Seawater: an explanation of differential isothermal compressibility measurements in terms of hydration and ion-water interactions

Hydration, ion-water interactions, and water structure effects in seawater were studied by determining differences (Δβ) between the compressibilities of test salt solutions and the compressibilities of reference solutions. The reference solutions were distilled water and seawater (35%0), and the test salt solutions were either 0.13 m or 0.26m with respect to one of the following test salts: LiCl, NaCl, KCl, CsCl, NaF, NaI, MgCl₂, CaCl₂, BaCl₂, Na₂SO₄, K₂SO₄, and MgSO₄. The compressibility measurements (to 900 bars) were carried out at 2°C and also at 15°C using a differential method in which a pressure increase or a temperature increase causes Δβ to become less negative. At 1 bar and 15°C, the Δβ (0.26 m, distilled water reference) values ranged from ?1.14 × 10^?6 bar^? for NaI to ?3.84 × 10^?6 bar^?1 for Na₂SO₄, and the Δβ (0.26 m, seawater reference) values ranged from ?1.30 × 10^?6 bar^?1 for NaCl to ?3.04 × 10^?6 bar^?1 for Na₂SO₄. The Δβ values were used to calculate hydration numbers. Entropy of transfer, excess hydrogen bond breaking (determined by NMR), and effective radii of ions are properties which can be used to describe the influence of ions on water structure. The extent to which these properties correlate with Δβ values depends upon whether the ion is an anion or a cation, and this correlation forms the thesis that anions alter water structure in a different way than do cations.     

Chlorinated hydrocarbons in the seawater and surface sediments of Blanca Bay,Argentina

In order to characterize our study area and to provide reference values to be used in the future to measure the changes produced by an increase in contamination, the concentrations of chlorinated hydrocarbons have been investigated in fifty-one samples of seawater, taken at four different depths: air-sea interface, surface, one metre and bottom waters, and in twenty-three samples of surface sediments from Blanca Bay, Argentina. Of eleven organochlorine compounds we were looking for (α BHC, lindane, heptachlor, δ BHC. aldrin, heptachlor epoxide, dieldrin, o-p′DDD, p-p′DDD, o-p′DDT and p-p′DDT), seven could be detected in seawater and three in surface sediments with the following mean concentrations: α-BHC=48·2 ng l^?1; lindane=54·2 ng l^?1; heptachlor=45·0 ng l^?1; δ BHC=12·5 ng l^?1; aldrin=61·8 ng l^?1 and ΣDDT=67·0 ng l^?1; and δ BHC=3·2 ng g^?1; lindane=4·2 ng g^?1 and heptachlor=1·0 ng g^?1 for seawater, regarding the surface waters, and sediment samples, respectively.Concentration factors among the different water layers were also studied to see if there was any correlation between chlorinated hydrocarbon contents and the water depths from which the samples were taken. As a mean value, the air-sea interface water contains 18 times more of these compounds than that of the water near the bottom. A comparison of the values corresponding to seawater and surface sediments from our study area with those levels measured in samples from other geographic locations is also presented.With the purpose to detect a relationship between chlorinated hydrocarbon concentrations and the contents of particulate matter (PM) on the one hand, and particulate organic material (POM) on the other hand, four groups of samples containing different amounts of PM and POM, respectively were formed. From a comparison of the results obtained, lindane, heptachlor and δ BHC showed a tendency to lower concentrations in those samples containing little PM whereas α BHC and aldrin remained without important changes. No significant correlation was found between organochlorine levels and contents of POM.     

A sediment budget for the Choptank River estuary in Maryland,U.S.A.

A sediment budget for the Choptank River, one of the three largest estuaries on the eastern shore of Chesapeake Bay, was developed from measurements of sediment carried in upland runoff, shore erosion, sedimentation, and levels of suspended sediments in estuarine waters. Shore erosion was the major source of sediment (340 × 10⁶ kg y^?1), contributing seven times more sediment than upland runoff. Low relief, the rural character of the Coastal Plain drainage basin, and the susceptibility of poorly consolidated shoreline materials to erosion contributed to the dominance of shore erosion over runoff as a sediment source. Box modelling indicated a net annual flux (14–44 × 10⁶ kg y^?1) of sediment from the Choptank River to Chesapeake Bay. A mass balance estimate of sedimentation, calculated as the difference between total inputs and loss at the mouth of the estuary, (350 × 10⁶ kg y^?1) agreed well with an estimate based on ²¹⁰Pb profiles (340 × 10⁶ kg y^?1) measured along the longitudinal axis of the estuary. Lead-210 sedimentation rates correspond to accumulation rates of 1·5–7·9 mm y^?1.     

The partitioning of organic carbon fluxes and sedimentary organic matter decomposition rates in the ocean

The partitioning of annual organic carbon fluxes from five stations located in the vicinity of the Pacific-Antarctic Ridge and the Peru continental margin suggests that 35–85% of the total near-bottom organic carbon flux is utilized at or near the sediment-water interface. These estimates have large uncertainties, but illustrate that assessments of organic carbon utilization can be made by several stepwise approaches which are generally applicable to a wide spectrum of marine environments.In one approach, the mineralization of organic carbon from the sediments was predicted from both sedimentary organic carbon and pore water nutrient profiles with comparable results. Neglecting sediment mixing, the rate constants of the anoxic sediments off Peru range from 0.1 × 10^?3 to 4 × 10^?3 y^?1, and rate constants derived for oxic SW Pacific sediments range from 3 × 10^?4 to 7 × 10^?4 y^?1. As with other values reported for sulfate reducing sediments by Toth and Lerman (1977) and for oxic central Pacific sediments by Müller and Mangini (1980), log-log plots of rate constants vs. sedimentation rate define two parallel linear relationships for oxic and anoxic sediments, respectively. The apparently enhanced rates for oxic environments may result from large benthic organisms which redistribute a portion of the available detritus and in doing so convert it into more easily accessible and metabolizable organic matter. In low-oxygen environments, bottom feeders and infauna are less abundant and more likely to irrigate rapidly accumulating sediments.     

Chemical oceanography, vol. 8: Edited by J.P. Riley and R. Chester. Academic Press, London, 1983, xvi + 398 pp., £45.00/US $75.00 (hardcover)

Representative profiles of inorganic nitrogenous species dissolved in interstitial waters of coral reef sands are presented. Ammonium is the dominant nitrogenous species in these pore waters with concentrations of up to 40 μm. Nitrate is present but in lower concentrations. Nitrite is found only occasionally in trace amounts. Computations of diffusive fluxes and inferences concerning microbial activity are derived from the profile structures. Computed flux rates of nitrogenous species from the sediment to the water column range between 0.75 and 1.37 μM m^?1 h^?1. These inputs may represent a significant source of recycled nitrogen to the primary producers of the coral reef ecosystem.     

Metabolism and chemical composition of zooplankton from 500 to 5,000?m depth of the western subarctic Pacific Ocean

Respiration (=oxygen consumption) rates of 28 zooplankton species belonging to 10 taxa from 500 to 5,000?m depth of the western subarctic Pacific Ocean were determined as 0.027–0.44?μLO₂ mg dry mass^?1 h^?1 at in situ temperatures (1.5–3?°C), which are 80?% lower than the rates of the epipelagic Antarctic zooplankton with similar body mass and at a comparable temperature. In terms of adjusted metabolic rate to 1?mg body N (AMR; μLO₂?mg?N^?0.8?h^?1) at 1?°C, the present results (mean 1.66) fall well within the range (0.84–3.32) reported for copepods, chaetognaths, and mixed crustaceans from 500 to 7,000?m in the subarctic Pacific Ocean and Antarctic waters. Judging from their body C:N elemental ratios and ash-free dry mass (=organic matter) data, the major component of organic matter is deduced to be protein (C:N?=?3.4–8.1, by mass) for 19 out of 28 species and lipids (C:N?=?8.6–13.0) for the remaining 9 species.     

Experimental determination of the silica solubility and of the H4SiO 4 0 activity ratio in standard and desalinated seawater

The solubility of amorphous silica was studied in mixtures of riverine and marine waters simulating the water composition at the river-sea geochemical barrier. The value of the thermodynamical equilibrium constant was determined for the reaction of silicon solubility as K _r ⁰ = (1.71 ± 0.01) × 10^?3 at 22°C. A near-linear dependence was found for the activity ratio of the H₄SiO ₄ ⁰ and the salinity with the increase of this ratio from 1.00 in the riverine to 1.15 in the standard seawater.     

Hydrolytic ectoenzyme activity associated with suspended and sinking organic particles within the anoxic Cariaco Basin

Ectohydrolase activities of suspended microbiota were compared to those associated with sinking particles (sed-POM) retrieved from sediment traps deployed in the permanently anoxic Cariaco Basin. In shore-based assays, activities of aminopeptidase, β-glucosidase, chitinase and alkaline phosphatase were measured in samples obtained from oxic and anoxic depths using MUF- and MCA-labeled fluorogenic substrate analogs. Hydrolysis potentials for these enzymes in the seston varied widely over the nine cruises sampled (8 Nov 1996–3 May 2000) and among depths (15–1265 m); from <10 to over 1600 nM d^?1 hydrolysate released, generally co-varying with one another and with suspended particulate organic carbon (POC) and particulate nitrogen (PN). Hydrolytic potentials, prokaryotic abundances and POC/PN concentrations in sinking debris were 400–1.3×10⁷ times higher than in comparable volumes of seawater. However when normalized to PN, hydrolytic potentials in sediment trap samples were not demonstrably higher than in Niskin bottle samples. We estimate that PN pools in sediment trap samples were turned over 2–1400 times (medians=7–26x) slower by hydrolysis than were suspended PN pools. Median prokaryotic growth rates (divisions d^?1) in sinking debris were also ～150 times slower than for bacterioplankton. Hydrolytic potentials in surface oxic waters were generally faster than in underlying anoxic waters on a volumetric basis (nM hydrolysate d^?1), but were not significantly (p>0.05) different when normalized to PN or prokaryote abundances. Alkaline phosphatase was consistently the most active ectohydrolase in both sample types, suggesting that Cariaco Basin assemblages were adapted to decomposing phosphate esters in organic polymers. However, phosphorus limitation was not evident from nutrient inventories in the water column. Results support the hypothesis that efficiencies of polymer hydrolysis in anoxic waters are not inherently lower than in oxic waters.     

Thermal constraints on the respiration and excretion rates of krill,Euphausia hanseni and Nematoscelis megalops,in the northern Benguela upwelling system off Namibia

Rates of respiration and ammonia excretion of Euphausia hanseni and Nematoscelis megalops were determined experimentally at four temperatures representative of conditions encountered by these euphausiid species in the northern Benguela upwelling environment. The respiration rate increased from 7.7 µmol O₂ h^?1 g_ww ^?1 at 5 °C to 18.1 µmol O₂ h^?1 g_ww ^?1 at 20 °C in E. hanseni and from 7.0 µmol O₂ h^?1 g_ww ^?1 (5 °C) to 23.4 µmol O₂ h^?1 g_ww ^?1 (20 °C) in N. megalops. The impact of temperature on oxygen uptake of the two species differed significantly. Nematoscelis megalops showed thermal adaptations to temperatures between 5 °C and 10 °C (Q₁₀ = 1.9) and metabolic constraint was evident at higher temperatures (Q₁₀ = 2.6). In contrast, E. hanseni showed adaptations to temperatures of 10–20 °C (Q₁₀ = 1.5) and experienced metabolic depression below 10 °C (Q₁₀ = 2.6). Proteins were predominantly metabolised by E. hanseni in contrast to lipids by N. megalops. Carbon demand of N. megalops between 5 and 15 °C was lower than in E. hanseni versus equal food requirements at 20 °C. It is concluded that the two species display different physiological adaptations, based on their respective temperature adaptations, which are mirrored in their differential vertical positioning in the water column.     

Hydrogen ion exchange on amorphous silica in seawater

The amount of hydrogen ion exchange on the surface of amorphous silica in seawater was measured as a function of pH at 2 and 25°C. Hydrogen ion exchange with the cations present in seawater is pH dependent and at 25°C the fraction of the surface in the cation form increases from 9% at pH 7 to 22% at pH 8. The exchange is temperature dependent and at 2°C and pH 8, 14% of the exchange sites are occupied by cations, as opposed to 22% of the exchange sites at 25°C. These results were used to calculate the buffer capacity of a model sediment consisting of pore water and amorphous silica. For a sediment of 70% porosity, pH 7.7, and 25°C, the buffer capacity of sediment plus pore water is 67 times the buffer capacity of pure seawater.     

Microbial activity promotes the enrichment of cobalt over nickel on hydrogenetic ferromanganese crusts

The different mineral phases of the ferromanganese (Fe–Mn) crusts stem from the interaction of biotic and abiotic components. It is therefore vital to study the activity of these components to decipher their contribution to the enrichment/depletion of metals in the crust. Thus, the present study examined sorption and release of Co and Ni by Fe-Mn crusts with associated microbial communities in the presence and absence of the metabolic poison sodium azide (15?mM). The study was conducted in the presence (G⁺) and absence (G^?) of added glucose (0.1%) at temperatures of 4?±?1°C and 28?±?2°C. Results showed that the microbial community had maximal sorption of Co of 66.12?µg?g^?1 at 4?±?1°C in the absence of added glucose and 479.75?µg?g^?1 at 28?±?2°C in the presence of added glucose. Maximum sorption of Ni in the absence of added glucose was 1.89?µg?g^?1 at 4?±?1°C and release of Ni was 51.28?µg?g^?1 in the presence of added glucose. Under abiotic conditions with 15?mM sodium azide as a metabolic inhibitor, significant amounts of Co and Ni were released in the G⁺ medium. Total cell counts on the Fe-Mn crust in the presence of added glucose increased by an order of magnitude from 10⁶ to 10⁷ cells g^?1 and in the absence of added glucose remained within the order of 10⁶ cells?g^?1 irrespective of temperature of incubation. Microscopic observation of the samples from biotic incubations showed numerous bacterial cells, exopolysaccharides, and structures resembling secondary minerals formed by bacteria. The results indicate that bacteria promote the enrichment of Co and Ni on the hydrogenetic Fe-Mn crusts by sorption processes and release of Ni by reductive dissolution of the oxides. The higher enrichment of Co than Ni is attributed to the way in which microbes interact with the metals.     

Photochemical production of hydrogen peroxide in Antarctic Waters

Photochemical production rates of hydrogen peroxide (H₂O₂) were determined in Antarctic waters during two research cruises. The first cruise was from mid-October to mid-November, 1993, in the confluence of the Weddell and Scotia Seas, and the second cruise was in December, 1994, along the coast of the Antarctic Peninsula. During these cruises, midday sea-surface production rates ranged from 2.1 to 9.6 nM h⁻¹, with an average rate of 4.5 nM h⁻¹. Production rates were consistently smaller than rates determined at lower latitudes (>9 nM h⁻¹), primarily due to the colder temperatures and lower ultraviolet irradiances in polar waters. In situ production rates were determined with a free-floating drifter that was deployed for 12–14 h. Production rates, averaged over the deployment time, were highest at or near the surface (ca. 2.4–3.5 nM h⁻¹) and decreased rapidly with depth to 0.1–0.7 nM h⁻¹ at 10–20 m. The decrease in production rates with depth generally paralleled the decrease in ultraviolet irradiance in the water column. Production rates of hydrogen peroxide in Antarctic seawater were largely controlled by the ultraviolet irradiance in the water column, although there was some evidence for production in the blue region of the solar spectrum. A laboratory study was conducted to determine the wavelength dependence of the apparent quantum yield for the photochemical formation of hydrogen peroxide in Antarctic waters. Apparent quantum yields determined at 0°C decreased from 0.74×10⁻³ mol einstein⁻¹ at 290 nm to 1.0×10⁻⁵ mol einstein⁻¹ 410 nm. At 20°C, apparent quantum yields for the photochemical production of hydrogen peroxide were within a factor of two of apparent quantum yields determined in temperate waters at 20–25°C. Sunlight-normalized H₂O₂ production rates were determined as a function of wavelength using noontime irradiance data from Palmer Station, Antarctica. A decrease in stratospheric ozone from 336 to 151 Dobson units resulted in a predicted 19–42% increase in the photoproduction of H₂O₂ at the sea surface in Antarctic waters. The magnitude of this increase depends on the concentration and absorbance characteristics of dissolved organic matter in the photic zone, as well as on other factors such as cloudiness and decreasing solar zenith angle that tend to lower photochemical rates offsetting increases due to stratospheric ozone depletion.     

A catalytic oxidation method for the determination of total nitrogen dissolved in seawater

A detailed examination of a high-temperature catalytic oxidation method for liquid samples in the analysis of total nitrogen dissolved in seawater is reported. The nitrogenous compounds in liquid samples are oxidized on a platinum catalyzer at 680°C under oxygen atmosphere and the generated NO₂ is absorbed into a chromogenic reagent, followed by a spectrophotometric determination. The results of this method are much higher than those of wet oxidation methods. Molecular size dependency of the results clearly indicates that the above discrepancy is caused by the low oxidation capacity of the wet oxidation method against high-polymer organic matter dissolved in seawater. The results revealed that the concentration of total nitrogen in seawater is nearly constant from surface to bottom, ranging from 30 to 40 μM 1^?1, which organic nitrogen concentration higher in the surface layer, and a rapid decrease with depth. An examination of molecular size distribution indicates that the concentration of high-polymer organic nitrogen decreases rapidly from surface to deeper layers, with molecular sizes ranging from 5 × 10³ to 3 × 10⁴. Because of the well-defined principle of the oxidation process, its reliability, ease of sample handling and of analytical procedure on board or in the land laboratory, the present method is much more suitable for the marine analytical chemistry of total and organic nitrogen than the other previous methods.     

The activity of NaCl in seawater of 10–40‰ salinity and 5–25°C at 1 atmosphere

The activity of NaCl in artificial seawater was measured potentiometrically with Na⁺- and Cl^? -sensitive electrodes. The salinity of the solutions, examined at 25°C, ranged from 10–40‰ salinity. The change in the activity from 5–25°C was measured at 35‰ salinity.The molal mean activity coefficient of NaCl in 35‰ seawater at 25°C is 0.667. The relative partial molal enthalpy of NaCl in 35‰ seawater is ?130 ±50 cal mol^?1. This value is in good agreement with the value measured in pure 0.72 M NaCl.The results were compared with activity coefficients predicted by a specific interaction model and by an ion association model. Good agreement was found in both cases.     

A seasonal comparison of prokaryote numbers,biomass and heterotrophic productivity in waters of the KwaZulu-Natal Bight,South Africa

The KwaZulu-Natal Bight is a shallow indentation of the eastern seaboard of South Africa, characterised by a narrow (45 km wide) extension of the continental shelf, with a shelf break at about 100 m. It has a complex hydrography: the waters of the bight are derived from the fast-flowing, southward-trending Agulhas Current, which is fed mostly by the tropical and subtropical surface waters of the South-West Indian Ocean subgyre, which are generally oligotrophic in nature, notably depleted in reduced nitrogen and phosphate except at river mouths and during periodic upwelling of deeper nutrient-rich water. Despite this, the bight is believed to be relatively productive, and it is suggested that efficient nutrient recycling by prokaryotes may sustain primary productivity efficiently, even in the absence of new nutrient inputs. Here we have measured bacterial numbers, biomass and heterotrophic productivity during summer and winter in conjunction with phytoplankton standing stock and factors that influence it. Bacterial distribution closely matched phytoplankton distribution in surface waters, and was highest close to the coast. Bacterial standing stocks were similar to those of oligotrophic systems elsewhere (0.5–5.0 × 10⁵ cells ml^–1; 1 × 10^–8 to 1.25 × 10^–7 g C ml^–1) and increased in association with the development of phytoplankton blooms offshore and with inputs of allochthonous material by rivers at the coast. Heterotrophic productivity in summer was lowest in the far south and north of the bight (0.5 × 10^–10 g C ml^–1 h^–1) but higher close to the shore, over shallow banks, and in association with increased phytoplankton abundance over the midshelf (1.0–3.5 × 10^–9 g C ml^–1 h^–1). There were marked seasonal differences with lower bacterial standing stocks (5 × 10⁴ to 2 × 10⁵ cells ml^–1; 4–5 × 10^–9 to 1–2 × 10^–8 g C ml^–1) and very low bacterial productivity (4 × 10^–11 to 1 × 10^–10 g C ml^–1 h^–1) in winter, probably resulting from lowered rates of primary productivity and dissolved organic matter release as well as reduced riverine allochthonous inputs during the winter drought.     

The effects of tropical storm Dennis on coastal phytoplankton

The effects of tropical storm Dennis were documented in the coastal waters of South Carolina during August 1981. Phytoplankton photosynthesis vs. irradiance curves showed initial depression of the parameter a followed by three- to five-fold increase of both a and the asymptotic maximum rate of photosynthesis P_m^B. Productivity rates were depressed in most samples immediately after the storm. Surface samples at the inshore stations were around 50 mg C m^?3 h^?1 at saturating light intensities, while the offshore station rates were around 10 mg C m^?3 h^?1. After a 10-day lag these rates had increased to about 200 mg C m^?3 h^?1 inshore and 75 mg C m^?3 h^?1 offshore. These changes are thought to be primarily caused by changes in species composition. Some of the dominant diatom species changed and dinoflagellate species were introduced. No significant changes in nutrient concentrations were observed. Transient depressions of water temperature, salinity and light intensity may have contributed to the observed changes.     

Stoichiometry among bioactive trace metals in the Chukchi and Beaufort Seas

The distribution of Al, Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb in seawater was investigated in the Chukchi and Beaufort Seas of the western Arctic Ocean in September 2000. The unfiltered and filtered seawater samples were used for determination of total dissolvable metal (TDM) and dissolved metal (DM), respectively. The concentration of labile particulate metal (LPM) was estimated with the difference between that of TDM and DM. The concentrations of TDAl, TDMn, TDFe, TDCo and TDPb varied substantially in the study area. The high concentrations occurred at stations near the Bering Strait, in the Mackenzie delta, and above reductive sediments on the shelf and slope. These elements were mostly dominated by labile particulate species, such as Fe?CMn oxides and species adsorbed on terrestrial clay. DCo was correlated with DMn over the study area (r?=?0.78, n?=?135), and the slope of the regression line was 27 times higher at a pelagic station than at a shelf station. TDNi, TDCu, TDZn and TDCd showed relatively small variations and were generally dominated by dissolved species. There was a moderate correlation between DCd and phosphate for all samples (r?=?0.79), whereas there were no significant correlation between the other DMs and nutrients. TDNi and TDCu showed a remarkable linearity for most stations except those near the Bering Strait (R ²?=?0.95, n?=?126). These results suggest that biogeochemical cycling including uptake by phytoplankton and remineralization from settling particles has only minor control over the distribution of trace metals in this area. Using the present data, the annual input of bioactive trace metals form the Bering Strait and the Mackenzie River was estimated. Also, the trace metal compositions of major water masses were evaluated. The dissolved elemental ratio was P:Al:Mn:Fe:Co:Ni:Cu:Zn:Cd?=?1:1.2?×?10^?2:4.4?×?10^?4:1.4?×?10^?3:3.7?×?10^?5:3.7?×?10^?3:1.4?×?10^?3:4.5?×?10^?3:2.2?×?10^?4 for Canada Basin deep water (CBDW). This ratio was significantly different from that for Pacific deep water and Bering Sea water, suggesting substantial modification of the trace metal compositions of seawater in the study area.     

Metabolic adaptations and reduced respiration of the copepod Calanoides carinatus during diapause at depth in the Angola-Benguela Front and northern Benguela upwelling regions

Stage C5 copepodids and adult females of the herbivorous copepod Calanoides carinatus were sampled in the Angola-Benguela frontal region and northern Benguela upwelling area off Namibia in February–March 2002, using a multiple opening/closing net system. Respiration rates of C5s collected between 400m and 700m were measured onboard at the simulated in situ temperature of 8°C and at sea surface temperature (SST ≥20°C). These data were compared to the oxygen demand of epipelagic individuals of C. carinatus caught in the upper 30m and incubated at ambient SST. Deep-living C5s consumed 0.21 ± 0.08ml O₂ h^?1 (g dry mass)^?1 at 8°C and 0.96ml O₂ h^?1 (g dry mass)^?1 (range 0.84–1.09) at 25.9°C. These results were substantially lower than respiration rates of 5.23 ± 0.55ml O₂ h^?1 (g dry mass)^?1 in epipelagic individuals incubated at SST. The results reveal a reduction by 96% of metabolic rate in deep-living, diapausing C5s relative to surface-dwelling, active individuals. Only 14.4% of this metabolic reduction is explained by the lower ambient temperature at depth and a Q₁₀ value of 2.34. Therefore, the major fraction (81.6%) of the metabolic reduction is attributable to active physiological changes or processes during diapause at depth. The study emphasises the importance for herbivorous copepods, in areas with a highly variable food supply, to adopt a dormant phase in their life cycle in order to survive long periods of starvation.     

Plankton productivity and biomass in a tributary of the upper Chesapeake Bay. I. Importance of size-fractionated phytoplankton productivity,biomass and species composition in carbon export

Phytoplankton productivity, community composition and biomass were determined over a nine-month period in brackish waters of the lower Gunpowder River, a tributary of Chesapeake Bay. Primary productivity followed expected seasonal magnitudes for temperate estuaries with rates exceeding 142·4 mg C m^?3 h^?1 in July through September 1979 and minimum rates of 1·6 mg C m^?3 h^?1 in February 1980. Annual primary production was estimated at 45·5 gC m^?2. Cell numbers were highest in August, September and November with cyanophytes dominating the planktonic algae. Primary productivity, chlorophyll concentrations and cell densities were dominated by nanoplanktonic forms (< 10 μm) through-out the study. Phytoplankton carbon calculated from cells volumes exceeded nutritional requirements of the pelagic herbivores in all months suggesting a mean daily export (to the bay or sediments) of 1607 mg C m^?3 d^?1.     

(Na,K)-phillipsite: Its stability conditions and geochemical role in the deep sea

Phillipsite occurs in the deep sea in areas of very slow sedimentation and as the final alteration product of basalt, suggesting that it is thermodynamically stable. The thermodynamic data for gibbsite, kaolinite, K-feldspar, Na-feldspar, analcime and H₄ SiO₄ (aq), as well as the activities of seawater constituents are reasonably well known. These values and estimated entropies for Na- and K-phillipsites permit an estimate of the free energy of formation (at 25°C) for Na-phillipsite (5337.6 ± 6.7 kcal/mole) and for K-phillipsite (5382.4 ± 1.9 kcal/mole). The decomposition of phillipsite to analcime at 250°C yields the same result, suggesting that phillipsite is indeed a stable mineral.Phillipsite does not regulate the concentration of Na⁺ and K⁺ in seawater, but probably affects the pH of bottom waters and the composition of interstitial waters. No indications exist of “frozen in” equilibria from hydrothermal reactions at 100–200°C as could be expected by submarine volcanism.