Krill Ocean Acidification Physiology Data
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Antarctic krill (Euphausia superba) have a keystone role in the Southern Ocean, as the primary prey of Antarctic predators. Any decreases in krill abundance could result in a major ecological regime shift, but there is currently limited information on how climate change may affect krill. Increasing anthropogenic carbon dioxide (CO2) emissions are causing ocean acidification, as absorption of atmospheric CO2 in seawater alters ocean chemistry. Ocean acidification increases mortality and negatively affects physiological functioning in some marine invertebrates, and is predicted to occur most rapidly at high latitudes. Here we show that, in the laboratory, adult krill are able to survive, grow, store fat, mature, and maintain respiration rates when exposed to near-future ocean acidification (1000 – 2000 μatm pCO2) for one year. Despite differences in seawater pCO2 incubation conditions, adult krill are able to actively maintain the acid-base balance of their body fluids in near-future pCO2, which enhances their resilience to ocean acidification.
Moulting and body shrinkage in the Antarctic krill, Euphausia superba
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Euphausia superba were collected from the Antarctic Ocean during the cruise by RV Kaiyo-Maru in January 1980, and were transported to the Australian Institute of Marine Science laboratories at Townsville in February 1980.Specimens of Euphausia superba were maintained in a cold room at -0.5°C (0 to -1.0°C) under continuous subdued light (Specimens were checked daily for moults, which were then preserved with a few drops of buffered formalin (40%) in seawater. The exopodite length of the moult uropod was later measured. Changes in body wet weight or length were then tracked by applying allometric equations derived from specimens sacrificed at the end of experiments. Preserved moults were later rinsed in distilled water to remove formalin and salts, and were dried in a desiccator over silica gel at room temperature to obtain dry weights. Fresh moults, collected from stock specimens were used for analysis of carbon and nitrogen using a elemental analyser (Perkin Elmer, model 240) with acetanilide as standard.In another experiment, conducted over a period of 211 days, using the same temperature, light and seawater conditions described above, 15 Euphausia superba of various sizes were maintained individually in sea water filtered through a HA Millipore filter, 0.45µm pore size (starved). Two control groups of 15 individuals each were fed, ad libitum, an artificial pet fish food (Tetra Marin) and frozen copepods (Calanus finmarchicus) or a mixture of microalgae (Dunaliella tertiolecta and Phaeodactylum tricornutum). During the experiment, handling of specimens was minimised to avoid possible damage. Changes in body wet weight were tracked as described above.At the end of the experiment, physiological rates (oxygen uptake, ammonia excretion, inorganic phosphate excretion, dissolved organic nitrogen (DON) excretion, dissolved organic phosphate (DOP) excretion) were measured by a water bottle method, where individual specimens were placed into 250 to 1000 ml glass bottles filled with the filtered sea water for 24 h in the dark at -0.5°C. Dissolved oxygen, ammonia, and inorganic phosphate were measured by Winkler titration, phenolhypochlorite, and molybdate methods, respectively. DON and DOP were determined by a UV irradiation method.The individuals were weighed (wet weight) and freeze-dried for the determination of dry weight and analyses of elemental composition (C, N, P). The analyses of C and N were made with an elemental analyzer (Perkin Ebner, Model 240) using acetanilide as standard. Determination of P was made by the molybdate method after digestion of samples in 50% (v/v) H2SO4 for 1 hour at ~ 100°C followed by neutralization with KOH. Laboratory experiments were undertaken to examine the relationship between different feeding regimes and/or body sizes and moulting in the krill, Euphausia superba. Experiments were also carried out to determine whether cessation of feeding could be a possible over-wintering mechanism for this species.
KRILLPODYM modelled estimates of Antarctic krill circumpolar distribution
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Robust prediction of population responses to changing environments requires the integration of factors controlling population dynamics with processes affecting distribution. This is true everywhere but especially in polar pelagic environments. Biological cycles for many polar species are synchronised to extreme seasonality, while their distributions may be influenced by both the prevailing oceanic circulation and sea-ice distribution. Antarctic krill (krill, Euphausia superba) is one such species exhibiting a complex life history that is finely tuned to the extreme seasonality of the Southern Ocean. Dependencies on the timing of optimal seasonal conditions has led to concerns over the effects of future climate on krill’s population status, particularly given the species’ important role within Southern Ocean ecosystems. Under a changing climate, established correlations between environment and species may breakdown. Developing the capacity for predicting krill responses to climate change therefore requires methods that can explicitly consider the interplay between life history, biological conditions, and transport. The Spatial Ecosystem And Population Dynamics Model (SEAPODYM) is one such framework that integrates population and general circulation modelling to simulate the spatial dynamics of key organisms. Here, we describe a modification to SEAPODYM, creating a novel model – KRILLPODYM – that generates spatially resolved estimates of krill biomass and demographics. This new model consists of three major components: (1) an age-structured population consisting of five key life stages, each with multiple age classes, which undergo age-dependent growth and mortality, (2) six key habitats that mediate the production of larvae and life stage survival, and (3) spatial dynamics driven by both the underlying circulation of ocean currents and advection of sea-ice. Here we present the first results of KRILLPODYM, using published deterministic functions of population processes and habitat suitability rules. Initialising from a non-informative uniform density across the Southern Ocean our model independently develops a circumpolar population distribution of krill that approximates observations. The model framework lends itself to applied experiments aimed at resolving key population parameters, life-stage specific habitat requirements, and dominant transport regimes, ultimately informing sustainable fishery management. This dataset represents KRILLPODYM modelled estimates of Antarctic krill circumpolar biomass distribution for the final year of a 12-year spin up. Biomass distributions are given for each of the five key life stages outlined above. The accompanying background, model framework and initialisation description can be found in the following reference paper: Green, D. B., Titaud, O., Bestley, S., Corney, S. P., Hindell, M. A., Trebilco, R., Conchon, A. and Lehodey, P. in review. KRILLPODYM: a mechanistic, spatially resolved model of Antarctic krill distribution and abundance. - Frontiers in Marine Science
Modelling growth and reproduction of Antarctic krill, Euphausia superba, based on temperature, food and resource allocation amongst life history functions
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This model was produced as part of Australian Antarctic Science project 4037 - Experimental krill biology: Response of krill to environmental change - The experimental krill research project is designed to focus on obtaining life history information of use in managing the krill fishery - the largest Antarctic fishery. In particular, the project will concentrate on studies into impacts of climate change on key aspects of krill biology and ecology. This metadata record is to reference the paper that describes the model. There is no archived data output from this data product. Taken from the abstract of the referenced paper: Estimates of productivity of Antarctic krill, Euphausia superba, are dependent on accurate models of growth and reproduction. Incorrect growth models, specifically those giving unrealistically high production, could lead to over-exploitation of the krill population if those models are used in setting catch limits. Here we review available approaches to modelling productivity and note that existing models do not account for the interactions between growth and reproduction and variable environmental conditions. We develop a new energetics moult-cycle (EMC) model which combines energetics and the constraints on growth of the moult-cycle. This model flexibly accounts for regional, inter- and intra-annual variation in temperature, food supply, and day length. The EMC model provides results consistent with the general expectations for krill growth in length and mass, including having thin krill, as well as providing insights into the effects that increasing temperature may have on growth and reproduction. We recommend that this new model be incorporated into assessments of catch limits for Antarctic krill.
Circumpolar Projections of Antarctic krill (Euphausia superba) growth potential
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These data represent the results of the first study to use Earth System Model (ESM) outputs of SST and chlorophyll-a to simulate circumpolar krill growth potential for the recent past (1960-1989) and future climate change scenarios (2070-2099). Growth potential is obtained using an empirically-derived krill growth model (Atkinson et al. 2006, Limnol. Oceanogr.), where growth is modeled as a function of SST and chlorophyll-a. It serves as an approximation of habitat quality, as areas that support high growth rates are assumed to be good habitat (see Murphy et al., 2017, Sci Rep). To increase confidence in the future projections, ESMs were selected and weighted for each season based on their skill at reproducing observation-based krill growth potential for the recent past. First, eleven ESMs which provided SST and chlorophyll-a outputs were obtained from the Coupled Model Inter-comparison Project 5 archive. These included: CanESM2, CMCC-CESM, CNRM-CM5, GFL-ESM2G, GFDL-ESM2M, GISS-E2-H-CC, HadGEM2-CC, IPSL-CM5A-LR, MPI-ESM-MR, MRI-ESM1 and NorESM1-ME. For each ESM, seasonal surface averages of SST and chlorophyll-a were used to calculate growth potential for the historical scenario (1960-1989), which was then bilinearly interpolated on to the same 1°x1° grid. Satellite observation-based datasets for SST and chlorophyll-a were used to calculate observation-based growth potential for the recent past (1997-2010). These comprised seasonal surface averages of SST (from the OISST v2 daily dataset, 1/4⁰ horizontal resolution) and chlorophyll-a (the mean of the SeaWiFS and Johnson et al. (2013) corrected estimate of SeaWiFS daily datasets, 1/12⁰ horizontal resolution). Observation-based growth potential was then bilinearly interpolated onto the same grid as the ESMs. ESM skill for each season was subsequently assessed against observation-based growth potential using a Taylor Diagram. The ESMs were selected and weighted according to their performance to produce a weighted subset (see "ESM_weighting_method.pdf" file). Of the netcdfs provided, "hist_mean_ensemble.nc" represents the unweighted mean of seasonal growth potential, calculated from the initial ensemble of eleven ESMs for the historical scenario. The "hist_mean_subset.nc" file represents the analogous output of the weighted subset. Future projections of seasonal growth potential for Representative Concentration Pathways (RCPs) 4.5 and 8.5 were obtained using the weighted subset for the period of 2070-2099. These projected seasonal surface averages are provided in the "rcp45_mean_subset.nc" and "rcp85_mean_subset.nc" files. RCPs represent standard climate change scenarios developed by the Intergovernmental Panel on Climate Change, with 4.5 reflecting some mitigation of carbon emissions, and 8.5 being the "business as usual" scenario. Analogous netcdfs for the weighted subset outputs of chlorophyll-a (chl) and SST (tos) for the historical and RCP scenarios are also provided in the "chl_tos_netcdfs.zip" file so that the driving environmental variables underlying growth potential can be examined.
Experimental studies into growth and ageing of krill 1993-2003
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Metadata record for data from ASAC Project 2337 See the link below for public details on this project. ---- Public Summary from Project ---- The experimental krill research program is focused on obtaining life history information of use in managing the krill fishery - the largest Antarctic fishery. In particular, the program will concentrate on studies into schooling, growth and ageing of krill. From the abstracts of some of the referenced papers: Nucleic acid contents of tissue were determined from field-caught Antarctic krill to determine whether they could be used as an alternative estimator of individual growth rates which can currently only be obtained by labour intensive on-board incubations. Krill from contrasting growth regimes from early and late summer exhibited differences in RNA-based indices. There was a significant correlation between the independently measured individual growth rates and the RNA-based indices. There was a significant correlation between the independently measured individual growth rates and the RNA:DNA ratio and also the RNA concentration of krill tissue, although the strength of the relationship was only modest. DNA concentration, on average, was relatively constant, irrespective of the growth rates. The moult stage did not appear to have a significant effect on the nucleic acid contents of tissue. Overall, the amount of both nucleic acids varied considerably between individuals. Nucleic acid-based indicators may provide information concerning the recent growth and nutritional status of krill and further experimentation under controlled conditions is warranted. The are, however, reasonably costly and time-consuming measurements. Growth rates of Antarctic krill Euphausia superba Dana in the Indian Ocean sector of the Southern Ocean were measured in 4 summers. Growth rate was measured using an 'instantaneous growth rate' technique which involved measuring the mean change in length if the uropods at moulting. In the first 4 days following collection mean growth rates ranged from 0.35 to 7.34% per moult in adults and 2.42 to 9.05% in juveniles. Mean growth rates of adult and juvenile krill differed between areas and between the different years of the investigation. When food was restricted under experimental conditions, individual krill began to shrink immediately and mean population growth rates decreased gradually, becoming negative after as little as 7 days. Populations of krill which exhibited initial growth rates began to shrink later than those which had initially been growing more slowly. Data were collected on growth rates of krill. These data were collected as part of ASAC projects 34, 1074, 2220 and 2337. ASAC_34 - Ecophysiology of Antarctic Krill 'Euphausia superba' ASAC_1074 - Seasonal growth in krill ASAC_2220 - Collection of live Antarctic krill ASAC_2337 - Experimental studies into growth and ageing of krill The fields in this dataset are: Field season (eg FS9596 = Field Season 1995-1996) Area (eg Indian Ocean) Cruise Month Date Latitude Longitude Total Number of Krill Dead Krill Moulted Krill Experiment ID Station ID Sample ID Sex Growth (IGR%) (% growth at time of moulting) Uropod Size (mm) Days after capture (when moulted) Standard length
Krill and zooplankton demography during K-Axis
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Distribution and abundance of zooplankton, krill and fish were observed on the K-axis transect using deployments of RMT1+8 net. Towing speed of the RMT1+8 were approximately 2 knots. All krill, fish and squid in the catch were sorted, identified to species and counted. The density at each station were determined from the counts per calibrated flow-meter readings attached to the net. Morphometric measures were taken and, for larger taxa. List of files K-Axis Morph combined_for data centre.xlsx: Morphological data for all krill and zooplankton captured in RMT-8 net haul. RMT data entry_v1_for data centre.xlsx: Trawl data. RMT8 filtered volume_for data centre.xlsx: Filtered volume for each haul. Map_all.tif: Map showing all trawl stations. Map_RMTR.tif: Map showing only regular trawl stations. Map_RMTT.tif: Mapn showing only target trawl stations. K-Axis description This dataset includes biological data from “K-Axis voyage, 2016 and “Voyage 3, 2015”. [Data from K-Axis voyage, 2016] Distribution and abundance of zooplankton, krill and fish were observed on the K-axis transect using deployments of RMT1+8 net. Towing speed of the RMT1+8 were approximately 2 knots. All krill, fish and squid in the catch were sorted, identified to species and counted. The density at each station were determined from the counts per calibrated flow-meter readings attached to the net. Morphometric measures were taken and, for larger taxa. -List of files- K-Axis Morph combined_for data centre.xlsx: Morphological data for all krill and zooplankton captured in RMT-8 net haul. Map_all.tif Map_RMTR.tif Map_RMTT.tif RMT data entry_v1_for data centre.xlsx: Trawl data. RMT8 filtered volume_for data centre.xlsx: Filtered volume for each haul. [Data from Voyage 3, 2015] The Australian Antarctic research and resupply vessel, RV Aurora Australis, was directed to undertake an opportunistic marine science survey for 17 days during 21 February to 10 March 2015 using ship time that became available due to unexpectedly favourable ice conditions for Mawson station resupply. The purpose of this opportunistic Marine Science work was to assess: 1. The spatial variability, particularly along the shelf break, of the prey field for penguins, flying seabirds and marine mammals in East Antarctica. 2. The small scale variability of prey in key foraging locations near to land-based colonies of penguins and flying seabirds in East Antarctica. 3. Feasibility and potential of utilising annual station resupply voyages as a cost effective means to undertake monitoring and research to better understand the ecosystem in the region. The survey completed 5 acoustic box surveys including a total of 53 RMT target and routine trawls, 6 demersal trawls, 131 phytoplankton samples from underway sampling, and 214 hourly observations of predators. These activities were successfully supervised remotely. -List of files- emm-15-22.pdf: Prelminary report of the voyage to CCAMLR WG-EMM Figure_V3_all_euphausiids.pdf: Map of Euphausiid abundance distribution. Figure_V3_Clione_antarctica.pdf: Map of Clione antarctica abundance distribution. Figure_V3_crystal_krill.pdf: Map of Euphausia crystallorophias abundance distribution. Figure_V3_frigida.pdf: Map of Euphausia frigida abundance distribution. Figure_V3_larval_fish_abundances.pdf: Map of fish larvae abundance distribution. Figure_V3_superba.pdf: Map of Antarctic krill abundance distribution. Figure_V3_tmacrura.pdf: Map of Thysanoessa macrura abundance distribution. V3_final_for data centre.xlsx: Trawl station data and density data of each taxa caught. Voyage 3 Marine Science Program Final.docx: Voyage report.
Krill Sterol and Lipid Class Fatty Acid Data
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Fatty acid analysis is a powerful tool in food web research for estimating dietary sources in marine predators. However, the utility of fatty acids as dietary indicators from whole lipid samples, rather than from separate lipid classes, has been questioned. Samples are often collected at a single time point, precluding seasonal dietary comparisons. We investigated variations in the fatty acid composition of structural (phospholipids) and storage lipids (triacylglycerols) of Antarctic krill (Euphausia superba) using fisheries samples obtained over one year. Seasonal variation was observed in fatty acid biomarkers within triacylglycerol and phospholipid fractions of krill. Fatty acids in krill triacylglycerols (thought to better represent recent diet), reflected omnivorous feeding with highest percentages of flagellate biomarkers (18:4n-3) in summer, and diatom biomarkers (16:1n-7c) in autumn, winter and spring. Carnivory biomarkers (∑ 20:1 + 22:1 and 18:1n-9c/18:1n-7c) in krill were greater in autumn. Phospholipid fatty acids were less variable and higher in 20:5n-3 and 22:6n-3, which are essential components of cell membranes. Sterol composition did not yield detailed dietary information, but percentages of the major krill sterol, cholesterol, were significantly higher in winter and spring compared with summer and autumn. Unexpectedly, 18:4n-3 and copepod markers ∑ 20:1 + 22:1 were not strongly associated with the triacylglycerol fraction during some seasons. Krill may mobilise 18:4n-3 to phospholipids for conversion to long chain polyunsaturated fatty acids, which would have implications for its role as a dietary biomarker. For the first time, we demonstrate the dynamic seasonal relationship between specific biomarkers and krill lipid classes.