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整合美国七个河口的高分辨率海岸酸化监测数据

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

作者信息

Rosenau Nicholas A, Galavotti Holly, Yates Kimberly K, Bohlen Curtis C, Hunt Christopher W, Liebman Matthew, Brown Cheryl A, Pacella Stephen R, Largier John L, Nielsen Karina J, Hu Xinping, McCutcheon Melissa R, Vasslides James M, Poach Matthew, Ford Tom, Johnston Karina, Steele Alex

机构信息

Ocean and Coastal Management Branch, Office of Wetlands Oceans and Watersheds, United States Environmental Protection Agency, Washington, DC, United States.

United States Geological Survey, St. Petersburg Coastal and Marine Science Center, St. Petersburg, FL, United States.

出版信息

Front Mar Sci. 2021 Aug 19;19:1-679913. doi: 10.3389/fmars.2021.679913.

Abstract

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 (CO) and pH. Analysis of high-frequency (hourly to sub-hourly) coastal acidification data including CO, 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 CO covaried, suggesting that CO variability was governed, in part, by seasonal temperature changes with average CO being lower in cooler, winter months and higher in warmer, summer months. Furthermore, the timing of seasonal shifts towards increasing (or decreasing) CO varied by location and appears to be related to regional climate conditions. Specifically, CO 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 CO 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 CO values in West Coast water bodies. The co-occurrence of high salinity, high CO, 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.

摘要

从2015年开始,美国环境保护局(EPA)的国家河口计划(NEP)与美国东海岸(巴尼加特湾;卡斯科湾)、西海岸(圣莫尼卡湾;旧金山湾;蒂拉穆克湾)以及墨西哥湾(GOM)海岸(坦帕湾;米申-阿兰萨斯河口)七个河口的合作伙伴展开合作,以扩大对二氧化碳(CO₂)分压和pH值的自主监测应用。对高频(每小时至亚小时)海岸酸化数据(包括CO₂、pH值、温度、盐度和溶解氧(DO))的分析表明,这些传感器在具有挑战性的环境条件下有效地获取了关键参数测量值,从而能够初步描绘出一系列河口环境中碳酸盐化学从每日到季节性的变化趋势。多年监测显示,在所有水体中,温度和CO₂相互关联,这表明CO₂的变化部分受季节性温度变化的影响,在较凉爽的冬季,平均CO₂较低,而在较温暖的夏季则较高。此外,季节性转向CO₂增加(或减少)的时间因地点而异,并且似乎与区域气候条件有关。具体而言,与东北部较凉爽、高纬度水体(巴尼加特湾;卡斯科湾)以及受上升流影响的西海岸水体(蒂拉穆克湾;圣莫尼卡湾;旧金山湾)相比,GOM中较温暖、低纬度水体(坦帕湾;米申-阿兰萨斯河口)的CO₂在一年中更早开始增加。结果表明,热影响和非热影响都是坦帕湾和米申-阿兰萨斯河口CO₂的重要驱动因素。相反,非热过程,最显著的是沿海上升流的生物地球化学结构,似乎在很大程度上决定了西海岸水体中观测到的CO₂值。圣莫尼卡湾和旧金山湾中高盐度、高CO₂、低DO和低温水的同时出现,体现了沿海上升流模式,当上升流主导淡水径流和局部过程时,这种模式在蒂拉穆克湾也很明显。这些数据表明,使用最初为公海环境设计的自主传感器,可以从河口环境中记录高质量的碳酸盐化学观测数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ece/9179233/7bc9c84c7812/nihms-1790793-f0001.jpg

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