The presence of anomalous trace element levels in present day Jamaican soils and the geochemistry of Late-Miocene or Pliocene phosphorites     

Robert G. Garrett  Anthony R.D. Porter  Patricia A. Hunt  Gerald C. Lalor 《Applied Geochemistry》2008

High levels of Cd and Zn in Jamaican soils observed in geochemical surveys are related to the presence of phosphorites of possible Late-Miocene or Pliocene age. The trace element and REE geochemistry of the phosphorites, together with SEM studies, indicate a guano origin for the phosphorites. No specific host minerals for Cd could be identified in the fossiliferous phosphorite which is characterized by uniquely high levels of Cd, Zn, Ag, Be, U and Y. However, in the soil Cd is present in lithiophorite and a complex history of pedological development is preserved in the aluminous–goethite present in the soil. The unique guano signature is preserved in the soil despite the fact that guanos themselves have either not been observed or have been destroyed by continuing karst and soil development. The phosphorite geochemical signature can be traced in the data of a 1988 island-wide soil geochemical survey, identifying areas where the Palaeo-environment that supported bird ‘rookeries’ existed in the Late-Miocene or Pliocene.  相似文献   

The hydrochemistry of a semi-arid pan basin case study: Sua Pan,Makgadikgadi, Botswana     

Frank D. Eckardt  Robert G. Bryant  Graham McCulloch  Baruch Spiro  Warren W. Wood 《Applied Geochemistry》2008

This study presents results on the fluid and salt chemistry for the Makgadikgadi, a substantial continental basin in the semi-arid Kalahari. The aims of the study are to improve understanding of the hydrology of such a system and to identify the sources of the solutes and the controls on their cycling within pans. Sampling took place against the backdrop of unusually severe flooding as well as significant anthropogenic extraction of subsurface brines. This paper examines in particular the relationship between the chemistry of soil leachates, fresh stream water, salty lake water, surface salts and subsurface brines at Sua Pan, Botswana with the aim of improving the understanding of the system’s hydrology. Occasionally during the short wet season (December–March) surface water enters the saline environment and precipitates mostly calcite and halite, as well as dolomite and traces of other salts associated with the desiccation of the lake. The hypersaline subsurface brine (up to TDS 190,000 mg/L) is homogenous with minor variations due to pumping by BotAsh mine (Botswana Ash (Pty) Ltd.), which extracts 2400 m³ of brine/h from a depth of 38 m. Notable is the decrease in TDS as the pumping rate increases which may be indicative of subsurface recharge by less saline water. Isotope chemistry for Sr (⁸⁷Sr/⁸⁶Sr average 0.722087) and S (δ³⁴S average 34.35) suggests subsurface brines have been subject to a lithological contribution of undetermined origin. Recharge of the subsurface brine from surface water including the Nata River appears to be negligible.  相似文献   

Solar research at The Mount Wilson and Palomar observatories     

Robert Howard 《Solar physics》1969,7(1):153-158

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Pole-to-pole moisture conditions for the IGY   总被引：1，自引：0，他引：1  

Victor P. Starr  José P. Peixoto  Robert G. McKean 《Pure and Applied Geophysics》1969,75(1):300-331

Summary A study of the mean atmospheric humidity conditions on a planetary scale during the IGY covering the calendar year 1958 is presented. The fields of mean precipitable water content and of the zonal and meridional transports of water vapor are analyzed for the entire globe. Zonally averaged values of the various quantities at several levels are presented in tabular form and compared whenever possible with previous results or indirectly are analyzed on the basis of information obtained from different sources. The structure of these fields is studied and the corresponding implications for the general circulations of the atmosphere are discussed. Finally the zonal water balance for all the globe is discussed and its implications analyzed.  相似文献   

COMMUNICATIONS FROM READERS     

Robert D. Mitchell 《The Professional geographer》1969,21(6):417-417

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Heat exchange between water and ice in the Arctic Ocean     

Robert Alan Lake 《Meteorology and Atmospheric Physics》1967,16(2-3):242-259

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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With 4 Figures

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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.  相似文献   

Artificial Recharge and pollution of Ground Water     

Robert H. Harmeson  Orville W. Vogel 《Ground water》1963,1(1):11-15

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Solubility of hydrous ferric oxide and iron speciation in seawater     

Robert H. Byrne  Dana R. Kester 《Marine Chemistry》1976,4(3):255-274

Iron solubility equilibria were investigated in seawater at 36.22‰ salinity and 25°C using several filtration and dialysis techniques. In simple filtration experiments with 0.05 μm filters and Millipore ultra-filters, ferric chlorides fluorides, sulfates, and FeOH²⁺ species were found to be insignificant relative to Fe(OH)₂⁺ at p[H⁺] = ?log [H⁺] greater than 6.0. Hydrous ferric oxide freshly precipitated from seawater yielded a solubility product of ${}^1\text{K}{}_{\mathrm{<mtext>so</mtext>}}\text{=}\text{[Fe}{}^{\mathrm{3+}}\text{][H}{}^{\mathrm{+}}\text{]}{}^{\mathrm{?3}}\text{= 4.7 · 10}{}^5$. Solubility studies based on the rates of dialysis of various seawater solutions and on the filtration of acidified seawater solutions indicated the existence of the Fe(OH)₃⁰ species. The formation constant for this species can be calculated as ${}^1\text{β}{}_3\text{=}\text{[Fe(OH)}{}_3{}^0\text{] [H}{}^{\mathrm{+}}\text{]}{}^3\text{/[Fe}{}^{\mathrm{3+}}\text{] = 2.4 · 10}{}^{\mathrm{?14}}$. The Fe(OH)₄^? species is present at concentrations which are negligible compared to Fe(OH)₂⁺ and Fe(OH)₃⁰ in the normal pH range of seawater. However, there is at least one other significant ferric complex in seawater above p[H⁺] = 8.0 (possibly with bicarbonate, carbonate, or borate ions) in addition to the Fe(OH)₂⁺ and Fe(OH)₃⁰ species.  相似文献   

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

Robert S Anderson  Marilyn A Angel  Francis L Rose 《Marine environmental research》1988,24(1-4)

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.  相似文献   

Toxicity of Santa Barbara seep oil to starfish embryos: Part 2—the growth bioassay     

Paul H. Davis  T. Wayne Schultz  Robert B. Spies 《Marine environmental research》1981,5(4):287-294

The asteroid Patiria miniata was used to develop a static bioassay for various crude oil water-soluble fractions (WSF). The criterion used is the size of 48-h exposed embryos. The reasons for choosing this species and the growth criterion are discussed. Experiments show that the body length of 48-h exposed embryos is inversely proportional to hydrocarbon concentration of the WSF and the time of exposure. It is also shown that the toxicity of the WSF decreases with the age of the preparation and that the first 12 h following fertilisation are most sensitive to the effects of WSF.  相似文献