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1.
Mol Ecol ; 21(8): 2017-30, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22250728

ABSTRACT

Earthworms are known for their important role within the functioning of an ecosystem, and their diversity can be used as an indicator of ecosystem health. To date, earthworm diversity has been investigated through conventional extraction methods such as handsorting, soil washing or the application of a mustard solution. Such techniques are time consuming and often difficult to apply. We showed that combining DNA metabarcoding and next-generation sequencing facilitates the identification of earthworm species from soil samples. The first step of our experiments was to create a reference database of mitochondrial DNA (mtDNA) 16S gene for 14 earthworm species found in the French Alps. Using this database, we designed two new primer pairs targeting very short and informative DNA sequences (about 30 and 70 bp) that allow unambiguous species identification. Finally, we analysed extracellular DNA taken from soil samples in two localities (two plots per locality and eight samples per plot). The two short metabarcode regions led to the identification of a total of eight earthworm species. The earthworm communities identified by the DNA-based approach appeared to be well differentiated between the two localities and are consistent with results derived from inventories collected using the handsorting method. The possibility of assessing earthworm communities from hundreds or even thousands of localities through the use of extracellular soil DNA will undoubtedly stimulate further ecological research on these organisms. Using the same DNA extracts, our study also illustrates the potential of environmental DNA as a tool to assess the diversity of other soil-dwelling animal taxa.


Subject(s)
DNA Barcoding, Taxonomic/methods , DNA, Mitochondrial/analysis , Ecosystem , Oligochaeta/classification , Oligochaeta/genetics , Soil/chemistry , Animals , DNA Primers , Electron Transport Complex IV/genetics , Molecular Sequence Data , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Species Specificity
2.
Mol Ecol ; 21(8): 1951-65, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22250784

ABSTRACT

Diet analysis is a prerequisite to fully understand the biology of a species and the functioning of ecosystems. For carnivores, traditional diet analyses mostly rely upon the morphological identification of undigested remains in the faeces. Here, we developed a methodology for carnivore diet analyses based on the next-generation sequencing. We applied this approach to the analysis of the vertebrate component of leopard cat diet in two ecologically distinct regions in northern Pakistan. Despite being a relatively common species with a wide distribution in Asia, little is known about this elusive predator. We analysed a total of 38 leopard cat faeces. After a classical DNA extraction, the DNA extracts were amplified using primers for vertebrates targeting about 100 bp of the mitochondrial 12S rRNA gene, with and without a blocking oligonucleotide specific to the predator sequence. The amplification products were then sequenced on a next-generation sequencer. We identified a total of 18 prey taxa, including eight mammals, eight birds, one amphibian and one fish. In general, our results confirmed that the leopard cat has a very eclectic diet and feeds mainly on rodents and particularly on the Muridae family. The DNA-based approach we propose here represents a valuable complement to current conventional methods. It can be applied to other carnivore species with only a slight adjustment relating to the design of the blocking oligonucleotide. It is robust and simple to implement and allows the possibility of very large-scale analyses.


Subject(s)
DNA Barcoding, Taxonomic/methods , DNA, Mitochondrial/genetics , Felidae/physiology , Predatory Behavior , RNA, Ribosomal/genetics , Sequence Analysis, DNA/methods , Animals , Behavior, Animal , DNA, Mitochondrial/analysis , Diet , Feces/chemistry , Oligonucleotides/genetics , Species Specificity
3.
Conserv Biol ; 24(2): 621-6, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20105205

ABSTRACT

Assessing conservation strategies requires reliable estimates of abundance. Because detecting all individuals is most often impossible in free-ranging populations, estimation procedures have to account for a <1 detection probability. Capture-recapture methods allow biologists to cope with this issue of detectability. Nevertheless, capture-recapture models for open populations are built on the assumption that all individuals share the same detection probability, although detection heterogeneity among individuals has led to underestimating abundance of closed populations. We developed multievent capture-recapture models for an open population and proposed an associated estimator of population size that both account for individual detection heterogeneity (IDH). We considered a two-class mixture model with weakly and highly detectable individuals to account for IDH. In a noninvasive capture-recapture study of wolves we based on genotypes identified in feces and hairs, we found a large underestimation of population size (27% on average) occurred when IDH was ignored.


Subject(s)
Biometry/methods , Population Density , Wolves , Animal Identification Systems , Animals , Feces , France , Hair , Models, Statistical
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