Seeking for the best conditions for fish fossil preservation in Las Hoyas Konservat-Lagerstätte using microbial mats

References

• Abed RMM, Polerecky L, Al Najjar M, de Beer D. 2006. Effect of temperature on photosynthesis, oxygen consumption and sulfide production in an extremely hypersaline cyanobacterial mat. Aquat Microb Ecol. 44:21–30. doi:10.3354/ame044021.
   Web of Science ®Google Scholar
• Abramoff MD, Magalhaes PJ, Ram SJ. 2004. Image Processing with ImageJ. Biophotonics International. 11(7):36–42.
   Google Scholar
• Adamczuk M, Ferencz B, Mieczan T, Dawidek J. 2019. Allochthonous subsidies as driving forces for development of plankton in an autotrophic, temperate, and small lake. Hydrobiologia. 846(1):59–73. doi: 10.1007/s10750-019-04052-9.
   Web of Science ®Google Scholar
• Alfonso MB, Brendel AS, Vitale AJ, Seitz C, Piccolo MC, Perillo GME. 2018. Drivers of ecosystem metabolism in two managed shallow lakes with different salinity and trophic conditions: The sauce grande and La Salada lakes (Argentina). Water (Switzerland). 10(9):1136. doi: 10.3390/w10091136.
   Google Scholar
• Alfonso MB, Vitale AJ, Menéndez MC, Perillo VL, Piccolo MC, Perillo GME. 2015. Estimation of ecosystem metabolism from diel oxygen technique in a saline shallow lake: La Salada (Argentina). Hydrobiologia. 752(1):223–237. doi: 10.1007/s10750-014-2092-1.
   Web of Science ®Google Scholar
• Babcock LE, Leslie SA, Elliot DH, Stigall AL, Ford LA, Briggs DE, Goodbred S, Miller M, Furbish D. 2006. The “preservation paradox”: microbes as a key to exceptional fossil preservation in the Kirkpatrick Basalt (Jurassic), Antarctica. Antarctica Sediment Rec. 4(4):4–8. doi: 10.2110/sedred.2006.4.4.
   Google Scholar
• Barral A, Gómez B, Fourel F, Daviero-Gomez V, Lécuyer C. 2017. CO2 and temperature decoupling at the million-year scale during the Cretaceous Greenhouse. Sci Rep. 7(1):8310. doi: 10.1038/s41598-017-08234-0.
   PubMedGoogle Scholar
• Berlanga M, Palau M, Guerrero R. 2022. Community homeostasis of coastal microbial mats from the Camargue during winter (cold) and summer (hot) seasons. Ecosphere. 13(2):e3922. doi: 10.1002/ecs2.3922.
   Web of Science ®Google Scholar
• Brett MT, Bunn SE, Chandra S, Galloway AWE, Guo F, Kainz MJ, Kankaala P, Lau DCP, Moulton TP, Power ME. 2017. How important are terrestrial organic carbon inputs for secondary production in freshwater ecosystems? Freshwater Biol. 62(5):833–853. doi: 10.1111/fwb.12909.
   Web of Science ®Google Scholar
• Burgener L, Hyland E, Reich BJ, Scotese C. 2023. Cretaceous climates: Mapping paleo-Köppen climatic zones using a bayesian statistical analysis of lithologic, paleontologic, and geochemical proxies. Palaeogeo, Palaeoclimat, Palaeoecol. 613:111373. doi:10.1016/j.palaeo.2022.111373.
   Google Scholar
• Buscalioni AD, Fregenal-Martínez M. 2010. A holistic approach to the palaeoecology of Las Hoyas Konservat-Lagerstätte (La Huérguina Formation, Lower Cretaceous, Iberian Ranges, Spain). J Iber Geol. 36(2):297–326. doi: 10.5209/rev_JIGE.2010.v36.n2.13.
   Web of Science ®Google Scholar
• Buscalioni AD, and Poyato-Ariza F. 2016. Las Hoyas: A unique Cretaceous Ecosystem. New Mexico Museum of Natural History and Science Bulletin: Cretaceous period: biotic diversity and biogeography. 71:51–63.
   Google Scholar
• Decker KLM, Potter CS, Bebout BM, Des Marais DJ, Carpenter S, Discipulo M, Hoehler TM, Miller SR, Thamdrup B, Turk KA, et al. 2005. Mathematical simulations of the O, S and C biogeochemistry of a hypersaline microbial mat. FEMS Microbiol Ecol. 52(3):377–395. doi:10.1016/j.femsec.2004.12.005.
   PubMed Web of Science ®Google Scholar
• De Kluijver A, Soetaert K, Czerny J, Schulz KG, Boxhammer T, Riebesell U, Middelburg JJ. 2013. A 13C labelling study on carbon fluxes in Arctic plankton communities under elevated CO2 levels. Biogeosciences. 10(3):1425–1440. doi: 10.5194/bg-10-1425-2013.
   Web of Science ®Google Scholar
• De Luca EH, Hamilton JG, Naidu S, Thomas RB, Andrews JA, Finzi A, Lavine M, Matamala R, Mohan JE, Hendrey GR, et al. 1999. Net Primary Production of a forest ecosystem with experimental CO2 enrichment. Science. 284(5417):1177–1179. doi: 10.1126/science.284.5417.1177.
   PubMed Web of Science ®Google Scholar
• De Wit R. 2016. Lake La Salada de Chiprana (NE Spain), an example of an athalassic salt lake in a cultural landscape. In: Nageeb RM, editor Lake sciences and climate change IntechOpen; pp. 43–60. doi:10.5772/64443.
   Google Scholar
• Dupraz C, Reid PR, Braissant O, Decho AW, Norman RS, Visscher PT. 2009. Processes of carbonate precipitation in modern microbial mats. Earth Sci Rev. 96(3):141–162. doi: 10.1016/j.earscirev.2008.10.005.
   Web of Science ®Google Scholar
• Epping E, Kúhl M. 2000. The responses of photosynthesis and oxygen consumption to short-term changes in temperature and irradiance in a cyanobacterial mat (Ebro Delta, Spain). Environ Microbiol. 2(4):465–474. doi: 10.1046/j.1462-2920.2000.00129.x.
   PubMed Web of Science ®Google Scholar
• Florín M, Montes C. 1998. Which are the relevant scales to assess primary production of Mediterranean semi-arid salt lakes? Int J Ecol Environ Sci. 24:161–177.
   Google Scholar
• Fregenal-Martínez M, Melendez N. 2016. Environmental reconstruction: a historical review. In: Poyato-Ariza F, and Buscalioni A, editors. Rhoyas: a Cretaceous wetland. Munchen: Friedrich Pfeil, Verlag; p. 14–28.
   Google Scholar
• Gromiec MJ. 1989. Reaeration. In: Jørgensen S Gromiec M, editors. Mathematical submodels in water quality systems. developments in environmental modelling 14. Amsterdam: Elsevier; pp. 33–64. doi: 10.1016/B978-0-444-88030-7.50002-0.
   Google Scholar
• Guerrero MC. 1991. Caracterización limnológica de la laguna Salada de Chiprana (Zaragoza, España) y sus comunidades de bacterias fototróficas. Limnetica. 7(1):83–96. doi: 10.23818/limn.07.07.
   Google Scholar
• Hall CAS, Moll R. 1975. Methods of assessing aquatic primary productivity. In: Lieth H Whittaker R, editors. Primary productivity of the biosphere. New York (NY): Springer Verlag; pp. 19–53. doi: 10.1007/978-3-642-80913-2_3.
   Google Scholar
• Haworth M, Hesselbo SP, McElwain JC, Robinson SA, James W. 2005. Mid-Cretaceous pCO2 based on stomata of the extinct conifer Pseudofrenelopsis (Cheirolepidiaceae). Geology. 33(9):749–752. doi: 10.1130/G21736.1.
   Web of Science ®Google Scholar
• Haywood AM, Valdes PJ, Markwick PJ. 2004. Cretaceous (Wealden) climates: a modelling perspective. Cretac Res. 25(3):303–311. doi: 10.1016/j.cretres.2004.01.005.
   Web of Science ®Google Scholar
• Iniesto M, Blanco-Moreno C, Villalba A, Buscalioni AD, Guerrero MC, López-Archilla AI. 2018. Plant tissue decay in long-term experiments with microbial mats. Geosciences. 8(11):387–408. doi: 10.3390/geosciences8110387.
   Web of Science ®Google Scholar
• Iniesto M, Buscalioni AD, Guerrero MC, Benzerara K, Moreira D, López-Archilla AI. 2016. Involvement of microbial mats in early fossilization by decay delay and formation of impressions and replicas of vertebrates and invertebrates. Sci Rep. 6(1):25716. doi: 10.1038/srep25716.
   PubMedGoogle Scholar
• Iniesto M, López-Archilla AI, Fregenal-Martínez MA, Buscalioni AD, Guerrero MC. 2013. Involvement of microbial mats in delayed decay: an experimental essay on fish preservation. Palaios. 28(1–2):56–66. doi: 10.2110/palo.2011.p11-099r.
   Web of Science ®Google Scholar
• Iniesto M, Laguna C, Florín F, Guerrero MC, Chicote A, Buscalioni AD, López-Archilla AI. 2015a. The impact of microbial mats and their microenvironmental conditions in early decay of fish. Palaios. 30(11):792–801. doi: 10.2110/palo.2014.086.
   Web of Science ®Google Scholar
• Iniesto M, Nina Z, López-Archilla AI, Sylvain B, Buscalioni AD, Guerrero MC, Benzerara K. 2015b. Preservation in microbial mats: mineralization by a talc-like phase of a fish embedded in a microbial sarcophagus. Front Earth Sci. 3(51):1–13. doi: 10.3389/feart.2015.00051.
   Google Scholar
• Iniesto M, Villalva I, Buscalioni AD, López-Archilla AI, López-Archilla AI. 2017. The effect of microbial mats in the decay of anurans with implications for understanding taphonomic processes in the fossil record. Sci Rep. 7(1):45160. doi: 10.1038/srep45160.
   PubMedGoogle Scholar
• Janssen K, Mähler B, Rust J, Bierbaum G, McCoy VE. 2022. The complex role of microbial metabolic activity in fossilization. Biol Rev. 97(2):449–465. doi: 10.1111/brv.12806.
   PubMed Web of Science ®Google Scholar
• Jodloswska S, Latala A. 2013. Combined effects of light and temperature on growth, photosynthesis, and pigment content in the mat-forming cyanobacterium Geitlerinema amphibium. Photosynthetica. 51(2):202–214. doi: 10.1007/s11099-013-0019-0.
   Web of Science ®Google Scholar
• Jonkers HM, Koh IO, Behrend P, Muyzer G, De BD. 2005. Aerobic organic carbon mineralization by sulfate-reducing bacteria in the oxygen-saturated photic zone of a hypersaline microbial mat. Microb Ecol. 49:291–300. doi:10.1007/s00248-004-0260-y.
   PubMed Web of Science ®Google Scholar
• Jonkers HM, Ludwig R, De Wit R, Pringault O, Muyzer G, Niemann H, Finke N, De Beer D. 2003. Structural and functional analysis of a microbial mat ecosystem from a unique permanent hypersaline inland lake: ‘La Salada de Chiprana’(NE Spain). FEMS Microbiol Ecol. 44(2):175–189. doi: 10.1016/S0168-6496(02)00464-6.
   PubMed Web of Science ®Google Scholar
• Kelly MG, Hornberger GM, Cosby BJ. 1974. Continuous automated measurement of rates of photosynthesis and respiration in an undisturbed river community. Limnol Oceanogr. 19(2):305–312. doi: 10.4319/lo.1974.19.2.0305.
   Web of Science ®Google Scholar
• Laas A, Nõges P, Kõiv T, Nõges T. 2012. High-frequency metabolism study in a large and shallow temperate lake reveals seasonal switching between net autotrophy and net heterotrophy. Hydrobiologia. 694(1):57–74. doi: 10.1007/s10750-012-1131-z.
   Web of Science ®Google Scholar
• Landwehrs J, Feulner G, Petri S, Sames B, Wagreich M. 2021. Investigating Mesozoic climate trends and sensitivities with a large ensemble of climate model simulations. Paleoceanogr Paleoclimatol. 36(6):e2020PA004134. doi: 10.1029/2020PA004134.
   PubMed Web of Science ®Google Scholar
• Lepock JR. 2005. How do cells respond to their thermal environment? Int J Hyperth. 21(8):681–687. doi: 10.1080/02656730500307298.
   PubMed Web of Science ®Google Scholar
• López-Archilla AI, Mollá S, Coleto MC, Guerrero MC, Montes C. 2004. Ecosystem metabolism in a Mediterranean shallow lake (Laguna de Santa Olalla, Doñana National Park, SW Spain). Wetlands. 24(4):848–858. doi: 10.1672/0277-5212(2004)024[0848:EMIAMS]2.0.CO;2.
   Web of Science ®Google Scholar
• Ludwig R, Al-Horani FA, de Beer D, Jonkers HM. 2005. Photosynthesis-controlled calcification in a hypersaline microbial mat. Limnol Oceanogr. 50(6):1836–1843. doi: 10.4319/lo.2005.50.6.1836.
   Web of Science ®Google Scholar
• Markager S, Sand-Jensen K. 1989. Patterns of night-time respiration in a dense phytoplankton community under a natural light regime. J Ecol. 44(1):49–61. doi: 10.2307/2260915.
   Google Scholar
• Mazière C, Bodo M, Perdrau MA, Cravo-Laureau C, Duran R, Dupuy C, Hubas C. 2022. Climate change influences chlorophylls and bacteriochlorophylls metabolism in hypersaline microbial mat. Sci Total Environ. 802:149787. doi:10.1016/j.scitotenv.2021.149787.
   PubMed Web of Science ®Google Scholar
• Mukundan MK, Antony PD, Nair MR. 1986. A review on autolysis in fish. Fish Res. 4(3–4):259–269. doi: 10.1016/0165-7836(86)90007-X.
   Web of Science ®Google Scholar
• [NOAA GML] National oceanic and atmospheric administration global monitoring laboratory. 2022. https://gml.noaa.gov/ccgg/
   Google Scholar
• Noffke N. 2021. Microbially induced sedimentary structures in clastic deposits: implication for the prospection for fossil life on Mars. Astrobiol. 21(7):866–892. doi: 10.1089/ast.2021.0011.
   PubMed Web of Science ®Google Scholar
• Noll P, Lilge L, Hausmann R, Henkel M. 2020. Modeling and exploiting microbial temperature response. Processes. 8(1):121. doi: 10.3390/pr8010121.
   Web of Science ®Google Scholar
• Odum EP. 1971. Fundamentals of ecology. 3 ed. Philadelphia: W.B. Saunders Copp. 1–574 pp.
   Google Scholar
• Odum HT. 1956. Primary production in flowing water. Limnol Oceanogr. 1(2):102–117. doi: 10.4319/lo.1956.1.2.0102.
   Web of Science ®Google Scholar
• Retallack GJ. 2011. Exceptional fossil preservation during CO2 greenhouse crises?: Palaeogeography, Palaeoclimatology. Palaeoecology. 307:59–74.
   Web of Science ®Google Scholar
• Russell BD, Connell SD, Findlay HS, Tait K, Widdicombe S, Mieszkowska N. 2013. Ocean acidification and rising temperatures may increase biofilm primary productivity but decrease grazer consumption. Phil Trans R Soc B. 368(1627):20120438. doi: 10.1098/rstb.2012.0438.
   PubMed Web of Science ®Google Scholar
• Sand-Jensen K, Staehr P. 2009. Net heterotrophy in Small Danish Lakes: A Widespread feature over gradients in trophic status and land cover. Ecosystems. 12(2):336–348. doi: 10.1007/s10021-008-9226-0.
   Web of Science ®Google Scholar
• Scharfenberger U, Jeppesen E, Beklioglu M, Søndergaard M, Angeler DG, Çakıroglu AI, Drakare S, Hejzlar J, Mahdy A, Papastergiadou E, et al. 2019. Effects of trophic status, water level, and temperature on shallow lake metabolism and metabolic balance: A standardized pan-European mesocosm experiment. Limnol Oceanogr. 64(2):616–631. doi: 10.1002/lno.11064.
   Web of Science ®Google Scholar
• Thyssen N, Erlandsen M, Jeppesen E, Ursin C. 1987. Reaeration of oxygen in shallow, macrophyte rich streams: I-Determination of the reaeration rate coefficient. Int Rev Gesamten Hydrobiol. 72(4):405–429. doi: 10.1002/iroh.19870720403.
   Google Scholar
• Visscher PT, Stolz JF. 2005. Microbial mats as bioreactors: populations, processes and products. Paelogeogr Paleoclimatol Paleoecol. 219(1–2):87–100. doi: 10.1016/j.palaeo.2004.10.016.
   Web of Science ®Google Scholar
• Zhang Y, Qi X, Wang S, Wu G, Briggs BR, Jiang H, Dong H, Hou W. 2020. Carbon fixation by photosynthetic mats along a temperature gradient in a Tengchong hot spring. JGR Biogeosciences. 125(9):e2020JG005719. doi: 10.1029/2020JG005719.
   Web of Science ®Google Scholar
• Zoboli O, Schilling K, Ludwig AL, Kreuzinger N, Zessner M. 2018. Primary productivity and climate change in Austrian lowland rivers. Water Sci Technol. 77(2):417–425. doi: 10.2166/wst.2017.553.
   PubMed Web of Science ®Google Scholar