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Creators/Authors contains: "Manne, Lisa L"

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  1. Abstract Habitat loss due to changes in land cover is one of the main causes of biodiversity decline worldwide. Habitat loss occurs disproportionately in areas of high biodiversity because these same areas are particularly suitable for development. We assessed the effect of development risk on the biodiversity of breeding birds in the United States. We compared the effect of two predictors of habitat loss on the richness, abundance, and rarity of woodland, open-habitat, and urban birds at the local and regional levels. We used the House Price Index—as a measure of development risk—and primary productivity as predictors in simulations of habitat loss. For local scale analysis, we used generalized regression models. For regional-scale habitat loss simulations, we statistically compared the results obtained from each predictor. Locally, development risk and primary productivity interacted in their effect on the richness, abundance, and rarity index of all birds. At the regional level, developme 
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  2. European gulls Chroicocephalus ridibundus, Larus canus, and L. graellsii have dispersed to North America and C. ridibundus and L. graellsii have bred or attempted to breed. North American gulls L. delawarensis, Leucophaeus atricilla, Leucophaeus pipixcan, and Chroicocephalus philadelphia have dispersed to Europe, although no successful breeding by non-hybrid pairs has yet occurred. We hypothesized that as gull population sizes increase, the number of birds exploring potential new breeding sites also increases. To test our hypothesis, we compared the number of transatlantic vagrants to the population size on the previous year using generalized linear models. We found an increasing number of transatlantic vagrants moving in both directions, which suggests that vagrancy is not a random phenomenon driven by strong winds nor caused by reverse migration. Population size predicted transatlantic vagrancy in four of the seven species. However, our hypothesis that increases in population size drive increases in vagrancy was only supported in two of these instances. We further looked at sub-populations of L. delawarensis in North America and tested our hypothesis for each subpopulation. We found partial support for our hypothesis for these data. Even within one species, we observed multiple relationships between vagrancy and population size. Our results showed that size or trend in source population size—in some circumstances—is clearly a driver of vagrancy, but other factors must play an important role too. As anthropogenic development continues, and high-quality habitats become farther apart, it is important that we continue to investigate all drivers of vagrancy because the persistence of a species may depend crucially on its longest-distance dispersers. 
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  3. Tropical Kingbird (Tyrannus melancholicus) is an abundant and widespread Neotropical species with an extended history of vagrancy to temperate North America (Pranty et al. 2016). One at Mount Loretto Unique Area, Staten Island, NY (40.503575, -74.218169) on 26 September 2021 was just the second for New York State, less than a year after the first, at Dobbs Ferry, Westchester County, 27-29 October 2020 (Tom Warren, Julien Ansellem, eBird). These New York records follow scores of records from Florida since 1982 and at least 25 from northeastern North America through 2020. Here we provide details for the Staten Island record, describe the broader recent increase in northward occurrence of vagrant Tropical Kingbirds, and address what could be responsible for this change. Specifically, we tested the hypothesis that the occurrence of Tropical Kingbirds in northeastern North America could be predicted by their occurrence in Florida and confirmed that this was so, supporting the notion that vagrancy to northeastern North America is the result of an ongoing process of population growth, exploratory behavior, and colonization. 
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  4. Elegant terns Thalasseus elegans breed in a very limited area of the northern Gulf of California and the Pacific coast of southern California, with up to 95% (mean 78%, 1991–2014, Perez et al., 2020 ) of the population nesting on Isla Rasa in the northern Gulf of California. On Isla Rasa, the primary nesting colony, elegant terns suffered predation by rodents which raised the possibility of population extinction, with a substantial proportion of the world population nesting on this single island. Because of this threat, rodents were successfully removed from Isla Rasa in 1995. The removal of rodents from Isla Rasa led to a near immediate increase in the population of elegant terns. That increase was associated with a changing pattern in dispersal by the terns, including extraordinary movements to the Gulf of Mexico, the Atlantic coast of the United States north to Massachusetts, and, remarkably, to western Europe. A few elegant terns successfully bred at these European localities during 2009 to the present. In this paper we use this exceptional example of long-distance dispersal to illustrate how rapid population growth during ∼ 1995 to present can lead to successful colonization of remote sites through repeated instances of vagrancy. We tested four Hypotheses that together support the idea that the growing population of elegant terns has produced increasing numbers of young, and these young have spread, through the mechanism of vagrancy, to the Pacific Northwest, the east coast of the United States, and western Europe. Our Hypotheses are: (1) The nesting population of elegant terns within their core nesting range has increased since removal of rodents from Isla Rasa; (2) Occurrence of vagrant elegant terns in the Pacific Northwest is driven by population growth within the core breeding range. (3) Occurrence of vagrant elegant terns at the east coast of the United States is driven by population growth within the core breeding range. (4) Occurrence and colonization of western Europe by elegant terns is driven by nesting population size within the core breeding range. Corollaries of these Hypotheses are, (i) that there is a time lag in occurrence of vagrants at each of these areas, based on increasing distance from the core breeding range and (ii) the number of vagrants in any given year is also related to sea surface temperature (SST), as expressed by Oceanic Niño Index, a proxy for food resource levels. Generally we found strong statistical support for each of these Hypotheses; an exception was for the occurrence of elegant terns in the Pacific Northwest, which initially occurred following El Niño events (low food supply) and profound breeding failure, but later corresponding to cold water years with high breeding success. We use elegant terns, exceptional for the highly restricted breeding range and sustained population growth over 25 years, to illustrate how growing populations may colonize very distant habitats through repeated instances of vagrancy. 
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  5. Abstract We studied positive associations among seabirds and marine mammals at South Georgia on research cruises during the Austral winters of 1985, 1991 and 1993 and found statistically significant differences. We collected data on abundance and distribution, providing a critical reference for sub-Antarctic conservation in anticipation of future environmental changes. We found significant changes in the abundance of 29% of species surveyed and a consequent change in species diversity. We postulate that the resulting altered community composition may have previously unanticipated population effects on the component species, due to changes in positive interactions among species which use each other as cues to the presence of prey. We found a near threefold reduction in spatial overlap among vertebrate predators, associated with warming sea temperatures. As the strength and opportunity for positive associations decreases in the future, feeding success may be negatively impacted. In this way, environmental changes may disproportionately impact predator abundances and such changes are likely already underway, as Southern Ocean temperatures have increased substantially since our surveys. Of course the changes we describe are not solely due to changing sea temperature or any other single cause—many factors are important and we do not claim to have removed these from consideration. Rather, we report previously undocumented changes in positive associations among species, and argue these changes may continue into the future, given near-certain continued increases in climate-related changes. 
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