Heat exchange between water and ice in the Arctic Ocean

Summary The heat balance equation for the bottom surface of floating sea ice is evaluated on the basis of observations of ice temperature, water temperature, current velocity, and ablation or accretion of ice. Assuming equality of the eddy diffusivities for momentum, heat, and salt (average 24 cm² sec^–1) it is shown that the temperature gradient in the oceanic boundary layer is extremely small (averages between 2.10^–5 and 4.10^–4°C/meter) and difficult to measure directly. It is suggested that a large part of the heat transfer from the relatively warm Atlantic water to the arctic atmosphere may occur through open leads in the ice cover.

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Zusammenfassung Die Wärmebilanzgleichung für die Unterseite von schwimmendem Meereis wird an Hand von Beobachtungen der Eistemperatur, der Wassertemperatur, der Strömungsgeschwindigkeit und der Eisdickenänderung ausgewertet. Unter der Annahme gleicher Austauschkoeffizienten für Bewegungsgröße, Wärme und Salzgehalt (im Mittel 24 cm² sec^–1) ergibt sich für die ozeanische Grenzschicht ein außerordentlich kleiner Gradient der Wassertemperatur (durchschnittlich zwischen 2.10^–5 und 4.10^–4°C/Meter), der durch direkte Beobachtungen schwer nachzuweisen ist. Es ist zu vermuten, daß ein beträchtlicher Teil der Wärmeabgabe von der relativ warmen atlantischen Wassermasse an die arktische Atmosphäre durch Öffnungen in der Meereisdecke erfolgt.

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Résumé On établit l'équation du bilan thermique valable pour la surface inférieure de la glace marine dérivante. Pour ce faire, on se sert d'observations de la température de la glace, de celle de l'eau, de la vitesse du courant et des variations de l'épaisseur de la glace. En admettant que les coefficients d'échange sont les mêmes pour la quantité de mouvement, la chaleur et le taux de salinité (en moyenne 24 cm² sec^–1), il résulte pour la couche limite un gradient extrêmement faible de la température de l'eau (situé en moyenne entre 2·10^–5 et 4·10^–4°C/m); un tel gradient est difficile à prouver au moyen d'observations directes. On peut supposer qu'une partie importante de la chaleur transmise par l'eau relativement chaude de l'Atlantique à l'atmosphère arctique passe au travers des lacunes de la couche de glace recouvrant l'océan.

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Contribution 141, Department of Atmospheric Sciences, University of Washington, Seattle. This is a thesis submitted by the author in partial fulfillment of the requirements for the degree of Master of Science.     

Metabolism of perylene by monooxygenases of the skin and liver of Ambystoma tigrinum

The prevalence of dermal neoplasia among neotenic tiger salamanders (Ambystoma tigrinum) collected from the Reese Air Force Base sewage lagoon far exceeded that among salamanders from nearby uncontaminated lagoons. Perylene was the predominant pglycyclic aromatic hydrocarbon contaminant in this lagoon. Perylene was shown to be a substrate for monooxygenases in skin and liver homogenates and formed DNA-binding metabolites. Perylene exposure appeared to augment subsequent perylene metabolism by dermal enzymes but it was not a strong inducer of hepatic monooxygenases. Aroclor 1254 induced benzo(a)pyrene and perylene metabolism by both skin and liver enzymes. However, perylene apparently was not activated by salamander enzymes, as suggested by its lack of in vitro mutagenicity and failure to induce tumors.     

The sea-surface microlayer of puget sound: Part I. Toxic effects on fish eggs and larvae

The sea surface is an important habitat for the developmental stages (eggs and larvae) of many fish and invertebrates; it is also a concentration point for anthropogenic contaminants entering the sea. Studies were conducted to determine the extent to which the sea surface of Puget Sound was toxic to the early life history stages of fish. Three urban bays with suspected contamination, a rural reference bay, and a Central Sound site were compared. Surface-dwelling eggs and organisms (zooneuston) were collected with a surface-skimming neuston net and their densities enumerated. Sand sole (Psettichthys melanostictus) embryos were exposed in the field and laboratory to the sea-surface microlayer. To develop a useful year-round approach to monitoring sea-surface toxicity, larval development of anchovies, kelp bass, and sea urchins was also evaluated as an indication of sea-surface microlayer toxicity.During the spawning season (February and March), urban boys in Puget Sound had lower concentrations of sand sole eggs and neustonic organisms on the sea surface than did the rural bayor Central Sound reference sites. Compared to the reference sites, laboratory exposure to surface microlayer samples collected from urban bay sites generally resulted in more chromsomal aberrations in developing sole embryos, reduced hatching success of sole larvae, and reduced growth in trout cell cultures. In situ hatching success of sole eggs was reduced by half or more in urban bays compared to reference sites.Toxicity was associated with visible surface slicks and, in urban bays, increased with increasing surface pressure (dynes cm⁻¹). Results to be reported separately (Part II) indicate that toxicity is strongly correlated with the presence of high concentrations of polycyclic aromatic hydrocarbons and metals in the sea-surface microlayer. The toxicity of SMIC samples was similar when evaluated by sole, anchovy, kelp bass, or sea urchin tests. A sea-surface monitoring program could use sea urchin embryos to evaluate site-specific sea-surface toxicity throughout the year.     

A New Genus and Species of Rhynchonellid (Brachiopoda, Recent) from Submarine Caves in the Mediterranean Sea

Abstract. A new rhynchonellid brachiopod genus Tethyrhynchia , with type species Tethyrhynchia mediterranea n. sp., is described from specimens discovered in dark zones of submarine caves along the Mediterranean coast of France between Marseille and La Ciotat, and also at Zembra Island, off the Gulf of Tunis, Tunisia. Other brachiopods occurring with this diminutive rhynchonellid are also small and include the megathyridids Argyrotheca cistellula and Megathiris detruncata . This is the first recorded occurrence of a rhynchonellid from the Mediterranean Sea. The new form is apparently neotenous, in that the lophophore in adults never develops beyond the trocholophous stage. A new type of rhynchonellid crus, crescentic in profile and here named the lunifer type, is described. The new genus is assigned to the new family Tethyrhynchiidae , and comparisons are made with other extant rhynchonellid genera.     

Glutathione S-transferase from an antarctic fish, Dissostichus mawsoni

Glutathione S-transferase activity was measured in the hepatic cytosol front Dissostichus mawsoni and Pagothenia borchgrevinki. Activity measures with 1-chloro-2,4-dinitrobenzene as substrate were 11·2 and 16·7 μmol/min/g tissue respectively. Little or no activity was detected when p-nitrobenzyl chloride or 3,4-dichloro-1-nitrobenzene were used as substrate. The hepatic glutathione S-transferases from D. mawsoni were partially purified using gel filtration and chromatofocusing. Three peaks of activity were resolved. The major isozyme (158-fold purification) eluting at pH7·1 appeared to be catalytically a homodimer. The isozyme was highly inhibited by triphenyltin chloride (IC₅₀ = 0·1 μ) while inhibition constants for Cibicron Blue 3GA, bromosulphophalein and hematin were 1·1, 20 and 34 μ respectively.     

On the sulphur chemistry of a super-anoxic fjord, Framvaren, South Norway

The concentrations of total carbonate (C_t), sulphate, sulphide, thiols and oxygen, the ratio between the stable sulphur isotopes ³⁴S and ³²S in sulphate and sulphide, and the density (used to calculate salinity) were determined on samples from the water column of Framvaren, a superanoxic fjord in southern Norway. From a depth of 18m (the oxic-anoxic boundary) the initial sulphate concentration, ([SO₄]_init), as calculated from salinity, is significantly higher than the sum of the measured sulphur species. This is attributed to a loss of sulphur from the water column. The amount of total carbonate produced, corrected for the initial concentration (C_t - 2.4 Sal/35) is found to be proportional to the amount of sulphate consumed, ([SO₄]_init - [SO₄]), according to the following relation C_t- 2.4 Sal/35 = 1.84 ([SO₄]_init - [SO₄]). Isotopic fractionation caused by bacterial sulphate reduction in the anoxic part of the water column produces sulphide with a δ³⁴S 40‰ lower than the δ³⁴S for sulphate at corresponding depths. The isotopic fractionation also results in δ³⁴S value for the remaining sulphate at depths below 80 m being considerably higher than the mean value for ocean water, which is close to + 20‰. The δ³⁴S values for sulphate at depths between 10 and 50 m were lower than + 20‰ which indicates oxidation of sulphide, which follows upon diffusion of sulphide from deeper parts of the water column and inflow of oxygenated seawater over the sill into the anoxic water of the fjord. A conclusive scenario of the Framvaren sulphur chemistry is presented.     

Environmental overview of Eckernförde Bay,northern Germany

This environmental overview of Eckernförde Bay (northern Germany) summarizes the results of previous studies relevant to the Office of Naval Research's Coastal Benthic Boundary Layer (CBBL) Baltic field exercise conducted during 1993–1994. Significant environmental characteristics include the following: (1) surface sediment distribution is related to water depth, dictated primarily by hydrodynamic reworking of older glacial deposits; (2) the origin and characteristics of small-scale sedimentary structures depend on storm-generated waves and currents; (3) the proximity of the sea surface and sediment —water interface results in a pelagic—benthic coupling that drives biogeochemical processes and produces organicrich, acoustically turbid sediments; and (4) the bay floor is complicated topographically by pockmarks and manmade sedimentary structures.     

Direct determination of organic carbon in modern reef sediments and calcareous organisms after dissolution of carbonate

An improved method for the direct determination of organic carbon in calcareous marine sediments, organisms and particulate matter is described. Samples are dissolved in phosphoric acid to remove carbonates, purged with oxygen to remove CO₂, and the resulting acidic solution is analysed for total (dissolved and particulate) organic carbon. The method is rapid, involves minimal sample manipulation, and is both accurate (better than ± 2%) and precise (better than ± 0.2 mg organic carbon/g sediment). The method is especially suitable for modern carbonate sediments which have low levels of predominantly acid-soluble organic carbon.