica, lowering its [[chemical activity]] to the lowest values seen in common rocks of the [[Earth's crust]].<ref name=FrostBeard2007>{{cite journal |last1=Frost |first1=B. R. |last2=Beard |first2=J. S. |title=On Silica Activity and Serpentinization |journal=Journal of Petrology |date=3 April 2007 |volume=48 |issue=7 |pages=1351–1368 |doi=10.1093/petrology/egm021|url=http://petrology.oxfordjournals.org/content/48/7/1351.full.pdf }}</ref> Serpentinization then continues through the hydration of olivine to yield serpentine and brucite (Reaction 1b).<ref name="Coleman77">{{cite book|last=Coleman|first=Robert G.|title=Ophiolites|date=1977|publisher=Springer-Verlag|isbn=978-3540082767|pages=100–101}}</ref> The mixture of brucite and serpentine formed by Reaction 1b has the lowest silica activity in the [[serpentinite]], so that the brucite phase is very important in understanding serpentinization.<ref name=FrostBeard2007/> However, the brucite is often blended in with the serpentine such that it is difficult to identify except with [[X-ray diffraction]], and it is easily altered under surface weathering conditions.{{sfn|Moody|1976|p=127}} |
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A similar suite of reactions involves [[pyroxene]]-group minerals: |
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{{NumBlk|: |
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|{{overset|[[Enstatite]]|3 {{chem|Mg|SiO|3}}}} + {{overset|silicon dioxide|{{chem|SiO|2}}}} + {{chem|H|2|O}} → {{overset|[[talc]]|{{chem|Mg|3|Si|4|O|10|(OH)|2}}}} |
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|{{EquationRef|Reaction 2a}}}} |
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{{NumBlk|: |
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|{{overset|[[Enstatite]]|6 {{chem|Mg|SiO|3}}}} + 3 {{chem|H|2|O}} → {{overset|serpentine|{{chem|Mg|3|Si|2|O|5|(OH)|4}}}} + {{overset|[[talc]]|{{chem|Mg|3|Si|4|O|10|(OH)|2}}}} |
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|{{EquationRef|Reaction 2b}}}} |
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Reaction 2a quickly comes to a halt as silica becomes unavailable, and Reaction 2b takes over.{{sfn|Frost|Beard|2007|p=1355}} When olivine is abundant, silica activity drops low enough that talc begins to react with olivine: |
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{{NumBlk|: |
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|{{overset|[[Forsterite]]|6 {{chem|Mg|2|SiO|4}}}} + {{overset|[[talc]]|{{chem|Mg|3|Si|4|O|10|(OH)|2}}}} + {{overset|water|9 {{chem|H|2|O}}}} → {{overset|serpentine|5 {{chem|Mg|3|Si|2|O|5|(OH)|4}}}} |
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|{{EquationRef|Reaction 3}}}} |
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This reaction requires higher temperatures than those at which brucite forms.{{sfn|Moody|1976|p=127}} |
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The final mineralogy depends both on rock and fluid compositions, temperature, and pressure. Antigorite forms in reactions at temperatures that can exceed {{convert|600|C|F|abbr=on}} during metamorphism, and it is the serpentine group mineral stable at the highest temperatures. Lizardite and chrysotile can form at low temperatures very near the Earth's surface.{{sfn|Moody|1976|p=125, 127, 131}} |
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===Breakdown of diopside and formation of rodingites=== |
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Ultramafic rocks often contain calcium-rich pyroxene ([[diopside]]), which breaks down according to the reaction: |
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{{NumBlk|: |
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|{{overset|[[Diopside]]|3 {{chem|Ca|Mg|Si|2|O|6}}}} + 6 {{chem|H|+}} → {{overset|serpentine|{{chem|Mg|3|Si|2|O|5|(OH)|4}}}} + 3 {{chem|Ca|2+}} + {{chem|H|2|O}} + {{overset|silicon dioxide|4 {{chem|SiO|2}}}} |
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|{{EquationRef|Reaction 4}}}} |
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This raises both the [[pH]], often to very high values, and the calcium content of the fluids involved in serpentinization. These fluids are highly reactive and may transport [[calcium]] and other elements into surrounding [[mafic]] rocks. Fluid reaction with these rocks may create [[metasomatism|metasomatic]] reaction zones enriched in calcium and depleted in silica, called [[rodingite]]s.{{sfn|Frost|Beard|2007|pp=1360-1362}} |
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===Formation of magnetite and hydrogen=== |
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{{See also|Schikorr reaction}} |
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In most crustal rock, the chemical activity of oxygen is prevented from dropping to very low values by the [[Mineral redox buffer#Common redox buffers and mineralogy|fayalite-magnetite-quartz (FMQ) buffer]].{{sfn|Moody|1976|p=129}} The very low chemical activity of silica during serpentinization eliminates this buffer, allowing serpentinization to produce highly [[Reduction (chemistry)|reducing]] conditions.<ref name=FrostBeard2007/> Under these conditions, water is capable of oxidizing ferrous ({{chem|Fe|2+}}) ions in fayalite. The process is of interest because it generates hydrogen gas:<ref name=":0" /><ref>{{cite web| title = Methane and hydrogen formation from rocks – Energy sources for life| url = http://www.lostcity.washington.edu/science/chemistry/methane.html| access-date = 2011-11-06}}</ref><ref>{{Cite journal| last = Sleep| first = N.H.| author2 = A. Meibom, Th. Fridriksson, R.G. Coleman, D.K. Bird| year = 2004| title = H<sub>2</sub>-rich fluids from serpentinization: Geochemical and biotic implications| journal = Proceedings of the National Academy of Sciences of the United States of America| volume = 101| issue = 35| pages = 12818–12823| doi = 10.1073/pnas.0405289101|bibcode = 2004PNAS..10112818S| pmid=15326313| pmc=516479| doi-access = free}}</ref> |
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{{NumBlk|: |
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|{{overset|[[Fayalite]]|3 {{chem|Fe|2|SiO|4}}}} + {{overset|water|2 {{chem|H|2|O}}}} → {{overset|[[magnetite]]|2 {{chem|Fe|3|O|4}}}} + {{overset|silicon dioxide|3 {{chem|SiO|2}}}} + {{overset|hydrogen|2 {{chem|H|2}}}} |
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|{{EquationRef|Reaction 5}}}} |
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However, studies of serpentinites suggest that iron minerals are first converted to [[wikt:ferroan|ferroan]] brucite, that is, brucite containing {{chem2|Fe(OH)2}},<ref>{{cite journal |last1=Bach |first1=Wolfgang |last2=Paulick |first2=Holger |last3=Garrido |first3=Carlos J. |last4=Ildefonse |first4=Benoit |last5=Meurer |first5=William P. |last6=Humphris |first6=Susan E. |title=Unraveling the sequence of serpentinization reactions: petrography, mineral chemistry, and petrophysics of serpentinites from MAR 15°N (ODP Leg 209, Site 1274) |journal=Geophysical Research Letters |date=2006 |volume=33 |issue=13 |pages=L13306 |doi=10.1029/2006GL025681|bibcode=2006GeoRL..3313306B |hdl=1912/3324 |s2cid=55802656 |hdl-access=free }}</ref> which then undergoes the [[Schikorr reaction]] in the anaerobic conditions of serpentinization:<ref name=Esource>{{cite journal |doi=10.1111/j.1472-4669.2010.00249.x|title=Serpentinization as a source of energy at the origin of life|year=2010|last1=Russell|first1=M. J.|last2=Hall|first2=A. J.|last3=Martin|first3=W.|journal=Geobiology|volume=8|issue=5|pages=355–371|pmid=20572872|s2cid=41118603 }}</ref><ref>{{cite journal |doi=10.2138/rmg.2013.75.18|title=Serpentinization, Carbon, and Deep Life|year=2013|last1=Schrenk|first1=M. O.|last2=Brazelton|first2=W. J.|last3=Lang|first3=S. Q.|journal=Reviews in Mineralogy and Geochemistry|volume=75|issue=1|pages=575–606|bibcode=2013RvMG...75..575S}}</ref> |
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{{NumBlk|: |
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|{{underset|ferrous hydroxide|6 {{chem|Fe|(OH)|2}}}} → {{underset|magnetite|2 {{chem|Fe|3|O|4}}}} + {{underset|water|4 {{chem|H|2|O}}}} + {{underset|hydrogen|2 {{chem|H|2}}}} |
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|{{EquationRef|Reaction 6}}}} |
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Maximum reducing conditions, and the maximum rate of production of hydrogen, occur when the temperature of serpentinization is between {{convert|200 and 315|C||sp=us}}<ref>{{cite journal |last1=McCollom |first1=Thomas M. |last2=Bach |first2=Wolfgang |title=Thermodynamic constraints on hydrogen generation during serpentinization of ultramafic rocks |journal=Geochimica et Cosmochimica Acta |date=February 2009 |volume=73 |issue=3 |pages=856–875 |doi=10.1016/j.gca.2008.10.032|bibcode=2009GeCoA..73..856M }}</ref> and when fluids are carbonate undersaturated.<ref name=":0" /> If the original ultramafic rock (the ''[[protolith]]'') is peridotite, which is rich in olivine, considerable magnetite and hydrogen are produced. When the protolith is pyroxenite, which contains more pyroxene than olivine, iron-rich talc is produced with no magnetite and only modest hydrogen production. Infiltration of silica-bearing fluids during serpentinization can suppress both the formation of brucite and the subsequent production of hydrogen.<ref>{{cite journal |last1=Klein |first1=Frieder |last2=Bach |first2=Wolfgang |last3=McCollom |first3=Thomas M. |title=Compositional controls on hydrogen generation during serpentinization of ultramafic rocks |journal=Lithos |date=September 2013 |volume=178 |pages=55–69 |doi=10.1016/j.lithos.2013.03.008|bibcode=2013Litho.178...55K }}</ref> |
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Chromite present in the protolith will be altered to chromium-rich magnetite at lower serpentinization temperatures. At higher temperatures, it will be altered to iron-rich chromite (ferrit-chromite).{{sfn|Moody|1976|p=128}} During serpentinization, the rock is enriched in [[chlorine]], [[boron]], [[fluorine]], and sulfur. Sulfur will be reduced to hydrogen sulfide and sulfide minerals, though significant quantities are incorporated into serpentine minerals, and some may later be reoxidized to sulfate minerals such as [[anhydrite]].<ref>{{Cite journal |last1=Debret |first1=Baptiste |last2=Andreani |first2=Muriel |last3=Delacour |first3=Adélie |last4=Rouméjon |first4=Stéphane |last5=Trcera |first5=Nicolas |last6=Williams |first6=Helen |date=2017-05-15 |title=Assessing sulfur redox state and distribution in abyssal serpentinites using XANES spectroscopy |url=https://www.sciencedirect.com/science/article/pii/S0012821X17300973 |journal=Earth and Planetary Science Letters |language=en |volume=466 |pages=1–11 |doi=10.1016/j.epsl.2017.02.029 |bibcode=2017E&PSL.466....1D |issn=0012-821X|doi-access=free |hdl=20.500.11850/207239 |hdl-access=free }}</ref> The sulfides produced include nickel-rich sulfides, such as [[mackinawite]].<ref>{{cite journal |last1=Delacour |first1=Adélie |last2=Früh-Green |first2=Gretchen L. |last3=Bernasconi |first3=Stefano M. |title=Sulfur mineralogy and geochemistry of serpentinites and gabbros of the Atlantis Massif (IODP Site U1309) |journal=Geochimica et Cosmochimica Acta |date=October 2008 |volume=72 |issue=20 |pages=5111–5127 |doi=10.1016/j.gca.2008.07.018|bibcode=2008GeCoA..72.5111D }}</ref> |
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===Methane and other hydrocarbons=== |
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Laboratory experiments have confirmed that at a temperature of {{convert|300|C||sp=us}} and pressure of 500 bars, olivine serpentinizes with release of hydrogen gas. In addition, methane and complex hydrocarbons are formed through reduction of carbon dioxide. The process may be catalyzed by magnetite formed during serpentinization.<ref name=BerndtEtal1996/> One reaction pathway is:<ref name=Esource/> |
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{{NumBlk|: |
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|{{overset|forsterite|18 {{chem|Mg|2|SiO|4}}}} + {{overset|fayalite|6 {{chem|Fe|2|SiO|4}}}} + 26 {{chem|H|2|O}} + {{chem|CO|2}} → {{overset|serpentine|12 {{chem|Mg|3|Si|2|O|5|(OH)|4}}}} + {{overset|magnetite|4 {{chem|Fe|3|O|4}}}} + {{overset|methane|{{chem|CH|4}}}} |
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|{{EquationRef|Reaction 7}}}} |
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===Metamorphism at higher pressure and temperature=== |
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Lizardite and chrysotile are stable at low temperatures and pressures, while antigorite is stable at higher temperatures and pressure.<ref>{{Cite journal |last=Evans |first=Bernard W. |date=2004-06-01 |title=The Serpentinite Multisystem Revisited: Chrysotile Is Metastable |journal=International Geology Review |volume=46 |issue=6 |pages=479–506 |doi=10.2747/0020-6814.46.6.479 |bibcode=2004IGRv...46..479E |s2cid=98271088 |issn=0020-6814}}</ref> Its presence in a serpentinite indicates either that serpentinization took place at unusually high pressure and temperature or that the rock experienced higher grade metamorphism after serpentinization was complete.<ref name="Moody1976" /> |
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Infiltration of {{CO2}}-bearing fluids into serpentinite causes distinctive ''[[Talc carbonate|talc-carbonate alteration]]''.<ref>{{cite journal |last1=Naldrett |first1=A. J. |title=Tale-Carbonate Alteration of some Serpentinized Ultramafic Rocks south of Timmins, Ontario |journal=Journal of Petrology |date=1 October 1966 |volume=7 |issue=3 |pages=489–499 |doi=10.1093/petrology/7.3.489}}</ref> Brucite rapidly converts to [[magnesite]] and serpentine minerals (other than antigorite) are converted to talc. The presence of [[pseudomorph]]s of the original serpentinite minerals shows that this alteration takes place after serpentinization.<ref name="Moody1976" /> |
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Serpentinite may contain [[chlorite group|chlorite]] (a [[phyllosilicate]] mineral), [[tremolite]] (Ca<sub>2</sub>(Mg<sub>5.0-4.5</sub>Fe<sup>2+</sup><sub>0.0-0.5</sub>)Si<sub>8</sub>O<sub>22</sub>(OH)<sub>2</sub>), and metamorphic olivine and [[diopside]] (calcium-rich pyroxene). This indicates that the serpentinite has been subject to more intense metamorphism, reaching the upper [[greenschist]] or [[amphibolite]] [[metamorphic facies]].<ref name="Moody1976" /> |
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Above about {{convert|450|C||sp=us}}, antigorite begins to break down. Thus serpentinite does not exist at higher metamorphic facies.<ref name=FruhGreenEtal2004/> |
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===Extraterrestrial production of methane by serpentinization=== |
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The presence of traces of [[Methane on Mars|methane in the atmosphere of Mars]] has been hypothesized to be a possible evidence for [[life on Mars (planet)|life on Mars]] if methane was produced by [[bacteria]]l activity. Serpentinization has been proposed as an alternative non-biological source for the observed methane traces.<ref>{{cite journal|jstor=27858733|title=Life on Mars?|date=March–April 2006|journal=American Scientist|volume=94|issue=2|pages=119–120|last1=Baucom|first1=Martin|doi=10.1511/2006.58.119}}</ref><ref>{{Cite web|url=https://www.esa.int/Our_Activities/Human_and_Robotic_Exploration/Exploration/ExoMars/The_methane_mystery|title=The methane mystery|last=esa|website=European Space Agency|language=en-GB|access-date=2019-04-22}}</ref> In 2022 it was reported that microscopic examination of the [[ALH 84001]] meteorite, which came from Mars, shows that indeed the organic matter it contains was formed by serpentinization, not by life processes.<ref>{{cite journal |display-authors=etal|last1=Andrew Steele |title=Organic synthesis associated with serpentinization and carbonation on early Mars |journal=Science |date=13 January 2022 |volume=375 |issue=6577 |pages=172–177 |doi=10.1126/science.abg7905|pmid=35025630 |bibcode=2022Sci...375..172S |s2cid=245933224 }}</ref><ref>{{cite journal |last1=Leah Crane |title=Mars: Organic compounds were made by water interacting with rocks |journal=New Scientist |date=22 January 2022 |url=https://www.newscientist.com/article/2304270-organic-compounds-on-mars-were-produced-by-water-and-rocks-not-life/}}</ref> |
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Using data from the [[Cassini–Huygens|Cassini]] probe flybys obtained in 2010–12, scientists were able to confirm that Saturn's moon [[Enceladus]] likely has a liquid water ocean beneath its frozen surface. A model suggests that the ocean on Enceladus has an alkaline [[pH]] of 11–12.<ref name="pH 2015">{{cite journal |title=The pH of Enceladus' ocean |journal=Geochimica et Cosmochimica Acta |date=16 April 2015 |last1=R. Glein |first1=Christopher |last2= Baross |first2= John A. |last3=Waite |first3=Hunter |doi=10.1016/j.gca.2015.04.017 |bibcode=2015GeCoA.162..202G |volume=162 |pages=202–219|arxiv=1502.01946 |s2cid=119262254 }}</ref> The high pH is interpreted to be a key consequence of serpentinization of [[chondrite|chondritic rock]], that leads to the generation of {{chem|H|2}}, a geochemical source of energy that can support both abiotic and biological synthesis of organic molecules.<ref name="pH 2015"/><ref>{{cite news |last=Wall |first=Mike |url=http://www.space.com/29334-enceladus-ocean-energy-source-life.html |title=Ocean on Saturn Moon Enceladus May Have Potential Energy Source to Support Life |work=Space.com |date=7 May 2015 |access-date=2015-05-08 }}</ref> |
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==Environment of formation== |
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[[Image:Gros Morne moho.jpg|thumb|Ophiolite of the [[Gros Morne National Park]], Newfoundland. Ophiolites characteristically have a serpentinite component.]] |
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Serpentinization occurs at [[mid-ocean ridges]], in the [[forearc]] mantle of [[subduction zone|subduction]] zones, in ophiolite packages, and in ultramafic intrusions. <ref name="GeologyDictionary" /><ref name=":2" /> |
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=== Mid-ocean ridges === |
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Conditions are highly favorable for serpentinization at slow to ultraslow spreading mid-ocean ridges.<ref name=Mevel2003/> Here the rate of [[crustal extension]] is high compared with the volume of magmatism, bringing ultramafic mantle rock very close to the surface where fracturing allows seawater to infiltrate the rock.<ref name=Lowell2002/> |
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Serpentinization at slow spreading mid-ocean ridges can cause the seismic Moho discontinuity to be placed at the serpentinization front, rather than the base of the crust as defined by normal petrological criteria.<ref>{{cite journal |last1=Minshull |first1=T. A. |last2=Muller |first2=M. R. |last3=Robinson |first3=C. J. |last4=White |first4=R. S. |last5=Bickle |first5=M. J. |title=Is the oceanic Moho a serpentinization front? |journal=Geological Society, London, Special Publications |date=1998 |volume=148 |issue=1 |pages=71–80 |doi=10.1144/GSL.SP.1998.148.01.05|bibcode=1998GSLSP.148...71M |s2cid=128410328 }}</ref><ref name="Mevel2003" /> The Lanzo Massif of the Italian Alps shows a sharp serpentinization front that may be a relict seismic Moho.<ref>{{cite journal |last1=Debret |first1=B. |last2=Nicollet |first2=C. |last3=Andreani |first3=M. |last4=Schwartz |first4=S. |last5=Godard |first5=M. |title=Three steps of serpentinization in an eclogitized oceanic serpentinization front (Lanzo Massif - Western Alps): ECLOGITIZED SERPENTINIZATION FRONT (LANZO) |journal=Journal of Metamorphic Geology |date=February 2013 |volume=31 |issue=2 |pages=165–186 |doi=10.1111/jmg.12008|s2cid=140540631 }}</ref> |
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=== Subduction Zones === |
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==== Forearc mantle ==== |
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Serpentinization is an important phenomenon in subduction zones that has a strong control on the water cycle and geodynamics of a subduction zone. <ref name=":3">{{Cite journal |last1=Xia |first1=Shaohong |last2=Sun |first2=Jinlong |last3=Huang |first3=Haibo |date=2017-05-31 |title=Degree of serpentinization in the forearc mantle wedge of Kyushu subduction zone |url=http://dx.doi.org/10.1190/igc2017-238 |journal=International Geophysical Conference, Qingdao, China, 17-20 April 2017 |pages=941–943 |publisher=Society of Exploration Geophysicists and Chinese Petroleum Society |doi=10.1190/igc2017-238}}</ref> Here mantle rock is cooled by the subducting slab to temperatures at which serpentinite is stable, and fluids are released from the subducting slab in great quantities into the ultramafic mantle rock.<ref name=":3" /> Direct evidence that serpentinization is taking place in the [[Mariana Islands]] [[island arc]] is provided by the activity of serpentinite [[mud volcano]]es. [[Xenolith]]s of harzburgite and (less commonly) dunite are occasionally erupted by the mud volcanoes, giving clues to the nature of the protolith.<ref name=HyndmanPeacock2003>{{cite journal |last1=Hyndman |first1=Roy D |last2=Peacock |first2=Simon M |title=Serpentinization of the forearc mantle |journal=Earth and Planetary Science Letters |date=July 2003 |volume=212 |issue=3–4 |pages=417–432 |doi=10.1016/S0012-821X(03)00263-2|bibcode=2003E&PSL.212..417H }}</ref> |
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Because serpentinization lowers the density of the original rock, serpentinization may lead to uplift or exhumation of serpentinites to the surface, as has taken place with the serpentinite exposed at the [[Presidio of San Francisco]] following cessation of subduction.<ref name="Presidio">{{cite web |title=Serpentinite |url=https://www.nps.gov/prsf/learn/nature/serpentinite.htm |website=Presidio of San Francisco |publisher=National Park Service |access-date=3 September 2021}}</ref> |
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Serpentinized ultramafic rock is found in many [[ophiolite]]s. Ophiolites are fragments of oceanic [[lithosphere]] that has been thrust onto continents, a process called ''[[obduction]]''. <ref>{{Cite web |date=2010-04-15 |title=Ophiolites |url=https://volcano.oregonstate.edu/volcanic-minerals/ophiolites |access-date=2022-11-20 |website=Volcano World |language=en}}</ref> They typically consist of a layer of serpentinized harzburgite (sometimes called ''alpine peridotite'' in older writings), a layer of hydrothermally altered [[diabase]]s and [[pillow basalt]]s, and a layer of deep water sediments containing radiolarian ribbon [[chert]].<ref>{{cite book |last1=Philpotts |first1=Anthony R. |last2=Ague |first2=Jay J. |title=Principles of igneous and metamorphic petrology |date=2009 |publisher=Cambridge University Press |location=Cambridge, UK |isbn=9780521880060 |edition=2nd |pages=370–372}}</ref> |
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[[File:Serpentinization Process at Subduction Zone.jpg|thumb|Hydration of [[forearc]] mantle due to the water expelled from deeper part of the subducting plate. Adapted from Hyndman and Peacock (2003)]] |
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=== Implications === |
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==== Limitation on earthquake depth ==== |
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[[Seismic wave]] studies can detect the presence of large bodies of serpentinite in the crust and upper mantle, since serpentinization has a huge impact on [[shear wave]] velocity. A higher degree of serpentinization will lead to lower shear wave velocity and higher [[Poisson's ratio]].<ref name=":1" /> Seismic measurements confirm that serpentinization is pervasive in forearc mantle.<ref name="HyndmanPeacock200322">{{cite journal |last1=Hyndman |first1=Roy D |last2=Peacock |first2=Simon M |date=July 2003 |title=Serpentinization of the forearc mantle |journal=Earth and Planetary Science Letters |volume=212 |issue=3–4 |pages=417–432 |bibcode=2003E&PSL.212..417H |doi=10.1016/S0012-821X(03)00263-2}}</ref> The serpentinization can produce an inverted [[Moho discontinuity]], in which seismic velocity abruptly ''decreases'' across the crust-mantle boundary, which is the opposite of the usual behavior. The serpentinite is highly deformable, creating an aseismic zone in the forearc, at which serpentinites slide at stable plate velocity. The presence of serpentinite may limit the maximum depth of [[Megathrust earthquake|megathrust earthquakes]] as they impede rupture into the forearc mantle.<ref name=":1">{{cite journal |last1=Bostock |first1=M. G. |last2=Hyndman |first2=R. D. |last3=Rondenay |first3=S. |last4=Peacock |first4=S. M. |date=May 2002 |title=An inverted continental Moho and serpentinization of the forearc mantle |journal=Nature |volume=417 |issue=6888 |pages=536–538 |bibcode=2002Natur.417..536B |doi=10.1038/417536a |pmid=12037564 |s2cid=3113794}}</ref> |
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==See also== |
==See also== |
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* [[Schikorr reaction]] |
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*[[Lost City (hydrothermal field)]] |
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* [[Serpentine subgroup]] |
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* [[Serpentinite]] |
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* [[Soapstone]] |
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* [[Hydrogen cycle]] |
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* [[Forearc]] |
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== References == |
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{{reflist}} |
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== External links == |
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{{commons category|Serpentinite}} |
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* [http://www.lostcity.washington.edu/story/Serpentinization] The Lost City hydrothermal field, [[Mid-Atlantic Ridge]]: serpentinization, the driving force of the system. |
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* [http://www.pnas.org/cgi/content/full/101/35/12818 H<sub>2</sub>-rich fluids from serpentinization: Geochemical and biotic implications]: [[Proceedings of the National Academy of Sciences]]. |
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{{Authority control}} |
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==References== |
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*[http://www.lostcity.washington.edu/science/chemistry/serpentinization.html Serpentinization: The Heat Engine at Lost City and Sponge of the Oceanic Crust] |
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*[http://www.pnas.org/cgi/content/full/101/35/12818 H2-rich fluids from serpentinization: Geochemical and biotic implications] |
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[[Category: |
[[Category:Metamorphic petrology]] |
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[[Category:Geological processes]] |
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{{geol-stub}} |
Latest revision as of 03:37, 13 November 2024
Serpentinization is a hydration and metamorphic transformation of ferromagnesian minerals, such as olivine and pyroxene, in mafic and ultramafic rock to produce serpentinite.[1] Minerals formed by serpentinization include the serpentine group minerals (antigorite, lizardite, chrysotile), brucite, talc, Ni-Fe alloys, and magnetite.[1][2] The mineral alteration is particularly important at the sea floor at tectonic plate boundaries.[3][4]
Formation and petrology
[edit]Serpentinization is a form of low-temperature (0 to ~600 °C) [5] metamorphism of ferromagnesian minerals in mafic and ultramafic rocks, such as dunite, harzburgite, or lherzolite. These are rocks low in silica and composed mostly of olivine ((Mg2+, Fe2+)2SiO4), pyroxene (XY(Si,Al)2O6), and chromite (approximately FeCr2O4). Serpentinization is driven largely by hydration and oxidation of olivine and pyroxene to serpentine group minerals (antigorite, lizardite, and chrysotile), brucite (Mg(OH)2), talc (Mg3Si4O10(OH)2), and magnetite (Fe3O4).[2] Under the unusual chemical conditions accompanying serpentinization, water is the oxidizing agent, and is itself reduced to hydrogen, H
2. This leads to further reactions that produce rare iron group native element minerals, such as awaruite (Ni
3Fe) and native iron; methane and other hydrocarbon compounds; and hydrogen sulfide.[1][6]
During serpentinization, large amounts of water are absorbed into the rock, increasing the volume, reducing the density and destroying the original structure.[7] The density changes from 3.3 to 2.5 g/cm3 (0.119 to 0.090 lb/cu in) with a concurrent volume increase on the order of 30-40%.[8] The reaction is highly exothermic, releasing up to 40 kilojoules (9.6 kcal) per mole of water reacting with the rock, and rock temperatures can be raised by about 260 °C (500 °F),[9][10] providing an energy source for formation of non-volcanic hydrothermal vents.[11] The hydrogen, methane, and hydrogen sulfide produced during serpentinization are released at these vents and provide energy sources for deep sea chemotroph microorganisms.[12][9]
Formation of serpentine minerals
[edit]Olivine is a solid solution of forsterite, the magnesium endmember of (Mg2+, Fe2+)2SiO4, and fayalite, the iron endmember, with forsterite typically making up about 90% of the olivine in ultramafic rocks.[13] Serpentine can form from olivine via several reactions:
+ + 4 H 2O → | (Reaction 1a) |
+ → + | (Reaction 1b) |
Reaction 1a tightly binds silica, lowering its chemical activity to the lowest values seen in common rocks of the Earth's crust.[14] Serpentinization then continues through the hydration of olivine to yield serpentine and brucite (Reaction 1b).[15] The mixture of brucite and serpentine formed by Reaction 1b has the lowest silica activity in the serpentinite, so that the brucite phase is very important in understanding serpentinization.[14] However, the brucite is often blended in with the serpentine such that it is difficult to identify except with X-ray diffraction, and it is easily altered under surface weathering conditions.[16]
A similar suite of reactions involves pyroxene-group minerals:
+ + H 2O → | (Reaction 2a) |
+ 3 H 2O → + | (Reaction 2b) |
Reaction 2a quickly comes to a halt as silica becomes unavailable, and Reaction 2b takes over.[17] When olivine is abundant, silica activity drops low enough that talc begins to react with olivine:
+ + → | (Reaction 3) |
This reaction requires higher temperatures than those at which brucite forms.[16]
The final mineralogy depends both on rock and fluid compositions, temperature, and pressure. Antigorite forms in reactions at temperatures that can exceed 600 °C (1,112 °F) during metamorphism, and it is the serpentine group mineral stable at the highest temperatures. Lizardite and chrysotile can form at low temperatures very near the Earth's surface.[18]
Breakdown of diopside and formation of rodingites
[edit]Ultramafic rocks often contain calcium-rich pyroxene (diopside), which breaks down according to the reaction:
+ 6 H+ → + 3 Ca2+ + H 2O + | (Reaction 4) |
This raises both the pH, often to very high values, and the calcium content of the fluids involved in serpentinization. These fluids are highly reactive and may transport calcium and other elements into surrounding mafic rocks. Fluid reaction with these rocks may create metasomatic reaction zones enriched in calcium and depleted in silica, called rodingites.[19]
Formation of magnetite and hydrogen
[edit]In most crustal rock, the chemical activity of oxygen is prevented from dropping to very low values by the fayalite-magnetite-quartz (FMQ) buffer.[20] The very low chemical activity of silica during serpentinization eliminates this buffer, allowing serpentinization to produce highly reducing conditions.[14] Under these conditions, water is capable of oxidizing ferrous (Fe2+
) ions in fayalite. The process is of interest because it generates hydrogen gas:[1][21][22]
+ → + + | (Reaction 5) |
However, studies of serpentinites suggest that iron minerals are first converted to ferroan brucite, that is, brucite containing Fe(OH)2,[23] which then undergoes the Schikorr reaction in the anaerobic conditions of serpentinization:[24][25]
→ + + | (Reaction 6) |
Maximum reducing conditions, and the maximum rate of production of hydrogen, occur when the temperature of serpentinization is between 200 and 315 °C (392 and 599 °F)[26] and when fluids are carbonate undersaturated.[1] If the original ultramafic rock (the protolith) is peridotite, which is rich in olivine, considerable magnetite and hydrogen are produced. When the protolith is pyroxenite, which contains more pyroxene than olivine, iron-rich talc is produced with no magnetite and only modest hydrogen production. Infiltration of silica-bearing fluids during serpentinization can suppress both the formation of brucite and the subsequent production of hydrogen.[27]
Chromite present in the protolith will be altered to chromium-rich magnetite at lower serpentinization temperatures. At higher temperatures, it will be altered to iron-rich chromite (ferrit-chromite).[28] During serpentinization, the rock is enriched in chlorine, boron, fluorine, and sulfur. Sulfur will be reduced to hydrogen sulfide and sulfide minerals, though significant quantities are incorporated into serpentine minerals, and some may later be reoxidized to sulfate minerals such as anhydrite.[29] The sulfides produced include nickel-rich sulfides, such as mackinawite.[30]
Methane and other hydrocarbons
[edit]Laboratory experiments have confirmed that at a temperature of 300 °C (572 °F) and pressure of 500 bars, olivine serpentinizes with release of hydrogen gas. In addition, methane and complex hydrocarbons are formed through reduction of carbon dioxide. The process may be catalyzed by magnetite formed during serpentinization.[6] One reaction pathway is:[24]
+ + 26 H 2O + CO 2 → + + | (Reaction 7) |
Metamorphism at higher pressure and temperature
[edit]Lizardite and chrysotile are stable at low temperatures and pressures, while antigorite is stable at higher temperatures and pressure.[31] Its presence in a serpentinite indicates either that serpentinization took place at unusually high pressure and temperature or that the rock experienced higher grade metamorphism after serpentinization was complete.[2]
Infiltration of CO2-bearing fluids into serpentinite causes distinctive talc-carbonate alteration.[32] Brucite rapidly converts to magnesite and serpentine minerals (other than antigorite) are converted to talc. The presence of pseudomorphs of the original serpentinite minerals shows that this alteration takes place after serpentinization.[2]
Serpentinite may contain chlorite (a phyllosilicate mineral), tremolite (Ca2(Mg5.0-4.5Fe2+0.0-0.5)Si8O22(OH)2), and metamorphic olivine and diopside (calcium-rich pyroxene). This indicates that the serpentinite has been subject to more intense metamorphism, reaching the upper greenschist or amphibolite metamorphic facies.[2]
Above about 450 °C (842 °F), antigorite begins to break down. Thus serpentinite does not exist at higher metamorphic facies.[12]
Extraterrestrial production of methane by serpentinization
[edit]The presence of traces of methane in the atmosphere of Mars has been hypothesized to be a possible evidence for life on Mars if methane was produced by bacterial activity. Serpentinization has been proposed as an alternative non-biological source for the observed methane traces.[33][34] In 2022 it was reported that microscopic examination of the ALH 84001 meteorite, which came from Mars, shows that indeed the organic matter it contains was formed by serpentinization, not by life processes.[35][36]
Using data from the Cassini probe flybys obtained in 2010–12, scientists were able to confirm that Saturn's moon Enceladus likely has a liquid water ocean beneath its frozen surface. A model suggests that the ocean on Enceladus has an alkaline pH of 11–12.[37] The high pH is interpreted to be a key consequence of serpentinization of chondritic rock, that leads to the generation of H
2, a geochemical source of energy that can support both abiotic and biological synthesis of organic molecules.[37][38]
Environment of formation
[edit]Serpentinization occurs at mid-ocean ridges, in the forearc mantle of subduction zones, in ophiolite packages, and in ultramafic intrusions. [3][4]
Mid-ocean ridges
[edit]Conditions are highly favorable for serpentinization at slow to ultraslow spreading mid-ocean ridges.[8] Here the rate of crustal extension is high compared with the volume of magmatism, bringing ultramafic mantle rock very close to the surface where fracturing allows seawater to infiltrate the rock.[11]
Serpentinization at slow spreading mid-ocean ridges can cause the seismic Moho discontinuity to be placed at the serpentinization front, rather than the base of the crust as defined by normal petrological criteria.[39][8] The Lanzo Massif of the Italian Alps shows a sharp serpentinization front that may be a relict seismic Moho.[40]
Subduction Zones
[edit]Forearc mantle
[edit]Serpentinization is an important phenomenon in subduction zones that has a strong control on the water cycle and geodynamics of a subduction zone. [41] Here mantle rock is cooled by the subducting slab to temperatures at which serpentinite is stable, and fluids are released from the subducting slab in great quantities into the ultramafic mantle rock.[41] Direct evidence that serpentinization is taking place in the Mariana Islands island arc is provided by the activity of serpentinite mud volcanoes. Xenoliths of harzburgite and (less commonly) dunite are occasionally erupted by the mud volcanoes, giving clues to the nature of the protolith.[42]
Because serpentinization lowers the density of the original rock, serpentinization may lead to uplift or exhumation of serpentinites to the surface, as has taken place with the serpentinite exposed at the Presidio of San Francisco following cessation of subduction.[43]
Serpentinized ultramafic rock is found in many ophiolites. Ophiolites are fragments of oceanic lithosphere that has been thrust onto continents, a process called obduction. [44] They typically consist of a layer of serpentinized harzburgite (sometimes called alpine peridotite in older writings), a layer of hydrothermally altered diabases and pillow basalts, and a layer of deep water sediments containing radiolarian ribbon chert.[45]
Implications
[edit]Limitation on earthquake depth
[edit]Seismic wave studies can detect the presence of large bodies of serpentinite in the crust and upper mantle, since serpentinization has a huge impact on shear wave velocity. A higher degree of serpentinization will lead to lower shear wave velocity and higher Poisson's ratio.[46] Seismic measurements confirm that serpentinization is pervasive in forearc mantle.[47] The serpentinization can produce an inverted Moho discontinuity, in which seismic velocity abruptly decreases across the crust-mantle boundary, which is the opposite of the usual behavior. The serpentinite is highly deformable, creating an aseismic zone in the forearc, at which serpentinites slide at stable plate velocity. The presence of serpentinite may limit the maximum depth of megathrust earthquakes as they impede rupture into the forearc mantle.[46]
See also
[edit]References
[edit]- ^ a b c d e Holm, N.G.; Oze, C.; Mousis, O.; Waite, J.H.; Guilbert-Lepoutre, A. (1 July 2015). "Serpentinization and the Formation of H2 and CH4 on Celestial Bodies (Planets, Moons, Comets)". Astrobiology. 15 (7): 587–600. Bibcode:2015AsBio..15..587H. doi:10.1089/ast.2014.1188. ISSN 1531-1074. PMC 4523005. PMID 26154779.
- ^ a b c d e Moody, Judith B. (April 1976). "Serpentinization: a review". Lithos. 9 (2): 125–138. Bibcode:1976Litho...9..125M. doi:10.1016/0024-4937(76)90030-X.
- ^ a b "Serpentine definition". Dictionary of Geology. Retrieved 23 October 2018.
- ^ a b Holm, N.g.; Oze, C.; Mousis, O.; Waite, J.h.; Guilbert-Lepoutre, A. (1 July 2015). "Serpentinization and the Formation of H2 and CH4 on Celestial Bodies (Planets, Moons, Comets)". Astrobiology. 15 (7): 587–600. Bibcode:2015AsBio..15..587H. doi:10.1089/ast.2014.1188. ISSN 1531-1074. PMC 4523005. PMID 26154779.
- ^ Evans, Bernard W. (1 June 2004). "The Serpentinite Multisystem Revisited: Chrysotile Is Metastable". International Geology Review. 46 (6): 479–506. Bibcode:2004IGRv...46..479E. doi:10.2747/0020-6814.46.6.479. ISSN 0020-6814. S2CID 98271088.
- ^ a b Berndt, Michael E.; Allen, Douglas E.; Seyfried, William E. (1 April 1996). "Reduction of CO2 during serpentinization of olivine at 300 °C and 500 bar". Geology. 24 (4): 351–354. Bibcode:1996Geo....24..351B. doi:10.1130/0091-7613(1996)024<0351:ROCDSO>2.3.CO;2.
- ^ Moody 1976, p. 128-129.
- ^ a b c Mével, Catherine (September 2003). "Serpentinization of abyssal peridotites at mid-ocean ridges". Comptes Rendus Geoscience. 335 (10–11): 825–852. Bibcode:2003CRGeo.335..825M. doi:10.1016/j.crte.2003.08.006.
- ^ a b Serpentinization: The heat engine at Lost City and sponge of the oceanic crust
- ^ Früh-Green, Gretchen L.; Connolly, James A.D.; Plas, Alessio; Kelley, Deborah S.; Grobéty, Bernard (2004). "Serpentinization of oceanic peridotites: Implications for geochemical cycles and biological activity". Geophysical Monograph Series. 144: 119–136. Bibcode:2004GMS...144..119F. doi:10.1029/144GM08. ISBN 0-87590-409-2.
- ^ a b Lowell, R. P. (2002). "Seafloor hydrothermal systems driven by the serpentinization of peridotite". Geophysical Research Letters. 29 (11): 1531. Bibcode:2002GeoRL..29.1531L. doi:10.1029/2001GL014411.
- ^ a b Früh-Green, Gretchen L.; Connolly, James A.D.; Plas, Alessio; Kelley, Deborah S.; Grobéty, Bernard (2004). "Serpentinization of oceanic peridotites: Implications for geochemical cycles and biological activity". Geophysical Monograph Series. 144: 119–136. Bibcode:2004GMS...144..119F. doi:10.1029/144GM08. ISBN 0-87590-409-2.
- ^ Snow, Jonathan E.; Dick, Henry J.B. (October 1995). "Pervasive magnesium loss by marine weathering of peridotite". Geochimica et Cosmochimica Acta. 59 (20): 4219–4235. Bibcode:1995GeCoA..59.4219S. doi:10.1016/0016-7037(95)00239-V.
- ^ a b c Frost, B. R.; Beard, J. S. (3 April 2007). "On Silica Activity and Serpentinization" (PDF). Journal of Petrology. 48 (7): 1351–1368. doi:10.1093/petrology/egm021.
- ^ Coleman, Robert G. (1977). Ophiolites. Springer-Verlag. pp. 100–101. ISBN 978-3540082767.
- ^ a b Moody 1976, p. 127.
- ^ Frost & Beard 2007, p. 1355.
- ^ Moody 1976, p. 125, 127, 131.
- ^ Frost & Beard 2007, pp. 1360–1362.
- ^ Moody 1976, p. 129.
- ^ "Methane and hydrogen formation from rocks – Energy sources for life". Retrieved 6 November 2011.
- ^ Sleep, N.H.; A. Meibom, Th. Fridriksson, R.G. Coleman, D.K. Bird (2004). "H2-rich fluids from serpentinization: Geochemical and biotic implications". Proceedings of the National Academy of Sciences of the United States of America. 101 (35): 12818–12823. Bibcode:2004PNAS..10112818S. doi:10.1073/pnas.0405289101. PMC 516479. PMID 15326313.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - ^ Bach, Wolfgang; Paulick, Holger; Garrido, Carlos J.; Ildefonse, Benoit; Meurer, William P.; Humphris, Susan E. (2006). "Unraveling the sequence of serpentinization reactions: petrography, mineral chemistry, and petrophysics of serpentinites from MAR 15°N (ODP Leg 209, Site 1274)". Geophysical Research Letters. 33 (13): L13306. Bibcode:2006GeoRL..3313306B. doi:10.1029/2006GL025681. hdl:1912/3324. S2CID 55802656.
- ^ a b Russell, M. J.; Hall, A. J.; Martin, W. (2010). "Serpentinization as a source of energy at the origin of life". Geobiology. 8 (5): 355–371. doi:10.1111/j.1472-4669.2010.00249.x. PMID 20572872. S2CID 41118603.
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External links
[edit]- [1] The Lost City hydrothermal field, Mid-Atlantic Ridge: serpentinization, the driving force of the system.
- H2-rich fluids from serpentinization: Geochemical and biotic implications: Proceedings of the National Academy of Sciences.