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At least 541 records · Page 30Linked to original sources

USGS2013

Emissions of carbon dioxide and methane from a headwater stream network of interior Alaska

Boreal ecosystems store significant quantities of organic carbon (C) that may be vulnerable to degradation as a result of a warming climate. Despite their limited coverage on the landscape, streams play a significant role in the processing, gaseous emission, and downstream export of C, and small streams are thought to be particularly important because of their close connection with the surrounding landscape. However, ecosystem carbon studies do not commonly incorporate the role of the aquatic conduit. We measured carbon dioxide (CO 2 ) and methane (CH 4 ) concentrations and emissions in a headwater stream network of interior Alaska underlain by permafrost to assess the potential role of stream gas emissions in the regional carbon balance. First-order streams exhibited the greatest variability in fluxes of CO 2 and CH 4, and the greatest mean p CO 2 . High-resolution time series of stream p CO 2 and discharge at two locations on one first-order stream showed opposing p CO 2 responses to storm events, indicating the importance of hydrologic flowpaths connecting CO 2 -rich soils with surface waters. Repeated longitudinal surveys on the stream showed consistent areas of elevated p CO 2 and p CH 4 , indicative of discrete hydrologic flowpaths delivering soil water and groundwater having varying chemistry. Up-scaled basin estimates of stream gas emissions suggest that streams may contribute significantly to catchment-wide CH 4 emissions. Overall, our results indicate that while stream-specific gas emission rates are disproportionately high relative to the terrestrial landscape, both stream surface area and catchment normalized emission rates were lower than those documented for the Yukon River Basin as a whole. This may be due to limitations of C sources and/or C transport to surface waters.

Journal of Geophysical Research G: Biogeosciences↗

USGS2016

Intertidal salt marshes as an important source of inorganic carbon to the coastal ocean

Dynamic tidal export of dissolved inorganic carbon (DIC) to the coastal ocean from highly productive intertidal marshes and its effects on seawater carbonate chemistry are thoroughly evaluated. The study uses a comprehensive approach by combining tidal water sampling of CO 2 parameters across seasons, continuous in situ measurements of biogeochemically-relevant parameters and water fluxes, with high-resolution modeling in an intertidal salt marsh of the U.S. northeast region. Salt marshes can acidify and alkalize tidal water by injecting CO 2 (DIC) and total alkalinity (TA). DIC and TA generation may also be decoupled due to differential effects of marsh aerobic and anaerobic respiration on DIC and TA. As marsh DIC is added to tidal water, the buffering capacity first decreases to a minimum and then increases quickly. Large additions of marsh DIC can result in higher buffering capacity in ebbing tide than incoming tide. Alkalization of tidal water, which mostly occurs in the summer due to anaerobic respiration, can further modify buffering capacity. Marsh exports of DIC and alkalinity may have complex implications for the future, more acidified ocean. Marsh DIC export exhibits high variability over tidal and seasonal cycles, which is modulated by both marsh DIC generation and by water fluxes. The marsh DIC export of 414 g C m −2 yr −1 , based on high-resolution measurements and modeling, is more than twice the previous estimates. It is a major term in the marsh carbon budget and translates to one of the largest carbon fluxes along the U.S. East Coast.

Massachusetts↗

USGS2023

High-frequency variability of carbon dioxide fluxes in tidal water over a temperate salt marsh

Existing analyses of salt marsh carbon budgets rarely quantify carbon loss as CO 2 through the air–water interface in inundated marshes. This study estimates the variability of partial pressure of CO 2 ( p CO 2 ) and air–water CO 2 fluxes over summer and fall of 2014 and 2015 using high-frequency measurements of tidal water p CO 2 in a salt marsh of the U.S. northeast region. Monthly mean CO 2 effluxes varied in the range of 5.4–25.6 mmol m −2 marsh d −1 (monthly median: 4.8–24.7 mmol m −2 marsh d −1 ) during July to November from the tidal creek and tidally-inundated vegetated platform. The source of CO 2 effluxes was partitioned between the marsh and estuary using a mixing model. The monthly mean marsh-contributed CO 2 effluxes accounted for a dominant portion (69%) of total CO 2 effluxes in the inundated marsh, which was 3–23% (mean 13%) of the corresponding lateral flux rate of dissolved inorganic carbon (DIC) from marsh to estuary. Photosynthesis in tidal water substantially reduced the CO 2 evasion, accounting for 1–86% (mean 31%) of potential CO 2 evasion and 2–26% (mean 11%) of corresponding lateral transport DIC fluxes, indicating the important role of photosynthesis in controlling the air–water CO 2 evasion in the inundated salt marsh. This study demonstrates that CO 2 evasion from inundated salt marshes is a significant loss term for carbon that is fixed within marshes.

Massachusetts↗

USGS2014

Distribution of soil organic carbon in the conterminous United States

The U.S. Soil Survey Geographic (SSURGO) database provides detailed soil mapping for most of the conterminous United States (CONUS). These data have been used to formulate estimates of soil carbon stocks, and have been useful for environmental models, including plant productivity models, hydrologic models, and ecological models for studies of greenhouse gas exchange. The data were compiled by the U.S. Department of Agriculture Natural Resources Conservation Service (NRCS) from 1:24,000-scale or 1:12,000-scale maps. It was found that the total soil organic carbon stock in CONUS to 1 m depth is 57 Pg C and for the total profile is 73 Pg C, as estimated from SSURGO with data gaps filled from the 1:250,000-scale Digital General Soil Map. We explore the non-linear distribution of soil carbon on the landscape and with depth in the soil, and the implications for sampling strategies that result from the observed soil carbon variability.

Book chapter↗

USGS1995

Interlaboratory study of a method for determining nonvolatile organic carbon in aquifer materials

The organic carbon fraction in aquifer materials exerts a major influence on the subsurface mobilities of organic and organic-associated contaminants. The spatial distribution of total organic carbon (TOC) in aquifer materials must be determined before the transport of hydrophobic organic pollutants in aquifers can be modeled accurately. Previous interlaboratory studies showed that it is difficult to measure TOC concentrations <0.1% in aquifer materials, when total inorganic carbon (TIC) concentrations are >1%. We have tested a new analytical method designed to improve the accuracy and precision of nonvolatile TOC quantitation in geologic materials that also contain carbonate minerals. Four authentic aquifer materials and one NIST standard reference material were selected as test materials for a blind collaborative study. Nonvolatile TOC in these materials ranged from 0.05 to 1.4%, while TIC ranged from 0.46 to 12.6%. Sample replicates were digested with sulfurous acid, dried at 40??C, and then combusted at 950??C using LECO or UIC instruments. For the three test materials that contained >2% TIC, incomplete acidification resulted in a systematic positive bias of TOC values reported by five of the six laboratories that used the test method. Participants did not have enough time to become proficient with the new method before they analyzed the test materials. A seventh laboratory successfully used an alternative method that analyzed separate liquid and solid fractions of the acidified sample residues. ?? 1995 Springer-Verlag.

Environmental Geology↗

USGS1985

Carbon, oxygen and hydrogen isotope abundances inStylites reflect its unique physiology

Natural abundances of oxygen-18, carbon-14, carbon-13 and deuterium were measured in Stylites andicola , a terrestrial vascular plant lacking stomates, and two terrestrial plant species having stomates that grew nearby. No substantial differences in oxygen-18 and carbon-13 abundances were observed among the three species. The deuterium concentration in Stylites was much higher than in the other species, confirming a previous report of CAM in Stylites. Stylites was depleted in carbon-14 relative to the present day atmosphere, consistent with the proposal that it fixes CO 2 derived from decomposing peat.

Oecologia↗

USGS1981

210 Pb method for estimating the rate of carbonate sand sedimentation

The plot of 210 Pb activity against depth in carbonate sands on the Virgin Island Bank is a negative asymmetric hyperbolic curve. As depth increases, an initial rapid decrease in 210 Pb activity caused by the decay of unsupported 210 Pb and 226 Ra is followed by increasing activity as a result of 210 Pb achieving equilibrium with in growing 230 Th. As this curve is time dependent, an estimate of the relative ages in carbonate sequences and the rates of net carbonate accumulation can be made. The ease of 210 Pb activity determinations makes this procedure an attractive method in obtaining carbonate sand accumulation rates.

Geo-Marine Letters↗

USGS2009

Basanite-nephelinite suite from early Kilauea: Carbonated melts of phlogopite-garnet peridotite at Hawaii's leading magmatic edge

A basanite-nephelinite glass suite from early submarine Kilauea defines a continuous compositional array marked by increasing concentrations of incompatible components with decreasing SiO 2 , MgO, and Al 2 O 3 . Like peripheral and post-shield strongly alkalic Hawaiian localities (Clague et al. in J Volcanol Geotherm Res 151:279-307, 2006; Dixon et al. in J Pet 38:911-939, 1997), the early Kilauea basanite-nephelinite glasses are interpreted as olivine fractionation products from primary magnesian alkalic liquids. For early Kilauea, these were saturated with a garnet-phlogopite-sulfide peridotite assemblage, with elevated dissolved CO 2 contents responsible for the liquids' distinctly low-SiO 2 concentrations. Reconstructed primitive liquids for early Kilauea and other Hawaiian strongly alkalic localities are similar to experimental 3 GPa low-degree melts of moderately carbonated garnet lherzolite, and estimated parent magma temperatures of 1,350-1,400??C (olivine-liquid geothermometry) match the ambient upper mantle geotherm shortly beneath the base of the lithosphere. The ???3 GPa source regions were too hot for stable crystalline carbonate and may have consisted of ambient upper mantle peridotite containing interstitial carbonate-silicate or carbonatitic liquid, possibly (Dixon et al. in Geochem Geophys Geosyst 9(9):Q09005, 2008), although not necessarily, from the Hawaiian mantle plume. Carbonate-enriched domains were particularly susceptible to further melting upon modest decompression during upward lithospheric flexure beneath the advancing Hawaiian Arch, or by conductive heating or upward drag by the Hawaiian mantle plume. The early Kilauea basanite-nephelinite suite has a HIMU-influenced isotopic character unlike other Hawaiian magmas (Shimizu et al. in EOS Tran Amer Geophys Union 82(47): abstr V12B-0962, 2001; Shimizu et al. in Geochim Cosmochim Acta 66(15A):710, 2002) but consistent with oceanic carbonatite involvement (Hoernle et al. in Contrib Mineral Petrol 142:520-542, 2002). It may represent the melting products of a fertile domain in the ambient upper mantle impinged upon and perturbed by the sustained plume source that feeds later shield-stage magmatism. ?? US Government 2009.

Contributions to Mineralogy and Petrology↗

USGS2025

Variation in soil organic carbon across a latitudinal chronosequence of mangrove poleward expansion

The critical carbon sink provided by coastal wetlands, known as blue carbon, can be affected by multiple aspects of climate change. One important example is warming-induced mangrove poleward expansion, which is shifting dominant plant cover across tropical–temperate transitional zones and altering ecosystem structure and function. We examined how mangrove expansion affects soil organic carbon (SOC) quantity and source, using measurements of SOC density and isotopic signatures (δ 13 C and δ 15 N) at 15 sites across Florida’s west coast (USA). The sampled sites represent examples of three expansion stages: a latitudinal chronosequence of mangrove expansion, spanning mature mangroves in the south, former ecotones at mid latitudes, and current ecotones in the north. Our analyses of soil core data indicate that mangrove expansion stage is a significant predictor of SOC density, δ 13 C, and δ 15 N, but not C:N ratio. Current ecotones exhibited significantly lower SOC density but higher δ 13 C, suggesting a greater contribution of preexisting C 4 salt marshes, while no difference was found between former ecotones and mature mangroves. SOC density, δ 13 C, and δ 15 N were found to vary with mangrove aboveground biomass, stage, and sedimentary setting along the latitudinal gradient. For all three mangrove expansion stages, SOC density decreased with depth, but δ 13 C showed no vertical trend, suggesting that mangroves contributed organic carbon to the entire 20-cm soil profile. The observed regional trend of SOC across mangrove expansion stages highlights the ecological impacts of warming-driven vegetation shifts in coastal wetlands, though further evidence is needed to determine the primary drivers and mechanisms, while also considering local and regional environmental factors.

Florida↗

USGS2009

Identifying sources of dissolved organic carbon in agriculturally dominated rivers using radiocarbon age dating: Sacramento-San Joaquin River Basin, California

We used radiocarbon measurements of dissolved organic carbon (DOC) to resolve sources of riverine carbon within agriculturally dominated landscapes in California. During 2003 and 2004, average Δ 14 C for DOC was −254‰ in agricultural drains in the Sacramento–San Joaquin Delta, −218‰ in the San Joaquin River, −175‰ in the California State Water Project and −152‰ in the Sacramento River. The age of bulk DOC transiting the rivers of California’s Central Valley is the oldest reported for large rivers and suggests wide-spread loss of soil organic matter caused by agriculture and urbanization. Using DAX 8 adsorbent, we isolated and measured 14 C concentrations in hydrophobic acid fractions (HPOA); river samples showed evidence of bomb-pulse carbon with average Δ 14 C of 91 and 76‰ for the San Joaquin and Sacramento Rivers, respectively, with older HPOA, −204‰, observed in agricultural drains. An operationally defined non-HPOA fraction of DOC was observed in the San Joaquin River with seasonally computed Δ 14 C values of between −275 and −687‰; the source of this aged material was hypothesized to be physically protected organic-matter in high clay-content soils and agrochemicals (i.e., radiocarbon-dead material) applied to farmlands. Mixing models suggest that the Sacramento River contributes about 50% of the DOC load in the California State Water Project, and agricultural drains contribute approximately one-third of the load. In contrast to studies showing stabilization of soil carbon pools within one or two decades following land conversion, sustained loss of soil organic matter, occurring many decades after the initial agricultural-land conversion, was observed in California’s Central Valley.

California↗

USGS2026

Water table rise sustains carbon release from soils in wetland-dominated landscapes: An intact soil core study

Wetland-dominated landscapes influence carbon cycling through their potential to act as both carbon sinks and sources. Wetlands in low-relief landscapes have dynamic terrestrial-aquatic interfaces that change seasonally with variable surface water and groundwater levels. However, few studies have directly quantified dissolved organic matter (DOM) release and greenhouse gas (CO 2 , CH 4 ) fluxes from wetland soils along terrestrial-aquatic interfaces as they are seasonally re-saturated by groundwater. To estimate groundwater-mediated soil DOM and gas fluxes, we performed laboratory simulations of vertical groundwater rise on intact soil cores collected from four Delmarva bay wetlands located in the Mid-Atlantic United States. At each wetland, one core was collected from within the wetland basin and the other from the transitional zone at the basin edge. Cores were re-saturated with groundwater over 15 days and then kept fully saturated for an additional 25 days. Source groundwater, soil porewater, and exfiltrated surface water samples were collected and analyzed for pH, ORP, DOM concentration, and DOM optical indices. In both the wetland and transition zone cores, porewater DOM concentrations increased over the wet up and were sustained during prolonged saturation. Optical indices shifted from recently produced, microbial-like signatures towards aromatic, terrestrial-like signatures. Fluxes of CO 2 decreased as the duration of soil saturation increased and soil cores switched from CH 4 sinks to sources upon full soil core saturation. Results indicate that groundwater rise sustains carbon mobilization from soils in wetland-dominated landscapes, emphasizing the need to understand how climate-driven changes to groundwater dynamics may affect carbon fluxes along terrestrial-aquatic interfaces.

Delaware, Maryland↗

USGS2012

Influence of dietary carbon on mercury bioaccumulation in streams of the Adirondack Mountains of New York and the Coastal Plain of South Carolina, USA

We studied lower food webs in streams of two mercury-sensitive regions to determine whether variations in consumer foraging strategy and resultant dietary carbon signatures accounted for observed within-site and among-site variations in consumer mercury concentration. We collected macroinvertebrates (primary consumers and predators) and selected forage fishes from three sites in the Adirondack Mountains of New York, and three sites in the Coastal Plain of South Carolina, for analysis of mercury (Hg) and stable isotopes of carbon (δ 13 C) and nitrogen (δ 15 N). Among primary consumers, scrapers and filterers had higher MeHg and more depleted δ 13 C than shredders from the same site. Variation in δ 13 C accounted for up to 34 % of within-site variation in MeHg among primary consumers, beyond that explained by δ 15 N, an indicator of trophic position. Consumer δ 13 C accounted for 10 % of the variation in Hg among predatory macroinvertebrates and forage fishes across these six sites, after accounting for environmental aqueous methylmercury (MeHg, 5 % of variation) and base-N adjusted consumer trophic position (Δδ 15 N, 22 % of variation). The δ 13 C spatial pattern within consumer taxa groups corresponded to differences in benthic habitat shading among sites. Consumers from relatively more-shaded sites had more enriched δ 13 C that was more similar to typical detrital δ 13 C, while those from the relatively more-open sites had more depleted δ 13 C. Although we could not clearly attribute these differences strictly to differences in assimilation of carbon from terrestrial or in-channel sources, greater potential for benthic primary production at more open sites might play a role. We found significant variation among consumers within and among sites in carbon source; this may be related to within-site differences in diet and foraging habitat, and to among-site differences in environmental conditions that influence primary production. These observations suggest that different foraging strategies and habitats influence MeHg bioaccumulation in streams, even at relatively small spatial scales. Such influence must be considered when selecting lower trophic level consumers as sentinels of MeHg bioaccumulation for comparison within and among sites.

New York;South Carolina↗

USGS2007

Mercury and organic carbon dynamics during runoff episodes from a northeastern USA watershed

Mercury and organic carbon concentrations vary dynamically in streamwater at the Sleepers River Research Watershed in Vermont, USA. Total mercury (THg) concentrations ranged from 0.53 to 93.8 ng/L during a 3-year period of study. The highest mercury (Hg) concentrations occurred slightly before peak flows and were associated with the highest organic carbon (OC) concentrations. Dissolved Hg (DHg) was the dominant form in the upland catchments; particulate Hg (PHg) dominated in the lowland catchments. The concentration of hydrophobic acid (HPOA), the major component of dissolved organic carbon (DOC), explained 41–98% of the variability of DHg concentration while DOC flux explained 68–85% of the variability in DHg flux, indicating both quality and quantity of the DOC substantially influenced the transport and fate of DHg. Particulate organic carbon (POC) concentrations explained 50% of the PHg variability, indicating that POC is an important transport mechanism for PHg. Despite available sources of DHg and wetlands in the upland catchments, dissolved methylmercury (DmeHg) concentrations in streamwaters were below detection limit (0.04 ng/L). PHg and particulate methylmercury (PmeHg) had a strong positive correlation ( r 2 = 0.84, p < 0.0001), suggesting a common source; likely in-stream or near-stream POC eroded or re-suspended during spring snowmelt and summer storms. Ratios of PmeHg to THg were low and fairly constant despite an apparent higher methylmercury (meHg) production potential in the summer. Methylmercury production in soils and stream sediments was below detection during snowmelt in April and highest in stream sediments (compared to forest and wetland soils) sampled in July. Using the watershed approach, the correlation of the percent of wetland cover to TmeHg concentrations in streamwater indicates that poorly drained wetland soils are a source of meHg and the relatively high concentrations found in stream surface sediments in July indicate these zones are a meHg sink.

Water, Air, & Soil Pollution↗

USGS2016

Nitrate removal from agricultural drainage ditch sediments with amendments of organic carbon: Potential for an innovative best management practice

Agricultural fertilizer applications have resulted in loading of nutrients to agricultural drainage ditches in the Lower Mississippi Alluvial Valley. The purpose of this study was to determine effects of dissolved organic carbon (DOC) and particulate organic carbon (POC) amendments on nitrate-nitrogen (NO 3 − -N) removal from overlying water, pore water, and sediment of an agricultural drainage ditch. Two experiments were conducted. In experiment 1, control (i.e., no amendment), DOC, and POC treatments were applied in laboratory microcosms for time intervals of 3, 7, 14, and 28 days. In experiment 2, control, DOC, and POC treatments were applied in microcosms at C/N ratios of 5:1, 10:1, 15:1, and 20:1. There were statistically significant effects of organic carbon amendments in experiment 1 ( F 2,71 = 27.1, P < 0.001) and experiment 2 ( F 2,53 = 39.1, P < 0.001), time ( F 1,71 = 14.5, P < 0.001) in experiment 1, and C/N ratio ( F 1,53 = 36.5, P < 0.001) in experiment 2. NO 3 − -N removal varied from 60 to 100 % in overlying water among all treatments. The lowest NO 3 − -N removals in experiment 1 were observed in the control at 14 and 28 days, which were significantly less than in DOC and POC 14- and 28-day treatments. In experiment 2, significantly less NO 3 − -N was removed in overlying water of the control compared to DOC and POC treatments at all C/N ratios. Amendments of DOC and POC made to drainage ditch sediment: (1) increased NO 3 − -N removal, especially over longer time intervals (14 to 28 days); (2) increased NO 3 − -N removal, regardless of C/N ratio; and (3) NO 3 − -N removal was best at a 5:1 C/N ratio. This study provides support for continued investigation on the use of organic carbon amendments as a best management practice for NO 3 − -N removal in agricultural drainage ditches.

Water, Air, & Soil Pollution↗

USGS2009

Effects of vegetation restoration and slope positions on soil aggregation and soil carbon accumulation on heavily eroded tropical land of Southern China

Background aim and scope Soil organic carbon (SOC) accumulation is strongly affected by soil erosion and deposition that differ at slope positions of a watershed. However, studies on the effects of topography on soil aggregation and SOC dynamics, especially after the implementation of vegetation restoration, are rare. Poorly understood mechanisms and a lack of quantification for the suite of ecological benefits brought by the impacts of topography after planting further obstructed our understanding of terrestrial ecosystem carbon (C) sequestration. The purposes of this study are to (1) quantify the impacts of vegetation restoration on size and stability of soil aggregates and the sequestration of C in soil and (2) to address the impacts of various slope locations on aggregates and SOC distribution. Materials and methods The experimental sites were set up in 1959 on a highly disturbed barren land in a tropical and coastal area of Guangdong province in South China. One site received human-induced vegetation restoration (the restored site), while the other received no planting and has remained as barren land (the barren site). The soil in the study sites was a latosol developed from granite. Soil samples were taken from 0 to 20 and 20 to 40 cm soil layer at shoulder and toe slope positions at both sites for comparisons. Soils were analyzed for proportion of soil macroaggregates (>0.25 mm), the SOC in soil layers, and the aggregate soil organic carbon (AOC) at different aggregate sizes. Results and discussion Measurements in 2007 showed that fractions of water stable macroaggregates in 0–40 cm at shoulder and toe slope ranged from 28% to 45%, about one third to one half of those of dry macroaggregates (91–95%) at the restored site. Soil macroaggregates were not detected at barren site in 2007. Average SOC storage in 0–40 cm soil layer of shoulder and toe slope positions at the restored site was 56.5 ± 10.9 Mg C ha −1 , about 2.4 times of that (23.4 ± 4.6 Mg C ha −1 ) at barren site in 2007. Since 1959, the soil aggregation and SOC storage are significantly improved at the restored site; opposite to that, soil physical and chemical quality has remained low on the barren land without planting. SOC storage in 0–40 cm at toe slope was 15.9 ± 1.8 Mg C ha −1 , which is only half of that (30.9 ± 9 Mg C ha −1 ) at shoulder slope of the barren site; this is opposite to the pattern found at restored site. The ratios of AOC in 0–20 cm to AOC in 20–40 cm at toe slope were lower than those at shoulder slope of the restored site. The comparison of organic carbon sequestered in soils at different slope positions suggest that soil aggregates played a role in sequestering C based upon landscape positions and soil profile depth as a consequence of soil erosion and deposition. Conclusions Results indicate that vegetation restoration and SOC accumulation significantly enhance soil aggregation, which in turn promotes further organic C accumulation in the aggregates via physical protection. Soil aggregation and soil C accumulation differed between slope positions. Soil aggregation was significantly enhanced in 0–20 cm layer and aggregates absorb C into deep layers in depositional environment (toe slope) under protection from human disturbances. The interactions of erosion–deposition, soil aggregates, and vegetation restoration play important roles on SOC accumulation and redistribution on land. Recommendations and perspectives The positive feedback between SOC and soil aggregates should be evaluated for improving the quantification of the impacts of land use change, erosion, and deposition on the dynamics of SOC and soil structure under the global climate change.

Guandong Province↗

USGS2011

Plant allocation of carbon to defense as a function of herbivory, light and nutrient availability

We use modeling to determine the optimal relative plant carbon allocations between foliage, fine roots, anti-herbivore defense, and reproduction to maximize reproductive output. The model treats these plant components and the herbivore compartment as variables. Herbivory is assumed to be purely folivory. Key external factors include nutrient availability, degree of shading, and intensity of herbivory. Three alternative functional responses are used for herbivory, two of which are variations on donor-dependent herbivore (models 1a and 1b) and one of which is a Lotka–Volterra type of interaction (model 2). All three were modified to include the negative effect of chemical defenses on the herbivore. Analysis showed that, for all three models, two stable equilibria could occur, which differs from most common functional responses when no plant defense component is included. Optimal strategies of carbon allocation were defined as the maximum biomass of reproductive propagules produced per unit time, and found to vary with changes in external factors. Increased intensity of herbivory always led to an increase in the fractional allocation of carbon to defense. Decreases in available limiting nutrient generally led to increasing importance of defense. Decreases in available light had little effect on defense but led to increased allocation to foliage. Decreases in limiting nutrient and available light led to decreases in allocation to reproduction in models 1a and 1b but not model 2. Increases in allocation to plant defense were usually accompanied by shifts in carbon allocation away from fine roots, possibly because higher plant defense reduced the loss of nutrients to herbivory.

Theoretical Ecology↗

USGS2008

Increased terrestrial to ocean sediment and carbon fluxes in the northern Chesapeake Bay associated with twentieth century land alteration

We calculated Chesapeake Bay (CB) sediment and carbon fluxes before and after major anthropogenic land clearance using robust monitoring, modeling and sedimentary data. Four distinct fluxes in the estuarine system were considered including (1) the flux of eroded material from the watershed to streams, (2) the flux of suspended sediment at river fall lines, (3) the burial flux in tributary sediments, and (4) the burial flux in main CB sediments. The sedimentary maximum in Ambrosia (ragweed) pollen marked peak land clearance (~1900 a.d.). Rivers feeding CB had a total organic carbon (TOC)/total suspended solids of 0.24??0.12, and we used this observation to calculate TOC fluxes from sediment fluxes. Sediment and carbon fluxes increased by 138-269% across all four regions after land clearance. Our results demonstrate that sediment delivery to CB is subject to significant lags and that excess post-land clearance sediment loads have not reached the ocean. Post-land clearance increases in erosional flux from watersheds, and burial in estuaries are important processes that must be considered to calculate accurate global sediment and carbon budgets. ?? 2008 Coastal and Estuarine Research Federation.

Estuaries and Coasts↗

USGS2016

Ecosystem level methane fluxes from tidal freshwater and brackish marshes of the Mississippi River Delta: Implications for coastal wetland carbon projects

Sulfate from seawater inhibits methane production in tidal wetlands, and by extension, salinity has been used as a general predictor of methane emissions. With the need to reduce methane flux uncertainties from tidal wetlands, eddy covariance (EC) techniques provide an integrated methane budget. The goals of this study were to: 1) establish methane emissions from natural, freshwater and brackish wetlands in Louisiana based on EC; and 2) determine if EC estimates conform to a methane-salinity relationship derived from temperate tidal wetlands with chamber sampling. Annual estimates of methane emissions from this study were 62.3 g CH 4 /m 2 /yr and 13.8 g CH 4 /m 2 /yr for the freshwater and brackish (8–10 psu) sites, respectively. If it is assumed that long-term, annual soil carbon sequestration rates of natural marshes are ~200 g C/m 2 /yr (7.3 tCO 2 e/ha/yr), healthy brackish marshes could be expected to act as a net radiative sink, equivalent to less than one-half the soil carbon accumulation rate after subtracting methane emissions (4.1 tCO 2 e/ha/yr). Carbon sequestration rates would need case-by-case assessment, but the EC methane emissions estimates in this study conformed well to an existing salinity-methane model that should serve as a basis for establishing emission factors for wetland carbon offset projects.

Louisiana↗