<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Juarez-Rivera, M.</style></author><author><style face="normal" font="default" size="100%">Mackey, Tyler J.</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author><author><style face="normal" font="default" size="100%">Sumner, Dawn Y.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Morphology and distribution of bubble-supported microbial mats from ice-covered Antarctic lakes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Geophysical Research: Biogeosciences</style></secondary-title><short-title><style face="normal" font="default" size="100%">JGR Biogeosciences</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">biosediments</style></keyword><keyword><style  face="normal" font="default" size="100%">bubble-driven morphology</style></keyword><keyword><style  face="normal" font="default" size="100%">gas-supersaturation</style></keyword><keyword><style  face="normal" font="default" size="100%">ice-covered lakes</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mats</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">03/2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://agupubs.onlinelibrary.wiley.com/doi/10.1029/2024JG008516</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">130</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Gas bubbles directly influence the macromorphology of benthic microbial mats resulting in preservable biosedimentary structures. This study characterizes the morphology and distribution of microbial mats growing in gas-supersaturated, perennially ice-covered lakes Fryxell, Joyce, and Hoare of the McMurdo Dry Valleys of Antarctica. Photosynthetic benthic mats within the gas-supersaturated zone trap oxygen-rich bubbles and become buoyant, tearing off the bottom as &amp;ldquo;liftoff mats.&amp;rdquo; These liftoff mats form a succession of morphologies starting with bubble-induced deformation of flat mats into tent, ridge, and finger liftoff mat. With progressive deformation, mats tear, forming sheet liftoff, while multiple cycles of deformation and tearing transform sheet into strip liftoff. Some mats detach from the substrate and float to the underside of the ice. The depth range of the liftoff zone has varied over time at each lake. Downslope expansion of bubble formation brings previously bubble-free, deep-water pinnacle mats into the liftoff zone. When the liftoff zone shallows, liftoff mats at the deeper end deflate and can become scaffolding for additional mat growth. The superposition and relative orientation of liftoff and pinnacle mats can be used to track the maximum depth of the liftoff zone and changes in gas saturation state in these lakes through time. Our results demonstrate that gas bubbles, even when they are transitory, can exert a significant impact on the morphology of microbial mats at larger scales. This provides a way to identify similar structures and gas supersaturated environments in the biosedimentary record.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Evans, Thomas W.</style></author><author><style face="normal" font="default" size="100%">Kalambokidis, Maria J.</style></author><author><style face="normal" font="default" size="100%">Jungblut, Anne D.</style></author><author><style face="normal" font="default" size="100%">Millar, Jasmin L.</style></author><author><style face="normal" font="default" size="100%">Bauersachs, Thorsten</style></author><author><style face="normal" font="default" size="100%">Grotheer, Hendrik</style></author><author><style face="normal" font="default" size="100%">Mackey, Tyler J.</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author><author><style face="normal" font="default" size="100%">Summons, Roger E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Lipid biomarkers from microbial mats on the McMurdo Ice Shelf, Antarctica: Signatures for life in the cryosphere</style></title><secondary-title><style face="normal" font="default" size="100%">Frontiers in Microbiology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Front. Microbiol.</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">bacteriohopanepolyol</style></keyword><keyword><style  face="normal" font="default" size="100%">cyanobacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">heterocyte glycolipids</style></keyword><keyword><style  face="normal" font="default" size="100%">homeoviscous adaptation</style></keyword><keyword><style  face="normal" font="default" size="100%">intact polar lipid</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mats</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">06/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.frontiersin.org/articles/10.3389/fmicb.2022.903621/full</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">903621</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Persistent cold temperatures, a paucity of nutrients, freeze-thaw cycles, and the strongly seasonal light regime make Antarctica one of Earth&amp;rsquo;s least hospitable surface environments for complex life. Cyanobacteria, however, are well-adapted to such conditions and are often the dominant primary producers in Antarctic inland water environments. In particular, the network of meltwater ponds on the &amp;lsquo;dirty ice&amp;rsquo; of the McMurdo Ice Shelf is an ecosystem with extensive cyanobacteria-dominated microbial mat accumulations. This study investigated intact polar lipids (IPLs), heterocyte glycolipids (HGs), and bacteriohopanepolyols (BHPs) in combination with 16S and 18S rRNA gene diversity in microbial mats of twelve ponds in this unique polar ecosystem. To constrain the effects of nutrient availability, temperature and freeze-thaw cycles on the lipid membrane composition, lipids were compared to stromatolite-forming cyanobacterial mats from ice-covered lakes in the McMurdo Dry Valleys as well as from (sub)tropical regions and hot springs. The 16S rRNA gene compositions of the McMurdo Ice Shelf mats confirm the dominance of Cyanobacteria and Proteobacteria while the 18S rRNA gene composition indicates the presence of Ochrophyta, Chlorophyta, Ciliophora, and other microfauna. IPL analyses revealed a predominantly bacterial community in the meltwater ponds, with archaeal lipids being barely detectable. IPLs are dominated by glycolipids and phospholipids, followed by aminolipids. The high abundance of sugar-bound lipids accords with a predominance of cyanobacterial primary producers. The phosphate-limited samples from the (sub)tropical, hot spring, and Lake Vanda sites revealed a higher abundance of aminolipids compared to those of the nitrogen-limited meltwater ponds, affirming the direct affects that N and P availability have on IPL compositions. The high abundance of polyunsaturated IPLs in the Antarctic microbial mats suggests that these lipids provide an important mechanism to maintain membrane fluidity in cold environments. High abundances of HG keto-ols and HG keto-diols, produced by heterocytous cyanobacteria, further support these findings and reveal a unique distribution compared to those from warmer climates.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dillon, Megan L.</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author><author><style face="normal" font="default" size="100%">Jungblut, Anne D.</style></author><author><style face="normal" font="default" size="100%">Mackey, Tyler J.</style></author><author><style face="normal" font="default" size="100%">Eisen, Jonathan A.</style></author><author><style face="normal" font="default" size="100%">Peter T. Doran</style></author><author><style face="normal" font="default" size="100%">Sumner, Dawn Y.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Energetic and environmental constraints on the community structure of benthic microbial mats in Lake Fryxell, Antarctica</style></title><secondary-title><style face="normal" font="default" size="100%">FEMS Microbiology Ecology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antarctica</style></keyword><keyword><style  face="normal" font="default" size="100%">energy</style></keyword><keyword><style  face="normal" font="default" size="100%">Lake Fryxell</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mat</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxygen</style></keyword><keyword><style  face="normal" font="default" size="100%">Photosynthetically Active Radiation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">02/2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://academic.oup.com/femsec/article/96/2/fiz207/5697196</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">96</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Ecological communities are regulated by the flow of energy through environments. Energy flow is typically limited by access to photosynthetically active radiation (PAR) and oxygen concentration (O&lt;sub&gt;2&lt;/sub&gt;). The microbial mats growing on the bottom of Lake Fryxell, Antarctica, have well-defined environmental gradients in PAR and (O&lt;sub&gt;2&lt;/sub&gt;). We analyzed the metagenomes of layers from these microbial mats to test the extent to which access to oxygen and light controls community structure. We found variation in the diversity and relative abundances of Archaea, Bacteria and Eukaryotes across three (O&lt;sub&gt;2&lt;/sub&gt;) and PAR conditions: high (O&lt;sub&gt;2&lt;/sub&gt;) and maximum PAR, variable (O&lt;sub&gt;2&lt;/sub&gt;) with lower maximum PAR, and low (O&lt;sub&gt;2&lt;/sub&gt;) and maximum PAR. We found distinct communities structured by the optimization of energy use on a millimeter-scale across these conditions. In mat layers where (O&lt;sub&gt;2&lt;/sub&gt;) was saturated, PAR structured the community. In contrast, (O&lt;sub&gt;2&lt;/sub&gt;) positively correlated with diversity and affected the distribution of dominant populations across the three habitats, suggesting that meter-scale diversity is structured by energy availability. Microbial communities changed across covarying gradients of PAR and (O&lt;sub&gt;2&lt;/sub&gt;). The comprehensive metagenomic analysis suggests that the benthic microbial communities in Lake Fryxell are structured by energy flow across both meter- and millimeter-scales.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record></records></xml>