Assessing Decomposition Rates of Rhizophora mangle and Laguncularia racemosa Leaves in a Tropical Mangrove

Studies exploring leaf decomposition in mangroves in the Brazilian northeast are scarce. Therefore, in a mangrove of the Cachoeira River estuary at Ilhéus, Bahia, the decomposition of senescent leaves of Rhizophora mangle L. and Laguncularia racemosa Gaertn was studied. The litter-bag method and the Olson exponential model were applied to estimate the decomposition rates. The decay pattern of leaf material of both species was similar to those reported in the literature, with rapid initial weight loss, followed by a deceleration and period of slow weight loss. L. racemosa had the highest decay constants at all the study sites which suggest that their leaves are more easily degraded than those of R. mangle. The constantly submerged site presented the highest decay constants of 0.022 g g^?1 day^?1 for R. mangle and 0.031 g g^?1 day^?1 for L. racemosa. Most (95 %) of the leaf material of the two species was lost in 135 and 98 days, respectively. Benthic macrofauna organisms were recorded in the litter bags from the fifth day after the start of the experiment. Such organisms play a key role in the first phase of decomposition in this mangrove system. The decay constants of the leaf litter were generally higher than those reported in other tropical and subtropical regions. This suggests that differences in the process of decomposition are in response to environmental conditions at each location.     

Distribution and migrations of the prawnPalaemon longirostris in the Mira River estuary (southwest Portugal)

Palaemon longirostris was sampled monthly at 12 sites in the Mira River estuary (southwest Portugal) from October 1990 to September 1991. Animals were counted, measured, and sexed. The estuarine distribution of prawns appeared to follow the salinity displacement, the animals being found at river stations during summer and autumn when saline encroachment up the estuary was greater. During winter and spring when freshwater input from the river was greatest, and thus moving the salinity gradient toward the mouth, the prawns migrated downstream to brackish areas. Ovigerous females were collected only from estuarine areas (January to August), suggesting that reproduction does not take place in freshwater habitats. Higher percentages of females than males were generally observed. Females, particularly ovigerous ones, were larger than males.     

A chemical and thermodynamic model of oil generation in hydrocarbon source rocks

Thermodynamic calculations and Gibbs free energy minimization computer experiments strongly support the hypothesis that kerogen maturation and oil generation are inevitable consequences of oxidation/reduction disproportionation reactions caused by prograde metamorphism of hydrocarbon source rocks with increasing depth of burial.These experiments indicate that oxygen and hydrogen are conserved in the process.Accordingly, if water is stable and present in the source rock at temperatures ?25 but ?100 °C along a typical US Gulf Coast geotherm, immature (reduced) kerogen with a given atomic hydrogen to carbon ratio (H/C) melts incongruently with increasing temperature and depth of burial to produce a metastable equilibrium phase assemblage consisting of naphthenic/biomarker-rich crude oil, a type-II/III kerogen with an atomic hydrogen/carbon ratio (H/C) of ∼1, and water. Hence, this incongruent melting process promotes diagenetic reaction of detritus in the source rock to form authigenic mineral assemblages.However, in the water-absent region of the system CHO (which is extensive), any water initially present or subsequently entering the source rock is consumed by reaction with the most mature kerogen with the lowest H/C it encounters to form CO₂ gas and a new kerogen with higher H/C and O/C, both of which are in metastable equilibrium with one another.This hydrolytic disproportionation process progressively increases both the concentration of the solute in the aqueous phase, and the oil generation potential of the source rock; i.e., the new kerogen can then produce more crude oil.Petroleum is generated with increasing temperature and depth of burial of hydrocarbon source rocks in which water is not stable in the system CHO by a series of irreversible disproportionation reactions in which kerogens with higher (H/C)s melt incongruently to produce metastable equilibrium assemblages consisting of crude oil, CO₂ gas, and a more mature (oxidized) kerogen with a lower H/C which in turn melts incongruently with further burial to produce more crude oil, CO₂ gas, and a kerogen with a lower H/C and so forth.The petroleum generated in the process progresses from heavy naphthenic crude oils at low temperatures to mature petroleum at ∼150 °C. For example, the results of Computer Experiment 27 (see below) indicate that the overall incongruent melting reaction in the water-absent region of the system C-H-O at 150 °C and a depth of ∼4.3 km of an immature type-II/III kerogen with a bulk composition represented by C₂₉₂H₂₈₈O_12(c) to produce a mature (oxidized) kerogen represented by C₁₂₈H₆₈O_7(c), together with a typical crude oil with an average metastable equilibrium composition corresponding to C_8.8H_16.9 (C_8.8H_16.9(l)) and CO₂ gas (CO_2(g)) can be described by writing

(A)     

Electrodialytic remediation of CCA-treated waste wood in pilot scale

When chromated copper arsenate (CCA)-treated wood is removed from service and turns into waste, the contents of Cu, Cr and As remain high due to the strong fixation of CCA in the wood. This high content of toxic compounds presents a disposal challenge. Incineration of CCA-treated waste wood is not allowed in Denmark; instead, the wood is to be land-filled until new methods for handling the wood are available. Since the amounts of CCA-treated wood being removed from service is expected to increase in the years to come, the need for finding alternative handling methods is very relevant. In this study, the usefulness of Electrodialytic Remediation was demonstrated for handling of CCA-treated waste wood in pilot scale. The electrodialytic remediation method, which uses a low-level direct current (DC) as the cleaning agent, combines electrokinetic movement of ions in the wood matrix with the principles of electrodialysis. It has previously been shown that it is possible to remove Cu, Cr and As from CCA-treated wood using electrodialytic remediation in laboratory scale, but until now, the method had not been studied in large scale. The pilot-scale plant used in this study was designed to contain up to 2 m³ wood chips. Six remediation experiments were carried out. In these experiments, the process was up-scaled stepwise by increasing the distance between the electrodes from initially 60 cm to finally 150 cm. The remediation time was varied between 11 and 21 days, and phosphoric acid and/or oxalic acid was used to facilitate the desorption of CCA from the wood. In the most successful of the experiments carried out, the concentration of CCA in the wood was reduced by up to 82% for Cr, 88% for Cu and at least 96% for As.     

Intrinsic groundwater vulnerability determination at the aquifer scale: a methodology coupling travel time estimation and rating methods

Groundwater vulnerability has been subject of much research due to the valuable information it provides concerning groundwater protection and exploitation potential. Up to now, most groundwater vulnerability studies adopt subjective systems of rating the various factors and subsequently, their results are often ambiguous and contradicting. Within the present study a methodology for the estimation of intrinsic groundwater vulnerability at the aquifer scale is presented. The methodology is based on travel time estimation from specified sources of pollution to the aquifer. Besides the deterministic calculation of travel times, the methodology provides a rating system for each pollution source, based on its relative severity and the estimated threat that it poses to the aquifer. Therefore, it can be regarded as a hybrid method that couples the advantages provided by the physically based methods with those of the subjective rating systems. The methodology is applied to the Neon Sidirochorion aquifer, Northeastern Greece, an overexploited aquifer where river waters, sea waters and lake waters interact, causing groundwater quality deterioration to the aquifer. The results indicated that the proposed groundwater vulnerability assessment methodology is well capturing pollution related to saltwater intrusion and agricultural activities, while it is concluded that the conceptual model is significantly affecting the vulnerability assessment results and therefore has to be previously developed.     

Progress and new directions in high temperature calorimetry revisited

 High temperature reaction calorimetry has seen considerable advances over the past twenty years. New and more sensitive calorimeters, improved sample handling techniques, and better control of the final dissolved state has made solution calorimetry and drop solution calorimetry, using molten lead borate and other solvents, very versatile and reliable techniques. This paper summarizes these advances and presents examples of specific applications to problems of transition metal oxide chemistry, high pressure geophysics, melt and glass energetics, and metastable materials relevant to the earth sciences. Received June 3, 1996 / Revised, accepted Spetember 23, 1996     

Transition enthalpies and entropies of high pressure zinc metasilicates and zinc metagermanates

The enthalpies of transition at T= 298 K between zinc metasilicate assemblages, measured by molten oxide solution calorimetry, are:

Derivation Of Refractive Index And Temperature Gradients From Optical Scintillometry To Correct Atmospherically Induced Errors For Highly Precise Geodetic Measurements

Refraction effects of optical beams are generally caused by an inhomogeneous propagation medium and are a major source of systematic errors in the precise optical determination of angles and distances in the atmospheric surface layer. In this contribution a method for deriving vertical temperature and refractive index gradients from optical scintillation is presented. Knowledge of these gradients is required for the compensation of atmospherically induced errors for highly precise terrestrial geodetic measurements, like direct transfer and levelling. The advantage of the present optical method is, that temperature and refractive index gradients can be derived as line-averaged values over the propagation path, which is not possible by meteorological point measurements. Field observations have been carried out with a displaced-beam scintillometer over flat terrain and under different atmospheric conditions in order to verify this method. The experiments show, that this method allows to derive accurate correction values for precise terrestrial geodetic measurements.     

Calorimetry of silicate melts at 1773 K: measurement of enthalpies of fusion and of mixing in the systems diopside-anorthite-albite and anorthite-forsterite

Transposed-temperature-drop calorimetry, using a Setaram HT 1500 calorimeter, was used to study directly the melting at 1773 K of mixtures of crystalline albite, anorthite, and diopside and of anorthite and forsterite. The enthalpy of albite at 1000–1773 K, starting with both crystalline and glassy samples, was also measured. The results confirm previously measured enthalpies of fusion of albite, diopside and anorthite (Stebbins et al. 1982, 1983; Richet and Bottinga 1984,1986). The new results use thermochemical cycles which completely avoid the glassy state by transforming crystals directly to melts. The enthalpy of fusion of forsterite is estimated to be 89±12 kJ/mol at 1773 K and 114±20 kJ/mol at its melting point of 2163 K. The data allow semiquantitative evaluation of heats of mixing in the molten silicates. Along the Ab-An join, enthalpies of mixing in the liquid at 773 K are the same or somewhat more negative than those in the glass at 986 K, whereas along Ab-Di and An-Di, enthalpies of mixing in the liquid are distinctly more positive than in the glass. These differences correlate with excess heat capacities in the liquids suggested by Stebbins et al. (1984).