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智利中部沿海大陆边缘沉积物中的碳氧化途径。

Pathways of carbon oxidation in continental margin sediments off central Chile.

作者信息

Thamdrup B, Canfield D E

机构信息

Max Planck Institute for Marine Microbiology, Bremen, Germany.

出版信息

Limnol Oceanogr. 1996 Dec;41(8):1629-50. doi: 10.4319/lo.1996.41.8.1629.

Abstract

Rates and oxidative pathways of organic carbon mineralization were determined in sediments at six stations on the shelf and slope off Concepcion Bay at 36.5 degrees S. The depth distribution of C oxidation rates was determined to 10 cm from accumulation of dissolved inorganic C in 1-5-d incubations. Pathways of C oxidation were inferred from the depth distributions of the potential oxidants (O2, NO3-, and oxides of Mn and Fe) and from directly determined rates of SO4(2-) reduction. The study area is characterized by intense seasonal upwelling, and during sampling in late summer the bottom water over the shelf was rich in NO3- and depleted of O2. Sediments at the four shelf stations were covered by mats of filamentous bacteria of the genera Thioploca and Beggiatoa. Carbon oxidation rates at these sites were extremely high near the sediment surface (>3 micromol cm-3 d-1) and decreased exponentially with depth. The process was entirely coupled to SO4(2-) reduction. At the two slope stations where bottom-water O2 was > 100 microM, C oxidation rates were 10-fold lower and varied less with depth; C oxidation coupled to the reduction of O2, NO3-, and Mn oxides combined to yield an estimated 15% of the total C oxidation between 0 and 10 cm. Carbon oxidation through Fe reduction contributed a further 12-29% of the depth-integrated rate, while the remainder of C oxidation was through SO4(2-) reduction. The depth distribution of Fe reduction agreed well with the distribution of poorly crystalline Fe oxides, and as this pool decreased with depth, the importance of SO4(2-) reduction increased. The results point to a general importance of Fe reduction in C oxidation in continental margin sediments. At the shelf stations, Fe reduction was mainly coupled to oxidation of reduced S. These sediments were generally H2S-free despite high SO4(2-) reduction rates, and precipitation of Fe sulfides dominated H2S scavenging during the incubations. A large NO3- pool was associated with the Thioploca, and the shelf sediments were thus enriched in NO3- relative to the bottom water, with maximum concentrations of 3 micromol cm-3. The NO3- was consumed during our sediment incubations, but no effects on either C or S cycles could be discerned.

摘要

在南纬36.5度康塞普西翁湾陆架和陆坡的六个站点的沉积物中,测定了有机碳矿化速率和氧化途径。通过在1 - 5天的培养中溶解无机碳的积累,确定了碳氧化速率在10厘米深度范围内的分布。碳氧化途径是根据潜在氧化剂(O2、NO3-以及锰和铁的氧化物)的深度分布以及直接测定的SO4(2-)还原速率推断出来的。研究区域的特点是强烈的季节性上升流,在夏末采样期间,陆架上的底层水富含NO3-且O2含量较低。四个陆架站点的沉积物被硫丝菌属和贝氏硫菌属的丝状细菌垫覆盖。这些站点沉积物表面附近的碳氧化速率极高(>3微摩尔·厘米-3·天-1),并随深度呈指数下降。该过程完全与SO4(2-)还原耦合。在两个底层水O2含量>100微摩尔的陆坡站点,碳氧化速率低10倍,且随深度变化较小;与O2、NO3-和锰氧化物还原耦合的碳氧化在0至10厘米深度范围内估计占总碳氧化的15%。通过铁还原的碳氧化在深度积分速率中又占12 - 29%,而其余的碳氧化则通过SO4(2-)还原。铁还原的深度分布与结晶度差的铁氧化物分布非常吻合,并且随着该库随深度减少,SO4(2-)还原的重要性增加。结果表明铁还原在陆缘沉积物碳氧化中具有普遍重要性。在陆架站点,铁还原主要与还原态硫的氧化耦合。尽管SO4(2-)还原速率很高,但这些沉积物通常不含H2S,并且在培养期间硫化铁沉淀主导了H2S清除。一个大的NO3-库与硫丝菌有关,因此陆架沉积物相对于底层水富含NO3-,最大浓度为3微摩尔·厘米-3。在我们的沉积物培养过程中NO3-被消耗,但未发现对碳或硫循环有任何影响。

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