Sulphonated aromatic pollutants

Many synthetic sulphonated aromatic compounds are used as starting material to produce dyes and pigments, or are released as by-products in the effluents of the textile and dye industry. A large number of these chemicals are poorly biodegradable and cannot be eliminated by classical wastewater treatment plants. To limit the impact of these pollutants on the environment, new processes, based on the use of higher plants (constructed wetlands or hydroponic systems), are under development. Detergents and surfactants are essential for both industrial and domestic applications, the most important family being the alkylbenzene sulphonates. Originally, the alkyl side chains were branched and thus recalcitrant to biodegradation. Therefore, they have been replaced by linear alkylbenzene sulphonates. Although more acceptable, present formulations still have adverse environmental and toxic effects. In this context, phytoremediation appears to be a promising approach to remove these compounds from contaminated soils and waters.     

The contribution from shipping emissions to air quality and acid deposition in Europe

A global three-dimensional Lagrangian chemistry-transport model STOCHEM is used to describe the European regional acid deposition and ozone air quality impacts along the Atlantic Ocean seaboard of Europe, from the SO2, NOx, VOCs and CO emissions from international shipping under conditions appropriate to the year 2000. Model-derived total sulfur deposition from international shipping reaches over 200 mg S m(-2) yr(-1) over the southwestern approaches to the British Isles and Brittany. The contribution from international shipping to surface ozone concentrations during the summertime, peaks at about 6 ppb over Ireland, Brittany and Portugal. Shipping emissions act as an external influence on acid deposition and ozone air quality within Europe and may require control actions in the future if strict deposition and air quality targets are to be met.     

Assessment of the importance of sorption for steroid estrogens removal during activated sludge treatment

Distribution coefficients (K(d)) between water and activated sludge particles (f(oc)=27.7+/-0.1%) were measured for the steroid estrogens (SE), estrone (E1), 17beta-estradiol (E2) and 17alpha-ethinylestradiol (EE2) in batch experiments. Experimental concentration levels ranged from environmentally realistic low ng/l to the high microg/l. In this range K(d)s were independent of their water concentration. The experimentally obtained K(d)s (with 95% confidence intervals) were 402+/-126 l/kg, 476+/-192 l/kg and 584+/-136 l/kg for E1, E2 and EE2, respectively. K(d)s were used to estimate the fraction of the total SE concentration that is expected to be sorbed in the activated sludge treatment tanks of a typical STP assuming equilibrium conditions. Assuming a suspended solids concentration of 4 g/l dissolved solids (ds), it was estimated that 61+/-9%, 66+/-13% and 70+/-6% of the total concentration of E1, E2 and EE2, respectively, would be sorbed during activated sludge treatment. The fraction of the SEs that was expected to be sorbed to suspended sludge particles in the effluents from a typical Danish STP was estimated to be only 0.20+/-0.06%, 0.24+/-0.10% and 0.29+/-0.07% of the total concentration of E1, E2 and EE2, respectively, at a suspended solids concentration of 5 mg/lds. For a typical STP the removal of steroid estrogens with excess sludge was estimated to be only 1.5-1.8% of the total loading if equilibrium conditions exists. Sorption is therefore not important for the fate of SEs in STPs compared to biodegradation.     

Modeling the Effects of Habitat Fragmentation on Source and Sink Demography of Neotropical Migrant Birds

Many songbird populations in the midwestem United States are structured as a network of sources and sinks that are linked by dispersal. We used a modeling approach to examine explicitly how populations respond to incremental fragmentation of source habitat and how this response may vary depending upon two life-history attributes: fidelity to natal habitat type and reproductive strength of the source. Fragmentation of source habitat led to a predictable decline in population for both attributes examined, but the manner in which populations declined varied depending upon the reproductive strength of the source and the level of fidelity. When the source was weak and produced few excess individuals, fragmentation of source habitats resulted in a predictable and parallel population decline of adults in both the source and the sink. In this situation high fidelity to natal habitats was important for maintenance of population size and structure. Low fidelity to weak sources resulted in population extinction; populations experienced a demographic cost by dispersing from high quality source habitat to low quality sink habitat. In contrast, when the source was strong and produced many excess individuals, fragmentation of the source led to population declines in both the source and the sink, but this decline was more abrupt in sink habitats. When the source was strong and produced a large excess of individuals, nonfidelity to natal habitats had little effect on metapopulation size and structure.     

Synergism between sib-rearing and sex ratio in Hymenoptera

Summary In many bees and wasps, solitary females produce offspring without help from other females. The transition from lone mothers producing offspring to situations in which females often help to rear siblings is an important step in the origins of complex sociality and nonreproductive castes. Recent work on Hymenoptera has stressed the role of sex ratio variation in this transition; when a mother's brood is more female biased than average, older daughters are favored to help rear their younger siblings because they are more closely related to sisters than to their own offspring. Here the direction of causality is from biased sex ratios, which arise by some extrinsic mechanism, to the origins of sib-rearing (eusociality). We present a model in which there is a synergism between sib-rearing and female-biased sex ratios, which may either complement the sex ratio variation idea by increasing the rate at which helping spreads or be an alternative hypothesis about the origins of eusociality. The synergism in our model depends on three conditions. 1) Daughters that help cause more food to be provisioned per offspring, which in turn causes larger offspring. 2) Females gain more than males by being large, which favors mothers with helpers to produce a higher proportion of daughters. 3) A helper's inclusive fitness rises as her mother's brood becomes increasingly female biased because a female helper is more closely related to her sisters than to her brothers. A female helper may also be more closely related to her sisters than to her own offspring, but this particular sibling-offspring relatedness asymmetry is not required by the synergism model. These three conditions create a synergism which favors a rapid transition from solitary (subsocial) to eusocial. Demographic and ecological factors that facilitate the evolution of eusociality reduce the stringency of the relatedness asymmetry condition (3) required by our idea. The synergism model therefore complements factors other than relatedness that may have been important during the evolution of eusociality.     

Spectral composition of bioluminescence of epipelagic organisms from the Sargasso Sea

The spectral characteristics of single identified epipelagic sources of bioluminescence from the western Sargasso Sea were measured with an optical multichannel analyzer (OMA) system during the April, 1985, Biowatt cruise. The emission spectra of specimens representing 45 species from 8 phyla were measured. Peak bioluminescence emissions typically occurred between 440 and 500 nm, in the blue region of the visible spectrum. Three exceptions involved emission in the green, yellow, and red spectral regions. Intraspectific variability in spectra, was noted in several species. One shrimp species exhibited two modes of light emission, each with different emission spectra. Other cases involved dynamic color shifts of 10 to 14 nm; the source of the spectral variability is unknown, but may involve optical filtering or differences in the color of luminescence from multiple sites of light emission. Measurements from independent samples of unsorted plankton revealed different spectral distributions. This suggests that the spectral emissions of bioluminescence in the upper water column will vary, based on species assemblage.     

Untersuchungen zur Aufnahme von HCB und Pyren durch den KompostwurmEisenia fetida und ausgewählte Regenwurmwildarten

The main issues of the studies described were the validation of a test design for the assessment of the bioaccumulation potential of environmental pollutants and the applicability ofEisenia fetida as a model-organism and artificial soil (OECD) as a standard test substrate. The test organisms used wereE. fetida of our own breeding stock andAllolobophora caliginosa, Allolobophora chlorotica, Allolobophora longa and Lumbricus rubellus sampled from a field site. Test soils used were the artificial soil (OECD) and a BBA field soil. Soils were each contaminated with 10 mg HCB and Pyrene per soil dry-weight. Within the test period of 4 weeks, samples were taken weekly for residue analysis in the worms and soils. Bioaccumulation factors (AF) calculated forE. fetida and the free-living species were in the range of 10–17 (HCB) and 0.9–1.7 (Pyrene) depending on the soil used. By re-calculation of the concentrations in soil to concentrations in soil water, the resulting bioconcentration factors are compared with published BCF values determined from QSAR’s of other worm species and fresh water fish. It could be concluded that the existing earthworm tests (OECD 1984, ISO 1998) represent an appropriate design for testing the bioconcentration potential of chemicals in soil.