An inverse method for determining wind stress from water-level fluctuations

The hydrodynamic equations governing the water-level response of a lake to wind stress are inverted to determine wind stress from water-level fluctuations. In order to obtain a unique solution, the wind-stress field is represented in terms of a finite number of spatially dependent basis functions with time-dependent coefficients. The discretized version of the inverse equation is solved by a least-squares procedure to obtain the coefficients, and thereby the stress. The method is tested for several ideal cases with Lake Erie topography. Real water-level data is then used to determine hourly values of vector wind stress over Lake Erie for the period 5 May–31 October, 1979. Results are compared with measurements of wind speed and direction from buoys deployed in the lake. Calculated stress direction agrees with observed wind direction for wind speeds > 7.5 m s⁻¹. Under neutral conditions, calculated drag coefficients increase with the wind speed from 1.53 × 10⁻³ for 7.5−10 m s⁻¹ winds to 2.04 × 10⁻³ for 15−17.5 m s⁻¹ winds. Drag coefficients are lower for stable conditions and higher for unstable conditions.     

Patterns in seasonal abundance,growth and biomass of the atlantic silverside,Menidia menidia,in a New England estuary

Patterns in seasonal abundance (no. per m² surface area), growth and biomass (g per m² surface area) of an annual fish, the Atlantic silverside, Menidia menidia (L.) were investigated in a marsh and more seaward bay region of Essex Bay, Massachusetts from August 1976 to May 1978 using a quantitative beach seining technique. Silverside abundance varied greatly by season and year class during the study period. Abundance was high in 1976 but winter mortality (99%) left an adult density of only .01 per m² surface area in the marsh during spring 1977. Resultant 1977 year class density in the marsh was 1.88 per m² by late fall 1977 but winter mortality again produced an adult density of .01 per m² in spring 1978. Abundance was generally higher in the marsh than in the bay region especially during spring and late fall when catches in the bay were negligible. Based on catch rate comparisons, the summer and fall juvenile abundance of the 1976 year class was much higher than the juvenile abundance of the 1977 year class. Coincidentally, mean lengths and condition of the abundant 1976 year class in the late fall were significantly lower than those of the 1977 year class, suggesting density dependent population regulation. In both years, juveniles grew rapidly and reached full adult size by November when an offshore movement to deeper waters outside Essex Bay occurred. Biomass peaked in the marsh region in late fall 1977 at 7.8 g per m² wet weight. Winter mortality was size selective, favoring larger individuals. The annual life history design of M. menidia including an offshore winter movement and high winter mortality suggests that silversides represent an important pathway of energy flow from marsh to offshore trophic systems.     

The American oyster as a coastal zone pollution monitor: A pilot study

The Condition Index [(dry meat weight)(100)/(internal cavity volume)] has been analyzed and compared in the American oyster,Crassostrea virginica, from two South Carolina estuaries, one of which was considered polluted by coliform bacteria standards. During the warmer months, oysters from the unpolluted habitat showed a consistently and significantly higher Condition Index. Best fit and power function regressions of Condition Index on total coliform bacteria levels conform with previously cited effects of pollutants on oysters. Condition Index droped markedly as the incidence of total coliforms increased toward levels of 100 per 100 ml of water. Our results and the known sensitivity of oysters to a spectrum of pollutants suggest that their condition could be used to monitor waterborne pollution in coastal zone areas.     

Strontium-calcium ratios in Cenozoic planktonic foraminifera

The $\text{Sr}\text{Ca}$ ratio and other parameters have been measured in fossil planktonic foraminifera from the Atlantic and Pacific Ocean basins in order to evaluate the $\text{Sr}\text{Ca}$ ratio of seawater during the last 75 million years. Results on well-preserved samples indicate that the ratio has increased to its present value by 10–15% during the Cenozoic, and that minima occurred between 55-45 Ma and 10-5 Ma, when the ratio was 15–25% less than at present. The long-term increase may reflect either decreasing deposition of aragonite with a high $\text{Sr}\text{Ca}$ ratio in shallow seas, or decreasing seafloor spreading rates and consequently decreasing hydrothermal supply of Ca during the Cenozoic. Other geologic evidence suggests that the Eocene minimum (near 50 Ma) may have resulted from increased aragonite sedimentation, while the Late Miocene minimum (between 10-5 Ma) may have been caused by an increased rate of seawater-basalt exchange when seafloor spreading rates increased on the East Pacific Rise near 10 Ma.     

Copper in surface waters of the Bering Sea

Copper concentrations have been measured in surface <75 m waters of the central Bering Sea. Concentrations of 2–4 nmole kg^?1 were measured in the Zhemchung Canyon region where water depths are greater than 1000 m. Concentrations are higher 2–25 nmole kg^?1 on the shallow <100 m continental shelf, inshore of a hydrographic front at the 100 m isobath. Copper-depth profiles on the continental shelf water mass are dominated by Cu concentrations increasing toward the sediments. These trends may be maintained by a flux of Cu from surficial sediments. A frontal system over the 100 m isobath acts to control the flux of Cu, a significant part of which apparently emanates from the sediments, between the continental shelf and the central Bering Sea basin. The benthic shelf Cu flux was constrained to be less than 3 nmole cm^?2 yr^?1.     

An electrochemical study of Ni2+, Co2+, and Zn2+ ions in melts of composition CaMgSi2O6

Cyclic voltammetry has been done for Ni²⁺, Co²⁺, and Zn²⁺ in melts of diopside composition in the temperature range 1425 to 1575°C. Voltammetric curves for all three ions excellently match theoretical curves for uncomplicated, reversible charge transfer at the Pt electrode. This implies that the neutral metal atoms remain dissolved in the melt. The reference electrode is a form of oxygen electrode. Relative to that reference assigned a reduction potential of 0.00 volt, the values of standard reduction potential for the ions are $\text{E}{}^1\text{(}\text{Ni}{}^{\mathrm{2+}}\text{Ni}{}^0\text{,}\text{diopside}\text{, 1500°C) = ?0.32 ± .01}\text{V}$, $\text{E}{}^1\text{(}\text{Co}{}^{\mathrm{2+}}\text{Co}{}^0\text{,}\text{diopside}\text{, 1500°C) = ?0.45 ± .02}\text{V}$, and $\text{E}{}^1\text{(}\text{Zn}{}^{\mathrm{2+}}\text{Zn}{}^0\text{,}\text{diopside}\text{, 1500°C) = ?0.53 ± .01}\text{V}$. The electrode reactions are rapid, with first order rate constants of the order of 10^?2 cm/sec. Diffusion coefficients were found to be 2.6 × 10^?6 cm²/sec for Ni²⁺, 3.4 × 10^?6 cm²/sec for Co²⁺, and 3.8 × 10^?6 cm²/sec for Zn²⁺ at 1500°C. The value of $\text{E1}$ ($\text{Ni}{}^{\mathrm{2+}}\text{Ni}{}^0$, diopside) is a linear function of temperature over the range studied, with values of ?0.35 V at 1425°C and ?0.29 V at 1575°C. At constant temperature the value of $\text{E}{}^1\text{(}\text{Ni}{}^{\mathrm{2+}}\text{Ni}{}^0\text{, 1525°C}$) was not observed to vary with composition over the range CaO · MgO · 2SiO₂ to CaO·MgO·3SiO₂ or from 1.67 CaO·0.33MgO·2SiO₂ to 0.5 CaO·1.5MgO·2SiO₂. The value for the diffusion coefficient for Ni²⁺ decreased by an order of magnitude at 1525°C over the compositional range CaO · MgO · 1.25SiO₂ to CaO · MgO · 3SiO₂. This is consistent with a mechanism by which Ni²⁺ ions diffuse by moving from one octahedral coordination site to another in the melt, with the same Ni²⁺ species discharging at the cathode regardless of the SiO₂ concentration in the melt.     

Production and pelagic dissolution of biogenic silica in the Southern Ocean

Vertical distributions of particulate silica, and of production and dissolution rates of biogenic silica, were determined on two N-S transects across the Pacific sector of the Antarctic Circumpolar Current during the austral spring of 1978. Particulate silica profiles showed elevated levels in surface water and near the bottom, with low (35–110 nmol Si · 1^?1) and vertically uniform values through the intervening water column. Both the particulate silica content of the upper 200 m and the production rate of biogenic silica in the photic zone increased from north to south, reaching their highest values near the edge of the receding pack ice. A significant, but variable, fraction (18–58%) of the biogenic silica produced in the surface layer was redissolving in the upper 90–98 m. Net production of biogenic silica in the surface layer (production minus dissolution) was proceeding at a mean rate of ca. 2 mmol Si · m^?2 · day^?1. This is ca. 4 times greater than the most recent estimate of the mean accumulation rate of siliceous sediments beneath the ACC. We estimate, based on mass balance, that the mean dissolution rate of biogenic silica in subsurface water column in the Southern Ocean is 1.2–2.9 mmol Si · m^?2 · day^?1.     

40Ar39Ar and KAr dating of altered glassy volcanic rocks: the Dabi Volcanics,P.N.G.

KAr and ${}^{40}\text{Ar}{}^{39}\text{Ar}$ ages have been determined for altered submarine tholeiitic and boninite (high-Mg andesite) lavas from the Dabi Volcanics, Cape Vogel Peninsula, Papua New Guinea. ${}^{40}\text{Ar}{}^{39}\text{Ar}$ whole rock total fusion and plateau ages identify a Late Paleocene age for the tholeiitic lavas (58.9 ± 1.1 Ma) and also for the boninitic lavas (58.8 ± 0.8 Ma). Apparent KAr ages for the same samples range from 27.2 ± 0.7 to 63.9 ± 4.5 Ma, and young KAr ages for glassy boninites are probably due to variable radiogenic ⁴⁰Ar (⁴⁰Ar¹) loss. These new ages effectively reconcile previously ambiguous age data for the Dabi Volcanics and indicate contemporaneous tholeiitic and boninitic volcanism occurring in southeast PNG during the Late Paleocene.Smectites, developed as alteration products after glass in oceanic lavas commonly do not retain ³⁹Ar during or subsequent to irradiation, but in some cases may contain ⁴⁰Ar1. In the absence of other factors modifying K and Ar contents, samples which have not lost ⁴⁰Ar¹ from smectite and suffer ³⁹Ar loss only, are interpreted to have been altered immediately subsequent to the crystallization of the lava; whereas samples which have lost ⁴⁰Ar¹ as well as ³⁹Ar may be the result of either recent alteration, or of continuous ⁴⁰Ar¹ loss since the time of crystallization.     

Mass transfer and volume change during alkali metasomatism at Kisingiri,Western Kenya

Mass transfer estimates for metasomatic rocks are dependent on volume-change determinations and a knowledge of the original composition. In particular, such estimates are highly sensitive to uncertainties in the original rock composition. A volume-change model is derived for Kisingiri fenites by considering textural evidence, the known transfer of SiO₂ to the crystallizing ijolite magma, the immobility of Al in low grade fenites, the effect of the stress field around an intrusion, and by considering major element ‘ion content’ concentration gradients across the fenites for various degrees of volume change. The model suggests volume decreases of up to 20% in a zone adjacent to the intrusions and approximately constant volume beyond this zone. Such volume decreases are explained by the removal of quartz by dissolution and diffusion into the crystallizing magma. Aluminium was almost immobile according to this model.