A chemical view of the most ancient metazoa--biomarker chemotaxonomy of hexactinellid sponges

Hexactinellid sponges are often considered to be the most ancient metazoans. Lipid biomarkers from 23 species were studied for information on their phylogenetic properties, particularly their disputed relation to the two other sponge classes (Demospongiae, Calcarea). The most prominent lipid compounds in the Hexactinellida comprise C28 to C32 polyenoic fatty acids. Their structures parallel the unique patterns found in demosponge membrane fatty acids ('demospongic acids') and strongly support a close phylogenetic association of the Demospongiae and the Hexactinellida. Both taxa also show unusual mid-chain methylated fatty acids (C15-C25) and irregular C25- and C40-isoprenoid hydrocarbons, tracers for specific eubacteria and Archaea, respectively. These biomarkers indicate a similar, highly conservative symbiont community, although some shift in the abundance of the associated microbiota was observed. The lack of these features in calcareous sponges further contradicts the still common view that Calcarea and Demospongiae are more closely related to each other than either is to the Hexactinellida.     

Input of trichloroacetic acid into the vegetation of various climate zones--measurements on several continents

Trichloroacetic acid (TCA, CCl(3)COOH) is a phytotoxic chemical. Although TCA salts and derivates were once used as herbicides to combat perennial grasses and weeds, they have since been banned because of their indiscriminate herbicidal effects on woody plant species. However, TCA can also be formed in the atmosphere. For instance, the high-volatile C(2)-chlorohydrocarbons tetrachloroethene (TECE, C(2)Cl(4)) and 1,1,1-trichloroethane (TCE, CCl(3)CH(3)) can react under oxidative conditions in the atmosphere to form TCA and other substances. The ongoing industrialisation of Southeast Asia, South Africa and South America means that use of TECE as solvents in the metal and textile industries of these regions in the southern hemisphere can be expected to rise. The increasing emissions of this substance--together with the rise in the atmospheric oxidation potential caused by urban activities, slash and burn agriculture and forest fires in the southern hemisphere--could lead to a greater input/formation of TCA in the vegetation located in the lee of these emission sources. By means of biomonitoring studies, the input/formation of TCA in vegetation was detected at various locations in South America, North America, Africa, and Europe.     

Heavy metals and arsenic fixation into freshwater organic matter under Gammarus pulex L. influence

Organic sediments are a main sink for metal pollutants in aquatic systems. However, factors that make sediments a sink of metals and metalloids are still not clear. Consequently, we investigate the role of invertebrate shredders (Gammarus pulex L.) on quality of metal and arsenic fixation into organic partitions of sediment in the course of litter decay with laboratory microcosm experiments. During the decomposition of leaf litter, G. pulex significantly facilitated the development of small particles of organic matter. The capacity of metal fixation was significantly higher in smaller particles than leaf litter and litter residuals. Thus, G. pulex enhanced metal fixation into the organic partition of sediments by virtue of increasing the amount smaller particles in the aquatic system. Furthermore, invertebrates have a significant effect on formation of dissolved organic matter and remobilization of cobalt, molybdenum and cesium, but no significant effect on remobilization of all other measured elements.     

The phytotoxic effect of C(1)/C(2)-halocarbons and trichloroacetic acid on the steppe plant Artemisia lerchiana

Artemisia lerchiana is a wormwood species of the Central Asian steppe regions, where it completely cover whole areas. For the first time it was possible to show through field experiments that C(1)/C(2) halocarbons (VCHCs), such as chloroform (CHL), tetrachloroethene (PER) and hexachloroethane (HEX), can be taken up by test plants of the species A. lerchiana via the soil/root pathway and metabolised inter alia into trichloroacetic acid (TCA) under semi-aride conditions. At the same time, chlorophyll a fluorescence measurements carried out on the test plants revealed a phytotoxic influence on plant vitality (max. decline in vitality of 52% with application of CHL) and less efficient energy flows in the photosynthesis mechanism of the A. lerchiana test plants. The authors examine possible links between the simultaneous appearance of VCHCs and additional drought stress in the acceleration of desertification processes.     

PROBLEMS IN WEIGHTING OF HYETOGRAPHS1

ABSTRACT: It was found that the conventional weighting factor application to hyetograph ordinates results in artificially attenuated storm patterns. A modified weighting procedure is suggested which allows adjustments in the storm timing, peak intensity, and volume but conserves the storm pattern observed at the raingage nearest to the watershed point of interest. The systematic underestimation of peak flood flows, which result from conventional hyetograph weighting, can be avoided by conserving the hyetograph shape from the raingage nearest to any subarea of a modeled watershed and merely applying weighting factors to the rainfall volumes and temporal center of gravity of several hyetographs.     

PARAMETER ESTIMATION IN HYDROLOGY: THE STATE OF THE ART1

ABSTRACT A detailed review of current methods and criteria used in parameter estimation in hydrology is presented. The effect of errors in the data set and the effect of interactions between methods of analysis, criteria, data set errors, and modeling assumptions are reviewed and discussed briefly. It is concluded that study of techniques, criteria, data set errors and particularly interactions between these, is essential to further progress in hydrologic modeling.     

REGIONAL RAINFALL INTENSITY-DURATION-FREQUENCY CURVES FOR PENNSYLVANIA1

ABSTRACT: A statistical analysis of all available continuous hourly and 15-minute duration rainfall records for Pennsylvania was performed to develop an updated procedure to estimate design storms. As a resuit of this study, Pennsylvania was divided into five homogeneous rainfall regions and a set of rainfall intensity-duration curves developed for each region, for return periods of 1 to 100 years and durations ranging from 5 minutes to 24 hours. The PDT-IDF curves were judged to be a better representation of Pennsylvania rainfall than the nationwide TP-40 maps, particularly for storm events of 10-years and lower return periods. The average time distribution of 24-hour storms in Pennsylvania was found to be well represented by the SCS Type II distribution. The Corps of Engineers SPS 24-hour distribution was found to differ appreciably from both the SCS Type H and the Pennsylvania 24-hour storm distribution. For storm durations between 15 and 90 minutes the standard Yarnell intensity-duration curves closely resemble Pennsylvania storm distributions.     

The environmental photolysis of perfluorooctanesulfonate,perfluorooctanoate, and related fluorochemicals

A field study on the photolysis of perfluoroalkyl substances (PFASs) was conducted at high altitudes in Mt. Mauna Kea (Hawaii, USA; 4200 m) and Mt. Tateyama (Toyama, Japan; 2500 m). Results of photolysis of PFASs in the field were further confirmed in laboratory studies. Perfluorooctanesulfonate (PFOS), which is perceived as a non-degradable chemical in the environment, can undergo photolysis. Long chain PFASs can be successively dealkylated to short chain compounds such as perfluorobutyric acid (PFBA) and perfluorobutane sulfonate (PFBS), but the short chain compounds were relatively more resistant to photodegradation. These results suggest that environmental levels of short chain PFASs would increase both due to their formation from photolysis of long chain PFASs and from direct releases. Earlier studies on photolysis of PFASs were focused on the formation of perfluorocarboxylic acids (PFCAs) and perfluorosulfonic acids (PFSAs) from precursor compounds (such as fluorotelomer alcohols) under laboratory conditions. Our study suggests that PFSAs and PFCAs themselves can undergo photodegradation in the environment.