Macrofaunal density and biomass in the Campeche Canyon, Southwestern Gulf of Mexico

The composition, density and community structure of the benthic macrofauna were investigated in sediments of the Campeche Canyon in the SW Gulf of Mexico. Total macrofaunal density ranged from 9466±2736 ind m⁻² at the continental shelf station to 1550±195 ind m⁻² in the canyon. Density values significantly diminished with distance from the coast and depth; only a few stations in the center of the canyon displayed larger density values (E-37 with 4666±1530 ind m⁻², E-36 with 5791±642 ind m⁻² and E-26 with 6925±2258 ind m⁻²). Densities were positively correlated to organic nitrogen in the sediment (r=0.82) and coarse silt (r=0.43), and negatively with depth (r=−0.74) and distance from the coast (r=−0.68). At all stations, the polychaete worms contributed most to the multi-species community structure. The nematodes and Foraminifera displayed their highest densities in the center of the canyon. The biomass values declined significantly with depth. We conclude that the macrofauna density and biomass changed in response to organic matter contents in the sediment, both with distance from the coast and with depth.     

LMWOA (low molecular weight organic acid) exudation by salt marsh plants: Natural variation and response to Cu contamination

This work aimed to evaluate, in vitro, the capability of roots of two salt marsh plants to release low molecular weight organic acids (LMWOAs) and to ascertain whether Cu contamination would stimulate or not organic acids exudation. The sea rush Juncus maritimus and the sea-club rush Scirpus maritimus, both from the lower Douro river estuary (NW Portugal), were used. Plants were collected seasonally, four times a year in 2004, during low tide. After sampling, plant roots were washed for removal of adherent particles and immersed for 2 h in a solution that matched salinity (3) and pH (7.5) of the pore water from the same location to obtain plant exudates. In one of the seasons, similar experiments were carried out but spiking the solution with different amounts of Cu in order to embrace the range between 0 and 1600 nM. In the final solutions as well as in sediment pore water LMWOAs were determined by high performance liquid chromatography. Plants were able to release, in a short period of time, relatively high amounts of LMWOAs (oxalate, citrate, malate, malonate, and succinate). In the sediment pore water oxalate, succinate and acetate were also detected. Therefore, plant roots probably contributed to the presence of some of these organic compounds in pore water. Exudation differed between the plant species and also showed some seasonally variation, particularly for S. maritimus. The release of oxalate by J. maritimus increased with Cu increase in the media. However, exudation of the other LMWOAs did not seem to be stimulated by Cu contamination in the media. This fact is compatible with the existence of alternative internal mechanisms for Cu detoxification, as denoted by the fact that in media contaminated with Cu both plant species accumulated relatively high amounts (29–83%) of the initially dissolved Cu. This study expands our knowledge on the contribution of globally dominant salt marsh plants to the release of LMWOAs into the environment.     

Ammonium excretion by benthic invertebrates and sediment-water nitrogen flux in the Gulf of Mexico near the Mississippi River outflow

Benthic macroinvertebrate biomass and ammonium excretion rates were measured at four stations in the Gulf of Mexico near the Mississippi River mouth. Calculated areal excretion rates were then compared to sediment-water nitrogen fluxes measured in benthic bottom lander chambers at similar stations to estimate the potential importance of macroinvertebrate excretion to sediment nitrogen mineralization. Excretion rates for individual crustaceans (amphipods and decapods) was 2–21 nmoles NH₄ ⁺ (mg dry weight)^?1 h^?1. The mean excretion rates for the polychaetes, Paraprionaspio pinnata [6–12 nmoles NH₄ ⁺ (mg dry weight)^?1h^?1] and Magelona sp. [27–53 nmoles NH₄ ⁺ (mg dry weight)^?1h^?1], were comparable or higher than previous measurements for similar size benthic or pelagic invertebrates incubated at the same temperature (22±1°C). Although the relatively high rates of excretion by these selective feeders may have been partially caused by experimental handling effects (e.g., removal from sediment substrates), they probably reflected the availability of nitrogen-rich food supplies in the Mississippi River plume. When the measured weight-specific rates were extrapolated to total areal biomass, areal macroinvertebrate excretion estimates ranged from 7 μmole NH₄ ⁺ m^?2h^?1 at a 40-m deep station near the river mouth to 18 μmole NH₄ ⁺ m^?2h^?1 at a shallower (28-m deep) station further from the river mouth. The net flux of ammonium and nitrate from the sediments to the water measured in bottom lander chambers in the same region were 15–53 μmole NH₄ ⁺ m^?2h^?1 and ?25–21 μmole NO₃ ^? m^?2h^?1. These results suggest that excretion of NH₄ ⁺ by macroinvertebrates could be a potentially important component of benthic nitrogen regeneration in the Mississippi River plume-Gulf shelf region.     

A model for adjustment of differential gravity measurements with simultaneous gravimeter calibration

 A mathematical model is proposed for adjustment of differential or relative gravity measurements, involving simultaneously instrumental readings, coefficients of the calibration function, and gravity values of selected base stations. Tests were performed with LaCoste and Romberg model G gravimeter measurements for a set of base stations located along a north–south line with 1750 mGal gravity range. This line was linked to nine control stations, where absolute gravity values had been determined by the free-fall method, with an accuracy better than 10 μGal. The model shows good consistence and stability. Results show the possibility of improving the calibration functions of gravimeters, as well as a better estimation of the gravity values, due to the flexibility admitted to the values of the calibration coefficients. Received: 15 November 1999 / Accepted: 31 October 2000     

Comparison of heat and bromide as ground water tracers near streams

Heat and bromide were compared as tracers for examining stream/ground water exchanges along the middle reaches of the Santa Clara River, California, during a 10-hour surface water sodium bromide injection test. Three cross sections that comprise six shallow (<1 m) piezometers were installed at the upper, middle, and lower sections of a 17 km long study reach, to monitor temperatures and bromide concentrations in the shallow ground water beneath the stream. A heat and ground water transport simulation model and a closely related solute and ground water transport simulation model were matched up for comparison of simulated and observed temperatures and bromide concentrations in the streambed. Vertical, one-dimensional simulations of sediment temperature were fitted to observed temperature results, to yield apparent streambed hydraulic conductivities in each cross section. The temperature-based hydraulic conductivities were assigned to a solute and ground water transport model to predict sediment bromide concentrations, during the sodium bromide injection test. Vertical, one-dimensional simulations of bromide concentrations in the sediments yielded a good match to the observed bromide concentrations, without adjustment of any model parameters except solute dispersivities. This indicates that, for the spatial and temporal scales examined on the Santa Clara River, the use of heat and bromide as tracers provide comparable information with respect to apparent hydraulic conductivities and fluxes for sediments near streams. In other settings, caution should be used due to differences in the nature of conservative (bromide) versus nonconservative (heat) tracers, particularly when preferential flowpaths are present.     

Multivariate statistical analysis of some recent volcanics from the Central Andes of Southern Peru

The application of Principal Component and Discriminant analysis to the major and minor oxides of recent volcanics from the Central Andes (S-Peru, N-Chile, Bolivia and Argentina) illustrates a variation in chemical composition related to geographical distribution, mainly in terms of TiO₂ and K₂O. A relationship between chemistry and distance from the Peru-Chile trench, dependent on P, Ti and Sr content of some cenozoic lavas from Southern Peru is also illustrated, by means of Multilinear Standardized Regressions and Partial Correlation analysis.

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Zusammenfassung Die Anwendung zweier statistischer Methoden (Principal Component und Discriminant Analysis) zur Erfassung der Oxidverteilung in den rezenten Vulkaniten der zentralen Anden (S-Peru, N-Chile, Bolivien und Argentinien) hat gezeigt, daß die Variation der chemischen Zusammensetzung, hauptsächlich bei TiO₂ und K₂O, abhängig von der geographischen Position der Ausbruchzentren ist.Eine Beziehung zwischen Geochemie und Entfernung vom Peru-Chile Tief-Seegraben für die rezenten Laven in S-Peru wird ferner mit multilinearen standardisierten Regressionen und Korrelationsanalysen, mit Schwerpunkt bei den Elementen P, Ti und Sr, aufgezeigt.

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Resume L'application de deux méthodes statistiques multivariées (Principal Component et Discriminant Analysis) à la distribution des éléments majeurs et mineurs dans les roches volcaniques récentes des Andes centrales (S-Pérou, N-Chili, Bolivie et Argentine) montre une variation de la composition chimique en fonction de la distribution géographique, surtout en ce qui concerne TiO₂ et K₂O.Une relation entre la variation de composition chimique de quelques laves récentes du Pérou du Sud et la distance du fossé océanique du Pérou-Chili est aussi montrée, à l'aide des Regressions Multilinéaires Standardisées et de l'Analyse de Corrélation partielle. Cette relation concerne spécialment les teneurs en P, Ti et Sr des laves étudiées.

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— Principal Component, Discriminant Analysis ( , , ) , . . . iO₂, K₂, . - . T Sr