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Experimental Set-up: An unreplicated, 6-level, dose-response experiment was conducted on a natural microbial community over a range of pCO2 levels (343, 506, 634, 953, 1140 and 1641 micro atm). Seawater was collected on the 19th November 2014 approximately 1 km offshore from Davis Station, Antarctica (68 degrees 35' S, 77 degrees 58' E) from an area of ice-free water amongst broken fast-ice. The seawater was collected using a thoroughly rinsed 720L Bambi bucket slung beneath a helicopter and transferred into a 7000 L polypropalene reservoir tank. Six 650 L polyethene tanks (minicosms), located in a temperature-controlled shipping container, were immediately filled via teflon lined house via gravity with an in-line 200 micron Arkal filter to exclude metazooplankton. The minicosms were simultaneously filled to ensure they contained the same starting community. The ambient water temperature at time of collection was -1.0 degrees C and the minicosms were maintained at a temperature of 0 degrees C plus or minus 0.5 degrees C. At the centre of each minicosm there was an auger shielded for much of its length by a tube of polythene. This auger was rotated at 15 rpm to gently mix the contents of the tanks. Each minicosm tank was covered with an acrylic air-tight lid to prevent pCO2 off-gasing outside of the minicosm headspace. The minicosm experiment was conducted between the 19th November and the 7th December 2014. Initially, the contents of the tanks were given a day to equibrate to the minicosms. This was followed by a five day acclimation period to increasing pCO2 at low light (0.8 plus or minus 0.2 micro mol m-1 s-1), allowing cell physiology to acclimated to the pCO2 increase (days 1-5). During this period the pCO2 was progressively adjusted over five days to the target level for each tank (343 - 1641 micro atm). Thereafter pCO2 was adjusted daily to maintain the pCO2 level in each treatment (see carbonate chemistry section below). Following acclimation to the various pCO2 treatments light was progressively adjusted to 89 plus or minus 16 micro mol m-2 s-1 at a 19 h light:5 h dark cycle. The community was incubated and allowed to grow for a further 10 days (days 8-18) with target pCO2 adjusted back to target each day (see carbonate chemistry section below). For a more detailed description of minicosm set-up, lighting and carbonate chemistry see; Davidson, A. T., McKinlay, J., Westwood, K., Thomson, P. G., van den Enden, R., de Salas, M., Wright, S., Johnson, R., and Berry, K.:Enhanced CO2 concentrations change the structure of Antarctic marine microbial communities, Mar. Ecol. Prog. Ser., 552, 93-113, 2016. Deppeler, S. L., Petrou, K., Westwood, K., Pearce, I., Pascoe, P., Schulz, K. G., and Davidson, A. T.: Ocean acidification effects on productivity in a coastal Antarctic marine microbial community, Biogeosciences, 2017. Light microscopy sampling and analysis: Samples from each minicosm were collected on days 1, 3, 5, 8, 10, 12, 14, 16 and 18 for microscopic analysis to determine protistan identity and abundance. Approximately 960 mL were collected from each tank, on each day. Samples were fixed with 20 40 mL of Lugol's iodine and allowed to sediment out at 4 degrees C for greater than or equal to 4 days. Once cells had settled the supernatant was gently aspirated till approximately 200 mL remained. This was transferred to a 250 mL measuring cylinder, again allowed to settle (as above), and the supernatant gently aspirated. The remaining 20 mL. This final 20 mL was transferred into a 30 mL amber glass bottle. All samples were stored and transported at 4 degrees C to the Australian Antarctic Division, Hobart, Australia for analysis. Lugols-fixed and sedimented samples were analysed by light microscopy between July 2015 and February 2017. Between 2 to 10 mL (depending on cell-density) of lugols-concentrated samples was placed into a 10 mL Utermohl cylinder (Hydro-Bios, Keil) and the cells allowed to settle overnight. Due to the large variation in size and taxa, a stratified counting procedure was employed to ensure both accurate identification of small cells and representative counts of larger cells. All cells greater than 20 microns were identified and counted at 20x magnification; those less than 20 microns at 40x magnification. For larger cells (greater than 20 microns), 20 randomly chosen fields of view (FOV) at 3.66 x 106 microns2 counted to gain an average cells per L. For smaller cells (less than 20 microns), 20 randomly chosen FOVs at 2.51 x 105 microns2 were counted. Counts were conducted on an Olympus IX 81 microscope with Nomarski interference optics. Identifications were determined using (Scott and Marchant, 2005) and FESEM images. Autotrophic protists were distinguished from heterotrophs via the presence of chloroplasts and based on their taxonomic identity. Electron microscopy sampling and analysis: A further 1 L was taken on days 0, 6, 13 and 18 for analysis by Field Emission Scanning Electron Microscope (FESEM). 25 These samples were concentrated to 5 mL by filtration over a 0.8 micron polycarbonate filter. Cells were resuspended, the concentrate transferred to a glass vial and fixed to a final concentration of 1% EM-grade gluteraldehyde (ProSciTech Pty Ltd). All samples were stored and transported at 4 degrees C to the Australian Antarctic Division, Hobart, Australia for analysis. Gluteraldehyde-fixed samples were prepared for FESEM imaging using a modified polylysine technique (Marchant and Thomas, 30 1983). In brief, a few drops of gluteraldehyde-fixed sample were placed on polylysine coated cover slips and post-fixed with OsO4 (4%) vapour for 30 min, allowing cells to settle onto the coverslips. The coverslips were then rinsed in distilled water and dehydrated through a graded ethanol series ending with emersion in 100% dry acetone before being critically point dried in a Tousimis Autosamdri-815 Critical Point Drier. The coverslips were mounted onto 12.5 mm diameter aluminium stubs and sputter-coated with 7 nm of platinum/palladium in a Cressington 208HRD coater. Imaging of stubs was conducted by JEOL JSM6701F FESEM and protists identified using (Scott and Marchant, 2005). All units are in cells per L estimates from individual field of view counts (FOV) Protistan taxa and functional group descriptions and abbreviations: Autotrophic Dinoflagellate (AD) - including Gymnodinium sp., Heterocapsa and other unidentified autotrophic dinoflagellates Bicosta antennigera (Ba) Chaetoceros (Cha) - mainly Chaetoceros castracanei and Chaetoceros tortissimus but also other Chaetoceros present including C. aequatorialis var antarcticus, C. cf. criophilus, C. curvisetus, C. dichaeta, C. flexuosus, C. neogracilis, C. simplex Choanoflagellates (except Bicosta) (Cho) - mainly Diaphanoeca multiannulata but also Parvicorbicula circularis and Parvicorbicula socialis present in low numbers Ciliates (Cil) - mostly cf. Strombidium but other ciliates also present Discoid Centric Diatoms greater than 40 microns (DC.l) - unidentified centrics of the genera Thalassiosira, Landeria, Stellarima or similar Discoid Centric Diatoms 20 to 40 microns (DC.m) - unidentified centrics of the genera Thalassiosira, Landeria, Stellarima or similar Discoid Centric Diatoms less than 20 microns (DC.s) - unidentified centrics of the genera Thalassiosira Euglenoid (Eu) - unidentified Fragilariopsis greater than 20 microns (F.l) - mainly Fragilariopsis cylindrus, some Fragilariopsis kerguelensis and potentially some Fragilariopsis curta present in very low numbers Fragilariopsis less than 20 microns (F.s) - mainly Fragilariopsis cylindrus, and potentially some Fragilariopsis curta present in very low numbers Heterotrophic Dinoflagellates (HD) - including Gyrodinium glaciale, Gyrodinium lachryma, other Gyrodinium sp., Protoperidinium cf. antarcticum and other unidentified heterotrophic dinoflagellates Landeria annulata (La) Other Centric Diatoms (OC) - Corethronb pennatum, Dactyliosolen tenuijuntus, Eucampia antarctica var recta, Rhizosolenia imbricata and other Rhizosolenia sp. Odontella (Od) - Odontella weissflogii and Odontella litigiosa Other Flagellates (OF) - Dictyocha speculum, Chrysochromulina sp., unknown haptophyte, Phaeocystis antarctica (flagellate and gamete forms), Mantoniella sp., Pryaminmonas gelidicola, Triparma columaceae, Triparma laevis subsp ramispina, Geminigera sp., Bodo sp., Leuocryptos sp., Polytoma sp., cf. Protaspis, Telonema antarctica, Thaumatomastix sp. and other unidentified nano- and picoplankton Other Pennate Diatoms (OP) - Entomonei kjellmanii var kjellmanii, Navicula gelida var parvula, Nitzschia longissima, other Nitzschia sp., Plagiotropus gaussi, Pseudonitzschia prolongatoides, Synedropsis sp. Phaeocystis antarctica (Pa) - colonial form only Proboscia truncata (Pro) Pseudonitzschia subcurvata (Ps) Pseudonitzschia turgiduloies (Pt) Stellarima microtrias (Sm) Thalassiosira antarctica (Ta) Thalassiosira ritscheri (Tr) *.se = standard error for mean cell per L estimate ie. Tr.se = standard error for the mean cells per L for Thalassiosira ritscheri based on individual FOV estimates as described in methods above. Davis Station Antarctica Experiment conducted between 19th November and 7th December 2014.
An unreplicated, six-level dose-response experiment was conducted using 650 L incubation tanks (minicosms) adjusted to fugacity of carbon dioxide (fCO2) from 343 to 11641 uatm. The minicosms were filled with near-shore water from Prydz Bay, East Antarctica and the protistan composition and abundance was determined by microscopy analysis of samples collected during the 18 day incubation. Abundant taxa with low variance were examined separately, but rare taxa with high variance were combined into functional groups (descriptions below). Cluster analyses and ordinations were performed on Bray-Curtis resemblance matrixes formed from square-root transformated abundance data. This transformation was assessed as appropriate for reducing the influence of abundance species, as judged from a one-to-one relationship between observed dissimilarities and ordination distances (ie. Shepard diagram, not shown). The Bray-Curtis metric was used as it is recommended for ecological data due to its treatment of joint absences (ie. these do not contribute towards similarity), and giving more weight to abundant taxa rather than rare taxa. The data days 1 to 8 and then days 8 to 18 were analysed separately to distinguish community structure in the acclimation period and in the exponential growth phase during the incubation period of the experiment. Hierarchical agglomerative cluster analyses, based on the Bray-Curtis resemblance matrix, was performed using group-average linkage. Significantly different clusters of samples were determined using SIMPROF (similarity profile permutations method) with an alpha value of 0.05 and based on 1000 permutations. An unconstrained ordination by non-metric multidimensional scaling (nMDS) was performed on the resemblance matrix with a primary (`weak') treatment of ties. This was repeated over 50 random starts to ensure a globally optimal solution according to . Clusters are displayed in the nMDS using colour. Weighted average of sample scores are shown in the nMDS to show the approximate contribution of each species to each sample. The assumption of a linear trend for predictors within the ordination was checked for each covariate, and in all instances was found to be justified. A constrained canonical analysis of principal coordinates (CAP) was conducted according to the Vegan protocol using the Bray-Curtis resemblance matrix. This analysis was used to assess the significance of the environmental covariates, or constraints, in determining the microbial community structure. Unlike the nMDS ordination, the CAP analysis uses the resemblance matrix to partition the total variance in the community composition into unconstrained and constrained components, with the latter comprising only the variation that can be attributed to the constraining variables, fCO2, Si, P and NOx. Random reassignment of sample resemblance was performed over 199 permutations to compute the pseudo-F statistic as a measure of significance of each environmental constraint in the structural change of the microbial community. A forward selection strategy was used to choose a minimum subset of significant constraints that still account for the majority of the variation within the microbial community. All analysis were performed using R v1.0.136 and the add-on package vegan v2.4-2. Protistan taxa and functional group descriptions and abbreviations: Autotrophic Dinoflagellate (AD) - including Gymnodinium sp., Heterocapsa and other unidentified autotrophic dinoflagellates Bicosta antennigera (Ba) Chaetoceros (Cha) - mainly Chaetoceros castracanei and Chaetoceros tortissimus but also other Chaetoceros present including C. aequatorialis var antarcticus, C. cf. criophilus, C. curvisetus, C. dichaeta, C. flexuosus, C. neogracilis, C. simplex Choanoflagellates (except Bicosta) (Cho) - mainly Diaphanoeca multiannulata but also Parvicorbicula circularis and Parvicorbicula socialis present in low numbers Ciliates (Cil) - mostly cf. Strombidium but other ciliates also present Discoid Centric Diatoms greater than 40 microns (DC.l) - unidentified centrics of the genera Thalassiosira, Landeria, Stellarima or similar Discoid Centric Diatoms 20 to 40 microns (DC.m) - unidentified centrics of the genera Thalassiosira, Landeria, Stellarima or similar Discoid Centric Diatoms less than 20 microns (DC.s) - unidentified centrics of the genera Thalassiosira Euglenoid (Eu) - unidentified Fragilariopsis greater than 20 microns (F.l) - mainly Fragilariopsis cylindrus, some Fragilariopsis kerguelensis and potentially some Fragilariopsis curta present in very low numbers Fragilariopsis less than 20 microns (F.s) - mainly Fragilariopsis cylindrus, and potentially some Fragilariopsis curta present in very low numbers Heterotrophic Dinoflagellates (HD) - including Gyrodinium glaciale, Gyrodinium lachryma, other Gyrodinium sp., Protoperidinium cf. antarcticum and other unidentified heterotrophic dinoflagellates Landeria annulata (La) Other Centric Diatoms (OC) - Corethronb pennatum, Dactyliosolen tenuijuntus, Eucampia antarctica var recta, Rhizosolenia imbricata and other Rhizosolenia sp. Odontella (Od) - Odontella weissflogii and Odontella litigiosa Other Flagellates (OF) - Dictyocha speculum, Chrysochromulina sp., unknown haptophyte, Phaeocystis antarctica (flagellate and gamete forms), Mantoniella sp., Pryaminmonas gelidicola, Triparma columaceae, Triparma laevis subsp ramispina, Geminigera sp., Bodo sp., Leuocryptos sp., Polytoma sp., cf. Protaspis, Telonema antarctica, Thaumatomastix sp. and other unidentified nano- and picoplankton Other Pennate Diatoms (OP) - Entomonei kjellmanii var kjellmanii, Navicula gelida var parvula, Nitzschia longissima, other Nitzschia sp., Plagiotropus gaussi, Pseudonitzschia prolongatoides, Synedropsis sp. Phaeocystis antarctica (Pa) - colonial form only Proboscia truncata (Pro) Pseudonitzschia subcurvata (Ps) Pseudonitzschia turgiduloies (Pt) Stellarima microtrias (Sm) Thalassiosira antarctica (Ta) Thalassiosira ritscheri (Tr) *.se = standard error for mean cell per L estimate ie. Tr.se = standard error for the mean cells per L for Thalassiosira ritscheri based on individual FOV estimates as described in methods above.
The collection aims to showcase the range of Southern Ocean diatom species found in the major hydrological provinces of the Australian Sector of the Southern Ocean along the 140 degrees E. The collection includes specimens collected in the Sub-Antarctic Zone (SAZ), Polar Frontal Zone (PFZ) and Antarctic Zone (AZ). Samples were collected with McLane Parflux time series sediment traps placed at several depths in the SAZ (47 degrees S site), PFZ (54 degrees S site) and AZ and (61 degrees S site) during the decade 1997-2007. The shortest sampling intervals were eight days and corresponded with the austral summer and autumn, whereas the longest interval was 60 days and corresponded with austral winter. Split aliquots were obtained for taxonomic analysis via scanning electron microscopy (SEM). For improved taxonomic imaging, samples were treated with hydrochloric acid and hydrogen peroxide to remove carbonates and organic matter, respectively. A micropipette was used to transfer the suspension of selected samples to a round-glass cover slip following standard decantation method outlined by Barcena and Abrantes (1998). Samples were air-dried and coated with gold for SEM analysis. SEM analysis was carried out using a JEOL 6480LV scanning electron microscope. Taxonomy Diatoms include all algae from the Class Bacillariophyceae and follow the standardised taxonomy of World Register of Marine Species (WoRMS). Order Asterolamprales Family Asterolampraceae Asteromphalus hookeri Ehrenberg Asteromphalus hyalinus Karsten Order Achnanthales Family Cocconeidaceae Cocconeis sp. Order Bacillariales Family Bacillariaceae Fragilariopsis curta (Van Heurck) Hustedt Fragilariopsis cylindrus (Grunow) Krieger Fragilariopsis kerguelensis (O'Meara) Hustedt Fragilariopsis pseudonana (Hasle) Hasle Fragilariopsis rhombica (O'Meara) Hustedt Fragilariopsis separanda Hustedt Nitzschia bicapitata Cleve Nitzschia kolaczeckii Grunow Nitzschia sicula (Castracane) Husted var. bicuneata (Grunow) Hasle Nitzschia sicula (Castracane) Husted var. rostrata Hustedt Pseudo-nitzschia heimii Manguin Pseudo-nitzschia lineola (Cleve) Hasle Pseudo-nitzschia turgiduloides Hasle Order Chaetocerotanae incertae sedis Family Chaetoceraceae Chaetoceros aequatorialis var. antarcticus Cleve Chaetoceros atlanticus Cleve Chaetoceros dichaeta Ehrenberg Chaetoceros peruvianus Brightwell Chaetoceros sp. Order Corethrales Family Corethraceae Corethron spp. Order Coscinodiscales Family Coscinodiscaceae Stellarima stellaris (Roper) Hasle et Sims Family Hemidiscaceae Actinocyclus sp. Azpeitia tabularis (Grunow) Fryxell et Sims Hemidiscus cuneiformis Wallich Roperia tesselata (Roper) Grunow Order Hemiaulales Family Hemiaulaceae Eucampia antarctica (Castracane) Mangin Order Naviculales Family Plagiotropidaceae Tropidoneis group Family Naviculaceae Navicula directa (Smith) Ralfs Family Pleurosigmataceae Pleurosigma sp. Order Rhizosoleniales Family Rhizosoleniaceae Dactyliosolen antarcticus Castracane Rhizosolenia antennata f. semispina Sundstrom Rhizosolenia antennata (Ehrenberg) Brown f. antennata Rhizosolenia cf. costata Gersonde Rhizosolenia polydactyla Castracane f. polydactyla Rhizosolenia simplex Karsten Proboscia alata (Brightwell) Sundstrom Proboscia inermis (Castracane) Jordan Ligowski Order Thalassiosirales Family Thalassiosiraceae Porosira pseudodenticulata (Hustedt) Jouse Thalassiosira ferelineata Hasle et Fryxell Thalassiosira gracilis (Karsten) Hustedt Thalassiosira lentiginosa (Janisch) Fryxell Thalassiosira oestrupii (Ostenfeld) Hasle var. oestrupii Fryxell et Hasle Thalassiosira oliveriana (O'Meara) Makarova et Nikolaev Thalassiosira tumida (Janisch) Hasle Order Thalassionematales Family Thalassionemataceae Thalassionema nitzschioides var. lanceolatum Grunow Thalassiothrix antarctica Schimper ex Karsten Data available: 73 SEM images of the most abundant diatom species found at the three sampling sites. Samples were collected by several sediment traps placed at different depths in the Subantarctic Zone (47 degrees S site), Polar Frontal Zone (54 degrees S site) and Antarctic Zone (61 degrees S site) during the decade 1997-2007. The collection site and date for each species image can be found in Table 1 (see the word document in the download file).
Diatom and biogenic particle fluxes were investigated over a one-year period (2001-02) at the southern Antarctic Zone in the Australian Sector of the Southern Ocean. Two vertically moored sediment traps were deployed at 60 degrees 44.43'S 139 degrees 53.97' E at 2000 and 3800 m below sea-level. In these data sets we present the results on the temporal and vertical variability of total diatom flux, species composition and biogenic particle fluxes during a year. A detailed description of the field experiment, sample processing and counting methods can be found in Rigual-Hernandez et al. (2015). Total fluxes of particulates at both traps were highly seasonal, with maxima registered during the austral summer (up to 1151 mg m-2 d-1 at 2000 m and 1157 mg m-2 d-1 at 3700 m) and almost negligible fluxes during winter (up to 42 mg m-2 d-1 at 2000 m and below detection limits at 3700 m). Particulate fluxes were slightly higher at 2000 m than at 3700 m (deployment average = 261 and 216 mg m-2 d-1, respectively). Biogenic silica (SiO2) was the dominant bulk component, regardless of the sampling period or depth (deployment average = 76% at 2000 and 78% at 3700 m). Highest relative contribution of opal was registered from the end of summer through early-autumn at both depths. Secondary contributors were carbonate (CaCO3) (7% at 2000 m and 9% at 3700 m) and particulate organic carbon (POC) (1.4% at 2000 m and 1.2% at 3700 m). The relative concentration of carbonate and POC was at its highest in austral spring and summer. Diatom frustules from 61 taxa were identified over the entire experiment. The dominant species of the diatom assemblage was Fragilariopsis kerguelensis with a mean flux between 53 x 106 and 60 x 106 valves m-2 day-1 at 2000 m (annualized mean and deployment average, respectively). Secondary contributors to the diatom assemblage at 2000 and 3700 m were Thalassiosira lentiginosa, Thalassiosira gracilis var. gracilis, Fragilariopsis separanda, Fragilariopsis pseudonana, Fragilariopsis rhombica, Fragilariopsis curta and Azpeitia tabularis. Data available: two excel files containing sampling dates and depths, raw counts, relative abundance and fluxes (valves m-2 d-1) of the diatom species, and biogenic particle fluxes found at 2000 m and 3700 m depth. Each file contains four spreadsheets: raw diatom valve counts, relative abundance of diatom species and valve flux of diatom species and biogenic particle composition and fluxes. Detailed information of the column headings is provided below. Cup - Cup (=sample) number Depth - vertical location of the sediment trap in meters below the surface Mid-point date - Mid date of the sampling interval Length (days) - number of days the cup was open Girdle bands instead of valves were counted for Dactyliosolen antarcticus Castracane. Therefore, D. antarcticus girdles counts were not included in relative abundance calculations
Diatom and biogenic particle fluxes were investigated over a two-year and six-year periods at the Subantarctic and Polar Frontal Zones, respectively, in the Australian Sector of the Southern Ocean. Both sites were located along ~ 140 degrees E: station 47 degrees S was set on the abyssal plain of the central SAZ whereas station 54 degrees S was placed on a bathymetric high of the Southeast Indian Ridge in the PFZ. The data sets contain diatom species and biogeochemical flux data measured at 1000 m at the 47 degrees S site between 1999-2001 and at 800 m at the 54 degrees S site during six selected years between 1997-2007. All traps were MacLane Parflux sediment traps: conical in shape with a 0.5 m2 opening area and equipped with a carousel of 13 or 21 sampling cups. Shortest intervals corresponded with the austral summer and autumn ranging typically between 4.25 and 10 days, whereas the longest intervals were 60 days and corresponded with winter. Total fluxes of particulates at both traps were highly seasonal, with maxima registered during the austral spring and summer and very low fluxes during winter. Seasonality was more pronounced in the 54 degrees S site. Biogenic silica (SiO2) was the dominant bulk component in the PFZ while carbonate (CaCO3) dominated the particle fluxes at the SAZ. POC export was relatively similar between sites despite significant differences in the total diatom flux. Diatom frustules from 94 taxa were identified over the entire experiment. The dominant species of the diatom assemblage was Fragilariopsis kerguelensis at both sites, representing 43% and 59% of the integrated diatom assemblage at the 47 degrees S and 54 degrees S sites, respectively. Secondary contributors to the diatom assemblage at the 47 degrees S were Azpeitia tabularis, Thalassiosira sp. 1, Nitzschia bicapitata, resting spores of Chaetoceros spp., Thalassiosira oestrupii var. oestrupii, Hemidiscus cuneiformis and Roperia tesselata. Subordinate contributions to the diatom assemblage correspond to Pseudo-nitzschia lineola cf. lineola, Pseudo-nitzschia heimii, Thalassiosira gracilis group and Fragilariopsis pseudonana, Fragilariopsis rhombica and Thalassiosira lentiginosa. Data available: two excel files containing sampling dates and depths, raw counts, relative abundance and fluxes (valves m-2 d-1) of the diatom species, and biogenic particle fluxes measured at 1000 m and 800 m depth at the 47 degrees S and 54 degrees S sites, respectively. Each file contains four spreadsheets: raw diatom valve counts, relative abundance of diatom species and valve flux of diatom species and biogenic particle composition and fluxes. Detailed information of the column headings is provided below. Cup - Cup (=sample) number Depth - vertical location of the sediment trap in meters below the surface Mid-point date - Mid date of the sampling interval Length (days) - number of days the cup was open Girdle bands instead of valves were counted for Dactyliosolen antarcticus Castracane. Therefore, D. antarcticus girdles counts were not included in relative abundance calculations. Dates of data collection: 47 degrees S site: July 1999 - October 2001 (two-year record) 54 degrees S site: September 1997 - February 1998, July 1999 - August 2000, November 2002 - October 2004 and December 2005 - October 2007 (six-year record).
We studied the gut contents of four dominant copepod species (Calanoides acutus, Calanus propinquus, Calanus simillimus and Rhincalanus gigas) during the summer (2014-2015) along a latitudinal gradient (sampled every 5° between 40°S and 65°S) in the Indian sector of the SO. Diatoms were the most abundant food item found in the guts, comprising 24 of the 25 species found, and 15 were common to the four species of copepod studied. Diatoms accounted for the lowest proportion of the diet in the warmer, northern waters while all the large diatoms (e.g. Chaetoceros atlanticus, C. criophilus, C. dichaeta, Corethron spp.) were only found at 65oS. The most frequent species in the guts were the centric diatoms Thalassiosira spp. (4 to 57%) and the pennate diatoms Fragilariopsis kerguelensis (27 to 80%) and Trichoctoxon reinboldii (2 to 50%); proportions varied within a species across locations. These species were found at all sites examined, whereas some diatoms were specific to one copepod species: Asteromphalus spp. (in R. gigas), C. criophilus and C. dichaeta (in C. acutus), Nitzschia lecointei and N. sicula (in C. propinquus).
Metadata record for data from ASAC Project 492 See the link below for public details on this project. From the abstracts of the referenced papers: Diatom assemblages in two Holocene sediment cores (GC1 and GC2) from the Mac. Robertson Shelf, East Antarctica, are compared with modern sedimentary diatom assemblages from the same area. Open marine deposition commenced in Iceberg Alley (GC1), on the outer continental shelf, greater than 10.7 adj. 14C kyr BP. Chaetoceros resting spores, which may indicate water-column stabilsation from melting glacial and/or sea ice or the maximum summer sea-ice retreat, dominate the diatom assemblage. Approximately 7.5 adj. 14C kyr BP, a sea-ice diatom assemblage was deposited. This assemblage is similar to that being deposited in the surface sediments of the Mac. Robertson Shelf today and suggests that perennial sea ice has persisted in the vicinity of Iceberg Alley since that time. Interbedded within the sea-ice assemblage, however, are Corethron-rich sediment layers that suggest mid- to late-Holocene high-productivity events associated with a climatic optimum. The diatom record from Nielsen Basin (GC2), on the inner continental shelf, is relatively uniform compared to that in GC1. Glacial ice was present over the region c. greater than 5.6 adj. 14C kyr BP and a dissolution diatom assemblage was deposited beneath it. following ice retreat, an ice-edge diatom assemblage was deposited briefly before sea-ice conditions similar to that on the continental shelf today developed. There is no evidence in GC2 for the mid- to late-Holocene high-productivity events identified in GC1. Four diatom assemblages are identified from the surface sediments of Prydz Bay and the Mac. Robertson Shelf using multivariate analysis. A coastal assemblage is characterised by the sea-ice diatoms Fragilariopsis curta, F. angulata, F. cylindrus and Pseudonitzschia turgiduloides. A continental shelf assemblage is characterised by the open-water diatoms Fragilariopsis kerguelensis, Thalassiosira lenuginosa, T. gracilis var. expecta and Trichotoxin reinboldii. The Cape Darnley assemblage contains both sea-ice and open-water diatoms, but all are characteristically large and heavily silicified. Multiple regression has been used to identify the relationships between the diatom assemblages and known environmental variables. There are strong correlations between the coastal, shelf and oceanic assemblages and ecological conditions, including latitude, sea-ice distribution and ocean currents. The Cape Darnley assemblage is thought to represent an assemblage from which the smaller and more lightly silicified species have been removed by current winnowing. The palaeo-depositional environment of inner Prydz Bay, East Antarctica, has been reconstructed for the past 21,320 14C yr B.P., using diatom assemblages and sediment facies from a short, 352 cm long gravity core. Between 21,320 and 11,650 14C yr B.P., compact tillite and diamicton are present in the core, and diatom frustules are rare to absent. These data suggest that an ice sheet grounded over the site during the last glacial maximum. Following glacial retreat, siliceous muddy ooze was deposited, from 11,650 to 2600 14C yr B.P., in an open marine setting. During this stage, diatom frustules are abundant and well preserved, and Thalassiosira antarctica resting spores and Fragilariopsis curta dominate the assemblage. This assemblage suggests open marine deposition in an environment where the spatial and temporal distribution of sea ice is less than today. Since 2600 14C yr B.P., sea-ice and ice-edge diatom species have become more abundant, and neoglacial cooling is inferred. The assemblage is similar to that forming currently in Prydz Bay, where sea-ice is absent (less than 10% cover) for 2-3 months of the year and permanent ice edge and/or multiyear sea ice remains in close proximity to the site.
Locations of sampling sites for ASAC project 40 on voyage 3 of the Aurora Australis in the 2005/2006 season (the BROKE-West voyage). Samples were collected between January and March of 2008. Three datasets are currently included in this download - an excel spreadsheet and a draft publication providing details on the methodology, etc employed, as well as two copies of corrected fluoro data for BROKE-West (BW_UwayFLuChla - in excel and csv formats). Public Summary from the project: This program aims to determine the role of single celled plants, animals, bacteria and viruses in Antarctic waters. We quantify their vital role as food for other organisms, their potential influence in moderating global climate change through absorption of CO2 and production of DMS, and determine their response to effect of climate change. For more information, see the other metadata records related to ASAC project 40 (ASAC_40). ###### Taken from the abstract of the draft paper: The geographic distribution, stocks and vertical profiles of phytoplankton of the seasonal ice zone off east Antarctica were determined during the 2005-2006 austral summer as part of the Baseline Research on Oceanography, Krill and the Environment-West (BROKE-West) survey. CHEMTAX analysis of HPLC pigment samples, coupled with microscopy, permitted a detailed survey along eight transects covering an extensive area between 30 degrees E and 80 degrees E, from 62 degrees S to the fast ice. Significant differences were found in the composition and stocks of populations separated by the Southern Boundary of the Antarctic Circumpolar Current (SB), as well as a small influence of the Weddell Gyre in the western sector of the zone south of the SB (SACCZ). Within the SACCZ, we identified a primary bloom under the ice, a secondary bloom near the ice edge, and an open ocean deep population. The similarity of distribution patterns across all transects allowed us to generalise a hypothesized sequence for the season. The primary bloom was initiated by release of cells and detritus from melting sea ice, some 35 days before ice melting, with stocks of Chl a ranging from 115-239 mg.m-2, apart one leg (41 mg.m-2), which was sampled late in the season. The bloom was dominated by haptophytes (in particular, colonies and gametes of Phaeocystis antarctica), diatoms and cryptophytes (or Myrionecta rubrum). The detrital material quickly sank from the upper water column, but the bloom of diatoms and, to a lesser extent cryptophytes, continued until 20 days after ice melt. Average Chl a stocks during this bloom ranged from 56-92 mg.m-2 between transects. A bloom of Phaeocystis gametes immediately after ice melt lasted for about 10 days. Grazing activity, as indicated by phaeophytin a, also increased at the same time. The diatom bloom became senescent, probably as a result of iron exhaustion, as indicated by chlorophyllides, which reached 45% of total Chl a. The bloom then rapidly declined, apparently due to grazing krill. Well-defined 'holes' in the chlorophyll distribution of most suggested that the krill were moving southward following the retreating sea ice and clearing the ice edge bloom. There was no evidence that blooms had been terminated by sinking or by vertical mixing. It appears that grazing of the bloom and export of cellular material as faecal pellets stripped the upper water column of iron, preventing its normal recycling via the microbial network. Thus, export of iron by grazing, and possibly sedimentation, created a southward migrating iron front, limiting growth in the upper water column. North of the iron front, a recycling nanoflagellate community developed at depth, sustained by residual iron, as indicated by a close correspondence between distributions of Chl a and profiles of Fv/Fm. Its depth was independent of the mixed layer and the pycnoclines. This community consisted of haptophytes (chiefly Phaeocystis gametes), dinoflagellates, prasinophytes, cryptophytes, and some small diatoms. The community may have derived from, and was possibly sustained by, selective grazing by krill. Average stocks of Chl a ranged from 36-49 mg.m-2 between transects. North of the SB, communities were found in the mixed layer, although they still had low Fv/Fm ratios. Populations were dominated by Phaeocystis gametes (with colonies north of the southern ACC front), diatoms such as Pseudonitzschia sp., Fragilariopsis pseudonana, F. kerguelensis, F. curta, and Gymnodinium sp. Average stocks of Chl a ranged from 40-67 mg.m-2 between transects.These appeared to be recycling communities that had been advected into the BROKE-West study region. These interpretations provide a cogent explanation for the composition and structure of microbial populations in the marginal ice zone during the latter half of the summer. ###### The fields in this dataset are: Peak Pigment name Retention times Visible maxima Comments Leg Zone Latitude Longitude CTD Julian Day Date Ice free days Pigment concentrations Protists