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Lisa M. Pajot

Publications and source records attributed to Lisa M. Pajot.

3 recordsLinked to original sources

After-hatch and hatch year Buff-breasted Sandpipers (Calidris subruficollis) can be sexed accurately using morphometric measures

Determining the sex of birds quickly in the field can help in studies of behavior and distribution, and when selecting particular sexes for deploying tracking devices or collecting samples. However, discerning males from females is difficult in species that are plumage monomorphic and have overlapping sexual-size dimorphism, as in Buff-breasted Sandpipers Calidris subruficollis . We developed three discriminant functions to sex Buff-breasted Sandpipers based on measurements of live birds captured in Brazil whose sex was confirmed with molecular techniques. We validated these discriminant functions using morphometric measures from other independent samples of known-sex live birds from wintering (Brazil), migration (Texas), and breeding (Alaska) sites. Discriminant functions derived from birds captured in Brazil accurately sexed ≥88% of the validation sample from Brazil, Texas, and Alaska. Errors in classification occurred among males on the wintering (0–5%) and breeding (8–12%) grounds, and females during migration (0–11%). Discriminant functions worked well because of the substantial sexual size dimorphism present in the species, with male traits being in general 5.2–10.4% larger than female traits. The size of morphological traits did not vary by age (after controlling for sex) for birds sampled on the wintering grounds and during migration. Our results indicate that discriminant functions can be used to sex after-hatch year (AHY) Buff-breasted Sandpipers throughout their range, and for hatch year (HY) birds during their first southbound migration and winter. Being able to accurately sex both AHY and HY birds using only morphological measurements will improve studies of the ecology and population structure of this species and enhance the application of conservation measures.

Wader Study

Epizootic of beak deformities among wild birds in Alaska: An emerging disease in North America?

The sudden appearance of a large cluster of animals with gross abnormalities may signal a significant change in an ecosystem. We describe an unusual concentration of beak deformities that appear to have arisen rapidly within Alaska and now extend southward along the Pacific Coast. In Alaska we have documented 2,160 Black-capped Chickadees ( Poecile atricapillus ) and 435 individuals of 29 other species of birds, primarily during the past decade, with grossly overgrown and often crossed beaks. The annual prevalence of beak abnormalities among adult Black-capped Chickadees in south-central Alaska varied from 3.6% to 9.7% and averaged 6.5 ± 0.5% between 1999 and 2008. Only 0.05 ± 0.05% of nestlings and 0.3 ± 0.2% of juveniles <6 months old had abnormal beaks, which suggests that this is either a latent developmental or an acquired condition. We documented 80 cases in which a Black-capped Chickadee captured with an apparently normal beak was subsequently recaptured with a beak abnormality and 8 cases in which a beak deformity was no longer detectable upon recapture. Necropsy and histopathology of a sample of affected individuals provided no conclusive evidence of the etiology of this condition. Deformities appear to affect primarily the keratin layer of the beak and may result from abnormally rapid growth of the rhamphotheca. Some affected birds also exhibited lesions in other keratinized tissues of the skin, legs, feet, claws, and feathers, which may represent a systemic disorder or secondary conditions. Additional studies are currently underway to determine diagnostic signs and the underlying cause of this avian keratin disorder.

Alaska

Use of buccal swabs for sampling DNA from nestling and adult birds

We evaluated the feasibility and efficiency of using swabs to collect buccal epithelial cells from small (2‐ to 13‐ g ) birds as a source of DNA for genetic studies. We used commercially available buccal swab kits to collect samples from 42 adult and 39 nestling (4‐ to 8‐day‐old) black‐capped chickadees (Poecile atricapillus) and from 6 4‐day‐old nestling boreal chickadees (P. hudsonica). We compared DNA from buccal epithelial samples to that from blood samples from the same individuals. We extracted sufficient quantities of DNA for analysis from all buccal samples, and samples remained viable even after being stored in original plastic sampling tubes at room temperature for up to 18 months. Yields were equivalent whether extracted using the proprietary quick‐extraction solution provided with buccal swab kits or using a salt‐extraction process with inexpensive reagents. Yields of DNA from buccal samples were consistently lower than those from blood samples, but quantities were sufficient for all analyses. Assignment of sex, based on DNA extracted from paired buccal and blood samples, was identical for all 87 birds. We found no difference in the genotypes obtained from buccal and blood samples for 12 individuals tested using 5 microsatellite loci and found perfect concordance in sequencing of an 823‐base‐pair segment within the control region of mitochondrial DNA for 7 individuals tested. Use of buccal swabs is highly recommended as a rapid, noninvasive technique for sampling avian genomic DNA, especially for extremely young altricial nestlings or small‐bodied adults, or for any birds for which blood sampling may be impossible or stressful.

Wildlife Society Bulletin