Soil Phosphorus Characteristics of Natural and Created Wetlands in the Atchafalaya Delta, Louisiana.

Quantitative comparisons of artificially created and natural wetlands are typically confounded by differences in wetland age, with created wetlands being younger than their natural counterparts. Observed differences between these wetlands may be attributed to either age differences or an inability to reproduce natural wetland characteristics. The objectives of this research were to: compare the phosphorus characteristics of similarly aged, created and natural wetlands in the Atchafalaya Delta, Louisiana and determine the controls over phosphorus retention in these wetlands. A phosphorus fractionation procedure was used to identify the phosphorus fractions in sediments from natural and artificially created wetlands in the Atchafalaya Delta belonging to three age classes: young (\u3c1--3 years old), intermediate (5--10 years old), and old (15--20 years old). The young, created wetland was lower in total phosphorus than its natural counterpart due to its higher sand content. The intermediate-aged, created wetland had lower phosphorus contents than its natural counterpart due to higher organic matter and lower bulk density. Phosphorus contents of the old created and natural wetlands were similar. These differences between the created wetlands and their natural counterparts can be explained by the design of the created wetlands. Bedload sediment from the Atchafalaya River, which is dredged to form the created wetlands, had lower phosphorus and oxalate-extractable iron than the river\u27s suspended sediment, which forms the natural wetlands. Sediment recently deposited at both created and natural wetlands had similar phosphorus contents. In the Atchafalaya Delta, wetlands created with dredge sediment will have less phosphorus upon formation than natural wetlands of the same age, but if they are built to mimic the elevation gradient, shape and orientation of the natural wetlands they can develop phosphorus characteristics similar to natural wetlands through the deposition of river sediment

Understanding, characterizing, and communicating responses to ocean acidification : challenges and uncertainties

Author Posting. © The Oceanography Society, 2015. This article is posted here by permission of The Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 28, no. 2 (2015): 30-39, doi:10.5670/oceanog.2015.29.Over the past decade, ocean acidification (OA) has emerged as a major concern in ocean science. The field of OA is based on certainties—uptake of carbon dioxide into the global ocean alters its carbon chemistry, and many marine organisms, especially calcifiers, are sensitive to this change. However, the field must accommodate uncertainties about the seriousness of these impacts as it synthesizes and draws conclusions from multiple disciplines. There is pressure from stakeholders to expeditiously inform society about the extent to which OA will impact marine ecosystems and the people who depend on them. Ultimately, decisions about actions related to OA require evaluating risks about the likelihood and magnitude of these impacts. As the scientific literature accumulates, some of the uncertainty related to single-species sensitivity to OA is diminishing. Difficulties remain in scaling laboratory results to species and ecosystem responses in nature, though modeling exercises provide useful insight. As recognition of OA grows, scientists’ ability to communicate the certainties and uncertainties of our knowledge on OA is crucial for interaction with decision makers. In this regard, there are a number of valuable practices that can be drawn from other fields, especially the global climate change community. A generally accepted set of best practices that scientists follow in their discussions of uncertainty would be helpful for the community engaged in ocean acidification.NOAA Ocean Acidification Program and National Marine Fisheries Service (DSB, MP), NSF-supported Center for Climate and Energy Decision Making (SCD), and NASA Ocean Biology and Biogeochemistry Program (SS)

Recommended Priorities for Research on Ecological Impacts of Ocean and Coastal Acidification in the U.S. Mid-Atlantic

The estuaries and continental shelf system of the United States Mid-Atlantic are subject to ocean acidification driven by atmospheric CO2, and coastal acidification caused by nearshore and land-sea interactions that include biological, chemical, and physical processes. These processes include freshwater and nutrient input from rivers and groundwater; tidally-driven outwelling of nutrients, inorganic carbon, alkalinity; high productivity and respiration; and hypoxia. Hence, these complex dynamic systems exhibit substantial daily, seasonal, and interannual variability that is not well captured by current acidification research on Mid-Atlantic organisms and ecosystems. We present recommendations for research priorities that target better understanding of the ecological impacts of acidification in the U. S. Mid-Atlantic region. Suggested priorities are: 1) Determining the impact of multiple stressors on our resource species as well as the magnitude of acidification; 2) Filling information gaps on major taxa and regionally important species in different life stages to improve understanding of their response to variable temporal scales and sources of acidification; 3) Improving experimental approaches to incorporate realistic environmental variability and gradients, include interactions with other environmental stressors, increase transferability to other systems or organisms, and evaluate community and ecosystem response; 4) Determining the capacity of important species to acclimate or adapt to changing ocean conditions; 5) Considering multi-disciplinary, ecosystem-level research that examines acidification impacts on biodiversity and biotic interactions; and 6) Connecting potential acidification-induced ecological impacts to ecosystem services and the economy. These recommendations, while developed for the Mid-Atlantic, can be applicable to other regions will help align research towards knowledge of potential larger-scale ecological and economic impacts

Integrating High-Resolution Coastal Acidification Monitoring Data Across Seven United States Estuaries.

Beginning in 2015, the United States Environmental Protection Agencys (EPAs) National Estuary Program (NEP) started a collaboration with partners in seven estuaries along the East Coast (Barnegat Bay; Casco Bay), West Coast (Santa Monica Bay; San Francisco Bay; Tillamook Bay), and the Gulf of Mexico (GOM) Coast (Tampa Bay; Mission-Aransas Estuary) of the United States to expand the use of autonomous monitoring of partial pressure of carbon dioxide (pCO2) and pH. Analysis of high-frequency (hourly to sub-hourly) coastal acidification data including pCO2, pH, temperature, salinity, and dissolved oxygen (DO) indicate that the sensors effectively captured key parameter measurements under challenging environmental conditions, allowing for an initial characterization of daily to seasonal trends in carbonate chemistry across a range of estuarine settings. Multi-year monitoring showed that across all water bodies temperature and pCO2 covaried, suggesting that pCO2 variability was governed, in part, by seasonal temperature changes with average pCO2 being lower in cooler, winter months and higher in warmer, summer months. Furthermore, the timing of seasonal shifts towards increasing (or decreasing) pCO2 varied by location and appears to be related to regional climate conditions. Specifically, pCO2 increases began earlier in the year in warmer water, lower latitude water bodies in the GOM (Tampa Bay; Mission-Aransas Estuary) as compared with cooler water, higher latitude water bodies in the northeast (Barnegat Bay; Casco Bay), and upwelling-influenced West Coast water bodies (Tillamook Bay; Santa Monica Bay; San Francisco Bay). Results suggest that both thermal and non-thermal influences are important drivers of pCO2 in Tampa Bay oxygen, National Estuary Program and Mission-Aransas Estuary. Conversely, non-thermal processes, most notably the biogeochemical structure of coastal upwelling, appear to be largely responsible for the observed pCO2 values in West Coast water bodies. The co-occurrence of high salinity, high pCO2, low DO, and low temperature water in Santa Monica Bay and San Francisco Bay characterize the coastal upwelling paradigm that is also evident in Tillamook Bay when upwelling dominates freshwater runoff and local processes. These data demonstrate that high-quality carbonate chemistry observations can be recorded from estuarine environments using autonomous sensors originally designed for open-ocean settings

Integrating high-resolution coastal acidification monitoring data across seven United States estuaries

Beginning in 2015, the United States Environmental Protection Agency’s (EPA’s) National Estuary Program (NEP) started a collaboration with partners in seven estuaries along the East Coast (Barnegat Bay; Casco Bay), West Coast (Santa Monica Bay; San Francisco Bay; Tillamook Bay), and the Gulf of Mexico (GOM) Coast (Tampa Bay; Mission-Aransas Estuary) of the United States to expand the use of autonomous monitoring of partial pressure of carbon dioxide (pCO2) and pH. Analysis of high-frequency (hourly to sub-hourly) coastal acidification data including pCO2, pH, temperature, salinity, and dissolved oxygen (DO) indicate that the sensors effectively captured key parameter measurements under challenging environmental conditions, allowing for an initial characterization of daily to seasonal trends in carbonate chemistry across a range of estuarine settings. Multi-year monitoring showed that across all water bodies temperature and pCO2 covaried, suggesting that pCO2 variability was governed, in part, by seasonal temperature changes with average pCO2 being lower in cooler, winter months and higher in warmer, summer months. Furthermore, the timing of seasonal shifts towards increasing (or decreasing) pCO2 varied by location and appears to be related to regional climate conditions. Specifically, pCO2 increases began earlier in the year in warmer water, lower latitude water bodies in the GOM (Tampa Bay; Mission-Aransas Estuary) as compared with cooler water, higher latitude water bodies in the northeast (Barnegat Bay; Casco Bay), and upwelling-influenced West Coast water bodies (Tillamook Bay; Santa Monica Bay; San Francisco Bay). Results suggest that both thermal and non-thermal influences are important drivers of pCO2 in Tampa Bay and Mission-Aransas Estuary. Conversely, non-thermal processes, most notably the biogeochemical structure of coastal upwelling, appear to be largely responsible for the observed pCO2 values in West Coast water bodies. The co-occurrence of high salinity, high pCO2, low DO, and low temperature water in Santa Monica Bay and San Francisco Bay characterize the coastal upwelling paradigm that is also evident in Tillamook Bay when upwelling dominates freshwater runoff and local processes. These data demonstrate that high-quality carbonate chemistry observations can be recorded from estuarine environments using autonomous sensors originally designed for open-ocean settings.This publication was developed in part under Assistance Agreement No. 83588701 awarded by U.S. Environmental Protection Agency (US EPA) to the American Association for the Advancement of Science (AAAS). Monitoring in Tillamook Bay was funded through US EPA Regional Applied Research Effort (RARE) and Office of Research and Development funding. In Mission-Aransas Estuary, funding for autonomous sensors and sensor deployment was provided by the US EPA’s National Estuary Program via the Coastal Bend Bays and Estuaries Program Contract No. 1605. Funding in Tampa Bay was provided by the Tampa Bay Estuary Program (TBEP; 2017 Tampa Bay Environmental Restoration Fund) and US EPA Section 320 Grants through multiple TBEP Workplans. Funding in Barnegat Bay was provided by US EPA under cooperative agreement CE98212312 to Ocean County College and Barnegat Bay Partnership. Funding in Casco Bay was provided by the EPA National Estuary Program to the Casco Bay Estuary Partnership at the University of Southern Maine through multiple cooperative agreements (CE96185501, CE96190301, CE 00A00063, CE 00A00299, and CE 00A00319) beginning in 2014, and subcontracted to the University of New Hampshire. Partial funding in San Francisco Bay was from the Central and Northern California Ocean Observing System (CeNCOOS), EPA Region 9 Section 320 (Grant No. 00T74501 - some equipment), and complementary funding was from San Francisco State University and University of California, Davis

Seawater carbonate chemistry and scope for growth for juvenile Atlantic sea scallops (Placopecten magellanicus)

This study assessed the energy budget for juvenile Atlantic Sea Scallop, Placopecten magellanicus, during a natural drop in temperature (15.6°C to 5.8°C) over an 8-week time period during the fall at three different enrichment levels of carbon dioxide (CO2). Every 2 weeks, individuals were sampled for ecophysiological measurements of feeding activity, respiration rate (RR) and excretion rate (ER) to enable the calculation of scope for growth (SFG) and atomic oxygen:nitrogen ratios (O:N). In addition, 36 individuals per treatment were removed for shell height, dry tissue weight (DTW) and dry shell weight (DSW). We found a significant decrease in feeding rates as CO2 increased. Those rates also were significantly affected by temperature, with highest feeding at 9.4°C. No significant CO2 effect was observed for catabolic energy processes (RR and ER); however, these rates did increase significantly with temperature. The O:N ratio was not significantly affected by CO2, but was significantly affected by temperature. There was a significant interaction between CO2 and temperature for ER and the O:N ratio, with low CO2 levels resulting in a U-shaped response that was not sustained as CO2 levels increased. This suggests that the independent effects of CO2 and temperature observed at low levels are different once a CO2 threshold is reached. Additionally, there were significant differences in growth estimators (shell height and DSW), with the best growth occurring at the lowest CO2 level. In contrast to temperature variations that induced a trade-off response in energy acquisition and expenditure, results from this research support the hypothesis that sea scallops have a limited ability to alter physiological processes to compensate for increasing CO2

Integrating High-Resolution Coastal Acidification Monitoring Data Across Seven United States Estuaries

Beginning in 2015, the United States Environmental Protection Agency’s (EPA’s) National Estuary Program (NEP) started a collaboration with partners in seven estuaries along the East Coast (Barnegat Bay; Casco Bay), West Coast (Santa Monica Bay; San Francisco Bay; Tillamook Bay), and the Gulf of Mexico (GOM) Coast (Tampa Bay; Mission-Aransas Estuary) of the United States to expand the use of autonomous monitoring of partial pressure of carbon dioxide (pCO2) and pH. Analysis of high-frequency (hourly to sub-hourly) coastal acidification data including pCO2, pH, temperature, salinity, and dissolved oxygen (DO) indicate that the sensors effectively captured key parameter measurements under challenging environmental conditions, allowing for an initial characterization of daily to seasonal trends in carbonate chemistry across a range of estuarine settings. Multi-year monitoring showed that across all water bodies temperature and pCO2 covaried, suggesting that pCO2 variability was governed, in part, by seasonal temperature changes with average pCO2 being lower in cooler, winter months and higher in warmer, summer months. Furthermore, the timing of seasonal shifts towards increasing (or decreasing) pCO2 varied by location and appears to be related to regional climate conditions. Specifically, pCO2 increases began earlier in the year in warmer water, lower latitude water bodies in the GOM (Tampa Bay; Mission-Aransas Estuary) as compared with cooler water, higher latitude water bodies in the northeast (Barnegat Bay; Casco Bay), and upwelling-influenced West Coast water bodies (Tillamook Bay; Santa Monica Bay; San Francisco Bay). Results suggest that both thermal and non-thermal influences are important drivers of pCO2 in Tampa Bay and Mission-Aransas Estuary. Conversely, non-thermal processes, most notably the biogeochemical structure of coastal upwelling, appear to be largely responsible for the observed pCO2 values in West Coast water bodies. The co-occurrence of high salinity, high pCO2, low DO, and low temperature water in Santa Monica Bay and San Francisco Bay characterize the coastal upwelling paradigm that is also evident in Tillamook Bay when upwelling dominates freshwater runoff and local processes. These data demonstrate that high-quality carbonate chemistry observations can be recorded from estuarine environments using autonomous sensors originally designed for open-ocean settings