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Jorge W. Santo Domingo

Researcher at United States Environmental Protection Agency

Publications -  120
Citations -  6385

Jorge W. Santo Domingo is an academic researcher from United States Environmental Protection Agency. The author has contributed to research in topics: Fecal coliform & Bacteroidales. The author has an hindex of 43, co-authored 116 publications receiving 5672 citations.

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Microbial source tracking: state of the science.

TL;DR: This review provides an outline of the main methods that either have been used or have been suggested for use in microbial source tracking and some of the limitations associated with those methods.
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Comparative fecal metagenomics unveils unique functional capacity of the swine gut.

TL;DR: The results from this metagenomic survey demonstrated the presence of genes associated with resistance to antibiotics and carbohydrate metabolism suggesting that the swine gut microbiome may be shaped by husbandry practices.
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Host Distributions of Uncultivated Fecal Bacteroidales Bacteria Reveal Genetic Markers for Fecal Source Identification

TL;DR: Examination of host distribution patterns among fecal bacteria in the order Bacteroidales revealed both endemic and cosmopolitan distributions among the eight hosts, with the goal of using endemic sequences as markers for fecal source identification in aquatic environments.
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Quo vadis source tracking? Towards a strategic framework for environmental monitoring of fecal pollution.

TL;DR: It is proposed that it is necessary to consider each of these aspects in order to advance towards a unifying framework in source identification, so that fecal pollution monitoring can be reliably used for comprehensive environmental microbial monitoring, to develop risk assessment models, and to implement and validate adequate management practices.
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Phylogenetic diversity of drinking water bacteria in a distribution system simulator

TL;DR: To characterize the composition of microbial populations in a distribution system simulator (DSS) by direct sequence analysis of 16S rDNA clone libraries by direct sequences analysis of16S r DNA clone libraries.