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1.
Braz J Microbiol ; 55(3): 2437-2452, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38758507

ABSTRACT

The active layer is the portion of soil overlaying the permafrost that freezes and thaws seasonally. It is a harsh habitat in which a varied and vigorous microbial population thrives. The high-altitude active layer soil in northern India is a unique and important cryo-ecosystem. However, its microbiology remains largely unexplored. It represents a unique reservoir for microbial communities with adaptability to harsh environmental conditions. In the Changthang region of Ladakh, the Tsokar area is a high-altitude permafrost-affected area situated in the southern part of Ladakh, at a height of 4530 m above sea level. Results of the comparison study with the QTP, Himalayan, Alaskan, Russian, Canadian and Polar active layers showed that the alpha diversity was significantly higher in the Ladakh and QTP active layers as the environmental condition of both the sites were similar. Moreover, the sampling site in the Ladakh region was in a thawing condition at the time of sampling which possibly provided nutrients and access to alternative nitrogen and carbon sources to the microorganisms thriving in it. Analysis of the samples suggested that the geochemical parameters and environmental conditions shape the microbial alpha diversity and community composition. Further analysis revealed that the cold-adapted methanogens were present in the Ladakh, Himalayan, Polar and Alaskan samples and absent in QTP, Russian and Canadian active layer samples. These methanogens could produce methane at slow rates in the active layer soils that could increase the atmospheric temperature owing to climate change.


Subject(s)
Altitude , Bacteria , Microbiota , Soil Microbiology , Bacteria/classification , Bacteria/genetics , Bacteria/isolation & purification , India , Permafrost/microbiology , Soil/chemistry , Archaea/classification , Archaea/genetics , Archaea/isolation & purification , Archaea/metabolism , Computer Simulation , Phylogeny , Ecosystem , Biodiversity
2.
Environ Sustain (Singap) ; 4(3): 489-501, 2021.
Article in English | MEDLINE | ID: mdl-38624658

ABSTRACT

Permanently frozen environments (glaciers, permafrost) are considered as natural reservoirs of huge amounts of microorganisms, mostly dormant, including human pathogens. Due to global warming, which increases the rate of ice-melting, approximately 4 × 1021 of these microorganisms are released annually from their frozen confinement and enter natural ecosystems, in close proximity to human settlements. Some years ago, the hypothesis was put forward that this massive release of potentially-pathogenic microbes-many of which disappeared from the face of the Earth thousands and even millions of years ago-could give rise to epidemics. The recent anthrax outbreaks that occurred in Siberia, and the presence of bacterial and viral pathogens in glaciers worldwide, seem to confirm this hypothesis. In that context, the present review summarizes the currently available scientific evidence that allows us to imagine a near future in which epidemic outbreaks, similar to the abovementioned, could occur as a consequence of the resurrection and release of microbes from glaciers and permafrost. Supplementary Information: The online version of this article (10.1007/s42398-021-00184-8) contains supplementary material, which is available to authorized users.

3.
Isotopes Environ Health Stud ; 56(5-6): 480-494, 2020.
Article in English | MEDLINE | ID: mdl-32951462

ABSTRACT

Glacial and periglacial basins contain the largest reserves of fresh water in the world. These areas are extremely sensitive to global warming and climate change. The dry Andes of South America are characterized by large periglacial areas. This study focuses on the water isotopic composition and hydrochemistry of a typical periglacial environment of the Andes, in the Vallecitos catchment (2400-5500 m a.s.l.), Cordillera Frontal, Argentina. Detailed fieldwork was conducted between 2013 and 2017 with 240 samples collected for major ions and physicochemical parameters, and 67 samples analysed for 2H and 18O. The chemical composition of precipitation is typical Ca-HCO3, while streams and groundwaters are Ca-MgSO4 type. The isotope content of precipitation shows a wide dispersion. The snow samples are in general more depleted than the rainfall. Some springs vary their composition seasonally, associated to the melting of perennial snow patches. In general, all samples from the upper basin present depleted isotope contents related to recharge at higher altitudes, whereas samples from the lower basin show more enriched values. Intermediate compositions reflect the melting of snow and degrading ice-rich permafrost. These results will give a better understanding of the dynamics of water to manage water resources.


Subject(s)
Environmental Monitoring/methods , Groundwater/chemistry , Rain/chemistry , Rivers/chemistry , Snow/chemistry , Water Resources/supply & distribution , Altitude , Argentina , Climate Change , Deuterium/analysis , Natural Springs/chemistry , Oxygen Isotopes/analysis , Permafrost/chemistry
4.
Astrobiology ; 20(6): 754-765, 2020 06.
Article in English | MEDLINE | ID: mdl-32525738

ABSTRACT

Microbial ecology of permafrost, due to its ecological and astrobiological importance, has been in the focus of studies in past decades. Although permafrost is an ancient and stable environment, it is also subjected to current climate changes. Permafrost degradation often results in generation of thaw ponds, a phenomenon not only reported mainly from polar regions but also present in high-altitude permafrost environments. Our knowledge about microbial communities of thaw ponds in these unique, remote mountain habitats is sparse. This study presents the first culture collection and results of the next-generation DNA sequencing (NGS) analysis of bacterial communities inhabiting a high-altitude permafrost thaw pond. In February 2016, a permafrost thaw pond on the Ojos del Salado at 5900 m a.s.l. (meters above sea level) was sampled as part of the Hungarian Dry Andes Research Programme. A culture collection of 125 isolates was established, containing altogether 11 genera belonging to phyla Bacteroidetes, Actinobacteria, and Proteobacteria. Simplified bacterial communities with a high proportion of candidate and hitherto uncultured bacteria were revealed by Illumina MiSeq NGS. Water of the thaw pond was dominated by Bacteroidetes and Proteobacteria, while in the sediment of the lake and permafrost, members of Acidobacteria, Actinobacteria, Bacteroidetes, Patescibacteria, Proteobacteria, and Verrucomicrobia were abundant. This permafrost habitat can be interesting as a potential Mars analog.


Subject(s)
Altitude , Bacteria/genetics , Genetic Variation , Permafrost/microbiology , Ponds/microbiology , Bacteria/growth & development , Bacteria/isolation & purification , Colony Count, Microbial , Geologic Sediments/microbiology , High-Throughput Nucleotide Sequencing , Phylogeny , Principal Component Analysis , South America , Water
5.
Extremophiles ; 24(4): 565-576, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32405812

ABSTRACT

We evaluated the diversity and distribution of viable fungi present in permafrost and active layers obtained from three islands of Maritime Antarctica. A total of 213 fungal isolates were recovered from the permafrost, and 351 from the active layer, which were identified in 58 taxa; 27 from permafrost and 31 from the active layer. Oidiodendron, Penicillium, and Pseudogymnoascus taxa were the most abundant in permafrost. Bionectriaceae, Helotiales, Mortierellaceae, and Pseudeurotium were the most abundant in the active layer. Only five shared both substrates. The yeast Mrakia blollopis represented is the first reported on Antarctic permafrost. The fungal diversity detected was moderate to high, and composed of cosmopolitan, cold-adapted, and endemic taxa, reported as saprobic, mutualistic, and parasitic species. Our results demonstrate that permafrost shelters viable fungi across the Maritime Antarctica, and that they are contrasting to the overlying active layer. We detected important fungal taxa represented by potential new species, particularly, those genetically close to Pseudogymnoascus destructans, which can cause extinction of bats in North America and Eurasia. The detection of viable fungi trapped in permafrost deserves further studies on the extension of its fungal diversity and its capability to expand from permafrost to other habitats in Antarctica, and elsewhere.


Subject(s)
Ascomycota , Permafrost , Antarctic Regions , Ecosystem , Fungi , Islands
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