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Chloe Apelgren

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Knemidokoptic mange was first observed on two Hawai‘i ‘Amakihi (Hemignathus virens) mist netted in Manuka Natural Area Reserve (NAR) on the Island of Hawai‘i in June 2007. Microscopic examination of skin scrapings from lesions of the infested individuals revealed the scaley-leg mite, Knemidokoptes jamaicensis. Continued surveillance at Manuka NAR (2007-2009) documented a 24% (15/63) prevalence of mange among Hawai‘i ‘Amakihi distributed from coastal habitat to 1,500 m above sea level (asl). From 2012-2014, we conducted an island-wide survey of wild passerine birds from several leeward sites (Manuka NAR, Kahuku Unit of Hawai‘i Volcanoes National Park (HAVO), Pu‘u Wa‘awa‘a Forest Bird Sanctuary, and Kipahoehoe NAR)...
Categories: Publication; Types: Citation; Tags: Technical Report
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The indigenous forest birds of American Samoa are increasingly threatened by changing patterns of rainfall and temperature that are associated with climate change as well as environmental stressors associated with agricultural and urban development, invasive species, and new introductions of avian diseases and disease vectors. Long term changes in their distribution, diversity, and population sizes could have significant impacts on the ecological integrity of the islands because of their critical role as pollinators and seed dispersers. We documented diversity of vector borne parasites on Tutuila and Ta‘u Islands over a 10-year period to expand earlier observations of Plasmodium, Trypanosoma, and filarial parasites,...
Categories: Publication; Types: Citation; Tags: Technical Report
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Microscopic examination of blood smears can be effective at diagnosing and quantifying hematozoa infections. However, this method requires highly trained observers, is time consuming, and may be inaccurate for detection of infections at low levels of parasitemia. To develop a molecular methodology for identifying and quantifying Leucocytozoon parasite infection in wild waterfowl (Anseriformes), we designed a real-time, quantitative PCR protocol to amplify Leucocytozoon mitochondrial DNA using TaqMan fluorogenic probes and validated our methodology using blood samples collected from waterfowl in interior Alaska during late summer and autumn (n = 105). By comparing our qPCR results to those derived from a widely used...
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