ABSTRACT
Although many studies have been conducted on the use of median and transverse incisions in various surgeries in the field of human medicine, related studies in veterinary medicine are lacking. This study aimed to present treatment options for dogs requiring cholecystectomy by reporting the pros and cons of 121 cholecystectomies performed via transverse incision at our hospital over 10 years. In most included cases, nonelective cholecystectomy was performed in an unstable emergency situation. The perioperative mortality rate was 23.14%, which was not significantly different from that of cholecystectomy performed via the conventional midline approach. However, the overall operation time (46.24 ± 6.13 min; range 35-65 min) was shortened by securing an adequate surgical field of view. The transverse incision approach facilitates fast and accurate surgery without increasing the fatality rate in small-breed dogs, in whom securing an adequate surgical field of view is difficult. Thus, transverse incision should be actively considered in dogs undergoing cholecystectomy due to emergency conditions, such as bile leakage or biliary tract obstruction, since prolonged anesthesia can be burdensome. This study may improve cholecystectomy outcomes in small-breed dogs with difficult-to-secure surgical fields.
ABSTRACT
OBJECTIVE: Skin-brightening agents prevent melanogenesis and reduce melanin production. However, a lower melanin content leads to weaker protection against sunlight. In this study, we evaluated the effect of lysophosphatidylcholine (LPC) and its commercial-grade product, Lysofix Dry™ (LD), on heat shock protein 70 (HSP70) expression in epidermal cells and their anti-skin photoaging effect against ultraviolet B (UVB) and blue light. METHODS: The HSP70 induction was detected using ELISA. To confirm the inhibition of melanin synthesis by LPC or LD, the melanin content assay and gene expression were analyzed. Cell viability was assessed to verify whether LPC or LD prevents photo-induced skin damage. The split-face test was performed to confirm skin-brightening effect of LD. Cream formulation with 2% of LD and placebo were used for 8 weeks, and skin brightness (L) was measured with chromameter (CR-400, Konica Minolta). RESULTS: LPC- and LD-induced HSP70 expression in epidermal cells. LPC and LD effectively suppressed melanogenesis provoked by α-MSH in B16 cells. They also inhibited the mRNA transcription of MITF and tyrosinase under blue light irradiation. LD increased the viability of B16 and HaCaT cells after UVB and blue light irradiation in vitro. The cream containing 2% LD increased ΔL by 1.7 after 8 weeks of use, whereas the placebo led to an increase of 0.7. CONCLUSION: LPC and LD were effective in suppressing melanogenesis and enhancing cell viability under UVB and blue light via HSP70 expression. Thus, they can be considered as potent skin-brightening agents with protective effects against skin photoaging.
Subject(s)
Skin Aging , HSP70 Heat-Shock Proteins/genetics , Lysophosphatidylcholines , Melanins , Monophenol Monooxygenase , Ultraviolet Rays/adverse effectsABSTRACT
One year after the Deepwater Horizon oil spill accident, semipermeable membrane devices (SPMDs) and polyethylene devices (PEDs) were deployed in wetland areas and coastal areas of the Gulf of Mexico (GOM) to monitor polycyclic aromatic hydrocarbons (PAHs). The measured PAH levels with the PEDs in coastal areas were 0.05-1.9 ng/L in water and 0.03-9.7 ng/L in sediment porewater. With the SPMDs, the measured PAH levels in wetlands (Barataria Bay) were 1.4-73 ng/L in water and 3.3-107 ng/L in porewater. The total PAH concentrations in the coastal areas were close to the reported baseline PAH concentrations in GOM; however, the total PAH concentrations in the wetland areas were one or two orders of magnitude higher than those reported in the coastal areas. In light of the significant spatial variability of PAHs in the Gulf's environments, baseline information on PAHs should be obtained in specific areas periodically.
Subject(s)
Environmental Monitoring/methods , Geologic Sediments/chemistry , Petroleum Pollution/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Seawater/chemistry , Water Pollutants, Chemical/analysis , Gulf of Mexico , Southeastern United States , Spatial Analysis , WetlandsABSTRACT
BACKGROUND: Phthalates are endocrine-disrupting chemicals that influence thyroid hormones and sex steroids, both critical for brain development. AIM: We studied phthalate concentrations in house dust in relation to the risks of developing autism spectrum disorder (ASD) or developmental delay (DD). METHODS: Participants were a subset of children from the CHARGE (CHildhood Autism Risks from Genetics and the Environment) case-control study. ASD and DD cases were identified through the California Department of Developmental Services system or referrals; general population controls were randomly sampled from state birth files and frequency-matched on age, sex, and broad geographic region to ASD cases. All children (50 ASD, 27 DD, 68 typically developing (TD)) were assessed with Mullen Scales of Early Learning, Vineland Adaptive Behavior Scales (VABS) and Aberrant Behavior Checklist. We measured 5 phthalates in dust collected in the child's home using a high volume small surface sampler. RESULTS: None of the phthalates measured in dust was associated with ASD. After adjustment, we observed greater di(2-ethylhexyl) phthalate (DEHP) and butylbenzyl phthalate (BBzP) concentrations in indoor dust from homes of DD children: Odds ratios (OR) were 2.10 (95% confidence interval (CI); 1.10; 4.09) and 1.40 (95% CI; 0.97; 2.04) for a one-unit increase in the ln-transformed DEHP and BBzP concentrations, respectively. Among TD children, VABS communication, daily living, and adaptive composite standard scores were lower, in association with increased diethyl phthalate (DEP) concentrations in dust. Participants with higher dibutyl phthalate (DBP) concentrations in house dust also trended toward reduced performance on these subscales. Among ASD and DD boys, higher indoor dust concentrations of DEP and DBP were associated with greater hyperactivity-impulsivity and inattention. DISCUSSION AND CONCLUSION: House dust levels of phthalates were not associated with ASD. The inability to distinguish past from recent exposures in house dust and the fact that house dust does not capture exposure from all sources, limit the interpretation of both positive and null findings and further work is needed. However, the associations observed for DEP and DBP with impairments in several adaptive functions and greater hyperactivity, along with evidence for increased risk of DD raise concerns that these chemicals may affect neurodevelopment in children.
Subject(s)
Air Pollution, Indoor/adverse effects , Autistic Disorder/chemically induced , Developmental Disabilities/chemically induced , Dust/analysis , Environmental Exposure/adverse effects , Environmental Pollutants/adverse effects , Phthalic Acids/analysis , Air Pollution, Indoor/analysis , Autistic Disorder/epidemiology , California/epidemiology , Case-Control Studies , Child, Preschool , Developmental Disabilities/epidemiology , Environmental Exposure/analysis , Environmental Pollutants/analysis , Female , Humans , Male , Odds RatioABSTRACT
Following the spill of bunker fuel oil (intermediate fuel oil 380, approximately 1500-3000 L) into San Francisco Bay in October 2009, polycyclic aromatic hydrocarbon (PAH) concentrations in mussels from moderately oiled areas increased up to 87 554 ng/g (dry wt) and, 3 mo later, decreased to concentrations found in mussels collected prior to oiling, with a biological half-life of approximately 16 d. Lysosomal membrane destabilization increased in mussels with higher PAH body burdens.
Subject(s)
Bivalvia/chemistry , Petroleum Pollution , Polycyclic Aromatic Hydrocarbons/analysis , Water Pollutants, Chemical/analysis , Animals , Bays , Half-Life , Intracellular Membranes/drug effects , Lysosomes/drug effects , Polycyclic Aromatic Hydrocarbons/toxicity , Water Pollutants, Chemical/toxicityABSTRACT
The objective of this study was to evaluate the efficacy of integrating a traditional sediment quality triad approach with selected sublethal chronic indicators in resident species in assessing sediment quality in four salt marshes in northern California, USA. These included the highly contaminated (Stege Marsh) and relatively clean (China Camp) marshes in San Francisco Bay and two reference marshes in Tomales Bay. Toxicity potential of contaminants and benthic macroinvertebrate survey showed significant differences between contaminated and reference marshes. Sublethal responses (e.g., apoptotic DNA fragmentation, lipid accumulation, and glycogen depletion) in livers of longjaw mudsucker (Gillichthys mirabilis) and embryo abnormality in lined shore crab (Pachygrapsus crassipes) also clearly distinguished contaminated and reference marshes, while other responses (e.g., cytochrome P450, metallothionein) did not. This study demonstrates that additional chronic sublethal responses in resident species under field exposure conditions can be readily combined with sediment quality triads for an expanded multiple lines of evidence approach. This confirmatory step may be warranted in environments like salt marshes in which natural variables may affect interpretation of toxicity test data. Qualitative and quantitative integration of the portfolio of responses in resident species and traditional approach can support a more comprehensive and informative sediment quality assessment in salt marshes and possibly other habitat types as well.
Subject(s)
Environmental Monitoring/methods , Geologic Sediments/analysis , Seawater/analysis , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/toxicity , Animals , Biota , California , Environmental Monitoring/economics , Invertebrates/drug effects , Invertebrates/embryology , Liver/drug effects , Liver/metabolism , Perciformes/metabolism , WetlandsABSTRACT
We demonstrate a controlled, systematic method to tune the charge transport in graphene field-effect transistors based on alternating layer-by-layer assembly of positively and negatively charged graphene oxide followed by thermal reduction. Surprisingly, tuning the number of bilayers of thermally reduced graphene oxide multilayer films allowed achieving either ambipolar or unipolar (both n- and p-type) transport in graphene transistors. On the basis of X-ray photoemission spectroscopy, Raman spectroscopy, time-of-flight secondary ion mass spectrometry, and temperature-dependent charge transport measurements, we found that nitrogen atoms from the functional groups of positively charged graphene oxide are incorporated into the reduced graphene oxide films and substitute carbon atoms during the thermal reduction. This nitrogen-doping process occurs in different degrees for graphene multilayers with varying numbers of bilayers and thereby results in the interesting transition in the electrical behavior in graphene multilayer transistors. We believe that such a versatile method to control the charge transport in graphene multilayers will further promote their applications in solution-processable electronic devices based on graphene.
ABSTRACT
Sub-micron sized airborne particulate matter (PM) is not collected well on regular quartz or glass fiber filter papers. We used a micro-orifice uniform deposit impactor (MOUDI) to fractionate PM into six size fractions and deposit it on specially designed high purity thin aluminum disks. The MOUDI separated PM into fractions 56-100 nm, 100-180 nm, 180-320 nm, 320-560 nm, 560-1000 nm, and 1000-1800 nm. Since the MOUDI has a low flow rate (30 L/min), it takes several days to collect sufficient carbon on 47 mm foil disks. The small carbon mass (20-200 microgram C) and large aluminum substrate (~25 mg Al) present several challenges to production of graphite targets for accelerator mass spectrometry (AMS) analysis. The Al foil consumes large amounts of oxygen as it is heated and tends to melt into quartz combustion tubes, causing gas leaks. We describe sample processing techniques to reliably produce graphitic targets for (14)C-AMS analysis of PM deposited on Al impact foils.
ABSTRACT
Sedimentation of metals preserves historical records of contaminant input from local and regional sources, and measurement of metals in sediment cores can provide information for reconstruction of historical changes in regional water and sediment quality. Sediment core was collected from Stege Marsh located in central San Francisco Bay (California, USA) to investigate the historical input of trace metals. Aluminum-normalized enrichment factors indicate that inputs from anthropogenic sources were predominant over natural input for Ag, Cu, Pb, and Zn. Among these, lead was the most anthropogenically impacted metal with enrichment factors ranging from 32 to 108. Depth profiles and coefficients of variation show that As, Cd, and Se were also influenced by anthropogenic input. The levels of these anthropogenically impacted metals decline gradually towards the surface due to regulation of the use of leaded gasoline, municipal and industrial wastewater discharge control, and closure of point sources on the upland of Stege Marsh. Although trace metal contamination is expected to be continuously declining, the rates of decline have slowed down. For lead, it is estimated to take 44, 82, and 153 years to decrease to probable effects level (112 microg/g), the San Francisco Bay ambient surface sediment level (43.2 microg/g), and the local baseline levels (5 microg/g), respectively. Some metals in surface sediments (0-6 cm) are still higher than sediment quality guidelines such as the probable effects level. To further facilitate the recovery of sediment quality, more efficient management plans need to be developed and implemented to control trace metals from non-point sources such as stormwater runoff.
Subject(s)
Geologic Sediments/chemistry , Trace Elements/analysis , Water Pollutants, Chemical/analysis , Water Pollution, Chemical/statistics & numerical data , Wetlands , Environmental Monitoring , Forecasting , San Francisco , Seawater/chemistryABSTRACT
To investigate the occurrence of contaminants and to assess their toxicity potential to benthic organisms, streambed sediments were collected from three agricultural and one urban influenced small waterways in the lower Sacramento River watershed and analyzed for PAHs, organochlorine (OC) and organophosphorus (OP) pesticides, pyrethroids, and metals. These sites had low benthic biotic index scores in earlier field surveys. The occurrence patterns of these contaminants and iron normalized enrichment factors of metals reflect the land use patterns around study sites. DDTs were detected in all samples while chlordanes were found only at the urban influenced site. No OP pesticides were found in any sediment presumably due to their high water solubilities and low solid-water partitioning. DDTs, PAHs, and metals at sites in the Biggs/West Gridley Canal showed a gradient increasing toward downstream. Distribution patterns of individual PAHs and their ratios found in sediment from the Biggs/West Gridley Canal downstream site resemble those of petroleum. PAHs in this site might originate from petroleum oils that have been used as agricultural pesticides. The enrichment factor of vanadium, which is an indicator of petroleum residue, was also higher in this site. The anthropogenic enrichment of copper at all Biggs/West Gridley Canal sites might be because of significant use of copper based pesticides. The high enrichment factor of lead at the urban influenced Dry Creek site might be related to historical use of leaded gasoline. All sediment samples had at least one chemical that exceed the threshold effects concentration (TEC). Total probable effects concentration quotients (tPECQs) were greater than 1 at all sites, indicating that sediment bound contaminants in the study sites can possibly pose toxic effects. This finding can be linked to lower biotic index scores observed in previous regional monitoring studies.
Subject(s)
Agriculture , Fresh Water/chemistry , Geologic Sediments/chemistry , Industry , California , Particle Size , Water Pollutants, Chemical/analysisABSTRACT
This study was undertaken to establish residue-response relationship between lysosomal destabilization and body residues of multiple PAHs in eastern oysters (Crassostrea virginica) exposed to a mixture of PAHs for 25 days in laboratory aquariums. The contaminated oysters were then placed in clean aquariums for 20 days to allow them to depurate and recover. The lysosomal destabilization was linearly correlated with the PAH body burdens. Regression analysis showed that critical body residue (CBR), in terms of lysosomal destabilization (at least 50% of destabilized cells), was found at 2,100 ng/g (9.32 nmol/g) of total PAHs. This CBR is much lower than the CBRs for reproduction and death, confirming that lysosomal destabilization, as a cellular level biomarker, appears to be functioning as an early warning indicator that can be used to detect aquatic contamination much before severe effects are observed. During 25 days of exposure, the lysosomal destabilization and PAH body burdens increased from 32 to 75% and 77 to 5,925 ng/g, respectively. After 20 days of elimination period, the lysosomal destabilization and PAH body burdens decreased to 49% and 2,350 ng/g, respectively. Uptake rates of PAHs showed parabolic shaped correlation with hydrophobicity (K(ow)). Uptake rate constants of more hydrophobic PAHs (log K(ow) > 4.6) had a negative correlation with K(ow), implying that hydrophobicity alone is not a satisfactory predictor for these PAHs. Elimination half-lives varied from 4 to 96 days and bioconcentration factors ranged from 650 to 160,000. Fugacity ratios (f(o)/f(w)) indicated that equilibrium still was not reached at the end of the uptake period. Data obtained from the three replicate aquariums, which were operated at the same time under the same condition, showed good replicability (RPD < 30%).
Subject(s)
Intracellular Membranes/drug effects , Lysosomes/drug effects , Ostreidae/metabolism , Polycyclic Aromatic Hydrocarbons/pharmacokinetics , Polycyclic Aromatic Hydrocarbons/toxicity , Animals , Lysosomes/metabolism , Regression AnalysisABSTRACT
To investigate the aerial distribution, seasonal variation, and sources of polycyclic aromatic hydrocarbons (PAHs), pine needles were collected from 18 sites in the Houston metropolitan area, Texas, USA. Total PAHs ranged from 209 to 2,226 ng/g (dry wt.), which were similar to those found in other urban areas. The highest and lowest concentrations were found in samples from the inner city of Houston and the outer edge of suburban area, respectively. Aerial distribution of PAHs in pine needles was closely correlated to the proximity to densely occupied residential area and traffic volumes around sampling sites. Seasonal changes of PAHs in pine needles were inversely correlated with ambient temperature with lower levels in warmer months. Calculated concentrations of 3-ring PAHs in the air had a positive correlation with ambient temperature with higher levels in warmer months. Ratios of PAHs in pine needles to PAHs in the air decreased as ambient temperature increased because fugacity (escaping tendency) of PAHs in pine needles is greater in warmer months. The PAH patterns and ratios were fairly constant in all samples, indicating that the whole study area was influenced by the same emission sources, most importantly gasoline vehicle emission. Phenanthrene was the predominant PAH and 3- and 4-ring PAHs were the most abundant in all samples, accounting for 79 to 97% of the total PAHs. The present study provides evidence that pine needle monitoring can be used as a good screening method to assess the atmospheric PAH contamination quickly and at low cost.
Subject(s)
Pinus/chemistry , Plant Leaves/chemistry , Polycyclic Compounds/analysis , Seasons , Temperature , Mass Spectrometry , TexasABSTRACT
Human exposure to indoor dust enriched with endocrine-disrupting chemicals released from numerous indoor sources has been a focus of increasing concern. Longer residence times and elevated contaminant concentrations in the indoor environment may increase chances of exposure to these contaminants by 1000-fold compared to outdoor exposure. To investigate the occurrence of semi-volatile endocrine-disrupting chemicals, including PBDEs (polybrominated diphenyl ethers), PCBs (polychlorinated biphenyls), phthalates, pyrethroids, DDT (dichlorodiphenyltrichloroethane) and its metabolites, and chlordanes, indoor dust samples were collected from household vacuum cleaner bags provided by 10 apartments and 1 community hall in Davis, California, USA. Chemical analyses show that all indoor dust samples are highly contaminated by target analytes measured in the present study. Di-(2-ethylhexyl)phthalate was the most abundant (104-7630 microg/g) in all samples and higher than other target analytes by 2 to 6 orders of magnitude. PBDEs were also found at high concentrations (1780-25,200 ng/g). Although the use of PCBs has been banned or restricted for decades, some samples had PCBs at levels that are considered to be concerns for human health, indicating that the potential risk posed by PCBs still remains high in the indoor environment, probably due to a lack of dissipation processes and continuous release from the sources. Although the use of some PBDEs is being phased out in some parts of the U.S., this trend may apply to PBDEs as well. We can anticipate that exposure to PBDEs will continue as long as the general public keeps using existing household items such as sofas, mattresses, and carpets that contain PBDEs. This study provides additional information that indoor dust is highly contaminated by persistent and endocrine-disrupting chemicals.
Subject(s)
Air Pollutants/analysis , Air Pollution, Indoor/analysis , Dust/analysis , Endocrine Disruptors/analysis , California , Environmental Monitoring , Halogenated Diphenyl Ethers , Insecticides/analysis , Phenyl Ethers/analysis , Phthalic Acids/analysis , Polybrominated Biphenyls/analysis , Polychlorinated Biphenyls/analysisABSTRACT
To investigate the loadings, solid-water partitioning, transport dynamics, and sources of polychlorinated biphenyls (PCBs) in urban stormwater runoff entering into the lower tidal Anacostia River, which flows south of Washington, DC, USA, storm and base flow samples were collected in six branches. Stormwater runoff contained elevated levels of PCBs (9.82 to 211 ng/L) higher than base flow by up to 80-fold. The present study suggests that input of PCBs from Lower Beaverdam Creek is likely to be greater than those from the two major branches (Northeast and Northwest Branches) that were believed as primary source areas. PCBs in storm flow were significantly enriched in the particle phase, which accounted for more than 90% of the total PCBs. Particles were the primary vector transporting PCBs into the Anacostia River, suggesting that removal of particles in stormwater runoff using best management practices (BMPs) such as post treatment system likely decrease PCBs significantly. PCB congener patterns found in stormwater samples clearly explain stormwater runoff is a major transport pathway adding substantial amount of PCBs to the tidal Anacostia River.
Subject(s)
Polychlorinated Biphenyls/analysis , Water Pollutants, Chemical/analysis , Chromatography, Gas , District of Columbia , Fresh WaterABSTRACT
To assess potential health risks to benthic organisms from exposure to toxic contaminants, sediment chemistry data from five salt marshes along the coast of California were compared with threshold effects levels (TELs) and probable effects levels (PELs). As an integrated estimate of toxicity potential of multiple contaminants, mean PEL quotients (mPELQs) were used to categorize sampling stations into three groups: high (>0.5), medium (0.1-0.5) and low (<0.1). In all sediments from Stege Marsh located in San Francisco Bay, at least one contaminant exceeded PELs by up to 18-fold and mPELQs were higher than 0.7. Mean PELQs in two core sediments from eastern Stege Marsh ranged from 0.7 to 2.1, indicating that benthic organisms in Stege Marsh may have been adversely affected for several decades. To investigate bioavailability and bioaccumulation of contaminants in sediments, longjaw mudsuckers (Gillichthys mirabilis) were transplanted to six Stege Marsh stations for 60 days. Body burdens of organic contaminants clearly showed that they were readily available for benthic organisms. Measured concentrations of organic contaminants in mudsuckers were similar to estimated levels computed using a theoretical bioaccumulation potential model. Levels of PCBs and arsenic in mudsuckers were higher than screening values set as guidelines for the protection of humans and levels of PCBs and DDTs were higher than criteria for wildlife. The results of this study indicate that the levels of contaminants in Stege Marsh sediments may not fully support the well-being of benthic organisms and also may provoke adverse effects on fish-eating animals and humans through trophic transfer.
Subject(s)
Geologic Sediments/analysis , Water Pollution/analysis , Wetlands , Animals , California , Perciformes/growth & development , Perciformes/metabolism , Seawater/analysis , United StatesABSTRACT
The Pacific Estuarine Ecosystem Indicators Research Consortium seeks to develop bioindicators of toxicant-induced stress and bioavailability for wetland biota. Within this framework, the effects of environmental and pollutant variables on microbial communities were studied at different spatial scales over a 2-year period. Six salt marshes along the California coastline were characterized using phospholipid fatty acid (PLFA) analysis and terminal restriction fragment length polymorphism (TRFLP) analysis. Additionally, 27 metals, six currently used pesticides, total polychlorinated biphenyls and polycyclic aromatic hydrocarbons, chlordanes, nonachlors, dichlorodiphenyldichloroethane, and dichlorodiphenyldichloroethylene were analyzed. Sampling was performed over large (between salt marshes), medium (stations within a marsh), and small (different channel depths) spatial scales. Regression and ordination analysis suggested that the spatial variation in microbial communities exceeded the variation attributable to pollutants. PLFA analysis and TRFLP canonical correspondence analysis (CCA) explained 74 and 43% of the variation, respectively, and both methods attributed 34% of the variation to tidal cycles, marsh, year, and latitude. After accounting for spatial variation using partial CCA, we found that metals had a greater effect on microbial community composition than organic pollutants had. Organic carbon and nitrogen contents were positively correlated with PLFA biomass, whereas total metal concentrations were positively correlated with biomass and diversity. Higher concentrations of heavy metals were negatively correlated with branched PLFAs and positively correlated with methyl- and cyclo-substituted PLFAs. The strong relationships observed between pollutant concentrations and some of the microbial indicators indicated the potential for using microbial community analyses in assessments of the ecosystem health of salt marshes.
Subject(s)
Bacteria/isolation & purification , Ecosystem , Fresh Water/microbiology , Geologic Sediments/microbiology , Sodium Chloride , Bacteria/classification , Bacteria/genetics , California , Fatty Acids/analysis , Genetic Variation , Metals, Heavy/pharmacology , Phospholipids/analysis , Polymorphism, Restriction Fragment Length , Seasons , Water Pollutants, Chemical/pharmacologyABSTRACT
Surface sediment samples (0-5 cm) from 5 tidal salt marshes along the coast in California, USA were analyzed to investigate the occurrence and anthropogenic input of trace metals. Among study areas, Stege Marsh located in the central San Francisco Bay was the most contaminated marsh. Concentrations of metals in Stege Marsh sediments were higher than San Francisco Bay ambient levels. Zinc (55.3-744 microg g(-1)) was the most abundant trace metal and was followed by lead (26.6-273 microg g(-1)). Aluminum normalized enrichment factors revealed that lead was the most anthropogenically impacted metal in all marshes. Enrichment factors of lead in Stege Marsh ranged from 8 to 49 (median=16). Sediments from reference marshes also had high enrichment factors (2-8) for lead, indicating that lead contamination is ubiquitous, possibly due to continuous input from atmospherically transported lead that was previously used as a gasoline additive. Copper, silver, and zinc in Stege Marsh were also enriched by anthropogenic input. Though nickel concentrations in Stege Marsh and reference marshes exceeded sediment quality guidelines, enrichment factors indicated nickel from anthropogenic input was negligible. Presence of nickel-rich source rock such as serpentinite in the San Francisco Bay watershed can explain high levels of nickel in this area. Coefficients of variation were significantly different between anthropogenically impacted and non-impacted metals and might be used as a less conservative indicator for anthropogenic input of metals when enrichment factors are not available.
Subject(s)
Geologic Sediments/chemistry , Metals/analysis , Trace Elements/analysis , Water Pollutants, Chemical/analysis , CaliforniaABSTRACT
Surface sediment samples (0-5 cm) from five tidal marshes along the coast of California, USA were analyzed for organic pollutants to investigate their relationship to land use, current distribution within marshes, and possible sources. Among the study areas, Stege Marsh, located in San Francisco Bay, was the most contaminated. Compared to San Francisco Bay, Stege Marsh had much higher levels of organic contaminants such as PCBs (polychlorinated biphenyls), DDTs, and chlordanes. At reference marshes (Tom's Point and Walker Creek in Tomales Bay), organic contaminants in sediments were very low. While PAHs (polycyclic aromatic hydrocarbons) were found at all of the study areas (22-13,600 ng g(-1)), measurable concentrations of PCBs were found only in the sediments from Stege Marsh (80-9,940 ng g(-1)). Combustion related (pyrogenic) high molecular weight PAHs were dominant in sediments from Stege and Carpinteria Marshes, while in sediments from Tom's Point and Walker Creek petroleum related (petrogenic) low molecular weight PAHs and alkyl-substituted PAHs were much more abundant than pyrogenic PAHs. PCB congener patterns in all of the Stege Marsh samples were the same and revealed that Aroclor 1248 was a predominant source. In all marshes, the sum of DDE and DDD accounted for more than 90% of total DDTs, indicating that DDT has degraded significantly. The ratios of p,p'-DDE to p,p'-DDD in sediments from Stege Marsh provide evidence of possible previous use of technical DDD. Chlordane ratios indicated that chlordanes have degraded slightly. Bis(2-ethylhexyl)phthalate (280-32,000 ng g(-1)) was the most abundant phthalate. The data indicates that Stege Marsh may be a source of contaminants that continue to be discharged into San Francisco Bay.
Subject(s)
Environmental Monitoring , Geologic Sediments/chemistry , Organic Chemicals/analysis , Salts/analysis , Water Pollutants, Chemical/analysis , CaliforniaABSTRACT
To investigate the sources, fate, and transport dynamics of PAHs (polycyclic aromatic hydrocarbons) in stormwater runoff that is a leading source of pollution in urban watersheds, storm and base flow samples were collected in six branches along the lower Anacostia River. PAHs in storm flow (1510-12,500 ng/L) were significantly enriched in the particle phase, which accounted for 68-97% of the total PAHs. It suggests that reducing particles in stormwater using post-treatment system would decrease PAHs considerably. The solid-water distribution coefficients (KD) of PAHs in the storm flow samples were up to 340 times higher than predicted values. A greater portion of high molecular weight PAHs and their distribution patterns indicate higher contribution of automobile originated pyrogenic PAHs. Total suspended solids in storm flow had a positive relationship with flow rates and exceeded benchmark level for the protection of aquatic biota in some samples.
Subject(s)
Polycyclic Aromatic Hydrocarbons/analysis , Rivers/chemistry , Water Pollutants, Chemical/analysis , District of Columbia , Environmental Monitoring/methods , Geologic Sediments , Molecular Weight , Urban Health , Vehicle Emissions/analysis , Water Movements , Water Purification/methodsABSTRACT
Contaminated oysters from near the Galveston Bay Ship Channel ([GBSC], TX, USA) were transplanted into clean aquariums in order to investigate the recovery of their lysosomal health. Destabilized lysosomes in the oyster hemocytes recovered from 81% to 34% after 23 d of elimination. Chemical analyses showed that transplanted oysters eliminated organic chemicals they had accumulated in their tissue. Enhanced lysosomal health (i.e., decreased lysosomal destabilization) was correlated positively with lower tissue concentrations of chemicals. This study indicates that lysosomal destabilization is a transient biomarker, which indicates only the current status (e.g., within one month) of chemical exposure and potential adverse biological effects. Analytical measurements revealed that polycyclic aromatic hydrocarbons (PAHs) generally were eliminated faster than polychlorinated biphenyls (PCBs) by a factor of 5 to 7. Body burdens of PCBs decreased exponentially, while the elimination pattern of PAHs were biphasic, representing a faster elimination during the early phase of elimination and, subsequently, a much slower elimination. This indicates that elimination of PAHs in the oysters is more complex and may include additional mechanisms compared to the uptake and elimination of PCBs.