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Stromatolite-thrombolite associations in a modern environment, Lee Stocking Island, Bahamas
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inferred← citeshttps://doi.org/10.1002/9781118280874.ch16openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118280874.ch8openalex-snapshot
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Do stromatolites need tides to trap ooids? Insights from a Cretaceous system of coastal‐wetlands
inferred← citeshttps://doi.org/10.1002/9781444312065.ch10openalex-snapshot
Microbes versus Metazoans as Dominant Reef Builders: Insights from Modern Marine Environments in the Exuma Cays, Bahamas
inferred← citeshttps://doi.org/10.1002/dep2.108openalex-snapshot
Controls on microbial and oolitic carbonate sedimentation and stratigraphic cyclicity within a mixed carbonate‐siliciclastic system: Upper Cambrian Wilberns Formation, Llano Uplift, Mason County, Texas, USA
inferred← citeshttps://doi.org/10.1002/gj.2663openalex-snapshot
Evolution of depositional settings in the Torrey area during the Smithian (Early Triassic, Utah, USA) and their significance for the biotic recovery
inferred← citeshttps://doi.org/10.1002/gj.4146openalex-snapshot
Microbial carbonate sequence architecture and depositional environments of Member IV of the Late Ediacaran Dengying Formation, Gaoshiti–Moxi area, Sichuan Basin, Southwest China
inferred← citeshttps://doi.org/10.1002/mmng.200600007openalex-snapshot
A Maastrichtian microbial reef and associated limestones in the Roca Formation of Patagonia (Neuquén Province, Argentina)
inferred← citeshttps://doi.org/10.1007/978-1-4020-8306-8_6openalex-snapshot
Diversity of Bahamian Microbialite Substrates
inferred← citeshttps://doi.org/10.1007/978-1-4020-9212-1_196openalex-snapshot
Microbialites, Stromatolites, and Thrombolites
inferred← citeshttps://doi.org/10.1007/978-3-319-13512-0_1openalex-snapshot
Interpreting Evaporite Textures
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Colonisation and bioerosion of marine bivalve shells from the Baltic Sea by euendolithic cyanobacteria: an experimental study
inferred← citeshttps://doi.org/10.1007/978-3-642-10415-2_16openalex-snapshot
Microbial Euendolithic Assemblages and Microborings in Intertidal and Shallow Marine Habitats: Insight in Cyanobacterial Speciation
inferred← citeshttps://doi.org/10.1007/978-3-642-10415-2_4openalex-snapshot
Modern Marine Stromatolites of Little Darby Island, Exuma Archipelago, Bahamas: Environmental Setting, Accretion Mechanisms and Role of Euendoliths
inferred← citeshttps://doi.org/10.1007/978-94-007-0397-1_10openalex-snapshot
Microbialites in the Middle–Upper Jurassic Ammonitico Rosso of the Southern Alps (Italy)
inferred← citeshttps://doi.org/10.1007/978-94-007-0397-1_13openalex-snapshot
Modern Marine Stromatolitic Structures: The Sediment Dilemma
inferred← citeshttps://doi.org/10.1007/bf02536885openalex-snapshot
Biosedimentology of Microbial Buildups IGCP Project No. 380 Proceedings of 2nd Meeting, Göttingen/Germany 1996
inferred← citeshttps://doi.org/10.1007/bf02537471openalex-snapshot
Microbialites and micro-encrusters in shallow coral bioherms (Middle to Late Oxfordian, Swiss Jura mountains)
inferred← citeshttps://doi.org/10.1007/s00442-016-3683-5openalex-snapshot
Coexisting living stromatolites and infaunal metazoans
inferred← citeshttps://doi.org/10.1007/s00531-001-0244-9openalex-snapshot
Stromatolitic fabric of authigenic carbonate crusts: result of anaerobic methane oxidation at cold seeps in 4,850 m water depth
inferred← citeshttps://doi.org/10.1007/s00531-012-0817-9openalex-snapshot
Mesoproterozoic biogenic thrombolites from the North China platform
inferred← citeshttps://doi.org/10.1007/s10347-007-0116-2openalex-snapshot
The role of microbes in reef-building communities of the Cannindah limestone (Mississippian), Monto region, Queensland, Australia
inferred← citeshttps://doi.org/10.1007/s10347-012-0321-5openalex-snapshot
Carnian (Triassic) aridization on the Levant margin: evidence from the M1 member, Mohilla Formation, Makhtesh Ramon, south Israel
inferred← citeshttps://doi.org/10.1007/s10347-013-0391-zopenalex-snapshot
Stromatolites in the Paratethys Sea during the Middle Miocene climate transition as witness of the Badenian salinity crisis
inferred← citeshttps://doi.org/10.1007/s10347-014-0417-1openalex-snapshot
Depositional facies and stratal cyclicity of dolomites in the Lower Qiulitag Group (Upper Cambrian) in northwestern Tarim Basin, NW China
inferred← citeshttps://doi.org/10.1007/s10347-016-0469-5openalex-snapshot
Microbialite elongation by means of coalescence: an example from the middle Furongian (upper Cambrian) Notch Peak Formation of western Utah
inferred← citeshttps://doi.org/10.1007/s10347-019-0572-5openalex-snapshot
Microbial-dominated carbonate depositional systems: a biosedimentary and stratigraphic reconstruction in the Late Triassic of Western Tethys (northern Calabria, Italy)
inferred← citeshttps://doi.org/10.1007/s10347-023-00661-yopenalex-snapshot
Bryoherms from the lower Sarmatian (upper Serravallian, Middle Miocene) of the Central Paratethys
inferred← citeshttps://doi.org/10.1007/s10347-025-00715-3openalex-snapshot
Exploring the influence of microbialite microfabrics and diagenetic evolution on reservoir quality: the key role of detailed petrography
inferred← citeshttps://doi.org/10.1007/s10347-026-00741-9openalex-snapshot
High-resolution facies analysis of the Upper Cambrian Pilgrim Limestone at Rendezvous Peak, Western Wyoming: Implications for carbonate factory dynamics and lithostratigraphic correlation
inferred← citeshttps://doi.org/10.1007/s11430-007-0132-7openalex-snapshot
Microbial carbonates in Holocene beachrocks, Shuiweiling, Luhuitou Peninsula, Hainan Island
inferred← citeshttps://doi.org/10.1007/s11430-008-0035-2openalex-snapshot
Modern microbialites and their environmental significance, Meiji reef atoll, Nansha (Spratly) Islands, South China Sea
inferred← citeshttps://doi.org/10.1007/s12549-016-0263-yopenalex-snapshot
New data on the incertae sedis biota and foraminifera of the mid-Famennian Baelen Member (Late Devonian, eastern Belgium)
inferred← citeshttps://doi.org/10.1007/s13146-021-00717-6openalex-snapshot
Microbiogenic thrombolites from the Cambrian Miaolingian Series of southern North China Craton
inferred← citeshttps://doi.org/10.1007/s13146-026-01314-1openalex-snapshot
Paleoenvironmental conditions recorded in a microbialitic level from the Paleocene–Eocene Maíz Gordo Formation, Northwestern Argentina
inferred← citeshttps://doi.org/10.1016/j.chemgeo.2013.10.002openalex-snapshot
Uranium concentrations and 238U/235U isotope ratios in modern carbonates from the Bahamas: Assessing a novel paleoredox proxy
inferred← citeshttps://doi.org/10.1016/j.crpv.2006.07.005openalex-snapshot
High-frequency palaeoenvironmental fluctuations recorded in Jurassic coral- and sponge-microbialite bioconstructions
inferred← citeshttps://doi.org/10.1016/j.crte.2003.10.024openalex-snapshot
Les microbialites de l'Anti-Atlas occidental (Maroc) : marqueurs stratigraphiques et témoins des changements environnementaux au Cambrien inférieur
inferred← citeshttps://doi.org/10.1016/j.earscirev.2019.05.007openalex-snapshot
‘Trapping and binding’: A review of the factors controlling the development of fossil agglutinated microbialites and their distribution in space and time
inferred← citeshttps://doi.org/10.1016/j.earscirev.2019.103065openalex-snapshot
Carbonates before skeletons: A database approach
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2019.103006openalex-snapshot
Short-term variation of ooid mineralogy in the Triassic-Jurassic boundary interval and its environmental implications: Evidence from the equatorial Ghalilah Formation, United Arab Emirates
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2021.103586openalex-snapshot
Microbialite development through the Ediacaran–Cambrian transition in China: Distribution, characteristics, and paleoceanographic implications
inferred← citeshttps://doi.org/10.1016/j.jop.2024.11.005openalex-snapshot
Origin and depositional environments of mounded, banded and bedded dolostones in the clastic deposits of the Paleoproterozoic Chuanlinggou Formation in Beijing, North China
inferred← citeshttps://doi.org/10.1016/j.jsames.2018.04.013openalex-snapshot
Biohermal thrombolites of the crater lake Rincón de Parangeo in Central México
inferred← citeshttps://doi.org/10.1016/j.margeo.2012.02.009openalex-snapshot
Characteristics, distribution and morphogenesis of subtidal microbial systems in Shark Bay, Australia
inferred← citeshttps://doi.org/10.1016/j.marpetgeo.2010.11.002openalex-snapshot
Sedimentation patterns during the Precambrian: A unique record?
inferred← citeshttps://doi.org/10.1016/j.marpetgeo.2016.07.003openalex-snapshot
Sequence stratigraphy of the Red River Formation, Williston Basin, USA: Stratigraphic signature of the Ordovician Katian greenhouse to icehouse transition
inferred← citeshttps://doi.org/10.1016/j.marpetgeo.2022.106085openalex-snapshot
Sedimentological and petrophysical heterogeneities controls on reservoir characterization of the Upper Triassic shallow marine carbonate Kurra Chine Formation, Northern Iraq: Integration of outcrop and subsurface data
inferred← citeshttps://doi.org/10.1016/j.marpetgeo.2024.106987openalex-snapshot
Diagenetic archives of the deeply-buried Cambrian Xiaoerbulake Formation microbialite reservoirs, Bachu-Tazhong area, Tarim Basin, China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2004.06.003openalex-snapshot
Palaeoenvironmental control on sponge-microbialite reefs and contemporaneous deep-shelf marl-limestone deposition (Late Oxfordian, southern Germany)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.08.030openalex-snapshot
Microbial deposits in upper Miocene carbonates, Mallorca, Spain
inferred← citeshttps://doi.org/10.1016/j.palaeo.2013.06.015openalex-snapshot
Geobiology of a lower Cambrian carbonate platform, Pedroche Formation, Ossa Morena Zone, Spain
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.06.007openalex-snapshot
Evidence for rapid precipitation of calcium carbonate in South China at the beginning of Early Triassic
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.05.015openalex-snapshot
A Permian-Triassic boundary microbialite deposit from the eastern Yangtze Platform (Jiangxi Province, South China): Geobiologic features, ecosystem composition and redox conditions
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.08.007openalex-snapshot
Environmental covariation of metazoans and microbialites in the Lower Ordovician Boat Harbour Formation, Newfoundland
inferred← citeshttps://doi.org/10.1016/j.palaeo.2018.01.043openalex-snapshot
The evolution of microbialite forms during the Early Triassic transgression: A case study in Chongyang of Hubei Province, South China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.109242openalex-snapshot
Interplay between biotic and environmental conditions in pre-salt Messinian microbialites of the western Mediterranean (Upper Miocene, Mallorca, Spain)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2025.113323openalex-snapshot
Palaeoenvironment and conodonts from the southern end of the Lower Ordovician carbonate platform of the Cuyania terrane, Central Argentina
inferred← citeshttps://doi.org/10.1016/j.palwor.2015.02.002openalex-snapshot
Microbialite concretions in a dolostone crust at the Permian–Triassic boundary of the Xishan section in Jiangsu Province, South China
inferred← citeshttps://doi.org/10.1016/j.palwor.2019.05.009openalex-snapshot
Stromatolite-dominated microbialites at the Permian–Triassic boundary of the Xikou section on South Qinling Block, China
inferred← citeshttps://doi.org/10.1016/j.precamres.2019.105593openalex-snapshot
Diverse thrombolites from the c. 2.4 Ga Turee Creek Group, Western Australia
inferred← citeshttps://doi.org/10.1016/j.quaint.2017.06.015openalex-snapshot
AMS Carbon-14 dating of microbial carbonates in Holocene coral reefs, Western Luzon, Philippines
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2004.02.004openalex-snapshot
An unusual Messinian succession in the Sinis Peninsula, western Sardinia, Italy
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2004.12.033openalex-snapshot
Steep microbial boundstone-dominated platform margins—examples and implications
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2011.06.014openalex-snapshot
An Upper Turonian fine-grained shallow marine stromatolite bed from the Muñecas Formation, Northern Iberian Ranges, Spain
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2011.09.006openalex-snapshot
Lagoon microbialites on Isla Angel de la Guarda and associated peninsular shores, Gulf of California (Mexico)
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2011.12.006openalex-snapshot
Dynamic controls on accretion and lithification of modern gypsum-dominated thrombolites, Los Roques, Venezuela
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2012.07.007openalex-snapshot
Impacts of flamingos on saline lake margin and shallow lacustrine sediments in the Kenya Rift Valley
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2013.05.008openalex-snapshot
Alternation of microbial mounds and ooid shoals (Middle Jurasssic, Morocco): Response to paleoenvironmental changes
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2013.11.003openalex-snapshot
Origin and significance of lamination in Lower Cretaceous stromatolites and proposal for a quantitative approach
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2014.08.006openalex-snapshot
Diversity and factors controlling widespread occurrence of syn-rift Ladinian microbialites in the western Tethys (Triassic Catalan Basin, NE Spain)
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2019.06.003openalex-snapshot
Microbialite fields developed in a protected rocky coastline: The shallow carbonate ramp of the Aptian Romualdo Formation (Araripe Basin, NE Brazil)
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2022.106257openalex-snapshot
Formation and preservation of Eocene lacustrine microbialites in the western Qaidam Basin (northeastern Qinghai-Tibetan Plateau, China): Petrological, mineralogical, and geochemical constraints
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2024.106781openalex-snapshot
Influence of stromatolites on petrophysical properties within stratigraphic contexts: A case study from the Dam Formation, eastern Saudi Arabia
inferred← citeshttps://doi.org/10.1016/j.sedgeo.2025.106847openalex-snapshot
Carbonate sedimentation and early diagenesis of the Doushantuo Formation, South China: A window into the terminal Proterozoic
inferred← citeshttps://doi.org/10.1016/s0016-7878(05)80043-4openalex-snapshot
Thrombolitic-Ortonella reefs and their bacterial diagenesis, Upper Visean Clifton Down Limestone, Bristol area, SW England
inferred← citeshttps://doi.org/10.1016/s0031-0182(01)00476-xopenalex-snapshot
Microbial carbonates as indicators of environmental change and biotic crises in carbonate systems: examples from the Late Devonian, Alberta basin, Canada
inferred← citeshttps://doi.org/10.1016/s0032-0633(99)00090-2openalex-snapshot
An ESA study for the search for life on Mars
inferred← citeshttps://doi.org/10.1016/s0037-0738(01)00146-4openalex-snapshot
Are reefs and mud mounds really so different?
inferred← citeshttps://doi.org/10.1016/s0037-0738(02)00319-6openalex-snapshot
Stratigraphic architecture and gamma ray logs of deeper ramp carbonates (Upper Jurassic, SW Germany)
inferred← citeshttps://doi.org/10.1016/s0037-0738(02)00379-2openalex-snapshot
Apparently homogenous “reef”-limestones built by high-frequency cycles
inferred← citeshttps://doi.org/10.1016/s0264-8172(03)00093-xopenalex-snapshot
Dynamic stratigraphy as a tool in economic mineral exploration: ultra-pure limestones (Upper Jurassic, SW Germany)
inferred← citeshttps://doi.org/10.1016/s0920-5446(08)00002-2openalex-snapshot
Chapter 2 The Palaeozoic larger benthic foraminifera: the Carboniferous and Permian
inferred← citeshttps://doi.org/10.1016/s1251-8050(01)01577-4openalex-snapshot
Implications de la présence de mud-mounds microbiens au Messinien (Sicile, Italie)
inferred← citeshttps://doi.org/10.1016/s1876-3804(25)60556-8openalex-snapshot
Lithofacies types, sedimentary cycles, and facies models of saline lacustrine hybrid sedimentary rocks: A case study of Neogene in Fengxi area, Qaidam Basin, NW China
inferred← citeshttps://doi.org/10.1017/s0016756805000907openalex-snapshot
Microbial–metazoan reefs of the terminal Proterozoic Nama Group ( c. 550–543 Ma), Namibia
inferred← citeshttps://doi.org/10.1023/a:1012229412462openalex-snapshot
The fauna of thrombolitic microbialites, Lake Clifton, Western Australia
inferred← citeshttps://doi.org/10.1038/ismej.2013.130openalex-snapshot
Active eukaryotes in microbialites from Highborne Cay, Bahamas, and Hamelin Pool (Shark Bay), Australia
inferred← citeshttps://doi.org/10.1038/s43247-025-02764-6openalex-snapshot
Seasonal biogeochemical variations in a modern microbialite reef under early Earth-like conditions
inferred← citeshttps://doi.org/10.1038/srep12601openalex-snapshot
Inner workings of thrombolites: spatial gradients of metabolic activity as revealed by metatranscriptome profiling
inferred← citeshttps://doi.org/10.1046/j.1365-3091.1997.d01-53.xopenalex-snapshot
Messinian stromatolite‐thrombolite associations, Santa Pola, SE Spain: an analogue for the Palaeozoic?
inferred← citeshttps://doi.org/10.1046/j.1365-3091.1999.00255.xopenalex-snapshot
Petrology of Lower Cretaceous carbonate mud mounds (Albian, N. Spain): insights into organomineralic deposits of the geological record
inferred← citeshttps://doi.org/10.1046/j.1365-3091.2000.00003.xopenalex-snapshot
Microbial carbonates: the geological record of calcified bacterial–algal mats and biofilms
inferred← citeshttps://doi.org/10.1046/j.1365-3091.2001.00372.xopenalex-snapshot
Microbial–silica interactions in Icelandic hot spring sinter: possible analogues for some Precambrian siliceous stromatolites
inferred← citeshttps://doi.org/10.1046/j.1365-3091.2003.00589.xopenalex-snapshot
Carbonate platform growth and cyclicity at a terminal Proterozoic passive margin, Infra Krol Formation and Krol Group, Lesser Himalaya, India
inferred← citeshttps://doi.org/10.1046/j.1365-3091.2003.00620.xopenalex-snapshot
Tepee‐shaped agglutinated microbialites: an example from a Famennian carbonate platform on the Lennard Shelf, northern Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.1080/00241160310004648openalex-snapshot
Patterns of Phanerozoic carbonate platform sedimentation
inferred← citeshttps://doi.org/10.1080/01490450590922532openalex-snapshot
Nonphotosynthetic Bacteria and the Formation of Carbonates and Evaporites Through Time
inferred← citeshttps://doi.org/10.1111/1462-2920.13094openalex-snapshot
Characterization of the stromatolite microbiome from L ittle D arby I sland, T he B ahamas using predictive and whole shotgun metagenomic analysis
inferred← citeshttps://doi.org/10.1111/1755-6724.12659openalex-snapshot
Reefs in the Early Paleozoic Taebaek Group, Korea: A Review
inferred← citeshttps://doi.org/10.1111/bre.12125openalex-snapshot
Stratigraphic modelling of platform architecture and carbonate production: a Messinian case study (Sorbas Basin, SE Spain)
inferred← citeshttps://doi.org/10.1111/gbi.12145openalex-snapshot
Grain trapping by filamentous cyanobacterial and algal mats: implications for stromatolite microfabrics through time
inferred← citeshttps://doi.org/10.1111/j.1365-3091.2003.00605.xopenalex-snapshot
Famennian microbial reef facies, Napier and Oscar Ranges, Canning Basin, western Australia
inferred← citeshttps://doi.org/10.1111/j.1365-3091.2006.00776.xopenalex-snapshot
Microbial primary dolomite from a Norian carbonate platform: northern Calabria, southern Italy
inferred← citeshttps://doi.org/10.1111/j.1365-3091.2011.01228.xopenalex-snapshot
Microbialites of the Neoproterozoic Beck Spring Dolomite, Southern California
inferred← citeshttps://doi.org/10.1111/j.1365-3091.2012.01336.xopenalex-snapshot
Lithofacies and cyclicity of Mohilla evaporite basins on the rifted margin of the Levant in the Late Triassic, Makhtesh Ramon, southern Israel
inferred← citeshttps://doi.org/10.1111/j.1472-4669.2010.00245.xopenalex-snapshot
Biogeochemical cycling and microbial diversity in the thrombolitic microbialites of Highborne Cay, Bahamas
inferred← citeshttps://doi.org/10.1111/j.1472-4669.2011.00279.xopenalex-snapshot
Discovery of large conical stromatolites in Lake Untersee, Antarctica
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1999.tb00550.xopenalex-snapshot
The term stromatolite: towards an essential definition
inferred← citeshttps://doi.org/10.1111/let.12378openalex-snapshot
Microbialites and trace fossils from a Middle Triassic restricted carbonate ramp in the Catalan Basin, Spain: evaluating environmental and evolutionary controls in an epicontinental setting
inferred← citeshttps://doi.org/10.1111/sed.12023openalex-snapshot
Controls on microbial activity and tidal flat evolution in Shark Bay, Western Australia
inferred← citeshttps://doi.org/10.1111/sed.12166openalex-snapshot
Microbial deposits in the aftermath of the end‐Permian mass extinction: A diverging case from the Mineral Mountains (Utah, USA )
inferred← citeshttps://doi.org/10.1111/sed.12304openalex-snapshot
Thrombolite fabrics and origins: Influences of diverse microbial and metazoan processes on Cambrian thrombolite variability in the Great Basin, California and Nevada
inferred← citeshttps://doi.org/10.1111/sed.12679openalex-snapshot
Late Cambrian microbial build‐ups, Llano Area, Central Texas: A three‐phase morphological evolution
inferred← citeshttps://doi.org/10.1111/sed.13048openalex-snapshot
Stromatolite‐rimmed thrombolite columns and domes constructed by microstromatolites, calcimicrobes and sponges in late Cambrian biostromes, Texas, USA
inferred← citeshttps://doi.org/10.1111/sed.13125openalex-snapshot
Sedimentary evolution and sequence stratigraphy of Ediacaran high‐grade phosphorite–dolomite–shale successions of the Bocaina Formation (Corumbá Group), Central Brazil: Implications for the Neoproterozoic phosphogenic event
inferred← citeshttps://doi.org/10.1111/sed.13185openalex-snapshot
Carbonate microbialites and chemotrophic microbes: Insights from caves from south‐east China
inferred← citeshttps://doi.org/10.1111/sed.13189openalex-snapshot
The hidden biotic face of microbialite morphogenesis – a case study from Laguna de Los Cisnes, southernmost Patagonia (Chile)
inferred← citeshttps://doi.org/10.1111/sed.13264openalex-snapshot
Carbonates and microbialites record a dynamic lake basin evolution in the Late Cretaceous to Eocene Sheep Pass Formation, Nevada, USA
inferred← citeshttps://doi.org/10.1130/0091-7613(2000)028<0919:moosrc>2.3.co;2openalex-snapshot
Microscale observations of sulfate reduction: Correlation of microbial activity with lithified micritic laminae in modern marine stromatolites
inferred← citeshttps://doi.org/10.1144/sp418.10openalex-snapshot
Pre-salt microbialites from the Campos Basin (offshore Brazil): image log facies, facies model and cyclicity in lacustrine carbonates
inferred← citeshttps://doi.org/10.1146/annurev-earth-042711-105327openalex-snapshot
The Meaning of Stromatolites
inferred← citeshttps://doi.org/10.1146/annurev.earth.27.1.313openalex-snapshot
STROMATOLITES IN PRECAMBRIAN CARBONATES: Evolutionary Mileposts or Environmental Dipsticks?
inferred← citeshttps://doi.org/10.1155/2020/6959532openalex-snapshot
Oceans, Lakes, and Stromatolites on Mars
inferred← citeshttps://doi.org/10.1306/02271412063openalex-snapshot
Depositional facies and platform architecture of microbialite-dominated carbonate reservoirs, Ediacaran–Cambrian Ara Group, Sultanate of Oman
inferred← citeshttps://doi.org/10.1306/06191312170openalex-snapshot
Topographic and sea level controls on oolite-microbialite-coralgal reef sequences: The terminal carbonate complex of southeast Spain
inferred← citeshttps://doi.org/10.1306/06261312174openalex-snapshot
Sedimentary features, occurrence, and cyclicity of microbialite facies in the Roubidoux and Jefferson City Formations of Missouri and Kansas
inferred← citeshttps://doi.org/10.1306/06261312182openalex-snapshot
Reservoir analog model for oolite-microbialite sequences, Miocene terminal carbonate complex, Spain
inferred← citeshttps://doi.org/10.1306/122903740479openalex-snapshot
Digital Reconstruction and Stratigraphic Evolution of a Microbial-Dominated, Isolated Carbonate Platform (Terminal Proterozoic, Nama Group, Namibia)
inferred← citeshttps://doi.org/10.1360/04yd0165openalex-snapshot
Middle and Late Devonian microbial carbonates, reefs and mounds in Guilin, South China and their sequence stratigraphic, paleoenvironmental and paleoclimatic significance
inferred← citeshttps://doi.org/10.14807/ijmp.v13i1.1573openalex-snapshot
Stromatolites - A life form that has witnessed the entire evolution of our planet
inferred← citeshttps://doi.org/10.1666/0094-8373(2000)026<0334:cmitsr>2.0.co;2openalex-snapshot
Calcified metazoans in thrombolite-stromatolite reefs of the terminal Proterozoic Nama Group, Namibia
inferred← citeshttps://doi.org/10.1669/0883-1351(2000)015<0087:tcomie>2.0.co;2openalex-snapshot
Taphonomic Control on Microstructure in Early Neoproterozoic Reefal Stromatolites and Thrombolites
inferred← citeshttps://doi.org/10.18261/9788294167128-2025-01openalex-snapshot
Ichnology of the Ediacaran–Cambrian Chapel Island Formation of Newfoundland, Canada: unraveling bioturbation at the onset of the Cambrian Explosion
inferred← citeshttps://doi.org/10.2110/jsr.2005.068openalex-snapshot
Quantitative Analysis and Paleoecology of Earliest Mississippian Microbial Reefs, Gudman Formation, Queensland, Australia: Not Just Post-Disaster Phenomena
inferred← citeshttps://doi.org/10.2110/jsr.2009.079openalex-snapshot
Insights on a Proposed Mid-Holocene Highstand Along the Northwestern Gulf of Mexico from the Evolution of Small Coastal Ponds
inferred← citeshttps://doi.org/10.2110/jsr.2020.166openalex-snapshot
Composite microbialites: Thrombolite, dendrolite, and stromatolite associations in a modern environment, Pozo Bravo lake, Salar de Antofalla, Catamarca Puna, Argentina
inferred← citeshttps://doi.org/10.2110/jsr.2020.74openalex-snapshot
The influence of benthic diatoms on the textures of carbonate-coated grains from a fluvial tufa spring in northern California
inferred← citeshttps://doi.org/10.2110/palo.2008.p08-001ropenalex-snapshot
TAPHONOMY OF MODERN MARINE BAHAMIAN MICROBIALITES
inferred← citeshttps://doi.org/10.2110/palo.2012.p12-022ropenalex-snapshot
CALCAREOUS TUBEWORMS AS DISASTER FORMS AFTER THE END-PERMIAN MASS EXTINCTION IN SOUTH CHINA
inferred← citeshttps://doi.org/10.2113/34.3.232openalex-snapshot
NEW SEM OBSERVATIONS OF KERIOTHECAL WALLS: IMPLICATIONS FOR THE EVOLUTION OF FUSULINIDA
inferred← citeshttps://doi.org/10.2113/gsrocky.36.2.81openalex-snapshot
Middle Cambrian offshore microbialites and shoaling successions, western Wyoming: Implications for regional paleography
inferred← citeshttps://doi.org/10.2113/gssajg.109.1-2.87openalex-snapshot
Affect of Sedimentation on Stromatolite Reef Growth and Morphology, Ediacaran Omkyk Member (Nama Group), Namibia
inferred← citeshttps://doi.org/10.2113/gssajg.117.2.173openalex-snapshot
DEPOSITIONAL ENVIRONMENT AND LITHOSTRATIGRAPHY OF THE PALEOPROTEROZOIC MOOIDRAAI FORMATION, KALAHARI MANGANESE FIELD, SOUTH AFRICA
inferred← citeshttps://doi.org/10.2139/ssrn.5735861openalex-snapshot
Controls on permeability variation of grain-dominated stromatolitic carbonates: Insights from high-resolution CT scanning
inferred← citeshttps://doi.org/10.2205/2025es001045openalex-snapshot
Middle Darriwilian Small Stromatolite Bioherms and Spheroids (Oncoids) From the Moyero River Section (Siberian Platform)
inferred← citeshttps://doi.org/10.3354/ame01895openalex-snapshot
Benthic microalgal variability associated with peritidal stromatolite microhabitats along the South African coast
inferred← citeshttps://doi.org/10.3354/meps12741openalex-snapshot
Macroinvertebrate variability between microhabitats of peritidal stromatolites along the South African coast
inferred← citeshttps://doi.org/10.3354/meps14585openalex-snapshot
Nutritional qualities partially predict diet of amphipod grazers: implications for modern coastal biofilms in microbialite pools
inferred← citeshttps://doi.org/10.3389/fmicb.2022.913452openalex-snapshot
Biospeleothems Formed by Fungal Activity During the Early Holocene in the “Salar de Uyuni”
inferred← citeshttps://doi.org/10.33899/earth.2019.170330openalex-snapshot
Sedimentary Environment of Naokelekan Formation (Late Oxfordian – Early Kimmeridgian) of Selected Surface Sections from Northern-East of Iraq
inferred← citeshttps://doi.org/10.35463/j.apr.2019.02.03openalex-snapshot
FACIES ASSOCIATIONS AND MICROFOSSILS FROM THE MIDDLE-UPPER TRIASSIC LIMESTONES OF THE TRANSILVANIAN NAPPES (PERȘANI MOUNTAINS, EASTERN CARPATHIANS, ROMANIA)
inferred← citeshttps://doi.org/10.3724/sp.j.1261.2013.00031openalex-snapshot
Environment controls on Mesoproterozoic thrombolite morphogenesis:A case study from the North China Platform
inferred← citeshttps://doi.org/10.3844/ojbsci.2022.87.111openalex-snapshot
About the Cyanobacteria and Stromatolites
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amr.734-737.388openalex-snapshot
Microbialites from the Upper Cambrian in the Tarim Basin, Northwest China: Implication for Depositional Environments
inferred← citeshttps://doi.org/10.4154/gc.2008.10openalex-snapshot
Abiogenic, microbial and hybrid authigenic crusts: components of Precambrian stromatolites
inferred← citeshttps://doi.org/10.5194/fr-9-183-2006openalex-snapshot
A Maastrichtian microbial reef and associated limestones in the Roca Formation of Patagonia (Neuquén Province, Argentina)
inferred← citeshttps://doi.org/10.5467/jkess.2013.34.5.381openalex-snapshot
Possibility for Heliotropism from Inclined Columns of Stromatolites, Socheong Island, Korea
inferred← citeshttps://doi.org/10.63313/cess.4006openalex-snapshot
Research Status and Progress of Thrombolite
inferred← citeshttps://doi.org/10.70675/1bb7cc95z8902z4904z81b8z7bf49d5038c5openalex-snapshot
4D paleoenvironmental evolution of the Early Triassic Sonoma Foreland Basin (western USA)
inferred← citeshttps://doi.org/10.70675/fdb2442ez35e8z469fz9df9z4a138be77b10openalex-snapshot
Facteurs de contrôle extrinsèques des dépôts microbiens récents en domaine de transition continental-marin
inferred← citeshttps://doi.org/10.7854/jpsk.2015.24.4.291openalex-snapshot
A Review on Microbialites: a Korean Perspective
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Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
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