Mississippian (Early Carboniferous) stromatolite mounds in a fore-reef slope setting, Laibin, Guangxi, South China

The Mississippian (Early Carboniferous) is generally a period of scarce carbonate buildups in South China. This study documents outcrops of stromatolite mounds at Mengcun and Helv villages, in Laibin City, Guangxi Province, South China. The stromatolite mounds contain various stromatolite morphologies including laminar, wavy-laminar, domal or hemispheroidal, bulbous, and flabellate-growth columns. Intramound rocks are brachiopod floatstone and dark thin-bedded laminated micrite limestone. Individual stromatolites at Mengcun village are generally 3–6 cm thick and morphologically represent relatively shallow-water laminar (planar and wavy-undulated stromatolites) and deeper-water domal, bulbous and columnar forms. Where mounds were formed, the stromatolites continued growing upward up to 60 cm thick. Thrombolitic fabrics also occur but are not common. Stromatolite microscopic structure shows the bulk of the lamination to consist of wavy microbialite and discrete thin micritic laminae. These mounds are intercalated in deep-water fore-reef talus breccia, packstone formed as a bioclastic debris flow and thin-bedded limestone containing common chert layers of the Tatang Formation (late Viséan). Further evidence supporting the deep-water setting of the stromatolite mounds are: (1) a laterally thinning horizon of brachiopod floatstone containing deep-water, small, thin-shelled brachiopods, peloidal micritic sediments and low-diversity, mixed fauna (e.g., thin-shelled brachiopods, tube-like worms and algae) that have been interpreted as storm deposits, (2) common fore-reef talus breccias, (3) lack of sedimentary structures indicating current action, (4) preservation of lamination with sponge spicules, and (5) lack of bioturbation suggesting that the stromatolites grew in a relatively low energy, deep-water setting. The stromatolite mounds are the first described stromatolite mounds in Mississippian strata of South China and contain evidence that supports interpretations of (1) growth history of Mississippian microbial buildups and (2) environmental controls on stromatolite growth and lithification.     

Fine‐grained agglutinated elongate columnar stromatolites: Tieling Formation,ca 1420 Ma,North China

The Mesoproterozoic Tieling Formation, near Jixian, northern China, contains thick beds of vertically branched, laterally elongate, columnar stromatolites. Carbonate mud is the primary component of both the stromatolites and their intervening matrix. Mud abundance is attributed to water column ‘whiting’ precipitation stimulated by cyanobacterial photosynthesis. Neomorphic microspar gives the stromatolites a ‘streaky’ microfabric and small mud flakes are common in the matrix. The columns consist of low‐relief, mainly non‐enveloping, laminae that show erosive truncation and well‐defined repetitive lamination. In plan view, the columns form disjunct elongate ridges <10 cm wide separated by narrow matrix‐filled runnels. The stromatolite surfaces were initially cohesive, rather than rigid, and prone to scour, and are interpreted as current aligned microbial mats that trapped carbonate mud. The pervasive ridge–runnel system suggests scale‐dependent biophysical feedback between: (i) carbonate mud supply; (ii) current duration, strength and direction; and (iii) growth and trapping by prolific mat growth. Together, these factors determined the size, morphology and arrangement of the stromatolite columns and their laminae, as well as their branching patterns, alignment and ridge–runnel spacing. Ridge–runnel surfaces resemble ripple mark patterns, but whether currents were parallel and/or normal to stromatolite alignment remains unclear. The formation and preservation of Tieling columns required plentiful supply of carbonate mud, mat‐building microbes well‐adapted to cope with this abundant sediment, and absence of both significant early lithification and bioturbation. These factors were time limited, and Tieling stromatolites closely resemble coeval examples in the Belt‐Purcell Supergroup of Laurentia. The dynamic interactions between mat growth, currents and sediment supply that determined the shape of Tieling columns contributed to the morphotypical diversity that characterizes mid–late Proterozoic branched stromatolites.     

Late Precambrian tidal-flat deposits and algal stromatolites in the Båtsfjord formation,East Finnmark,North Norway

The Annijokka Member of the Late Precambrian Båtsfjord Formation consists of about 300 m of siliciclastic and carbonate deposits which accumulated on tidal flats, and includes several horizons of stromatolite biostromes. Seven main lithofacies are arranged in fining-up cycles a few metres thick. The cycles are terrigenous in the lower part and carbonate-rich higher up and are interpreted as reflecting shallowing-up conditions of deposition. Lithofacies distribution in the member as a whole also shows an upward decrease in the terrigenous component and grain size and increase in carbonates, thus suggesting that the Annijokka Member is regressive.The stromatolite biostromes of the member contain domal forms composed of calcite while the non-stromatolitic, though possibly in part algal-laminated, carbonate-rich beds of the member are dolomitic. This contrasting mineralogy suggests (1) penecontemporaneous supratidal dolomitization, and (2) a possibly freshwater-influenced origin of the domal stromatolites.     

The role of endolithic cyanobacteria in the formation of lithified laminae in Bahamian stromatolites

The microboring activity of endolithic cyanobacteria plays a major role in the formation of the dominant lithified laminae in modern marine stromatolites in the Exuma Cays, Bahamas. These stromatolites are composed primarily of fine-grained carbonate sand that is trapped and bound by the filamentous cyanobacteria Schizothrix sp.. Periodic introduction of coccoid endolithic cyanobacteria Solentia sp. during hiatuses in stromatolite growth associated with very low rates of sedimentation results in the formation of lithified horizons, 200–1000 μm thick. These layers consist of micritized grains that are welded together at point contacts. The micritization is caused by extensive microboring and carbonate precipitation within boreholes concurrent with endolithic activity. Grain welding occurs when boreholes cross from one grain to another at point contacts. Thus, microboring destroys original grain textures but, at the same time, plays a constructional role in stromatolite growth by forming lithified layers of welded grains. These lateral bands of fused carbonate grains help to stabilize and preserve the stromatolite deposits.     

贺兰山地区中元古代微生物席成因构造

贺兰山中段中元古界黄旗口组石英砂岩中发现丰富的微生物席成因构造(MISS),包括由微生物席生长、破坏和腐烂过程形成的3种类型、9种不同形态的构造;与华北大红峪组发现的同类构造在成因类型与多样性方面具有很强的可对比性.砂岩中发育双向交错层理、冲洗层理、高角度单斜层理系和波痕,泥质粉砂岩夹层中发育波痕与泥裂,表明微生物席主要发育于潮间带上部至潮上带下部环境.MISS构造在华北地台长城系下部砂岩中的广泛存在表明在1.6 Ga前以蓝细菌为主的微生物群在环潮坪碎屑环境也很活跃.可能代表了微生物由海洋向陆地环境发展的过渡阶段.具光合作用功能的制氧蓝细菌的蓬勃发展可能是引发中元古代海洋化学条件发生转变、含氧量增高的重要原因,并为真核生物及宏观藻类的兴起创造了条件.研究表明,黄旗口组与华北大红峪组大致同时,反映了Columbia超大陆裂解期华北地台开始拉伸-张裂、缓慢沉降的构造古地理背景.     

Recent analog of gypsified microbial laminites and stromatolites in solar salt works and the Miocene gypsum deposits of Saudi Arabia and Egypt

Accumulation of microbial mats and stromatolites dominate in the crystallization ponds of solar salt works west of Alexandria, Egypt. These microbial mats are laminar in the permanent submerged part of the ponds. The microbial mats commonly form sites for growth of gypsum crystals during periods having higher salinity. In the dominant submerged part of the pond, domal stromatolites are common around groundwater seepage holes. In the shallow, intermittent margin of the ponds, the laminated microbial structure forms laterally close-linked hemispheroidal stromatolite type, with unidirectional and multidirectional ripple mark-like morphology on their surface. The microbial laminite and stromatolite types in the modern solar salt works are similar to the organic-rich Miocene gypsum beds of El-Barqan (west Alexandria, Egypt) and Rabigh (north Jeddah, Saudi Arabia). The Miocene organic-rich beds consist of interlayered dark-colored microbial laminae and light-colored gypsum laminae. These beds may have three different variations: regular even lamination, laterally closed-linked hemispheroidal stromatolites, and/or discrete hemispheroidal stromatolites. Petrographic examination of the microbial laminites and stromatolites in the solar salt works and the Miocene gypsum beds indicate that the dark-colored, organic-rich laminae are composed of micritized microbial laminae and/or brown organic filaments. In El-Barqan area, the light-colored gypsum-rich laminae are composed of either gypsum crystal fragments, or lenticular and prismatic gypsum. These gypsum crystals are either entrapped within the microbial filaments or are nucleated at the surface of the microbial laminae to form a radial pattern, whereas in Rabigh area, the light-colored gypsum-rich laminae are composed of secondary porphyrotopic, poikilotopic, or granular gypsum crystals. By comparison of the microbial structure in the Miocene gypsum beds with the recent occurrence of the microbial laminites and stromatolites in the solar salt works, it is demonstrated that the organic-rich Miocene gypsum beds were formed in a very shallow salina with slightly fluctuating brine levels.     

Possible indicators of microbial mat deposits in shales and sandstones: examples from the Mid-Proterozoic Belt Supergroup, Montana, U.S.A.

It has been suspected for some time that microbial mats probably colonized sediment surfaces in many terrigenous clastic sedimentary environments during the Proterozoic. However, domination of mat morphology by depositional processes, post-depositional compaction, and poor potential for cellular preservation of mat-building organisms make their positive identification a formidable challenge. Within terrigenous clastics of the Mid-Proterozoic Belt Supergroup, a variety of sedimentary structures and textural features have been observed that can be interpreted as the result of microbial colonization of sediment surfaces. Among these are: (a) domal buildups resembling stromatolites in carbonates; (b) cohesive behaviour of laminae during soft-sediment deformation, erosion, and transport; (c) wavy–crinkly character of laminae; (d) bed surfaces with pustular–wrinkled appearance; (e) rippled patches on otherwise smooth surfaces; (f) laminae with mica enrichment and/or randomly oriented micas; (g) irregular, curved–wrinkled impressions on bedding planes; (h) uparched laminae near mud-cracks resembling growth ridges of polygonal stromatolites; and (i) lamina-specific distribution of certain early diagenetic minerals (dolomite, ferroan carbonates, pyrite). Although in none of the described examples can it irrefutably be proven that they are microbial mat deposits, the observed features are consistent with such an interpretation and should be considered indicators of possible microbial mat presence in other Proterozoic sequences.     

Biostratigraphy and depositional environment of algal stromatolites from the Mescal Limestone (Proterozoic) of central Arizona

The Apache Group of central Arizona is subdivided into, from base upward, the Pioneer Formation, the Dripping Spring Quartzite and the Mescal Limestone. Radiometric age determinations by Silver, and Livingston and Damon indicate an age of 1.2–1.4 billion years. Within the Mescal Limestone, algal stromatolites form a conspicuous biostrome, commonly 20–25 m thick. The basal 1–5 m of the biostrome consists of up to three zones of digitate stromatolites, which often form discrete bush-like bioherms. These forms are interpreted as Baicalia baicalica, Parmites sp. and Tungussia sp.; the latter form previously reported by Cloud and Semikhatov (1969). The form Parmites is interpreted as a modification of digitate stromatolites probably by decrease in current velocity within the shallow marine environment, which allowed discrete heads to coalesce. Basal digitate forms are replaced upward in the biostrome by domal and undulatory laminated (stratiform) stromatolites, interpreted to represent gradual upward shoaling, with lower intertidal and subtidal forms (digitate morphology) being replaced by upper intertidal and possibly supratidal forms (stratiform types).The digitate form B. baicalica is suggested by Soviet workers to be indicative of Middle Riphean time (1350-950 m.y.). While many empirical data suggest the possibility of gross subdivision of Late Proterozoic time on the basis of algal stromatolite “zones”, the intercontinental applicability and the ultimate validity of this concept in unresolved.     

Comparative study of two relatives,MISS and Stromatolites: example from the Proterozoic Kunihar Formation,Simla Group,Lesser Himalaya

Comparison of microbially induced sedimentary structures (MISS) and stromatolitic bearing horizons from the Proterozoic Kunihar Formation, Simla Group, Lesser Himalaya, has been scrutinised to understand the formative processes and controls on MISS and stromatolites in the context of sedimentary facies and response to sea level fluctuations. MISS structures recorded are wrinkle structures, Kinneyia ripples, load casts, domal structures, sand chips, palimpsest and patchy ripples with limited desiccation cracks. Stromatolitic morphotypes recorded are solitary, branching, wavy and domal forms of stromatolites associated with ooids, peloids and fenestral laminae. MISS structures flourished within tidal flats to shallow intertidal while stromatolites mushroomed in environments ranging from tidal to deep subtidal. MISS structures were favoured by resistant substratum, low energy conditions, consistent water supply and low terrigenous input. Stromatolites boomed when the volume of carbonate accumulation exceeded siliciclastic deposition. Fluctuating environmental conditions and sediment budget controlled morphology of stromatolites. Owing to limited siliciclastic input during deposition of dolomudstones (characterizes transgressive systems tract), microbial growth was enhanced. Calcareous shales were deposited over dolomudstones which marks the maximum flooding surface (MFS) indicating the culmination of transgression. Deposition of storm-dominated sandstone-siltstone (FA1), wave-rippled sandstones (FA2), tide-dominated sandstones (FA3), heteroliths (FA4), wackestone-packestone (FA6), boundstone (FA7) and ooid-peloid grainstone (FA8) on top of the MFS reflects initiation of highstand systems tract (HST) which is mainly characterized by stromatolitic horizons, alternation of carbonates and siliciclastics with flourishing microbial activity. Eventually, increased sedimentation in upper part of Kunihar Formation marks late stage of regression.     

河北承德寒武系凤山组叠层石生物丘中的沉积组构

河北承德路通沟剖面芙蓉统凤山组中部发育厚层块状叠层石生物丘,构成一个淹没不整合型层序的强迫型海退体系域,指示这些叠层石形成于中高能浅海环境。该生物丘宏观上主要由柱状叠层石组成,叠层石内部纹层较粗糙,在构成叠层石的致密泥晶和微亮晶组构中,还见到球粒、底栖鲕粒及凝聚颗粒等多种生物成因颗粒类型,代表着复杂的微生物活动特征,以此而区别于前寒武纪的叠层石。更为重要的是,叠层石生物丘中的致密泥晶基质中发育一些“石松藻(Lithocodium)”状的钙化蓝细菌菌落残余物,以及一些丝状钙化蓝细菌化石,指示了形成叠层石的微生物席为蓝细菌所主导的微生物席。因此,凤山组叠层石生物丘内复杂而特殊的碳酸盐岩沉积组构为研究叠层石形成过程中复杂的微生物代谢活动所产生的钙化作用机制提供了一个宝贵的地质实例。     

Microbial mat structures in profile: The Neoproterozoic Sonia Sandstone,Rajasthan, India

Ubiquitous microorganisms, especially cyanobacteria preferably grow on the sediment surface thereby producing microbial mats. In the absence of grazers and bioturbators, microbial mat is a unique feature of the Proterozoic. Most of the papers so far published described a wide variety of bed surface microbial mat structures with rare illustrations from sections perpendicular to bedding. Nonetheless, bed surface exposures are relatively rare in rock records. This limitation of bed surface exposures in rock records suggest that a study of microbial mats in bed-across sections is needed. The 60 m thick coastal marine interval of the Sonia Sandstone Formation is bounded between two terrestrial intervals, a transgressive lag at the base and an unconformity at the top, and has been chosen for exploration of microbial mat structures in bed-across sections. A wide variety of microbial mat-induced structures in bed-across sections are preserved within the coastal interval of the Sonia Sandstone. Though many of these structures are similar in some aspects with bed surface structures, some of those presented here are new. The palaeogeographic range of these microbial structures extends from supralittoral to neritic. Diagenetic alterations of microbial mats produce pyrite and those zones are suitable for the preservation of microbial remains. SEM and EDAX analyses show fossil preservation of filamentous microbial remains that confirm the presence of microbial mats within the coastal interval of the Sonia Sandstone. Effects of proliferation of microbial mats in the siliciclastic depositional setting are numerous. The mat-cover on sediment surfaces hinders reworking and/or erosion of the sediments thereby increases the net sedimentation rate. Successive deposition and preservation of thick microbial mat layer under reducing environments should have a great potential for hydrocarbon production and preservation and therefore these Proterozoic formations could be a target for exploration.     

Origin of Cretaceous phosphorites from the onshore of Tamil Nadu,India

Cretaceous phosphorites from the onshore of Tamil Nadu have been investigated for their origin and compared with those in the offshore. Cretaceous phosphorites occur as light brown to yellowish brown or white nodules in Karai Shale of the Uttatur Group in the onshore Cauvery basin. Nodules exhibit phosphatic nucleus encrusted by a chalky shell of carbonate. The nucleus of the nodules consists of light and dark coloured laminae, phosphate peloids/coated grains and detrital particles interspersed between the laminae. Scanning electron microscope (SEM) studies reveal trapping and binding activity of microbial filaments. A mat structure with linearly arranged microbial filaments and hollow, cell-based coccoid cyanobacterial mat are present. Nodules contain abundant carbonate fluorapatite, followed by minor calcite, quartz and feldspar. The P₂O₅ content of the phosphorites ranges from 18 to 26%. The CaO/P₂O₅, Sr and F contents are higher than that of pure carbonate fluorapatite. Concentrations of Si, Al, K, Fe, and Ti are low. We suggest that the nuclei of the nodules represent phosphate clasts related to phosphate stromatolites formed at intertidal conditions. At high energy levels the microbial mats were disintegrated into phosphate clasts, coated with carbonate and then reworked into Karai Shale. On the other hand, Quaternary phosphorites occur as irregular to rounded, grey coloured phosphate clasts at water depths between 180 and 320m on the continental shelf of Tamil Nadu. They exhibit grain-supported texture. Despite Quaternary in age, they also resemble phosphate stromatolites of intertidal origin and reworked as phosphate clasts onto the shelf margin depressions. Benthic microbial mats probably supplied high phosphorus to the sediments. Availability of excess phosphorus seems to be a pre-requisite for the formation of phosphate stromatolites.     

The preservation potential of some recent stromatolites

Stromatolites are laminated organo-sedimentary structures, generally compared to present day blue-green algal mats. Their morphology, species composition and overall extent are largely governed by the amount of wetting, although other factors such as competition, predation and desiccation, also contribute. The Trucial Coast mats are essentially intertidal. Stromatolite accretion rates in this area are of the order of 0·2 mm p.a. but lamina growth is far from regular. The area is also characterized by the development of evaporites, especially gypsum which proves to be an important agent of mat destruction. The growth of crystals causes disruption within the upper portions of the stromatolite section with the result that none of the upper intertidal mat forms are preserved. Other agencies of destruction include bacterial decay, desiccation and dehydration, and compaction under burial which may depress and deform the original mat relief. Decay results in the almost total loss of cellular contents, only a few empty sheaths and the pigment surviving into the fossil record. Preservation may be effected via (a) burial or (b) lithification. However, few modern algal mat structures bear any resemblance to fossil stromatolite heads with the exception of those from Shark Bay. From this, one might infer that pene-contemporaneous lithification is a prerequisite for their preservation.     

豫西寒武纪叠层石演化特征及其与后生动物的耦合关系

作为微生物席建造物的叠层石记录了大量的古环境和古地理信息,在豫西寒武系出露18层叠层石,以宏观和微观沉积特征为基础,依据各组段叠层石丰度(层厚度)和分异度(形态类型)的演化,将豫西寒武纪叠层石划分为6个演化组合。从叠层石组合的微观纹层、微生物化石及其微生物席演化等方面,结合沉积学和生物化石特征,探讨了豫西寒武纪叠层石的幕式演化,分别为微生物岩-叠层石演化幕和微生物岩-灰岩演化幕。以中寒武世灰岩中微生物岩与遗迹化石的密度关系为例,并从整个寒武纪微生物岩与后生动物化石之间关系的角度分析,认为叠层石微生物岩演化与后生动物之间并非只是简单的“此消彼长”,而是一种动态平衡的耦合关系。     

Temporal and environmental significance of microbial lamination: Insights from Recent fluvial stromatolites in the River Piedra,Spain

Despite extensive research, the environmental and temporal significance of microbial lamination is still ambiguous because of the complexity of the parameters that control its development. A 13 year monitored record of modern fast‐accreting calcite stromatolites (mean 14 mm year^?1) from artificial substrates installed in rapid flow in the River Piedra (north‐east Spain) allows comparison of the sedimentological attributes of successive six‐month depositional packages with the known climatic, hydrophysical and hydrochemical parameters of the depositional system. The stromatolites are formed of dense, porous and macrocrystalline composite laminae. The dense and porous composite laminae, which are composed of two to eight laminae consisting largely of calcified cyanobacteria, are characterized by: (i) dense composite laminae, up to 15 mm thick, mostly with successive dense laminae and minor alternating dense and porous laminae; and (ii) porous composite laminae, up to 12 mm thick, consisting mainly of porous laminae alternating with thinner dense laminae. Most of the dense composite laminae formed during the warm periods (April to September), whereas most of the porous composite laminae developed in the cool periods (October to March). Each dense and porous composite lamina represents up to or slightly longer than six months. The alternation of these two types of composite laminae parallels seasonal changes in temperature. The dense and porous laminae result from shorter (for example, intraseasonal) variations in temperature, insolation and hydrological conditions. The macrocrystalline laminae, with crystals >100 μm long, occur isolated and grouped into composite laminae up to 1·7 mm thick. Their occurrence suggests the absence or poor development of microbial mats over periods of weeks to several months. Thus, stromatolite lamination can record different‐order, periodic and non‐periodic changes in the magnitude of environmental parameters over a single year. These results hold important implications for the temporal and environmental interpretation of lamination in microbial structures.     

现代叠层石的多样化构成:认识古代叠层石形成的关键和窗口*

自从Kalkowsky在1908年构筑了叠层石的术语之后,叠层石一直是地质学家采用不同方法研究和思考的主题,而且一直被当作证明地球早期生命历史的代表物而得到深入调查。叠层石确实为地球早期生命历史提供了间接而且复杂的证据,所以,现代叠层石确实代表着明显的生物信号而成为研究的焦点。最为引人注目的是,现代叠层石的多样化构成,确实表明了蓝细菌生物席建造了叠层石,而且进一步表明了微生物席转化成叠层石不是一个直接的作用过程。那些反映现代叠层石多样化构成的典型实例包括:(1)南极Untersee地区的湖泊相锥状泥质叠层石;(2)新西兰North群岛被称为煎锅湖的热水湖泊中以及美国黄石国家公园热泉中的硅质叠层石;(3)巴哈马台地、澳大利亚鲨鱼湾以及巴西东南部海湾碳酸盐沉积物构成的叠层石。由于蓝细菌微生物席是否代表了古代叠层石的形态学前体总是存在争议,而且在生命的图像中叠层石一直是一个迷惑的关键片段,因此,现代叠层石的多样化构成,将成为认识古代叠层石形成的关键和窗口。立足于前人的研究成果,追踪和总结现代叠层石的多样化构成,以及它们所代表的沉积作用和微生物新陈代谢活动丰富而复杂的信息,将不但丰富微生物沉积学的研究内容,还将拓宽沉积相分析的基本内容,对深入了解叠层石复杂的沉积学特征和生物学属性具有重要的科学意义。     

微生物席沉积学:一个年轻的沉积学分支

现代实例和岩石记录的研究表明,微生物席是一个特别的微生物群落,这个特殊的微生物群落就像一个复杂的食物网一样,群落中的每一个组成成员紧密相互依赖,从而构成了地球上形成最早、延续时间最长的生态系.微生物席在沉积岩中留下了丰富而且复杂的记录,在碳酸盐岩中最为典型的产物就是叠层石,在碎屑岩中最具有代表性的产物就是"微生物诱发的...     

The calcium carbonate saturation state in cyanobacterial mats throughout Earth’s history

Through early lithification, cyanobacterial mats produced vast amounts of CaCO₃ on Precambrian carbonate platforms (before 540 Myr ago). The superposition of lithified cyanobacterial mats forms internally laminated, macroscopic structures known as stromatolites. Similar structures can be important constituents of Phanerozoic carbonate platforms (540 Myr to present). Early lithification in modern marine cyanobacterial mats is thought to be driven by a metabolically-induced increase of the CaCO₃ saturation state (Ω_CaCO3) in the mat. However, it is uncertain which microbial processes produce the Ω_CaCO3 increase and to which extent similar Ω_CaCO3 shifts were possible in Precambrian oceans whose chemistry differed from that of the modern ocean. I developed a numerical model that calculates Ω_CaCO3 in cyanobacterial mats and used it to tackle these questions. The model is first applied to simulate Ω_CaCO3 in modern calcifying cyanobacterial mats forming at Highborne Cay (Bahamas); it shows that while cyanobacterial photosynthesis increases Ω_CaCO3 considerably, sulphate reduction has a small and opposite effect on mat Ω_CaCO3 because it is coupled to H₂S oxidation with O₂ which produces acidity. Numerical experiments show that the magnitude of the Ω_CaCO3 increase is proportional to DIC in DIC-limited waters (DIC < 3-10 mM), is proportional to pH when ambient water DIC is not limiting and always proportional to the concentration of Ca²⁺ in ambient waters. With oceanic Ca²⁺ concentrations greater than a few millimolar, an appreciable increase in Ω_CaCO3 occurs in mats under a wide range of environmental conditions, including those supposed to exist in the oceans of the past 2.8 Gyr. The likely lithological expression is the formation of the microsparitic stromatolite microtexture—indicative of CaCO₃ precipitation within the mats under the control of microbial activity—which is found in carbonate rocks spanning from the Precambrian to recent. The model highlights the potential for an increase in the magnitude of the Ω_CaCO3 shift in cyanobacterial mats throughout Earth’s history produced by a decrease in salinity and temperature of the ocean, a decrease in atmospheric pCO₂ and an increase in solar irradiance. Such a trend would explain how the formation of the microsparitic stromatolite microtexture was possible as the Ω_CaCO3 of the ocean decreased from the Paleoproterozoic to the Phanerozoic.     

Stromatolites of the lower Missoula Group (Middle Proterozoic), Belt Supergroup,Glacier National Park,Montana

The mode of formation and environmental setting of stromatolites from the lower Missoula Group (ca. 1.1·10⁹ years old) in Glacier National Park, Montana, have been determined. The stromatolite-bearing interval in the lower Missoula Group was deposited in a shallow, intermittently exposed setting of very low relief, the stromatolites forming during periods of submergence. In situ carbonate precipitation was the dominant process involved in the formation of encrusting stromatolitic laminae. This precipitate was deposited within, and probably beneath, algal mats, most likely as a result of the photosynthetic removal of carbon dioxide by the mat-building microscopic algae. Calcite also was precipitated in several types of open-space structures occurring within these stromatolites. Other laminae were produced by the organic stabilization of detrital particles; by the solely physical accumulation of terrigenous material; and probably, by bacterially induced precipitation of iron sulfide which was later oxidized to form hematite layers.Three forms of filamentous microfossils, two of which appear to be oscillatoriacean cyanophytes and the third of which is probably either a cyanophyte or filamentous bacterium, have been detected in these structures. In addition, hematitic pillar-shaped microstructures, interpreted to have been produced by filamentous bacteria, are abundant locally.In gross morphology, the lower Missoula Group stromatolites are simple, unbranched, domal structures ranging from several millimeters to several decimeters in both height and diameter. Physical conditions played a major role in determining the macrostructure of these stromatolites. Of particular importance were the shape of the positive sediment-surface irregularities upon which the stromatolites initially formed, the rate of sedimentation between stromatolite colonies, and the deposition of layers of terrigenous material on stromatolite growth surfaces. The effect of biological factors on stromatolite structure is clearly seen in those portions of stromatolites relatively free of terrigenous material; biological activity was apparently greatest on positive irregularities of the growth surface, resulting in preferential enhancement of such irregularities and development of second- and higher-order hemispheroidal structures.