Municipal wastewater treatment cost

The cost of control for conventional pollutants at municipal wastewater treatment plants is examined. Empirical estimates of the effect of performance measures as well as the flow size of the waste stream are obtained for both the capital and the operation and maintenance components of total facility cost. These estimates are used to calculate the marginal cost per pound of pollution control over the range of effluent concentration beyond secondary treatment. The implications of the results for current environmental policy issues are outlined.     

Urbanization affects stream ecosystem function by altering hydrology, chemistry, and biotic richness.

Catchment urbanization can alter physical, chemical, and biological attributes of stream ecosystems. In particular, changes in land use may affect the dynamics of organic matter decomposition, a measure of ecosystem function. We examined leaf-litter decomposition in 18 tributaries of the St. Johns River, Florida, USA. Land use in all 18 catchments ranged from 0% to 93% urban which translated to 0% to 66% total impervious area (TIA). Using a litter-bag technique, we measured mass loss, fungal biomass, and macroinvertebrate biomass for two leaf species (red maple [Acer rubrum] and sweetgum [Liquidambar styraciflua]). Rates of litter mass loss, which ranged from 0.01 to 0.05 per day for red maple and 0.006 to 0.018 per day for sweetgum, increased with impervious catchment area to levels of approximately 30-40% TIA and then decreased as impervious catchment area exceeded 40% TIA. Fungal biomass was also highest in streams draining catchments with intermediate levels of TIA. Macroinvertebrate biomass ranged from 17 to 354 mg/bag for red maple and from 15 to 399 mg/bag for sweetgum. Snail biomass and snail and total invertebrate richness were strongly related to breakdown rates among streams regardless of leaf species. Land-use and physical, chemical, and biological variables were highly intercorrelated. Principal-components analysis was therefore used to reduce the variables into several orthogonal axes. Using stepwise regression, we found that flow regime, snail biomass, snail and total invertebrate richness, and metal and nutrient content (which varied in a nonlinear manner with impervious surface area) were likely factors affecting litter breakdown rates in these streams.     

Modelling algal blooms in the Dutch coastal waters by integrated numerical and fuzzy cellular automata approaches

In this paper, an integrated numerical and fuzzy cellular automata model was developed to predict possible algal blooms in Dutch coastal waters basing on the irradiance, nutrients and neighbourhood conditions. The numerical module used Delft3D-WAQ to compute the abiotic conditions, and fuzzy cellular automata approach was applied to predict the algal biomass that was indicated by chlorophyll a concentration. The simulated results of year 1995 were compared with that from BLOOM II model, and the advantages, disadvantages as well as future improvement were presented. In general, through this study, it is seen that the integrated modelling deserves more research inputs because: (1) the hydrodynamic processes and nutrients concentrations can be simulated in details by numerical method; (2) the irregular and sparse water quality and biological data, and the empirical knowledge from experts can be explored by the fuzzy logic technique; (3) the spatial heterogeneity, local interactions and the emerge of patchiness could be well captured through the cellular automata paradigm.     

Natural food,foregut clearance-rate and activity of the crab Scylla serrata

The natural diet, rate of foregut clearance and diurnal activity of the crab Scylla serrata were determined. The gut volume is related to size of crab as gut volume (ml)=0.07e^0.033x , where x=carapace width in millimetres. Fifty per cent of crabs collected in Australia and South Africa contained molluscan remains and about 21% contained crustacean remains — chiefly grapsid crabs. Fish remains were rarely found, and it was concluded that S. serrata does not normally catch mobile forms such as fish and penaeid prawns. Gut clearance of organic tissue was rapid and almost complete after 12 h. Fish bone was retained for a mean time of 2 to 3 days, and shell for 5 to 6 days. Time-lapse photography, using infra-red light, was used to record activity. Visible light flashes reduced activity. S. serrata remained buried during the day, emerging at sunset to spend the night feeding, which occurred intermittently even when unlimited food was available. If no food was present the amount of time spent on the substrate surface was halved.     

Abundance,breeding and growth of the crab Scylla serrata in two South African estuaries

Populations of the crab Scylla serrata (Forskal) were studied in two South African estuaries from 1971 until 1974. One estuary was open to the sea, the other was closed by a sandbar. Population density in the closed estuary was estimated by means of mark-release-recapture data from tagged crabs. The population of S. serrata was estimated as 1 crab/124m² and the production at 3.4 g/m²/annum. Catch per unit effort data from the closed estuary indicated a natural mortality of 41% in the crabs' second year and 60% in the third. Growth was studied in both estuaries by means of size-frequency analysis and from tagging returns. Growth was rapid in the first 12 to 15 months, when the crabs attained a carapace width of 80 to 160 mm. Thereafter growth slowed, and after 3 years crabs were between 140 and 180 mm in carapace width. Females mated in summer at a carapace width of 103 to 148 mm, males at 141 to 166 mm. After mating, females migrated out of both estuaries into the sea.     

Chlorcarbazole in Böden

Goal and Scope

In soil samples taken from several locations throughout Bavaria, the detection of p,p′-DDT by GC/MS was impeded by a superimposed peak. The authenticity of this compound, which has been identified as dichlorocarbazole by mass spectra databases, is confirmed and some characteristics of its occurrence in soils are described.

Methods

The authenticity of the unknown compound has been checked by comparing the low resolution mass spectra and chromatographic retention times with those of standard compounds. Some methodical studies concerning extraction and clean-up were also carried out.

Results and Conclusion

Mass spectra and retention of the unknown compound are identical with that of the 3,6-dichlorocarbazole standard compound; additionally, a second chlorocarbazole was found with mass spectrum and retention similar to 3-chlorocarbazole. In many topsoils (A-horizons) and subsoils (B-horizons) from 200 locations of different land-uses, the dichlorocarbazole could be detected. In contrast to PAH and other POPs, maximum concentrations occurred in the A- and upper B-horizons of forest soils rather than in the organic layers. Assuming the environmental distribution properties of the chlorocarbazoles to be similar to those of the PAH, this could indicate that the chlorocarbazoles are not deposited from the atmosphere as a result of anthropogenic activities but might be generated by natural processes in situ.

Recommendation and Perspective

To our knowledge, the occurrence of chlorocarbazoles in soils of unpolluted sites has not been previously described. Their widespread occurrence in relatively high concentrations and their detection using analytical standard procedures is surprising and requires further examination.     

Sexual selection and cuckoldry in a monogamous songbird: implications for sexual selection theory

Sexual selection is generally assumed to be weaker in monogamous than in polygynous animals. Recently, though, extra-pair fertilizations have been hailed as an important force in generating variance in reproductive success among males in socially monogamous species, thereby increasing the intensity of sexual selection. To see if extra-pair copulations contribute to variance in male reproductive success in the house finch (Carpodacus mexicanus), we used DNA fingerprinting to determine the paternity of chicks from 35 nests. This species is a socially monogamous passerine in which plumage brightness serves as a sexually selected indicator of male quality. Out of 119, nestlings 10 (8.3%) were fathered by a male other than the attending male, but cuckoldry occurred randomly with respect to the plumage colouration, size, or age of the attending male. Thus extra-pair fertilizations do not generate variance in male reproductive success with respect to plumage colour. On the other hand, a strongly male-biased sex ratio and asynchronous breeding by females may generate substantial variance in male reproductive success and could explain the evolution of ornamental colouration.     

Distribution of Juvenile,subadult and adult Scylla serrata (Crustacea: Portunidae) on tidal flats in Australia

In Deception Bay, northern Australia, during 1979–1981, a study was made of the distribution of Scylla serrata (Forskal) in an area having a broad intertidal zone. Juveniles (20 to 99 mm carapace width) were resident in the mangrove zone, remaining there during low tide. The majority of subadult crabs (100 to 149 mm) migrated into the intertidal zone to feed at high tide and retreated to subtidal waters at low tide. Adults (150 mm and larger) were caught mainly subtidally and only small numbers were captured in the intertidal at high tide. Few crabs were captured in the coolest months (May to August). Adults were captured on the flats mainly in the warmest months (January to April), but subadults could be captured over the entire summer (September to March). Juveniles were found in the upper intertidal throughout the year.     

Salinity and temperature tolerance of zoeae of the portunid crab Scylla serrata

The tolerances of the first zoeal stage of the crab Scylla serrata (Forskal) have been investigated in 64 different temperature-salinity combinations. Exposure to temperatures above 25°C or to salinities below 17.5 caused considerable mortality; therefore, zoeae are unsuited to estuarine conditions. The larvae can tolerate temperatures down to 5°C is they are inactive below 10°C. It is suggested that 10°C is probably a lower limit and that female crabs which migrate to sea to release their eggs do not enter water with a temperature below 12°C. Hydrological conditions along the south-east coast of Africa indicate that females would, therefore, migrate less than 10 km offshore.