However, in mature mats net growth of cyanobaceria appears to be of minor importance. Most of the organic matter produced from photosynthetic CO 2 fixation is liberated in the sediment by oneof the following: fermentation, photorespiration, pouring out of solutes or secretion of mucus.
This organic matter is degraded by chemotrophic microorganisms, among which sulfate-reducing bacteria are particularly important. The combined activities of the cyanobacteria and sulfate-reducing bacteria result in steep and fluctuating gradients of sulfide and oxygen. Cyanobacteria may thus have to cope with high concentrationsof sulfide and oxygen but also with anoxic conditions.
The physicochemicalgradients force different functional groups of microorganisms to particular vertical stratified positions in the mat. This, and the fact that accretion of sediment fluctuates, gives rise to one of the most conspicuous properties of microbial mats,namely their laminated structure.
Modern microbial mats have this laminated structure in common with Precambrian stromatolites. However, the great majority of modern mats do not lithify. Only a few examples of recent calcifying stromatolithic microbial matsare known. A hypothesis has been developed which conceives a role for extracellular polysaccharides in calcification.
These moleculesmayserve as inhibitors of calcification. Extracellular polysaccharides in cyanobacterial mats are probably produced as a result of unbalanced growth caused by nitrogen limitation. Although nitrogen fixation is an important process in many marine microbial mats, in only a few cases the specialized nitrogen-fixing hetero cystouscyanobacteria are present. Non-heterocystous diazotrophic cyanobacteria are less efficient in nitrogen fixation.
The possible reasons for the exclusion of heterocystous species in many mats are discussed. Unable to display preview. Download preview PDF. Skip to main content. This service is more advanced with JavaScript available.
Advertisement Hide. Cyanobacterial Mats and Stromatolites. Authors Authors and affiliations Lucas J. This process is experimental and the keywords may be updated as the learning algorithm improves. This is a preview of subscription content, log in to check access. Albertano P and Kovacik L Light and temperature responses of terrestrial sciaphilous strains of Leptolyngbya sp.
Algol Stud 17—28 Google Scholar. Awramik SM Ancient stromatolites and microbial mats. Liss Inc. Plant Physiol — Google Scholar. Bar-Or Y and Shilo M The role of cell-bound flocculants in coflocculation of benthic cyanobacteria with clay particles.
Appl Environ Microbiol — Google Scholar. Bender J, Rodriguezeaton S, Ekanemesang UM and Phillips P Characterization of metal-binding bioflocculants produced by the cyanobacterial component of mixed microbial mats. Cytobios 7—18 Google Scholar. J Phycol — Google Scholar. Geochim Cosmochim Acta — Google Scholar. Springer Verlag, New York, pp. Google Scholar.
Eur J Phycol 99— Google Scholar. Phycologia — PubMed Google Scholar. Cairns-Smith AG Precambrian solution photochemistry, inverse segregation, and banded iron formations. Nature Google Scholar. Campbell SE Soil stabilization by a prokaryotic desert crust: implications for Precambrian land biota. Origins of Life 9: — Science — PubMed Google Scholar. Structure, Development and Environmental Significance pp. Its relevance to fossil preservation.
Topics in Geobiology Vol. Castenholz RW Movements. Castenholz RW The effect of sulfide on the blue green algae of hot springs. New Zealand and Iceland. J Phycol 54—68 Google Scholar.
Castenholz RW The effect of sulfide on the blue-green algae of hot springs. Yellowstone National Park. Castenholz RW Motility and taxes. Arch Microbiol Google Scholar. Chafetz HS Bacterially induced precipitates of calcium carbonate and lithification of microbial mats.
Palaios 7: — Google Scholar. Christensen BE, Kjosbakken J and Smidsrod O Partial chemical and physical characterization of two extracellular polysaccharides produced by marine periphytic Pseudomonas sp. Am J Sci — Google Scholar. Cohen Y Photosynthesis in cyanobacterial mats and its relation to the sulfur cycle: a model for microbial sulfur interactions.
Physiological Ecology of Benthic Microbial Communities pp. Alan R. Physiological Ecology of Benthic Microbial Communities. Cypionka H, Widdel F and Pfennig N Survival of sulfatereducing bacteria after oxygen stress and growth in sulfate-free oxygen-sulfide gradients. Davey A Effects of abiotic factors on nitrogen fixation by blue-green algae in Antarctica.
As well, since they also fix CO 2 , they are able to synthesize the acceptor molecules for the fixed nitrogen. However, it is also feasible that other diazotrophs in a joint venture with cyanobacteria are responsible for the bulk of the fixed nitrogen.
In this review we discuss the importance of cyanobacteria as diazotrophs in microbial mats, their interactions with other potential N 2 -fixing microorganisms, and the factors that control their activities. Ramsing NB, Prufert-Bebout L Motility of Microcoleus chthonoplastes subjected to different light intensities quantified by digital image analysis. Springer, Heidelberg, pp — Google Scholar.
Clarendon, Oxford, pp —, pp Google Scholar. Rees DA Structure, conformation and mechanism in the formation of polysaccharide gels and network. Geology —18 CrossRef Google Scholar.
Reinhold L, Kosloff R, Kaplan A A model for inorganic carbon fluxes and photosynthesis in cyanobacterial carboxysomes. Nitrogen controls excretion and metabolism of glycolate in Anabaena cylindrica. Uptake, growth and metabolic pathways. Richardson LL, Castenholz RW a Diel vertical movements of the cyanobacterium Oscillatoria terebriformis in a sulfide-rich hot spring microbial mat.
Richardson LL, Castenholz RW b Enhanced survival of the cyanobacterium Oscillatoria terebriformis in darkness under anaerobic conditions.
Robbins LL, Blackwelder PL Biochemical and ultrastructural evidence for the origin of whitings: a biologically induced calcium carbonate precipitation mechanism.
Geology — CrossRef Google Scholar. Biochemistry — CrossRef Google Scholar. The role of glycolic acid. Hydrobiologia — CrossRef Google Scholar. Schmetterer G Cyanobacterial respiration. Cyanobacteria : morphological and molecular criteria for revision of the genus Microcoleus Gomont.
Smith AJ Modes of cyanobacterial carbon metabolism. Blackwell, Oxford, pp 47—85, pp Google Scholar. Srivastava P Vindhyan akinetes: an indicator of mesoproterozoic biosphere evolution. Sroga GE Regulation of nitrogen fixation by different nitrogen sources in the filamentous non-heterocystous cyanobacterium Microcoleus sp. Stal LJ Mikrobielle Matten. Gustav Fischer, Jena, pp —, pp Google Scholar. Stal LJ Microbial mats in coastal environments. Springer, Heidelberg, pp 21—32 Google Scholar.
Stal LJ Physiological ecology of cyanobacteria in microbial mats and other communities. Stal LJ Cyanobacterial mats and stromatolites. Their diversity in time and space. Stal LJ Coastal microbial mats: the physiology of a small-scale ecosystem. Stal LJ Microphytobenthos as a biogeo-morphological force in intertidal sediment stabilization.
Stal LJ, Krumbein WE Temporal separation of nitrogen fixation and photosynthesis in the filamentous, non-heterocystous cyanobacterium Oscillatoria sp. Stal LJ, Reed RH Low-molecular mass carbohydrate accumulation in cyanobacteria from a marine microbial mat in response to salt. Stolz JF Magnetosomes. Sutherland IW Biofilm exopolysaccharides: a strong and sticky framework. Microbiology —9 PubMed Google Scholar.
Tabita FR Molecular and cellular regulation of autotrophic carbon dioxide fixation in microorganisms. Tago Y, Aida K Exocellular mucopolysaccharide closely related to bacterial floc formation. Taiz L Plant cell expansion: regulation of cell wall mechanical properties. Utkilen HC Thiosulphate as electron donor in the blue-green alga Anacystis nidulans. Van Bergeijk SA, Stal LJ The role of oxygenic phototrophic microorganisms in production and conversion of dimethylsulfonio-propionate and dimethylsulfide in microbial mats.
Van Gemerden H Competition between purple sulfur bacteria and green sulfur bacteria: role of sulfide, sulfur and polysulfides.
Acta Acad Abo —27 Google Scholar. Van Gemerden H Microbial mats: a joint venture. Naturwissenschaften — CrossRef Google Scholar. Villbrandt M Interactions of nitrogen fixation and photosynthesis in marine cyanobacterial mats Mellum, Southern North Sea. Villbrandt M, Stal LJ The effect of sulfide on nitrogen fixation in heterocystous and non-heterocystous cyanobacterial mat communities. Algol Stud — Google Scholar. Visscher PT Microbial sulfur cycling in laminated marine ecosystems.
In: Oremland RS ed Biogeochemistry of global change: radiatively active trace gases. Am Mineral — Google Scholar. Visscher PT, Reid RP, Bebout BM Microscale observations of sulfate reduction: correlation of microbial activity with lithified micritic laminae in modern marine stromatolites.
Walsby AE The permeability of heterocysts to the gases nitrogen and oxygen. Walter MR ed Stromatolites. Elsevier, Amsterdam, pp Google Scholar. Biochem Z — Google Scholar. Z Naturforsch B— Google Scholar. PDF 7. PDF 34K. PDF 1. XLSX 60K. PDF 41K. Abstract Microbial mats are complex, micro-scale ecosystems that can be found in a wide range of environments.
Keywords: cyanobacteria, microbial mats, hypersaline, diversity, morphological characterization, 16S rRNA gene, phylogeny, next-generation sequencing. Introduction Photosynthetic microbial mats are complex, micro-scale ecosystems that can be found globally in a wide range of environments and are a major driving force in the formation of some modern microbialites, i. Open in a separate window. Figure 1. Field sampling, sample processing, and study design Mat samples from each site were collected from an area of 1 m 2 Supplementary Image S1D , in February during the rainy season Supplementary Images S1D—F.
Within parentheses are average values for the 13 months prior to sampling. Figure 2. Schematic overview of the experimental design. See text for methodological details. Isolation, culturing, and morphological-based characterization of cyanobacteria For the isolation of cyanobacteria, subsamples were subjected to liquid culture enrichment, streaking in agar plates or micromanipulation Rippka, ; Waterbury, ; see also Brito et al.
Survey of cyanobacterial taxa from previous publications A primary literature search was performed to assess the cyanobacterial species richness previously recorded in the Araruama's complex. Denaturing gradient gel electrophoresis, and cloning After gel visualization, PCR products from the same mat sample were pooled. Sanger sequencing Purified plasmids and PCR products obtained from isolates purified with the same spin columns mentioned above were sent for sequencing at Macrogen Amsterdam, Netherlands.
Table 2 Number of cyanobacterial 16S rRNA gene sequences used in or discarded from phylogeny, by sample. Results Characterization of microbial mats Morphologically, the cyanobacterial mats found at the sampling sites belonged to the smooth EB1 or polygonal EB2 and EB3 types, while structurally they were layered Supplementary Table S1 and Supplementary Image S1.
Table 3 Species composition and morphological-based characterization of cyanobacteria observed in the upper layer of the microbial mats collected at Araruama EB1 , Pitanguinha EB2 , and Pernambuco EB3 lagoons. Black circles or squares denote first reported observations of a species for that water body. White circles or squares indicate that the species was also observed in previous studies see also the full checklist available in Supplementary Table S1. Squares mean that the taxon was found to dominate or was abundant in samples from this study.
Figure 3. Table 4 List of cyanobacterial strains isolated from hypersaline microbial mats collected at the Araruama lagoon system RJ, Brazil. Strain Order Sampling site Figure Leptolyngbya aff. Figure 4. Molecular and phylogenetic characterization The pyrosequencing generated 10, high quality reads in total, for the three mat samples. Figure 5. Figure 6. Table 5 Taxon richness comparison, by taxonomic order, of morphospecies and phylotypes identified in this study and morphospecies previously reported for lagoons from the Araruama's entire complex, as retrieved from the literature survey see Supplementary Table S1 for the full checklist.
Number of genera shown in parentheses. Some OTUs belonging to this lineage were previously detected by Clementino et al. Moreover, the genus Halothece may actually contain some species of Aphanothece order Synechococcales , including A. Discussion In this work, we have attempted to uncover the cyanobacterial diversity present in hypersaline mats from three lagoons of the Araruama system, while exploring the impact of different classification methods or procedures to evaluate such diversity.
Culture-dependent approach Five of the nine isolates corresponded to a single species, Geitlerinema cf. Comparison between molecular- and morphological-based approaches For the first time, a molecular study was performed in order to characterize and classify the cyanobacterial diversity present in microbial mats from the Araruama's lagoons. Classification and identification issues The assignment of taxa to sequences is often a challenge in molecular-based classification methods, chiefly in the analysis of metagenomic data directly retrieved from environmental samples Mobberley et al.
Conflict of interest statement The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Footnotes Funding.
Click here for additional data file. References Abed R. Polyphasic characterization of benthic, moderately halophilic, moderately thermophilic cyanobacteria with very thin trichomes and the proposal of Halomicronema excentricum gen.
Diazotrophic microbial community of coastal microbial mats of the southern North Sea. Geobiology 9 , — Barcoded primers used in multiplex amplicon pyrosequencing bias amplification. Metagenomics using next-generation sequencing. Methods Mol. Culture-dependent characterization of cyanobacterial diversity in the intertidal zones of the Portuguese coast: a polyphasic study.
BMC Bioinformatics 10 Phylum BX. New York, NY: Springer; , — Oxynema, a new genus separated from the genus Phormidium Cyanophyta. Cryptogamie Algol. Prokaryotic diversity in one of the largest hypersaline coastal lagoons in the world. Extremophiles 12 , — Overview of biopolymer-induced mineralization: what goes on in biofilms? Epilithic cyanobacterial communities of a marine tropical beach rock Heron Island, Great Barrier Reef : diversity and diazotrophy.
Processes of carbonate precipitation in modern microbial mats. Species concepts and speciation factors in cyanobacteria, with connection to the problems of diversity and classification. The NCBI taxonomy database. Nucleic Acids Res. Flat laminated microbial mat communities. Consistency of metagenomic assignment programs in simulated and real data. BMC Bioinformatics 15 The phylogeny of unicellular, extremely halotolerant cyanobacteria.
Phenotypic and phylogenetic analyses show Microcoleus chthonoplastes to be a cosmopolitan cyanobacterium. Determining the specific microbial populations and their spatial distribution within the stromatolite ecosystem of Shark Bay. ISME J. Timmis K. Berlin; Heidelberg: Springer; , — Harris J. Phylogenetic stratigraphy in the Guerrero Negro hypersaline microbial mat. Hydrology and salt balance in a large, hypersaline coastal lagoon: Lagoa de Araruama, Brazil. Shelf Sci.
A polyphasic approach for the taxonomy of cyanobacteria: principles and applications. Cyanoprokaryota 1. Jena: Gustav Fischer; , 1—
0コメント