Spectrophotometric determination of trifluralin in commercial formulations and agricultural samples using factorial design

A simple spectrophotometric method was developed for determination of trifluralin in commercial formulation and food samples. The method was based on the hydrolysis of trifluralin with sodium hydroxide to form 2,6-dinitro-4-trifluoromethylaniline. The resultant aniline group was diazotized with nitrate in acidic media and the diazotized product was coupled with β-naphthol to form red colored product having λ_max 550 nm. The reaction conditions were optimized for hydrolysis as well as for the diazotization reaction. The Beer’s law was obeyed over the range of 0.2–17 μg mL⁻¹ with molar absorptivity of 1.5 × 10⁴ L mol⁻¹ cm⁻¹. The relative standard deviation was found to be 3.6%. A two level factorial design of 2³ was used for optimization of all parameters. The influence of different factors and their interactions on the final azo dye formation were also studied from these factorial designs. The method has been applied successfully for the analysis of commercial formulations and agricultural samples. The recovery for the determination of trifluralin was found to be in the range 95–97%.     

Residues of fluoroquinolones in marine aquaculture environment of the Pearl River Delta, South China

Concentrations and distributions of selected fluoroquinolones (norfloxacin, ciprofloxacin and enrofloxacin) in water, sediments and nine kinds of fish species collected from 6 sites in two marine aquaculture regions of the Pearl River Delta, China, were analyzed by using high-performance liquid chromatography with fluorescence detector (HPLC). The results showed that the concentrations of ciprofloxacin and enrofloxacin were below the limits of quantification (LOQ) in all water samples except for norfloxacin. Norfloxacin and ciprofloxacin concentrations ranged from 1.88 to 11.20 ng g⁻¹ dry wt, 0.76–2.42 ng g⁻¹ dry wt in sediments collected from the Dapeng’ao region (sites 1–3) and ranged from 2.31 to 4.75 ng g⁻¹ dry wt, 1.26–1.76 ng g⁻¹ dry wt in sediments collected from the Hailing Island region (sites 4–6), respectively. However, no enrofloxacin was found in all sediment samples. The three fluoroquinolones (FQs) were detected in all fish samples, and the concentrations were higher in liver tissues than those in muscle tissues. The levels of norfloxacin were higher than ciprofloxacin and enrofloxacin in both liver and muscle tissues. Among the nine marine fish species, Siganus fuscescens from Hailing Island had a significantly high level of norfloxacin in liver tissue (254.58 ng g⁻¹ wet wt), followed by Sparus macrocephalus (133.15 ng g⁻¹ wet wt) from Dapeng’ao, and the lowest value was Lutianus argentimaculatus (5.18 ng g⁻¹ wet wt) from Hailing Island. The obtained results of FQs in present study do not represent a risk to the human health in Guangdong coastal area, based on the maximum residue limits (MRLs) established by Chinese Government and the acceptable daily intake (ADI) recommended by the Food and Agriculture Organization and World Health Organization (FAO/WHO).     

Determination trace amounts of copper, nickel, cobalt and manganese ions in water samples after simultaneous separation and preconcentration

In the present article, a simple, rapid, sensitive and economical method has been developed for the simultaneous separation and preconcentration of the trace amounts of copper, nickel, cobalt and manganese in water samples by using modified XAD-4 resins. The sorption was quantitative in the pH range 6.0–9.0, whereas quantitative desorption occurred instantaneously with 5.0 mL of 2 M HNO₃, and selected elements have been determined by using flame atomic absorption spectrometry. Dynamic ranges were 0.04–3.5, 0.1–6.0, 0.04–4.5 and 0.04–4.0 μg/mL for copper, nickel, cobalt and manganese, respectively. The detection limits were 9.2, 28.6, 12.3 and 5.7 ng/mL for Cu(II), Ni(II), Co(II) and Mn(II), respectively. The effects of the experimental parameters, including the sample pH, eluent type, interference ions and breakthrough volume, were studied for separation and preconcentration of Cu(II), Ni(II), Co(II) and Mn(II) ions. Determination of these ions in standard samples confirmed that the proposed method has good accuracy. The proposed method was used for the determination of these ions in water samples.     

Automated method for the determination of total arsenic and selenium in natural and drinking water by HG-AAS

A multicommutated flow system was designed and evaluated for the determination of total arsenic and selenium by Hydride Generation Atomic Absorption Spectrometry (HG-AAS). It was applied to the determination of arsenic and selenium in samples of natural and drinking water. Detection limits were 0.46 and 0.08 μg l⁻¹ for arsenic and selenium, respectively; sampling frequency was 120 samples h⁻¹ for arsenic and 160 samples h⁻¹ for selenium. Linear ranges found were 1.54–10 μg l⁻¹ (R = 0.999) for arsenic and 0.27–27 μg l⁻¹ (R = 0.999) for selenium. Accuracy was evaluated by spiking various water samples and using a reference material. Recoveries were in the range 95–116%. Analytical precision (s _r (%), n = 10) was 6% for both elements. Compared with the Standard Methods, APHA, 3114B manual method, the system consumes at least 10 times less sample per determination, and the quantities of acid and reducing agent used are significantly lower with a reduction in the generation of pollutants and waste. As an additional advantage, the system is very fast, efficient and environmentally friendly for monitoring total arsenic and selenium levels in waters.     

A simple voltammetric procedure for speciation and evaluation of As removal from water

Here, we show a fast and sensitive method for the determination of inorganic arsenic in natural waters using differential pulse cathodic stripping voltammetry. All the arsenite determinations were done in 2.0 mol L⁻¹ HCl + 3.15 × 10⁻⁴ mol L⁻¹ Cu(II) supporting electrolyte. 1 × 10⁻³ mol L⁻¹ sodium thiosulphate was used as As(V) reducing agent. The detection limit was 0.5 μg L⁻¹ for both species. The method has been applied to water samples collected in an arsenic-contaminated region of Brazil, in particular, to verify the efficiency of the solar oxidation and removal of arsenic process applied to these waters.     

Characterization and sources of PAHs in an urban river system in Beijing,China

Water samples from 20 locations on rivers in the Tongzhou District of Beijing were collected four times from July 2005 to March 2006. In addition, sediment samples were collected in July 2005. All samples were analyzed for 16 US Environmental Protection Agency (EPA) priority pollutants polycyclic aromatic hydrocarbons (PAHs). The concentration, distribution, seasonal variation, and sources of the 16 PAH compounds identified in the water samples, suspended particles, and surface sediments were then evaluated. The concentrations of PAHs in the water and suspended particle and surface sediment samples ranged from 87.3 to 1,890 ng l⁻¹, 1,330 to 27,700 ng g⁻¹, and 156 to 8,650 ng g⁻¹, respectively. These results demonstrated that rivers in the Tongzhou District of Beijing had a high level of PAH pollution, especially in the suspended particles. The highest and lowest concentrations of PAHs in the water samples were observed in summer and spring. However, the seasonal variations in the concentration of PAHs in the suspended particles were more complicated. The dominant compounds in the water, suspended particle, and surface sediment samples were two-, three- and four-ring PAH compounds, respectively. Ratio analysis illustrated that fuel-burning was the primary source of PAHs in the study area. Gasoline, diesel, coal, and coke oven sources were identified and the contributions of the different fuel-burning sources were then calculated using factor analysis and multiple linear regression. These analyses revealed that coal combustion, gasoline combustion plus coke oven emission, and diesel combustion accounted for 38.8%, 38.5%, and 22.7% of the PAHs in suspended particles, respectively.     

Laser-induced fluorescence of polycyclic aromatic hydrocarbons: an approach to gas standards

Rapid methods are needed to analyse air pollutants such as polycyclic aromatic hydrocarbons (PAHs). Reliable semi-quantitative gas standards were required for the development of a laser-induced fluorescence (LIF) method for polycyclic aromatic hydrocarbon analysis, based on sampling of air onto multi-channel polydimethylsiloxane rubber traps. Easily constructed diffusion tubes provided naphthalene vapour at ~2 ng s⁻¹. A gas chromatographic fraction collection method for loading less volatile PAHs onto the traps from a flame ionization detector outlet was developed and optimized. The accuracy of the method, which can be further optimized, was sufficient for initial LIF screening tests to flag samples exceeding threshold PAH levels for subsequent quantitative GC–MS analysis.     

In situ net primary productivity and photosynthesis of Antarctic sea ice algal, phytoplankton and benthic algal communities

Primary production at Antarctic coastal sites is contributed from sea ice algae, phytoplankton and benthic algae. Oxygen microelectrodes were used to estimate sea ice and benthic primary production at several sites around Casey, a coastal area in eastern Antarctica. Maximum oxygen export from sea ice was 0.95 mmol O₂ m⁻² h⁻¹ (~11.7 mg C m⁻² h⁻¹) while from the sediment it was 6.08 mmol O₂ m⁻² h⁻¹ (~70.8 mg C m⁻² h⁻¹). When the ice was present O₂ export from the benthos was either low or negative. Sea ice algae assimilation rates were up to 3.77 mg C (mg Chl-a)⁻¹ h⁻¹ while those from the benthos were up to 1.53 mg C (mg Chl-a)⁻¹ h⁻¹. The contribution of the major components of primary productivity was assessed using fluorometric techniques. When the ice was present approximately 55–65% of total daily primary production occurred in the sea ice with the remainder unequally partitioned between the sediment and the water column. When the ice was absent, the benthos contributed nearly 90% of the primary production.     

Trace element concentration in wheat grain: results from the Swedish long-term soil fertility experiments and national monitoring program

Concentrations of trace elements in wheat grain sampled between 1967 and 2003 from the Swedish long-term soil fertility experiments were analyzed using ICP-MS. The long-term effect of inorganic and organic fertilization on trace metal concentrations was investigated including the impact of atmospheric deposition and myccorhiza, whereas other factors such as soil conditions, crop cultivar, etc. are not discussed in this paper. Mean values derived from 10 experimental sites were reported. Significantly declining Pb and Cd concentrations in wheat grain could be explained by lower atmospheric deposition. Mean Se contents in all samples were 0.031 mg kg⁻¹ grain dry weight. No samples had sufficiently high Se concentrations for human (0.05 mg Se kg⁻¹) or animal demand (0.1 mg Se kg⁻¹). Concentrations of Co in wheat grain were extremely low, 0.002–0.005 mg Co kg⁻¹ grain dry weight, and far below the minimum levels required by animals, which applied to all fertilizer treatments. A doubling of Mo concentrations in grain since 1975 resulted in Cu/Mo ratios often below one, which may cause molybdenosis in ruminants. The increase in Mo concentrations in crops correlated with the decline in sulfur deposition. Concentrations of Cu and Fe declined in NPK-fertilized wheat as compared to unfertilized or manure-treated wheat. Very low concentrations of Se and Co and low concentrations of Fe and Cu require attention to counteract risks for deficiencies. The main characteristic of the study is that there are few significant changes over time between different fertilizer treatments, but throughout there are low concentrations of most trace elements in all treatments. In general, good agreement between concentrations in wheat from the long-term fertility experiments and the national monitoring program indicate that values are representative.     

Natural radioactivity and trace metals in crude oils: implication for health

Crude oil samples were collected from six different fields in the central Niger Delta in order to determine their natural radioactivity and trace element contents, with the aim of assessing the radiological health implications and environmental health hazard of the metals, and also to provide natural radioactivity baseline data that could be used for more comprehensive future study in this respect. The activity concentrations of the radionuclides were measured using a well, accurately calibrated and shielded vertical cryostat, Canberra coaxial high-purity germanium (HPGe) detector system, and the derived doses were evaluated. The metal concentrations were determined by the graphite furnace atomic absorption spectroscopic (GFAAS) method. The radionuclides identified with reliable regularity belong to the decay series of naturally occurring radionuclides headed by ²³⁸U and ²³²Th along with the non-decay series radionuclide, ⁴⁰K. The averaged activity concentrations obtained were 10.52 ± 0.03 Bq kg⁻¹, 0.80 ± 0.37 Bq kg⁻¹ and 0.17 ± 0.09 Bq kg⁻¹ for ⁴⁰K, ²³⁸U and ²³²Th, respectively. The equivalent doses were very low, ranging from 0.0028 to 0.012 mSv year⁻¹ with a mean value of 0.0070 mSv year⁻¹. The results obtained were low, and hence, the radioactivity content from the crude oils in the Niger delta oil province of Nigeria do not constitute any health hazard to occupationally exposed workers, the public and the end user. The concentrations of the elements (As, Cd, Co, Fe, Mn, Ni, Se and V) determined ranged from 0.73 to 202.90 ppb with an average of 74.35 ppb for the oil samples analysed. The pattern of occurrence of each element agreed with the earlier studies from other parts of the Niger Delta. It was obvious from this study and previous ones that the Niger Delta oils have low metal contents. However, despite the low concentrations, they could still pose an intrinsic health hazard considering their cumulative effects in the environment. Also, various studies on the impact of oil spillage and activities of oil exploration and production on organisms in the immediate environment suggest this.     

The determination of fluoride in water in the presence of organic acids and iron using a fluoride-selective electrode

Surface waters in Scotland, notably from upland catchment areas, are commonly enriched in iron and organic acids. This study investigated the impact of these species on the direct potentiometric determination of fluoride using a fluoride-selective electrode. As the electrode technique is commonly used to monitor the fluoride content of potable waters, it is important that these effects are evaluated if such waters are to be fluoridated. The determination method used was that defined by Nicholson (1983) and Nicholson and Duff (1981) to minimise errors. This employs the TISAB III-TAC buffer system with the following composition (in 1L): 58.0 g sodium chloride, 57.0 mL glacial acetic acid, 4.0 g CDTA, 243.0 g tri-ammonium citrate adjusted to pH 5.4 with 10 M sodium hydroxide. Experimental solutions of fluoride with organic acid or iron were prepared, and the effect on fluoride concentration determined for each combination. Concentrations used: fluoride: 0.1, 1.0 mg L⁻¹; humic acid: 5, 10, 100, 1000, 10,000 mg L⁻¹; oxalic acid: 5, 10, 100, 1000, 10,000 mg L⁻¹; iron(III): 1, 10, 100, 500 mg L⁻¹; Humic acid (HA) concentrations had no impact on the determination of fluoride at the 1.0 mg L⁻¹ level. However, with 0.1 mg L⁻¹; F⁻, an increase in the apparent fluoride concentration was observed when HA > 1,000 mg L⁻¹; this increased with increasing HA content to a maximum of ∼600%. Oxalic acid (OA) generally had no impact on the fluoride determinations at the 1.0 mg L⁻¹; level, but at an OA concentration of 10,000 mg L⁻¹; fluoride concentrations were reduced by ∼50%. At 0.1 mg L⁻¹ F⁻, increasing OA concentrations produce a steady increase in the fluoride concentration of up to 200% with 1,000 mg L⁻¹; OA, greater OA contents produce a fall in the fluoride content. Iron had no effect on the fluoride determinations at both the 0.1 and 1.0 mg L⁻¹ levels. The causes of the apparent increases in fluoride concentration have not been determined, although fluoride contamination by the reagents has been ruled-out. However, the results demonstrate that the defined method and buffer system is suitable for the determination of fluoride in the presence of iron and organic acids at naturally occurring levels, and that fluoride will not be masked from detection.     

Production and fate of copepod fecal pellets across the Southern Indian Ocean

The vertical distribution of copepods, fecal pellets and the fecal pellet production of copepods were measured at seven stations across the Southern Indian Ocean from productive areas off South Africa to oligotrophic waters off Northern Australia during October/November 2006. We quantified export of copepod fecal pellet from surface waters and how much was retained. Furthermore, the potential impact of Oncaea spp. and harpacticoid copepods on fecal pellets degradation was evaluated and found to be regional substantial. The highest copepod abundance and fecal pellet production was found in the western nutrient-rich stations close to South Africa and the lowest at the central oligotrophic stations. The in situ copepod fecal pellet production varied between 1 and 1,000 μg C m⁻³ day⁻¹. At all stations, the retention of fecal pellets in the upper 400 m of the water column was more than 99% and the vertical export of fecal pellets was low (<0.02 mg m⁻² day⁻¹).     

Crop demand of manganese

The peri-urban soils of Huelva, one of the first industrial cities in Spain, are subject to severe pollution problems primarily due to past poor management of industrial wastes and effluents. In this study, soil cores were collected in seven sites potentially contaminated with toxic chemicals arising from multiple anthropogenic sources, in order to identify trace elements of concern and to assess human health risks associated with them. In most soil core samples, total concentrations of As (up to 4,390 mg kg⁻¹), Cd (up to 12.9 mg kg⁻¹), Cu (up to 3,162 mg kg⁻¹), Pb (up to 6,385 mg kg⁻¹), Sb (up to 589 mg kg⁻¹) and Zn (up to 4,874 mg kg⁻¹) were by more than one order of magnitude greater than the site-specific reference levels calculated on the basis of regional soil geochemical baselines. These chemicals are transferred from the hazardous wastes, mainly crude pyrite and roasted pyrite cinders, to the surrounding soils by acid drainage and atmospheric deposition of wind-blown dust. Locally, elevated concentrations of U (up to 96.3 mg kg⁻¹) were detected in soils affected by releases of radionuclides from phosphogypsum wastes. The results of the human health risk-based assessment for the hypothetical exposure of an industrial worker to the surface soils indicate that, in four of the seven sites monitored, cancer risk due to As (up to 4.4 × 10⁻⁵) is slightly above the target health risk limit adopted by the Spanish legislation (1 × 10⁻⁵). The cumulative non-carcinogenic hazard index ranged from 2.0 to 12.2 indicating that there is also a concern for chronic toxic effects from dermal contact with soil.     

Photolytical property of L(+)-α-phenylglycine in aqueous solution

A wide range of pharmaceutical compounds have been identified in the environment, and their existence is a topic of growing concern, both for human and ecological health. The work described here has investigated the photolytic properties of L(+)-α-phenylglycine (L-α-PG-H) in aqueous solution as it can be degraded by photo-catalysis. In 266 nm laser flash photolysis of aqueous solution of L-α-PG-H saturated with nitrogen, two transient absorption bands are observed at 280–330 nm and 450–800 nm, respectively, due to L-α-PG-H radical cation and hydrated electrons (e_aq⁻). Then e_aq⁻ reacts with L-α-PG-H to form the L-α-PG-H radical anion. Decaying rate constants of e_aq⁻ observed at 720 nm is to be 8.9 × 10⁸ dm³ mol⁻¹ s⁻¹. The rate constant for oxidation of L-α-PG-H by SO₄ ⁻ is calculated as 4.5 × 10⁸ and 4.3 × 10⁸ s⁻¹ mol⁻¹ dm³, respectively. The dissociation constants (pKa) of L-α-PG-H is 3. Excited triplet of L-α-PG-H in solution is formed by laser flash photolysis. The quench rate constant of L-α-PG-H excited triplet (k _s) is determined to be 1.3 × 10⁷ dm³ mol⁻¹ s⁻¹ and k ₀ is equal to 1.7 × 10⁵ s⁻¹.     

Modification of light utilization for skeletal growth by water flow in the scleractinian coral <Emphasis Type="Italic">Galaxea fascicularis</Emphasis>

In this study, we tested the hypothesis that the importance of water flow for skeletal growth (rate) becomes higher with increasing irradiance levels (i.e. a synergistic effect) and that such effect is mediated by a water flow modulated effect on net photosynthesis. Four series of nine nubbins of G. fascicularis were grown at either high (600 μE m⁻² s⁻¹) or intermediate (300 μE m⁻² s⁻¹) irradiance in combination with either high (15–25 cm s⁻¹) or low (5–10 cm s⁻¹) flow. Growth was measured as buoyant weight and surface area. Photosynthetic rates were measured at each coral’s specific experimental irradiance and flow speed. Additionally, the instantaneous effect of water flow on net photosynthetic rate was determined in short-term incubations in a respirometric flowcell. A significant interaction was found between irradiance and water flow for the increase in buoyant weight, the increase in surface area, and specific skeletal growth rate, indicating that flow velocity becomes more important for coral growth with increasing irradiance levels. Enhancement of coral growth with increasing water flow can be explained by increased net photosynthetic rates. Additionally, the need for costly photo-protective mechanisms at low flow regimes could explain the differences in growth with flow.     

A sensitive spectrophotometric method for the determination of arsenic in environmental samples

We developed a cost-effective and sensitive spectrophotometric method for the determination of arsenic at trace level using a new reagent, leuco malachite green. Here we show that, arsenic reacts with potassium iodate in acidic conditions to liberate iodine, and the liberated iodine selectively oxidizes leuco malachite green to malachite green dye. We studied the Beer’s law at 617 nm, which showed linearity over the concentration range 0.09–0.9 μg ml⁻¹ of arsenic. We show that the molar absorptivity, Sandell’s sensitivity and detection limit of the method are 6.1 × 10⁴ l mol⁻¹ cm⁻¹, 0.0012 μg cm⁻² and 0.025 μg ml⁻¹, respectively. We applied the developed method for the determination of arsenic in environmental samples.     

Microbial activity and carbon, nitrogen, and phosphorus content in a subtropical seagrass estuary (Florida Bay): evidence for limited bacterial use of seagrass production

Bacterial abundance, production, and extracellular enzyme activity were determined in the shallow water column, in the epiphytic community of Thalassia testudinum, and at the sediment surface along with total carbon, nitrogen, and phosphorus in Florida Bay, a subtropical seagrass estuary. Data were statistically reduced by principle components analysis (PCA) and multidimensional scaling and related to T. testudinum leaf total phosphorus content and phytoplankton biomass. Each zone (i.e., pelagic, epiphytic, and surface sediment community) was significantly dissimilar to each other (Global R = 0.65). Pelagic aminopeptidase and sum of carbon hydrolytic enzyme (esterase, peptidase, and α- and β-glucosidase) activities ranged from 8 to 284 mg N m⁻² day⁻¹ and 113–1,671 mg C m⁻² day⁻¹, respectively, and were 1–3 orders of magnitude higher than epiphytic and sediment surface activities. Due to the phosphorus-limited nature of Florida Bay, alkaline phosphatase activity was similar between pelagic (51–710 mg P m⁻² day⁻¹) and sediment (77–224 mg P m⁻² day⁻¹) zones but lower in the epiphytes (1.1–5.2 mg P m⁻² day⁻¹). Total (and/or organic) C (111–311 g C m⁻²), N (9.4–27.2 g N m⁻²), and P (212–1,623 mg P m⁻²) content were the highest in the sediment surface and typically the lowest in the seagrass epiphytes, ranging from 0.6 to 8.7 g C m⁻², 0.02–0.99 g N m⁻², and 0.5–43.5 mg P m⁻². Unlike nutrient content and enzyme activities, bacterial production was highest in the epiphytes (8.0–235.1 mg C m⁻² day⁻¹) and sediment surface (11.5–233.2 mg C m⁻² day⁻¹) and low in the water column (1.6–85.6 mg C m⁻² day⁻¹). At an assumed 50% bacterial growth efficiency, for example, extracellular enzyme hydrolysis could supply 1.8 and 69% of epiphytic and sediment bacteria carbon demand, respectively, while pelagic bacteria could fulfill their carbon demand completely by enzyme-hydrolyzable organic matter. Similarly, previously measured T. testudinum extracellular photosynthetic carbon exudation rates could not satisfy epiphytic and sediment surface bacterial carbon demand, suggesting that epiphytic algae and microphytobenthos might provide usable substrates to support high benthic bacterial production rates. PCA revealed that T. testudinum nutrient content was related positively to epiphytic nutrient content and carbon hydrolase activity in the sediment, but unrelated to pelagic variables. Phytoplankton biomass correlated positively with all pelagic components and sediment aminopeptidase activity but negatively with epiphytic alkaline phosphatase activity. In conclusion, seagrass production and nutrient content was unrelated to pelagic bacteria activity, but did influence extracellular enzyme hydrolysis at the sediment surface and in the epiphytes. This study suggests that seagrass-derived organic matter is of secondary importance in Florida Bay and that bacteria rely primarily on algal/cyanobacteria production. Pelagic bacteria seem coupled to phytoplankton, while the benthic community appears supported by epiphytic and/or microphytobenthos production.     

Feeding biology of a predatory and a facultatively predatory nematode (Enoploides longispiculosus and Adoncholaimus fuscus)

This paper reports on the feeding biology of a predatory and of a facultatively predatory nematode, Enoploides longispiculosus and Adoncholaimus fuscus, respectively. Both species represent genera which are common and abundant in the littoral of the North Sea and in adjacent estuaries. Observations on the foraging behaviour of both species are given, and for the former species, a range of prey from its natural habitat is identified. Respiration was determined using a polarographic oxygen electrode technique and compared to consumption determined as predation rates on the monhysterid nematode Diplolaimelloides meyli. The daily C-loss due to respiration accounted for 15% of the measured C-consumption in E. longispiculosus and for 111% in A. fuscus, proving the observed feeding rates in the latter species to have been inadequate for the maintenance of its aerobic metabolism. Daily respiration rates at an average environmental temperature were 219 ng C ind⁻¹d⁻¹ for adults of A. fuscus and 21.9 ng C ind⁻¹ d⁻¹ for adults of E. longispiculosus. Using radiotracer techniques, no uptake of bacterial cells or of organic matter in the dissolved phase was demonstrated for E. longispiculosus. In A. fuscus, however, a significant drinking of label in the dissolved or volatile fraction occurred; bacterial cells were taken up at a level insignificant to the nematode's daily C-ration. It is concluded that E. longispiculosus has a fairly strict predatory feeding strategy, while A. fuscus gains a majority of C from additional foraging strategies, among which the uptake of dissolved material and scavenging on macrofauna carcasses (as reported in the literature) may be of particular importance. Received: 28 August 1998 / Accepted: 8 March 1999     

Screening of phthalic acid esters in raw materials,premixes and feed additives

Phthalates are animal carcinogens and may cause death or tissue deformities. Samples of feedstuffs collected in 2005 and 2006 from industrial feed manufacturers in the Czech Republic were analysed for contamination with phthalic acid esters (PAEs), specifically di-2-ethylhexyl phthalate (DEHP) and di-n-butyl phthalate (DBP). Samples of feed additives, premixes and raw materials were collected (year 2005, n = 26). For soybean oil, the total volume of phthalates measured (DBP + DEHP) reached a level of 131.42 mg kg⁻¹; for rapeseed oil, fish meal and animal fats, the levels measured were 15.00, 7.96 and 58.87 mg kg⁻¹, respectively. The lowest level of DBP + DEHP was found in corn (2.03 mg kg⁻¹). Since phthalates were detected, samples of feed additives (n = 28) and raw materials (n = 28) were collected again in 2006. The highest levels of DBP + DEHP were found in raw materials containing fat. Phthalate levels in rapeseed oil samples ranged from 1.38 to 32.40 mg kg⁻¹ DBP + DEHP. For feed additives, contamination levels in vitamins and amino acids ranged from 0.06 to 3.15 and 1.76 to 4.52 mg kg⁻¹ DBP + DEHP, respectively. Here, we show that the levels of PAEs found in cereals such as wheat, barley and corn may be regarded as being alarmingly high, because cereals make up the largest proportion of compound feed of farm animals.     

Mercury contamination in agricultural soils from abandoned metal mines classified by geology and mineralization

Lead (Pb) contents and partition in soils collected from eleven vegetable-growing lands in Fujian Province, China, were investigated using a modification of the BCR (Community Bureau of Reference) sequential extraction procedure coupled with the Pb isotope ratio technique. Pb contents in Chinese white cabbage (B. Chinensis L.) grown on the lands for this study were also measured. Results showed that Pb concentrations in fifty samples of topsoil ranged from 456 to 21.5 mg kg⁻¹, with each mean concentration of six sampling lands exceeding the national standard (50 mg kg⁻¹); while Pb concentrations in edible portions of thirty-two vegetable samples ranged from 0.009 to 2.20 mg kg⁻¹, with four sampling sites exceeding the national sanitary standard (0.2 mg kg⁻¹). A significant correlation (r = 0.971, P < 0.01) of Pb contents in the acid-extractable fractions by BCR approach and the vegetables was observed, which indicates that the acid-extractable Pb is useful for evaluating the metal bioavailability for plants and potential risk for human health in soils. The determination of lead isotope ratios in different chemical forms of soils by BCR sequential extraction procedures provides useful information on the Pb isotopic composition associated with different soil fractions (especially in the acid-extractable fractions), and the result is helpful for the further study on controlling and reducing Pb contamination in vegetable-growing soils.