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Piping Plover - U.S. Fish and Wildlife Service

Piping Plover - U.S. Fish and Wildlife Service

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fidelity of Atlantic birds, potentially as a consequence of reduced spatiotemporal variability<br />

in habitat conditions. Conversely, greater temporal climatic variation may cause flooding or<br />

complete desiccation of habitats used by interior populations, thereby forcing more dispersal.<br />

This difference in genetic structure between C. m. melodus <strong>and</strong> circumcinctus may reflect<br />

important adaptations to differences in habitat stability, although we cannot exclude the<br />

possibility of a plastic (i.e., not hereditary) response to varying environments. Furthermore,<br />

while C. m. circumcinctus breed on a range of habitat types (see discussion in section<br />

2.1.3.1), habitat factors such as coastal tides, which affect C. m. melodus (but not C. m.<br />

circumcinctus) nest site selection <strong>and</strong> foraging behaviors during critical stages in the<br />

breeding cycle, may constitute an important ecological difference between subspecies.<br />

Casual comparison of studies suggests other possible behavioral differences (e.g., prevalence<br />

<strong>and</strong> timing of brood desertion by female parents, rates of inter-year mate retention) between<br />

subspecies, but no formal analyses have been conducted.<br />

In 2001, the Canadian Committee on the Status of Endangered <strong>Wildlife</strong> in Canada<br />

recognized C. m. melodus <strong>and</strong> C. m. circumcinctus as separate taxa <strong>and</strong> designated each<br />

subspecies as “Endangered” (Department of Justice Canada 2002). This superseded 1978<br />

<strong>and</strong> 1985 designations assigned to the entire Canadian population of piping plovers<br />

(COSEWIC 2001).<br />

We are not aware of any current publications in the peer-reviewed literature that reject these<br />

subspecies. S. M. Haig, first author of a 1988 allozyme study (Haig <strong>and</strong> Oring 1988a) that<br />

failed to detect differences supporting piping plover subspecies, is also a co-author of Miller<br />

et al. (2009). Thus, this more recent study employing modern <strong>and</strong> variable genetic<br />

information systems to analyze a substantially larger data set fully supersedes Haig <strong>and</strong><br />

Oring (1988a).<br />

The subspecies C. m. melodus exactly coincides with the geographic coverage of the Atlantic<br />

Coast piping plover recovery plan (USFWS 1996), while the Great Lakes plan (USFWS<br />

2003) <strong>and</strong> the Northern Great Plains plan (USFWS 1988b) pertain to C. m. circumcinctus.<br />

2.1.3 Application of the 1996 DPS policy<br />

Section 3 of the ESA defines “species” to include subspecies <strong>and</strong> “any distinct population<br />

segment of any species of vertebrate fish or wildlife which interbreeds when mature<br />

(emphasis added).” In 1996, the USFWS <strong>and</strong> the National Marine <strong>Fish</strong>eries <strong>Service</strong><br />

published a joint policy guiding the recognition of DPSs of vertebrate species (61 FR 4722).<br />

As discussed in section 2.1.2 above, new information supports subspecies designation for C.<br />

m. melodus <strong>and</strong> circumcinctus. However, because the piping plover is a vertebrate listed<br />

prior to 1996, we evaluate evidence for DPSs within these two subspecies (see 61 FR 4724:<br />

“The <strong>Service</strong>s maintain that the authority to address DPSs extends to species in which<br />

subspecies are recognized …”).<br />

The DPS policy specifies three elements to assess whether a population segment under<br />

consideration for listing may be recognized as a DPS: (1) the population segment’s<br />

discreteness from the remainder of the species to which it belongs, (2) the significance of the<br />

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