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Impact of chronic nitrogen loading on greenhouse gas fluxes in coastal wetlands

机译:慢性氮负荷对沿海湿地温室气体通量的影响

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Coastal wetlands are valuable ecosystems that historically have not been protected and have been lost at rapid rates. Recently, they have gained attention for their potential role in climate change mitigation given that they have the ability to sequester and store large amounts of atmospheric carbon dioxide (CO2). While other ecosystems can sequester and store carbon as well, salt marshes have the unique ability to store vast amounts of carbon while emitting relatively negligible amounts of methane (CH4) and nitrous oxide (N2O). These are additional greenhouse gases (GHGs) that can be emitted from ecosystems, particularly CH4 in large quantities from freshwater wetlands. These gases are 45 and 270 times, respectively, greater at trapping heat in the atmosphere than CO2.;However, anthropogenic nitrogen (N) inputs into coastal estuaries have the potential to shift biogeochemical cycling within coastal wetlands, possibly switching salt marshes from CO2 sinks to being sources of one or more of the three major GHGs. Excessive anthropogenic N inputs are a threat to overall ecosystem health on local, regional, and global scales. Salt marshes are natural and efficient filters of excess N entering into these systems, although they cannot filter out unlimited quantities. Excess N in coastal systems can lead to a suite of negative consequences including poor water quality as a result of over stimulation of primary productivity and overall habitat degradation. The threat of anthropogenic N to coastal areas is only increasing as populations grow and concentrate along desirable coastal locations. For coastal wetlands that already face threats of habitat loss from increased rates of sea level rise (SLR) and urban development, N inputs can exacerbate rates of marsh loss. As efforts expand to protect these valuable ecosystems through development of financial incentives, such as carbon trading markets, it is important to quantify how N loading impacts GHG fluxes within wetlands and rates of N transformation. Most research to date in salt marsh systems has focused on impacts from short-term N additions on GHG fluxes.;The goal of this research was to examine the role of chronic N loading on GHG fluxes in Spartina alterniflora-dominated marshes and to assess quantities of N available for transformation through measurement of denitrification enzyme activity (DEA). To accomplish these goals, we first examined the role of chronic N loading on GHG fluxes using three salt marshes located along a historic N gradient (high, medium, low) within Narragansett Bay, RI. Narragansett Bay is an ideal location for this work since it has received chronic N loading, mainly from wastewater inputs, since the late 1800s. To asses impacts of N loading on GHG fluxes, CO2, CH4 and N2O were measured for one field season in 2016. Along with measured fluxes, plant properties, edaphic parameters, and nutrient availability were measured. Relationships of fluxes to these additional parameters were then explored. We then compared rates of DEA at the opposite ends (high, low) of the N gradient within Narragansett Bay in 2017, focusing on four marsh zones (creekbank, mudflat, low marsh, high marsh) at two sites to assess any differences in N availability and rates of N transformation. Additionally, GHG fluxes were measured at the high N site in 2017 to explore relationships with DEA rates.;As a result of this work, we found that the site receiving the highest N loading experienced the highest CO2 uptake as well as the highest emissions of CH4 and N2O compared to the other two sites along the N gradient. However, these emissions were not on an order of magnitude to significantly offset CO2 uptake. This was as expected, however, the other measured parameters (plant properties and edaphic variables) and DEA did not necessarily fall along expected trends of the N gradient. There were no significant differences in DEA among sites or zones, suggesting each site had similar amounts of N available for transformation and that soil in each zone had equal ability to transform N. At the marsh with the highest historic N loading, GHG fluxes fell along expected trends among zones with increased uptake of CO2 within vegetated zones contrasting with CO2 emission in non-vegetated zones. CH4 fluxes were highest in the bare creekbank zone, but were similar among the three remaining zones. Surprisingly, no significant N2O fluxes were measured in any of the four zones, suggesting along with DEA results that most N inputs are completely reduced to N2 via denitrification.
机译:沿海湿地是宝贵的生态系统,历史上一直没有得到保护,而且已经迅速丧失。最近,由于它们具有隔离和储存大量大气二氧化碳(CO2)的能力,因此它们在缓解气候变化中的潜在作用已受到关注。尽管其他生态系统也可以隔离和存储碳,但盐沼具有独特的存储大量碳的能力,同时排放相对可忽略不计的甲烷(CH4)和一氧化二氮(N2O)。这些是可以从生态系统中排放的额外温室气体(GHG),尤其是淡水湿地中大量排放的CH4。这些气体在大气中的热量捕获分别是二氧化碳的45倍和270倍;但是,人为进入沿海河口的氮(N)输入有可能改变沿海湿地内的生物地球化学循环,可能会改变CO2汇的盐沼成为三种主要温室气体中一种或多种的来源。人为氮素输入过多对地方,区域和全球范围的整体生态系统健康构成威胁。盐沼是进入这些系统的自然而有效的多余氮过滤器,尽管它们不能过滤出无限量。沿海系统中过量的氮会导致一系列负面影响,包括过度刺激初级生产力和总体生境退化导致水质差。人为氮对沿海地区的威胁只会随着人口的增长并集中在理想的沿海地区而增加。对于已经面临因海平面上升速度和城市发展速度增加而造成生境丧失的威胁的沿海湿地,氮输入会加剧沼泽丧失的速度。随着通过诸如碳交易市场等金融激励措施的发展来保护这些有价值的生态系统的努力,重要的是量化氮负荷如何影响湿地中的GHG通量和氮转化率。迄今为止,盐沼系统中的大多数研究都集中在短期添加氮对温室气体通量的影响上;该研究的目的是研究长期氮负荷对以互花米草为主的沼泽中温室气体通量的作用并评估其数量。通过测量反硝化酶活性(DEA)可用于转化的氮为了实现这些目标,我们首先使用了三个盐沼,研究了长期氮负荷对温室气体通量的作用,这些盐沼位于罗德岛州纳拉甘西特湾沿历史N梯度(高,中,低)。纳拉甘西特湾(Narragansett Bay)是这项工作的理想地点,因为自1800年代后期以来,它一直承受长期的氮负荷,主要是来自废水的输入。为了评估氮负荷对温室气体通量的影响,在2016年的一个田间季节测量了CO2,CH4和N2O。连同测量的通量一起,还测量了植物性状,营养参数和养分利用率。然后研究通量与这些附加参数的关系。然后,我们比较了2017年纳拉甘塞特湾内N梯度相反两端(高,低)的DEA速率,重点研究了两个地点的四个沼泽地带(溪岸,滩涂,低沼泽,高沼泽),以评估N的任何差异N转化的可用性和速率。此外,2017年在高氮站点测量了温室气体通量,以探讨与DEA率的关系。作为这项工作的结果,我们发现,氮负荷最高的站点二氧化碳吸收量最高,二氧化碳排放量最高。 CH4和N2O与沿着N梯度的其他两个位置相比。但是,这些排放量并未明显抵消二氧化碳的吸收量。这与预期的一样,但是其他测得的参数(植物特性和水生变量)和DEA不一定会随N梯度的预期趋势而下降。站点或区域之间的DEA没有显着差异,表明每个站点具有可转换的相似量的N,并且每个区域中的土壤具有相等的N转换能力。在历史氮含量最高的沼泽,GHG通量沿植被带内二氧化碳吸收增加的地区之间的预期趋势与非植被带的二氧化碳排放形成对比。 CH4通量在裸溪岸区域最高,但在其余三个区域中相似。出乎意料的是,在四个区域中的任何一个区域都没有测量到明显的N2O通量,这与DEA结果一起表明,大多数N输入通过反硝化作用完全还原为N2。

著录项

  • 作者

    Szura, Katelyn Ann.;

  • 作者单位

    University of Rhode Island.;

  • 授予单位 University of Rhode Island.;
  • 学科 Environmental science.;Biogeochemistry.
  • 学位 M.S.
  • 年度 2017
  • 页码 59 p.
  • 总页数 59
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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