The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton
The actual piece of equipment used was an International Light IL 1700Radiometer equipped with broad band detectors to measure PAR, UV-A and erythemal UV-B. The effects of UV-B radiation on the fatty acid, total lipid and sterol composition and content of three Antarctic marine phytoplankton were exa...
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Format: | Dataset |
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Australian Antarctic Data Centre
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Online Access: | https://researchdata.ands.org.au/effects-uv-b-antarctic-phytoplankton/700331 https://data.aad.gov.au/metadata/records/ASAC_872 http://nla.gov.au/nla.party-617536 |
id |
ftands:oai:ands.org.au::700331 |
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record_format |
openpolar |
institution |
Open Polar |
collection |
Research Data Australia (Australian National Data Service - ANDS) |
op_collection_id |
ftands |
language |
unknown |
topic |
biota climatologyMeteorologyAtmosphere geoscientificInformation oceans ULTRAVIOLET RADIATION EARTH SCIENCE ATMOSPHERE ATMOSPHERIC RADIATION ORGANIC CARBON OCEAN CHEMISTRY PHYTOPLANKTON BIOSPHERE AQUATIC ECOSYSTEMS PLANKTON EARTH SCIENCE > BIOSPHERE > ECOSYSTEMS > MARINE ECOSYSTEMS > COASTAL ALGAE ANTARCTIC CHAEOTOCEROS DIATOMS ESSENTIAL FATTY ACIDS FATTY ACID LIPID ODONTELLA PAR PHAEOCYSTIS UV-B Radiometers CONTINENT > AUSTRALIA/NEW ZEALAND > AUSTRALIA ANTARCTICA GEOGRAPHIC REGION > POLAR |
spellingShingle |
biota climatologyMeteorologyAtmosphere geoscientificInformation oceans ULTRAVIOLET RADIATION EARTH SCIENCE ATMOSPHERE ATMOSPHERIC RADIATION ORGANIC CARBON OCEAN CHEMISTRY PHYTOPLANKTON BIOSPHERE AQUATIC ECOSYSTEMS PLANKTON EARTH SCIENCE > BIOSPHERE > ECOSYSTEMS > MARINE ECOSYSTEMS > COASTAL ALGAE ANTARCTIC CHAEOTOCEROS DIATOMS ESSENTIAL FATTY ACIDS FATTY ACID LIPID ODONTELLA PAR PHAEOCYSTIS UV-B Radiometers CONTINENT > AUSTRALIA/NEW ZEALAND > AUSTRALIA ANTARCTICA GEOGRAPHIC REGION > POLAR The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton |
topic_facet |
biota climatologyMeteorologyAtmosphere geoscientificInformation oceans ULTRAVIOLET RADIATION EARTH SCIENCE ATMOSPHERE ATMOSPHERIC RADIATION ORGANIC CARBON OCEAN CHEMISTRY PHYTOPLANKTON BIOSPHERE AQUATIC ECOSYSTEMS PLANKTON EARTH SCIENCE > BIOSPHERE > ECOSYSTEMS > MARINE ECOSYSTEMS > COASTAL ALGAE ANTARCTIC CHAEOTOCEROS DIATOMS ESSENTIAL FATTY ACIDS FATTY ACID LIPID ODONTELLA PAR PHAEOCYSTIS UV-B Radiometers CONTINENT > AUSTRALIA/NEW ZEALAND > AUSTRALIA ANTARCTICA GEOGRAPHIC REGION > POLAR |
description |
The actual piece of equipment used was an International Light IL 1700Radiometer equipped with broad band detectors to measure PAR, UV-A and erythemal UV-B. The effects of UV-B radiation on the fatty acid, total lipid and sterol composition and content of three Antarctic marine phytoplankton were examined in a preliminary culture experiment. Exponential growth phase cultures of the diatoms Odontella weissflogii and Chaetoceros simplex and the Haptophyte Phaeocystis antarctica were grown at 2 (plus or minus 1)degrees C and exposed to 16.3 (plus or minus 0.7) W.m-2 photosynthetically active radiation (PAR). UV-irradiated treatments were exposed to constant UV-A (4.39 (plus or minus 0.20) W.m-2) and low (0.37 W.m-2) or high UV-B (1.59 W.m-2). UV-B treatments induced species specific changes in lipid content and composition. The sterol, fatty acid and total lipid content and profiles for O. weissflogii changed little under low UV-B when compared with control conditions (PAR alone), but showed a decrease in the lipid content per cell under high UV-B treatment. In contrast, when P. antarctica was exposed to low UV-B irradiance, storage lipids were reduced and structural lipids increased indicating that low UV-B enhanced cell growth and metabolism. P. antarctica also contained a higher proportion of polyunsaturated fatty acids under low UV-B in comparison with PAR irradiated control cultures. The flagellate life stage of P. antarctica died under high UV-B irradiation. However, exposure of P. antarctica to high UV-B irradiance increased total lipid, triglyceride and free fat. The effect of UV-B irradiances on the lipid content of Antarctic marine phytoplankton is species specific. Changes in ambient UV-B may alter the nutritional quality of food available to higher trophic levels. EXPERIMENTAL All measurements of irradiance were made with an International Light IL 1700 Radiometer equipped with broad band detectors to measure PAR, UV-A and erythemal UV-B [14]. A National Institute of Standards and Technology intercomparison package (NIST Test #534/240436-88) was used to calibrate each light sensor. Unialgal cultures of the diatoms Odontella weissflogii and Chaetoceros simplex were isolated from sea ice collected in Prydz Bay, Antarctica during the 1990/91 austral summer. Phaeocystis antarctica was isolated from Prydz Bay in 1982/83 summer. Cultures of diatoms and Phaeocystis antarctica were maintained in 2 l glass flasks using f/2 growth medium [32] and GP5 medium [33] respectively at a temperature of 2 plus or minus 1 degrees C. Cool white fluorescent lights provided photosynthetically active radiation (PAR) intensity of 17.08 J.m-2.s-1 (84.7 micro E.m-2.s-1), with no UV-B enhancement, on a 12 h light : 12 h dark cycle. Immediately before experimental irradiation, three replicate subsamples of approximately 15 ml were obtained from each parental culture and fixed with Lugols iodine, a known sample volume sedimented, and cells counted over 15 replicate fields using a Labovert inverted microscope. Mean cell concentration and standard deviation were then computed. Each exponential growth phase parental culture was thoroughly mixed and 3 replicate 300 ml Costar polystyrene culture flasks (which completely absorbed wavelengths below 295 nm) established for each light treatment (control, low and high UV exposures). Cultures were irradiated for 24 hours in a 48 hour experimental period (6 h light : 12 h dark : 12 h light : 12 h dark : 6 h light) [14, 23]. Exposures were conducted in a Thermoline controlled environment cabinet at 2 plus or minus 1 degrees C with cool white fluorescent tubes to provide PAR and UV-A (320-400 nm), with UV-B provided by FS20T 12 UV-B Westinghouse sunlamps. PAR and UV-A irradiances were 16.3 plus or minus 0.7 W.m-2 (81.3 plus or minus 3.4 micro E.m-2.s-1) and 4.39 plus or minus 0.20 W.m-2 respectively. The spectral distribution and UV-B irradiance were varied by attenuation with glass filters [5] to provide low (0.37 W.m-2) or high UV-B (1.59 W.m-2). Sensors were each covered by an attenuating glass screen and a single layer of Costar culture flask to measure the experimental irradiances to which the algae were exposed. UV-B irradiances were chosen to reflect less than (74%) and greater than (318%) peak UV-B exposure as measured at an Antarctic coastal site (Casey station, 66 degrees S, [34]). Following irradiation each culture was well mixed and approximately 15 ml was fixed with Lugols Iodine for subsequent estimation of cell concentration (as above). Chlorotic and greatly vesicularised cells were considered to be dead [23]. The remainder of each experimental culture was filtered through Whatman GF/F filters. On completion of filtration, the filters were stored at -20C overnight before extraction of lipids the following day. |
author2 |
SKERRATT, JENNIFER HELEN (hasPrincipalInvestigator) DAVIDSON, ANDREW TIMOTHY (processor) Australian Antarctic Data Centre (publisher) |
format |
Dataset |
title |
The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton |
title_short |
The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton |
title_full |
The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton |
title_fullStr |
The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton |
title_full_unstemmed |
The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton |
title_sort |
effects of uv-b radiation on the nutritional composition of antarctic phytoplankton |
publisher |
Australian Antarctic Data Centre |
url |
https://researchdata.ands.org.au/effects-uv-b-antarctic-phytoplankton/700331 https://data.aad.gov.au/metadata/records/ASAC_872 http://nla.gov.au/nla.party-617536 |
op_coverage |
Spatial: northlimit=-54.0; southlimit=-70.0; westlimit=62.0; eastLimit=159.0; projection=WGS84 Temporal: From 1995-09-30 to 1996-03-31 |
long_lat |
ENVELOPE(110.528,110.528,-66.282,-66.282) ENVELOPE(62.0,159.0,-54.0,-70.0) |
geographic |
Antarctic Austral Casey Station New Zealand Prydz Bay |
geographic_facet |
Antarctic Austral Casey Station New Zealand Prydz Bay |
genre |
Antarc* Antarctic Antarctica Prydz Bay Sea ice |
genre_facet |
Antarc* Antarctic Antarctica Prydz Bay Sea ice |
op_source |
Australian Antarctic Data Centre |
op_relation |
https://researchdata.ands.org.au/effects-uv-b-antarctic-phytoplankton/700331 5049017f-5d93-41b8-9e48-d85574d1b0fb ASAC_872 https://data.aad.gov.au/metadata/records/ASAC_872 http://nla.gov.au/nla.party-617536 |
_version_ |
1766245913262555136 |
spelling |
ftands:oai:ands.org.au::700331 2023-05-15T13:46:58+02:00 The effects of UV-B radiation on the nutritional composition of Antarctic phytoplankton SKERRATT, JENNIFER HELEN (hasPrincipalInvestigator) DAVIDSON, ANDREW TIMOTHY (processor) Australian Antarctic Data Centre (publisher) Spatial: northlimit=-54.0; southlimit=-70.0; westlimit=62.0; eastLimit=159.0; projection=WGS84 Temporal: From 1995-09-30 to 1996-03-31 https://researchdata.ands.org.au/effects-uv-b-antarctic-phytoplankton/700331 https://data.aad.gov.au/metadata/records/ASAC_872 http://nla.gov.au/nla.party-617536 unknown Australian Antarctic Data Centre https://researchdata.ands.org.au/effects-uv-b-antarctic-phytoplankton/700331 5049017f-5d93-41b8-9e48-d85574d1b0fb ASAC_872 https://data.aad.gov.au/metadata/records/ASAC_872 http://nla.gov.au/nla.party-617536 Australian Antarctic Data Centre biota climatologyMeteorologyAtmosphere geoscientificInformation oceans ULTRAVIOLET RADIATION EARTH SCIENCE ATMOSPHERE ATMOSPHERIC RADIATION ORGANIC CARBON OCEAN CHEMISTRY PHYTOPLANKTON BIOSPHERE AQUATIC ECOSYSTEMS PLANKTON EARTH SCIENCE > BIOSPHERE > ECOSYSTEMS > MARINE ECOSYSTEMS > COASTAL ALGAE ANTARCTIC CHAEOTOCEROS DIATOMS ESSENTIAL FATTY ACIDS FATTY ACID LIPID ODONTELLA PAR PHAEOCYSTIS UV-B Radiometers CONTINENT > AUSTRALIA/NEW ZEALAND > AUSTRALIA ANTARCTICA GEOGRAPHIC REGION > POLAR dataset ftands 2020-01-05T21:17:29Z The actual piece of equipment used was an International Light IL 1700Radiometer equipped with broad band detectors to measure PAR, UV-A and erythemal UV-B. The effects of UV-B radiation on the fatty acid, total lipid and sterol composition and content of three Antarctic marine phytoplankton were examined in a preliminary culture experiment. Exponential growth phase cultures of the diatoms Odontella weissflogii and Chaetoceros simplex and the Haptophyte Phaeocystis antarctica were grown at 2 (plus or minus 1)degrees C and exposed to 16.3 (plus or minus 0.7) W.m-2 photosynthetically active radiation (PAR). UV-irradiated treatments were exposed to constant UV-A (4.39 (plus or minus 0.20) W.m-2) and low (0.37 W.m-2) or high UV-B (1.59 W.m-2). UV-B treatments induced species specific changes in lipid content and composition. The sterol, fatty acid and total lipid content and profiles for O. weissflogii changed little under low UV-B when compared with control conditions (PAR alone), but showed a decrease in the lipid content per cell under high UV-B treatment. In contrast, when P. antarctica was exposed to low UV-B irradiance, storage lipids were reduced and structural lipids increased indicating that low UV-B enhanced cell growth and metabolism. P. antarctica also contained a higher proportion of polyunsaturated fatty acids under low UV-B in comparison with PAR irradiated control cultures. The flagellate life stage of P. antarctica died under high UV-B irradiation. However, exposure of P. antarctica to high UV-B irradiance increased total lipid, triglyceride and free fat. The effect of UV-B irradiances on the lipid content of Antarctic marine phytoplankton is species specific. Changes in ambient UV-B may alter the nutritional quality of food available to higher trophic levels. EXPERIMENTAL All measurements of irradiance were made with an International Light IL 1700 Radiometer equipped with broad band detectors to measure PAR, UV-A and erythemal UV-B [14]. A National Institute of Standards and Technology intercomparison package (NIST Test #534/240436-88) was used to calibrate each light sensor. Unialgal cultures of the diatoms Odontella weissflogii and Chaetoceros simplex were isolated from sea ice collected in Prydz Bay, Antarctica during the 1990/91 austral summer. Phaeocystis antarctica was isolated from Prydz Bay in 1982/83 summer. Cultures of diatoms and Phaeocystis antarctica were maintained in 2 l glass flasks using f/2 growth medium [32] and GP5 medium [33] respectively at a temperature of 2 plus or minus 1 degrees C. Cool white fluorescent lights provided photosynthetically active radiation (PAR) intensity of 17.08 J.m-2.s-1 (84.7 micro E.m-2.s-1), with no UV-B enhancement, on a 12 h light : 12 h dark cycle. Immediately before experimental irradiation, three replicate subsamples of approximately 15 ml were obtained from each parental culture and fixed with Lugols iodine, a known sample volume sedimented, and cells counted over 15 replicate fields using a Labovert inverted microscope. Mean cell concentration and standard deviation were then computed. Each exponential growth phase parental culture was thoroughly mixed and 3 replicate 300 ml Costar polystyrene culture flasks (which completely absorbed wavelengths below 295 nm) established for each light treatment (control, low and high UV exposures). Cultures were irradiated for 24 hours in a 48 hour experimental period (6 h light : 12 h dark : 12 h light : 12 h dark : 6 h light) [14, 23]. Exposures were conducted in a Thermoline controlled environment cabinet at 2 plus or minus 1 degrees C with cool white fluorescent tubes to provide PAR and UV-A (320-400 nm), with UV-B provided by FS20T 12 UV-B Westinghouse sunlamps. PAR and UV-A irradiances were 16.3 plus or minus 0.7 W.m-2 (81.3 plus or minus 3.4 micro E.m-2.s-1) and 4.39 plus or minus 0.20 W.m-2 respectively. The spectral distribution and UV-B irradiance were varied by attenuation with glass filters [5] to provide low (0.37 W.m-2) or high UV-B (1.59 W.m-2). Sensors were each covered by an attenuating glass screen and a single layer of Costar culture flask to measure the experimental irradiances to which the algae were exposed. UV-B irradiances were chosen to reflect less than (74%) and greater than (318%) peak UV-B exposure as measured at an Antarctic coastal site (Casey station, 66 degrees S, [34]). Following irradiation each culture was well mixed and approximately 15 ml was fixed with Lugols Iodine for subsequent estimation of cell concentration (as above). Chlorotic and greatly vesicularised cells were considered to be dead [23]. The remainder of each experimental culture was filtered through Whatman GF/F filters. On completion of filtration, the filters were stored at -20C overnight before extraction of lipids the following day. Dataset Antarc* Antarctic Antarctica Prydz Bay Sea ice Research Data Australia (Australian National Data Service - ANDS) Antarctic Austral Casey Station ENVELOPE(110.528,110.528,-66.282,-66.282) New Zealand Prydz Bay ENVELOPE(62.0,159.0,-54.0,-70.0) |