Bartholomew G W, Pfaender F K
Appl Environ Microbiol. 1983 Jan;45(1):103-9. doi: 10.1128/aem.45.1.103-109.1983.
The influence of spatial and temporal environmental variations on rates of organic pollutant biodegradation were assessed by using heterotrophic uptake kinetics. These studies were conducted at three sites, representing the gradient from freshwater to estuarine to marine systems. Of the compounds tested, total uptake Vmax rates decreased in the order of nitrilotriacetic acid, m-cresol, chlorobenzene, and 1,2,4-trichlorobenzene. In general, the freshwater site exhibited the highest uptake rates, with somewhat lower rates at the estuarine site. Rates at the marine site were much lower than at the other sites, except during the winter. Metabolic rates at both the freshwater and estuarine areas were significantly decreased during periods of low water temperature. Rates at the marine site were relatively uniform throughout the year. Linear regression analysis was used to compare m-cresol biodegradation rates to characteristics of the microbial community, which included direct microscopic counts, CFU counts, and cellular incorporation of amino acids. The observed rates did not consistently correlate well with any of the measured characteristics of the microbial community.
利用异养吸收动力学评估了空间和时间环境变化对有机污染物生物降解速率的影响。这些研究在三个地点进行,代表了从淡水到河口再到海洋系统的梯度。在所测试的化合物中,总吸收Vmax速率按次氮基三乙酸、间甲酚、氯苯和1,2,4 - 三氯苯的顺序降低。一般来说,淡水地点的吸收速率最高,河口地点的速率略低。除冬季外,海洋地点的速率远低于其他地点。在水温较低的时期,淡水和河口地区的代谢速率均显著降低。海洋地点的速率全年相对稳定。使用线性回归分析将间甲酚生物降解速率与微生物群落特征进行比较,这些特征包括直接显微镜计数、CFU计数和氨基酸的细胞掺入。观察到的速率与微生物群落的任何测量特征均未始终呈现良好的相关性。