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Impacts of spatial and temporal variation of water column production and respiration on hypoxia in Narragansett Bay.

机译:Narragansett湾水柱生产和呼吸的时空变化对缺氧的影响。

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I begin by summarizing the impacts of climate change on Narragansett Bay (Chapter 1). Many of these changes in climate (increased temperature, increased rainfall, and decreased wind) impact mixing in the water column and thereby may exacerbate hypoxia in Narragansett Bay.;In order to examine the effects of metabolism on hypoxia, it was necessary to place metabolic rates into units of oxygen. To accurately convert measurements of carbon to oxygen, I used empirical measurements of production to calculate a photosynthetic quotient (Chapter 2). Specifically, I used concurrent 14C and light bottle oxygen net primary production measurements. The present summer PQ ratio for Narragansett Bay is 1.42 +/- 0.09.;A survey of spatial and temporal variation in water column metabolism was conducted over two years (2006--2008), in order to provide an annual perspective to metabolism in the summer (Chapter 3). This was particularly important given speculation that primary production has changed over the past several decades as a result of climate change. Spatially, primary production decreased exponentially down the Bay. Respiration was low in the Providence River Estuary, increased in the Upper Bay, and decreased down the West Passage. Based on net 24-hour metabolism, the Providence River was autotrophic, exporting organic matter into the heterotrophic Upper Bay. Production and respiration were comparable in the remainder of the Bay, yielding a net 24-hour metabolism near zero. Seasonally, the highest rates of production, respiration, and net 24-hour metabolism (autotrophy) were in the summer. The overall annual metabolism budget of the Providence River Estuary and the West Passage of the Bay was as follows: total production of 290 gC m-2 y-1 , total respiration of 320 gC m-2 y-1 , and slight net heterotrophy of 30 gC m-2 y -1.;Summer metabolism data were examined in conjunction with continuous oxygen sensor measurements in order to examine drivers of hypoxia in Narragansett Bay (Chapter 4). Little hypoxia occurred in summer 2007; summer 2008 had several short hypoxic episodes; and summer 2009 was hypoxic continuously through the latter half of summer. Summers with the most severe hypoxia (2008 & 2009 vs. 2007) had the highest bay-wide volume-weighted production (807 & 857 vs. 402 gO2 m-2 summer-1); respiration did not show the same variation (325 & 289 vs. 324 gO 2 m-2 summer-1). Hypoxia in the Providence River was controlled by stratification. Hypoxia in the well-mixed Upper Bay was caused by elevated respiration, which was fueled by advected organic matter from the Providence River. Hypoxia in the well-mixed, low respiration Mid Bay was caused by advected low oxygen water from Greenwich Bay and the Upper Bay. The Lower Bay had low stratification, respiration, and production, and hypoxia did not occur. Inter-summer variation of hypoxia was due to changes in riverflow driven stratification, water temperature, and wind.;To fully understand primary production in the Bay, an analysis was conducted comparing incubation metabolism estimations with estimations from in situ sensors (Chapter 5). In situ monitoring sensors have become increasingly utilized in coastal ecosystems due to their ability to capture highly resolved spatial and temporal dynamics within a system. I created three different algorithms to integrate oxygen fluctuations through night and day in order to calculate metabolism using in situ sensor measurements. By examining multiple methods of both incubations and in situ estimations, we were able to account for differences within in situ and incubation estimations. Incubation production estimations were significantly higher than in situ estimations differing in capturing bloom dynamics. The mechanism behind these differences can be attributed to the exclusion of grazers from bottle samples. Thus, incubation productivity estimations represent a measure of phytoplankton production, whereas in situ productivity estimations represent a measure of system apparent production. In terms of future analysis, the comparison of incubation and in situ metabolism estimations may provide a mechanism to quantitatively examine grazer dynamics. (Abstract shortened by UMI.)
机译:首先,我概述了气候变化对纳拉甘西特湾的影响(第1章)。气候中的许多这些变化(温度升高,降雨量增加和风的减少)都会影响水柱中的混合,从而可能加剧纳拉甘塞特湾的缺氧状态。为了检查新陈代谢对缺氧的影响,有必要进行新陈代谢速率以氧气为单位。为了将碳的测量值准确地转换为氧气,我使用了生产的经验测量值来计算光合商(第2章)。具体来说,我使用了同时进行的14C和轻瓶氧气净初级生产测量。目前纳拉甘西特湾的夏季PQ比为1.42 +/- 0.09 .;在过去两年(2006--2008年)中对水柱代谢的时空变化进行了调查,以提供年度角度的水质代谢研究。夏天(第3章)。鉴于人们猜测由于气候变化,过去几十年来初级生产发生了变化,这一点尤其重要。在空间上,海湾沿岸的初级生产呈指数下降。普罗维登斯河口的呼吸很低,上海湾的呼吸增加,西通道的呼吸减少。根据24小时的净新陈代谢,普罗维登斯河是自养的,将有机物输出到异养的上海湾。在海湾的其余部分,产量和呼吸作用相当,产生的净24小时新陈代谢几乎为零。季节性上,最高的生产率,呼吸作用和24小时净代谢(自养)发生在夏季。普罗维登斯河河口和海湾西通道的年度总代谢预算如下:总产量为290 gC m-2 y-1,总呼吸量为320 gC m-2 y-1,且净净异养30 gC m-2 y -1 .;结合连续的氧传感器测量,检查夏季代谢数据,以检查纳拉甘西特湾缺氧的驱动因素(第4章)。 2007年夏季几乎没有缺氧发生; 2008年夏季发生了几次短暂的低氧发作;在整个夏季的后半段,2009年夏季一直处于低氧状态。缺氧最严重的夏季(2008年和2009年与2007年相比)在海湾地区的体积加权产量最高(807和857年与402 gO2 m-2夏季-1);呼吸没有显示出相同的变化(325和289比324 gO 2 m-2 summer-1)。普罗维登斯河的缺氧是通过分层控制的。上层海湾混合不足的缺氧是由于呼吸增加引起的,而呼吸的增加是由普罗维登斯河的平流有机物推动的。混合海湾,低呼吸中海湾的缺氧是由于格林威治海湾和上海湾的平流低氧水引起的。下湾的分层,呼吸和生产能力较低,并且没有发生缺氧。夏季缺氧的变化是由于河水驱动的分层,水温和风的变化所致。为了充分了解海湾的初级生产,进行了分析,将孵化代谢估算值与现场传感器估算值进行了比较(第5章)。由于其能够捕获系统内高度解析的时空动态的能力,因此在沿海生态系统中已越来越多地使用现场监测传感器。我创建了三种不同的算法来整合夜间和白天的氧气波动,以便使用原位传感器测量来计算新陈代谢。通过研究孵化和原位估计的多种方法,我们能够解释原位和孵化估计中的差异。孵化产量估算值明显高于捕获大花动力学的原位估算值。这些差异背后的机制可以归因于瓶样品中排除了放牧者。因此,孵化生产力估计值代表浮游植物产量的度量,而原位生产力估计值代表系统表观产量的度量。就未来的分析而言,对孵化率和原位代谢估计值的比较可能提供一种定量检查放牧者动态的机制。 (摘要由UMI缩短。)

著录项

  • 作者

    Smith, Leslie Michelle.;

  • 作者单位

    University of Rhode Island.;

  • 授予单位 University of Rhode Island.;
  • 学科 Biology Oceanography.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 341 p.
  • 总页数 341
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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