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Journal articles on the topic 'Microcoleus'

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1

Rosowski, J. R., J. J. Shaffer, E. L. Martin, T. A. Kokjohn, and K. W. Lee. "First Report of a Putative Cyanophage, Mc-1, of Microcoleus Sp." Microscopy and Microanalysis 5, S2 (1999): 1142–43. http://dx.doi.org/10.1017/s1431927600019036.

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A current review (1) lists 21 cyanophages of coccoid and filamentous heterocystic and non-heterocystic blue-green algae (BGA). The capsid diameters of these viruses range from 50-90 nm, and none have been previously reported for Microcoleus,a sheath-producing, filamentous, surface colonizing BGA (Fig. 1), of the order Oscillatoriales, and class Cyanophyceae (= Cyanobacteria). From a freshwater culture of Microcoleussp. we report here a putative cyanophage with a side-to-side hexagonal capsid diameter of 140 nm, based on measurements from thin sections of algal filaments prepared for transmissi
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2

Trnková, Kateřina, and Nele Tschense. "Structure and function of biological soil crusts from Antarctica with a special respect to their microtopography and UV-B sensitivity." Czech Polar Reports 9, no. 2 (2019): 243–50. http://dx.doi.org/10.5817/cpr2019-2-20.

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Although an extensive professional literature exists on biological soil crusts (BSCs), especially on the species composition of hetero- and autotrophs forming the micro-biological comunity, micromorphological information on BSCs is extremely scarce. In our study, we focused on microstructure of the BSCs from the James Ross Island (Antarctica). We combined the approach of digital microscopy to study surface roughness of the BSCs with taxonomy of BSC-forming autotrophs and chlorophyll fluorescence study focused on the photosynthetic functioning of BSCs when exposed to controlled UV-B stress. Mic
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3

Hernández-Mariné, Mariona. "Electron microscopic characterization of Microcoleus chthonoplastes THUR. (Cyanobacteria)." Algological Studies/Archiv für Hydrobiologie, Supplement Volumes 83 (December 19, 1996): 347–65. http://dx.doi.org/10.1127/algol_stud/83/1996/347.

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4

Grimalt, Joan O., Rutger de Wit, Pilar Teixidor, and Joan Albaigés. "Lipid biogeochemistry of Phormidium and Microcoleus mats." Organic Geochemistry 19, no. 4-6 (1992): 509–30. http://dx.doi.org/10.1016/0146-6380(92)90015-p.

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5

Omoregie, Enoma O., Lori L. Crumbliss, Brad M. Bebout, and Jonathan P. Zehr. "Determination of Nitrogen-Fixing Phylotypes in Lyngbya sp. and Microcoleuschthonoplastes Cyanobacterial Mats from Guerrero Negro, Baja California, Mexico." Applied and Environmental Microbiology 70, no. 4 (2004): 2119–28. http://dx.doi.org/10.1128/aem.70.4.2119-2128.2004.

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ABSTRACT In many environments, biological nitrogen fixation can alleviate nitrogen limitation. The high rates of N2 fixation often observed in cyanobacterial mats suggest that N2 fixation may be an important source of N. In this study, organisms expressing nifH were identified in a Lyngbya sp.- and two Microcoleus chthonoplastes-dominated cyanobacterial mats. The pattern of nitrogenase activity was determined for the Lyngbya sp. mat and a Microcoleus chthonoplastes mat sampled directly in Guerrero Negro, Mexico. Their maximum rates were 23 and 15 μmol of C2H4 m−2 h−1, respectively. The second
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6

Wit, Rutger, Wim H. M. Boekel, and Hans Gemerden. "Growth of the cyanobacterium Microcoleus chtonoplastes on sulfide." FEMS Microbiology Letters 53, no. 3-4 (1988): 203–9. http://dx.doi.org/10.1111/j.1574-6968.1988.tb02665.x.

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7

Kupriyanova, E. V., A. G. Markelova, N. V. Lebedeva, L. M. Gerasimenko, G. A. Zavarzin, and N. A. Pronina. "Carbonic Anhydrase of the Alkaliphilic Cyanobacterium Microcoleus chthonoplastes." Microbiology 73, no. 3 (2004): 255–59. http://dx.doi.org/10.1023/b:mici.0000032233.36705.5a.

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8

Wit, Rutger, and Hans Gemerden. "Oxidation of sulfide to thiosulfate by Microcoleus chtonoplastes." FEMS Microbiology Letters 45, no. 1 (1987): 7–13. http://dx.doi.org/10.1111/j.1574-6968.1987.tb02332.x.

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9

MACHADO DE LIMA, NÁTHALI MARIA, and LUIS H. Z. BRANCO. "Biological soil crusts: new genera and species of Cyanobacteria from Brazilian semi-arid regions." Phytotaxa 470, no. 4 (2020): 263–81. http://dx.doi.org/10.11646/phytotaxa.470.4.1.

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In the uppermost millimeters of soils is commonly found a thin layer of cryptobiotic organisms, including cyanobacteria, microalgae, lichens, mosses, fungi, bacteria and archaea. These communities are called Biological Soil Crusts (BSCs) or biocrusts and perform important ecological functions, mainly attributed to their capacity of providing soil stability and incorporate nutrients through nitrogen and carbon fixation. Among all the organisms found in the biocrusts, the filamentous cyanobacteria Microcoleus vaginatus and M. steenstrupii are the best studied soil colonizers. The genus Microcole
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10

Davydov, Denis. "Cyanoprokaryotes of the west part of Oscar II Land, West Spitsbergen Island, Spitsbergen archipelago." Czech Polar Reports 7, no. 1 (2017): 94–108. http://dx.doi.org/10.5817/cpr2017-1-10.

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The present study provides new information about the diversity of freshwater and terrestrial cyanoprokaryotes of the western part of the Oscar II Land, Spitsbergen (Svalbard) archipelago. Altogether, and 51 taxa were found in different habitats (29 species was found on wet rocks, 21 on the seepages, 18 on the lakes, 11 on the moss tundra), mainly in wet ones. Nostoc commune, Gloeocapsa kuetzingiana, Microcoleus autumnalis, and Microcoleus vaginatus dominated almost all types of habitats. Aphanocapsa rivularis and Woronichinia karelica are reported for the first time for Spitsbergen flora. The
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11

Ghosh, Ashmita, Saumyakanti Khanra, Gopinath Haldar, Tridib Kumar Bhowmick, and Kalyan Gayen. "Diverse Cyanobacteria Resource from North East Region of India for Valuable Biomolecules: Phycobiliprotein, Carotenoid, Carbohydrate and Lipid." Current Biochemical Engineering 5, no. 1 (2019): 21–33. http://dx.doi.org/10.2174/2212711905666180817105828.

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Background: :North east region of India is well known as biodiversity hotspot with endemic flora and fauna. Organisms belonging to the cyanobacterial species are commonly known as blue green algae and are found in diverse categories in the environment of north-east India. Potentials of these cyanobacterial species are mostly unexplored. Present study aimed to isolate, identify and evaluate the potential cyanobacterial strains for the sustainable producers of biomolecules with agricultural, therapeutic and industrial significance.Methods::Growth and biochemical characterization were performed w
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12

Mehda, Smail, Maria Ángeles Muñoz-Martín, Mabrouka Oustani, Baelhadj Hamdi-Aïssa, Elvira Perona, and Pilar Mateo. "Microenvironmental Conditions Drive the Differential Cyanobacterial Community Composition of Biocrusts from the Sahara Desert." Microorganisms 9, no. 3 (2021): 487. http://dx.doi.org/10.3390/microorganisms9030487.

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The Sahara Desert is characterized by extreme environmental conditions, which are a unique challenge for life. Cyanobacteria are key players in the colonization of bare soils and form assemblages with other microorganisms in the top millimetres, establishing biological soil crusts (biocrusts) that cover most soil surfaces in deserts, which have important roles in the functioning of drylands. However, knowledge of biocrusts from these extreme environments is limited. Therefore, to study cyanobacterial community composition in biocrusts from the Sahara Desert, we utilized a combination of method
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13

Jose, Nicholas A., Rebecca Lau, Tami L. Swenson, et al. "Flux balance modeling to predict bacterial survival during pulsed-activity events." Biogeosciences 15, no. 7 (2018): 2219–29. http://dx.doi.org/10.5194/bg-15-2219-2018.

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Abstract. Desert biological soil crusts (BSCs) are cyanobacteria-dominated surface soil microbial communities common to plant interspaces in arid environments. The capability to significantly dampen their metabolism allows them to exist for extended periods in a desiccated dormant state that is highly robust to environmental stresses. However, within minutes of wetting, metabolic functions reboot, maximizing activity during infrequent permissive periods. Microcoleus vaginatus, a primary producer within the crust ecosystem and an early colonizer, initiates crust formation by binding particles i
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14

Ikoma, Misato, Yusuke Nakasone, and Masahide Terazima. "Photoreaction of photoactivated adenylate cyclase from cyanobacterium Microcoleus chthonoplastes." Journal of Photochemistry and Photobiology B: Biology 221 (August 2021): 112252. http://dx.doi.org/10.1016/j.jphotobiol.2021.112252.

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15

Arabadzhi, L. I., A. M. Solonenko, O. G. Bren та M. I. Holubev. "ЦИАНОПРОКАРИОТЫ УРОЧИЩА ТУБAЛЬСКИЙ ЛИМАН". Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University 6, № 3 (2016): 414–18. http://dx.doi.org/10.15421/2016112.

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<p>Information about species composition of Cyanoprocaryota representatives in the natural boundary of Tubalskyi Estuary within Pryazov National Natural Park is supplemented. Taxonomic structure of identified algae species is given, the data about occurrence of species in different habitats within national park is provided. We present a systematic structure and geographical affinity of discovered algae species. We registered 38 species of cyanoprocaryotic algae of orders: Chroococcales, Oscillatoriales and Nostocales with predominance of Oscillatoriales representatives in different habit
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16

McAllister, Tara G., Susanna A. Wood, Emma M. MacKenzie, and Ian Hawes. "Reach- and mat-scale differences in Microcoleus autumnalis (cyanobacterium) accrual along velocity and nitrate gradients in three New Zealand rivers." Canadian Journal of Fisheries and Aquatic Sciences 77, no. 2 (2020): 401–12. http://dx.doi.org/10.1139/cjfas-2019-0133.

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Proliferations of the toxic, mat-forming cyanobacterium Microcoleus autumnalis are an increasingly recognized problem in cobble-bed rivers worldwide. This study explored how flow and nutrient concentrations influence mat expansion. Microcoleus autumnalis was inoculated into cobbles placed in runs, riffles, and pools in three rivers with different nutrient conditions, and mat size was monitored over 21 days. The following hypotheses were tested: (i) mat expansion will reflect cover increases at the reach scale; (ii) biomass and cover will be highest in high-velocity habitats; and (iii) under si
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17

Kupriyanova, Elena, Arsenio Villarejo, Alexandra Markelova, et al. "Extracellular carbonic anhydrases of the stromatolite-forming cyanobacterium Microcoleus chthonoplastes." Microbiology 153, no. 4 (2007): 1149–56. http://dx.doi.org/10.1099/mic.0.2006/003905-0.

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18

Toledo, Gerardo, Yoav Bashan, and Al Soeldner. "In vitro colonization and increase in nitrogen fixation of seedling roots of black mangrove inoculated by a filamentous cyanobacteria." Canadian Journal of Microbiology 41, no. 11 (1995): 1012–20. http://dx.doi.org/10.1139/m95-140.

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An isolate of the filamentous cyanobacterium Microcoleus sp. was obtained from black mangrove aerial root (pneumatophore) and inoculated onto young mangrove seedlings to evaluate N2-fixation and root-colonization capacities of the bacterium under in vitro conditions in closed-system experiments. N2 fixation (acetylene reduction) gradually increased with time and reached its peak 5 days after inoculation. Later, it decreased sharply. The level of N2 fixation in the presence of the plant was significantly higher than the amount of nitrogen fixed by a similar quantity of cyanobacteria on a N-free
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19

Faluaburu, Merry Sailonga, Ryosuke Nakai, Satoshi Imura, and Takeshi Naganuma. "Phylotypic Characterization of Mycobionts and Photobionts of Rock Tripe Lichen in East Antarctica." Microorganisms 7, no. 7 (2019): 203. http://dx.doi.org/10.3390/microorganisms7070203.

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Saxicolous rock ripe lichens that grow on rocks in the East Antarctic fellfields were sampled for phylotypic characterization of its constituent mycobionts (fungi) and photobionts (algae and cyanobacteria). The rock tripe lichen-forming fungal and algal phylotypes were classified under the common lichen-forming genera of ascomycetes, namely, Umbilicaria, and green algae, namely, Trebouxia and Coccomyxa. However, phylotypes of the green algal chloroplasts and the lichen-associated cyanobacteria showed unexpectedly high diversity. The detected chloroplast phylotypes were not fully affiliated wit
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20

Kupriyanova, Elena V., Maria A. Sinetova, Alexandra G. Markelova, Suleyman I. Allakhverdiev, Dmitry A. Los та Natalia A. Pronina. "Extracellular β-class carbonic anhydrase of the alkaliphilic cyanobacterium Microcoleus chthonoplastes". Journal of Photochemistry and Photobiology B: Biology 103, № 1 (2011): 78–86. http://dx.doi.org/10.1016/j.jphotobiol.2011.01.021.

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21

Moezelaar, R., S. M. Bijvank, and L. J. Stal. "Fermentation and Sulfur Reduction in the Mat-Building Cyanobacterium Microcoleus chthonoplastes." Applied and environmental microbiology 62, no. 5 (1996): 1752–58. http://dx.doi.org/10.1128/aem.62.5.1752-1758.1996.

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22

Giloteaux, Ludovic, Antoni Solé, Isabel Esteve, and Robert Duran. "Bacterial community composition characterization of a lead-contaminated Microcoleus sp. consortium." Environmental Science and Pollution Research 18, no. 7 (2011): 1147–59. http://dx.doi.org/10.1007/s11356-010-0432-x.

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23

Toledo, Gerardo, Yoav Bashan, and Al Soeldner. "Cyanobacteria and black mangroves in Northwestern Mexico: colonization, and diurnal and seasonal nitrogen fixation on aerial roots." Canadian Journal of Microbiology 41, no. 11 (1995): 999–1011. http://dx.doi.org/10.1139/m95-139.

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Nitrogen fixation and colonization by associative cyanobacteria in the aerial roots (pneumatophores) of black mangrove trees was evaluated in situ at Balandra lagoon, Baja California Sur, Mexico, for 18 consecutive months. Year-round vertical zonation of cyanobacterial colonization was determined along the pneumatophores. The bottom part close to the sediment was colonized mainly by nonheterocystous, filamentous cyanobacteria resembling Lyngbya sp. and Oscillatoria sp. The central zone was colonized mainly by filaments resembling Microcoleus sp. and the upper part was colonized by coccoidal cy
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24

Strunecký, Otakar, Jiří Komárek, Jeffrey Johansen, Alena Lukešová, and Josef Elster. "Molecular and morphological criteria for revision of the genus Microcoleus (Oscillatoriales, Cyanobacteria)." Journal of Phycology 49, no. 6 (2013): 1167–80. http://dx.doi.org/10.1111/jpy.12128.

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25

Prasanth, S., K. R. Haridas, M. Haridas, and A. Sabu. "Novel lipoxygenase inhibitor, 1-ethenoxy-2-methylbenzene, from marine cyanobacteria Microcoleus chthonoplastes." Natural Product Research 32, no. 24 (2017): 2910–15. http://dx.doi.org/10.1080/14786419.2017.1392949.

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26

Jørgensen, Bo Barker, Yehuda Cohen, and Niels Peter Revsbech. "Transition from Anoxygenic to Oxygenic Photosynthesis in a Microcoleus chthonoplastes Cyanobacterial Mat." Applied and Environmental Microbiology 51, no. 2 (1986): 408–17. http://dx.doi.org/10.1128/aem.51.2.408-417.1986.

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Lodders, Nicole, Erko Stackebrandt, and Ulrich Nubel. "Frequent genetic recombination in natural populations of the marine cyanobacterium Microcoleus chthonoplastes." Environmental Microbiology 7, no. 3 (2005): 434–42. http://dx.doi.org/10.1111/j.1462-2920.2005.00730.x.

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28

Garcia-Pichel, F., L. Prufert-Bebout, and G. Muyzer. "Phenotypic and phylogenetic analyses show Microcoleus chthonoplastes to be a cosmopolitan cyanobacterium." Applied and environmental microbiology 62, no. 9 (1996): 3284–91. http://dx.doi.org/10.1128/aem.62.9.3284-3291.1996.

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29

Thomson-Laing, Georgia, Niamh Dyer, Ruby Whyte-Wilding, and Susanna A. Wood. "In situ river experiments to explore variability in Microcoleus autumnalis mat expansion." Hydrobiologia 848, no. 2 (2020): 445–67. http://dx.doi.org/10.1007/s10750-020-04453-1.

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30

Yeager, Chris M., Jennifer L. Kornosky, David C. Housman, Edmund E. Grote, Jayne Belnap, and Cheryl R. Kuske. "Diazotrophic Community Structure and Function in Two Successional Stages of Biological Soil Crusts from the Colorado Plateau and Chihuahuan Desert." Applied and Environmental Microbiology 70, no. 2 (2004): 973–83. http://dx.doi.org/10.1128/aem.70.2.973-983.2004.

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ABSTRACT The objective of this study was to characterize the community structure and activity of N2-fixing microorganisms in mature and poorly developed biological soil crusts from both the Colorado Plateau and Chihuahuan Desert. Nitrogenase activity was approximately 10 and 2.5 times higher in mature crusts than in poorly developed crusts at the Colorado Plateau site and Chihuahuan Desert site, respectively. Analysis of nifH sequences by clone sequencing and the terminal restriction fragment length polymorphism technique indicated that the crust diazotrophic community was 80 to 90% heterocyst
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31

Kelly, Laura, Susanna Wood, Tara McAllister, and Ken Ryan. "Development and Application of a Quantitative PCR Assay to Assess Genotype Dynamics and Anatoxin Content in Microcoleus autumnalis-Dominated Mats." Toxins 10, no. 11 (2018): 431. http://dx.doi.org/10.3390/toxins10110431.

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Microcoleus is a filamentous cyanobacteria genus with a global distribution. Some species form thick, cohesive mats over large areas of the benthos in rivers and lakes. In New Zealand Microcoleus autumnalis is an anatoxin producer and benthic proliferations are occurring in an increasing number of rivers nationwide. Anatoxin content in M. autumnalis-dominated mats varies spatially and temporally, making understanding and managing proliferations difficult. In this study a M. autumnalis-specific TaqMan probe quantitative PCR (qPCR) assay targeting the anaC gene was developed. The assay was asses
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32

XU, Juan-Juan, De-Lu ZHANG, Guo-Qiao WU, Gao-Hong WANG, Yong-Ding LIU, and Chun-Xiang HU. "EFFECT OF WIND STRESS ON PHOTOSYNTHETIC ACTIVITY OF MICROCOLEUS VAGINATUS CRUSTS." Acta Hydrobiologica Sinica 36, no. 3 (2010): 575–81. http://dx.doi.org/10.3724/sp.j.1035.2010.00575.

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33

Malin, G., and H. W. Pearson. "Aerobic Nitrogen Fixation in Aggregate-forming Cultures of the Nonheterocystous Cyanobacterium Microcoleus chthonoplastes." Microbiology 134, no. 7 (1988): 1755–63. http://dx.doi.org/10.1099/00221287-134-7-1755.

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34

Bolhuis, Henk, Ina Severin, Veronique Confurius-Guns, Ute I. A. Wollenzien, and Lucas J. Stal. "Horizontal transfer of the nitrogen fixation gene cluster in the cyanobacterium Microcoleus chthonoplastes." ISME Journal 4, no. 1 (2009): 121–30. http://dx.doi.org/10.1038/ismej.2009.99.

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35

Diaz, Mara R., Jorge E. Corredor, and Julio M. Morell. "Nitrogenase activity of Microcoleus lyngbyaceus mat communities in a eutrophic, tropical marine environment." Limnology and Oceanography 35, no. 8 (1990): 1788–95. http://dx.doi.org/10.4319/lo.1990.35.8.1788.

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Kelly, Laura T., Ken G. Ryan, and Susanna A. Wood. "Differential strain response in alkaline phosphatase activity to available phosphorus in Microcoleus autumnalis." Harmful Algae 89 (November 2019): 101664. http://dx.doi.org/10.1016/j.hal.2019.101664.

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Lan, Shubin, Li Wu, Delu Zhang, and Chunxiang Hu. "Effects of light and temperature on open cultivation of desert cyanobacterium Microcoleus vaginatus." Bioresource Technology 182 (April 2015): 144–50. http://dx.doi.org/10.1016/j.biortech.2015.02.002.

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38

Puddick, Jonathan, Roel van Ginkel, Carrie D. Page, et al. "Acute toxicity of dihydroanatoxin-a from Microcoleus autumnalis in comparison to anatoxin-a." Chemosphere 263 (January 2021): 127937. http://dx.doi.org/10.1016/j.chemosphere.2020.127937.

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Chen, L., T. Li, L. Guan, Y. Zhou, and P. Li. "Flocculating activities of polysaccharides released from the marine mat-forming cyanobacteria Microcoleus and Lyngbya." Aquatic Biology 11, no. 3 (2011): 243–48. http://dx.doi.org/10.3354/ab00309.

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Stielow, Stefanie, and David L. Ballantine. "Benthic cyanobacterial, Microcoleus lyngbyaceus, blooms in shallow, inshore Puerto Rican Seagrass habitats, Caribbean sea." Harmful Algae 2, no. 2 (2003): 127–33. http://dx.doi.org/10.1016/s1568-9883(03)00007-6.

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Chen, Lan-Zhou, Dun-Hai Li, Li-Rong Song, Chun-Xiang Hu, Gao-Hong Wang, and Yong-Ding Liu. "Effects of Salt Stress on Carbohydrate Metabolism in Desert Soil Alga Microcoleus vaginatus Gom." Journal of Integrative Plant Biology 48, no. 8 (2006): 914–19. http://dx.doi.org/10.1111/j.1744-7909.2006.00291.x.

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Nelson, Corey, Ana Giraldo-Silva, and Ferran Garcia-Pichel. "A symbiotic nutrient exchange within the cyanosphere microbiome of the biocrust cyanobacterium, Microcoleus vaginatus." ISME Journal 15, no. 1 (2020): 282–92. http://dx.doi.org/10.1038/s41396-020-00781-1.

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Dvořák, Petr, Petr Hašler, and Aloisie Poulíčková. "Phylogeography of the Microcoleus vaginatus (Cyanobacteria) from Three Continents – A Spatial and Temporal Characterization." PLoS ONE 7, no. 6 (2012): e40153. http://dx.doi.org/10.1371/journal.pone.0040153.

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Garcia-Pichel, Ferran, Virginia Loza, Yevgeniy Marusenko, Pilar Mateo, and Ruth M. Potrafka. "Temperature Drives the Continental-Scale Distribution of Key Microbes in Topsoil Communities." Science 340, no. 6140 (2013): 1574–77. http://dx.doi.org/10.1126/science.1236404.

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Global warming will likely force terrestrial plant and animal species to migrate toward cooler areas or sustain range losses; whether this is also true for microorganisms remains unknown. Through continental-scale compositional surveys of soil crust microbial communities across arid North America, we observed a latitudinal replacement in dominance between two key topsoil cyanobacteria that was driven largely by temperature. The responses to temperature of enrichment cultures and cultivated strains support this contention, with one cyanobacterium (Microcoleus vaginatus) being more psychrotolera
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45

Mühlsteinová, Radka, Jeffrey R. Johansen, Nicole Pietrasiak, and Michael P. Martin. "Polyphasic characterization of Kastovskya adunca gen. nov. et comb. nov. (Cyanobacteria: Oscillatoriales), from desert soils of the Atacama Desert, Chile." Phytotaxa 163, no. 4 (2014): 216. http://dx.doi.org/10.11646/phytotaxa.163.4.2.

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Recent taxonomic revisions within the cyanobacteria have shown that the traditional simple filamentous genera often represent large polyphyletic clusters of not-so-closely-related taxa. In this study, the new cyanobacterial genus Kastovskya is described based on a combination of morphological, molecular, and ecological evidence. Kastovskya was first described as Schizothrix adunca, a morphospecies discovered in the Atacama Desert, Chile more than 50 years ago. This species has been transferred to Kastovskya and serves as the generitype. Kastovskya adunca currently represents a unique and proba
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46

Jadhav, M. J., and Sunita V. Jawale. "House Dust Algae from Aurangabad City of Maharashtra." Plantae Scientia 4, no. 3 (2021): 160–62. http://dx.doi.org/10.32439/ps.v4i3.160-162.

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House dust contains different biocomponents. Algae are one of the important biocomponents of house dust and is present in the form of spores and filaments. Dust samples were collected from houses of patients suffering from respiratory allergy in Aurangabad city during September 2017 to August 2018. Total of 34 samples were collected and cultured in the petriplates containing agarized Bold’s basal medium (BBM). Algal forms belonged to Chlorophyceae, Bacillariophyceae and Cyanophyceae were cultured and identified. Cyanophycean algae dominated the algal flora of house dust. Algal taxa which were
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Carrasco, María, Jesús M. Mercado, and Francisco Xavier Niell. "Diversity of inorganic carbon acquisition mechanisms by intact microbial mats of Microcoleus chthonoplastes (Cyanobacteriae, Oscillatoriaceae)." Physiologia Plantarum 133, no. 1 (2008): 49–58. http://dx.doi.org/10.1111/j.1399-3054.2007.01032.x.

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Hasler, Petr, Petr Dvorak, Jeffrey R. Johansen, Miloslav Kitner, Vladan Ondrej, and Aloisie Poulickova. "Morphological and molecular study of epipelic filamentous genera Phormidium, Microcoleus and Geitlerinema (Oscillatoriales, Cyanophyta/Cyanobacteria)." Fottea 12, no. 2 (2012): 341–56. http://dx.doi.org/10.5507/fot.2012.024.

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Wood, Susanna A., Laura Biessy, and Jonathan Puddick. "Anatoxins are consistently released into the water of streams with Microcoleus autumnalis-dominated (cyanobacteria) proliferations." Harmful Algae 80 (December 2018): 88–95. http://dx.doi.org/10.1016/j.hal.2018.10.001.

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Khan, Zakaullah, and So Deuk Park. "Effects of Inoculum Level and Time of Microcoleus vaginatus on Control of Meloidogyne incognita on Tomato." Journal of Asia-Pacific Entomology 2, no. 2 (1999): 93–96. http://dx.doi.org/10.1016/s1226-8615(08)60036-9.

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