Forest carbon balance under elevated CO2

Free-air CO₂ enrichment (FACE) technology was used to expose a loblolly pine (Pinus taeda L.) forest to elevated atmospheric CO₂ (ambient + 200 µl l^-1). After 4 years, basal area of pine trees was 9.2% larger in elevated than in ambient CO₂ plots. During the first 3 years the growth rate of pine was stimulated by ~26%. In the fourth year this stimulation declined to 23%. The average net ecosystem production (NEP) in the ambient plots was 428 gC m^-2 year^-1, indicating that the forest was a net sink for atmospheric CO₂. Elevated atmospheric CO₂ stimulated NEP by 41%. This increase was primarily an increase in plant biomass increment (57%), and secondarily increased accumulation of carbon in the forest floor (35%) and fine root increment (8%). Net primary production (NPP) was stimulated by 27%, driven primarily by increases in the growth rate of the pines. Total heterotrophic respiration (R_h) increased by 165%, but total autotrophic respiration (R_a) was unaffected. Gross primary production was increased by 18%. The largest uncertainties in the carbon budget remain in separating belowground heterotrophic (soil microbes) and autotrophic (root) respiration. If applied to temperate forests globally, the increase in NEP that we measured would fix less than 10% of the anthropogenic CO₂ projected to be released into the atmosphere in the year 2050. This may represent an upper limit because rising global temperatures, land disturbance, and heterotrophic decomposition of woody tissues will ultimately cause an increased flux of carbon back to the atmosphere.     

The annual patterns of photosynthesis in two large, freshwater, ultra-oligotrophic Antarctic lakes

The phytoplankton productivity and biomass of two large, freshwater Antarctic lakes (Vestfold Hills, eastern Antarctica) were investigated over a 12-month period. Crooked Lake was sampled at one site, while Lake Druzhby, a complex lake with two shallow and one deep basin, was subject to a more detailed investigation. Concentrations of chlorophyll a were usually below 1 µg l^-1, indicating ultra-oligotrophic conditions. Despite periodic low nutrient levels, low temperatures (range 0.4-2.8°C) and periodic poor light climate, some degree of photosynthesis was measurable throughout the year, including the dark winter phase. Snow cover had a pronounced impact on the light climate of the water column and inhibited photosynthesis. Mean rates of carbon fixation in the 0- to 15-m water column varied between 0 and 38.47 µg C l^-1 day^-1 in Crooked Lake and 0.24 and 37.68 µg C l^-1 day^-1 in Lake Druzhby. There were significant differences in the seasonal patterns of primary production between the basins of Lake Druzhby. The shallow basins had highest productivity in August, whereas the deep basin had highest rates in summer. Chlorophyll specific rates of photosynthesis or assimilation numbers [µg C (chl. a)^-1 h^-1] varied between 0.05 and 44.9, and photosynthetic efficiency [µg C (chl. a)^-1 h^-1 µmol m^-2 s^-1] between 0.02 and 5.19. The data suggest that the phytoplankton of these lakes is adapted to low irradiance levels, low temperatures and nutrient limitation.     

Temperature and Antarctic plankton community respiration

Antarctic plankton community respiration rates were determinedfrom in vitro changes in dissolved oxygen. Oxygen consumptionrates, measured at in situ temperatures between 0 and 6°C,were found to lie in the range 0.3–3.7 µmol O₂ l^–1per 24 h. Water samples were collected between East FalklandIsland and South Georgia, South Atlantic Ocean, and incubatedshipboard in the dark at up to 36 temperatures between –2and 14–C. A respiration rate at each temperature was thendetermined and used to calculate the temperature coefficient(Q₁₀) of Antarctic planktonic community respiration from theArrhenius equation. Fourteen Q₀ values lay in the range 1–3,with four further values >5. This range of temperature coefficientvalues for community respiration is comparable to the publishedrange of values for plankton photosynthesis. Frequency distributionsof temperature coefficients for the two processes show similarmodal Q₁₀5 of 2–3. Thus, this study does not lend supportto the hypothesis of a differential response of photosynthesisand community respiration to low temperature.     

Dynamics of inorganic phosphorus in pelagic communities of the Sea of Okhotsk

Inorganic phosphorus uptake and regeneration in the OkhotskSea waters were investigated in July–August 1994 withthe use of radioisotopic techniques. The rates of PO₄-P uptakeby microplankton in the upper mixed layer were between 1.5 and6.6 µg P l^-1 day^-1 (average 2.75) in areas of diatom dominance,and between 0.68 and 1.68 µg P l^-1 day^-1 (average 1.16)in areas of intense warming and summer phytoplankton minimum.The residence time of PO₄-P standing stock in water at differentstations varied between 1.5 and 24 days (mean 9 days). The shareof bacterioplankton contributing to total PO₄-P uptake was 50%in areas of the summer phytoplankton minimum and 20–30%in areas of diatom dominance. The PO₄-P regeneration rate wasmeasured first time experimentally in the temperate sea. Itsrates varied from 0.30 to 1.65 µg P l^-1 day^-1. In areasof diatom dominance, it compensated with 30–60% of PO₄-Puptake. In zones of summer phytoplankton minimum and in thelayers of deep chlorophyll maxima at 10–25 m depths, thePO₄-P regeneration rate often exceeded its uptake. Primary phytoplanktonproduction correlated well with PO₄-P uptake values in the uppermixed layer, while no correlation was found between primaryproduction and the ambient PO₄-P content in water.     

Multiple subsurface phytoplankton blooms occurring simultaneously in the Skagerrak

The distribution and characteristics of phytoplankton in theSkagerrak in August–September 2000 were analysed in orderto evaluate the importance of subsurface phytoplankton peaksto water column ecology and primary production. In areas affectedby outflow from the Baltic, enhanced chlorophyll concentrationswere found in the warm surface waters (i.e. upper 10–20m). However, for the central Skagerrak, the major part (50–80%)of the chlorophyll in the water column was found below the warmsurface waters. The highest chlorophyll concentrations (up to>18 µg l^-1) in the study area were also found belowthe warm surface waters and up to 95% of total water columnprimary production was recorded below the warm surface waterlayer. Measurements of variable fluorescence (F_v/F_m) indicatedthe greatest potential capacity for electron flow in photosystemII in phytoplankton was located below the warm surface waters.Spectrophotometrically determined pigment ratios suggest thatthe enhanced capacity for photosynthesis in the deeper watersmay be related to greater nutrient availability here than insurface waters. Subsurface chlorophyll distributions seen inrelation to the different water masses identified in the area,as well as community analysis of the phytoplankton present inthe subsurface peaks, indicate the presence of at least threedistinct subsurface phytoplankton blooms in the Skagerrak duringthe study period. Local oxygen saturation maxima recorded immediatelyabove the subsurface peaks provide in situ evidence that thesepeaks are photosynthetically active. This suggests that newproduction is taking place in these peaks, although quantificationof this production is hampered due to a lack of informationconcerning the initial conditions in and lifetime of the subsurfacepeaks. The subsurface phytoplankton peaks were, generally, foundimmediately above an oxygen minimum that covered the entirestudy area. In the relatively cold deep Atlantic water foundbelow the oxygen minimum layer, no or very little chlorophyllwas recorded and oxygen concentrations increased. Thus, it isargued that the respiration of the organic material producedin the upper part of the water column during late summer mayprimarily occur in the intermediate layers of the water column.     

Microbial community composition and function beneath temperate trees exposed to elevated atmospheric carbon dioxide and ozone

We hypothesized that changes in plant growth resulting from atmospheric CO₂ and O₃ enrichment would alter the flow of C through soil food webs and that this effect would vary with tree species. To test this idea, we traced the course of C through the soil microbial community using soils from the free-air CO₂ and O₃ enrichment site in Rhinelander, Wisconsin. We added either ¹³C-labeled cellobiose or ¹³C-labeled N-acetylglucosamine to soils collected beneath ecologically distinct temperate trees exposed for 3 years to factorial CO₂ (ambient and 200 µl l^-1 above ambient) and O₃ (ambient and 20 µl l^-1 above ambient) treatments. For both labeled substrates, recovery of ¹³C in microbial respiration increased beneath plants grown under elevated CO₂ by 29% compared to ambient; elevated O₃ eliminated this effect. Production of ¹³C-CO₂ from soils beneath aspen (Populus tremuloides Michx.) and aspen-birch (Betula papyrifera Marsh.) was greater than that beneath aspen-maple (Acer saccharum Marsh.). Phospholipid fatty acid analyses (¹³C-PLFAs) indicated that the microbial community beneath plants exposed to elevated CO₂ metabolized more ¹³C-cellobiose, compared to the microbial community beneath plants exposed to the ambient condition. Recovery of ¹³C in PLFAs was an order of magnitude greater for N-acetylglucosamine-amended soil compared to cellobiose-amended soil, indicating that substrate type influenced microbial metabolism and soil C cycling. We found that elevated CO₂ increased fungal activity and microbial metabolism of cellobiose, and that microbial processes under early-successional aspen and birch species were more strongly affected by CO₂ and O₃ enrichment than those under late-successional maple.     

Respiratory ETS activity of plankton in the northwestern Alboran Sea: seasonal variability and relationship with hydrological and biological features

Respiratory electron transport system (ETS) activity was measuredin plankton samples (<200 µm) collected in the NW AlboranSea. Sampling was carried out during seasonal cruises (summerand autumn 2003 and winter and spring 2004) in 12 stations locatedin transects off the coast of Malaga (southern Spain). Thiswork reports for the first time seasonal variations of the Arrheniusactivation energy (Ea) as well as being the first study to addressCO₂ balance in the NW Alboran Sea. These variations were relatedto changes in the phytoplankton community assemblage, whichcould ultimately be caused by the seasonal variability of hydrologicalconditions. ETS activity was significantly higher in summer,coinciding with a higher chlorophyll a (Chl a) concentrationand relatively high levels of particulate organic matter. TheETS:Chl a_total ratios were low during the four seasons, suggestinga high contribution of autotrophic phytoplankton to the respiratoryactivity of planktonic community. Respiratory CO₂ production(RCP) calculated from ETS activity ranged from 4.6 to 28.1 mgC m^–3 day^–1 during the four cruises. Chl a-specificRCP was lower than the maximum photosynthetic rates reportedin the literature for the studied area, suggesting that primaryproduction (PP) and respiration in the water column might beunbalanced.     

Biomass, feeding and production of Noctiluca scintillans in the Seto Inland Sea, Japan

The abundance and biomass of the large heterotrophic dinoflagellateNoctiluca scintillans, together with the changes in its potentialprey items, were monitored in the Seto Inland Sea, Japan, duringsummer 1997 (17 July-11 August). Growth and grazing rates ofNscintillans fed natural plankton populations were also measuredeight and seven times, respectively, during the survey period.The abundance and biomass of N scintillans averaged over thewater column (19 m) were in the range 1–345 cells 1^–1(temporalaverage = 93 cell1^–1) and 0.1–49.6 µg C l^–1(temporalaverage = 13.8 µg C l^–1; three times higher thanthat of calanoid copepods during the same period). Noctilucascintillans populations followed the changes in phytoplankton:N.scintillans biomass was increasing during the period of diatomblooms and was at a plateau or decreasing during periods oflow chlorophyll a. The growth rates of N.scintillans (µ)were also consistent with the wax and wane of the N.scintillanspopulation: N.scintillans showed highest growth rates duringdiatom blooms. A simple relationship between µ and chlorophylla concentration was established, and the production of N.scintillanswas estimated using this relationship and the measured biomass.The estimated production averaged over the water column wasin the range >0.1–5.2 µg C l^–1 day^–1(temporalaverage = 1.4 µg C l^–1 day^–1; 64% of the productionof calanoid copepods during the same period). Diatom clearancerates by N.scintillans were in the range 0.10–0.35 mlcell^–1 day^–1, and the phytoplankton population clearanceby N.scintillans was >12% day^–1. Thus, although thefeeding pressure of N.scintillans on phytoplankton standingstock was low, N.scintillans was an important member of themesozooplank-ton in terms of biomass and production in the SetoInland Sea during summer.     

Plankton community respiration in Bransfield Strait (Antarctic Ocean) during austral spring

Community respiration (R) was determined in Bransfield Straitfrom oxygen changes in water samples incubated in borosilicatebottles maintained at in situ temperature. The respiratory electrontransport system (ETS) activity of seawater communities wasalso measured from the same samples. Both data sets were relatedby the regression equation: log R (mg O₂ m^–3 day^–1)=0.462+0.730xlogETS activity mg O₂ m^–3 day^–1) (r=0.80, n=23). Fromthis equation and 37 ETS activity depth profiles, we calculatedthe integrated (0–100 m) community respiration as beingin the range 1.2–4.5 g O₂ m^–2 day^–1 (mean=2.2).These values do not differ significantly from other publishedresults for the Arctic and Antarctic Oceans. Assuming a respiratoryquotient of unity, the areal respiration ranges between 0.45and 1.69 g C m^–2 day^–1 (mean=0.8). This would representan important sink for the primary production reported for BransStrait. The spatial distribution of community respiration showedhigher values associated with the warmer and phytoplankton-richwaters outflowing from Gerlache Strait into Bransfield Strait,and with the front that separates Bellingshausen Sea watersfrom Weddell Sea waters. We suggest that this pattern of distributionmay be related to the transport of organic matter by the BransfieldCurrent along the front.     

Primary production, light and vertical mixing in Potter Cove, a shallow bay in the maritime Antarctic

Phytoplankton photosynthesis was measured during spring-summer 1991-1992 in the inner and outer part of the shallow Potter Cove, King George Island. Strong winds characterise this area. Wind-induced turbulent mixing was quantified by means of the root-mean square expected vertical displacement depth of cells in the water column, Z_t. The light attenuation coefficient was used as a measure of the influence of the large amount of terrigenous particles usually present in the water column; 1% light penetration ranged between 30 and 9 m, and between 30 and 15 m for the inner and outer cove, respectively. Obvious differences between photosynthetic capacity [P*_max; averages 2.6 and 0.6 µg C (µg chlorophyll-a)^-1 h^-1] and photosynthetic efficiency {!*; 0.073 and 0.0018 µg C (µg chlorophyll-a)^-1 h^-1 [(µmol m^-2 s^-1)^-1]} values were obtained for both sites during low mixing conditions (Z_t from 10 to 20 m), while no differences were found for high mixing situations (Z_t>20 m). This suggests different photoacclimation of phytoplankton responses, induced by modifications of the light field, which in turn are controlled by physical forcing. Our results suggest that although in experimental work P*_max can be high, wind-induced mixing and low irradiance will prevent profuse phytoplankton development in the area.     

Underwater light field and phytoplankton absorbance in different surface water masses of the Atlantic sector of the Southern Ocean

Spectral water transparency and phytoplankton light absorbance were studied in the Atlantic sector of the Southern Ocean during the Southern Ocean JGOFS ANT XIII/2 cruise in early austral summer 1995/1996. The study area comprised three zones, which differed markedly with respect to their hydrographic and planktological characteristics: the Antarctic Polar Frontal Zone with adiatom bloom, the Antarctic Circumpolar Current outside frontal systems with phytoplankton-poor water and a higher flagellate abundance than in the other two areas, and the marginal ice zone with a Phaeocystis bloom. The influence of phytoplankton on spectral water transparency was assessed by two independent procedures: the pigment-specific beam absorption coefficient, a_J*[5], at all stations, as estimated by spectroscopy of in vivo light absorption of plankton on glass fibre filters, and the pigment-specific light attenuation, (k_c[5]), as derived by regression analysis of spectral in situ vertical light attenuation coefficients in the sea against concomitant pigment concentrations. Values of a_J*[5] and vertical profiles of light attenuation by phytoplankton exhibited regional differences that corresponded with the three zones from which samples had been collected. These differences can be related to the specific characteristics of the three zones with respect to cell size distribution, pigment composition and biomass. The observed variations in a_J*[5] values should be considered when oceanic primary production is to be estimated by biooptical modelling.     

Contribution of Picocyanobacteria to total primary production and community respiratory losses in a backwater system

The contribution of autotrophic picoplankton (APP) to phytoplanktonicprimary production, investigated during the phytoplankton growingseason (March–September) in a macrophyte-dominated backwatersystem near Vienna, showed that APP mainly consisted of rod-shapedand coccoid cyanobacteria. Two stations were examined, exhibitingsimilar seasonal patterns in the development of picocyanobacteria,although the two sites differed in picocyanobacterial cell numbersand biomass by a factor of 1.5. Cell numbers determined by epifluorescencemicroscopy varied between 0.29 x 10⁴ and 34.5 x 10⁴ cells ml^–1at Station 1, and between 0.23 x 10⁴ and 19.1 x 10⁴ cells ml^–1at Station 2. At both sites, the mean cell volume of picocyanobacteriawas 0.5 µm³. Carbon fixation in the planktonic communityof the Kühwörter Wasser was dominated primarily bylarger phytoplankton, although the picoplankton community sometimessupplied up to 74% (mean: 35%) of total primary production.Distinct differences in chlorophyll a concentrations and primaryproduction between the two sites refer to a greater competitionbetween phytoplankton and macrophytes at Station 2. Communityrespiration deviated greatly in time and in level at the twostations, showing a higher dynamic in community metabolism atStation 1. At this site, community respiration losses rangedbetween 12 and 100% of gross production. Hence, community metabolismcomprised net autotrophic, balanced, and net heterotrophic situationsover the investigation period, whereas at Station 2, only netautotrophic situations could be determined.     

Feeding rates of the woodlouse Armadillidium vulgare on herb litters produced at two levels of atmospheric CO2

The consumption and assimilation rates of the woodlouse Armadillidium vulgare were measured on leaf litters from five herb species grown and naturally senesced at 350 and 700 µl l^-1 CO₂. Each type of litter was tested separately after 12, 30 and 45 days of decomposition at 18°C. The effects of elevated CO₂ differed depending on the plant species. In Medicago minima (Fabaceae), the CO₂ treatment had no significant effect on consumption and assimilation. In Tyrimnus leucographus (Asteraceae), the CO₂ treatment had no significant effect on consumption, but the elevated CO₂ litter was assimilated at a lower rate than the ambient CO₂ litter after 30 days of decomposition. In the three other species, Galactites tomentosa (Asteraceae), Trifolium angustifolium (Fabaceae) and Lolium rigidum (Poaceae), the elevated CO₂ litter was consumed and/or assimilated at a higher rate than the ambient CO₂ litter. Examination of the nitrogen contents in these three species of litter did not support the hypothesis of compensatory feeding, i.e. an increase in woodlouse consumption to compensate for low nitrogen content of the food. Rather, the results suggest that in herbs that were unpalatable at the start of the experiment (Galactites, Trifolium and Lolium), more of the the litter produced at 700 µl l^-1 CO₂ was consumed than of that produced at 350 µl l^-1 because inhibitory factors were eliminated faster during decomposition.     

Plankton gross production and respiration in the shallow water hydrothermal systems of Milos, Aegean Sea

Plankton gross production, net community production and darkcommunity respiration were measured at coastal sites aroundthe island of Milos, Aegean Sea, during June and September 1996and June 1997. Sampling sites were chosen to include those withand without visible signs of hydrothermal activity. Planktongross production ranged from undetectable (<0.3 mmol O₂ m-³day-¹) to 3 mmol O₂ m-³ day-¹; respiration rates ranged from1 to 6 mmol O₂ m-³ day-¹. No significant difference was foundbetween gross production or respiration rates measured at hydrothermallyactive areas and gross production or respiration rates measuredat non-venting areas. The dissolved inorganic carbon concentrationvaried by ~200 mmol C m-³ between venting and non-venting sites.Temperature had a pronounced stimulatory effect on the rateof plankton dark community respiration. The T_opt for planktondark community respiration always lay above the highest incubationtemperature of 30°C (i.e. >6°C above in situ temperature).Temperature had less of a stimulatory effect on the rate ofgross production.     

Soil microbial community and bacterial functional diversity at Machu Picchu, King George Island, Antarctica

The objective of this study was to evaluate the potential contribution of the soil microbial community in the vicinity of two plant covers, Sanionia uncinata and Deschampsia antarctica, at Machu Picchu Station, King George Island, Antarctica. Soil samples were collected at the study site during the southern (pole) summer period from 0-5 cm and 5-10 cm depths, for chemical and biological analyses. Soil microbial biomass reached a maximal value of 144 µg g^-1 in soil samples taken from under the S. uncinata upper layer plant. qCO₂ ranged from 167 to 239 µg CO₂^.mgC_mic^.h^-1 at the 0-5 and 5-10 cm depths, respectively. CO₂ evolution showed values of 54.3 mg^.m^-2 h^-1 beneath plant cover and 55.9 mg^.m^-2 h^-1 in the open space. CO₂ evolved by substrate induced respiration in the soil samples taken under the plant cover in the summer period, oscillated between 0.25 and 4.78 µg CO₂ g^-1 h^-1. The data obtained from this short study may provide evidence that both activity and the composition and substrate utilization of the microbial community appear to change substantially across the moisture level and sample location.     

Lactate dehydrogenase from the Antarctic eelpout, Lycodichthys dearborni

As part of our studies to examine the molecular basis of cold-adaptation, we have determined the kinetic properties, thermal stability and deduced amino acid sequence of the enzyme lactate dehydrogenase (LDH) from an Antarctic zoarcid fish, Lycodichthys dearborni. Unlike Antarctic notothenioid fish which are endemic to the Southern Ocean, zoarcid fish are cosmopolitan and have a substantially longer evolutionary history as a sub-order. The A₄-LDH isoform was isolated and purified from the white muscle of L. dearborni. The kinetic parameters K_m^PYR and k_cat were determined at temperatures from 0 to 25°C. K_m^PYR was substantially higher at low temperatures than those from Antarctic and temperate notothenioid fish, whereas k_cat at these temperatures was essentially the same as those of the other fish LDH in this study. The sequence of L. dearborni A₄-LDH was determined from cDNA derived from white muscle RNA and found to be similar to, but distinct from, the A₄-LDH sequences of Antarctic notothenioid fish. Molecular modelling based on the structure of the A₄-LDH from Pagothenia borchgrevinki suggested that three conservative amino acid changes within the core of the protein that are not directly part of the active site but which might nonetheless influence the active site, may be important in cold-adaptation in L. dearborni A₄-LDH, and that several other changes on the surface of the protein might also play a role in cold-adaptation.     

Mesozooplankton community structure and grazing impact in the Polar Frontal Zone of the south Indian Ocean during austral autumn 2002

Mesozooplankton community structure and grazing impact were investigated at 13 stations in the Polar Frontal Zone during the second Marion Offshore Variability Ecosystem Study (MOVES II), conducted during April 2002. Total integrated chl- a biomass ranged between 11.17 and 28.34 mg chl- a m^-2 and was always dominated by nano- and picophytoplankton (<20 µm). Throughout the study, small copepods, mainly Oithona similis and Ctenocalanus vanus, numerically dominated the mesozooplankton community, composing up to 85% (range 30-85%) of the total abundance. Grazing activity of the four most abundant copepods ( O. similis, C. vanus, Calanus simillimus and Clausocalanus spp.), constituting up to 93% of total mesozooplankton abundance, was investigated using the gut fluorescence technique. Results of gut fluorescence analyses indicated that Calanus simillimus and Clausocalanus spp. exhibited diel variability in gut pigments with maximum values recorded at night. In contrast, O. similis and Ctenocalanus vanus did not demonstrate diel variation in gut pigment contents. Ingestion rates of the four copepods ranged from 23.23 to 1462,02 ng(pigm.)ind^-1day^-1. The combined grazing impact of the four copepods ranged between 1 and 36% of the phytoplankton standing stock per day, with the highest daily impact occurring at stations occupied in the vicinity of the Antarctic Polar Front (~35.86% at station 23). Among the copepods, O. similis and Ctenocalanus vanus represented the most important consumers of phytoplankton biomass, collectively responsible for up to 89% (range 15-89%) of the total daily grazing impact. Carbon specific ingestion rates of the copepods varied between 42 and 320% body carbon per day.     

Dynamics of microplankton communities at the ice-edge zone of the Lazarev Sea during a summer drogue study

Microzooplankton grazing and community structure were investigatedin the austral summer of 1995 during a Southern Ocean Drogueand Ocean Flux Study (SODOFS) at the ice-edge zone of the LazarevSea. Grazing was estimated at the surface chlorophyll maximum(5–10 m) by employing the sequential dilution technique.Chlorophyll a concentrations were dominated by chainformingmicrophytoplankton (>20 µm) of the genera Chaetocerosand Nitzschia. Microzooplankton were numerically dominated byaloricate ciliates and dinoflagellates (Protoperidinium sp.,Amphisoleta sp. and Gymnodinium sp.). Instantaneous growth ratesof nanophytoplankton (<20 µm) varied between 0.019and 0.080 day^–1, equivalent to between 0.03 and 0.12 chlorophylldoublings day^–1. Instantaneous grazing rates of microzooplanktonon nanophytoplankton varied from 0.012 to 0.052 day^–1.This corresponds to a nanophytoplankton daily loss of between1.3 and 7.0% (mean = 3.76%) of the initial standing stock, andbetween 45 and 97% (mean = 70.37%) of the daily potential production.Growth rates of microphytoplankton (>20 µm) were lower,varying between 0.011 and 0.070 day^–1, equivalent to 0.015–0.097chlorophyll doublings day^–1. At only three of the 10 stationsdid grazing by microzooplankton result in a decrease in microphytoplanktonconcentration. At these stations instantaneous grazing ratesof microzooplankton on microphytoplankton ranged between 0.009and 0.015 day^–1, equivalent to a daily loss of <1.56%(mean = 1.11%) of initial standing stock and <40% (mean =28.55%) of the potential production. Time series grazing experimentsconducted at 6 h intervals did not show any diel patterns ofgrazing by microzooplankton. Our data show that microzooplanktongrazing at the ice edge were not sufficient to prevent chlorophylla accumulation in regions dominated by rnicrophytoplankton.Here, the major biological routes for the uptake of carbon thereforeappear to be grazing by metazoans or the sedimentation of phytoplanktoncells. Under these conditions, the biological pump will be relativelyefficient in the drawdown of atmospheric CO₂.     

In situ oxygen microelectrode measurements of bottom-ice algal production in McMurdo Sound, Antarctica

In-situ estimates of fast-ice algal productivity at Cape Evans, McMurdo Sound, in 1999 were lower than at the same site in previous years. Under-ice irradiance was between 0 and 8 µmol photons m^-2 s^-1; the ice was between 1.9 and 2.0 m thick and the algal biomass averaged 150 mg chl a m^-2, although values as high as 378 mg chl a m^-2 were recorded. Production on 11 and 12 November was between 0.053 and 1.474 mg C m^-2 h^-1. When the data from 11 November were fitted to a hyperbolic tangent function, a multilinear regression gave estimates for P_max of 0.571 nmol O₂ cm^-2 s^-1, an ! of 0.167 nmol O₂ cm^-2 s^-1 µmol^-1 photons m^-2 s^-1 and an E_k of 3.419 µmol photons m^-2 s^-1. A P_max of 2.674 nmol O₂ cm^-2 s^-1, an ! of 0.275 nmol O₂ cm^-2 s^-1 µmol^-1 photons m^-2 s^-1, r of 0.305 nmol O₂ cm^-2 s^-1 and an E_k of 9.724 µmol^-1 photons m^-2 s^-1 were estimated from the 12 November data. The sea-ice algal community was principally comprised of Nitzschia stellata, Entomoneis kjellmanii and Berkeleya adeliensis. Other taxa present included N. lecointei, Fragilariopsis spp., Navicula glaciei, Pleurosigma spp. and Amphora spp. Variations in the method for estimating the thickness of the diffusive boundary layer were not found to significantly affect the measurements of oxygen flux. However, the inability to accurately measure fine-scale variations in biomass is thought to contribute to the scatter of the P versus E data.     

Distribution patterns of decapod crustaceans in polar areas: a result of magnesium regulation?

Nearly all decapod crustaceans found in Antarctic waters south of the Antarctic Convergence are caridean shrimps (Natantia) while the group of Reptantia is largely absent in this area. Progress in the development of a physiological hypothesis is reported, which explains this distribution pattern based on differences in the regulation of magnesium levels in the haemolymph ([Mg²⁺]_HL) and on the Mg²⁺ dependence of threshold temperatures below which cold-induced failure of cardiac and ventilatory performance occurs. Previous studies had shown that an increase in oxygen consumption and activity levels in the cold can be induced by experimental reduction of [Mg²⁺]_HL in different reptant decapod species. In the present study, we tested the potential of these experimental findings for predicting the effect of low [Mg²⁺]_HL in nature, and investigated temperature-induced changes in oxygen consumption in two species with low but different [Mg²⁺]_HL from southern Chile, Halicarcinus planatus and Acanthocyclus albatrossis ([Mg²⁺]_HL=10.7 and 21.6 mmol l^-1, respectively). In accordance with previous findings, low [Mg²⁺]_HL levels were associated with a reduction of thermal sensitivity and a higher metabolic rate in the cold. A model is developed which describes how [Mg²⁺]_HL reduction caused a threshold temperature (pejus temperature, Tp) to fall, which characterises the onset of cold-induced failure in oxygen supply to tissues. This threshold temperature is interpreted, not only to indicate the limits of cold tolerance, but also of geographical distribution. Tp is shifted towards lower temperatures in Natantia, which are efficient [Mg²⁺]_HL regulators. In contrast, Reptantia, which are poor [Mg²⁺]_HL regulators, appear unable to colonise the permanently cold water of the Antarctic due to insufficient capacity of cardiac performance and, therefore, largely reduced scope for activity at high [Mg²⁺]_HL.