TY - JOUR
T1 - Degrader density determines spatial variability of 2,6-dichlorobenzamide mineralisation in soil
AU - Sjøholm, Ole Rüdiger
AU - Aamand, Jens
AU - Sørensen, Jan
AU - Nybroe, Ole
N1 - Funding Information:
This work was supported by the Center for Environmental and Agricultural Microbiology, CREAM and the Ph.D. research school RECETO. We thank Pia B. Jacobsen and Christina R. Lynge (GEUS) for technical assistance.
PY - 2010/1
Y1 - 2010/1
N2 - The metabolite 2,6-dichlorobenzamide (BAM) is a frequent groundwater
pollutant produced during degradation of the herbicide
2,6-dichlorobenzonitrile (dichlobenile). Spatial variability of BAM
mineralisation is uncharacterized in surface soil, however, and factors
controlling the heterogeneity remain unknown. We addressed these issues
by sample-to-sample comparisons of BAM mineralisation rates and a range
of soil characteristics at spatial scales ranging from meters to
centimetres. For mineralisation assays nano-molar concentrations of
labelled BAM were added to determine mineralisation rates under
realistic conditions. We found a significant variability of BAM
mineralisation which increased with decreasing spatial scale. BAM
mineralisation rates were correlated to the density of BAM-degrading
bacteria but not to water content, TOC, NH4+, NO3−, or pH. The genus Aminobacter,
which contains the only BAM degraders known, was detected in MPN
samples of BAM degraders by a specific PCR assay targeting the 16S rRNA
gene, confirming a role of Aminobacter in BAM mineralisation.
AB - The metabolite 2,6-dichlorobenzamide (BAM) is a frequent groundwater
pollutant produced during degradation of the herbicide
2,6-dichlorobenzonitrile (dichlobenile). Spatial variability of BAM
mineralisation is uncharacterized in surface soil, however, and factors
controlling the heterogeneity remain unknown. We addressed these issues
by sample-to-sample comparisons of BAM mineralisation rates and a range
of soil characteristics at spatial scales ranging from meters to
centimetres. For mineralisation assays nano-molar concentrations of
labelled BAM were added to determine mineralisation rates under
realistic conditions. We found a significant variability of BAM
mineralisation which increased with decreasing spatial scale. BAM
mineralisation rates were correlated to the density of BAM-degrading
bacteria but not to water content, TOC, NH4+, NO3−, or pH. The genus Aminobacter,
which contains the only BAM degraders known, was detected in MPN
samples of BAM degraders by a specific PCR assay targeting the 16S rRNA
gene, confirming a role of Aminobacter in BAM mineralisation.
KW - 2,6-dichlorobenzamide
KW - 2,6-dichlorobenzonitrile
KW - Aminobacter
KW - Mineralisation
KW - Spatial heterogeneity
UR - http://www.scopus.com/inward/record.url?scp=74249097317&partnerID=8YFLogxK
U2 - 10.1016/j.envpol.2009.07.002
DO - 10.1016/j.envpol.2009.07.002
M3 - Article
SN - 0269-7491
VL - 158
SP - 292
EP - 298
JO - Environmental Pollution
JF - Environmental Pollution
IS - 1
ER -