Lisa W. von Friesen, Carolin R. Löscher, Stefan Bertilsson, Hanna Farnelid, Pauline Snoeijs-Leijonmalm, Marcus Sundbom, Sachia J. Traving, Flor Vermassen, Lasse Riemann
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引用次数: 0
摘要
由于气候变化,海冰更普遍地在北冰洋的大陆架断裂上退缩,影响了更深盆地的海冰-中上层-底栖生物耦合。据报道,北极陆架沉积物中存在固氮作用(重氮营养体微生物将二氮气体还原为生物可利用的氨),但北极深海中的固氮作用尚不清楚。我们在北冰洋中部冰层覆盖的深海(900-1500米)表层沉积物的5个地点取样,通过长期(>; 280天)稳定同位素(15N2)孵育来测量潜在的固氮作用,并通过功能标记基因nifH的扩增子测序来研究重氮营养菌群落组成。我们在罗蒙诺索夫海岭(0.6 pmol N g−1 day−1)和莫里斯杰瑟普海岭(0.4 pmol N g−1 day−1)测得低但可检测的固氮率。在有机质含量和细菌丰度最低的沉积物中,固氮作用最为明显,其中硫酸盐还原剂如desulfuromonadis和Desulfosporosinus sp.的作用最为突出。大多数nifH基因与已知重氮营养体有远亲关系。在这项研究中,我们展示了北极深海沉积物中固氮的潜力,大大扩展了已知的海洋固氮生物群系。它提出了深海沉积物中低但潜在广泛的固氮意义的问题。
Nitrogen Fixation Potential in Bathypelagic Sediment of the Ice-Covered Arctic Ocean Revealed Through Long-Term Stable Isotope Incubations
Due to climate change, sea ice more commonly retreats over the shelf breaks in the Arctic Ocean, impacting sea ice-pelagic-benthic coupling in the deeper basins. Nitrogen fixation (the reduction of dinitrogen gas to bioavailable ammonia by microorganisms called diazotrophs) is reported from Arctic shelf sediments but is unknown from the Arctic deep sea. We sampled five locations of deep-sea (900–1500 m) surface sediments in the central ice-covered Arctic Ocean to measure potential nitrogen fixation through long-term (> 280 days) stable-isotope (15N2) incubations and to study diazotroph community composition through amplicon sequencing of the functional marker gene nifH. We measured low but detectable nitrogen fixation rates at the Lomonosov Ridge (0.6 pmol N g−1 day−1) and the Morris Jessup Rise (0.4 pmol N g−1 day−1). Nitrogen fixation was observed in sediments with the lowest organic matter content and bacterial abundance, and where sulphate-reducers like Desulfuromonadia and Desulfosporosinus sp. were prominent. Most nifH genes were distantly related to known diazotrophs. In this study, we show a potential for nitrogen fixation in Arctic bathypelagic sediments, considerably extending the known biome of marine nitrogen fixation. It raises the question of the significance of low but potentially widespread nitrogen fixation in deep-sea sediments.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.