Modern and fossil siliciclastic sediments colonized by microbial mats. A comparative study for analog determination.

Authors

  • Diana G. Cuadrado Instituto Argentino de Oceanografía-CONICET- Florida 7000 - 8000, Bahía Blanca. Universidad Nacional del Sur. Dto Geología. San Juan 670 - 8000, Bahía Blanca.
  • Adriana M. Blasi CIC-Div. Miner. Petrol y Sedim. Museo de La Plata FCNYM-UNLP. Paseo del Bosque S/N -1900, La Plata.

Keywords:

Lamination, Bioestabilization, Ichnites preservation, Fossil and modern records, Atlantic coast, Argentina.

Abstract

The present study is based on the comparison between siliciclastic sedimentary deposits of both, paleo- and modern environments in which microbial activity has been recognized in sediments, leading to the establishment of analogues. This fact leads up to the characterization of microbial sedimentary structures and the comprehension of the physical- chemical and biological processes of their formation and modification. Different characteristics are com- pared in both environments: sedimentary fabrics, grain size, mineralogical composition presence of microorganisms or microbial activity remnants, and sedimentary structures. The objective is to under- stand the occurrence of such characteristics, the mechanisms of formation that acted in the past and their relationship with the environmental conditions. In addition, the presence of microbial mats in the fossil environment is discussed as an agent for the preservation of the ichnites and archaeological remains after an early lithification.

The archaeological localities of “La Olla” and “Monte Hermoso I” are studied (Fig. 1). They are characterized by an excellent conservation of organic remains associated with human activity, and the preservation of human footprints, respectively. Both deposits are Holocene sediments, currently located in the lower- and middle- intertidal area of a modern beach. The remarkable preservation of traces of extinct mammals (the most remarkable is the huge ground sloth Megatherium), birds, and vertebrates at

 

the Pehuen Có paleoichnological site, has also been documented. These sediments correspond to late Pleistocene, and are currently located in the upper- intertidal zone where is sometimes covered by sand after storm events. All these fossil sedimentary deposits are located on the coast of SE Buenos Aires. Modern environments, Bahía Blanca Estuary and the paleo-channel of Paso Seco, were studied (Fig. 1). Several microbial induced sedimentary structures have been found and were related to the hydrodynamic processes.

Direct observation of microbial sedimentary structures present in the supra-tidal zone of Bahia Blanca Estuary and coastal area in Paso Seco were compared with sedimentary structures expose in the fossil deposits. Also, various analyses to determine the sedimentary arrangement and textural features have been applied. Micrographs obtained from the scanning electron microscope (SEM) have allowed the identification of the interaction of the sediments with microorganisms, recognizing the substances generated by them (EPS, extracellular polymeric substances) and the presence of authigenic mine- rals, such as pyrite as geochemical product of the bacterial metabolism. Analysis of thin sections show the sedimentary fabric associated with the presence of cyanobacteria. X-ray analysis allowed determining authigenic minerals such as biogenic calcite, magnesian calcite, and dolomite.

The relevant characteristics of the deposits asso- ciated with the presence of microbial activity are documented in detail. The identification of millimeter to centimeter thickness lamination, fine and coarse sedimentation stands out (Fig. 2) which is the most remarkable characteristic of the presence of microbial activity recognized as biolamination (Fig. 4). This

alternation can be clearly documented in modern environment with specific details as light crinkled lamination and the presence of EPS that amalgamate the siliciclastic grains. Thin and coarse alternation contributes to another common characteristic that is the bimodal distribution in granulometric sediment analyses (Fig. 4). Petrographic thin sections were observed under a petrographic microscope (Fig. 5). Both environments, ancient and modern sediments, present similar characteristics. The biolamination with diffuse border in the fossil sample, sometimes waving, in light and dark brown laminae can be appreciated. The biolaminites can be discriminated in modern samples. The alternation with coarse sediment (sands) reflects the hydrodynamic condi- tions of the area, a change towards a greater energy level. Micrographs obtained from SEM under fossil samples reveal the presence of bacteria, EPS, diatoms, and authigenic minerals as pyrite (Figs. 6, 7). The micrographs from the modern environment show the sedimentological-biological relationship in the microbial mat and authigenic precipitates.

Several microbial sedimentary structures were recognized in La Olla site (Fig. 8). They are: a) biolamination; b) presence of bubbles generated by microorganism metabolisms and entrapped by biofilm; c) elephant skin texture; d) plant and arqueological rests entrapped by the microbial mat colonization; e) microbial folds; f) mat deformation. Also, in El Pisadero site in the archaeological locality Monte Hermoso I, an special configuration were observed that was defined as deformed structure by load pressure and injection of underlying mat, related to the weight of individuals that had walked on the microbial mat surface (Fig. 8h, i). In the Pehuen Có paleo-ichnological site, the most conspicuous structures are the huge ground sloths footprints with a marginal erosioned rim exposing the lamination (Fig. 9). There is also a high ichnodiversity preservation of mammal and bird tracks showing the high vertebrate biodiversity du- ring the late Pleistocene in southern South America. To confirm the presence of microbial mats, several others microbial sedimentary structures and textures were recognized, biolaminites, wrinkle marks, bubbles, colonized plant rests, mat chips, desiccation cracks, and preserved ripples. The laminated siltstone erosion is common. In the colonized modern supra-tidal plain in Bahía Blanca Estuary, several microbial sedimentary structures

related to physical processes as storm events were documented: flipped-over mats, erosional pockets, microbial mat chips, and desiccation cracks with recolonization due to successive inundation. In Paso Seco, the characteristic cohesive and flexible behavior of mats was recognized by the presence of microbial domes with diameter > 12 cm (Fig. 10), and deformed microbial structures as folds, and roll- ups. These structures are formed as a consequence of water friction associated to high tide-related currents flooding in an ancient channel. The mat growing in the supratidal area during calm conditions may involve several days or months when the tide reaches the zone during spring-tides. It can also grow over shells or plants in the modern or fossil sites (Figs. 8c, 11).

The mat activity can be inferred by the formation of bubbles or domes with different sizes depending on the microbial thickness and different stages of evolution (Fig. 12). Similar bubbles were found in the fossil environment and analogous process can be suggested to their formation (Fig. 13). Also, the ancient or modern desiccation cracks represent constant periods of exposition in a supratidal zone. Conversely, other sedimentary structures are formed as a response to physical process as water currents or waves acting on microbial mats (Fig. 14). In that case, erosional pockets and remnants, microbial chips, and folds were compared in the fossil and mo- dern environments. The characteristically plasticity and cohesiveness of the microbial mat under wet conditions favors mat deformation.

Finally, the relevance of microbial mats in modi- fying the erosional threshold, and the conditions needed for the formation of footprints over a microbial mat are discussed. Also, the role of microbial mats in the preservation of ichnites by means of stability and early lithification is recognized.

References

Andersen, T.J. y M. Pejrup, 2011. Biological influences on sedi- ment behavior and transport. En E. Wolanski y D.S. McLusky (Eds.), Treatise on Estuarine and Coastal Science 2. Academic Press, Waltham: 289-309.

Aramayo, S.A. y T. Manera de Bianco, 1987. Hallazgo de una icnofauna continental (Pleistoceno tardío) en la localidad de Pehuén Có, Provincia de Buenos Aires, Argentina. IV Congreso Latinoamericano de Paleontología Actas Parte II: Carnivora, Artiodactyla y Aves:532–547, Santa Cruz de la Sierra, Bolivia. Aramayo, S.A. y T. Manera de Bianco, 1989. Nuevos hallazgos de mamíferos pleistocénicos en el yacimiento de Playa del Barco, provincia de Buenos Aires. 1° Jornadas Geológicas Bonae­

renses Actas:701-712, Tandil.

Aramayo, S.A. y T. Manera de Bianco, 2009. Late Quaternary palaeoichnological sites from the southern Atlantic coast of Buenos Aires Province, Argentina: Mammal, Bird and Hominid Evidence. Ichnos 16:25-32.

Aramayo, S.A., T. Manera de Bianco, N. Bastianelli y R. Melchor,

Pehuen Có: Updated taxonomic review of a late Pleistocene ichnological site in Argentina. Palaeogeography, Palaeoclimatology, Palaeoecology 439:144-165.

Aref, M., M.H. Basyoni y G.H. Bachmann, 2014. Microbial and

physical sedimentary structures in modern evaporitic coastal environments of Saudi Arabia and Egypt. Facies 60:371-388.

Baumgartner, L.K., R.P. Reid, C. Dupraz, A.W. Decho, D.H.

Buckley, J.R. Spear, K.M. Przekop y P.T. Visscher, 2006. Sulfate reducing bacteria in microbial mats: Changing para- digms, new discoveries. Sedimentary Geology 185:131-145.

Bayon, C. y G. Politis, 1996. Estado actual de las investigaciones

en el sitio Monte Hermoso I. Revista Arqueología 6:83-115.

Bayón, C., T. Manera, G. Politis y S. Aramayo, 2011. Following the Tracks of the First South Americans. Evolution: Education and Outreach 4-2:205-216.

Blasi, A., G. Politis y M.C. Bayón, 2013. Palaeo-environmental reconstruction of La Olla, a Holocene archaeological site in the Pampean coast. Journal of Archaeological Science 40:1554- 1567.

Bose, S. y H.S. Chafetz, 2009. Topographic control on distribution of modern microbially induced sedimentary structures (MISS): a case study from Texas coast. Sedimentary Geology 213:136-149.

Bournod, C.N., D.G. Cuadrado, N.B. Carmona, J.J. Ponce y J. Pan, 2014. Estructuras sedimentarias inducidas por actividad microbiana (ESIAM) en la planicie de marea de Puerto Rosales, estuario de Bahía Blanca. Revista de la Asociación Geológica Argentina 71:331-344.

Carmona, N.B., C.A. Bournod, J.J. Ponce y D.G. Cuadrado, 2011. The role of microbial mats in the preservation of bird footprints: a case study from the mesotidal Bahia Blanca estuary (Argentina). En N. Noffke y H.S. Chafetz (Eds.), Microbial mats in siliciclastic depositional systems through time. Society for Sedimentary Geology, Special Publication 101:37-45.

Chafetz, H. y C. Buczynski, 1992. Bacterially Induced Lithification of Microbial Mats. Palaios 7:277-293.

Cuadrado, D.G. y J. Pan, 2018. Field observations on the evolution of microbial reticulates in a modern siliciclastic coastal environment. Journal of Sedimentary Research 88:24-37.

Cuadrado, D.G y N.V. Pisani, 2007. Identification of Microbially

Induced Sedimentary Structures over a tidal flat. Latin Ame­ rican Journal of Sedimentology and Basin Analysis 14:105-116. Cuadrado, D.G., N.B. Carmona y C.N. Bournod, 2011. Biostabili- zation of sediments by microbial mats in a temperate siliciclastic tidal flat, Bahia Blanca estuary (Argentina).

Sedimentary Geology 237:95-101.

Cuadrado, D.G., G.M.E. Perillo y A. Vitale, 2014. Modern micro- bial mats in siliciclastic tidal flats: Evolution, structure and the role of hydrodynamics. Marine Geology 352:367-380.

Cuadrado, D.G., J. Pan, E.A. Gómez y L. Maisano, 2015. Deformed

microbial mat structures in a semiarid temperate coastal setting. Sedimentary Geology 325:106-118.

Dai, H., L. Xing, D. Marty, J. Zhang, W. Persons, H. Hu y F. Wang,

Microbially-induced sedimentary wrinkle structures and possible impact of microbial mats for the enhanced preservation of dinosaur tracks from the Lower Cretaceous Jiaguan Formation near Qijiang (Chongqing, China). Creta­ ceous Research 53:98-109.

Davis, R.A., 1968. Algal stomatolites compossed of quartz

sandstone. Journal of Sedimentary Petrology 38:953-955.

Decho, A.W., 1990. Microbial exopolymer secretions in ocean environments: their role(s) in food webs and marine processes. Oceanography Marine Biology 28:73-153.

de Souza Carvalho, I., L. Borghia y G. Leonardi, 2013. Preser-

vation of dinosaur tracks induced by microbial mats in the Sousa Basin (Lower Cretaceous), Brazil. Cretaceous Research 44:112-121.

Dupraz, C. y P. Vissher, 2005. Microbial lithification in marine stromatolites and hypersaline mats.Trends in Microbiology 13:429-38.

Dupraz, C., R. Reid, O. Braissan, A. Decho, R. Norman y P. Visscher, 2009. Processes of carbonate precipitation in modern microbial mats. Earth­Science Reviews 96:141-162.

Eriksson, P.G., J. Schieber, E. Bouougri, G. Gerdes, H. Porada,

S. Banerjee, P.K. Bose y S. Sarkar, 2007. Classification of structures left by microbial mats in their host sediments. En

J. Schieber, P.K. Bose, P.G. Eriksson, S. Banerjee, S. Sarkar,

W. Altermann y O. Catuneanu (Eds.), Atlas of Microbial Mat Features Preserved Within the Siliciclastic Rock Record. Atlases in Geoscience 2. Elsevier, Amsterdam:39-52.

Eriksson, P.G., S. Sarkar, P. Samanta, S. Banerjee, H. Porada y O. Catuneanu, 2010. Paleoenvironmental Context of Microbial Mat-Related Structures in Siliciclastic Rocks. En J. Seckbach y A.Oren (Eds), Microbial Mats. Cellular Origin, Life in Extreme Habitats and Astrobiology vol. 14. Springer, Dordrecht: 73- 110.

Folk, R., 1954. The Distinction between grain size and mineral composition in sedimentary-rock nomenclature.The Journal of Geology 62:344-359.

Freytet, P., 2003. Analyse d’un exemple de fossilization d’une trace de pas de Dinosaure (Liasinférieur des Causses). Le Naturaliste Vendéen 3:63-67.

Gall, J.C., 1998. Paleoecologie: paysages et environnements disparus. Masson, Paris, 239 pp.

Gallagher K.L., C. Dupraz y P.T. Visscher, 2014. Two opposing effects of sulfate reduction on carbonate precipitation in normal marine, hypersaline, and alkaline environments: COMMENT. Geology 42: e313-e314.

Gerdes, G., W.E. Krumbein y N. Noffke, 2000. Microbial signatures

in peritidal siliciclastic sediments: a catalogue. Sedimentology

, 279-308.

Gerdes, G., 2010. What are microbial mats? En J. Seckbach y

A. Oren (Eds.), Microbial Mats. Modern and Ancient Micro­ organisms in Stratified Systems. Springer, Dordrecht: 5-28.

Hagadorn, J.W. y C. McDowell, 2012. Microbial influence on erosion, grain transport and bedform genesis in sandy subs- trates under unidirectional flow. Sedimentology 59:795-808.

Knoll, A., 2008. Cyanobacteria and Earth History. En A. Herrero

y E. Flores (Eds), The Cyanobacteria: Molecular Biology, Genomics and Evolution. Caister Academic Press, UK:1-20.

Krumbein, W.E., 1994. The year of the slime. En W.E. Krumbein,

D.M. Paterson y L.J. Stal (Eds.), Biostabilization of sediments. Biblioteks- und Information system der Carl von Ossietzky Universität Oldenberg, (BIS) -Verlag, Oldenburg: 1-7.

Maisano, L., I.E. Quijada, J. Pan y D.G. Cuadrado, 2017. Preci- pitación temprana de carbonato en presencia de matas microbianas en un ambiente silicoclástico. XX Congreso Geológico Argentino, Actas: 76-80, San Miguel de Tucumán.

Manera de Bianco, T. y S.A. Aramayo, 2003. Primer registro

de huellas de Equidae en el yacimiento paleoicnológico de Pehuen Có (Pleistoceno tardío) provincia de Buenos Aires, Argentina. Ameghiniana 40: Suplemento: 61R.

Margulis, L. y M.F. Dolan, 2002. Early life: evolution on the

Precambrian Earth. Jones and Bartlett Publishers, UK, 168 pp. Marty, D., A. Strasser y C.A. Meyer, 2009. Formation and taphonomy of human footprints in microbial mats of present- day tidal-flat environments: Implications for the study of

fossil footprints. Ichnos 16:127-142.

McNamara, M.E., P. J. Orr, S.L. Kearns, L. Alcalá, P. Anadón y E. Peñalver, 2009. Soft-tissue preservation in Miocene frogs from Libros, Spain: Insights into the genesis of decay microenvironments. Palaios 24:104-117.

Morrow, D., 1972.An injection structure in a Permian limestone.

Journal of Sedimentary Petrology 4:230-235.

Noffke, N., 1999. Erosional remnants and pockets evolving from biotic–physical interactions in a Recent lower supratidal envi- ronment. Sedimentary Geology 123:175-181.

Noffke, N., 2010. Microbial Mats in Sandy Deposits from the

Archean Era to Today. Springer-Verlag, Berlin, 200 pp.

Noffke, N. y D. Paterson, 2008. Microbial interactions with physical sediment dynamics, and their significance for the interpretation of Earth’s biological history. Geobiology 6:1-4.

Noffke, N., G.Gerdes, T. Klenke y W.E. Krumbein, 2001. Micro-

bially induced sedimentary structures - a new category within the classification of primary sedimentary structures. Journal of Sedimentary Research 71:649-656.

Noffke, N., G.Gerdes y T. Klenke, 2003. Benthic cyanobacteria

and their influence on the sedimentary dynamics of peritidal depositional systems (siliciclastic, evaporitic salty, and evaporitic carbonatic). Earth­Science Reviews 62:163-176.

Pan, J., C.N. Bournod, N.V Pizani, D.G. Cuadrado y N.B. Carmona,

Characterization of microbial mats from a siliciclastic tidal flat (Bahía Blanca estuary, Argentina). Geomicrobiology Journal 30:665-674.

Pan J., C.N. Bournod, D.G. Cuadrado, A. Vitale y M.C. Piccolo,

Interaction between estuarine microphytobenthos and physical forcings: the role of atmospheric and sedimentary factors. International Journal of Geosciences 4:352-361.

Pan J., Cuadrado D.G., Gómez E.A., Raniolo L.A. y Maisano

L., 2015. Tidal sedimentation under high-energy influence: physical and biological interactions. 9th International Confe­ rence on Tidal Sedimentology Actas en CD, Puerto Madryn, Argentina.

Paterson, D.M., 1994. Microbiological mediation of sediment

structure and behaviour. En L.J. Stal y P. Caumette (Eds.),

Microbial Mats. Springer-Verlag, Berlin: 97-109.

Pisani, N.V, D.G. Cuadrado y E.R. Parodi, 2006. Estudio preli- minar de los efectos del dragado sobre aspectos bio- sedimentológicos de las planicies de marea. Geoacta 31:33-39. Porada, H. y G. Druschel, 2010. Evidence for participation of microbial mats in the deposition of the siliciclastic “ore formation” in the Copperbelt of Zambia. Journal of African

Earth Sciences 58:427-444.

Quijada, I.E., D.G. Cuadrado, L. Maisano y J. Pan, 2017. Carbonate precipitation in microbial mats developed in a siliciclastic coastal environment. 33rd International Meeting of Sedimentology. IAS Abstract: 734, Tolousse, Francia.

Schieber, J., 1986. The possible role of benthic microbial mats

during the formation of carbonaceous shales in shallow Mid- Proterozoic basins. Sedimentology 33:521-536.

Schieber, J., 1999. Microbial mats in terrigenous clastics: the

challenge of identification in the rock record. Palaios 14:3-12. Schieber, J., 2004. Microbial mats in the siliciclastic rock record: a summary of diagnostic features. En P.G. Eriksson,

W. Altermann, D. Nelson, W.U. Mueller, O. Catuneanu y K. Strand (Eds.), The Precambrian Earth: Tempos and Events, Developments in Precambrian Geology, Elsevier: 663-272.

Shepard, R.N. y D.Y. Sumner, 2010. Undirected motility of filamentous cyanobacteria produces reticulate mats. Geobio­ logy 8:179-190.

Schnack, E.J., F.I. Isla, F.D. De Francesco y E.E. Fucks, 2005. Estratigrafía del Cuaternario marino tardío en la Provincia de Buenos Aires. En R.E. de Barrio, R.O. Etcheverry, M.F. Caballé

y E. Llambías, (Eds.), Geología y Recursos Minerales de la Provincia de Buenos Aires, Relatorio 16° Congreso Geológico Argentino: 159-182, La Plata.

Stolz, J.F., 2000. Structure of Microbial Mats and Biofilms. En R. Riding y S. Awramik (Eds.), Microbial Sediments, Springer- Verlag Berlin Heidelberg: 1-8.

Stoodley, P., I. Dodds, J.D. Boyle y H.M. Lappin-Scott, 1999. Influence of hydrodynamics and nutrients on biofilm structure. Journal of Applied Microbiology 85:19S-28S.

Stoodley, P., K. Sauer, D.G. Davies y J.W. Costerton, 2002. Biofilms

as complex differentiated communities. Annual Review of Microbiology 56:187-209.

Tanner, P.W., 1998. Interstratal dewatering origin for polygonal patterns of sand-filled cracks: a case study from late Prote- rozoic metasediments of Islay, Scotland. Sedimentology 45:71- 89.

Van Lith, Y.V., R. Warthmann, C. Vasconcelos y J.A. McKenzie, 2003. Microbial fossilization in carbonate sediments: a result of the bacterial surface involvement in dolomite precipitation. Sedimentology 50:237-245.

Walkley, A. y I.A. Black, 1934. An examination of Degtjareff

method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Science 37:29-38.

Zavala, C., S. Grill, D. Martínez, H. Ortiz y R. González, 1992. Análisis paleoambiental de depósitos cuaternarios. Sitio paleoicnológico Monte Hermoso I, Provincia de Buenos Aires. 3ras Jornadas Geológicas y Geofísicas Bonaerenses Actas: 31- 3, La Plata.

Published

2021-03-31

How to Cite

Cuadrado , D. G. ., & Blasi, A. M. . (2021). Modern and fossil siliciclastic sediments colonized by microbial mats. A comparative study for analog determination. Latin American Journal of Sedimentology and Basin Analysis, 24(2), 39-73. Retrieved from https://lajsba.sedimentologia.org.ar/index.php/lajsba/article/view/115

Issue

Section

Research Papers