Temporal Changes in Snow Albedo, Including the Possible Effects of Red
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Marine Ecology Progress Series 600:21
Vol. 600: 21–39, 2018 MARINE ECOLOGY PROGRESS SERIES Published July 30 https://doi.org/10.3354/meps12663 Mar Ecol Prog Ser OPENPEN ACCESSCCESS Short-term processing of ice algal- and phytoplankton- derived carbon by Arctic benthic communities revealed through isotope labelling experiments Anni Mäkelä1,*, Ursula Witte1, Philippe Archambault2 1School of Biological Sciences, University of Aberdeen, Aberdeen AB24 3UU, UK 2Département de biologie, Québec Océan, Université Laval, Québec, QC G1V 0A6, Canada ABSTRACT: Benthic ecosystems play a significant role in the carbon (C) cycle through remineral- ization of organic matter reaching the seafloor. Ice algae and phytoplankton are major C sources for Arctic benthic consumers, but climate change-mediated loss of summer sea ice is predicted to change Arctic marine primary production by increasing phytoplankton and reducing ice algal contributions. To investigate the impact of changing algal C sources on benthic C processing, 2 isotope tracing experiments on 13C-labelled ice algae and phytoplankton were conducted in the North Water Polynya (NOW; 709 m depth) and Lancaster Sound (LS; 794 m) in the Canadian Arc- tic, during which the fate of ice algal (CIA) and phytoplankton (CPP) C added to sediment cores was traced over 4 d. No difference in sediment community oxygen consumption (SCOC, indicative of total C turnover) between the background measurements and ice algal or phytoplankton cores was found at either site. Most of the processed algal C was respired, with significantly more CPP than CIA being released as dissolved inorganic C at both sites. Macroinfaunal uptake of algal C was minor, but bacterial assimilation accounted for 33−44% of total algal C processing, with no differences in bacterial uptake of CPP and CIA found at either site. -
Chilling Out: the Evolution and Diversification of Psychrophilic Algae with a Focus on Chlamydomonadales
Polar Biol DOI 10.1007/s00300-016-2045-4 REVIEW Chilling out: the evolution and diversification of psychrophilic algae with a focus on Chlamydomonadales 1 1 1 Marina Cvetkovska • Norman P. A. Hu¨ner • David Roy Smith Received: 20 February 2016 / Revised: 20 July 2016 / Accepted: 10 October 2016 Ó Springer-Verlag Berlin Heidelberg 2016 Abstract The Earth is a cold place. Most of it exists at or Introduction below the freezing point of water. Although seemingly inhospitable, such extreme environments can harbour a Almost 80 % of the Earth’s biosphere is permanently variety of organisms, including psychrophiles, which can below 5 °C, including most of the oceans, the polar, and withstand intense cold and by definition cannot survive at alpine regions (Feller and Gerday 2003). These seemingly more moderate temperatures. Eukaryotic algae often inhospitable places are some of the least studied but most dominate and form the base of the food web in cold important ecosystems on the planet. They contain a huge environments. Consequently, they are ideal systems for diversity of prokaryotic and eukaryotic organisms, many of investigating the evolution, physiology, and biochemistry which are permanently adapted to the cold (psychrophiles) of photosynthesis under frigid conditions, which has (Margesin et al. 2007). The environmental conditions in implications for the origins of life, exobiology, and climate such habitats severely limit the spread of terrestrial plants, change. Here, we explore the evolution and diversification and therefore, primary production in perpetually cold of photosynthetic eukaryotes in permanently cold climates. environments is largely dependent on microbes. Eukaryotic We highlight the known diversity of psychrophilic algae algae and cyanobacteria are the dominant photosynthetic and the unique qualities that allow them to thrive in severe primary producers in cold habitats, thriving in a surprising ecosystems where life exists at the edge. -
Hidden Food in the Coldest of Times the NUTRIENT ROLE of SEA ICE Copepods, Tiny Lipid-Rich Obtaining Sufficient Food Under Fig
UNDERSTANDING ECOSYSTEM PROCESSES IN THE BERING SEA 2007–2013 Hidden Food in the Coldest of Times THE NUTRIENT ROLE OF SEA ICE Copepods, tiny lipid-rich obtaining sufficient food under Fig. 1 crustaceans in the Bering Sea, the ice to initiate feeding and are a favored meal of larval and reproduction. A second question juvenile Pollock. One copepod is “what is this food source”? One that dominates the zooplankton possibility was the layer of ice on the Bering Sea shelf, and shelf algae—a diverse community of areas around the Arctic Ocean, microscopic plants and animals is Calanus glacialis (Figure 1). that grow under the ice during We know that the abundance of spring (Figure 2)—rather than this species fluctuates between from the more usual phytoplank- years. Surprisingly, colder years, ton community in the water when ice cover is more extensive column beneath. and persists longer during spring, appear to favor growth of the How We Did It copepod population. Why is this? We collected zooplankton We set out to answer this ques- samples to see what the C. glacialis Fig. 2 tion during a cruise in late winter population was doing, whether of 2009 through early spring of the adult females were laying eggs 2010, when ice covered most of or not, and how much food was the Bering Sea shelf. in their guts. We determined the Since reproduction and identity of individual prey spe- growth of this copepod is con- cies in their guts from their DNA trolled by the availability of food, and quantified the amount of this we thought that they must be continued on page 2 The Big Picture The high feeding rates of the copepod Calanus glacialis that we observed during a cruise in late Blocks of sea ice turned winter and early spring of 2009/2010 could not have been sustained by the low levels of phyto- upside down to reveal plankton in the water column. -
Photobiological Effects on Ice Algae of a Rapid Whole-Fjord Loss of Snow Cover During Spring Growth in Kangerlussuaq, a West Greenland Fjord
Journal of Marine Science and Engineering Article Photobiological Effects on Ice Algae of a Rapid Whole-Fjord Loss of Snow Cover during Spring Growth in Kangerlussuaq, a West Greenland Fjord Brian K. Sorrell 1,* , Ian Hawes 2 , Tanja Stratmann 3,4 and Lars Chresten Lund-Hansen 1 1 Arctic Research Centre, Department of Biology, Aarhus University, Aarhus C., DK-8000 Aarhus, Denmark; [email protected] 2 Coastal Marine Field Station, Environmental Research Institute, University of Waikato, Sulphur Point, Tauranga 3110, New Zealand; [email protected] 3 Department of Earth Sciences, Utrecht University, 3584 CB Utrecht, The Netherlands; [email protected] 4 HGF MPG Joint Research Group for Deep-Sea Ecology and Technology, Max Planck Institute for Marine Microbiology, 28359 Bremen, The Netherlands * Correspondence: [email protected] Abstract: Snow cover on sea ice is the most important factor controlling light availability for sea ice algae, but it is predicted by climate models to become more variable and stochastic. Here, we document effects of a sudden, complete loss of the entire snow cover on first-year sea ice at Kangerlussuaq Fjord, West Greenland, due to a natural Föhn wind event that caused a ca. 17 ◦C air temperature increase over 36 h. We applied Imaging-PAM fluorometry to examine effects of snow cover on algal distribution and photobiology and observed a rapid decrease in algal biomass associated with loss of the skeletal ice crystal layer on the underside of the ice that had supported most of the visible algae. Furthermore, the remaining algae were photobiologically stressed, as seen Citation: Sorrell, B.K.; Hawes, I.; in a significant decrease in the dark-acclimated fluorescence yield (F ) from 0.55 before snow Stratmann, T.; Lund-Hansen, L.C. -
A Taxonomic Reassessment of Chlamydomonas Meslinii (Volvocales, Chlorophyceae) with a Description of Paludistella Gen.Nov
Phytotaxa 432 (1): 065–080 ISSN 1179-3155 (print edition) https://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2020 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.432.1.6 A taxonomic reassessment of Chlamydomonas meslinii (Volvocales, Chlorophyceae) with a description of Paludistella gen.nov. HANI SUSANTI1,6, MASAKI YOSHIDA2, TAKESHI NAKAYAMA2, TAKASHI NAKADA3,4 & MAKOTO M. WATANABE5 1Life Science Innovation, School of Integrative and Global Major, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8577, Japan. 2Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8577, Japan. 3Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata, 997-0052, Japan. 4Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa, Kanagawa, 252-8520, Japan. 5Algae Biomass Energy System Development and Research Center, University of Tsukuba. 6Research Center for Biotechnology, Indonesian Institute of Sciences, Jl. Raya Bogor KM 46 Cibinong West Java, Indonesia. Corresponding author: [email protected] Abstract Chlamydomonas (Volvocales, Chlorophyceae) is a large polyphyletic genus that includes numerous species that should be classified into independent genera. The present study aimed to examine the authentic strain of Chlamydomonas meslinii and related strains based on morphological and molecular data. All the strains possessed an asteroid chloroplast with a central pyrenoid and hemispherical papilla; however, they were different based on cell and stigmata shapes. Molecular phylogenetic analyses based on 18S rDNA, atpB, and psaB indicated that the strains represented a distinct subclade in the clade Chloromonadinia. The secondary structure of ITS-2 supported the separation of the strains into four species. -
Occurrence of an Algal Bloom Under Arctic Pack Ice
MARINE ECOLOGY PROGRESS SERIES Vol. 131: 301-305, 1996 Published February 8 p-- Mar Ecol Prog Serpp p -- - l NOTE Occurrence of an algal bloom under Arctic pack ice R. Gradinger Institut fur Polarokologie, WischhofstraRe 1-3, Gebaude 12, D-24148 Kiel, Germany ABSTRACT: Summer melting of sea ice leads to the formation Materials and methods. The investigation was con- of under-rce melt ponds in Arctic seas. The biological char- ducted during the RV 'Polarstern' expedition ARK IX/4 acteristics of such a pond were studied in summer 1993. from August to October 1993. Sampling of ice cores The chlorophyte Pyramimonas sp. (Prasinophyceae) formed a unialgal bloom with cell densities of 19.1 X 103 cells ml-' and and under-ice water took place at Stns (station number a pigment concentration of 29.6 mg m-" comparison with = day of the year) 230 (82"45.4'N,40" 12.2' E) and 231 ice core data revealed differences in algal biomass and com- (82O23.2' N, 40°54.9'E) At Stn 230, ice was collected munity structure. Physical data indicate that under-ice ponds from a 2 m thick multi-year ice floe. At Stn 231, we are a common feature in the Arctic Ocean. Thus, communit~es encountered a layer of thin ice (grey ice of 21 to 60 cm within under-ice ponds, which have not been included in pro- duction estimates, may slgniflcantly contribute to the Arctrc thickness) between 2 multi-year ice floes, which were marine food web more than 4 m thick (Fig. -
The Symbiotic Green Algae, Oophila (Chlamydomonadales
University of Connecticut OpenCommons@UConn Master's Theses University of Connecticut Graduate School 12-16-2016 The yS mbiotic Green Algae, Oophila (Chlamydomonadales, Chlorophyceae): A Heterotrophic Growth Study and Taxonomic History Nikolaus Schultz University of Connecticut - Storrs, [email protected] Recommended Citation Schultz, Nikolaus, "The yS mbiotic Green Algae, Oophila (Chlamydomonadales, Chlorophyceae): A Heterotrophic Growth Study and Taxonomic History" (2016). Master's Theses. 1035. https://opencommons.uconn.edu/gs_theses/1035 This work is brought to you for free and open access by the University of Connecticut Graduate School at OpenCommons@UConn. It has been accepted for inclusion in Master's Theses by an authorized administrator of OpenCommons@UConn. For more information, please contact [email protected]. The Symbiotic Green Algae, Oophila (Chlamydomonadales, Chlorophyceae): A Heterotrophic Growth Study and Taxonomic History Nikolaus Eduard Schultz B.A., Trinity College, 2014 A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science at the University of Connecticut 2016 Copyright by Nikolaus Eduard Schultz 2016 ii ACKNOWLEDGEMENTS This thesis was made possible through the guidance, teachings and support of numerous individuals in my life. First and foremost, Louise Lewis deserves recognition for her tremendous efforts in making this work possible. She has performed pioneering work on this algal system and is one of the preeminent phycologists of our time. She has spent hundreds of hours of her time mentoring and teaching me invaluable skills. For this and so much more, I am very appreciative and humbled to have worked with her. Thank you Louise! To my committee members, Kurt Schwenk and David Wagner, thank you for your mentorship and guidance. -
The VIIRS Sea-Ice Albedo Product Generation and Preliminary Validation
remote sensing Article The VIIRS Sea-Ice Albedo Product Generation and Preliminary Validation Jingjing Peng 1,* , Yunyue Yu 2 , Peng Yu 1,2 and Shunlin Liang 3 1 Earth System Science Interdisciplinary Center/Cooperative Institute for Climate and Satellites-Maryland, University of Maryland, College Park, MD 20740, USA; [email protected] 2 NOAA NESDIS Center for Satellite Applications and Research, College Park, MD 20740, USA; [email protected] 3 Department of Geographical Sciences, University of Maryland, MD 20740, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-240-825-6625 Received: 14 September 2018; Accepted: 15 November 2018; Published: 17 November 2018 Abstract: Ice albedo feedback amplifies climate change signals and thus affects the global climate. Global long-term records on sea-ice albedo are important to characterize the regional or global energy budget. As the successor of MODIS (Moderate Resolution Imaging Spectroradiometer), VIIRS (Visible Infrared Imaging Radiometer Suite) started its observation from October 2011 on S-NPP (Suomi National Polar-orbiting Partnership). It has improved upon the capabilities of the operational Advanced Very High Resolution Radiometer (AVHRR) and provides observation continuity with MODIS. We used a direct estimation algorithm to produce a VIIRS sea-ice albedo (VSIA) product, which will be operational in the National Oceanic and Atmospheric Administration’s (NOAA) S-NPP Data Exploration (NDE) version of the VIIRS albedo product. The algorithm is developed from the angular bin regression method to simulate the sea-ice surface bidirectional reflectance distribution function (BRDF) from physical models, which can represent different sea-ice types and vary mixing fractions among snow, ice, and seawater. -
The Biogeography of Green Algae Associated with Red Snow in Japan
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by National Institute of Polar Research Repository The Biogeography of Green Algae Associated with Red Snow in Japan Ryota Ito1, Masashi Murakami1, Nozomu Takeuchi2 1Department of Biology, Graduate School of Science, Chiba University, Japan 2Department of Earth Science, Graduate School of Science, Chiba University, Japan Red snow is a world-wide phenomenon which is the changes in the color of snow surface into red. Red snow is known to be caused by the bloom of green algae, mainly Chlamydomonas nivalis (Takeuchi et al., 2006). Because a snow surface with red color decreases its albedo, it implies that red snow accelerates snow melting (Thomas and Duval, 1995, Yallop et al. 2012). Increasing melting of ice should be a big problem because it would lead to the loss of habitats of polar animals and a cause a flood and water-level elevation. Therefore, understanding the mechanism of the colonization and establishment of microbes associated with red snow is important in evaluating the risk of ice thawing. However, little is known about the mechanism of the determinants of their distribution. Two conflicting views exist in the mechanism of distribution of snow algae. First, snow algae is cosmopolitan with migrating widely through the atmosphere, which is implied by Baas-Becking hypothesis (Baas-Becking 1934). Another view is that the snow algae is endemic, which is an idea that snow algae keep resting in soil, and move up to snow surface from the soil when it is covered by snow (Hoham, 2001). -
Chilling Out: the Evolution and Diversification of Psychrophilic Algae with a Focus on Chlamydomonadales
Polar Biol (2017) 40:1169–1184 DOI 10.1007/s00300-016-2045-4 REVIEW Chilling out: the evolution and diversification of psychrophilic algae with a focus on Chlamydomonadales 1 1 1 Marina Cvetkovska • Norman P. A. Hu¨ner • David Roy Smith Received: 20 February 2016 / Revised: 20 July 2016 / Accepted: 10 October 2016 / Published online: 21 October 2016 Ó Springer-Verlag Berlin Heidelberg 2016 Abstract The Earth is a cold place. Most of it exists at or Introduction below the freezing point of water. Although seemingly inhospitable, such extreme environments can harbour a Almost 80 % of the Earth’s biosphere is permanently variety of organisms, including psychrophiles, which can below 5 °C, including most of the oceans, the polar, and withstand intense cold and by definition cannot survive at alpine regions (Feller and Gerday 2003). These seemingly more moderate temperatures. Eukaryotic algae often inhospitable places are some of the least studied but most dominate and form the base of the food web in cold important ecosystems on the planet. They contain a huge environments. Consequently, they are ideal systems for diversity of prokaryotic and eukaryotic organisms, many of investigating the evolution, physiology, and biochemistry which are permanently adapted to the cold (psychrophiles) of photosynthesis under frigid conditions, which has (Margesin et al. 2007). The environmental conditions in implications for the origins of life, exobiology, and climate such habitats severely limit the spread of terrestrial plants, change. Here, we explore the evolution and diversification and therefore, primary production in perpetually cold of photosynthetic eukaryotes in permanently cold climates. environments is largely dependent on microbes. -
Western Siberia)
BIO Web of Conferences 16, 00022 (2019) https://doi.org/10.1051/bioconf/20191600022 Results and Prospects of Geobotanical Research in Siberia The «red snow» of the Polar Urals (Western Siberia) Yuriy Naumenko* Central Siberian Botanical Garden, SB RAS, 630090, Zolotodolinskaja Str., 101, Novosibirsk, Russia Abstract: Pink-red colored snow fields were sampled in the area of Ochety Lake (the Polar Urals, West Siberia) at the altitude of 272 m above the sea level in August 2019. Zygospores of Chlamydomonas nivalis prevailed in plant communities. Altogether, 9 species of algae have been discovered in snow samples: 7 species of Cyanoprokaryota, 1 species of Bacillariophyta and 1 species of Chlorophyta. Tinted snow is observed rather frequently in the mountains and polar regions. Red snow was first scientifically mentioned by Horace de Saussure, a Swiss natural scientist, in 1760. He discovered it at the foot of the Alpes in the Duchy of Savoy in France [1]. Analogous findings were later noted in different areas of the Alpes, Pyrenees, in the north of Scandinavia, in Alyaska, in polar countries and other places. I. V. Palibin was the first who mention pink and red snow in the European part of Russia. In 1901, he took part in the polar expedition on “Yermak” icebreaker, where he studied flora of Franz Josef Land, Spitzbergen and Severny (Northern) island of Novaya Zemlya. He observed the red snow phenomenon on Novaya Zemlya near Mashigin Bay and in the area of Matochkin Strait where pink snow is encountered in ravines, mountain slopes, almost everywhere. Research demonstrated that the red tint of snow is caused by the development of Chlamydomonas nivalis (F.A.Bauer) Wille algae. -
"Phycology". In: Encyclopedia of Life Science
Phycology Introductory article Ralph A Lewin, University of California, La Jolla, California, USA Article Contents Michael A Borowitzka, Murdoch University, Perth, Australia . General Features . Uses The study of algae is generally called ‘phycology’, from the Greek word phykos meaning . Noxious Algae ‘seaweed’. Just what algae are is difficult to define, because they belong to many different . Classification and unrelated classes including both prokaryotic and eukaryotic representatives. Broadly . Evolution speaking, the algae comprise all, mainly aquatic, plants that can use light energy to fix carbon from atmospheric CO2 and evolve oxygen, but which are not specialized land doi: 10.1038/npg.els.0004234 plants like mosses, ferns, coniferous trees and flowering plants. This is a negative definition, but it serves its purpose. General Features Algae range in size from microscopic unicells less than 1 mm several species are also of economic importance. Some in diameter to kelps as long as 60 m. They can be found in kinds are consumed as food by humans. These include almost all aqueous or moist habitats; in marine and fresh- the red alga Porphyra (also known as nori or laver), an water environments they are the main photosynthetic or- important ingredient of Japanese foods such as sushi. ganisms. They are also common in soils, salt lakes and hot Other algae commonly eaten in the Orient are the brown springs, and some can grow in snow and on rocks and the algae Laminaria and Undaria and the green algae Caulerpa bark of trees. Most algae normally require light, but some and Monostroma. The new science of molecular biology species can also grow in the dark if a suitable organic carbon has depended largely on the use of algal polysaccharides, source is available for nutrition.