<?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%">Stone, Michael S.</style></author><author><style face="normal" font="default" size="100%">Devlin, Shawn</style></author><author><style face="normal" font="default" size="100%">Ian Hawes</style></author><author><style face="normal" font="default" size="100%">Kathleen A. Welch</style></author><author><style face="normal" font="default" size="100%">Michael N. Gooseff</style></author><author><style face="normal" font="default" size="100%">Cristina D. Takacs-Vesbach</style></author><author><style face="normal" font="default" size="100%">Rachael M. Morgan-Kiss</style></author><author><style face="normal" font="default" size="100%">Byron Adams</style></author><author><style face="normal" font="default" size="100%">John E. Barrett</style></author><author><style face="normal" font="default" size="100%">John C. Priscu</style></author><author><style face="normal" font="default" size="100%">Peter T. Doran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">McMurdo Dry Valley lake edge ‘moats’: The ecological intersection between terrestrial and aquatic polar desert habitat</style></title><secondary-title><style face="normal" font="default" size="100%">Antarctic Science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">connectivity</style></keyword><keyword><style  face="normal" font="default" size="100%">ecosystem</style></keyword><keyword><style  face="normal" font="default" size="100%">ice</style></keyword><keyword><style  face="normal" font="default" size="100%">microbial mats</style></keyword><keyword><style  face="normal" font="default" size="100%">transition</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">04/2024</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/journals/antarctic-science/article/mcmurdo-dry-valley-lake-edge-moats-the-ecological-intersection-between-terrestrial-and-aquatic-polar-desert-habitats/31D94DD51E651603482A3AE6E8A52A57</style></url></web-urls></urls><pages><style face="normal" font="default" size="100%">1 - 17</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Aquatic ecosystems - lakes, ponds and streams - are hotspots of biodiversity in the cold and arid environment of Continental Antarctica. Environmental change is expected to increasingly alter Antarctic aquatic ecosystems and modify the physical characteristics and interactions within the habitats that they support. Here, we describe physical and biological features of the peripheral &amp;lsquo;moat&amp;rsquo; of a closed-basin Antarctic lake. These moats mediate connectivity amongst streams, lake and soils. We highlight the cyclical moat transition from a frozen winter state to an active open-water summer system, through refreeze as winter returns. Summer melting begins at the lakebed, initially creating an ice-constrained lens of liquid water in November, which swiftly progresses upwards, creating open water in December. Conversely, freezing progresses slowly from the water surface downwards, with water at 1 m bottom depth remaining liquid until May. Moats support productive, diverse benthic communities that are taxonomically distinct from those under the adjacent permanent lake ice. We show how ion ratios suggest that summer exchange occurs amongst moats, streams, soils and sub-ice lake water, perhaps facilitated by within-moat density-driven convection. Moats occupy a small but dynamic area of lake habitat, are disproportionately affected by recent lake-level rises and may thus be particularly vulnerable to hydrological change.&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%">Patriarche, Jeffrey D.</style></author><author><style face="normal" font="default" size="100%">John C. Priscu</style></author><author><style face="normal" font="default" size="100%">Cristina D. Takacs-Vesbach</style></author><author><style face="normal" font="default" size="100%">Winslow, Luke A.</style></author><author><style face="normal" font="default" size="100%">Myers, Krista F.</style></author><author><style face="normal" font="default" size="100%">Heather N. Buelow</style></author><author><style face="normal" font="default" size="100%">Rachael M. Morgan-Kiss</style></author><author><style face="normal" font="default" size="100%">Peter T. Doran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Year‐round and long‐term phytoplankton dynamics in Lake Bonney, a permanently ice‐covered Antarctic lake</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%">J Geophys Res Biogeosci</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">algae</style></keyword><keyword><style  face="normal" font="default" size="100%">Antarctic</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorometry</style></keyword><keyword><style  face="normal" font="default" size="100%">ice</style></keyword><keyword><style  face="normal" font="default" size="100%">lakes</style></keyword><keyword><style  face="normal" font="default" size="100%">light</style></keyword><keyword><style  face="normal" font="default" size="100%">profiling</style></keyword><keyword><style  face="normal" font="default" size="100%">winter</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">04/2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://agupubs.onlinelibrary.wiley.com/doi/10.1029/2020JG005925</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">126</style></volume><pages><style face="normal" font="default" size="100%">e2020JG005925</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Lake Bonney (McMurdo Dry Valleys, east Antarctica) represents a year‐round refugium for life adapted to permanent extreme conditions. Despite intensive research since the 1960s, due to the logistical constraints posed by 4‐months of 24‐h darkness, knowledge of how the resident photosynthetic microorganisms respond to the polar winter is limited. In addition, the lake level has risen by more than 3 m since 2004: impacts of rapid lake level rise on phytoplankton community structure is also poorly understood. From 2004 to 2015 an in situ submersible spectrofluorometer (bbe FluoroProbe) was deployed in Lake Bonney during the austral summer to quantify the vertical structure of four functional algal groups (green algae, mixed algae, and cryptophytes, cyanobacteria). During the 2013&amp;ndash;2014 field season the Fluoroprobe was mounted on autonomous cable‐crawling profilers deployed in both the east and west lobes of Lake Bonney, obtaining the first daily phytoplankton profiles through the polar night. Our findings showed that phytoplankton communities were differentially impacted by physical and chemical factors over long‐term versus seasonal time scales. Following a summer of rapid lake level rise (2010&amp;ndash;2011), an increase in depth integrated chlorophyll a (chl‐a) occurred in Lake Bonney caused by stimulation of photoautotrophic green algae. Conversely, peaks in chl‐a during the polar night were associated with an increase in mixotrophic haptophytes and cryptophytes. Collectively our data reveal that phytoplankton groups possessing variable trophic abilities are differentially competitive during seasonal and long‐term time scales owing to periods of higher nutrients (photoautotrophs) versus light/energy limitation (mixotrophs).&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue></record></records></xml>