Photodegradation of sulfonamide antibiotics in simulated and natural sunlight: Implications for their environmental fate

The photochemical fate of seven sulfonamides was investigated in matrices representative of natural water bodies under various light sources. Fundamental photolysis parameters such as molar absorption coefficient, quantum yield (QY) and first-order rate constants were determined. The photolysis decay rate was dependent on the protonation state of the molecule, pH of the water sample and dissolved organic matter. Natural organic matter was the most significant factor in the indirect photolysis of sulfonamides. Half-lives were in the range of minutes at 254 nm to days under natural sunlight. Under natural sunlight, all sulfonamides showed higher removal rates in natural waters implying that indirect photolysis is the predominant mechanism.     

Concentration of trace metals in sediments and soils from protected lands in south Florida: background levels and risk evaluation

A comprehensive environmental evaluation was completed on 20 metals: two reference metals (Fe, Al) and several minor trace metals (As, Ba, Co, Cr, Cu, Mn, Ni, Pb, V, and Zn) for surface soils and sediments collected from 50 sites in Everglades National Park (ENP), the coastal fringes of Biscayne National Park (BNP), and Big Cypress National Preserve. Samples were prepared by acid digestion (EPA3050) and analyzed by ICP/MS detection (EPA6020). Although no widespread contamination was detected across the two parks and one preserve, there were some specific areas where metal concentrations exceeded Florida’s ecological thresholds, suggesting that some metals were of concern. A screening-level evaluation based on a proposed effect index grouped trace metals by their potential for causing negligible, possible, and probable effects on the biota. For example, Cu in BNP and Cr and Pb in ENP were considered of concern because their adverse effect likelihood to biota was assessed as probable; consequently, these trace metals were selected for further risk characterization. Also, stations were ranked based on a proposed overall contamination index that showed that: site BB10 in BNP and sites E3 and E5 in ENP had the highest scores. The first site was located in a marina in BNP, and the other two sites were along the eastern boundary of ENP adjacent to current or former agricultural lands. An assessment tool for south Florida protected lands was developed for evaluating impacts from on-going Everglades restoration projects and to assist State and Federal agencies with resource management. The tool consists of enrichment plots and statistically derived background concentrations based on soil/sediment data collected from the two national parks and one preserve. Finally, an equally accurate but much simplified approach is offered for developing enrichment plots for other environmental settings.     

Copper desorption in flooded agricultural soils and toxicity to the Florida apple snail (Pomacea paludosa): implications in Everglades restoration

Copper (Cu) desorption and toxicity to the Florida apple snail were investigated from soils obtained from agricultural sites acquired under the Comprehensive Everglades Restoration Plan. Copper concentrations in 11 flooded soils ranged from 5 to 234 mg/kg on day 0 and from 6.2 to 204 mg/kg on day 28 (steady-state). The steady-state Cu concentration in overlying water ranged from 9.1 to 308.2 microg/L. In a 28-d growth study, high mortality in snails occurred within 9 to 16 d in two of three soil treatments tested. Growth of apple snails over 28 d was affected by Cu in these two treatments. Tissue Cu concentrations by day 14 were 12-23-fold higher in snails exposed to the three soil treatments compared to controls. The endangered Florida snail kite and its main food source, the Florida apple snail, may be at risk from Cu exposure in these managed agricultural soil-water ecosystems.     

西安夏季大气亚微米颗粒物化学组成与来源的在线观测研究

西安作为汾渭平原地区最大的城市,大气颗粒物污染形势严峻.2017年夏季期间,在西安市浐灞生态园区运用气溶胶化学组分监测仪,对大气亚微米颗粒物中的非难挥发性组分(NR-PM1)进行了在线监测.观测期间NR-PM1的平均质量浓度为(30.1?±?15.4)μg???m?3.其中有机物含量最高,占NR-PM1总质量浓度的63％,其次为硫酸盐(18％)、铵盐(10％)和硝酸盐(9％).运用正交矩阵因子分析法共解析出两个主要因子,包括烃类有机组分(HOA)和含氧有机组分(OOA),分别占有机物总质量浓度的43％和55％.HOA主要由机动车排放贡献,而OOA主要由气态污染物的二次反应生成.气象因素对NR-PM1的浓度与化学组分的影响较为显著.高硝酸盐阶段发生在高湿、低温条件,可能是由氮氧化物的液相反应产生的.高硫酸盐阶段发生在低湿、高温条件,主要来自于大气光化学反应的贡献.该研究结果为西安及周边地区的空气污染治理决策提供重要的理论依据.     

Bioconcentration and depuration of endosulfan sulfate in mosquito fish (Gambusia affinis)

Endosulfan is an insecticide which has been widely used in agriculture. The technical grade material consists of two isomers (alpha and beta). Under natural environmental conditions, endosulfan is metabolized through oxidation and the main metabolite in the environment is endosulfan sulfate. Most ecotoxicology research has been conducted with technical grade endosulfan to determine effects on non-target aquatic organisms. Little data on the effects of endosulfan sulfate on aquatic organisms are available in the literature. This study characterizes endosulfan sulfate bioconcentration and depuration in mosquito fish (Gambusia affinis). During the study, G. affinis was exposed to an environmentally relevant endosulfan sulfate concentration of 0.25 μg L⁻¹ for 5 weeks (uptake phase) followed by a 3-week period (depuration phase) in clean water. This study found that G. affinis bioconcentrated endosulfan sulfate. During the exposure phase, fish tissue concentrations of endosulfan sulfate increased with time up to 730 μg kg⁻¹ dw or 215 μg kg⁻¹ ww. The bioconcentration data followed Michaelis-Menten kinetics better than the one-compartment first order kinetics (1-CFOK). Using these models, the bioconcentration factors for endosulfan sulfate-exposed G. affinis were from 687 to 888  L kg⁻¹ in wet weight or 2263 to 2936 L kg⁻¹ in dry weight. During the depuration phase, endosulfan sulfate concentrations in tissue significantly decreased and the data followed first order kinetics. The half-life of endosulfan sulfate in G. affinis was about 9 d. There was no significant difference in standard length or weight between control and exposed fish. The growth data followed the von Bertalanffy growth model. However, the condition factor of exposed fish increased with time during the exposure phase.     

Environmental Contaminants in Blood, Hair, and Tissues of Ocelots from the Lower Rio Grande Valley, Texas, 1986–1997

The ocelot (Felis pardalis) isan endangered neotropical cat distributed within asmall range in the Lower Rio Grande Valley (LRGV), inTexas, U.S.A. Studies of the impacts of environmentalcontaminants in wild cats are few. Approximately onefourth of the estimated population (about 100) ofocelots in the LRGV was sampled to evaluate theimpacts of chlorinated pesticides, polychlorinatedbiphenyls, and trace elements on the population. Hairwas collected from 32 ocelots trapped between 1986–1992,and blood was collected from 20 ocelots trappedbetween 1993–1997. A few blood samples were obtainedfrom individuals recaptured two or three times. Tissue samples from 4 road-killed ocelots were alsoanalyzed. DDE, PCBs, and Hg were some of the mostcommon contaminants detected in hair and blood. MeanHg levels in hair ranged from 0.5 to 1.25 g g^-1 dw,Se from 1.5 to 3.48 g g^-1 dw, and Pb from 0.56 to26.8 g g^-1 dw. Mean DDE concentrations in plasma ranged from 0.005 g g^-1 ww to 0.153 g g^-1 ww, and PCBs ranged from 0.006 g g^-1 ww to 0.092 g g^-1 ww. Mean Hg levels in red blood cells rangedfrom 0.056 g g^-1 dw to 0.25 g g^-1 dw. Concentrations of DDE, PCBs, or Hg, did not increasesignificantly with age, although the highestconcentrations of DDE and Hg were found in olderanimals. Overall, concentrations of DDE, PCBs, and Hgwere low and at levels that currently do not pose anythreat to health or survival of the ocelot. This isfurther supported by good reproduction of the ocelotin the LRGV, where adult females averaged about 1.5kittens/litter. Thus, it seems that the current majorthreat to recovery of the ocelot in the LRGV may behabitat loss, although potential impacts of newgeneration pesticides, such as organophosphorus andcarbamate insecticides need further study.     

Trace determination of caffeine in surface water samples by liquid chromatography--atmospheric pressure chemical ionization--mass spectrometry (LC-APCI-MS)

A new method based on liquid-liquid extraction (LLE) coupled to reverse phase liquid chromatography and atmospheric pressure chemical ionization mass spectrometry (LC-APCI-MS) has been applied to determine trace amounts of caffeine (1,3,7-trimethylxanthine) in surface water samples from a near coastal ecosystem such as Biscayne Bay, Florida. The rational behind the development of such method will be to evaluate the use of unmetabolized caffeine as a potential dissolved phase tracer of human waste contamination. The method allows for the determination of caffeine at levels as low as 4.0 ng/l (ppt) in both salt and freshwater by extracting and concentrating a 1-1 water sample to a final volume of 500 microl and using HPLC separation coupled to an atmospheric pressure chemical ionization mass spectrometry (APCI-MS) system operated in selected ion monitoring (SIM) for the protonated molecular ions (M + H(+)). Samples from different portions of Biscayne Bay and the Miami River, one of its major tributaries, were analyzed and caffeine was detected in those areas previously identified for consistently exceeding the water quality criteria for fecal coliform bacteria contamination. The caffeine concentration in the samples with positive detection was generally low at levels equal or lower than 41 ng/l. However, there is a marked difference between samples collected in open bay areas and those collected from the Miami River.     

Organic compounds and trace metals of anthropogenic origin in sediments from Montego Bay,Jamaica: assessment of sources and distribution pathways

Surface sediments throughout Montego Bay, Jamaica were collected in 1995 and analyzed for their trace metal and trace organic contaminant content. A variety of trace metals, petroleum hydrocarbons, polycyclic aromatic hydrocarbons, coprostanol as well as chlorinated hydrocarbons such as pesticides and polychlorinated biphenyls were detected and provide evidence for several anthropogenic inputs to the bay. Two main sources of these chemicals are the Montego River and the North Gully, the latter being more significant. Particle-associated pollutants were found to be distributed along the Montego River plume, as well as being transported by the prevailing water currents to the South-Western sections of the bay, probably through re-suspension of enriched fine sediments from the North Gully outfall area.     

Uptake and depuration of toxic halogenated aromatic hydrocarbons by the American oyster (Crassostrea virginica): a field study

Uptake and depuration of toxic chlorinated compounds such as planar polychlorinated biphenyls (PCBs 77, 126, 169), 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and 2,3,7,8-tetrachlorodibenzofuran (TCDF) were monitored during a 50-day field study where American oysters (Crassostrea virginica) were transplanted back and forth between a heavily polluted area (Houston Ship Channel, SC) and a relatively unimpacted area (Hanna's Reef, HR) within Galveston Bay, TX. In general, low molecular weight, less lipophilic compounds accumulated in the oysters to a larger extent than high molecular weight ones. Estimated half-lives for planar PCB congeners 77 and 126 were 28 and 51 days, respectively for depuration of newly contaminated oysters (HR-SC-HR) while longer half-lives (42 and 60 days, respectively) were observed for the same compounds as they were eliminated from chronically contaminated individuals (SC-HR). Estimated half-lives for 2,3,7,8-TCDD and 2,3,7,8-TCDF were 35 and 36 days, respectively and were similar to the tetrachlorinated biphenyls (PCBs 77 and 81). Compared with ortho-substituted PCB congeners of the same chlorination level, the more toxic PCBs take longer to depurate from the oysters. With few exceptions, elimination of all toxic compounds investigated proceeded at a slower rate from the chronically exposed population that from the newly contaminated one.