More accurate chronological age determination of crustaceans from field situations using the physiological age marker,lipofuscin

A captive population of Australian red-claw crayfish, Cherax quadricarinatus, of known age was used for the study. Lipofuscin concentration in the left olfactory lobe cell mass of the brain was measured using image analysis of fluorescence micrographs. Age predictions based on lipofuscin concentration were more accurate and had narrower 95% confidence limits than those derived from the more conventional body size and weight predictors for all age groups tested (180, 300, 420, 780 d). Overall, use of lipofuscin concentration produced a significantly lower (p0.001) mean age-prediction error (16.65%) than use of carapace length or body weight (32.45 and 32.3%, respectively). Carapace length was of little value for prediction of the age of older individuals. Mathematical models defining the relationships between temperature, age and lipofuscin accumulation were derived from laboratory-reared individuals. These models did not describe adequately the course of lipofuscin accumulation in crayfish from the field over the whole lifespan. Field data from three known year-classes were used to generate simulated size-frequency and lipofuscin concentration-frequency histograms. Year-classes in the lipofuscin concentration frequency-histogram were much more easily distinguished than in the size-frequency histogram. Under field conditions, lipofuscin concentration was a better predictor of chronological age than conventional morphometric measures.     

Nitrogen excretion by some demersal macrozooplankton in Heron and One Tree Reefs,Great Barrier Reef,Australia

Nitrogen excretion rates of demersal macrozooplankton were measured together with nitrogen concentrations in the water column and sediments in lagoons of Heron Reef and One Tree Reef, Great Barrier Reef, Australia, during August and November 1991. Excretion rates increased with body weight, and weight-specific excretion rates of the demersal macrozooplankton were comparable to those of pelagic zooplankton and meiofauna in the Great Barrier Reef. Values of demersal macrozooplankton abundance from previous studies and excretion rates from this study were combined to estimate fluxes of ammonium from demersal macrozooplankton in coral reef lagoons. The estimated fluxes in the water column and sediments were 12 M NH₄ m^-2 d^-1 and 34 M NH₄ m^-2d^-1, respectively. These fluxes were compared with reported fluxes of ammonium in coral reef lagoons in the Great Barrier Reef, Australia. The estimated flux from the demersal macrozooplankton in the water column was 29 and 9% of those reported for microheterotroph regeneration and phytoplankton utilization, respectively. It was 10% of the reported advective flux during periods of low advection and 13% of the maximum efflux from sediments computed from diffusion models. The estimated flux from the demersal macrozooplankton in the sediments exceeded those reported for meiofauna, and was 5 to 32% and 2 to 13% of those reported for ammonification and utilization in sediments, respectively. The potential importance of demersal macrozooplankton in mediating sediment-water column exchanges in the absence of diffusive effluxes and when they swarm is discussed.     

Spatial,temporal, and behavioral patterns in emergence of zooplankton in the lagoon of Heron Reef,Great Barrier Reef,Australia

A total of 34 zooplanktonic taxa were common in emergence trap, reentry trap, and net-tow samples taken in the lagoon of Heron Reef, Great Barrier Reef, between 27 February and 22 March and between 11 June and 4 July 1985. Twenty-nine of these taxa were classified as demersal (17 taxa), meroplanktonic and larval (10 taxa), or incidental (2 taxa). The remaining five multispecific groups yielded variable results. Differences were observed between two locations separated by 200 m, with emergence 2 to 62 times greater for 22 taxa at a deeper site with larger coral formations. Most zooplankters were more common (2 to 122 times) in samples from 1 m² areas around 0.25 to 0.5 m² patches of branching coral. However, two species of copepods, Pseudodiaptomus colefaxi and Metis holothuriae, were taken in greater numbers (3 to 12 times) from open sand. Seasonal increases (2 to 322 times) were observed for 13 adult taxa and 8 classes of larvae or juveniles in the summer and for 10 adult taxa and one larval group in the winter. Fourteen of the 17 demersal taxa and 4 groups of large larvae or juveniles emerged in numbers 2 to 323 times greater during lunar quarters or new moons. In contrast, 6 larval taxa and 4 groups of small or transparent adults displayed significant emergence during full moons. Five diurnal emergence patterns were shown by 27 taxa, with patterns varying primarily among lunar periods. The variety of taxon-specific patterns observed in this study highlight a need for caution when generalizing about demersal zooplankton.     

Effect of housing geometry on the performance of Chemcatcher passive sampler for the monitoring of hydrophobic organic pollutants in water

Passive sampling of pollutants in water has been gaining acceptance for environmental monitoring. Previously, an integrative passive sampler (the Chemcatcher) was developed and calibrated for the measurement of time weighted average concentrations of hydrophobic pollutants in water. Effects of physicochemical properties and environmental variables (water temperature and turbulence) on kinetic and thermodynamic parameters characterising the exchange of analytes between the sampler and water have been published. In this study, the effect of modification in sampler housing geometry on these calibration parameters was studied. The results obtained for polycyclic aromatic hydrocarbons show that reducing the depth of the cavity in the sampler body geometry increased the exchange kinetics by approximately twofold, whilst having no effect on the correlation between the uptake and offload kinetics of analytes. The use of performance reference compounds thus avoids the need for extensive re-calibration when the sampler body geometry is modified.     

Performance of an in situ passive sampling system for metals in stormwater

A passive sampler has been developed and is demonstrated in situ for urban runoff. The passive sampler is compared to conventional composite (time-dependent and flow-weighted) bottle sampling during and between storm events. The sampling was carried out at established stormwater stations; before and after a stormwater detention pond. In situ deployment of the passive sampler provides the metal concentrations, corresponding to the electrochemically available fraction of total metal, for time-dependent samples collected in parallel. The sampler provides improved accuracy compared to bottle sampling because contamination during sample transport and handling is minimised. Laboratory handling is reduced by direct analysis of the accumulated metals on the receiving membrane by laser ablation inductively coupled plasma mass spectrometry. Passive sampling also solves the problem of metal speciation change during transport to the laboratory, which is a potential problem for bottle samples. The low cost and convenience of the passive sampler and subsequent analysis should allow significantly more extensive spatial and temporal monitoring of metals in the aquatic environment than has previously been possible.     

Development of a novel passive sampling system for the time-averaged measurement of a range of organic pollutants in aquatic environments

A new sampling system has been developed for the measurement of time-averaged concentrations of organic micropollutants in aquatic environments. The system is based on the diffusion of targeted organic compounds through a rate-limiting membrane and the subsequent accumulation of these species in a bound, hydrophobic, solid-phase material. It provides a novel and robust solution to the problem of monitoring in situations where large temporal fluctuations in pollutant levels may occur. Accumulation rates are regulated by choice of diffusion-limiting membrane and bound solid-phase material and have been found to be dependent on the physico-chemical properties of individual target analytes. Two separate prototype systems are described: one suitable for the sampling of non-polar organic species with log octanol/water partition coefficient (log P) values greater than 4, the other for more polar species with log P values between 2 and 4. Both systems use the same solid-phase material (47 mm C18 Empore disk) as a receiving phase but are fitted with different rate-limiting membrane materials (polysulfone for the polar and polyethylene for the non-polar analytes). The two systems complement each other and together can be used for sampling a wider range of organic analytes than generally possible using current passive sampling techniques. Calibration data are presented for both devices. In each case, linear uptake kinetics were sustained, under constant conditions, for deployment periods of between 1 and 9 days. The effects of water temperature and turbulence on sampling rates have been quantitatively assessed. The performance of the system was further investigated by means of field exposures for one and two weeks in marine environments where calibrated samplers were used to determine the time-averaged concentrations of the polar biocides diuron and irgarol 1051. The quantitative results obtained using the passive sampler were compared with those obtained using spot sampling.     

Changes in the nature of dissolved organics during pulp and paper mill wastewater treatment: a multivariate statistical study combining data from three analytical techniques

The paper-making process can produce large amounts of wastewater (WW) with high particulate and dissolved organic loads. Generally, in developed countries, stringent international regulations for environmental protection require pulp and paper mill WW to be treated to reduce the organic load prior to discharge into the receiving environment. This can be achieved by primary and secondary treatments involving both chemical and biological processes. These processes result in complex changes in the nature of the organic material, as some components are mineralised and others are transformed. In this study, changes in the nature of organics through different stages of secondary treatment of pulp and paper mill WW were followed using three advanced characterisation techniques: solid-state ¹³C nuclear magnetic resonance (NMR) spectroscopy, pyrolysis-gas chromatography mass spectrometry (py-GCMS) and high-performance size-exclusion chromatography (HPSEC). Each technique provided a different perspective on the changes that occurred. To compare the different chemical perspectives in terms of the degree of similarity/difference between samples, we employed non-metric multidimensional scaling. Results indicate that NMR and HPSEC provided strongly correlated perspectives, with 86 % of the discrimination between the organic samples common to both techniques. Conversely, py-GCMS was found to provide a unique, and thus complementary, perspective.