4.2 Article

Spatio-temporal variability in ammonia oxidation and ammonia-oxidising bacteria and archaea in coastal sediments of the western English Channel

期刊

MARINE ECOLOGY PROGRESS SERIES
卷 511, 期 -, 页码 41-58

出版社

INTER-RESEARCH
DOI: 10.3354/meps10933

关键词

Coastal; Sediment; Ammonia oxidation; Archaeal amoA gene; Bacteria amoA gene

资金

  1. NERC programme Oceans, NERC National Capability
  2. US NSF Biocomplexity program
  3. NERC [pml010004, NE/L003279/1, pml010009] Funding Source: UKRI
  4. Natural Environment Research Council [NE/L003279/1, pml010009, pml010004] Funding Source: researchfish

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The abundance of ammonia-oxidising bacterial (AOB) and ammonia-oxidising archaeal (AOA) (amoA) genes and ammonia oxidation rates were compared bimonthly from July 2008 to May 2011 in 4 contrasting coastal sediments in the western English Channel. Despite a higher abundance of AOA amoA genes within all sediments and at all time-points, rates of ammonia oxidation correlated with AOB and not AOA amoA gene abundance. Sediment type was a major factor in determining both AOB amoA gene abundance and AOB community structure, possibly due to deeper oxygen penetration into the sandier sediments, increasing the area available for ammonia oxidation. Decreases in AOB amoA gene abundance were evident during summer and autumn, with maximum abundance and ammonia oxidation rates occurring in winter and early spring. PCR-DGGE of AOB amoA genes indicated that no seasonal changes to community composition occurred; however, a gradual movement in community composition occurred at 3 of the sites studied. The lack of correlation between AOA amoA gene abundance and ammonium oxidation rates, or any other environmental variable measured, may be related to the higher spatial variation amongst measurements, obscuring temporal trends, or the bimonthly sampling, which may have been too infrequent to capture temporal variability in the deposition of fresh organic matter. Alternatively, AOA may respond to changing substrate concentrations by an increase or decrease in transcript rather than gene abundance.

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