Polycyclic aromatic hydrocarbon residues in blood serum and human milk in Egypt,A pilot case study

This study was performed to monitor residues of polycyclic aromatic hydrocarbons (PAHs) in samples of human blood serum and human milk taken from volunteers from one rural area of Egypt. Extraction and clean-up processes were conducted using the Quick Easy Cheap Effective Safe methodology. PAH residue analysis was performed by Gas chromatography-flame ioninzation detector (GC-FID) and High performance liquid chromatography-fluorescence detector (HPLC-FLD) for blood and milk samples, respectively. Some confirmatory work was conducted using a mass spectrometer. The concentrations of PAH residues in blood samples were between 0.007 and 0.407 mg/l, with many of the congeners below detection limits. Residues of the most carcinogenic PAH congeners including benzo (a) pyrene were below the limits of detection in all blood samples, and total PAH concentrations have ranged between 0.156 and 3.61 mg/l. Regarding human milk samples, the sum of PAH concentrations ranged from 95.23 to 229.26 (µg/kg f.w.) with a mean of 154.35 (µg/kg f.w.). Benzo[a]pyrene was detected in concentrations ranging from 0.348 to 15.4, with a mean of 7.872 (µg/kg f.w.). Acenaphthylene, dibenzo [a,h]anthracene, acenaphthene, and naphthalene were the most abundant congeners in milk samples. Results indicated that the sources of PAHs in blood serum and human milk are of pyrogenic and petrogenic origin, respectively.     

Polycyclic Aromatic Hydrocarbons in Road-Deposited Sediments and Roadside Soil in Tijuana,Mexico

Road-deposited sediment and roadside soil in the urban area of the city of Tijuana were collected and analyzed for 16 polycyclic aromatic hydrocarbons (PAHs). The ΣPAH concentration for road-deposited sediment (RDS) ranged between 460 and 2027 µg/kg with an average of 933 µg/kg. The ΣPAH concentration in roadside soil was lower than in RDS, with a range between 54 and 1863 µg/kg and a mean value of 308 µg/kg. The diagnostic ratios showed that the PAHs originated mostly from pyrogenic sources such as gasoline and diesel combustion. The results show that PAH concentration in RDS and roadside soils is low when compared with other published studies. The low PAH levels found in this study are possibly related to differences in climate, urban features, and anthropogenic activities conducted in the studied areas. The toxicity equivalent concentrations (TEQ) of PAH calculated were also low in comparison with other studies. This is probably due to the lower concentration of total PAHs and the highly toxic high-molecular-weight PAHs.     

Polycyclic aromatic hydrocarbons and phthalic acid esters in the soil-radish (Raphanus sativus) system with sewage sludge and compost application

We studied the accumulation of polycyclic aromatic hydrocarbons (PAHs) and phthalic acid esters (PAEs) in a latosolic red soil and radish (Raphanus sativus) with application of sewage sludge at rates of 10, 20 and 40 g kg(-1) soil or compost at rate of 10 g kg(-1) soil. In radish the concentrations of individual PAHs and PAEs varied from non-detectable to 803 microg kg(-1) dry weight (d.w.) and from non-detectable to 2048 microg kg(-1) d.w., respectively. Compared to the control, higher application rates of sewage sludge resulted in pronounced increases in shoot, root and soil concentrations of PAHs and PAEs. PAE concentrations in radish grown in soil spiked with sludge compost were higher while the PAH concentrations were comparable to those receiving 10 g kg(-1) of sewage sludge. However, the root biomass of radish in soil amended with compost was significantly higher and the shoot-to-root ratio was significantly lower than in the other treatments. The bioconcentration factors (BCFs, the ratio of contaminant concentration in plant tissue to the soil concentration) of di-n-butyl phthalate and di(2-ethylhexyl) phthalate in both shoots and roots and of total PAH concentrations in roots were less than 1.0, but some BCFs for individual PAHs were high with a maximum value of 80.     

DNA damage measured by the single-cell gel electrophoresis (Comet) assay in mammals fed with mussels contaminated by the 'Erika' oil-spill

This research aimed to estimate potential genotoxicity for consumers resulting from the ingestion of seafood contaminated with polycyclic aromatic hydrocarbons (PAHs) released into the marine environment after the 'Erika' shipwreck along the coasts of south Brittany, in France. Mussels (Mytilus sp.) collected from sites on the Atlantic coast that were affected by the oil slick in various degrees, were used to feed rats daily for 2 and 4 weeks. DNA damage was measured by use of the Comet assay in the liver, bone marrow and blood of rats receiving food contaminated with 312 microg of 16PAHs/kg dry weight (d.w.) equivalent to 33.8 microg TEQs (toxic equivalent quantities to benzo(a)pyrene (BaP))/kg d.w. mussels, 569 microg/kg d.w. (83.6 microg TEQs/kg) and 870 microg/kg d.w. (180.7 microg TEQs/kg). A dose-effect-time relationship was observed between the amount of DNA damage in the liver and bone marrow of the rats and the PAH contamination level of the mussels. Genotoxicity increased during the period between 15 and 30 days in rats that received food at the highest two PAH levels. On the other hand, no significant change in liver and bone marrow of rats fed with mussels containing 33.8 microg TEQs/kg d.w. was recorded at 30 days compared with 15 days, indicating efficient DNA repair capacity at low levels of exposure. No signs of genotoxicity were found in peripheral blood. Globally, the observed effects were rather moderate. These results show that oil-contaminated food caused DNA damage in predators, and underline the bioavailability to consumers of pollutants in mussels contaminated with fuel oil. The usefulness of the Comet assay as a sensitive tool in biomonitoring studies analyzing responses of PAH transfer through food webs was also confirmed.     

褐菖鲉肝CYP 1A作为生物标志物监测厦门海域石油污染状况

以褐菖鲉为实验鱼类,以鱼肝微粒体CYP1A 生物标志物(EROD活性和CYP1A蛋白表达量)为指标,在厦门海域开展了两次野外监测实验,研究EROD活性和CYP1A蛋白表达量的变化,以及它们与海水和沉积物中石油类和重金属含量之间的相关性。结果表明,在现场属于一类海水的石油类浓度(0.0121-0.0242 mg/L)条件下,石油类就能够显著诱导褐菖鲉肝EROD活性和CYP1A蛋白表达量,鱼肝EROD活性和CYP1A蛋白表达量与海水中石油类含量均呈现极显著正相关,CYP1A蛋白表达量比EROD活性较为敏感和稳定。此外,在监测实验中,尚未发现这两种生物标志物受所监测海区的海水和沉积物重金属含量的影响。因此,利用褐菖鲉肝微粒体EROD活性和CYP1A蛋白表达量作为生物标志物监测海洋石油类及其PAHs污染是可行的,在海洋环境石油类污染监测及其生化效应评价中具有重要的应用价值。而且,把这两种生物标志物结合起来加以研究并推广应用将更有意义。     

Uptake and biotransformation of 2,4,6-trinitrotoluene (TNT) by microplantlet suspension culture of the marine red macroalga Portieria hornemannii

Microplantlets of the marine red macroalga Portieria hornemannii efficiently removed the explosive compound 2,4,6-trinitrotoluene (TNT) from seawater. Photosynthetic, axenic microplantlets (1.2 g FW/L) were challenged with enriched seawater medium containing dissolved TNT at concentrations of 1.0, 10, and 50 mg/L. At 22 degrees C and initial TNT concentrations of 10 mg/L or less, TNT removal from seawater was 100% within 72 h, and the first-order rate constant for TNT removal ranged from 0.025 to 0.037 L/gFW h under both illuminated conditions (153 microE/m(2)s, 14:10 LD photoperiod) and dark conditions. Two immediate products of TNT biotransformation, 2-amino-4,6-dinitrotoluene and 4-amino-2,6-dintrotoluene, were identified in the liquid culture medium, with a maximum material balance recovery of 29 mole%. Only trace levels of these products and residual TNT were found within the fresh cell biomass. Removal of TNT by P. hornemannii microplantlets at initial concentrations of 1.0 or 10 mg/L did not affect the respiration rate. At an initial TNT concentration of 10 mg/L, net photosynthesis decreased towards zero, commensurate with the removal of dissolved TNT from seawater, whereas at an initial TNT concentration of 1.0 mg/L, the net photosynthesis rate was not affected.     

Enhancing the intrinsic bioremediation of PAH-contaminated anoxic estuarine sediments with biostimulating agents

Estuarine sediments are frequently polluted with hydrocarbons from fuel spills and industrial wastes. Polycyclic aromatic hydrocarbons (PAHs) are components of these contaminants that tend to accumulate in the sediment due to their low aqueous solubility, low volatility, and high affinity for particulate matter. The toxic, recalcitrant, mutagenic, and carcinogenic nature of these compounds may require aggressive treatment to remediate polluted sites effectively. In petroleum-contaminated sediments near a petrochemical industry in Gwangyang Bay, Korea, in situ PAH concentrations ranged from 10 to 2,900 microg/kg dry sediment. To enhance the biodegradation rate of PAHs under anaerobic conditions, sediment samples were amended with biostimulating agents alone or in combination: nitrogen and phosphorus in the form of slow-release fertilizer (SRF), lactate, yeast extract (YE), and Tween 80. When added to the sediment individually, all tested agents enhanced the degradation of PAHs, including naphthalene, acenaphthene, anthracene, fluorene, phenanthrene, fluoranthene, pyrene, chrysene, and benzo[a]pyrene. Moreover, the combination of SRF, Tween 80, and lactate increased the PAH degradation rate 1.2-8.2 times above that of untreated sediment (0.01-10 microg PAH/kg dry sediment/day). Our results indicated that in situ contaminant PAHs in anoxic sediment, including high molecular weight PAHs, were degraded biologically and that the addition of stimulators increased the biodegradation potential of the intrinsic microbial populations. Our results will contribute to the development of new strategies for in situ treatment of PAH-contaminated anoxic sediments.     

Silver speciation during chronic toxicity tests with the mysid,Americamysis bahia

A 28-day chronic toxicity test and two 7-day chronic estimation toxicity tests were conducted with silver nitrate (AgNO(3)) and the marine invertebrate, Americamysis bahia, in 20 per thousand (parts-per thousand) salinity seawater. One 7-day test was initiated with 7-day-old mysids and the second was initiated with <24-h-old mysids. There was very good agreement between the three toxicity tests. The no-observed-effect concentration (NOEC) values from the 28-day test, the 7-day test initiated with 7-day-old mysids, and the 7-day test initiated with <24-h-old mysids were 34, 65 and 38 microg/l silver, respectively. The 96-h LC50 values from the 28-day toxicity test and the 7-day toxicity test initiated with 7-day old mysids were 260 microg/l, and the 96-h LC50 value from the 7-day toxicity test initiated with <24-h-old mysids was 280 microg/l. Free ionic silver, Ag(+), concentrations measured with a silver electrode were in good agreement with concentrations calculated using total dissolved silver and chloride concentrations. Mean measured concentrations of Ag(+) in the test solutions ranged from 0.99 to 25 ng/l for the dissolved silver concentrations that ranged from 34 to 410 microg/l silver, indicating that free ionic silver varied from 0.003 to 0.006% of the silver dissolved in the 20 per thousand salinity seawater. Understanding the relationship of salinity and silver speciation, and the effect of this relationship on chronic invertebrate toxicity, will be useful for development of a marine biotic ligand model (BLM) and a water quality criterion for silver. This model could provide an important tool for improving the relationship of laboratory toxicity test results and predicted effects in natural environments, where variations in salinity may act to modify the toxicity of silver and other metals.     

Pyrithiones as antifoulants: environmental fate and loss of toxicity

The environmental fate and the loss of toxicity of two important antifouling actives, zinc pyrithione (ZnPT) and copper pyrithione (CuPT), were investigated using a bioassay study and an outdoor microcosm study. The bioassay used inhibition of the growth of a marine diatom (Amphora coffeaeformis) to measure the toxicity of ZnPT and CuPT over time in sterile, natural, and sediment-supplemented seawater. In natural seawater and sediment-supplemented seawater in the dark and in sterile seawater exposed to light, growth inhibition was reduced at rates corresponding to the rapid degradation rates for ZnPT and CuPT measured in previous aquatic metabolism, die-away, and photolysis studies. Similarly, the bioassay results from sterile seawater in the dark were consistent with the slower degradation rates measured in abiotic hydrolysis studies. In addition to corroborating the rapid degradation of pyrithione upon exposure to light or sediment, the loss of toxicity indicated that the degradation products were not toxic at the concentrations produced from the dose, which was much higher than predicted environmental concentrations. To supplement environmental fate studies designed to elucidate single-pathway transformations, a microcosm study was conducted to integrate all of the degradation pathways. The study used two sediment and water systems, one of which was dosed during the day and the other at night. The pyrithione degraded rapidly in the water phase, with very little accumulation in the sediment. 2-Pyridine sulfonic acid (PSA) and carbon dioxide were the only detectable degradation products 30 d after dosing. Aquatic toxicity studies with PSA showed no observable effect at concentrations at least three orders of magnitude higher than those for either ZnPT or CuPT. As a result, the worst-case environmental concentration of PSA is expected to be far below the no observable effect concentration.     

Pyrithiones as antifoulants: Environmental fate and loss of toxicity

The environmental fate and the loss of toxicity of two important antifouling actives, zinc pyrithione (ZnPT) and copper pyrithione (CuPT), were investigated using a bioassay study and an outdoor microcosm study. The bioassay used inhibition of the growth of a marine diatom (Amphora coffeaeformis) to measure the toxicity of ZnPT and CuPT over time in sterile, natural, and sediment-supplemented seawater. In natural seawater and sediment-supplemented seawater in the dark and in sterile seawater exposed to light, growth inhibition was reduced at rates corresponding to the rapid degradation rates for ZnPT and CuPT measured in previous aquatic metabolism, die-away, and photolysis studies. Similarly, the bioassay results from sterile seawater in the dark were consistent with the slower degradation rates measured in abiotic hydrolysis studies. In addition to corroborating the rapid degradation of pyrithione upon exposure to light or sediment, the loss of toxicity indicated that the degradation products were not toxic at the concentrations produced from the dose, which was much higher than predicted environmental concentrations. To supplement environmental fate studies designed to elucidate single-pathway transformations, a microcosm study was conducted to integrate all of the degradation pathways. The study used two sediment and water systems, one of which was dosed during the day and the other at night. The pyrithione degraded rapidly in the water phase, with very little accumulation in the sediment. 2-Pyridine sulfonic acid (PSA) and carbon dioxide were the only detectable degradation products 30 d after dosing. Aquatic toxicity studies with PSA showed no observable effect at concentrations at least three orders of magnitude higher than those for either ZnPT or CuPT. As a result, the worst-case environmental concentration of PSA is expected to be far below the no observable effect concentration.     

Toxicity of dissolved Cu, Zn, Ni and Cd to developing embryos of the blue mussel (Mytilus trossolus) and the protective effect of dissolved organic carbon

Marine water quality criteria for metals are largely driven by the extremely sensitive embryo-larval toxicity of Mytilus sp. Here we assess the toxicity of four dissolved metals (Cu, Zn, Ni, Cd) in the mussel Mytilus trossolus, at various salinity levels while also examining the modifying effects of dissolved organic carbon (DOC) on metal toxicity. In 48 h embryo development tests in natural seawater, measured EC50 values were 6.9-9.6 microg L(-1) (95% C.I.=5.5-10.8 microg L(-1)) for Cu, 99 microg L(-1) (86-101) for Zn, 150 microg L(-1) (73-156) for Ni, and 502 microg L(-1) (364-847) for Cd. A salinity threshold of >20 ppt (approximately 60% full strength seawater) was required for normal control development. Salinity in the 60-100% range did not alter Cu toxicity. Experimental addition of dissolved organic carbon (DOC) from three sources reduced Cu toxicity; for example the EC50 of embryos developing in seawater with 20 mg C L(-1) was 39 microg Cu L(-1) (35.2-47.2) a 4-fold increase in Cu EC50. The protective effects of DOC were influenced by their distinct physicochemical properties. Protection appears to be related to higher fulvic acid and lower humic acid content as operationally defined by fluorescence spectroscopy. The fact that DOC from freshwater sources provides protection against Cu toxicity in seawater suggests that extrapolation from freshwater toxicity testing may be possible for saltwater criteria development, including development of a saltwater Biotic Ligand Model for prediction of Cu toxicity.     

Modelling of fish contamination with 90Sr in relation to the calcium concentrations in water

A set of data on the equilibrium concentration factors of 90Sr in fish in relation to the Ca concentrations in water was collected and analyzed. An empiric relationship was obtained on the basis of statistical processing of this dataset: CF(90Sr, Bq/kg w.w.) = 3940(1770-6110)/[Ca, mg/L]water. The range of observed data on the concentration factors of 90Sr in fish is from 20 to 4000 L/kg (about 200 times). The statistical relationship obtained in the paper allows one to reduce this uncertainty by more than 50 times. The formula adequately describes equilibrium concentration factors of 90Sr both in freshwater and in marine fish. A dynamics model approach is described for the cases of accidental contamination of water bodies, when the equilibrium approaches are not appropriate.     

海洋酸化条件下Cd2+和Hg2+对斧文蛤幼贝急性毒性效应

为研究在海洋酸化条件下重金属污染物对滩涂贝类的影响,采用半静态急性毒性实验的研究方法,利用海洋酸化人工模拟系统,分析了不同酸化条件下(对照组pH 8.20、酸化组pH分别为7.80、7.60和7.40)Cd2+和Hg2+对斧文蛤(Meretrix lamarckii)幼贝急性毒性效应的影响。实验结果表明:在实验设定的海洋酸化范围内,单一的海洋酸化对斧文蛤幼贝的存活没有显著性影响,但海洋酸化显著增强了Cd2+和Hg2+的急性毒性。与对照组相比,酸化组Cd2+和Hg2+的毒性随着酸化程度的加剧而呈现出逐渐增强的趋势; Cd2+和Hg2+均在pH 7.40时对斧文蛤的毒性最强,其96h半致死(96h LC50)浓度分别为4.068 mg/L(Cd2+)和10.332 mg/L(Hg2+),明显低于pH 8.20、7.80和7.60时其对斧文蛤幼贝的96h LC50浓度(其值分别为Cd2+ 6.458、5.947、4.728 mg/L和Hg2+ 12.027、11.169、10.595 mg/L)。研究有助于丰富海洋酸化与重金属毒理作用在海洋贝类中的研究内容,为斧文蛤资源恢复和海洋环境保护提供科学依据。     

The cytotoxic effect of heavy metals on an L-cell culture

The dependence of some parameters of L-cells culture viability on different concentrations of heavy metals was studied. Considerable cytotoxic effect of low concentrations of nickel (0.025 mcg/ml) and lead (0.05 mcg/ml) was shown. Copper and chrome at concentrations of 0.25-0.5 mcg/ml promote cells proliferation between third and fifth days of cultivation. Nickel at concentration 0.025 mcg/ml and lead at all investigated concentrations synchronize cells division in culture. Increasing of giant polynucleas cells level in culture was characteristic for investigated metals. The maximum levels of this type cells were caused by the action of nickel, chrome and copper.     

Assessing measurable adverse changes to benthic invertebrate communities based on site-specific sediment toxicity testing and community data at the Anniston,Alabama PCB site

Laboratory toxicity tests were conducted for polychlorinated biphenyl (PCB)-containing sediment from Choccolocco Creek at the Anniston PCB Site. The objective of this investigation was to develop a site-specific PCB concentration–response relationship for invertebrate test organisms. Test results from reference locations were used to develop background-adjusted 10% (EC10*) and 20% (EC20*) effect concentrations for a range of survival, growth, and reproduction endpoints. The EC20* values ranged from 4.43 to 114 milligrams of PCBs per kilogram (mg/kg) of sediment on a dry weight basis for reproductive endpoints, 28 to 67.7 mg/kg sediment for growth, and 123 to 165 mg/kg sediment for survival. The aggregate EC20* response range for endpoints that demonstrated good test performance with reasonable ranges in control variability (<20%) and reference sample responses was 14.3 to 165 mg/kg. The PCB concentrations in sediments for a majority of the Site rarely exceed even the lowest of these thresholds. Given the protective process used to develop these thresholds, there is a high level of confidence that benthic communities are not impacted. This finding is supported by direct measurements of the benthic communities that have been living and reproducing on the Site.     

Trace Metals (Cd,Co, Cr,Cu, Hg,Ni, Pb,and Zn) in Food Supplements of Marine Origin

We determined the concentrations of Cd, Co, Cr, Cu, Hg, Ni, Pb, and Zn in dietary supplements of marine origin. Four supplement categories were studied; algae, coral, krill, and shark cartilage. A direct mercury analyzer was used for Hg determinations while acid digestions and ICP-AES were used for Cr analysis and ICP-MS for the other trace metals. Algae are the supplements showing the highest concentrations of Pb, Cr, and Ni with respective means of 1.6 mg Pb/kg dry weight (d.w.), 3.2 Cr mg/kg d.w., and 8.0 mg Ni/kg d.w. Krill supplements have the highest levels of Cd, Cu, and Zn with 0.65 mg Cd/kg d.w., 63 mg Cu/kg d.w., and 50 mg Zn/kg d.w., respectively. Shark cartilage supplements show the highest levels of Hg and Co with mean concentrations of 160 μg Hg/kg d.w. and 73 ± 51 μg Co/kg d.w., respectively. No samples in our study exceeded the provisional tolerable daily intakes set by Health Canada, the joint committee of the World Health Organization/Food and Agricultural Organization, or the U.S. Environmental Protection Agency. Nevertheless, Ni and Pb in algae and Hg in shark cartilage may end up contributing to a very significant portion of the allowable daily intake—leaving little room for normal intake through food consumption and other exposure pathways.     

Accumulation and clearance of orally administered erythromycin and its derivative, azithromycin, in juvenile fall chinook salmon Oncorhynchus tshawytscha

Fall Chinook salmon Oncorhynchus tshawytscha were fed practical diets medicated with azithromycin (30 mg kg(-1) fish for 14 d) or erythromycin (100 mg kg(-1) fish for 28 d) either 1, 2, or 3 times beginning 14 d after initiation of exogenous feeding (February) and ending at smoltification (June). Average tissue concentrations of azithromycin increased from 19.0 microg g(-1) in fry to 44.9 microg g(-1) in smolts, and persisted in the tissues > 76 d after treatment ceased. Tissue concentrations of erythromycin were comparatively low, ranging from 0.2 microg g(-1) in fry to 10.4 microg g(-1) in smolts. Erythromycin was not detectable 21 d post-treatment. Neither antibiotic caused histopathologically significant lesions in the trunk kidney or other organ tissues. The high tissue concentrations and prolonged retention of azithromycin in Chinook may be factors that increase the efficacy of the antibiotic against Renibacterium salmoninarum, compared with erythromycin, particularly in early life history stages before covertly infected fish show clinical signs of disease.     

Acclimation of Daphnia magna to environmentally realistic copper concentrations

It may be hypothesised that as the bioavailable background concentration of an essential metal increases (within natural limits), the natural tolerance (to the metal) of the acclimated/adapted organisms and communities will increase. In this study the influence of acclimation to different copper concentrations on the sensitivity of the freshwater cladoceran Daphnia magna Straus was investigated. D. magna was acclimated over three generations to environmentally relevant copper concentrations ranging from 0.5 to 100 microg Cu/l (copper activity: 7.18 x 10(-15) to 3700 x 10(-12) M Cu2+). A modified standard test medium was used as culture and test medium. Medium modifications were: reduced hardness (lowered to 180 mg CaCO3/l) and addition of Aldrich humic acid at a concentration of 5 mg DOC/l (instead of EDTA). The effects of acclimation on these organisms were monitored using acute mortality assays and long-term assays in which life table parameters, copper body concentrations and energy reserves were used as test endpoints. Our results showed a two-fold increase in acute copper tolerance with increasing acclimation concentration for second and third generation organisms. Copper acclimation concentrations up to 35 microg Cu/l (80 pM Cu2+) did not affect the net reproduction and the intrinsic growth rate. The energy reserves of the acclimated daphnids revealed an Optimal Concentration range (OCEE) and concentrations between 5 and 12 microg Cu/l (0.5-4.1 pM Cu2+) and 1 and 35 microg Cu/l (0.023-80 pM Cu2+) seemed to be optimal for first and third generation daphnids, respectively. Lower and higher copper concentrations resulted in deficiency and toxicity responses. It was also demonstrated that up to 35 microg Cu/l, third generation daphnids were able to regulate their total copper body concentration. These results clearly indicate that bioavailable background copper concentrations present in culture media have to be considered in the evaluation of toxicity test results, especially when the toxicity data are used for water quality guideline derivation and/or ecological risk assessment for metals.     

Identification of juvenile hormone-active alkylphenols in the lobster Homarus americanus and in marine sediments

We have identified, by gas chromatography/mass spectrometry, four alkylphenols that are present in the hemolymph and tissues of the American lobster Homarus americanus and in marine sediments. These alkylphenols are used industrially in antioxidant formulations for plastic and rubber polymer manufacturing, and are similar in structure to a known endocrine disruptor, bisphenol A. The compound 2-t-butyl-4-(dimethylbenzyl)phenol was present at concentrations of 0.02 to 1.15 microg/ml in hemolymph and 8.95 to 21.58 microg/g in sediments. A second compound, 2,4-bis-(dimethylbenzyl)phenol, was present at concentrations between 0.07 and 19.78 microg/ml in hemolymph and 138.94 to 224.89 microg/g in sediment, while a third compound, 2,6-bis-(t-butyl)-4-(dimethylbenzyl)phenol, was found at concentrations between 0.01 and 13.00 microg/ml in hemolymph, 2.55 and 6.11 microg/g in hepatopancreas, and 47.85 and 74.66 microg/g in sediment. A fourth compound, 2,4-bis-(dimethylbenzyl)-6-t-butylphenol, was found at concentrations of 0.20 to 70.71 microg/ml in hemolymph, 23.56 to 26.89 microg/g in hepatopancreas, and 90.68 to 125.58 microg/g in sediment. These compounds, along with bisphenol A, 4-dimethylbenzylphenol, and nonylphenol, display high juvenile hormone activity in bioassays. Alkylphenols at high concentrations are toxic to crustaceans and may contribute significantly to lobster mortality; at lower concentrations, they are likely to have endocrine-disrupting effects.     

Selenium, zinc, and copper concentrations in the blood and milk of lactating women

The aim of the study was to determine Se, Zn, and Cu concentrations in blood plasma and milk of lactating women from central Poland who were in different stages of lactation and to investigate the relationship between the content of trace elements in mothers’ blood and concentrations of microelements in their milk. Se and Zn concentrations in blood plasma of mothers were the lowest and Cu was the highest on the first 4 d of lactation (colostrum, n=43) and were found to be 34.9±11.8 μg/L, 0.51±0.13 mg/L, and 1.70±0.55 mg/L, respectively. The highest plasma level of Se and Zn and the lowest content of Cu could be observed between d 10 and 30 of lactation (mature milk, n=41), and were found to be 54.3±14.6 μg/L for Se (p<0.001), 0.76±0.20 mg/L for Zn (p<0.001), and 1.03±0.30 mg/L (p<0.001) for Cu. The results of Se, Zn, and Cu determination in breast milk samples demonstrate a pattern of decline in their concentration with advancing stages of lactation. We found out that Se, Zn, and Cu concentrations were the highest in colostrum (n=43) and amounted to 24.8±10.1 μg/L, 8.2±2.8 mg/L, and 0.45±0.11 mg/L, respectively. The content of all determined microelements declined significantly during the time of lactation. Statistically significant linear correlation was found between concentrations of Zn in blood plasma and milk in the first stage of lactation. Weak but statistically significant linear correlations were also found between plasma Se content in plasma and in transitional and mature milk of breast-feeding women.