Regional geochemistry of metals in organic-rich sediments, sawgrass and surface water, from Taylor Slough, Florida
No abstract available.
Florida↗
SEARCH · USGS Science
Results for “Organic Geochemistry”
Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Tracking riverborne sediment and contaminants in Commencement Bay, Washington, using geochemical signatures
Large rivers carry terrestrial sediment, contaminants, and other materials to the coastal zone where they can affect marine biogeochemical cycles and ecosystems. This U.S. Geological Survey study combined river and marine sediment geochemistry and organic contaminant analyses to identify riverborne sediment and associated contaminants at shoreline sites in Commencement Bay, Puget Sound, Washington, that could be used by adult forage fish and other marine organisms. Geochemical signatures distinguished the fine fraction (<0.063 millimeter, mm) of Puyallup River sediment—which originates from Mount Rainier, a Cascade volcano—from glacial fine sediment in lowland bluffs that supply sediment to beaches. In combination with activities of beryllium-7 ( 7 Be), a short-lived radionuclide, geochemical signatures showed that winter 2013–14 sediment runoff from the Puyallup River was transported to and deposited along the north shore of Commencement Bay, then mixed downward into the sediment column. The three Commencement Bay sites at which organic contaminants were measured in surface sediment did not have measurable 7 Be activities in that layer, so their contaminant assemblages were attributed to sources from previous years. Concentrations of organic contaminants (the most common of which were polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and fecal sterols) were higher in the <0.063-mm fraction compared to the <2-mm fraction, in winter compared to summer, in river suspended sediment compared to river bar and bank sediment, and in marine sediment compared to river sediment. The geochemical property barium/aluminum (Ba/Al) showed that the median percentage of Puyallup River derived fine surface sediment along the shoreline of Commencement Bay was 77 percent. This finding, in combination with higher concentrations of organic contaminants in marine rather than river sediment, indicates that riverborne sediment-bound contaminants are retained in shallow marine habitats of Commencement Bay. The retention of earlier inputs complicates efforts to identify recent inputs and sources. Understanding modern sources and fates of riverborne sediment and contaminants and their potential ecological impacts will therefore require a suite of targeted geochemical studies in such marine depositional environments.
Washington↗
Isotope geochemistry and fluxes of carbon and organic matter in tropical small mountainous river systems and adjacent coastal waters of the Caribbean
Recent studies have shown that small mountainous rivers (SMRs) may act as sources of aged and/or refractory carbon (C) to the coastal ocean, which may increase organic C burial at sea and subsidize coastal food webs and heterotrophy. However, the characteristics and spatial and temporal variability of C and organic matter (OM) exported from tropical SMR systems remain poorly constrained. To address this, the abundance and isotopic character (δ13C and Δ14C) of the three major C pools were measured in two Puerto Rico SMRs with catchments dominated by different land uses (agricultural vs. non-agricultural recovering forest). The abundance and character of C pools in associated estuaries and adjacent coastal waters were also examined. Riverine dissolved and particulate organic C (DOC and POC, respectively) concentrations were highly variable with respect to land use and sampling month, while dissolved inorganic C (DIC) was significantly higher at all times in the agricultural catchment. In both systems, riverine DOC and POC ranged from modern to highly aged (2,340 years before present), while DIC was always modern. The agricultural river and irrigation canals contained very old DOC (1,184 and 2,340 years before present, respectively), which is consistent with findings in temperate SMRs and indicates that these tropical SMRs provide a source of aged DOC to the ocean. During months of high river discharge, OM in estuarine and coastal waters had C isotope signatures reflective of direct terrestrial input, indicating that relatively unaltered OM is transported to the coastal ocean at these times. This is also consistent with findings in temperate SMRs and indicates that C transported to the coastal ocean by SMRs may differ from that of larger rivers because it is exported from smaller catchments that have steeper terrains and fewer land-use types.
Puerto Rico↗
An integrated perspective of paleoenvironmental change in the Western Interior Seaway before and during OAE-2 reveals how organic-rich mudstones form in dynamic environments
Organic and inorganic geochemistry was integrated with sedimentology from the Eagle Ford Group in the U.S. Geological Survey Gulf Coast-3 drill core to investigate why organic matter enrichment and anoxia predate the Cenomanian–Turonian oceanic anoxic event (OAE-2) at the southern Western Interior Seaway (WIS). The relationship between the degree of organic matter sulfurization and preservation in the southern WIS is comparable to OAE-2 sites outside of the WIS, but enhanced organic matter sulfurization and preservation predated OAE-2, distinguishing the southern WIS from other OAE-2 localities. Persistent euxinia and organic matter sulfurization before and during the mid-Cenomanian event (MCE) facilitated maximum organic matter enrichment and preservation to coincide with extensive lateral sediment transport. The new perspective detailed here reconciles geochemical evidence of depositional euxinia with sedimentological evidence of sediment transport, which informs how organic-rich mudstones form in dynamic environments. After the MCE but before OAE-2, reducing conditions weakened as relative sea-level continued to rise, resulting in an oxygen-depleted environment that was prone to transient euxinia. The extent of organic matter sulfurization, preservation, and enrichment declined as euxinia became intermittent. As maximum sea-level was established during OAE-2, boreal water masses flowed into the southern WIS and unrestricted, oxygenated marine conditions developed, which resulted in degradation of marine organic matter and less organic enrichment. The highest relative contribution of marine bacterial organic matter occurred during the persistently euxinic interval before and during the MCE. The relative input of algal organic matter increased as the depositional conditions became less reducing after the MCE but before OAE-2. Prasinophyte green algae contributed to the consistent dominance of C 28 steranes preceding OAE-2, which is becoming a widely observed feature across the southern and central WIS. A sharp drop in the C 28 sterane relative abundance reflects a decline in the abundance of prasinophytes as oxic depositional conditions developed during OAE-2. Relative abundances of 2-methylhopanes increased during OAE-2, which is a common signature of OAEs, suggesting a modified nitrogen cycle in the offshore southern WIS despite oxic depositional conditions during OAE-2.
Arkansas, Louisiana, Oklahoma, Texas↗
An integrated mudstone facies classification scheme and revised interpretation of the sedimentologic processes driving carbon burial in the Cenomanian–Turonian Greenhorn Formation, Colorado, U.S.A.
Standardizing facies descriptions has proven key to integrating interpretations of depositional processes and environments from sedimentologic observations with geochemistry data for mudstone lithologies. Because of their fine-grained nature, high degree of compaction, and heterogeneous composition, standardizing methods for mudstone descriptions has proven difficult, but it is critical to formulating meaningful interpretations of the processes that govern the accumulation of organic-rich lithologies and their role in both petroleum systems and the global carbon cycle. In this study, we have developed a modified facies classification scheme for mudstone lithologies that incorporates sedimentologic and compositional observation at the hand-sample and thin-section scales with geochemical measurements, including bulk organic and inorganic geochemistry, to characterize these rocks and their variability more completely for improved interpretations of depositional environments during a low-order sea-level transgression. The facies described in this study are of the Cenomanian–Turonian Greenhorn Formation in the USGS #1 Portland Core drilled in Fremont County, Colorado. Strata of the Greenhorn Formation span Oceanic Anoxic Event 2 (OAE-2) and the preceding interval. Lithologies range from organic-rich argillaceous mudstones with varied sedimentary structures to organic-lean, highly bioturbated limestones. Six facies were identified, each differentiated by varied sedimentary structures and geochemical composition. These facies occur in a predictable stratigraphic stacking pattern that represents a low-order sea-level transgression with interpreted depositional environments ranging from terrigenous-dominated pro-delta and muddy continental shelf at the base of the interval to pelagic offshore marine at the top of the Greenhorn Formation. Though the facies are consistent with previous interpretations of depositional environments at this locale in the Cretaceous Western Interior Seaway during the Greenhorn cyclothem, the sedimentary processes governing the accumulation of organic-rich strata that have defined this interval are significantly revised. Variability in the proximity and intensity of bottom currents driven by storms and geostrophic flows were key to the accumulation of each facies, with significant sediment transport occurring even through deposition in the most oxygen-depleted bottom waters. The methodology and interpretations provided here are now being employed to basin-scale predictions of organic enrichment utilizing calibrated petrophysical methods. The approach and results from this study improve understanding of how organic and inorganic carbon was sequestered during perturbations to the global carbon cycle associated with events such as OAE-2.
Colorado↗
The geochemistry of water near a surficial organic-rich uranium deposit, northeastern Washington State, U.S.A.
The chemistry of three stream, three spring and six near-surface waters in the vicinity of a Holocene organic-rich uranium deposit is described, with particular emphasis on the chemistry of U. Results characterize the solution behavior of uranium as U-bearing water interacts with relatively undecomposed, surficial organic matter. Of the measured major and trace chemical species, only U is consistently highly enriched (17-318 ppb) relative to reported values for regional waters, or to literature values for waters in largely granitic terrains. R-mode factor analysis of the chemical data suggests that most U is present in a soluble form, but that some U is also associated with fine suspended particulates of clay, organic matter, or hydrous oxides. Calculations that apply thermodynamic data to predict U speciation in solution indicate the relative importance of uranyl carbonate and uranyl phosphate complexes. Analysis of more finely filtered samples (0.05 ??m vs. 0.45 ??m), and direct radiographic observations using fission-track detectors suspended in the waters indicate the presence of some uraniferous particulate matter. Application of existing thermodynamic data for uranous- and uranyl-bearing minerals indicates that all waters are undersaturated with U minerals as long as ambient Eh ??? +0.1 v. If coexisting surface and near-surface waters are sufficiently oxidizing, initial fixation of U in the deposit should be by a mechanism of adsorption. Alternatively, more reducing conditions may prevail in deeper pore waters of the organic-rich host sediments, perhaps leading to direct precipitation or diagenetic formation of U4+ minerals. A 234U 238U alpha activity ratio of 1.08 ?? 0.02 in a spring issuing from a hillslope above the deposit suggests a relatively soluble source of U. In contrast, higher activity ratios of 234U 238U (??? 1.3) in waters in contact with the uraniferous valley-fill sediments suggest differences in the nature of interaction between groundwater and the local, U-rich source rocks. ?? 1987.
Chemical Geology↗
Geochemistry of deep-sea manganese nodules; organic involvement
No abstract available.
Conference Paper↗
Contribution of deep-sourced carbon from hydrocarbon seeps to sedimentary organic carbon: Evidence from radiocarbon and stable isotope geochemistry
Sulfate-driven anaerobic oxidation of methane (AOM) limits the release of methane from marine sediments and promotes the formation of carbonates close to the seafloor in seepage areas along continental margins. It has been established that hydrocarbon seeps are a source of methane, dissolved inorganic carbon, and dissolved organic carbon to marine environments. However, questions remain about the contribution of deep-sourced carbon from hydrocarbon seeps to the sedimentary organic carbon pool. In this study, we analyzed carbon quantity, radiocarbon content (as percent modern carbon, pMC), stable carbon isotopic compositions (as δ 13 C) of organic matter enclosed within seep carbonates from the Gulf of Mexico and the South China Sea to assess if sediment organic matter may be used as a proxy for methane seepage intensity. The δ 13 C values of organic matter (δ 13 C org ) exhibited a large range from −81.4‰ to −23.9‰. Radiocarbon contents of the carbonate-bound organic matter in seep carbonates ranged from 6% to 28% pMC, suggesting organic matter of the carbonates is a mixture of marine particulate organic matter (δ 13 C = −22‰ VPDB and 90% modern carbon) and biomass resulting from methane oxidation (assumed to have 0% modern carbon). Assuming constant productivity in the marine photic zone, it is proposed that seepage intensity and duration are the most important factors controlling the contribution of methane-derived carbon to the sedimentary column. This study reinforces the potential for using δ 13 C values of organic carbon to discern methane-rich environments in ancient sedimentary environments where authigenic carbonate is not present and to constrain the record of AOM through Earth history.
Chemical Geology↗
The interaction of natural organic matter with iron in a wetland (Tennessee Park, Colorado) receiving acid mine drainage
Pore water from a wetland receiving acid mine drainage was studied for its iron and natural organic matter (NOM) geochemistry on three different sampling dates during summer 1994. Samples were obtained using a new sampling technique that is based on screened pipes of varying length (several centimeters), into which dialysis vessels can be placed and that can be screwed together to allow for vertical pore-water sampling. The iron concentration increased with time (through the summer) and had distinct peaks in the subsurface. Iron was mainly in the ferrous form; however, close to the surface, significant amounts of ferric iron (up to 40% of 2 mmol L-1 total iron concentration) were observed. In all samples studied, iron was strongly associated with NOM. Results from laboratory experiments indicate that the NOM stabilizes the ferric iron as small iron oxide colloids (able to pass a 0.45μm dialysis membrane). We hypothesize that, in the pore water of the wetland, the high NOM concentrations (>100 mg C L-1) allow formation of such colloids at the redoxcline close to the surface and at the contact zone to the adjacent oxic aquifer. Therefore, particle transport along flow paths and resultant export of ferric iron from the wetland into ground water might be possible.
Aquatic Geochemistry↗
Factors influencing the biogeochemistry of sedimentary carbon and phosphorus in the Sacramento-San Joaquin Delta
This study characterizes organic carbon (C organic ) and phosphorus (P) geochemistry in surface sediments of the Sacramento-San Joaquin Delta, California. Sediment cores were collected from five sites on a sample transect from the edge of the San Francisco Bay eastward to the freshwater Consumnes River. The top 8 cm of each core were analyzed (in 1-cm intervals) for C organic , four P fractions, and redox-sensitive trace metals (uranium and manganese). Sedimentary C organic concentrations and C organic : P ratios, decreased, while reactive P concentrations increased moving inland in the Delta. The fraction of total P represented by organic P increased inland, while that of authigenic P was higher bayward than inland reflecting increased diagenetic alteration of organic matter toward the bayward end of the transect. The redox indicator metals are consistent with decreasing sedimentary suboxia inland. The distribution of P fractions and C:P ratios, reflect the presence of relatively labile organic matter in upstream surface sediments. Sediment C and P geochemistry is influenced by site-specific particulate organic matter sources, the sorptive power of the sedimentary material present, physical forcing, and early diagenetic transformations presumably driven by C organic oxidation.
California↗
Petrography of Permian “Gondwana” coals from boreholes in northwestern Bangladesh, based on semiautomated reflectance scanning
Drilling through Quaternary alluvium and Tertiary cover at low-gravity anomalies in northwestern Bangladesh showed the presence of Permian sedimentary rocks in depressions that may be as much as a thousand meters deep in the crystalline basement. These Permian strata include low-sulfur, high-volatile bituminous coals in beds as thick as 15 m. The maceral group composition of these coals was determined by semiautomated reflectance scanning with a motorized microscope stage, rather than by point counting. This method was chosen to give objectively recorded raw analytical data and to provide a graphical picture of each sample. The coals are mostly “Gondwana” type (poorly layered “plum pudding” with abundant minerals and inertinite in a vitrinite groundmass) that would be classed as semi-dull (inerto-gelitite) coals. However, six samples have more than 70% vitrinite. None of the samples would be classed as sapropelic (liptinitic). The upper, middle, and lower main seams in borehole GDH-45 were sampled in 10 benches (0.1–3 m thick) each. Inertinite ranges from 7 to 100 vol% (mineral free basis) in individual benches, but composite seam averages are 41, 54 and 67%. Inertinite increases toward the top of two main seams so the bottom would yield the most valuable first mine slices. Some benches with extremely high inertinite content, such as the top 7 m of the lower thick seam, might be mined specially for blending with foreign low-inert coals to increase coke strength. The free swelling index reaches 7.5 in several vitrinite-rich benches, which can indicate good coking coal. Much of the vitrinite is fluorescent, which indicates secondary bituminization characteristic of vitrinite in good coking coals. Ash yields range from 8 to 52%, with composite seam averages of 15, 14 and 24%. Rare visible pyrite is in veinlets or small nodules; framboids and dispersed pyrite are absent. In borehole GDH-40 near Barapukuria (200–500 m depth), the mean random reflectance of vitrinite “A” ranges from 0.60 to 0.80% R o and vitrinite “B” ranges from 0.55 to 0.65%. In borehole GDH-45 near Khalaspir (287–442 m), the reflectance of vitrinite ranges from 0.79 to 0.94%. In individual cases, the vitrinite is difficult to define because of semivitrinite at higher reflectance (forming a separate peak on several reflectograms) and because of surface bitumen films or resinous (?) inclusions at lower reflectance. On the basis of vitrinite reflectance, the coals can be considered to have entered the “main phase of bitumen generation” of organic thermal maturation as understood in petroleum geochemistry.
Organic Geochemistry↗
Geochemistry of coastal permafrost and erosion-driven organic matter fluxes to the Beaufort Sea near Drew Point, Alaska
Accelerating erosion of the Alaska Beaufort Sea coast is increasing inputs of organic matter from land to the Arctic Ocean, and improved estimates of organic matter stocks in eroding coastal permafrost are needed to assess their mobilization rates under contemporary conditions. We collected three permafrost cores (4.5–7.5 m long) along a geomorphic gradient near Drew Point, Alaska, where recent erosion rates average 17.2 m year −1 . Down-core patterns indicate that organic-rich soils and lacustrine sediments (12–45% total organic carbon; TOC) in the active layer and upper permafrost accumulated during the Holocene. Deeper permafrost (below 3 m elevation) mainly consists of Late Pleistocene marine sediments with lower organic matter content (∼1% TOC), lower C:N ratios, and higher δ 13 C values. Radiocarbon-based estimates of organic carbon accumulation rates were 11.3 ± 3.6 g TOC m −2 year −1 during the Holocene and 0.5 ± 0.1 g TOC m −2 year −1 during the Late Pleistocene (12–38 kyr BP). Within relict marine sediments, porewater salinities increased with depth. Elevated salinity near sea level (∼20–37 in thawed samples) inhibited freezing despite year-round temperatures below 0°C. We used organic matter stock estimates from the cores in combination with remote sensing time-series data to estimate carbon fluxes for a 9 km stretch of coastline near Drew Point. Erosional fluxes of TOC averaged 1,369 kg C m −1 year −1 during the 21st century (2002–2018), nearly doubling the average flux of the previous half-century (1955–2002). Our estimate of the 21st century erosional TOC flux year −1 from this 9 km coastline (12,318 metric tons C year −1 ) is similar to the annual TOC flux from the Kuparuk River, which drains a 8,107 km 2 area east of Drew Point and ranks as the third largest river on the North Slope of Alaska. Total nitrogen fluxes via coastal erosion at Drew Point were also quantified, and were similar to those from the Kuparuk River. This study emphasizes that coastal erosion represents a significant pathway for carbon and nitrogen trapped in permafrost to enter modern biogeochemical cycles, where it may fuel food webs and greenhouse gas emissions in the marine environment.
Alaska↗
Deposition of sedimentary organic matter in black shale facies indicated by the geochemistry and petrography of high-resolution samples, blake nose, western North Atlantic
A transect of three holes drilled across the Blake Nose, western North Atlantic Ocean, retrieved cores of black shale facies related to the Albian Oceanic Anoxic Events (OAE) lb and ld. Sedimentary organic matter (SOM) recovered from Ocean Drilling Program Hole 1049A from the eastern end of the transect showed that before black shale facies deposition organic matter preservation was a Type III-IV SOM. Petrography reveals that this SOM is composed mostly of degraded algal debris, amorphous SOM and a minor component of Type III-IV terrestrial SOM, mostly detroinertinite. When black shale facies deposition commenced, the geochemical character of the SOM changed from a relatively oxygen-rich Type III-IV to relatively hydrogen-rich Type II. Petrography, biomarker and organic carbon isotopic data indicate marine and terrestrial SOM sources that do not appear to change during the transition from light-grey calcareous ooze to the black shale facies. Black shale subfacies layers alternate from laminated to homogeneous. Some of the laminated and the poorly laminated to homogeneous layers are organic carbon and hydrogen rich as well, suggesting that at least two SOM depositional processes are influencing the black shale facies. The laminated beds reflect deposition in a low sedimentation rate (6m Ma-1) environment with SOM derived mostly from gravity settling from the overlying water into sometimes dysoxic bottom water. The source of this high hydrogen content SOM is problematic because before black shale deposition, the marine SOM supplied to the site is geochemically a Type III-IV. A clue to the source of the H-rich SOM may be the interlayering of relatively homogeneous ooze layers that have a widely variable SOM content and quality. These relatively thick, sometimes subtly graded, sediment layers are thought to be deposited from a Type II SOM-enriched sediment suspension generated by turbidities or direct turbidite deposition.
Special Papers of the Geological Society of London↗
Microbial production of organic acids in aquitard sediments and its role in aquifer geochemistry
Microbial activity in aquifers plays an important part in the chemical evolution of ground water 1–5 . The most important terminal electron-accepting microbial processes in deeply buried anaerobic aquifers are iron reduction, sulphate reduction and methanogenesis 5–8 , each of which requires simple organic compounds or hydrogen (H 2 ) as electron donors. Until now, the source of these compounds was unknown because the concentrations of dissolved organic carbon and sedimentary organic carbon in aquifers are extremely low 9–11 . Here we show that rates of microbial fermentation exceed rates of respiration in organic-rich aquitards (low-permeability sediments stratigraphically adjacent to higher-permeability aquifer sediments), resulting in a net accumulation of simple organic acids in pore waters. In aquifers, however, respiration outpaces fermentation, resulting in a net consumption of organic acids. The concentration gradient that develops in response to these two processes drives a net diffusive flux of organic acids from aquitards to aquifers. Diffusion calculations demonstrate that rates of organic acid transport are sufficient to account for observed rates of microbial respiration in aquifers. This overall process effectively links the large pool of sedimentary organic carbon in aquitards to microbial respiration in aquifers, and is a principal mechanism driving groundwater chemistry changes in aquifers.
Nature↗
The aqueous geochemistry of uranium in a drainage containing uraniferous organic-rich sediments, Lake Tahoe area, Nevada, USA
Anomalously uraniferous waters occur in a small (4.2 km2) drainage in the west-central Carson Range, Nevada, on the eastern side of Lake Tahoe. The waters transport uranium from local U-rich soils and bedrock to organic-rich valley-fill sediments where it is concentrated, but weakly bound. The dissolved U and the U that is potentially available from coexisting sediments pose a threat to the quality of drinking water that is taken from the drainage. The U concentration in samples of 6 stream, 11 spring and 7 near-surface waters ranged from <1 to 177 ??g l-1 with an average value of 17 ?? 14 ??g l-1 for stream and spring waters. This value significantly exceeds a reported regional average value of ~5 ??g l-1, and is comparable to proposed maximum contaminant levels of U in drinking water. Calculations that utilize chemical compositions of the waters and thermodynamic data indicate that uranyl-carbonate and uranyl-phosphate complexes are the major inorganic species of dissolved U. In addition, dialysis experiments suggest an association of at least some dissolved U with macromolecular organic matter, particularly in near-surface waters that are in contact with organic-rich sediments. Calculations of the saturation index for uranous and uranyl-bearing minerals indicate that all of the waters are undersaturated with uranium minerals as long as ambient Eh is oxidizing (i.e. > 0.1 V). Possible precipitation of U(IV) minerals is predicted under the more reducing conditions that are particularly likely in near-surface waters, but the inhibitory effects of sluggish kinetics or organic complexing are not considered. These combined results suggest that a process such as adsorption or ion exchange, rather than mineral saturation, is the most probable mechanism for uranium fixation in the sediments. -Authors
Uranium↗
Early developments in petroleum geochemistry
Petroleum geochemistry is the outgrowth of the application of the principles and methods of organic chemistry to petroleum refining and petroleum geology . This paper reviews 120 years of petroleum geochemistry, from about 1860 to 1980, and includes a discussion of the formal recognition of petroleum geochemistry as an earth-science discipline starting in 1959 when a general petroleum geochemistry symposium was first organized at Fordham University, New York. A chronology of significant events, including concepts, techniques, and textbook publications, is presented. Because petroleum geochemistry has been a tool for petroleum exploration from the beginning, the early developments of surface prospecting, source-rock identification, and oil/oil and oil/source correlation are discussed, along with the application of geochemistry to petroleum migration, accumulation, and alteration. In addition the paper deals with the biomarker revolution, which began in earnest about 1964, and with early models of geothermal history. Concepts in petroleum geochemistry have continually evolved, enhanced by the development of new analytical techniques, leading to new discoveries concerning the origin and occurrence of petroleum.
Organic Geochemistry↗
Using multiple metal mixture models to predict toxicity of riverine sediment porewater to the benthic life stage of juvenile white sturgeon (Acipenser transmontanus)
Five metal mixture dose–response models were used to predict the toxicity of porewater to young sturgeon at areas of interest in the Upper Columbia River (WA, USA/BC, Canada) and to evaluate these models as tools for risk assessments. Dose components of metal mixture models included exposure to free metal ion activities or metal accumulation by biotic ligands or humic acid, and links of dose to response used logistic equations, independent joint action equations, or additive toxicity functions. Laboratory bioassay studies of single metal exposures to juvenile sturgeon, porewater collected in situ in the fast-flowing Upper Columbia River, and metal mixture models were used to evaluate toxicity. The five metal mixture models were very similar in their predictions of adverse response of juvenile sturgeon and in identifying copper (Cu) as the metal responsible for the most toxic conditions. Although the modes of toxic action and the 20% effective concentration values were different among the dose models, predictions of adverse response were consistent among models because all doses were tied to the same biological responses. All models indicated that 56% ± 5% of 122 porewater samples were predicted to have <20% adverse response, 25% ± 5% of samples were predicted to have 20% to 80% adverse response, and 20% ± 4% were predicted to have >80% adverse response in juvenile sturgeon. The approach of combining bioassay toxicity data, compositions of field porewater, and metal mixture models to predict lack of growth and survival of aquatic organisms due to metal toxicity is an important tool that can be integrated with other information (e.g., survey studies of organism populations, life cycle and behavior characteristics, sediment geochemistry, and food sources) to assess risks to aquatic organisms in metal-enriched ecosystems. Environ Toxicol Chem 2023;00:1–12. Published 2023. This article is a U.S. Government work and is in the public domain in the USA.
Environmental Toxicology & Chemistry↗
Using multiple environmental proxies and hydrodynamic modeling to investigate Late Holocene climate and coastal change within a large Gulf of Mexico estuarine system (Mobile Bay, Alabama, USA)
A high degree of uncertainty exists for understanding and predicting coastal estuarine response to changing climate, land-use, and sea-level conditions, leaving geologic records as a best-proxy for constraining potential outcomes. With the majority of the world's population focused in coastal regions, understanding how local systems respond to global, regional, and even local pressures is key in developing mitigation, adaptation, and management plans. The geomorphology of Mobile Bay in southeast Alabama (USA) has evolved considerably (e.g., bayhead delta back-stepping) over the late Holocene in response to global and regional sea-level and climate change. Smaller-scale geomorphic changes (e.g., spit and beach ridge development) have also had a significant influence on the evolution of the estuary. Organic matter characteristics, inorganic sediment geochemistry, benthic microfossils, and pollen in a ~ 3500 cal yr BP sediment sequence recovered in a gravity core (20GC) from Bon Secour Bay, a small sub-bay in the southeast corner of Mobile Bay, record time-varying marine influence. Increases in marine influence during ~3500 to 2300 cal yr BP and 1930 to 1160 cal yr BP are defined as zones with high-density and pre-dominantly calcareous foraminiferal species, abundant sand (>10%) and more marine-like geochemical signatures, which contrast the low-density and pre-dominantly agglutinated foraminiferal and more terrestrially influenced estuarine muds observed in other intervals of the sedimentary record (2300–1930 and 1160–400 cal yr BP) and the modern bay. Hydrodynamic models constrained by geomorphic boundary conditions for the time ~ 3500 cal yr BP, consistent with the most prominent marine-influenced sediment, provide insight to potential coastal configuration that might have permitted such marine water intrusion into the bay. Of several scenarios evaluated, a breach in Morgan Peninsula produces tidal circulation within the basin supportive of persistent marine incursions in the bay between ~3500 to 2300 cal yr BP. The findings show that slight variations in coastal configuration can have broad-scale effects on bays and estuaries with consequences that may relate to water quality, vertebrate and invertebrate habitat, and coastal vulnerability to episodic events like (extra)tropical storms.
Alabama, Mississippi↗