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Piping Plover - U.S. Fish and Wildlife Service

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A recently completed study (Miller et al. 2009, discussed below) provides new insight into<br />

piping plover taxonomy. Furthermore, notwithst<strong>and</strong>ing a 22-year history of recovery<br />

programs predicated on three populations, no formal analysis of these populations has been<br />

conducted pursuant to the 1996 DPS policy. We therefore review these interrelated issues in<br />

light of currently available scientific information.<br />

2.1.2 Taxonomic classification or changes in nomenclature<br />

A molecular genetic-based investigation of piping plovers, including mitochondrial DNA<br />

sequences (580 bp, n = 245 individuals) <strong>and</strong> eight nuclear microsatellite loci (n = 229<br />

individuals) from 15 U.S. states <strong>and</strong> eight Canadian provinces, was completed in 2009<br />

(Miller et al. 2009). Only four of 70 unique mitochondrial haplotypes were shared between<br />

interior (i.e., Northern Great Plains <strong>and</strong> Great Lakes) <strong>and</strong> Atlantic groups, <strong>and</strong> four<br />

phylogenetic reconstruction procedures revealed strong differentiation between interior <strong>and</strong><br />

Atlantic populations. Consistent with these analyses, a Bayesian clustering procedure<br />

implemented using STRUCTURE (version 2.2.3) found that the most likely partitioning of<br />

the data supported two groups, Atlantic <strong>and</strong> interior. Differential genetic structure patterns<br />

were also observed within the two groups, with stronger spatial genetic structure in both<br />

mitochondrial <strong>and</strong> microsatellite data sets for Atlantic birds. Miller et al. (2009) confirmed<br />

separate Atlantic <strong>and</strong> interior piping plover subspecies (C. m. melodus <strong>and</strong> C. m.<br />

circumcinctus, respectively). This study found that birds from the Great Lakes region were<br />

allied with the interior subspecies group <strong>and</strong> should be taxonomically referred to as C. m.<br />

circumcinctus.<br />

Genetic evidence for the two subspecies described above is consistent with data from<br />

resightings of b<strong>and</strong>ed piping plovers (Table 1). Despite intensive surveys of breeding sites<br />

<strong>and</strong> marking of at least 7,374 birds (1,424 Atlantic Coast; 5,950 Great Lakes <strong>and</strong> Northern<br />

Great Plains combined) between 1982 <strong>and</strong> 2007, no interchange between subspecies has been<br />

reported. Although the subspecies mix to varying extents on their wintering grounds (Gratto-<br />

Trevor et al. 2009) <strong>and</strong> interior birds have been observed at migration stopovers in the<br />

Atlantic breeding range as far north as New Jersey (Stucker <strong>and</strong> Cuthbert 2006), they form<br />

pairs on the breeding grounds (Elliott-Smith <strong>and</strong> Haig 2004). We do not completely discount<br />

the possibility that a very few undetected birds could occasionally move between the<br />

breeding ranges of the two subspecies, but complete lack of observed exchanges of b<strong>and</strong>ed<br />

birds, coupled with genetic differences, provide further evidence of existence of separate<br />

subspecies.<br />

Ecological exchangeability (e.g., life history traits, morphology, habitat) of coastal <strong>and</strong><br />

interior breeders has received little explicit attention in recent scientific literature. Moser<br />

(1942) found no differences in measurements of birds with different plumage types. As<br />

noted in section 2.1.1 of this review, Wilcox (1959) rejected assertions by Moser (1942)<br />

regarding differences in extent of breast b<strong>and</strong>s. However, the differences in genetic structure<br />

between C. m. melodus <strong>and</strong> circumcinctus observed by Miller et al. (2009) may be<br />

evolutionarily important. Atlantic birds demonstrated the signature of a genetic isolation-bydistance<br />

pattern that was not apparent among interior birds. Miller et al. (2009) suggested<br />

that these genetic structure differences may reflect relatively higher breeding <strong>and</strong> natal site<br />

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