RATES OF PHOTOADAPTATION IN SEA ICE DIATOMS FROM MCMURDO SOUND,ANTARCTICA1

Sea ice microalgae are released from their relatively stable light environment to the water column seasonally, and any subsequent growth in a vertically mixed water column may depend, in part, on their photoadaptation rates. In this study we followed the time course of photoadaptation in natural sea ice algal communities from bottom ice and surface ice by measuring their photophysiological response to an artificial shift in the ambient irradiance field. Microalgae from under-ice habitats, were incubated under full sunlight (LL-HL) and microalgae from surface ice habitats were incubated under artificial light to mimic under-ice irradiance (HL-LL). During 3- to 4-day time course studies, opposite shifts in chlorophyll: carbon, α, P^B_m, and I_k were observed, depending on the direction of the irradiance change. First-order rate constants (k) ranged from 0.0067 to 0.29 h^?1 for photosynthetic parameters, although P^B_m did not always show a clear change over time. Rates of photoadaptation for ice algae are comparable to k values reported for temperate phytoplankton, suggesting that sea ice algae may be equally capable of adapting to the light conditions experienced in a vertically mixed water column. This study presents the first evidence that sea ice microalgae are physiologically capable of adapting to a planktonic life and thus could serve as a seed population for polar marine phytoplankton blooms.     

THE INFLUENCE OF SALINITY AND TEMPERATURE COVARIATION ON THE PHOTOPHYSIOLOGICAL CHARACTERISTICS OF ANTARCTIC SEA ICE MICROALGAE1

The responses of sea ice microalgae to variation in ambient irradiance (0 to 150 μE · m^?2· s^?1), temperature (–6° to + 6° C), and salinity (0 to 100 ppt) were tested to determine whether these variables act independently or in concert to influence rates of microalgal photosynthesis. The photosynthetic efficiency and maximum photosynthetic rate for sea ice microalgae increased as a function of incubation temperature between -6° and + 6° C. Furthermore, photosynthetic efficiency, maximum photosynthetic rate, and quantum yield were greatest at salinities between SO and 50 ppt. In contrast, the mean specific absorption coefficients were lowest near seawater salinities, and the saturating irradiance, I_s, appeared to be inversely proportional to salinity. Results also suggest that the effects of salinity on the growth of sea ice microalgae are independent of those elicited by temperature or light, and that the functional relationship between salinity and light or temperature is multiplicative. This information is essential to the proper formulation of algorithms used to describe algal growth in environments where light, temperature, and salinity are changing simultaneously, such as within sea ice or within the water column at the marginal ice edge zone.     

POPULATION DYNAMICS OF MICROALGAE IN THE UPPER LAND-FAST SEA ICE AT A SNOW-FREE LOCATION

The population dynamics of interior ice microalgae were investigated at a snow-free site on annual land-fast sea ice in McMurdo Sound, Antarctica, during the austral spring and summer of 1995 – 96. A dynamic successional sequence was observed with life history transformations playing an important role. During late November and early December (austral spring), cryo- and halotolerant dinoflagellates and chrysophytes bloomed in brine channels within the upper ice. At this time, competition and grazing pressure are low because of the inability of most marine species to grow under the extreme environmental conditions found in the upper ice during the austral spring. In November and December, dinoflagellates, chrysophytes, and prasinophytes contributed an average of 66%, 44%, and < 1% of the phytoflagellate biomass, respectively. Both the dinoflagellates and the chrysophytes encysted in December, with cyst formation most intense just prior to surface melt and flushing of the ice. The cysts appear to be an adaptation for survival and dispersal in the plankton during ice decay and/or overwintering in the sea ice. In January (austral summer), when ice temperatures were similar to those in the water column, pennate diatoms replaced flagellates as the photosynthetic dominants in the upper sea ice. The upper land-fast sea ice undergoes dramatic seasonal changes in light availability, temperature, brine salinity, and inorganic nutrient availability. Ephemeral blooms of cyst-forming phytoflagellates exploit this habitat in the austral spring, when both inorganic nutrients and light are available but temperatures <− 2° C and brine salinities elevated.     

PHOTOSYNTHESIS AND CELL DIVISION BY ANTARCTIC MICROALGAE: COMPARISON OF BENTHIC,PLANKTONIC AND ICE ALGAE1

Irradiance-dependent rates of photosynthesis and cell division of six species of microalgae isolated from the benthos, plankton and sea ice microbial community in McMurdo Sound, Antarctica were compared. Microalgae isolated from different photic environments had distinct photosynthetic and growth characteristics. For benthic and ice algae, photosynthesis saturated at 6 to 20 μE.m^?2.s^?1 and was photoinhibited at 10 to 80 μE.m^?2.s^?1 while for the planktonic algae, saturation irradiances were up to 13 times higher and photoinhibition was not detected. The slope of the light-limited portion of the P-I relationship was up to 50 times greater for the benthic algae than for either the ice or planktonic algae suggesting that benthic algae used the low irradiances more efficiently for carbon uptake. Cell division was dependent on the incubation irradiance for all but one microalga examined. The dependence of division rates on irradiance was however much smaller than for carbon uptake, suggesting that cell division buffers the influence of short term variations of irradiance on cellular metabolism.     

ICE‐BINDING PROTEINS FROM SEA ICE DIATOMS (BACILLARIOPHYCEAE)1

Sea ice diatoms thrive under conditions of low temperature and high salinity, and as a result are responsible for a significant fraction of polar photosynthesis. Their success may be owing in part to secretion of macromolecules that have previously been shown to interfere with the growth of ice and to have the ability to act as cryoprotectants. Here we show that one of these molecules, produced by the sea ice diatom Navicula glaciei Vanheurk, is a ～25 kDa ice‐binding protein (IBP). A cDNA obtained from another sea ice diatom, Fragilariopsis cylindrus Grunow, was found to encode a protein that closely matched the partially sequenced N. glaciei IBP, and enabled the amplification and sequencing of an N. glaciei IBP cDNA. Similar proteins are not present in the genome of the mesophilic diatom Thalassiosira pseudonana. Both proteins closely resemble antifreeze proteins from psychrophilic snow molds, and as a group represent a new class of IBPs that is distinct from other IBPs found in fish, insects and plants, and bacteria. The diatom IBPs also have striking similarities to three prokaryotic hypothetical proteins. Relatives of both snow molds and two of the prokaryotes have been found in sea ice, raising the possibility of a fungal or bacterial origin of diatom IBPs.     

PHOTOPHYSIOLOGICAL EVIDENCE OF NUTRIENT LIMITATION OF PLATELET ICE ALGAE IN MCMURDO SOUND, ANTARCTICA

Seasonally changing photophysiological and biochemical characteristics of sea ice microalgae are interpreted with respect to light availability and measurements of nutrient concentration made at high vertical resolution (12.5 cm) during a dense bloom in the platelet ice layer of McMurdo Sound during a 6-week study in austral spring of 1989. Platelet ice algae remained highly shade adapted throughout the spring as shown by their low photoadaptive index (E_k, 3.7–8.4 μmol photons·m⁻²·s⁻¹), low mean specific absorption coefficient (<0.009 m² mg⁻¹ Chl a), high optical cross-sectional area of photosystem II (σ_PSII, 3.0–8.2), and high molar ratio of fucoxanthin:chlorophyll a (mean = 1.62 ± 0.15 SD). Between 24 October and 8 November, the algae exhibited a photoacclimative response that was marked by a 30% decrease in photosynthetic efficiency (α^B), a 75% decrease in maximum photosynthetic rate (P^B/_m), and a 60% increase in σ_PSII. The photochemical conversion efficiency at photosystem II (F_v/F_m= ca. 0.5) and the quantum yield of photosynthesis (Ø_C= 0.062– 0.078 mol C mol⁻¹ photons) were ca. 80% of their maximal values. After 8 November, changes in algal photophysiology and biochemistry, which were inconsistent with a photoacclimation response, suggest that the platelet ice algae near the platelet/congelation ice interface became increasingly nutrient limited. The number of pennate diatoms increased threefold to 150 × 10⁹ cells m⁻³ between 8 and 14 November, then remained unchanged throughout the remainder of the field season. Following the increase in cell number, F_v/F_m, Ø_C, and C:Chla decreased by >40%, σ_PSII increased by 70%; and the biochemical ratios C:N and C:Si increased 25%–30%. Nutrient depletion was apparent from the high-resolution vertical profiles, but nutrient concentrations limiting algal growth were not observed. However, nutrient concentrations at the likely site of nutrient limitation near the platelet/congelation ice interface were not measured, indicating that higher resolution sampling is necessary to fully characterize this highly variable habitat.     

SHORT‐TERM EFFECT OF TEMPERATURE ON THE PHOTOKINETICS OF MICROALGAE FROM THE SURFACE LAYERS OF ANTARCTIC PACK ICE1

Microalgae growing within brine channels (85 psu salinity) of the surface ice layers of Antarctic pack ice showed considerable photosynthetic tolerance to the extreme environmental condition. Brine microalgae exposed to temperatures above ?5°C and at irradiances up to 350 μmol photons·m^?2·s^?1 showed no photosynthetic damage or limitations. Photosynthesis was limited (but not photoinhibited) when brine microalgae were exposed to ?10°C, provided the irradiance remained under 50 μmol photons·m^?2·s^?1. The highest level of photosynthetic activity (maximum relative electron transport rate [rETR_max]) in brine microalgae growing within the surface layer of sea ice was at approximately 18 μmol electrons·m^?2·s^?1, which occurred at ?1.8°C. Effective quantum yield of PSII and rETR_max of the halotolerant brine microalgae exhibited a temperature‐dependent pattern, where both parameters were higher at ?1.8°C and lower at ?10°C. Relative ETR_max at temperatures above ?5°C were stable across a wide range of irradiance.     

A DINOFLAGELLATE CYST FROM ANTARCTIC SEA ICE1

The small (< 15 μm) hypnozygote of an autotrophic athecate dinofiagellate found in association with Antarctic sea ice had an external covering composed of approximately 60 plates, each of which was bounded by sutural ridging and possessed an intratabular process. A cingulum and sulcus were also evident. The ultrastructure of the cyst was increasingly dominated by storage bodies as the cyst matured, and the cell wall thickened from 0.2 to 0.8 μm over 2 months. This cyst has been encountered often but usually at low abundances (10³?10⁴ cells·L^?1); however, the maximum abundances observed (10⁶ cells·L^?1) indicate that the formation of this cyst may play an important part in the ecology of sea ice communities.     

PHOTOSYNTHESIS-IRRADIANCE RELATIONSHIPS IN PHYTOPLANKTON FROM THE PHYSICALLY STABLE WATER COLUMN OF A PERENNIALLY ICE-COVERED LAKE (LAKE BONNEY,ANTARCTICA)1

The perennially ice-covered lakes of Antarctica have hydrodynamically stable water columns with a number of vertically distinct phytoplankton populations. We examined the photosynthesis-irradiance characteristics of phytoplankton from four depths of Lake Bonney to determine their physiological condition relative to vertical gradients in irradiance and temperature. All populations studied showed evidence of extreme shade adaptation, including low I_k values (15–45 μE · m^?2· s^?1) and extremely low maximal photosynthetic rates (P^B_m less than 0.3 μg C ·μg chl a^?1· h^?1). Photosynthetic rates were controlled by temperature as well as light variations with depth. Lake Bonney has an inverted temperature profile within the trophogenic zone that increased from 0° C at the ice-water interface to 6° C from 10 to 18 m. Deeper phytoplankton (10 m and 17 m) were found to have photosynthetic capacities (P^B_m) and efficiences (α) three to five times higher than those at the ice-water interface. However, Q₁₀ values were only ca. 2 for P^B_m (no temperature dependence was evident for α), suggesting that a simple temperature response cannot explain all the differences between populations. Lake Bonney phytoplankton (primarily cryptophytes and chlorophytes) had photosynthetic characteristics similar to diatoms from other physically stable environments (e.g. sea ice, benthos) and may be ecologically analogous to multiple deep chlorophyll maxima.     

EFFECT OF SEASONAL SEA ICE BREAKOUT ON THE PHOTOSYNTHESIS OF BENTHIC DIATOM MATS AT CASEY,ANTARCTICA1

Photosynthesis of marine benthic diatom mats was examined before and after sea ice breakout at a coastal site in eastern Antarctica (Casey). Before ice breakout the maximum under‐ice irradiance was between 2.5 and 8.2 μmol photons·m^?2·s^?1 and the benthic microalgal community was characterized by low E_k (12.1–32.3 μmol photons·m^?2·s^?1), low relETR_max (9.2–32.9), and high alpha (0.69–1.1). After breakout, 20 days later, the maximum irradiance had increased to between 293 and 840 μmol photons·m^?2·s^?1, E_k had increased by more than an order of magnitude (to 301–395 μmol photons·m^?2·s^?1), relETR_max had increased by more than five times (to 104–251), and alpha decreased by approximately 50% (to 0.42–0.68). During the same time interval the species composition of the mats changed, with a decline in the abundance of Trachyneis aspera (Karsten) Hustedt, Gyrosigma subsalsum Van Heurck, and Thalassiosira gracilis (Karsten) Hustedt and an increase in the abundance of Navicula glaciei Van Heurck. The benthic microalgal mats at Casey showed that species composition and photophysiology changed in response to the sudden natural increase in irradiance. This occurred through both succession shifts in the species composition of the mats and also an ability of individual cells to photoacclimate to the higher irradiances.     

EFFECT OF HYPEROXIA ON THE GROWTH AND PHOTOSYNTHESIS OF POLAR SEA ICE MICROALGAE1

Sea ice algal communities are naturally exposed to very high concentrations of dissolved oxygen, which are likely to lead to increasing stress levels and declines in productivity. To test this hypothesis, cultures of Fragilariopsis cylindrus (Grun?) Hasle, Pseudo‐nitzschia sp., Fragilariopsis curta (Van Heurch), Porosira glacialis (Grunow), and Entomoneis kjellmannii (Cleve) from Antarctic sea ice and Nitzschia frigida from Arctic sea ice were exposed to elevated dissolved oxygen levels, and their growth, maximum quantum yield, relative maximum electron transport rate, and photosynthetic efficiency were measured. At oxygen concentrations equivalent to approximately four times air saturation (89% oxygen), the growth rate and maximum quantum yield were significantly reduced in all taxa. When the oxygen concentration was regularly allowed to drop, the effect on growth and quantum yield was reduced. At lower dissolved oxygen concentrations (52%), the declines in growth and quantum yield were reduced but were still mostly significantly different from the controls (21% oxygen). It is likely that the generation of excess active oxygen radicals in the presence of free oxygen is responsible for most of the decline in growth, maximum quantum yield, relative maximum electron transport rate, and photosynthetic efficiency in all species.     

SHADE ADAPTED BENTHIC DIATOMS BENEATH ANTARCTIC SEA ICE1

A dense community of shade adapted microalgae dominated by the diatom Trachyneis aspera is associated with a siliceous sponge spicule mat in McMurdo Sound, Antarctica. Diatoms at a depth of 20 to 30 m were found attached to spicule surfaces and in the interstitial water between spicules. Ambient irradiance was less than 0.6 μE · m^?2· s^?1 due to light attenuation by surface snow, sea ice, ice algae, and the water column. Photosynthesis-irradiance relationships determined by the uptake of NaH¹⁴CO₃ revealed that benthic diatoms beneath annual sea ice were light-saturated at only 11 μE·m^?2·s^?1, putting them among the most shade adapted microalgae reported. Unlike most shade adapted microalgae, however, they were not photoinhibited even at irradiances of 300 μE·m^?2·s^?1. Although in situ primary production by benthic diatoms was low, it may provide a source of fixed carbon to the abundant benthic invertebrates when phytoplankton or ice algal carbon is unavailable.     

THE BOTTOM-ICE MICROALGAL COMMUNITY FROM ANNUAL ICE IN THE INSHORE WATERS OF EAST ANTARCTICA1

The structure, productivity and heterotrophic potential of an extensive microalgal community growing on the underside of sea ice near the Australian Antarctic Station of Casey, are described. Underwater observations made near the Australian Antarctic stations of Davis and Mawson are also reported. This community develops during September, is largely suspended from the bottom surface of annual sea ice and often extends into the underlying water column as conspicuous strands up to 15 cm long. The algal community structure in the strands is dominated by an unidentified tube diatom belonging to the Amphipleura/Berkeleya group and chains of a species of Entomoneis cf. Amphiprora paludosa var. hyperborea (Grunow) Cleve. Unlike previously described bottom ice environments, a brash ice layer under the hard sea ice is absent. Living cells, predominantly Nitzschia frigida Grunow, also occur in microbrine channels in the bottom 3 cm of the ice. Maximal primary production rates of 81 μg C · L^-1· h^-1 occurred during November, then began declining near the end of December. Minimal rates (2.8 μg C · L^-1· h^-1) were reached in mid-January and coincided with changes in the physical structure of the sea ice and in the stability of the water column. An abundant epibacterial community associated with the microalgal strands assimilated ³H-labelled amino acids suggesting significant heterotrophic recycling of dissolved organic matter. Turnover times of assimilated amino acids in the bottom ice community averaged 55 h during November while negligible turnover of these substrates occurred in the water column 1.5 m below the ice. These bottom ice communities have higher primary productivity than typical brash ice communities; they are also accessible to marine herbivores and so may be more important to the Antarctic marine food chain than previously supposed.     

MICROALGAL LIGHT-HARVESTING IN EXTREME LOW-LIGHT ENVIRONMENTS IN MCMURDO SOUND, ANTARCTICA1

Microalgal pigment composition, photosynthetic characteristics, single-cell absorption efficiency (Qa_(λ)) spectra, and fluorescence-excitation (FE) spectra were determined for platelet ice and benthic communities underlying fast ice in Mc Murdo Sound, Antarctica, during austral spring 1988. Measurements of spectral irradiance (E_(λ)) and photosynthetically active radiation (PAR) as well as samples for particulate absorption measurements were taken directly under the congelation ice, within the platelet layer, as profiles vertically through the water column, and at the benihic surface. Light attenuation by.sea ice, algal pigments, and particulates reduced PAR reaching the platelet ice layer to 3%(9–33 fimol photons m-²-^?s-¹) of surface values and narrowed its spectral distribution to a band between 400 and 580 nm. Attenuation by the water column further reduced PAR reaching the sea floor (28–m depth) to 0.05% of surface levels (< 1 μmol photons m-² s-¹), with a spectral distribution dominated by 470–580–nm wavelengths. The photoadaptive index (I) for platelet ice algae (5.9–12.6 μmol photons m-^2.s-¹) was similar to ambient PAR, indicating that algae had acclimated to their light environment (i.e. the algae were light-replete). Maximum Qa_(λ) at the blue absorption peak (440 nm) was 0.63, and enhanced absorption was observed from 460–500 nm and was consistent with observed high cellular chlorophyll (chi) c:chl a and fucoxanthin: chl a molar ratios (0.4 and 1.2, respectively). Benthic algae were light-limited despite the maintenance of very low I_k values (4–11 μmol photons.m-^2.s-¹). Extremely high fucoxanthin: chi a ratios (1.6) in benthic algae produced enhanced green light absorption, resulting in a high degree of complementation between algal absorption and ambient spectral irradiance. Qa_(λ) values for benthic algae were maximal (0.9) between 400 and 510 nm but remained >0.35 even at absorption minima. Strong spectral flattening, a characteristic of intense pigment packaging, was also apparent in the Qa_(λ) spectra for benthic algae. FE and Qa_(λ) spectra were similar in shape for platelet ice algae, indicating that the efficiency at which absorbed energy was transferred to photosystem II (PSII) was independent of wavelength. Fluorescence emission by benthic algae was greatest for the 500–560–nm excitation wavelengths, suggesting that most energy absorbed by accessory pigments was transferred to PSII. These results suggest that under ice algae employ complementary pigmentation and maximize absorption efficiency as adaptive strategies to low-light stress. Regulating the distribution of absorbed energy between PSI and PSII may be an adaptive response to the restricted spectral distribution of irradiance.     

GROWTH RESPONSES TO SALINITY VARIATION IN FOUR ARCTIC ICE DIATOMS1,2

During spring, extensive blooms of microalgae grow on the underside of arctic sea ice. The brownish, algal layer penetrates ca. 2 cm into the bottom surface of the ice and the algae are potentially exposed to very high salinities. Four diatom species, Melosira juergensii Ag., Porosira glacialis (Grun.) Jørg., Navicula transitans var. derasa (Grun.) Cleve, and Coscinodiscus lacustris Grun., isolated from, sea ice samples taken from the Beaufort and Chukchi seas near Barrow, Alaska, were grown at 11 salinities ranging from 5 to 70‰ at 5 C under constant illumination. All of the species grew at 5‰ except N. transitans whose lower growth limit was 15‰. Growth was high over a broad range of salinities, but none of the species grew at salinities above 60‰. These diatom species appear to be well suited to tolerate the salinities in the brine pockets near the bottom of annual arctic sea ice where they are found. High brine-cell salinity, however, may limit the upward, penetration of ice algae into the bottom of sea ice.     

PHOTOADAPTATION,GROWTH AND PRODUCTION OF BOTTOM ICE ALGAE IN THE ANTARCTIC1

Biomass, chemical composition, growth rates and the photosynthetic response of natural populations of sea ice algae in McMurdo Sound, Antarctica were followed over most of the spring bloom to examine temporal variability under a relatively constant incident irradiance (ca. 1500–1700 μE · m^-2· s^-1 at solar noon). Collection were restricted to bottom 20 cm of the ice sheet in an area with little or no snow (0–5 cm). At low temperature and irradiance these algae normally exhibited low assimilation numbers (ca. 0.1–0.4 mg C · mg Chl^-1· h^-1). Average growth rates (0.02–0.45 d^-1), based on changes in standing stocks, were also low. Biomass, biochemical composition, growth rates, assimilation numbers and photosynthetic efficiencies (mg C · mg Chl^-1· h^-1 (μE · m^-2· s^-1)^-1) displayed large fluctuations over periods of several days during the growth season. On the other hand, I_k which is an index of photoadaptation, and I_m, the optimal irradiance for photosynthesis, were relatively constant with less than twofold variation throughout our study. Substantial nutrient fluxes (3.3–8.0 mmol Si or N · m^-2· d^-1) were necessary to satisfy the minimum nutrient demand for the observed biomass levels and population growth rates; over the 41 days of our study, integrated nutrient demand represented 69–150 mmol N or Si · m^-2, Only 5–25% of this total demand could be met by all of the nutrients in the ice sheet, if they were readily available. However, adequate amounts were present in the top few meters of the water column. With small nutrient gradients in surface waters below the sea ice, vertical eddy diffusivities on the order of 3.8–9.3 cm²· s^- should supply sufficient nutrients to meet algal demand.     

PHYSIOLOGY OF SEA ICE DIATOMS. I. RESPONSE OF THREE POLAR DIATOMS TO A SIMULATED SUMMER-WINTER TRANSITION1

Three axenic polar sea ice diatom cultures were subjected to a 30 day simulated summer-winter transition in which light and temperature were decreased and salinity was increased to mimic seasonal changes previously reported for ice-covered polar seas. The diatoms responded to these changes by a reduction in cellular metabolism as indicated by: 1) A decline in growth rate and photosynthetic rate; 2) a decrease in cellular ATP; and 3) the storage and subsequent utilization of endogenous carbon reserves. In addition, heterotrophic potential of the three clones increased by as much as 60-fold. In some cases, the decrease in light intensity characteristic of the onset of polar winter was alone sufficient to trigger these physiological changes.     

CYANOBACTERIAL ASSEMBLAGES IN PERMANENT ICE COVERS ON ANTARCTIC LAKES: DISTRIBUTION, GROWTH RATE, AND TEMPERATURE RESPONSE OF PHOTOSYNTHESIS

The proliferation of microalgae in the McMurdo Dry Valleys of Antarctica is intricately linked to the seasonal cycle involving the freezing and melting of water. Anecdotal observations and preliminary sampling have found cyanobacterial cells in ice covers on lakes in the McMurdo Dry Valleys, and several of these ice covers are known to undergo seasonal freeze–thaw cycles. Therefore, we sought to determine the distribution and abundance of cyanobacterial assemblages in several permanent ice covers throughout the McMurdo Dry Valleys and to determine their rates of growth and their photosynthetic physiologies upon encountering liquid water. We found that the majority of the permanent ice covers contained cyanobacterial assemblages in close association with sedimentary material. Cyanobacterial biomass was conspicuously absent in sediment-free ice covers, suggesting that the seasonal interaction between the sediments, ice, and solar radiation present the necessary liquid water environment for cyanobacterial growth. All assemblages exhibited extremely low rates of photosynthesis when first exposed to liquid water. Despite the low rates of photosynthesis, a large proportion (41%) of the photosynthate was incorporated into protein, indicating that the cells were undergoing efficient net cellular growth. The short-term response (24 h) of photosynthesis to a range of temperatures showed optimum rates occurring at temperatures >15° C, which is similar to those of psychrotrophic cyanobacteria isolates from soil and stream habitats, which we believe provides the inoculum for the in- ice habitats.     

SEA ICE MICROBIAL COMMUNITIES. V. THE VERTICAL ZONATION OF DIATOMS IN AN ANTARCTIC FAST ICE COMMUNITY1

A distinct vertical zonation was observed among diatoms in a bottom congelation ice community at McMurdo Sound, Antarctica during the 1981 spring bloom. The bottom 20 cm of ice collected in December from four stations with variable snow cover was subdivided into 5 cm sections for analysis of algal distribution. Algal abundance was inversely related to the depth of snow cover, and generally decreased with increasing distance above the ice-water interface. Most diatoms, including the dominant species Nitzschia stellata Manguin, Amphiprora kufferathii Manguin and Fragilaria islandica var. adeliae Manguin showed peak abundance in the bottom 10 cm of the ice, where the proportion of living to empty cells was also highest. Two species, however, an Auricula Castracane sp. and Navicula glaciei van Heurck, reached highest concentrations at depths 10–20 cm above the ice-water interface. We considered two factors as contributing to the observed vertical zonation: (1) successive blooms at the ice-water interface become spatially stratified within the ice by further accretion below; (2) a differential growth of species occurs along physicochemical gradients within the ice column. A comparison of early versus late season profiles suggests the latter mechanism may prevail once ice accretion has ceased.     

ABUNDANCE OF A NOVEL DINOFLAGELLATE PHYLOTYPE IN THE ROSS SEA,ANTARCTICA1

The biodiversity of protistan assemblages present in microhabitats of the Ross Sea, Antarctica, was examined using molecular biological methods to obtain a greater understanding of the genetic diversity present. Sequencing of 18S clone libraries indicated genetically diverse collections of organisms in the water column, ice, and meltwater layer (slush), but a single small subunit ribosomal DNA (srDNA) sequence type dominated clone libraries (>30%) from seawater and slush samples taken within the ice pack of this ecosystem. The BLAST searches indicated that this dominant clone was derived from a dinoflagellate, and that it shared sequence similarity (97.6%–98.3%) with both Karenia and Karlodinium species. Phylogenetic analyses based on small subunit ribosomal gene sequences supported its placement as a sister group to these taxa, and suggested that it represented a novel genus. The dinoflagellate was successfully recovered in culture, and morphological analyses have shown that it contains chloroplasts, is gymnodinoid, appears not to have thecal plates, and has an apical groove and sulcal structure that confirm its placement as a relative of the Karenia/Karlodinium group. The abundance of this phylotype in natural samples was confirmed by quantitative PCR analyses of water and slush communities, and suggests that this dinoflagellate can be a major constituent of the protistan assemblages of some Antarctic microhabitats of the Ross Sea.