Geology Reports⌕ Search

SEARCH · Geology Reports

Results for “Auk”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 163 records · Page 9Linked to original sources
USGS2004

How we can learn more about the Cerulean Warbler ( Dendroica cerulea )

A sense of urgency attends the study of species of concern, like the Cerulean Warbler ( Dendroica cerulea ). Sharpened by Robbins et al. (1992) and Hamel (1992), such concern prompted the U.S. Department of the Interior, Fish and Wildlife Service (USFWS) to commission a status assessment of the Cerulean Warbler (Hamel 2000a). Shortly after the status review was published, a petition (Ruley 2000) was delivered to the USFWS urging that the species be listed as “threatened” under the Endangered Species Act of 1973. The account of the Cerulean Warbler in the Birds of North America series also appeared that year (Hamel 2000b). Substantial attention is currently focused on the species, and the Cerulean Warbler Technical Group (CWTG) was formed in 2002 (see Appendix). This overview consists of two parts. The first, prepared primarily by P.B.H., attempts to summarize current knowledge and suggest productive avenues to pursue in our efforts to understand the biology and conserve populations of Cerulean Warblers. The second, written by D.K.D. and P.D.K., is a summary of the structure and priorities of the CWTG, an organization that can spur and facilitate research and conservation action directed at this species and serve as a model for conservation of other forest birds (Appendix). Further information on Cerulean Warblers and activities of the Cerulean Warbler Technical Group can be found on the CWTG website (see Acknowledgments).

The Auk↗
USGS2004

Early environment and recruitment of black brant ( Branta bernicla nigricans ) into the breeding population

In geese, growth regulates survival in the first year. We examined whether early growth, which is primarily governed by environmental conditions, also affects the probability that individuals that survive their first year enter the breeding population. We used logistic regression on a sample of Black Brant ( Branta bernicla nigricans ) that were weighed at a known age in their first summer and observed during winter (indicating that they had survived the principal mortality period in their first year) to study whether early growth influenced the probability that those individuals would be recruited into the breeding population. We also examined the effects of cohort (1986-1996), sex, age when measured, and area where individuals were reared. The model with the lowest Akaike's Information Criterion score contained body mass, age (days) at measurement, cohort, sex, and brood-rearing area. Models that included variable mass had 85% of the cumulative model weight of the models we considered, indicating that gosling mass had a substantial effect on probability of them entering the breeding population. Females were more likely to be detected breeding than males, which is consistent with the differential fidelity of the sexes. Of individuals that survived the first year, larger goslings were more likely to become breeders. More recent cohorts were less likely to have been detected as breeders. Our findings indicate that environment during the growth period affects the ability of individuals to enter the breeding population, even after accounting for the effects of growth on survival.

Alaska↗
USGS2004

Nutrient reserves of Lesser Scaup ( Aythya affinis ) during spring migration in the Mississippi Flyway: A test of the spring condition hypothesis

The continental scaup population (Lesser [ Aythya affinis ] and Greater [ A. marila ] combined) has declined markedly since 1978. One hypothesis for the population decline states that reproductive success has decreased because female scaup are arriving on breeding areas in poorer body condition than they did historically (i.e. spring condition hypothesis). We tested one aspect of that hypothesis by comparing body mass and nutrient reserves (lipid, protein, and mineral) of Lesser Scaup at four locations (Louisiana, Illinois, Minnesota, and Manitoba) between the 1980s and 2000s. We found that mean body mass and lipid and mineral reserves of females were 80.0, 52.5, and 3.0 g higher, respectively, in the 2000s than in the 1980s in Louisiana; similarly, body mass and lipid and mineral reserves of males were 108.8, 72.5, and 2.5 g higher, respectively. In Illinois, mean body mass and lipid reserves of females were 88.6 and 56.5 g higher, respectively, in the 2000s than in the 1980s; similarly, body mass and lipid and mineral reserves of males were 80.6, 76.0, and 2.7 g higher, respectively. Mean body mass of females were 58.5 and 58.9 g lower in the 2000s than in the 1980s in Minnesota and Manitoba, respectively; mean body mass of males, similarly, were 40.7 g lower in Minnesota. Mean lipid reserves of females in the 2000s were 28.8 and 27.8 g lower than those in the 1980s in Minnesota and Manitoba, respectively. Mean mineral reserves of females in the 2000s were 3.2 g lower than those in the 1980s in Manitoba. Consequently, females arriving to breed in Manitoba in the 2000s had accumulated lipid reserves for 4.1 fewer eggs and mineral reserves for 0.8 fewer eggs than those arriving to breed there in the 1980s. Accordingly, our results are consistent with the spring condition hypothesis and suggest that female body condition has declined, as reflected by decreases in body mass, lipids, and mineral reserves that could cause reductions in reproductive success and ultimately a population decline.

The Auk↗
USGS2005

Enhancing the scientific value of the Christmas Bird Count

T he C hristmas B ird C ount (CBC), conducted by the National Audubon Society (NAS) since 1900, constitutes the longest-running and geographically most widespread survey of bird life in the Western Hemisphere. Starting with 25 count locations in its first year, the program has grown continuously ever since, with 20–30 locations currently being added annually. Each CBC consists of a tally of all birds detected within a circle 24.1 km (15 miles) in diameter, on a single day within a few weeks around Christmas (current allowable dates are 14 December through 5 January). More than 50,000 observers now take part each year, in close to 2,000 count circles spread across the U.S. and its territories, southern Canada, and, increasingly, Latin America.

The Auk↗
USGS2005

[Book review] The history of ornithology in Virginia

Virginia is arguably the birthplace of ornithology in North America. Captain John Smith and naturalist Mark Catesby were among the early describers of Virginia's common birds. David Johnston's book, however, begins by taking the reader back to the Tertiary period, some 65 million years ago, with Storrs Olson's description of fossils from tidewater Virginia. John Guilday, studying bone deposits in mountain caves, identified 80 species of birds, including Rock Ptarmigan and Spruce Grouse, from a time when Virginia's climate differed greatly from that of today. Archaeological studies and accounts of aboriginals in the 17th century complete Chapter 1.

The Auk↗
USGS2005

Parental nest defense on videotape: More reality than "myth"

Predation is recognized as the primary source of nest mortality in most passerine species (e.g. Ricklefs 1969, Martin 1992a); thus, it is no surprise that parental nest defense has received considerable scientific attention (see below). By nest defense, we refer to any parental behavior that decreases the probability that a predator (or brood parasite) will harm the nest contents and that simultaneously entails some cost to the bird engaged in the behavior—either by increasing the bird's risk of injury or death (Montgomerie and Weatherhead 1988) or by at least increasing its expenditure of time and energy (Buitron 1983).

The Auk↗
USGS2005

Phylogeography of the American woodcock ( Scolopax minor ): Are management units based on band recovery data reflected in genetically based management units?

Information on population connectivity throughout the annual cycle has become more crucial, because populations of many migratory birds are in decline. One such species is the American Woodcock ( Scolopax minor ), which inhabits early-successional forests in eastern North America. Although band recoveries have proved useful for dividing populations of this game bird species into an Eastern Region and Central Region for management purposes, these data do not provide enough detail to determine the breeding population of origin of birds recovered on stopover and wintering areas. To obtain more fine-scale data, we undertook a phylogeographic study of American Woodcock populations throughout their primary breeding range in the eastern United States and Canada using mitochondrial DNA (mtDNA) sequences from the hypervariable control region I (CRI) and ND6 gene. Despite high haplotype diversity, nucleotide diversity was low and there was no phylogeographic structure among American Woodcock populations across the species range, with birds from many states and provinces in both management regions sharing identical haplotypes. Results suggest recent or ongoing gene flow among populations, with asymmetric movement of birds between migration flyways. As has been demonstrated for several other avian species in North America, American Woodcock appear to have undergone a rapid population expansion following the late Pleistocene glacial retreat. Thus, a combination of historical demographic factors and recent or ongoing gene flow mask any population structure based on mtDNA that might accrue from philopatry to breeding areas observed in studies of marked birds.

The Auk↗
USGS2005

Habitat and sex differences in physiological condition of breeding Southwestern Willow Flycatchers ( Empidonax traillii extimus )

The Southwestern Willow Flycatcher ( Empidonax traillii extimus ; here- after “flycatcher”) is a federally listed endangered species that breeds in densely vegetated riparian habitats dominated by native and exotic plants, including introduced monotypic saltcedar (Tamarix ramosissima) . Some workers have theorized that saltcedar is unsuitable habitat for the flycatcher, primarily because it generally supports a smaller and less diverse invertebrate community (the flycatcher's food base) than native habitats (e.g. Salix spp.). However, differences in insect communities between native and saltcedar habitats are not proof that saltcedar habitats are inferior. The only way to evaluate whether the habitats differ in dietary or energetic quality is to document actual food limitation or its manifestations. Measurements of an individual's body condition and metabolic state can serve as indicators of environmental stressors, such as food limitation and environmental extremes. We captured 130 flycatchers breeding in native and saltcedar habitats in Arizona and New Mexico and measured 12 variables of physiological condition. These variables included body mass, fat level, body condition index, hematocrit, plasma triglycerides, plasma free fatty acids and glycerol, plasma glucose and beta-hydroxybutyrate, plasma uric acid, total leukocyte count, and heterophil-to-lymphocyte ratio. We found substantial sex-based differences in the condition of male and female flycatchers. Ten of the 12 measures of physiological condition differed significantly between the sexes. In all cases where male and female condition differed (except mass), the differences suggest that males were in poorer condition than females. We found few habitat-based differences in flycatcher condition. Only 3 of the 12 physiological condition indices differed significantly between habitats. Our data show that, at least in some parts of the flycatcher's range, there is no evidence that flycatchers breeding in saltcedar habitats exhibit poorer nutritional condition or are suffering negative physiological affects.

The Auk↗
USGS2005

[Book review] Massachusetts breeding bird atlas

A glance at the dust jacket of this handsome volume drives home the conservation message that breeding bird atlases are designed to promote—that bird populations are changing over vast areas and, unless we become aware of changes in status and take remedial action, some species will disappear from our neighborhoods and even our county or state. A case in point involves the closely related Golden-winged Warbler ( Vermivora chrysoptera ) and Blue- winged Warbler ( Vermivora pinus ). The males are shown in the atlas with their breeding distribution maps. When I was an active birder in the Boston suburbs in the 1930s, the Golden-winged Warbler was a common breeder and it was a treat to find a Blue-winged Warbler. The atlas map 40 years later (1974–1979) shows only five confirmed records statewide for the Golden-winged Warbler, compared with 73 for the Blue-winged Warbler, and the Golden-winged Warbler is now listed as endangered by the Massachusetts Division of Fisheries and Wildlife. Nationally, it is a species of management concern.

The Auk↗
USGS2006

Nest survival in dusky Canada geese ( Branta canadensis occidentalis ): Use of discrete-time models

The Dusky Canada Goose ( Branta canadensis occidentalis ) population that breeds in the Copper River Delta, Alaska, has declined substantially since the late 1970s. Persistent low numbers have been attributed to low productivity in recent years. We examined patterns in survival rates of 1,852 nests to better understand ecological processes that influenced productivity during 1997-2000. We compared 10 nonparametric models of daily survival rate of nests (DSR) that included variation among years, calendar dates, nest initiation dates, and nest ages with equivalent models based on parametric functions. The unequivocal best model included patterns of DSR that varied among discrete periods of years, calendar dates, and nest ages. Generally, DSR was low early in the nesting season and higher midseason. Across years, patterns in DSR were most variable early and late in the nesting season. Daily survival rates of nests declined between the first and second week after initiation, increased until the fourth week, and then declined during the last week before hatch. Nest survival probability estimates ranged from 0.07 to 0.71 across years and nest initiation dates. Mean rates of nest survival ranged between 0.21 and 0.31 each year. We suggest (1) considering models that do not limit estimates of daily nest survival to parametric forms; (2) placing greater emphasis on sample size when nests are rare, to obtain accurate estimates of nest survival; and (3) developing new techniques to estimate the number of nests initiated.

The Auk↗
USGS2006

Fat dynamics of arctic-nesting sandpipers during spring in mid-continental North America

We measured fresh body mass, total body fat, and fat-free dry mass (FFDM) of three species of Arctic-nesting calidrid sandpipers (Baird's Sandpiper [ Calidris bairdii ], hereafter “BASA”; Semipalmated Sandpiper [ C. pusilla ], hereafter “SESA”; and White-rumped Sandpiper [ C. fuscicollis ], hereafter “WRSA”) during spring stopovers in the Prairie Pothole Region (PPR) of North Dakota, and evaluated the contribution of stored fat to (1) energy requirements for migration to their Arctic-breeding grounds and (2) nutrient needs for reproduction. All spring migrant WRSA ( n = 124) and BASA ( n = 111), and all but 2 of 99 SESA we collected were ≥2 years old. Male and female BASA migrated through North Dakota concurrently, male SESA averaged earlier than females, and WRSA males preceded females. Fat indices (ratio of fat to FFDM) of male and female SESA and WRSA averaged approximately twice those of male and female BASA. Total body fat of male and female BASA increased with date in spring 1980, but not in 1981; slopes were similar for both sexes each year. Male and female SESA arrived lean in 1980 and 1981, and total body fat increased with date in both years, with similar slopes for all combinations of sex and year. Male and female WRSA arrived lean in 1980–1981 and 1981, respectively, and total body fat increased with date, whereas females arrived with fat reserves already acquired in 1980. Interspecific and sex differences in migration schedules probably contributed to variation in fat storage patterns by affecting maintenance energy costs and food availability. Estimated flight ranges of BASA suggest that few could have met their energy needs for migration to the breeding grounds exclusively from fat stored by the time of departure from North Dakota. Estimated flight ranges of SESA and WRSA, along with fresh body masses of both species when live-trapped on or near their breeding grounds in northern Canada, suggest that major parts of both populations stored adequate fat by departure from temperate mid-continental North America to meet their energy requirements for migration and part of their nutrient needs for reproduction.

The Auk↗
USGS2006

Ecological and physiological factors affecting brood patch area and prolactin levels in arctic-nesting geese

We investigated effects of ecological and physiological factors on brood patch area and prolactin levels in free-ranging Lesser Snow Geese ( Chen caerulescens caerulescens ; hereafter “Snow Geese”) and Ross's Geese ( C. rossii ). On the basis of the body-size hypothesis, we predicted that the relationships between prolactin levels, brood patch area, and body condition would be stronger in Ross's Geese than in the larger Snow Geese. We found that brood patch area was positively related to clutch volume and inversely related to prolactin levels in Ross's Geese, but not in Snow Geese. Nest size, nest habitat, and first egg date did not affect brood patch area in either species. Prolactin levels increased as incubation progressed in female Snow Geese, but this relationship was not significant in Ross's Geese. Prolactin levels and body condition (as indexed by size-adjusted body mass) were inversely related in Ross's Geese, but not in Snow Geese. Our findings are consistent with the prediction that relationships between prolactin levels, brood patch area, and body condition are relatively stronger in Ross's Geese, because they mobilize endogenous reserves at faster rates than Snow Geese.

The Auk↗
USGS2006

Breeding biology and success of a reintroduced population of the critically endangered Puaiohi ( Myadestes palmeri )

The ultimate success of reintroduction programs for endangered species depends on the ability of reintroduced animals to breed in the wild. We studied the nesting success and breeding biology of a reintroduced population of Puaiohi ( Myadestes palmeri ) on the island of Kaua'i, Hawaii. Thirty-four captive-bred Puaiohi were released into the Alaka'i Swamp in 1999-2001 and monitored using radiotelemetry. Ten females and two males paired with wild and other released birds, including one polygynous trio. From March to September, 31 nests were built. Mean clutch size was 2.0 eggs, daily nest survival was 0.97 ± 0.01 (mean ± SE) and overall nest success was 0.40 ± 0.02. We confirmed predation, most probably by rats ( Rattus spp.), as the greatest cause of nest failure, occurring at 38% of active nests with known fates, and causing the death of two nesting adult females. Ground-based rodent control proved ineffective at protecting nest attempts. Successful nests fledged an average of 1.4 young each ( n = 10), and 85% of fledglings survived at least two weeks. Importantly, breeding behavior and success were comparable to those of wild Puaiohi. This is the first record of breeding in the wild from captive-bred endangered Hawaiian passerines. The ability of captive-bred Puaiohi to survive and breed successfully in the wild bodes well for future releases of this and other endangered passerines, but high predation rates on nests and nesting females highlights the importance of maintaining and restoring safe habitat for recovery.

The Auk↗
USGS2006

A review of the population estimation approach of the North American landbird conservation plan

As part of their development of a continental plan for monitoring landbirds (Rich et al. 2004), Partners in Flight (PIF) applied a new method to make preliminary estimates of population size for all 448 species of landbirds present in the continental United States and Canada (Table 1). Estimation of the global population size of North American landbirds was intended to (1) identify the degree of vulnerability of each species, (2) provide estimates of the current population size for each species, and (3) provide a starting point for estimating population sizes in states, provinces, territories, and Bird Conservation Regions (Rich et al. 2004). A method proposed by Rosenberg and Blancher (2005) was used to derive population estimates from available survey data. To enhance the credibility of these estimates, PIF organized a review of the methodology used to estimate North American landbird population sizes. A planning committee selected members from the ornithological and biometrical communities (hereafter “the panel”), with the aim of selecting individuals from academia, state natural-resource agencies, and the U.S. and Canadian federal governments, including the Canadian Wildlife Service, the U.S. Geological Survey, and the U.S. Department of Agriculture Forest Service. The panel addressed three questions: (1) Were the methods of population estimation proposed by PIF reasonable? (2) What actions could be taken to improve the data or analyses on which the PIF population estimates were based? and (3) How should the PIF population estimates be interpreted?

The Auk↗
USGS2006

[Book review] Birds in Europe: Population estimates, trends and conservation status

Effective bird conservation requires knowledge of distribution, relative abundance, and population trends at multiple geographic scales. Obtaining this information for a continental avifauna poses considerable challenges, especially in Europe with its 52 countries, numerous languages and cultures, and disparate resources available for monitoring bird populations within each country. Synthesizing the available information on the status and trends of all European birds into a single volume is an enormous yet essential task necessary to direct bird conservation activities across the continent.

The Auk↗
USGS2007

Philopatry: A return to origins

The word “philopatry” is a combination of the prefix philo (from the Greek philos, “beloved”) and the Latin patria, which means “fatherland” or “homeland.” Since the first English-language use of “philopatry” in an ornithological context by Huntington (1951) , the term has been applied to two types of site-faithful behavior in birds. Closest to the etymological meaning is the first, “natal philopatry,” which means not dispersing far from, or returning to, a birthplace for reproduction. The second is “breeding philopatry,” which means returning to the same breeding area each year, though that area may not be an individual’s birth place ( Shields 1982 , Anderson et al. 1992 ). Therefore, any assessment of breeding philopatry likely includes some immigrant individuals, whereas assessments of natal philopatry include only locally hatched or born individuals. In the past several years, the use of philopatry in the ornithological literature has widened further, to include site fidelity to nonbreeding areas, such as sites used for molting ( Iverson et al. 2004 ), wintering ( Robertson and Cooke 1999 , Mehl et al. 2004 ), or stopover during migration ( Merom et al. 2000 ). Use of the term “philopatry” to describe not only natal homing, but general site fidelity to both breeding and nonbreeding sites of individuals whose natal areas are unknown is, I believe, problematic and warrants reconsideration. This is because there are substantial genetic and demographic implications of philopatry in its purest and historical sense (i.e., natal philopatry), such as increased relatedness and population differentiation ( Greenwood 1980 , Quinn and White 1987 , Avise et al. 1992 ). Indeed, the historical and theoretical discussions of natal philopatry focus on the behavior of limited dispersal from a birth place, how this promotes inbreeding, why inbreeding might be adaptive, and how a lack of gene flow might promote speciation ( Mayr 1963 , Shields 1982 , Anderson et al. 1992 ). I believe that these population-genetic and demographic implications are potentially misapplied when “philopatry” is used to describe site-faithful behavior in general (see Pearce and Talbot 2006 ). The potential danger of applying philopatry to non-natal and nonbreeding conditions is that it creates the expectation of certain outcomes, such as low dispersal rates, population genetic differentiation, and unique population segments, when such conditions may not exist. Given that most avian species do not molt, winter, or have migratory stopovers where they breed, I propose that the term “philopatry” and its genetic expectations be used only in relation to natal philopatry and not extended to (1) breeding- site fidelity of individuals whose natal areas are unknown and (2) nonbreeding areas where site- faithful behavior is observed. I believe this correctly distinguishes natal philopatry as a specific type of site fidelity with its own implications for population genetics and dynamics. Thus, philopatry should be viewed as synonymous and interchangeable with the terms “natal-site fidelity” and “natal philopatry,” and the term “breeding-site fidelity” should replace “breeding philopatry,” because it reflects the unknown natal origins of birds captured as adults. Although the broader condition of site fidelity may have implications for fitness, mate pairing, and population delineation—as examined in several studies ( Robertson and Cooke 1999 , Merom et al. 2000 , Iverson et al. 2004 , Mehl et al. 2004 )—future investigations of site fidelity should be pursued without automatically invoking the term “philopatry” and assuming that the genetic and demographic connotations of natal philopatry also apply. In contrast to philopatry, the probability of fidelity ( F ) and dispersal (1 − F ) are estimable parameters ( Burnham 1993 , Kendall and Nichols 2004 ), and the demographic and genetic consequences of site fidelity, regardless of where it occurs, can serve as hypotheses for testing with multiple data types (e.g., Arsenault et al. 2005 ). Such data mergers should enhance our understanding of the demographic, behavioral, and genetic implications of natal philopatry and site fidelity.

The Auk↗