Dong, LF and Smith, CJ and Papaspyrou, S and Stott, A and Osborn, AM and Nedwell, DB (2009) Changes in Benthic Denitrification, Nitrate Ammonification, and Anammox Process Rates and Nitrate and Nitrite Reductase Gene Abundances along an Estuarine Nutrient Gradient (the Colne Estuary, United Kingdom). Applied And Environmental Microbiology, 75 (10). pp. 3171-3179. DOI https://doi.org/10.1128/aem.02511-08
Dong, LF and Smith, CJ and Papaspyrou, S and Stott, A and Osborn, AM and Nedwell, DB (2009) Changes in Benthic Denitrification, Nitrate Ammonification, and Anammox Process Rates and Nitrate and Nitrite Reductase Gene Abundances along an Estuarine Nutrient Gradient (the Colne Estuary, United Kingdom). Applied And Environmental Microbiology, 75 (10). pp. 3171-3179. DOI https://doi.org/10.1128/aem.02511-08
Dong, LF and Smith, CJ and Papaspyrou, S and Stott, A and Osborn, AM and Nedwell, DB (2009) Changes in Benthic Denitrification, Nitrate Ammonification, and Anammox Process Rates and Nitrate and Nitrite Reductase Gene Abundances along an Estuarine Nutrient Gradient (the Colne Estuary, United Kingdom). Applied And Environmental Microbiology, 75 (10). pp. 3171-3179. DOI https://doi.org/10.1128/aem.02511-08
Abstract
Estuarine sediments are the location for significant bacterial removal of anthropogenically derived inorganic nitrogen, in particular nitrate, from the aquatic environment. In this study, rates of benthic denitrification (DN), dissimilatory nitrate reduction to ammonium (DNRA), and anammox (AN) at three sites along a nitrate concentration gradient in the Colne estuary, United Kingdom, were determined, and the numbers of functional genes (narG, napA, nirS, and nrfA) and corresponding transcripts encoding enzymes mediating nitrate reduction were determined by reverse transcription-quantitative PCR. In situ rates of DN and DNRA decreased toward the estuary mouth, with the findings from slurry experiments suggesting that the potential for DNRA increased while the DN potential decreased as nitrate concentrations declined. AN was detected only at the estuary head, accounting for similar to 30% of N(2) formation, with 16S rRNA genes from anammox-related bacteria also detected only at this site. Numbers of narG genes declined along the estuary, while napA gene numbers were stable, suggesting that NAP-mediated nitrate reduction remained important at low nitrate concentrations. nirS gene numbers (as indicators of DN) also decreased along the estuary, whereas nrfA (an indicator for DNRA) was detected only at the two uppermost sites. Similarly, nitrate and nitrite reductase gene transcripts were detected only at the top two sites. A regression analysis of log(n + 1) process rate data and log(n + 1) mean gene abundances showed significant relationships between DN and nirS and between DNRA and nrfA. Although these log-log relationships indicate an underlying relationship between the genetic potential for nitrate reduction and the corresponding process activity, fine- scale environmentally induced changes in rates of nitrate reduction are likely to be controlled at cellular and protein levels.
Item Type: | Article |
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Subjects: | Q Science > QH Natural history > QH301 Biology |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 23 Sep 2011 09:06 |
Last Modified: | 16 May 2024 18:12 |
URI: | http://repository.essex.ac.uk/id/eprint/891 |