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Biogeochemistry Of Methane And Nitrous Oxide In The Water And Sediments Of JiaoZhou Bay

Posted on:2010-11-17Degree:MasterType:Thesis
Country:ChinaCandidate:J YangFull Text:PDF
GTID:2121360275485730Subject:Analytical Chemistry
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CH4 and N2O are important greenhouse gases, which play significant roles in the global warming and atmospheric chemistry. Global oceans are net natural sources of atmospheric CH4 and N2O. Although continental shelves, estuaries and bays only occupy a small part of the world ocean, they appear to be responsible for a large part of the oceanic CH4 and N2O emission. Therefore studies on the biogeochemistry of dissolved CH4 and N2O in coastal waters, especially on the production and consumption mechanism, will be helpful to enrich the list about sources and sinks of global atmospheric CH4 and N2O, and to expand the studies about biogeochemistry of dissolved CH4 and N2O in continental shelves, estuaries and bays.In this dissertation, the production and consumption mechanism, sediment-water flux, distributions, sources and sinks in Jiaozhou Bay which is impacted by human activities severely, are studied detailedly.1. Nitrification rates, denitrification rates and the sediment-water fluxs were determined during surveys at Dagu estuary and Loushan estuary in December 2007, Septemberand November 2008 and February 2009. The results showed that the nitrification rates and denitrification rates in tidal flat sediment had obviously seasonal and spatialvariations, and the latter is higher than the former. At Dagu estuary, the denitrification rates ranged from 9.55 to 104.43μmol·N·m-2·h-1 with maximum values occurring in spring and lowest values occurring in winter due to the influence of temperature and biomass. The maximum nitrification rate was determined in spring, but it hardly happened in summer. Based on the denitrification rates, the area of the Jiaozhou Bay and mean inputs of nitrate from Dagu river into the Jiaozhou Bay, the proportion of the nitrate inputs removed via denitrification is estimated to be 18% in spring, 5% in summer, 10% in autumn and 2% in winter. At Loushan estuary, the denitrification rate in summer was higher than that in winter due to the influence of organic matterand the concentration of nitrate in the overlying water. The nitrification hardly happened in summer also. The sediment-water N2O fluxes showed obvious seasonal variations. At Dagu estuary, the sediment released N2O into the overlying water allthe year except in winter. The sediment at Loushan estuary released N2O not only in summer but also in winter. On an annual scale, the tidal flat sediments surroundingJiaozhou Bay is a main source of N2O in the water column. The sediment-water CH4fluxes showed obvious seasonal variations. At Dagu estuary, the sediment absorbede CH4 from the overlying water in all seasons. But the sediment at Loushan estuary release CH4 in summer and winter.2. CH4 and N2O concentrations in surface waters of the Jiaozhou Bay, riverine water and sewage water were determined during surveys between December 2007 and February 2009., Concentrations and saturations of CH4 showed obvious seasonal variation with maximum values occurring in summer and lowest values occurring in winter. The seasonal variations of dissolved N2O concentrations in the the Jiaozhou Bay were not obvious, but the saturations showed obvious seasonal variations with higher values occurring in autumn. The dissolved CH4 in the water column showed an obvious decrease from eastern and northern to western and southern part of the bay, while N2O showed decreases from both the eastern and northwestern coast to the central part. The distribution of CH4 and N2O in the Jiaozhou Bay are influenced strongly by the land-soure input. In situ incubation experiments of sediment cores in April 2008 showed that the CH4 release rates from two stations were 0.07 and 0.29μmol·CH4·m-2·h-1, and the N2O release rates were 0.04 and 0.11μmol·m-2·h-1, which indicates that the sediment of the Jiaozhou Bay could can act as a source of dissolved CH4 and N2O in the water column. The annual flux from sediments is estimated to be 1.11×106mol·a-1 for CH4 and 0.46×106mol·a-1 for N2O. Biological activities in the surface waters of the Jiaozhou Bay varied seasonally and spatially, The production of N2O by biological activities was estimated to be 0.31×106 mol·a-1. Concentrations of CH4 and N2O in the riverine water around the Jiaozhou Bay ranged from 500 to 5000 nmol/L and 9.8 to 1400 nmol/L, and the annual riverine input was estimated to be 2.69×106 mol·a-1 and 0.25×106 mol·a-1, respectively. The annual input via sewage water is estimated to be 0.02×106 mol·a-1 and 0.29×106 mol·a-1, respectively. So the primary source of the dissolved CH4 in the water of the Jiaozhou Bay is the riverine water input, while N2O is the sewage water input.Air-sea fluxes of dissolved CH4 and N2O showed obvious seasonal and spatial variations. The studied area is a net source of atmospheric CH4 all the year around, while from winter till autumn, it transforms from sink of atmospheric N2O to source. The annual CH4 and N2O emission from the Jiaozhou Bay are estimated to be 10×106 -17.4×106 mol·a-1and 0.76×106 -1.40×106 mol·a-1.
Keywords/Search Tags:methane, nitrous oxide, denitrification, nitrification, sediment-water flux, Jiaozhou Bay
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