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Identification of a novel arsenite oxidase gene, arxA, in the haloalkaliphilic, arsenite-oxidizing bacterium alkalilimnicola ehrlichii strain MLHE-1

Although arsenic is highly toxic to most organisms, certain prokaryotes are known to grow on and respire toxic metalloids of arsenic (i.e., arsenate and arsenite). Two enzymes are known to be required for this arsenic-based metabolism: (i) the arsenate respiratory reductase (ArrA) and (ii) arsenite oxidase (AoxB). Both catalytic enzymes contain molybdopterin cofactors and form distinct phylogenetic clades (ArrA and AoxB) within the dimethyl sulfoxide (DMSO) reductase family of enzymes. Here we report on the genetic identification of a “new” type of arsenite oxidase that fills a phylogenetic gap between the ArrA and AoxB clades of arsenic metabolic enzymes. This “new” arsenite oxidase is referred to as ArxA and was identified in the genome sequence of the Mono Lake isolate Alkalilimnicola ehrlichii MLHE-1, a chemolithoautotroph that can couple arsenite oxidation to nitrate reduction. A genetic system was developed for MLHE-1 and used to show that arxA (gene locus ID mlg _ 0216 ) was required for chemoautotrophic arsenite oxidation. Transcription analysis also showed that mlg _ 0216 was only expressed under anaerobic conditions in the presence of arsenite. The mlg _ 0216 gene is referred to as arxA because of its greater homology to arrA relative to aoxB and previous reports that implicated Mlg_0216 (ArxA) of MLHE-1 in reversible arsenite oxidation and arsenate reduction in vitro . Our results and past observations support the position that ArxA is a distinct clade within the DMSO reductase family of proteins. These results raise further questions about the evolutionary relationships between arsenite oxidases (AoxB) and arsenate respiratory reductases (ArrA). Arsenic is toxic to most organisms and is known to cause cancer in humans. However, bacteria have adapted several biotransformation pathways that function to either couple the reduction or oxidation of arsenicals to energy conservation and growth (1). The enzymologies of these two pathways have several features in common. The arsenate respiratory reductase (ArrAB) and arsenite oxidase (AoxAB) enzymes are usually composed of at least two subunits, a small iron-sulfur cluster-containing subunit (ArrB and AoxA) and a larger molybdopterin-containing catalytic subunit (ArrA and AoxB). Although they catalyze arsenic redox chemistry, ArrA and AoxB form distinct phylogenetic clades within the dimethyl sulfoxide (DMSO) reductase family of molybdenum-containing enzymes (16, 24). Culture-dependent approaches have resulted in the isolation of a variety of diverse bacteria that metabolize arsenic (reviewed in reference 26). Many of these isolates have had their genomes sequenced, which has been insightful for understanding the composition and diversity of arr and aox gene clusters. In the arsenite-oxidizing nitrate reducer Alkalilimnicola ehrlichii strain MLHE-1 (a haloalkaliphile isolated from Mono Lake [CA]) (10, 15), bioinformatic analysis of its genome revealed the absence of genes homologous to the arsenite oxidase genes of the aoxB type. Instead, two genes ( mlg _ 0216 and mlg _ 2426 ) were identified that better resembled the catalytic subunit of the arsenate respiratory reductase (20); however, MLHE-1 has not been shown to respire (or reduce) arsenate (15). Recent work by Richey et al. (20) showed that the Mlg_0216 protein (and not Mlg_2426) was expressed under chemolithoautotrophic (10 mM arsenite and 10 mM nitrate) growth conditions. Moreover, it was shown that Mlg_0216 exhibits both arsenate reductase and arsenite oxidase activities in vitro . These observations raised the question, is the mlg _ 0216 gene required for arsenite oxidation in vivo ? In this report, we addressed this question by developing a genetic system in MLHE-1, generating strains with mutations in mlg _ 0216 and mlg _ 2426 , and physiologically characterizing the resulting strains. Our results implicate mlg _ 0216 in chemolithoautotrophic arsenite oxidation coupled to nitrate respiration.

Journal of Bacteriology↗

Gas-water-rock interactions in Frio Formation following CO 2 injection: Implications for the storage of greenhouse gases in sedimentary basins

To investigate the potential for the geologic storage of CO 2 in saline sedimentary aquifers, 1600 t of CO 2 were injected at 1500 m depth into a 24-m-thick sandstone section of the Frio Formation, a regional brine and oil reservoir in the U.S. Gulf Coast. Fluid samples obtained from the injection and observation wells before CO 2 injection showed a Na-Ca-Cl–type brine with 93,000 mg/L total dissolved solids (TDS) at near saturation with CH 4 at reservoir conditions. Following CO 2 breakthrough, samples showed sharp drops in pH (6.5–5.7), pronounced increases in alkalinity (100–3000 mg/L as HCO 3 ) and Fe (30–1100 mg/L), and significant shifts in the isotopic compositions of H 2 O, dissolved inorganic carbon (DIC), and CH 4 . Geochemical modeling indicates that brine pH would have dropped lower but for the buffering by dissolution of carbonate and iron oxyhydroxides. This rapid dissolution of carbonate and other minerals could ultimately create pathways in the rock seals or well cements for CO 2 and brine leakage. Dissolution of minerals, especially iron oxyhydroxides, could mobilize toxic trace metals and, where residual oil or suitable organics are present, the injected CO 2 could also mobilize toxic organic compounds. Environmental impacts could be major if large brine volumes with mobilized toxic metals and organics migrated into potable groundwater. The δ 18 O values for brine and CO 2 samples indicate that supercritical CO 2 comprises ∼50% of pore-fluid volume ∼6 mo after the end of injection. Postinjection sampling, coupled with geochemical modeling, indicates that the brine gradually will return to its preinjection composition.

Geology↗

Introduction

Ecotoxicology is the study of the movement of environmental contaminants through ecosystems and their effects on plants and animals. Examining tissue residues of these contaminants in biota is basic to ecotoxicology, both for understanding the movement of contaminants within organisms and through food chains, and for understanding and quantifying injuries to organisms and their communities. This book provides guidance on interpreting tissue concentrations of environmental contaminants. Tissue concentrations have long been used both to identify the cause of toxicity in animals and as a measure of the severity of toxicity. More recently, they have been incorporated into environmental models, tying together exposure, kinetics, and toxic effects. Measuring tissue concentrations is basic to studies on the kinetics of contaminants, which entails characterizing the rates of uptake and elimination in organisms, as well as redistribution (organs, lipid, and plasma) within them. Tissue concentrations are also used in ecological studies examining the movement of contaminants between organisms and within biological communities.

Book chapter↗

Studies of certain sulfonamide drugs for use in juvenile chinook salmon

Sulfamethazine, introduced to fishery medicine by Snieszko and Friddle in 1950, has been widely accepted for treatment of systemic bacterial infections of fish. When administered to fish in their diet, this drug is effective against susceptible bacteria but has the disadvantages of being slowly absorbed (Snieszko and Friddle, 1951) and relatively toxic (Wood, Yasutake, and Johnson, 1957). Today there are many sulfonamides which are more efficacious than sulfamethazine. In domestic animals, sulfisoxazole and sulfadimethoine are absorbed quickly from the gastrointestinal tract and have fewer toxic side reactions, a wider antibacterial spectrum, and better bacteriostatic activity. In the work described in this paper, the efficacies of sulfisoxazole and sulfadimethoxine were compared to the efficacy of sulfamethazine. Experiments were designed to determine the rate of intestinal absorption, the rate of elimination from the blood, the effect on growth, and the toxicity of each drug in juvenile chinook salmon ( Oncorhynchus tshawytscha ). The comparative bacteriostatic activity against two common fish pathogens was also determined for each drug.

Progressive Fish-Culturist↗

Experiments upon the control of Trichodiniasis of salmonid fishes by the prolonged recirculation of formalin solutions

In a search for more effective disinfectants to combat parasitic diseases of hatchery fish, the authors report results from a series of experiments designed to determine the toxicity of varying exposures to concentrations of formalin, sodium p‐phenolsulphonate, ammonium sulphate, and sodium benzoate. Non‐toxic concentrations of these disinfectants were tested, in addition to the usual hatchery methods of salt treatment and hand dipping in copper sulphate and acetic acid solutions, on No. 1 brook trout fingerlings which had been experimentally infected with the protozoan parasite Trichodina sp. (previously known as Cyclochaeta sp.). Of the disinfectants tested, only formalin completely removed all parasites. Salt treatment in a 5 per cent solution, by weight, as well as hand dipping in 1:500 acetic acid, failed to eradicate all parasites present, although a marked reduction in their numbers did occur. The hand dipping in a 1:2,000 copper sulphate solution was found to be without practical value for the removal of parasites. The authors recommend a prolonged treatment for sixty minutes by recirculating a 1:4,000 solution of formalin, or, where circumstances permit, a 120‐ to 150‐minute exposure to a 1:6,000 concentration of formalin, as the most effective, most economical, and least toxic treatments for combating infections of Trichodina sp., and presumably those of other external parasites as well, among hatchery fish.

Transactions of the American Fisheries Society↗

Selective control of common carp: Ineffectiveness of 2-(digeranylamino)-ethanol (GD-174) in pond trials

The candidate piscicide, 2‐(digeranylamino)‐ethanol, (commonly known as GD‐174) was subjected to efficacy trials in ponds under a wide variety of conditions. Results of the trials were disappointing considering that laboratory tests had shown the compound to be selectively toxic to common carp ( Cyprinus carpio ). Results of pretreatment, on‐site toxicity tests were misleading and indicated concentrations that failed to kill all of the carp in 19 of 23 ponds. In a few instances, the chemical killed the carp with little or no effect on nontarget fishes. No fish were killed in some trials and large numbers of nontarget fishes were killed in others. Twenty of 25 pond trials were judged to be unsuccessful. Success or failure of pond treatments could not be correlated with any particular combination of physical, chemical, and biological factors. Because the activity of GD‐174 against mixed populations of fish cannot be predicted, further development of this compound as a selective toxicant for carp has been discontinued at the National Fishery Research Laboratory.

North American Journal of Fisheries Management↗

Mercury and selenium in American White Pelicans breeding at Pyramid Lake, Nevada

American White Pelicans (Pelecanus erythrorhynchos) that breed on Anaho Island, Pyramid Lake, Nevada, are potentially exposed to a variety of contaminants. Therefore, the reproductive success of this colony was monitored in 1996 and eggs, blood and feathers from nestlings, livers from adults and nestlings, regurgitated fish from nestlings, and fish from representative feeding areas were collected and analyzed for mercury and selenium to determine exposure to the pelicans and sources of contamination. Additional samples were collected and analyzed in 1988, 1992, and 2004. Reproductive success at the Anaho Island colony was normal in 1996 based on hatching rates of eggs (???75% in undisturbed areas) and survival of nestlings. Mercury and selenium concentrations in eggs were generally below known effect levels and did not appear to have an adverse impact on hatching success. Mercury and selenium concentrations in fish ranged widely, with mercury of greatest concern. Microscopic lesions characteristic of mercury toxicity were absent in pre-fledging nestlings in 1996. Some adult pelicans had elevated mercury concentrations in their livers; however, the potential toxic effects were difficult to evaluate because of probable demethylation of mercury, thereby possibly providing protection from toxicity. Exposure of pelicans to mercury varied among years, most likely in relation to wet-dry cycles and available feeding areas.

Waterbirds↗

Lethal and sublethal effects of ammonia to juvenile Lampsilis mussels (Unionidae) in sediment and water-only exposures

We compared the sensitivity of two juvenile unionid mussels (Lampsilis cardium and Lampsilis higginsii) to ammonia in 96-h water-only and sediment tests by use of mortality and growth measurements. Twenty mussels were placed in chambers buried 2.5 cm into reference sediments to approximate pore-water exposure (sediment tests) or elevated above the bottom of the experimental units (water-only tests). In the sediment tests, a pH gradient existed between the overlying water (mean 8.0), sediment-water interface (mean 7.7), and 2.5 cm depth (mean 7.4). We assumed that mussels were exposed to ammonia in pore water and report effect concentrations in pore water, but if they were exposed to the higher pH water, more of the ammonia would be in the toxic un-ionized (NH 3) form. The only differences in toxicity and growth between mussel species occurred in some of the water-only tests. In sediment tests, median lethal concentrations (LC50s) ranged from 124 to 125 ??g NH3-N/L. In water-only tests, LC50s ranged from 157 to 372 ??g NH3-N/L. In sediment tests, median effective concentrations (EC50s based on growth) ranged from 30 to 32 ??g NH3-N/L. Juvenile mussels in the water-only tests grew poorly and did not exhibit a dose-response relation. These data demonstrate that growth is a sensitive and valuable endpoint for studies on ammonia toxicity with juvenile freshwater mussels and that growth should be measured via sediment tests. ?? 2007 SETAC.

Environmental Toxicology and Chemistry↗

Prediction of lethal/effective concentration/dose in the presence of multiple auxiliary covariates and components of variance

Predictors of the percentile lethal/effective concentration/dose are commonly used measures of efficacy and toxicity. Typically such quantal-response predictors (e.g., the exposure required to kill 50% of some population) are estimated from simple bioassays wherein organisms are exposed to a gradient of several concentrations of a single agent. The toxicity of an agent may be influenced by auxiliary covariates, however, and more complicated experimental designs may introduce multiple variance components. Prediction methods lag examples of those cases. A conventional two-stage approach consists of multiple bivariate predictions of, say, medial lethal concentration followed by regression of those predictions on the auxiliary covariates. We propose a more effective and parsimonious class of generalized nonlinear mixed-effects models for prediction of lethal/effective dose/concentration from auxiliary covariates. We demonstrate examples using data from a study regarding the effects of pH and additions of variable quantities 2???,5???-dichloro-4???- nitrosalicylanilide (niclosamide) on the toxicity of 3-trifluoromethyl-4- nitrophenol to larval sea lamprey (Petromyzon marinus). The new models yielded unbiased predictions and root-mean-squared errors (RMSEs) of prediction for the exposure required to kill 50 and 99.9% of some population that were 29 to 82% smaller, respectively, than those from the conventional two-stage procedure. The model class is flexible and easily implemented using commonly available software. ?? 2007 SETAC.

Environmental Toxicology and Chemistry↗

An enriched stable-isotope approach to determine the gill-zinc binding properties of juvenile rainbow trout (Oncorhynchus mykiss) during acute zinc exposures in hard and soft waters

The objective of the present study was to employ an enriched stable-isotope approach to characterize Zn uptake in the gills of rainbow trout (Oncorhynchus mykiss) during acute Zn exposures in hard water (???140 mg/L as CaCO 3 ) and soft water (???30 mg/L as CaCO 3 ). Juvenile rainbow trout were acclimated to the test hardnesses and then exposed for up to 72 h in static exposures to a range of Zn concentrations in hard water (0-1,000 ??g/L) and soft water (0-250 ??g/L). To facilitate detection of new gill Zn from endogenous gill Zn, the exposure media was significantly enriched with 67 Zn stable isotope (89.60% vs 4.1% natural abundance). Additionally, acute Zn toxicity thresholds (96-h median lethal concentration [LC50]) were determined experimentally through traditional, flow-through toxicity tests in hard water (580 ??g/L) and soft water (110 ??g/L). Following short-term (???3 h) exposures, significant differences in gill accumulation of Zn between hard and soft water treatments were observed at the three common concentrations (75, 150, and 250 ??g/L), with soft water gills accumulating more Zn than hard water gills. Short-term gill Zn accumulation at hard and soft water LC50s (45-min median lethal accumulation) was similar (0.27 and 0.20 ??g/g wet wt, respectively). Finally, comparison of experimental gill Zn accumulation, with accumulation predicted by the biotic ligand model, demonstrated that model output reflected short-term (<1 h) experimental gill Zn accumulation and predicted observed differences in accumulation between hard and soft water rainbow trout gills. Our results indicate that measurable differences exist in short-term gill Zn accumulation following acclimation and exposure in different water hardnesses and that short-term Zn accumulation appears to be predictive of Zn acute toxicity thresholds (96-h LC50s). ?? 2009 SETAC.

Environmental Toxicology and Chemistry↗

Potential impact of Dare County landfills on Alligator River National Wildlife Refuge

Runoff of leachate from East Lake and Dare County Construction and Demolition Debris landfills has the potential to impact wildlife resources at Alligator River National Wildlife Refuge, Dare and Hyde Counties, North Carolina. Sediment quality of samples collected in August 2000 at 14 locations down-gradient from the landfills was assessed by measuring metal and organic contaminants in the sediments, chronic toxicity of solid-phase sediment (28-d static-renewal exposures; survival and growth as test endpoints) and acute toxicity of sediment porewater (96-h static exposures) to Hyalella azteca (Crustacea: Amphipoda). In addition, contaminant bioaccumulation from 4 sediments was determined using 28-d exposures of Lumbriculus variegatus (freshwater oligochaete). Although survival was not impaired, length of H. azteca was significantly reduced in sediments from 5 locations. Pore water from 4 locations was acutely toxic to H. azteca. Metals and a few polycyclic aromatic hydrocarbons (PAHs) were bioaccumulated by L variegatus from the sediments. Several metals and PAHs exceeded sediment quality guidelines, and metals in porewater from several sites exceeded water quality criteria for the protection of aquatic wildlife. Runoff of leachate from the landfills has reduced sediment quality and has the potential to adversely affect wildlife resources at Alligator River National Wildlife Refuge.

North Carolina↗

Calibrating biomonitors to ecological disturbance: a new technique for explaining metal effects in natural waters

Bioaccumulated toxic metals in tolerant biomonitors are indicators of metal bioavailability and can be calibrated against metal‐specific responses in sensitive species, thus creating a tool for defining dose–response for metals in a field setting. Dose–response curves that define metal toxicity in natural waters are rare. Demonstrating cause and effect under field conditions and integrated chemical measures of metal bioavailability from food and water is problematic. The total bioaccumulated metal concentration in any organism that is a net accumulator of the metal is informative about metal bioavailability summed across exposure routes. However, there is typically no one universal metal concentration that is indicative of toxicity, especially across species, largely because of interspecies differences in detoxification. Stressed organisms are also only present across a narrow range in the dose–response curve, limiting the use of singles species as both biomonitors and bioindicator of stress. Herein we show, in 3 field settings, that bioaccumulated Cu concentrations in a metal‐tolerant, riverine biomonitor (species of the caddisfly genus Hydropsyche spp.) can be calibrated against metal‐specific ecological responses across very wide ranges of contamination. Using the calibrated dose–response, we show that reduced abundance of species and individuals from particularly sensitive mayfly families (heptageniid mayflies) is more than 2‐fold more sensitive to bioavailable Cu than other traditional measures of stress like EPT or total number of benthic macroinvertebrate species. We propose that this field dose‐response curve be tested more widely for general application, and that calibrations against other stress responses be developed for biomonitors from lakes, estuaries, and coastal marine ecosystems.

Integrated Environmental Assessment and Management↗

Hazards to wildlife from soil-borne cadmium reconsidered

Cadmium is a toxic element that should be included in environmental risk assessments of contaminated soils. This paper argues, however, that hazards to wildlife from cadmium have often been overstated. The literature contains only meager evidence that wild animals have been seriously harmed by cadmium, even at severely contaminated sites. Although some researchers have reported that wildlife have accumulated concentrations of cadmium in their kidneys that were above suggested injury thresholds, the thresholds may be disputed, since they were well below the World Health Organization criterion of 200 mg/kg (wet weight) of cadmium in the renal cortex for protecting human health. Recent risk assessments have concluded that soil cadmium concentrations less than 1 mg/kg are toxic to soil organisms and wildlife, which implies that background concentrations of cadmium naturally found in soils are hazardous. An examination of the databases used to support these assessments suggested that the toxicity of cadmium has been exaggerated.

Journal of Environmental Quality↗

Dioxins and furans linked to reproductive impairment in wood ducks

A wetland in central Arkansas was contaminated with polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans and because the area was a major waterfowl habitat, we studied the effects of the contamination on nesting wood ducks ( Aix sponsa ) during 1988-90. Residues in wood duck eggs, based on toxicity equivalency factors (TEFs) for combined compounds, ranged from 0.2 to 611 parts per trillion (ppt) wet mass (70% were the toxic isomer 2,3,7,8-tetrachlorodibenzo-p-dioxin (tetraCDD)) and were 50 times higher in eggs from near the point source than from an uncontaminated reference site 111 km away. Nest success, hatching success, and duckling production were suppressed ( P < 0.05) at nesting sites 9 and 17 km downstream, as was hatching success 58 km downstream. Egg TEFs were inversely correlated ( P < 0.001) with productivity in corresponding nests. In addition, teratogenic effects occurred in ducklings at the more contaminated nesting site nearest the point source. The threshold range of toxicity (based on TEFs) where reduced productivity was evident in wood ducks was gt 20-50 ppt. Wood ducks were sensitive to dioxin and furan contamination, and we recommend it as an indicator species for monitoring biological impacts from these contaminants.

Arkansas↗

Pesticide mixtures in the Sacramento–San Joaquin Delta, 2016–17: Results from year 2 of the Delta Regional Monitoring Program

The Delta Regional Monitoring Program was developed by the Central Valley Regional Water Quality Control Board in response to the decline of pelagic fish species in the Sacramento–San Joaquin Delta that was observed in the early 2000s. The U.S. Geological Survey, in cooperation with the Delta Regional Monitoring Program, has been responsible for collecting and analyzing surface-water samples for a suite of 154 pesticides and pesticide degradates in surface water and in suspended sediment. Additional samples were collected for the analysis of dissolved organic carbon, dissolved copper, particulate organic carbon, particulate inorganic carbon, total particulate carbon, and total particulate nitrogen; and field water-quality indicators (water temperature, specific conductance, dissolved oxygen, pH, and turbidity) were measured at each site. Five integrator sites on streams draining mixed land-use watersheds were sampled monthly from July 2016 to June 2017. Two sites were sampled in the San Joaquin River watershed and one site was sampled in each of the Mokelumne River, Sacramento River, and Ulatis Creek watersheds. A total of 53 out of 154 pesticides (18 herbicides, 14 insecticides, 13 fungicides, 7 breakdown products, and 1 synergist) were detected in surface-water samples and 95 percent of samples contained mixtures of 2 or more pesticides. The most frequently detected pesticides were the herbicides hexazinone, metolachlor, and diuron (present in 83 percent, 72 percent, and 67 percent of water samples, respectively), the insecticide methoxyfenozide (present in 83 percent of samples), and the fungicides boscalid and azoxystrobin (present in 67 percent and 58 percent of samples, respectively). Pesticide concentrations detected in water samples ranged from below method detection limits to 1,300 nanograms per liter (ng/L) for the insecticide chlorantraniliprole. A total of 4 pesticides (2 herbicides and 2 insecticides) were detected in suspended-sediment samples and 13 percent of suspended-sediment samples contained at least 1 pesticide. Pesticide concentrations detected in suspended-sediment samples ranged from 4.1 to 750 ng/L, both for the herbicide pendimethalin. Six samples contained the insecticide imidacloprid at concentrations above the U.S. Environmental Protection Agency (EPA) Aquatic Life Benchmark (10 ng/L) for chronic toxicity to aquatic invertebrates. Three samples contained bifenthrin at concentrations above the EPA Aquatic Life Benchmark (1.3 ng/L) for chronic toxicity to invertebrates. One sample contained cyhalothrin at a concentration above the U.S. Aquatic Life Benchmark (3.5 ng/L) for acute toxicity to invertebrates.

California↗

Mercury studies in the Florida Everglades

Public concern for wildlife and human health problems due to mercury (Hg) toxicity has increased substantially since the mid-1980's. These concerns are manifested primarily by the issuance of fish consumption advisories in the majority of U.S. states, Canada, and several European countries because of high levels of mercury in game fish. Although the precise causes for this contamination problem are not completely understood, it appears that there are both source and ecosystem-specific factors that can result in elevated levels of mercury in game fish. Because mercury is known to adverse affect the human brain and nervous system, health concerns arise when elevated concentrations of mercury are detected in game fish from ecosystems where there is subsistence level consumption of fish. In extreme cases such as the Everglades, where mercury concentrations in fish consistently exceed the Florida advisory level of 1.5 parts per million, even occasional fish consumption is not recommended. For most aquatic ecosystems, atmospheric deposition is the primary source of mercury. although there are numerous instances of geologic and anthropogenic point-source contamination. There are many sources of mercury to the atmosphere, both natural and human related. Natural sources include outgassing from the oceans, volcanoes, and natural mercury deposits. Coal combustion, waste incineration, chloralkai production, and metal processing are the dominant human-related sources to the atmosphere. In ecosystems for which atmospheric deposition is the dominant source, resulting concentrations of total mercury in water are very low, generally less than 10 nanograms per liter (ng/L). The challenge to scientists is to explain the series of processes that lead to toxic or near-toxic levels of mercury in organisms near the top of the food chain (bioaccumulation), when aqueous concentrations and source-delivery rates are so low. To understand this phenomenon adequately, scientists must apply an interdisciplinary approach wherein various components of an ecosystem (atmosphere, biota, surface water, ground water, and sediments) are studied-contemporaneously. The purpose of this fact sheet is to describe the mercury contamination problem in south Florida, and the interdisciplinary project that was assembled under the auspices of the U.S. Geological Survey South Florida Ecosystem Program to investigate the underlying processes that cause mercury bioaccumulation.

Florida↗

Field and laboratory guide to freshwater cyanobacteria harmful algal blooms for Native American and Alaska Native communities

Cyanobacteria can produce toxins and form harmful algal blooms. The Native American and Alaska Native communities that are dependent on subsistence fishing have an increased risk of exposure to these cyanotoxins. It is important to recognize the presence of an algal bloom in a waterbody and to distinguish a potentially toxic harmful algal bloom from a non-toxic bloom. This guide provides field images that show cyanobacteria blooms, some of which can be toxin producers, as well as other non-toxic algae blooms and floating plants that might be confused with algae. After recognition of a potential toxin-producing cyanobacterial bloom in the field, the type(s) of cyanobacteria present needs to be identified. Species identification, which requires microscopic examination, may help distinguish a toxin-producer from a non-toxin producer. This guide also provides microscopic images of the common cyanobacteria that are known to produce toxins, as well as images of algae that form blooms but do not produce toxins.

Open-File Report↗

Mercury in U.S. coal—Priorities for new U.S. Geological Survey studies

In 2011, the U.S. Environmental Protection Agency (EPA) introduced emissions standards, known as Mercury and Air Toxics Standards (MATS), for a range of toxic constituents from coal-fired utility power stations and other combustion sources. This report presents the findings of an expert panel convened in September 2014 to assess the role of the U.S. Geological Survey (USGS) in new coal investigations that would be useful to stakeholders under MATS. Panel input is provided as summaries of responses to a questionnaire distributed to participants. The panel suggests that the USGS continue its work on trace elements in coal and include more information about delivered coals and boiler feed coals, in comparison to previous USGS compilations that emphasized sampling representative of coals in the ground. To be useful under multipollutant regulatory standards, investigation of a range of constituents in addition to mercury would be necessary. These include other toxic metals proposed for regulation, such as arsenic, nickel, cadmium, and chromium, as well as the halogens chlorine and fluorine, which upon emission form harmful acid gases. Halogen determinations are also important because they influence mercury speciation in flue gas, which allows the effectiveness of mercury controls to be assessed and predicted. The panel suggests that the Illinois Basin and the Powder River Basin should have the highest priority for new coal quality investigations in the near term by the USGS, on the basis of current economic conditions and overall economic importance, respectively. As a starting point for new investigations, brief summaries of the distribution of mercury in each coal basin, and their potential for further investigation, are presented.

Open-File Report↗