Total petroleum hydrocarbon distribution in soils and groundwater in Songyuan oilfield, Northeast China

In order to investigate the distribution of the total petroleum hydrocarbons (TPH) in groundwater and soil, a total of 71 groundwater samples (26 unconfined groundwater samples, 37 confined groundwater samples, and 8 deeper confined groundwater samples) and 80 soil samples were collected in the Songyuan oilfield, Northeast China, and the vertical variation and spatial variability of TPH in groundwater and soil were assessed. For the groundwater from the unconfined aquifer, petroleum hydrocarbons were not detected in three samples, and for the other 23 samples, concentrations were in the range 0.01–1.74 mg/l. In the groundwater from the confined aquifer, petroleum hydrocarbons were not detected in two samples, and in the other 35 samples, the concentrations were 0.04–0.82 mg/l. The TPH concentration in unconfined aquifer may be influenced by polluted surface water and polluted soil; for confined aquifer, the injection wells leakage and left open hole wells may be mainly responsible for the pollution. For soils, the concentrations of TPH varied with sampling depth and were 0–15 cm (average concentration, 0.63 mg/g), >40–55 cm (average concentration, 0.36 mg/g), >100–115 cm (average concentration, 0.29 mg/g), and >500–515 cm (average concentration, 0.26 mg/g). The results showed that oil spillage and losses were possibly the main sources of TPH in soil. The consequences concluded here suggested that counter measures such as remediation and long-term monitoring should be commenced in the near future, and effective measures should be taken to assure that the oilfields area would not be a threat to human health.     

Relative Phytoplankton growth responses to physically and chemically dispersed South Louisiana sweet crude oil

We conducted controlled laboratory exposure experiments to assess the toxic effects of water-accommodated fractions (WAFs) of South Louisiana sweet crude oil on five phytoplankton species isolated from the Gulf of Mexico. Experiments were conducted with individual and combinations of the five phytoplankton species to determine growth inhibitions to eight total petroleum hydrocarbon (TPH) equivalent concentrations ranging from 461 to 7,205 ppb. The composition and concentration of crude oil were altered by physical and chemical processes and used to help evaluate crude oil toxicity. The impact of crude oil exposure on phytoplankton growth varied with the concentration of crude oil, species of microalgae, and their community composition. At a concentration of TPH <?1,200 ppb, dinoflagellate species showed significantly better tolerance, while diatom species showed a higher tolerance to crude oil at higher concentrations of TPH. For both groups, the larger species were more tolerant to crude oil than smaller ones. The toxicity potential of crude oil seems to be strongly influenced by the concentration of polycyclic aromatic hydrocarbons (PAHs). The addition of the dispersant, Corexit® EC9500A, increased the amount of crude oil up to 50-fold in the water column, while the physical enhancement (vigorous mixing of water column) did not significantly increase the amount of TPH concentration in the water column. The species response to crude oil was also examined in the five-species community. Each phytoplankton species showed considerably less tolerance to crude oil in the five-species community compared to their individual responses. This study provides baseline information about individual phytoplankton responses to crude oil and dispersed crude oil for subsequent research efforts seeking to understand the impacts of oil on the phytoplankton in the bigger picture.     

Mercury in small Illinois fishes: historical perspectives and current issues

Documenting long-term trends in mercury deposition and/or accumulation is important in setting regulatory benchmarks, modeling contaminant transfer and flux, measuring success of environmental controls, and even assigning responsibility for pollution. We conducted a study to compare mercury concentrations in small fishes from “high-mercury” and “low-mercury” regions of Illinois, as well as to examine historic patterns of mercury availability using preserved fishes. Mercury concentrations were greater in four species of small fishes collected from a stream in a “high-mercury” region than in those same taxa collected from a stream in a “low-mercury” area in Illinois. Mercury concentrations in blackstripe topminnows (Fundulus notatus) declined dramatically between 1900 and 1961/2006 in the “high-mercury” stream, presumably due reductions in mercury releases from local and regional sources. Preserved fish had an apparent increase in mercury concentrations for up to 12 months, which is consistent with changes in mass and loss of proteins observed in other studies, and we recommend that recent samples be preserved for at least 12 months before comparison with older fluid-preserved material. Based on our results, further studies of mercury in small fishes in Illinois streams appear warranted.     

Release of arsenic (As) and lead (Pb) from quicklime-sulfate stabilized/solidified soils under diffusion-controlled conditions

A quicklime-sulfate-based stabilization/ solidification (S/S) process for arsenic (As) and lead (Pb) immobilization was evaluated under “semi-dynamic” leaching conditions. In order to simulate aggressive leaching conditions the semi-dynamic leaching tests was modified by using 0.014 N of acetic solution instead of distilled water. Kaolinite-sand and montmorillonite-sand soil samples were artificially contaminated with As and Pb, compacted and cured for 28 days. The semi-dynamic leaching tests were then conducted for 90 days. The effectiveness of the S/S treatment was evaluated by assessing the cumulative release of As and Pb as well as by determining the diffusion coefficients (D _eff) and leachability indices (LX). The release of As and Pb was greatly reduced by quicklime-sulfate treatment as compared to untreated samples. Moreover, the quicklime-sulfate treatment was more effective than the quicklime-only treatment in reducing both As and Pb release. The controlling leaching mechanisms were determined using a diffusion theory model. Upon S/S treatment, As and Pb release was diffusion controlled. The LX of all the treated samples were greater than nine, suggesting that S/S treated samples were suitable for “controlled utilization”.     

Spatial distribution and concentration assessment of total petroleum hydrocarbons in the intertidal zone surface sediment of Todos os Santos Bay, Brazil

The primary objective of this study was to investigate the concentrations and spatial distribution of the total petroleum hydrocarbons (TPHs) in the intertidal zone surface sediment of Todos os Santos Bay, Brazil, to assess the distribution and degree of contamination by TPHs, measure the level of TPH degradation in the surface sediment, and identify the organic matter sources. The surface sediment used in this study was collected in 50 stations, and TPHs, isoprenoid alkanes (pristane and phytane), and unresolved complex mixture (UCM) were analyzed by gas chromatography with a flame ionization detector. The total concentrations ranged from 0.22 to 40,101 μg g^?1 dry weight and showed a strong correlation with the total organic carbon (TOC) content. The highest TPH concentrations were observed in samples from the mangrove sediments of a river located near a petroleum refinery. Compared with other studies in the world, the TPH concentrations in the intertidal surface sediment of Todos os Santos Bay were below average in certain stations and above average in others. An analysis of the magnitude of UCM (0.11 to 17,323 μg g^?1 dry weight) and the ratios nC17/Pr and nC18/Ph suggest that an advanced state of oil weathering, which indicates previous contamination. The molar C/N ratios varied between 5 and 43, which indicate organic matter with a mixed origin comprising marine and continental contributions.     

Toxicity assessment for petroleum-contaminated soil using terrestrial invertebrates and plant bioassays

The assessment of soil quality after a chemical or oil spill and/or remediation effort may be measured by evaluating the toxicity of soil organisms. To enhance our understanding of the soil quality resulting from laboratory and oil field spill remediation, we assessed toxicity levels by using earthworms and springtails testing and plant growth experiments. Total petroleum hydrocarbons (TPH)-contaminated soil samples were collected from an oilfield in Sfax, Tunisia. Two types of bioassays were performed. The first assessed the toxicity of spiked crude oil (API gravity 32) in Organization for Economic Co-operation and Development artificial soil. The second evaluated the habitat function through the avoidance responses of earthworms and springtails and the ability of Avena sativa to grow in TPH-contaminated soils diluted with farmland soil. The EC₅₀ of petroleum-contaminated soil for earthworms was 644 mg of TPH/kg of soil at 14 days, with 67 % of the earthworms dying after 14 days when the TPH content reached 1,000 mg/kg. The average germination rate, calculated 8 days after sowing, varied between 64 and 74 % in low contaminated soils and less than 50 % in highly contaminated soils.     

GC estimation of organic hydrocarbons that threaten shallow Quaternary sandy aquifer Northwestern Gulf of Suez,Egypt

Soil and groundwater contamination is one of the important environmental problems at petroleum-related sites, which causes critical environmental and health defects. Severe petroleum hydrocarbon contamination from coastal refinery plant was detected in a shallow Quaternary sandy aquifer is bordered by Gulf in the Northwestern Gulf of Suez, Egypt. The overall objective of this investigation is to estimate the organic hydrocarbons in shallow sandy aquifers, released from continuous major point-source of pollution over a long period of time (91 years ago). This oil refinery contamination resulted mainly in the improper disposal of hydrocarbons and produced water releases caused by equipment failures, vandalism, and accidents that caused direct groundwater pollution or discharge into the gulf. In order to determine the fate of hydrocarbons, detailed field investigations were made to provide intensive deep profile information. Eight composite randomly sediment samples from a test plot were selected for demonstration. The tested plot was 50 m long?×?50 m wide?×?70 cm deep. Sediment samples were collected using an American auger around the point 29° 57′ 33″ N and 32° 30′ 40″ E in 2012 and covered an area of 2,500 m² which represents nearly 1/15 of total plant area (the total area of the plant is approximately 3.250 km²). The detected total petroleum hydrocarbons (TPHs) were 2.44, 2.62, 4.54, 4.78, 2.83, 3.22, 2.56, and 3.13 wt%, respectively. TPH was calculated by differences in weight and subjected to gas chromatography (GC). Hydrocarbons were analyzed on Hewlett–Packard (HP-7890 plus) gas chromatograph equipped with a flame ionization detector (FID). The percentage of paraffine of the investigated TPH samples was 7.33, 7.24, 7.58, 8.25, 10.25, 9.89, 14.77, and 17.53 wt%, respectively.     

Effects of crude oil residuals on soil chemical properties in oil sites, Momoge Wetland, China

Crude oil exploration and production has been the largest anthropogenic factor contributing to the degradation of Momoge Wetland, China. To study the effects of crude oil on wetland soils, we examined the total petroleum hydrocarbon (TPH), total organic carbon (TOC), total nitrogen (TN), and total phosphorus (TP), as well as pH and electricity conductivity (EC) from oil sites and uncontaminated areas in the Momoge Wetland. All contaminated areas had significantly higher (p < 0.05) contents of TPH and TOC, but significantly lower (p < 0.05) TN contents than those of the uncontaminated areas. Contaminated sites also exhibited significantly higher (p < 0.05) pH values, C/N and C/P ratios. For TP contents and EC, no significant changes were detected. The level of soil contamination and impact of oil residuals on soil quality greatly depended on the length of time the oil well was in production. Oil residuals had caused some major changes in the soils’ chemical properties in the Momoge Wetland.     

On the effects of the dispersant Corexit 9500© during the degradation process of n-alkanes and PAHs in marine sediments

In many coastal countries, oil spill contingency plans include several alternatives for removal of the spilled oil from the ocean. Frequently, these plans include dispersants. Because this process applies chemical substances that may add toxicity to oil that already contains toxic compounds, it is, at times, a controversial method to fight oil pollution. Additionally, local conditions may result in particular complications. We investigated the possible effects of the dispersant Corexit 9500© under conditions similar to those of subtropical oceans. We used fuel oil #6+ diesel as the test mixture. Under certain conditions, at least part of the dispersed oil may reach the sediment, particularly if the dispersant is applied in coastal waters. Nine experimental units were used in this experiment. Similar conditions of water temperature, salinity, air fluxes into the experimental units, and hydrocarbon concentrations in sediments were used. Two treatments and one control, each one with three replicates, were carried out. We concentrated our investigation on sediment, although measurements of water were also taken. Our results suggest that once the oil has penetrated the sediment, no significant differences exist between oil that contains dispersant and oil without dispersant. Noticeable degradation of aliphatic hydrocarbons occurred mainly in the low molecular weight aliphatic hydrocarbons and not in the others. Apparently, degradation of aromatics was easier than that of alkanes. However, some differences were noticed for the degradation of PAHs in the sediment, suggesting a faster degradation under particular conditions in aerobic environments such as under this experiment.     

Lead (Pb) quantification in potable water samples: implications for regulatory compliance and assessment of human exposure

Assessing the health risk from lead (Pb) in potable water requires accurate quantification of the Pb concentration. Under worst-case scenarios of highly contaminated water samples, representative of public health concerns, up to 71–98 % of the total Pb was not quantified if water samples were not mixed thoroughly after standard preservation (i.e., addition of 0.15 % (v/v) HNO₃). Thorough mixing after standard preservation improved recovery in all samples, but 35–81 % of the total Pb was still un-quantified in some samples. Transfer of samples from one bottle to another also created high errors (40–100 % of the total Pb was un-quantified in transferred samples). Although the United States Environmental Protection Agency’s standard protocol avoids most of these errors, certain methods considered EPA-equivalent allow these errors for regulatory compliance sampling. Moreover, routine monitoring for assessment of human Pb exposure in the USA has no standardized protocols for water sample handling and pre-treatment. Overall, while there is no reason to believe that sample handling and pre-treatment dramatically skew regulatory compliance with the US Pb action level, slight variations from one approved protocol to another may cause Pb-in-water health risks to be significantly underestimated, especially for unusual situations of “worst case” individual exposure to highly contaminated water.     

Assessment of organochlorine pesticides and plasticisers in the Selangor River basin and possible pollution sources

A study on the quality of water abstracted for potable use was conducted in the Selangor River basin from November 2008 to July 2009. Seven sampling sites representing the intake points of water treatment plants in the basin were selected to determine the occurrence and level of 15 organochlorine pesticides (OCPs), six phthalate esters (PAEs) and bisphenol A (BPA). Results indicated OCPs were still detected regularly in 66.1 % of the samples with the Σ₁₅OCPs ranging from 0.6–25.2 ng/L. The first data on PAEs contamination in the basin revealed Σ₆PAEs concentrations were between 39.0 and 1,096.6 ng/L with a median concentration of 186.0 ng/L while BPA concentration ranged from <1.2 to 120.0 ng/L. Although di-n-butyl phthalate was detected in all the samples, concentrations of di-ethyl(hexyl)phthalate were higher. Sampling sites located downstream recorded the highest concentrations, together with samples collected during the dry season. Comparison of the detected contaminants with the Department of Environment Water Quality Index (DOE-WQI) showed some agreement between the concentration and the current classification of stream water. While the results suggest that the sites were only slightly polluted and suitable to be used as drinking water source, its presence is cause for concern especially to the fragile firefly “Pteroptyx tener” ecosystem located further downstream.     

Performance of EIA authority and effectiveness of EIA system in Pakistan

Environmental Impact Assessment (EIA) agencies worldwide face multiple challenges that compromise their performance and in turn EIA procedural effectiveness. The current study aimed to evaluate the performance of the Environmental Protection Agency (EPA) of Punjab, Pakistan and the problems it faces whilst implementing EIA and ensuring EIA effectiveness. Semi-structured interviews were used to collect data for the study. EPA performance and procedural effectiveness were evaluated using the formal and informal roles of EPA and EIA good practices respectively. They were also linked to regulatory framework, capacities of actors and contextual factors. Study found that EPA and EIA system performance is weak. Consequently, procedural effectiveness is compromised. The main causes include limited capacities of EPA, consultants and proponents; lack of political will; political interference and outdated regulations. A strong political will of the government is required to enhance the capacity of EPA and other actors in terms of motivation or “the will to” and means or “the ability to”. Measures taken by international EIA agencies to improve performance and effectiveness have also been discussed. Based on this study, lessons can be learnt by not only EPA Punjab but also other agencies in Pakistan and international agencies facing similar challenges.     

Assessing soil and groundwater contamination in a metropolitan redevelopment project

The purpose of this study was to assess contaminated soil and groundwater for the urban redevelopment of a rapid transit railway and a new mega-shopping area. Contaminated soil and groundwater may interfere with the progress of this project, and residents and shoppers may be exposed to human health risks. The study area has been remediated after application of first remediation technologies. Of the entire area, several sites were still contaminated by waste materials and petroleum. For zinc (Zn) contamination, high Zn concentrations were detected because waste materials were disposed in the entire area. For petroleum contamination, high total petroleum hydrocarbon (TPH) and hydrocarbon degrading microbe concentrations were observed at the depth of 7 m because the underground petroleum storage tank had previously been located at this site. Correlation results suggest that TPH (soil) concentration is still related with TPH (groundwater) concentration. The relationship is taken into account in the Spearman coefficient (α).     

Detection of seasonal variations in surface water quality using discriminant analysis

In the study, discriminant analysis (DA) was applied to water quality data set monitored in winter and summer months along 3 years to investigate seasonal variations of Tahtali Reservoir water quality. The variables were divided into two categories as “parameters naturally found in surface waters—Al, Fe, Mn, F, Ba, Cl, and SO₄” and “pollutants—biochemical oxygen demand, chemical oxygen demand, and NO₃”. Linear discriminant functions were calculated to distinguish between winter and summer samples. Results revealed that water quality variables (naturally found in surface water and also pollutants) were distinctly different between two seasons. Seasonal changes of water quality caused by anthropogenic activities should be taken into consideration by the water managers especially in summer seasons in which higher concentrations were observed. The study showed that DA can be applied successfully to establish the seasonal variation in surface water quality and make it possible to design a future temporal sampling strategy in an optimal manner.     

Nutrient baselines of Cerrado low-order streams: comparing natural and impacted sites in Central Brazil

The aquatic systems responsible for water supply in the Brazilian Federal District (FD) have been threatened by anthropogenic pressures, especially considering the expressive demographic increase in the region during the last decades. The purposes of this research were: (a) to assess the water quality in streams located in the FD by monitoring physical–chemical variables; (b) to define baselines for these variables among different ecological status categories. The 14 investigated streams were sampled between 2006 and 2009, in the dry (August–September, 2006, 2008, 2009) and rainy (March–April, 2008, 2009) seasons. All sampling sites were classified in four categories (“very impacted”, “impacted”, “in transition” and “natural”) using an adaptation of a rapid habitat assessment protocol. Differences in water quality among sites were generally well predicted in the four ecological status categories defined by the protocol, which showed a gradient in nutrient concentrations from reference sites classified as “natural” (medians: electrical conductivity?=?7.3 μS cm^?1; nitrate?=?0.040 mg L^?1; ammonium?=?0.039 mg L^?1; soluble reactive phosphorus (SRP)?=?<0.001 mg L^?1; total phosphorus (TP)?=?0.006 mg L^?1; ) to those classified as “very impacted” (medians: electrical conductivity?=?87.7 μS cm^?1; nitrate?=?0.247 mg L^?1; ammonium?=?0.219 mg L^?1; SRP?=?0.010 mg L^?1; TP?=?0.035 mg L^?1). Point sources inputs were the main factor for water quality deterioration. The nutrient baselines reported were relatively low when compared to data collected from reference areas in Brazil (e.g., São Paulo State) or temperate regions, especially for TP.     

The use of sensory perception indicators for improving the characterization and modelling of total petroleum hydrocarbon (TPH) grade in soils

This paper proposes a multistep approach for creating a 3D stochastic model of total petroleum hydrocarbon (TPH) grade in potentially polluted soils of a deactivated oil storage site by using chemical analysis results as primary or hard data and classes of sensory perception variables as secondary or soft data. First, the statistical relationship between the sensory perception variables (e.g. colour, odour and oil–water reaction) and TPH grade is analysed, after which the sensory perception variable exhibiting the highest correlation is selected (oil–water reaction in this case study). The probabilities of cells belonging to classes of oil–water reaction are then estimated for the entire soil volume using indicator kriging. Next, local histograms of TPH grade for each grid cell are computed, combining the probabilities of belonging to a specific sensory perception indicator class and conditional to the simulated values of TPH grade. Finally, simulated images of TPH grade are generated by using the P-field simulation algorithm, utilising the local histograms of TPH grade for each grid cell. The set of simulated TPH values allows several calculations to be performed, such as average values, local uncertainties and the probability of the TPH grade of the soil exceeding a specific threshold value.     

Remediation of hydrocarbons in crude oil-contaminated soils using Fenton’s reagent

Sandy soil samples spiked with Bonny light crude oil were subsequently treated with Fenton's reagent at acidic, neutral, and basic pH ranges. Oil extracts from these samples including an untreated one were analyzed 1?week later with a gas chromatograph to provide evidence of hydrocarbon depletion by the oxidant. The reduction of three broad hydrocarbon groups-total petroleum hydrocarbon (TPH); benzene, toluene, ethylbenzene, and xylene (BTEX); and polycyclic aromatic hydrocarbon (PAH) were investigated at various pHs. Hydrocarbon removal was efficient, with treatment at the acidic pH giving the highest removal of about 96% for PAH, 99% for BTEX, and some TPH components experiencing complete disappearance. The four-ringed PAHs were depleted more than their three-ringed counterparts at the studied pH ranges.     

A Pilot Study on Using Urinary 1-Hydroxypyrene Biomarker for Exposure to PAHs in Beijing

To study whether the urinary 1-hydroxypyrene (1-OHP) could be the biomarker of atmospheric PAHs, a small-scale pilot study was carried out on the relation of 1-OHP vs PAHs with the traffic policemen in Beijing of smokers and nonsmokers to be subgroups in both the exposure and control groups. Both the PAHs and 1-OHP were analyzed with high performance liquid chromatography (HPLC). The ambient concentrations of PAHs were different at the different sites (the average sum of PAHs (TPAH) were 12.36, 16.27, 18.37 ng/m³ at the suburban residential, police station and high traffic area, respectively.), but considerably lower than the personal-exposure concentrations (the average TPAH were 65.84 and 47.28 ng/m³ for patrol cars and inspection station, respectively). Pyrene was correlated well with BaP and the summed PAHs (TPAH), with the correlation coefficients (R) of 0.79, 0.87 for ambient level and 0.92, 0.96 for personal exposure, respectively. The average of 1-hydroxypyrene of smokers and nonsmokers were 0.39, 0.15 μmol/mol creatinine in control group and 0.57, 0.33 μmol/mol creatinine in exposure group, respectively. The better correlation of pyrene to BaP and TPAH especially for personal exposure samples indicated that the probability of urinary 1-hydroxypyrene, the metabolite of pyrene, to be the biomarker of total PAH. Nonsmokers in the exposure and control groups had indistinguishable levels of 1-OHP, presumably because the ambient levels of pyrene were so similar (the average were 3.25, 3.20 ng/m³ at the police station and high traffic area, respectively.). Smokers in the control group had significantly higher 1-OHP than that of the nonsmokers, but showed indistinguishable differences in the exposure group. These results suggested that urinary 1-OHP could be a biomarker of PAHs only when the level of PAHs was at a relatively higher level. Smoking as an important influencing factor need to be controlled carefully.     

Determination of total petroleum hydrocarbons (TPH) in agricultural soils near a petrochemical complex in Guangzhou,China

The total petroleum hydrocarbons (TPH) pollution in regional agricultural soils was investigated. Seventy soil samples collected from surface layers (0–20 cm) and horizons of five selected pedons in the vicinity of a petrochemical complex in Guangzhou, China were analyzed, and the vertical variation and spatial variability of TPH were evaluated. The TPH concentration in top soils around the petrochemical complex ranged from 1,179.3 to 6,354.9 mg kg^− 1, with the average of 2,676.6 mg kg^− 1. Furthermore, significant differences between land-use types showed that the TPH concentration in top soils was strongly influenced by accidental spills. Both the TPH trends in pedons and the identified hot-spot areas also showed that the accidental explosions or burning accidents were mainly responsible for the pollution. The results reported here suggest that the regular monitoring and inspection shall be conducted for safety and to avoid or minimize the accidents, and the effective measures should be taken to remediate the contaminated areas and to assure that the important industrialization of Guangzhou area would not mean human health risks near the petrochemical complex.     

Snapshot of Vibrio parahaemolyticus densities in open and closed shellfish beds in Coastal South Carolina and Mississippi

Vibrio parahaemolyticus is a Gram negative, halophilic bacterium that is ubiquitous in warm, tropical waters throughout the world. It is a major cause of seafood-associated gastroenteritis and is generally associated with consumption of raw or undercooked seafood, especially oysters. This study presents a snapshot of total V. parahaemolyticus densities in surface waters and shellstock American oysters (Crassostrea virginica) from open and closed shellfish harvesting areas, as well as “more rural areas” on two different US coasts, the Atlantic and the Gulf. Sampling was conducted from 2001 to 2003 at five sites near Charleston/Georgetown, SC and at four locations in the Gulfport/Pascagoula, MS area. V. parahaemolyticus numbers were determined by a direct plating method using an alkaline-phosphatase-labeled DNA probe targeting the species-specific thermolabile hemolysin gene (tlh) that was used for identification of bacterial isolates. The greatest difference between the two coasts was salinity; mean salinity in SC surface waters was 32.9 ppt, whereas the mean salinity in MS waters was 19.2 ppt, indicating more freshwater input into MS shellfish harvesting areas during the study period. The mean V. parahaemolyticus numbers in oysters were almost identical between the two states (567.4 vs. 560.1 CFU/g). Bacterial numbers in the majority of surface water samples from both states were at or below the limit of detection (LOD?=?<10 CFU/mL). The bacterial concentrations determined during this study predict a low public health risk from consumption of oysters in shellfish growing areas on either the Gulf or the Atlantic US coast.