Front. Mar. Sci.Frontiers in Marine ScienceFront. Mar. Sci.2296-7745Frontiers Media S.A.10.3389/fmars.2021.793020Marine ScienceEditorialEditorial: Effects of Ice Loss on Marine BiodiversityLinseKatrin1*PeekenIlka2TandbergAnne Helene Solberg31Biodiversity, Evolution & Adaptation Team, British Antarctic Survey, Cambridge, United Kingdom2Polar Biological Oceanography, Helmholtz Centre for Polar and Marine Research, Alfred Wegener Institute, Bremerhaven, Germany3Natural History Department, University Museum, University of Bergen, Bergen, Norway
Edited and reviewed by: Thomas Wilke, University of Giessen, Germany
*Correspondence: Katrin Linse kl@bas.ac.uk
This article was submitted to Marine Evolutionary Biology, Biogeography and Species Diversity, a section of the journal Frontiers in Marine Science
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Editorial on the Research Topic Effects of Ice Loss on Marine Biodiversityzooplanktonphytoplanktonzoobenthosmeiofaunain-situ habitat images
The Arctic and Antarctic oceans are undergoing changes in the extent of their sea-ice and ice-shelves (IPCC, in press). These have important impacts on the biodiversity, structure, and function of sea ice biota, pelagic and benthic communities, and will change the composition, distribution, and productivity of all species in these ecosystems (Constable et al., 2014; Lannuzel et al., 2020). Decreasing Arctic sea ice has led to a northwards shift in phytoplankton distributions (Nöthig et al., 2015; Metfies et al., 2016) and phytoplankton blooms were discovered in autumn (Ardyna et al., 2014). Shifts were also observed in the vertical and horizontal distributions of zooplankton communities (Wassmann et al., 2015). In the Antarctic, gigantic icebergs have calved from ice shelves and in some cases, entire ice shelves have collapsed enabling sunlight and currents to reach the underlying benthic communities and providing new space for pelagic ecosystems (e.g., Vernet et al., 2019). The benthic habitats and their faunal inhabitants under floating Antarctic ice shelves are among the least known marine communities on Earth.
This Research Topic aimed to address all aspects of marine biodiversity science that introduce new knowledge to improve our understanding of the effects ice loss (sea ice and ice shelf) has on the pelagic and benthic communities in the polar oceans (Figure 1). Contributions were delivered by 61 participating authors providing up-to-date information on the species richness and biogeographic responses in marine biodiversity adapted to ice-covered environments, on their phylogeographic relationships and how they affect biogeochemical cycles, on the status of the effects of ice loss on marine biogeochemistry and biodiversity on regional and global scales, on how feedbacks and controls could change these systems and ultimately, on what new conditions might be present in these regions on decadal and longer time scales.
Locations of pelagic and benthic biodiversity study sites in the Arctic and Antarctic and current seasonal sea ice extent. (A) Arctic, (B) Antarctic and Southern Ocean. The maps are drawn to 55° latitude. Sea ice extent data are from https://nsidc.org/cryosphere/sotc/sea_ice.html.
Reduction of sea-ice in the Arctic resulted in a massive loss of the previous typical multiyear ice, with a reduction of biodiversity of the sea-ice associated protists (Hop et al., 2021) and an increase of primary production (Arrigo and Van Dijken, 2015). North of Svalbard Ehrlich et al. show loss in biodiversity for the sympagic meiofauna, with nematodes totally absent and only a low number of flatworms. In addition, hardly any sympagic amphipods were present, suggesting the strong connectivity of these organisms with multiyear ice. A study of lipid biomarkers gives further insight in the transfer of sea-ice derived carbon for higher trophic levels. While Kohlbach et al. (2016) demonstrated a strong dependence of the sympagic and pelagic organisms on sea-ice derived carbon in the Central Arctic, Kohlbach et al. suggest that for Barents Sea amphipods this is only a surplus food source. Calanoid copepods already shifted their food demand entirely on pelagic resources and thus might have already adapted to the changing sea ice conditions in this region. By applying high-throughput amplicon sequencing, Kalenitchenko et al. show a distinct difference of protists diversity between the Arctic Ocean and the Central Arctic suggesting a low connectivity between these regions and imply that the ongoing changes in sea ice cover will not result in a high productive Nares Strait ecosystem.
Moving to the Antarctic, particularly the western Antarctic Peninsula is the key region, where rapid sea ice loss has been reported with major consequences for the ecosystem (Constable et al., 2014). By applying whole community metatranscriptomic together with lipidomics Bowman et al. analyzed how lipid production and utilization was influenced by changing light conditions. They show an intrinsic adaptation behind various pelagic species, implying future changes in the phytoplankton composition, and the production of lipid-rich food sources with the ongoing change of the sea ice cover along the western Antarctic Peninsula.
Effects of changes and status-quo of benthic communities and their biodiversity were studied in the Antarctic Peninsula, Weddell, and Ross seas. The Prince Gustav Channel area had been influenced by the break-up of the Prince Gustav ice shelf, retreating glaciers, and changes in sea-ice cover but its benthic biodiversity had been never assessed. The meiobenthic and nematode communities, analyzed by Pantó et al. using metabarcoding and environmental proxy characterization, revealed high densities at all depths based on availability of fresh organic sedimentary matter. As shown by Di Franco et al. also abundance and community structure of macrobenthic peracarids were affected by length of sea ice cover and associated blooms of the primary producers. Drennan et al. reported a diverse and spatially heterogenous annelid fauna, including wide-spread, circum-Antarctic species as well as yet unnamed species in an area with dynamic recent glacial history. The in-situ habitat heterogeneity in the Prince Gustav Channel was illustrated by Almond et al. showing that locations previously covered by the ice shelf held distinct and unique communities. In the Ross Sea, Cummings et al. investigating macro-infaunal and mega-epifaunal benthos showed that organic seabed fluxes and sea ice cover were important for the community structure.
Describing and understanding the marine communities and their biodiversity under the floating ice shelves is still a gap in our knowledge, as these communities are mostly accessible to study after the collapse. Multidisciplinary collaborations with geological and glaciological scientists using shelf ice core bore holes gave a first glimpse into these unknown ecosystems as reviewed by Griffiths et al. who also presented the first record of hard rock suspension feeder community hundreds of kilometers away from the open ocean. These unique, unstudied ecosystems, like under the Filchner-Ronne Ice shelf, are under future climate threads as Naughten et al. (2021) are predicting significant changes in the oceanographic settings.
This volume provides a brief indication of the current state of the art and indicates some of the pressing issues and questions related to ice and biodiversity loss in the Polar Regions. We, the editors, hope that this Research Topic will form the basis of further discussion and will foster future cross-polar region research in the effects of ice loss on marine biodiversity.
Author Contributions
KL wrote the first draft of the manuscript KL, IP, and AT wrote sections of the manuscript. KL drafted the figure. All authors contributed to manuscript, read, and approved the submitted version.
Conflict of Interest
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.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
We thank our authors for submitting their research to our topic. We are especially grateful to the reviewers who returned their comments within the requested timeline. Special thanks to Huw J. Griffiths for providing the maps for the figure.
ReferencesArdynaM.BabinM.GosselinM.DevredE.RainvilleL.TremblayJ. E. (2014). Recent Arctic Ocean sea ice loss triggers novel fall phytoplankton blooms. Geophys. Res. Lett.41, 6207–6212. 10.1002/2014GL061047ArrigoK. R.Van DijkenG. L. (2015). Continued increases in Arctic Ocean primary production. Prog. Oceanogr.136, 60–70. 10.1016/j.pocean.2015.05.002ConstableA. J.Melbourne-ThomasJ.CorneyS. P.ArrigoK. R.BarbraudC.BarnesD. K. A.. (2014). Climate change and Southern Ocean ecosystems I: how changes in physical habitats directly affect marine biota. Glob. Change Biol.20, 3004–3025. 10.1111/gcb.1262324802817HopH.WoldA.MeyerA.BaileyA.HatlebakkM.KwasniewskiS.. (2021). Winter-spring development of the zooplankton community below sea ice in the Arctic Ocean. Front. Mar. Sci. 9, 1–21. 10.3389/fmars.2021.609480IPCC (in press). Climate change 2021: the physical science basis, in Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change, eds Masson-DelmotteV.ZhaiP.PiraniA.ConnorsS. L.PéanC.BergerS.CaudN.ChenY.GoldfarbL.GomisM. I.HuangM.LeitzellK.LonnoyE.MatthewsJ. B. R.MaycockT. K.WaterfieldT.YelekçiO.YuR.ZhouB. (Cambridge University Press).KohlbachD.GraeveM.LangeB. A.DavidC.PeekenI.FloresH. (2016). The importance of ice algae-produced carbon in the central Arctic Ocean ecosystem: food web relationships revealed by lipid and stable isotope analyses. Limnol. Oceanogr.61, 2027–2044. 10.1002/lno.10351LannuzelD.TedescoL.Van LeeuweM.CampbellK.FloresH.DelilleB.. (2020). The future of Arctic sea-ice biogeochemistry and ice-associated ecosystems. Nat. Clim. Change10, 983–992. 10.1038/s41558-020-00940-4MetfiesK.Von AppenW. J.KiliasE.NicolausA.NothigE. M. (2016). Biogeography and photosynthetic biomass of arctic marine pico-eukaroytes during summer of the record sea ice minimum 2012. PLoS ONE11:e0148512. 10.1371/journal.pone.014851226895333NaughtenK. A.De RydtJ.RosierS. H. R.JenkinsA.HollandP. R.RidleyJ. K. (2021). Two-timescale response of a large Antarctic ice shelf to climate change. Nat. Commun.12:1991. 10.1038/s41467-021-22259-033790289NöthigE. M.BracherA.EngelA.MetfiesK.NiehoffB.PeekenI.. (2015). Summertime plankton ecology in Fram Strait - a compilation of long- and short-term observations. Polar Res.34:23349. 10.3402/polar.v34.23349VernetM.GeibertW.HoppemaM.BrownP. J.HaasC.HellmerH. H.. (2019). The Weddell Gyre, Southern Ocean: present knowledge and future challenges. Rev. Geophys.57, 623–708. 10.1029/2018RG000604WassmannP.KosobokovaK. N.SlagstadD.DrinkvvaterK. F.HoperoftR. R.MooreS. E.. (2015). The contiguous domains of Arctic Ocean advection: trails of life and death. Prog. Oceanogr.139, 42–65. 10.1016/j.pocean.2015.06.011‘Oh, my dear Thomas, you haven’t heard the terrible news then?’ she said. ‘I thought you would be sure to have seen it placarded somewhere. Alice went straight to her room, and I haven’t seen her since, though I repeatedly knocked at the door, which she has locked on the inside, and I’m sure it’s most unnatural of her not to let her own mother comfort her. It all happened in a moment: I have always said those great motor-cars shouldn’t be allowed to career about the streets, especially when they are all paved with cobbles as they are at Easton Haven, which are{331} so slippery when it’s wet. He slipped, and it went over him in a moment.’ My thanks were few and awkward, for there still hung to the missive a basting thread, and it was as warm as a nestling bird. I bent low--everybody was emotional in those days--kissed the fragrant thing, thrust it into my bosom, and blushed worse than Camille. "What, the Corner House victim? Is that really a fact?" "My dear child, I don't look upon it in that light at all. The child gave our picturesque friend a certain distinction--'My husband is dead, and this is my only child,' and all that sort of thing. It pays in society." leave them on the steps of a foundling asylum in order to insure [See larger version] Interoffice guff says you're planning definite moves on your own, J. O., and against some opposition. Is the Colonel so poor or so grasping—or what? Albert could not speak, for he felt as if his brains and teeth were rattling about inside his head. The rest of[Pg 188] the family hunched together by the door, the boys gaping idiotically, the girls in tears. "Now you're married." The host was called in, and unlocked a drawer in which they were deposited. The galleyman, with visible reluctance, arrayed himself in the garments, and he was observed to shudder more than once during the investiture of the dead man's apparel. HoME香京julia种子在线播放
ENTER NUMBET 0016griven.com.cn www.jiahei.com.cn www.ilijia.com.cn www.kguedm.com.cn www.nrchain.com.cn ubdex.net.cn www.op8news.com.cn www.sbgdss.org.cn www.x-gnd.com.cn www.wuxibar.org.cn