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At least 1,189 records · Page 66Linked to original sources

USGS2013

Variations of iron flux and organic carbon remineralization in a subterranean estuary caused by interannual variations in recharge

We determine the inter-annual variations in diagenetic reaction rates of sedimentary iron (Fe ) in an east Florida subterranean estuary and evaluate the connection between metal fluxes and recharge to the coastal aquifer. Over the three-year study period (from 2004 to 2007), the amount of Fe-oxides reduced at the study site decreased from 192 g/yr to 153 g/yr and associated organic carbon (OC) remineralization decreased from 48 g/yr to 38 g/yr. These reductions occurred although the Fe-oxide reduction rates remained constant around 1 mg/cm 2 /yr. These results suggest that changes in flow rates of submarine groundwater discharge (SGD) related to changes in precipitation may be important to fluxes of the diagenetic reaction products. Rainfall at a weather station approximately 5 km from the field area decreased from 12.6 cm/month to 8.4 cm/month from 2004 to 2007. Monthly potential evapotranspiration (PET) calculated from Thornthwaite’s method indicated potential evapotranspiration cycled from about 3 cm/month in the winter to about 15 cm/month in the summer so that net annual recharge to the aquifer decreased from 40 cm in 2004 to -10 cm in 2007. Simultaneously, with the decrease in recharge of groundwater, freshwater SGD decreased by around 20% and caused the originally 25 m wide freshwater seepage face to decrease in width by about 5 m. The smaller seepage face reduced the area under which Fe-oxides were undergoing reductive dissolution. Consequently, the observed decrease in Fe flux is controlled by hydrology of the subterranean estuary. These results point out the need to better understand linkages between temporal variations in diagenetic reactions and changes in flow within subterranean estuaries in order to accurately constrain their contribution to oceanic fluxes of solutes from subterranean estuaries.

Florida↗

USGS2015

Uranium isotopes and dissolved organic carbon in loess permafrost: Modeling the age of ancient ice

The residence time of ice in permafrost is an indicator of past climate history, and of the resilience and vulnerability of high-latitude ecosystems to global change. Development of geochemical indicators of ground-ice residence times in permafrost will advance understanding of the circumstances and evidence of permafrost formation, preservation, and thaw in response to climate warming and other disturbance. We used uranium isotopes to evaluate the residence time of segregated ground ice from ice-rich loess permafrost cores in central Alaska. Activity ratios of 234 U vs. 238 U ( 234 U/ 238 U) in water from thawed core sections ranged between 1.163 and 1.904 due to contact of ice and associated liquid water with mineral surfaces over time. Measured ( 234 U/ 238 U) values in ground ice showed an overall increase with depth in a series of five neighboring cores up to 21 m deep. This is consistent with increasing residence time of ice with depth as a result of accumulation of loess over time, as well as characteristic ice morphologies, high segregated ice content, and wedge ice, all of which support an interpretation of syngenetic permafrost formation associated with loess deposition. At the same time, stratigraphic evidence indicates some past sediment redistribution and possibly shallow thaw among cores, with local mixing of aged thaw waters. Using measures of surface area and a leaching experiment to determine U distribution, a geometric model of ( 234 U/ 238 U) evolution suggests mean ages of up to &sim;200 ky BP in the deepest core, with estimated uncertainties of up to an order of magnitude. Evidence of secondary coatings on loess grains with elevated ( 234 U/ 238 U) values and U concentrations suggests that refinement of the geometric model to account for weathering processes is needed to reduce uncertainty. We suggest that in this area of deep ice-rich loess permafrost, ice bodies have been preserved from the last glacial period (10–100 ky BP), despite subsequent fluctuations in climate, fire disturbance and vegetation. Radiocarbon ( 14 C) analysis of dissolved organic carbon (DOC) in thaw waters supports ages greater than &sim;40 ky BP below 10 m. DOC concentrations in thaw waters increased with depth to maxima of >1000 ppm, despite little change in ice content or cryostructures. These relations suggest time-dependent production of old DOC that will be released upon permafrost thaw at a rate that is mediated by sediment transport, among other factors.

Alaska↗

USGS2019

A high carbon content of the Hawaiian mantle from olivine-hosted melt inclusions

The deep mantle carbon content and flux are fundamental quantities in understanding global volatile cycles and distributions. Here, we present CO2 concentrations measured in 407 olivine-hosted melt inclusions from Hualalai, Kilauea, Koolau, Loihi, and Mauna Loa to constrain the Hawaiian mantle CO2 content and flux. Quantification of melt inclusion CO2 is complicated by the ubiquitous presence of vapor or “shrinkage” bubbles. The contribution from exsolved shrinkage bubble CO2 was determined from the measured bubble size and a CO2 equation of state, and added to the dissolved CO2 to reconstruct total melt inclusion CO2 concentrations. Bubbles typically contain ~90% of melt inclusion C, much of which may be sequestered in precipitated phases on bubble walls, and thus not amenable to measurement by Raman spectroscopy. Based on our dataset of total (dissolved + bubble) CO2 concentrations, we estimate that parental melts from the five Hawaiian volcanoes have CO2 concentrations ranging from 3900 to 10,000 ppm CO2. Among the active volcanoes, CO2 concentrations decrease to the northwest, likely reflecting mantle source heterogeneity, although differences in the depths of the magma chambers may also play a role. Mantle sources of the Hawaiian volcanoes range from 380 to 480 ppm CO2 suggesting that the Hawaiian plume is at least a factor of ~4 more C-rich than the MORB mantle. This enrichment is likely due to the presence of recycled surficial C and/or C-rich primitive material in the Hawaiian mantle.

Hawaii↗

USGS2008

Distinguishing black carbon from biogenic humic substances in soil clay fractions

Most models of soil humic substances include a substantial component of aromatic C either as the backbone of humic heteropolymers or as a significant component of supramolecular aggregates of degraded biopolymers. We physically separated coarse (0.2–2.0 μm e.s.d.), medium (0.02–0.2 μm e.s.d.), and fine (> 0.02 μm e.s.d.) clay subfractions from three Midwestern soils and characterized the organic material associated with these subfractions using 13 C-CPMAS-NMR, DTG, SEM-EDX, incubations, and radiocarbon age. Most of the C in the coarse clay subfraction was present as discrete particles (0.2–5 μm as seen in SEM images) of black carbon (BC) and consisted of approximately 60% aromatic C, with the remainder being a mixture of aliphatic, anomeric and carboxylic C. We hypothesize that BC particles were originally charcoal formed during prairie fires. As the BC particles aged in soil their surfaces were oxidized to form carboxylic groups and anomeric and aliphatic C accumulated in the BC particles either by adsorption of dissolved biogenic compounds from the soil solution or by direct deposition of biogenic materials from microbes living within the BC particles. The biogenic soil organic matter was physically separated with the medium and fine clay subfractions and was dominated by aliphatic, anomeric, and carboxylic C. The results indicate that the biogenic humic materials in our soils have little aromatic C, which is inconsistent with the traditional heteropolymer model of humic substances.

Geoderma↗

USGS2014

Evaluation of a model framework to estimate soil and soil organic carbon redistribution by water and tillage using 137 Cs in two U.S. Midwest agricultural fields

Cultivated lands in the U.S. Midwest have been affected by soil erosion, causing soil organic carbon (SOC) redistribution in the landscape and other environmental and agricultural problems. The importance of SOC redistribution on soil productivity and crop yield, however, is still uncertain. In this study, we used a model framework, which includes the Unit Stream Power-based Erosion Deposition (USPED) and the Tillage Erosion Prediction (TEP) models, to understand the soil and SOC redistribution caused by water and tillage erosion in two agricultural fields in the U.S. Midwest. This model framework was evaluated for different digital elevation model (DEM) spatial resolutions (10-m, 24-m, 30-m, and 56-m) and topographic exponents ( m = 1.0–1.6 and n = 1.0–1.3) using soil redistribution rates from 137 Cs measurements. The results showed that the aggregated 24-m DEM, m = 1.4 and n = 1.0 for rill erosion, and m = 1.0 and n = 1.0 for sheet erosion, provided the best fit with the observation data at both sites. Moreover, estimated average SOC redistributions were 1.3 ± 9.8 g C m − 2 yr − 1 in field site 1 and 3.6 ± 14.3 g C m − 2 yr − 1 in field site 2. Spatial distribution patterns showed SOC loss (negative values) in the eroded areas and SOC gain (positive value) in the deposition areas. This study demonstrated the importance of the spatial resolution and the topographic exponents to estimate and map soil redistribution and the SOC dynamics throughout the landscape, helping to identify places where erosion and deposition from water and tillage are occurring at high rates. Additional research is needed to improve the application of the model framework for use in local and regional studies where rainfall erosivity and cover management factors vary. Therefore, using this model framework can help to improve the information about the spatial distribution of soil erosion across agricultural landscapes and to gain a better understanding of SOC dynamics within eroding and previously eroded fields.

Iowa↗

USGS2015

Long-term controls of soil organic carbon with depth and time: a case study from the Cowlitz River Chronosequence, WA USA

Over timescales of soil development (millennia), the capacity of soils to stabilize soil organic carbon (SOC) is linked to soil development through changes in soil mineralogy and other soil properties. In this study, an extensive dataset of soil profile chemistry and mineralogy is compiled from the Cowlitz River Chronosequence (CRC), WA USA. The CRC soils range in age from 0.25 to 1200 kyr, spanning a developmental gradient encompassing clear changes in soil mineralogy, chemistry, and surface area. Comparison of these and other metrics of soil development with SOC properties reveal several relationships that may be diagnostic of the long-term coupling of soil development and C cycling. Specifically, SOC content was significantly correlated with sodium pyrophosphate extractable metals emphasizing the relevance of organo-metal complexes in volcanic soils. The depth distributions of organo-metals and other secondary weathering products, including the kaolin and short-range order (SRO) minerals, support the so-called “binary composition” of volcanic soils. The formation of organo-metal complexes limits the accumulation of secondary minerals in shallow soils, whereas in deep soils with lower SOC content, secondary minerals accumulate. In the CRC soils, secondary minerals formed in deep soils (below 50 cm) including smectite, allophane, Fe-oxides and dominated by the kaolin mineral halloysite. The abundance of halloysite was significantly correlated with bulk soil surface area and 14 C content (a proxy for the mean age of SOC), implying enhanced stability of C in deep soils. Allophane, an SRO mineral commonly associated with SOC storage, was not correlated with SOC content or 14 C values in CRC soils. We propose conceptual framework to describe these observations based on a general understanding of pedogenesis in volcanic soils, where SOC cycling is coupled with soil development through the formation of and fate of organo-metal or other mobile weathering products. This framework highlights interactions between SOC and soil development, which may be applicable to other soils where organic inputs interact with the products of chemical weathering.

Washington↗

USGS2021

The trajectory of soil development and its relationship to soil carbon dynamics

It has been postulated that the amount of soil organic carbon (SOC) associated with soil minerals exhibits a threshold relationship in response to effective soil moisture (estimated as precipitation less evapotranspiration). To better characterize the role of moisture in influencing mechanisms of SOC storage during pedogenesis, we compare soils from two different chronosequence sites: the Santa Cruz and Mattole River marine terraces that together form a soil age-by-climate gradient (i.e., climo-chronosequence). Our results demonstrate how variation in the effective soil moisture may drive soil development along divergent pedogenic trajectories, resulting in variations in the form and depth distribution of secondary weathering products. In particular, the residual metals Fe and Al are directly related to the type of secondary minerals that accumulate during weathering, and these variations are coupled to differences in the storage and long-term preservation of SOC both within and between soils. Over time, these differences in soil development may lead to ‘pedogenic thresholds’ that further differentiate soil characteristics and influence SOC dynamics. In this case, the pedogenic threshold takes the form of clay-rich argillic horizons that once formed, inhibit aqueous transport, decouple shallow and deep soil environments, and potentially limit SOC inputs and increase microbial recycling in deep soils. Our data suggest argillic horizon development is favorable in the drier Santa Cruz soils, where kaolinite is the dominant secondary weathering product. In contrast, greater available moisture in soils of the Mattole chronosequence drive a different weathering trajectory characterized by the accumulation of more amorphous secondary minerals. As a result, the Mattole soils and do not exhibit argillic horizon development but are instead characterized by greater accumulation of SOC across all depths sampled. Overall, our results illustrate how the interaction of climate (i.e., moisture) and time may shape the trajectory of soil development and the dynamics of SOC storage and preservation.

California↗

USGS2022

Vertical movement of soluble carbon and nutrients from biocrusts to subsurface mineral soils

Dryland ecosystems can be constrained by low soil fertility. Within drylands, the soil nutrient and organic carbon (C) cycling that does occur is often mediated by soil surface communities known as biological soil crusts (biocrusts), which cycle C and nutrients in the top ca. 0–2 cm of soil. However, the degree to which biocrusts are influencing soil fertility and biogeochemical cycling in deeper, subsurface mineral soils is unclear. The movement of dissolved resources from biocrusts to deeper soil layers in leachate may be one of the main mechanisms through which biocrust fertility is transferred downward towards deeper microbial communities and plant roots occurring within mineral soil. Here we examined the role of biocrust leachate in contributing to subsurface nutrient and soluble C pools and subsurface microbial cycling. We collected biocrusts from three biocrust successional stages and explored resource pools in situ at multiple soil depths, while collecting leachate and measuring nutrient and organic C concentrations and metabolite composition from each successional stage in the laboratory. After four leachate collections, we conducted an incubation of mineral soil collected from below each biocrust successional stage to measure heterotrophic microbial CO 2 flux and biomass. Overall, our findings observed that the degree of nutrient and C connectivity between biocrusts and the sub-crust mineral soil depended on the biocrust successional stage and the element being considered, and the influence of biocrust successional stage on mineral soil CO 2 flux is likely related to long-term resource build up. Together, our results suggest that the influence of biocrust leachate on subsurface mineral soil is complex and context dependent, but, over longer time periods and at later successional stages, can have measurable effects on dryland soil biogeochemical cycling with feedbacks to resource availability and CO 2 flux.

Geoderma↗

USGS2012

Sequestration of non-pure carbon dioxide streams in iron oxyhydroxide-containing saline repositories

Iron oxyhydroxide, goethite (α-FeOOH), was evaluated as a potential formation mineral reactant for trapping CO 2 in a mineral phase such as siderite (FeCO 3 ), when a mixture of CO 2 -SO 2 flue gas is injected into a saline aquifer. Two thermodynamic simulations were conducted, equilibrating a CO 2 -SO 2 fluid mixture with a NaCl-brine and Fe-rich rocks at 150 °C and 300 bar. The modeling studies evaluated mineral and fluid composition at equilibrium and the influence of pH buffering in the system. Results show siderite precipitates both in the buffered and unbuffered system; however, the presence of an alkaline pH buffer enhances the stability of the carbonate. Based on the model, an experiment was designed to compare with thermodynamic predictions. A CO 2 -SO 2 gas mixture was reacted in 150 ml of NaCl-NaOH brine containing 10 g of goethite at 150 °C and 300 bar for 24 days. Mineralogical and brine chemistry confirmed siderite as the predominant reaction product in the system. Seventy-six mg of CO 2 are sequestered in siderite per 10 g of goethite.

International Journal of Greenhouse Gas Control↗

USGS2018

Using mercury injection pressure analyses to estimate sealing capacity of the Tuscaloosa marine shale in Mississippi, USA: Implications for carbon dioxide sequestration

This work used mercury injection capillary pressure (MICP) analyses of the Tuscaloosa Group in Mississippi, including the Tuscaloosa marine shale (TMS), to assess their efficacy and sealing capacity for geologic carbon dioxide (CO 2 ) sequestration. Tuscaloosa Group porosity and permeability from MICP were evaluated to calculate CO 2 column height retention. TMS and Lower Tuscaloosa shale samples have, respectively, Swanson permeability values less than 0.003 md and 0.00245 md; porosity from 3.86% to 9.86% and 1.34% to 7.96%; median pore throat sizes from 0.00342 to 0.0111 μm and 0.00311 to 0.017 μm; and pore radii from 0.0130 to 0.152 μm and 0.0132 to 0.149 μm. Mercury entry pressures for the TMS and Lower Tuscaloosa range from 4.9 to 57.1 MPa and 5.0 to 56.3 MPa, respectively. Calculated CO 2 column heights that the TMS sample set can retain in the reservoir range from 23 to 255 m when the TMS is near 100% water saturation. Potential top seal leakage is more likely to be influenced by the numerous well penetrations through the confining system of the TMS rather than capillary failure. Results of this study demonstrate desirable sealing capacity of the TMS for geologic CO 2 sequestration in reservoir sandstones of the Lower Tuscaloosa and could provide an analogue to other potential CO 2 sequestration top seals.

Louisiana, Mississippi↗

USGS2020

Corrigendum to "A remote sensing-based model of tidal marsh aboveground carbon stocks for the conterminous United States" [ISPRS J. Photogram. Rem. Sens.139 (2018) 255-271]

The authors regret that two thirds of the San Francisco Bay biomass data included in the Landsat random forest models were not scaled to the proper units of grams per square meter. This error affects the Landsat-only models in the article, which are models #1-4 shown in Table 6. The authors have thoroughly investigated the error and found that the final random forest model, including the selected dependent and independent variables, is still the most appropriate model for representing CONUS-wide tidal marsh aboveground biomass and carbon (C). Using the properly scaled biomass data we have corrected remote sensing-based estimates of tidal marsh aboveground biomass and C stocks, and we have corrected Tables 4, 6, 7 and 8 and Figures 5, 6, and 9 of the original article.

ISPRS Journal of Photogrammetry and Remote Sensing↗

USGS2004

Application of deterministic deconvolution of ground-penetrating radar data in a study of carbonate strata

We successfully applied deterministic deconvolution to real ground-penetrating radar (GPR) data by using the source wavelet that was generated in and transmitted through air as the operator. The GPR data were collected with 400-MHz antennas on a bench adjacent to a cleanly exposed quarry face. The quarry site is characterized by horizontally bedded carbonate strata with shale partings. In order to provide groundtruth for this deconvolution approach, 23 conductive rods were drilled into the quarry face at key locations. The steel rods provided critical information for: (1) correlation between reflections on GPR data and geologic features exposed in the quarry face, (2) GPR resolution limits, (3) accuracy of velocities calculated from common midpoint data and (4) identifying any multiples. Comparing the results of deconvolved data with non-deconvolved data demonstrates the effectiveness of deterministic deconvolution in low dielectric-loss media for increased accuracy of velocity models (improved at least 10-15% in our study after deterministic deconvolution), increased vertical and horizontal resolution of specific geologic features and more accurate representation of geologic features as confirmed from detailed study of the adjacent quarry wall. ?? 2004 Elsevier B.V. All rights reserved.

Journal of Applied Geophysics↗

USGS2006

Carbon and nitrogen fixation differ between successional stages of biological soil crusts in the Colorado Plateau and Chihuahuan Desert

Biological soil crusts (cyanobacteria, mosses and lichens collectively) perform essential ecosystem services, including carbon (C) and nitrogen (N) fixation. Climate and land-use change are converting later successional soil crusts to early successional soil crusts with lower C and N fixation rates. To quantify the effect of such conversions on C and N dynamics in desert ecosystems we seasonally measured diurnal fixation rates in different biological soil crusts. We classified plots on the Colorado Plateau (Canyonlands) and Chihuahuan Desert (Jornada) as early (Microcoleus) or later successional (Nostoc/Scytonema or Placidium/Collema) and measured photosynthesis (Pn), nitrogenase activity (NA), and chlorophyll fluorescence (Fv/Fm) on metabolically active (moist) soil crusts. Later successional crusts typically had greater Pn, averaging 1.2-1.3-fold higher daily C fixation in Canyonlands and 2.4-2.8-fold higher in the Jornada. Later successional crusts also had greater NA, averaging 1.3-7.5-fold higher daily N fixation in Canyonlands and 1.3-25.0-fold higher in the Jornada. Mean daily Fv/Fm was also greater in later successional Canyonlands crusts during winter, and Jornada crusts during all seasons except summer. Together these findings indicate conversion of soil crusts back to early successional stages results in large reductions of C and N inputs into these ecosystems.

Journal of Arid Environments↗

USGS2014

Integration of stable carbon isotope, microbial community, dissolved hydrogen gas, and 2 H H 2 O tracer data to assess bioaugmentation for chlorinated ethene degradation in fractured rocks

An in situ bioaugmentation (BA) experiment was conducted to understand processes controlling microbial dechlorination of trichloroethene (TCE) in groundwater at the Naval Air Warfare Center (NAWC), West Trenton, NJ. In the BA experiment, an electron donor (emulsified vegetable oil and sodium lactate) and a chloro-respiring microbial consortium were injected into a well in fractured mudstone of Triassic age. Water enriched in 2 H was also injected as a tracer of the BA solution, to monitor advective transport processes. The changes in concentration and the δ 13 C of TCE, cis-dichloroethene (cis-DCE), and vinyl chloride (VC); the δ 2 H of water; changes in the abundance of the microbial communities; and the concentration of dissolved H2 gas compared to pre- test conditions, provided multiple lines of evidence that enhanced biodegradation occurred in the injection well and in two downgradient wells. For those wells where the biodegradation was stimulated intensively, the sum of the molar chlorinated ethene (CE) concentrations in post-BA water was higher than that of the sum of the pre-BA background molar CE concentrations. The concentration ratios of TCE/(cis-DCE + VC) indicated that the increase in molar CE concentration may result from additional TCE mobilized from the rock matrix in response to the oil injection or due to desorption/diffusion. The stable carbon isotope mass-balance calculations show that the weighted average 13 C isotope of the CEs was enriched for around a year compared to the background value in a two year monitoring period, an effective indication that dechlorination of VC was occurring. Insights gained from this study can be applied to efforts to use BA in other fractured rock systems. The study demonstrates that a BA approach can substantially enhance in situ bioremediation not only in fractures connected to the injection well, but also in the rock matrix around the well due to processes such as diffusion and desorption. Because the effect of the BA was intensive only in wells where an amendment was distributed during injection, it is necessary to adequately distribute the amendments throughout the fractured rock to achieve substantial bioremediation. The slowdown in BA effect after a year is due to some extend to the decrease abundant of appropriate microbes, but more likely the decreased concentration of electron donor.

New Jersey↗

USGS2018

Variability of organic carbon content and the retention and release of trichloroethene in the rock matrix of a mudstone aquifer

Contaminants diffusing from fractures into the immobile porosity of the rock matrix are subject to prolonged residence times. Organic contaminants can adsorb onto organic carbonaceous materials in the matrix extending contaminant retention. An investigation of spatial variability of the fraction of organic carbon ( f oc ) is conducted on samples of rock core from seven closely spaced boreholes in a mudstone aquifer contaminated with trichloroethene (TCE). A total of 378 samples were analyzed at depths between 14 and 36 m below land surface. Mudstone units associated with deep water deposition have the largest f oc , with a maximum value of 0.0396, and units associated with shallow water deposition have the smallest f oc . Even though f oc correlates with depositional conditions, f oc still varies over more than an order of magnitude in continuous mudstone layers between boreholes, and there is large variability in f oc over short distances perpendicular to bedding. Simulations of diffusion and linear equilibrium adsorption of TCE using spatially variable f oc in the rock matrix show order of magnitude variability in the adsorbed TCE over short distances in the matrix and residence times extending to hundreds of years following remediation in adjacent fractures. Simulations using average values of f oc do not capture the range of TCE mass that can be retained in a rock matrix characterized by spatially variable f oc . Bounds on TCE mass within the rock matrix can be obtained by simulations with spatially uniform values of f oc equal to the maximum and minimum values of f oc for a given mudstone unit.

New Jersey↗

USGS2021

Telemetry evaluation of carbon dioxide as a behavioral deterrent for invasive carps

Carbon dioxide (CO 2 ) mixed into water is being explored as a possible management strategy to deter the upstream movements of invasive carps through navigation locks and other migratory pinch-points. This study used two-dimensional acoustic telemetry to assess the effectiveness of dissolved CO 2 as a chemosensory deterrent to two carp species in a large U-shaped pond. Free-swimming movements of telemetered bighead carp ( Hypophthalmichthys nobilis ) and grass carp ( Ctenopharyngodon idella ) were documented 24 h before treatment and 24 h during treatments at 60, 121 and 213 mg/L CO 2 (mean concentrations in pond water). Several behavioral endpoints were then quantified and compared to evaluate deterrence efficacy. In general, results showed that both carp species responded similarly to CO 2 treatments. Carps consistently relocated into areas away from the injection site and made fewer attempts to re-enter CO 2 treated areas. On average, CO 2 treatments reduced mid-line crosses between untreated and treated sides of the pond by 58% at 121 mg/L CO 2 and 78% at 213 mg/L CO 2 relative to normal swimming movements recorded before treatment. Fish swim speeds increased significantly when inside the CO 2 plume during treatments during 213 mg/L CO 2 trials relative to swim speeds outside the plume, possibly indicative of active searching and avoidance responses. Overall, this study found that CO 2 altered the behavior of bighead carp and grass carp. Natural resource agencies could consider the CO 2 concentrations identified in this study to inform future applications to deter invasive carps from locations where they are at-risk to move upstream.

Journal of Great Lakes Research↗

USGS2013

Export of dissolved organic carbon from the Penobscot River basin in north-central Maine

Dissolved organic carbon (DOC) flux from the Penobscot River and its major tributaries in Maine was determined using continuous discharge measurements, discrete water sampling, and the LOADEST regression software. The average daily flux during 2004–2007 was 71 kg C ha −1 yr −1 (392 Mt C d −1 ), an amount larger than measured in most northern temperate and boreal rivers. Distinct seasonal variation was observed in the relation between concentration and discharge (C–Q). During June through December (summer/fall), there was a relatively steep positive C–Q relation where concentration increased by a factor of 2–3 over the approximately 20-fold range of observed stream discharge for the Penobscot River near Eddington, Maine. In contrast, during January through May (winter/spring), DOC concentration did not increase with increasing discharge. In addition, we observed a major shift in the C–Q between 2004–2005 and 2006–2007, apparently resulting from unprecedented rainfall, runoff, and soil flushing beginning in late fall 2005. The relative contribution to the total Penobscot River basin DOC flux from each tributary varied dramatically by season, reflecting the role of large regulated reservoirs in certain basins. DOC concentration and flux per unit watershed area were highest in tributaries containing the largest areas in palustrine wetlands. Tributary DOC concentration and flux was positively correlated to percentage wetland area. Climatic or environmental changes that influence the magnitude or timing of river discharge or the abundance of wetlands will likely affect the export of DOC to the near-coastal ocean.

Maine↗

USGS2006

Drowned coralline algal dominated deposits off Lanai, Hawaii; carbonate accretion and vertical tectonics over the last 30 ka

We present detailed bathymetry, remotely operated vehicle (ROV) and submersible observations, and sedimentary and radiocarbon age data from carbonate deposits recovered from two submerged terraces at − 150 m (T1) and − 230 m (T2) off Lanai, Hawaii. The tops of the terraces are veneered by relatively thin (<5 m) in situ accumulations of coralline algal nodule, coralgal nodule, Halimeda and a derived oolitic facies deposited in intermediate (30–60 m) to deep fore-reef slope settings (60–120 m). The data are used to develop a sedimentary facies model that is consistent with eustatic sea-level variations over the last 30 ka. Both nodule facies on T1 and T2 initiated growth 30–29 ka following a fall in sea level of &sim;50 m and increase in bottom currents during the transition from Marine Isotope Stage 3 to 2. The nodules accreted slowly throughout the Last Glacial Maximum when sea-level was relatively stable. Drowning occurred during the early deglaciation (17–16 ka) and was marked by the complete drowning of coralline algal nodules facies on T2 and incipient drowning of coralgal facies on T1. Abrupt sea-level rise during the middle deglaciation, perhaps associated with global meltwater pulse 1A (14–15 ka), finally drowned the coralgal facies on T1, which in turn was overlain by a deep-water Halimeda facies or an oolitic facies derived from upslope. Our data indicates that Lanai has experienced relatively little vertical tectonic movement over the last 30 ka. Using paleobathymetric data derived from the sedimentary facies, age vs. depth relationships, and published sea-level curves, we estimate that Lanai could be either slowly uplifting or subsiding, but at rates <0.1 m/kyr (uplift) or <0.4 m/kyr (subsidence) over this 30 kyr period.

Hawai'i↗