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At least 703 records · Page 39Linked to original sources
USGS1993

Overwinter distribution of northern pintail populations in North America

Northern pintails ( Anas acuta ) exist as a single circumpolar breeding population but display weak fidelity to given breeding sites. If fidelity to wintering areas is strong, management on wintering grounds may allow local winter populations to increase. Thus, I delineated reference areas for wintering areas based on recovery data for pintails banded during the winter (Dec-Feb) in the United States. Fidelity to these reference areas varied with the strongest fidelity observed for pintails banded in areas along coastal areas or near large bodies of water such as western Washington-northwestern Oregon, central California, northwestern Utah, the Texas-Louisiana Gulf Coast, and the Greater Chesapeake Bay Region. My analysis suggests that pintails occurred in distinct wintering populations and that wintering ground affiliations to certain areas appear to be more stable population units than breeding ground affiliations. Consequently, winter banding programs may be useful in monitoring survival of specific wintering populations of concern.

North America↗
USGS1993

Survival of northern pintails banded during winter in North America, 1950-88

From 1950 through 1988, the continental breeding population of northern pintails ( Anas acuta ) varied from 2.0 million to 9.9 million. Because pintails have high fidelity to certain wintering grounds along coasts and large bodies of water, management on these wintering areas may increase population size if changes in winter survival rate are related to changes in population size. I used band-recovery data to estimate survival rates for winter-banded pintails and to test for sex-specific, temporal, and geographic variation in survival rates. Survival rate estimates varied between 0.632 and 0.806 for males, and 0.421 and 0.769 for females. Males had higher ( P < 0.0001) average annual survival rates than females. Limited geographic variation occurred in estimates of average annual survival rates for males, and no variation occurred for females. Males had lower average annual survival rates in the Imperial Valley than in central California ( P = 0.007) or in the Gulf Coast ( P = 0.092). Little annual variation was found within time periods. However, longer-term variation was found in survival rate estimates for males and females. Males had higher ( P = 0.054) average annual survival rates in the Pacific Flyway during 1959-61, a period of drought, breeding-population decline, and restrictive hunting regulations, than during 1950-58, a period with a higher breeding population and liberal regulations. The increase in wintering population size in the Pacific Flyway during the 1970's was associated with a higher average annual survival rate for females in the Pacific Flyway than during the 1950's. Results from the Pacific Flyway suggested that an interaction may exist between population size and the effect of harvest regulations on survival of males. Changes in harvest regulations appeared to have a greater effect at lower population levels.

North America↗
USGS1990

Recent trends in counts of migrant hawks from northeastern North America

Using simple regression, pooled-sites route-regression, and nonparametric rank-trend analyses, we evaluated trends in counts of hawks migrating past 6 eastern hawk lookouts from 1972 to 1987. The indexing variable was the total count for a season. Bald eagle ( Haliaeetus leucocephalus ), peregrine falcon ( Falco peregrinus ), merlin ( F. columbarius ), osprey ( Pandion haliaetus ), and Cooper's hawk ( Accipiter cooperii ) counts increased using route-regression and nonparametric methods (P < 0.05). Northern harrier ( Circus cyaneus ) counts increased based on the nonparametric method (P < 0.01) but not the route-regression method (P > 0.10). We found no consistent trends (P > 0.10) in counts of sharp-shinned hawks ( A. striatus ), northern goshawks ( A. gentilis ) red-shouldered hawks ( Buteo lineatus) , red-tailed hawks ( B. jamaicensis ), rough-legged hawsk ( B. lagopus ), and American kestrels ( F. sparverius ). Broad-winged hawk ( B. platypterus ) counts declined (P < 0.05) based on the route-regression method. Empirical comparisons of our results with those for well-studied species such as the peregrine falcon, bald eagle, and osprey indicated agreement with nesting surveys. We suggest that counts of migrant hawks are a useful and economical method for detecting long-term trends in species across regions, particularly for species that otherwise cannot be easily surveyed.

Michigan, Minnesota, New Jersey, New York, Pennsyl↗
USGS1970

Records of the brambling in North America

A Brambling, Fringella montifringella , was seen regularly in Portland, Oregon, from 22 November 1967 to 3 April 1968 and photographed by many people. First discovered at a feeder in the northeast section of the city by Jeff Gilligan and Ron Klein, from January on it was a daily visitor to the feeder of the Albert H. Praels in the same part of Portland. The bird, judged by plumage to be a male, fed regularly with House Finches ( Carpodacus mexicanus ) on sunflower seeds. The occurrence of this individual in Portland was recorded in Audubon Field Notes (22: 471, 1968) without detail.

The Auk↗
USGS2016

Avian fatalities at wind energy facilities in North America: A comparison of recent approaches

Three recent publications have estimated the number of birds killed each year by wind energy facilities at 2012 build-out levels in the United States. The 3 publications differ in scope, methodology, and resulting estimates. We compare and contrast characteristics of the approaches used in the publications. In addition, we describe decisions made in obtaining the estimates that were produced. Despite variation in the 3 approaches, resulting estimates were reasonably similar; about a quarter- to a half-million birds are killed per year by colliding with wind turbines.

Human-Wildlife Interactions↗
USGS2013

Amphibians and reptiles of Guyana, South America: illustrated keys, annotated species accounts, and a biogeographic synopsis

Guyana has a very distinctive herpetofauna. In this first ever detailed modern accounting, based on voucher specimens, we document the presence of 324 species of amphibians and reptiles in the country; 148 amphibians, 176 reptiles. Of these, we present species accounts for 317 species and color photographs of about 62% (Plates 1–40). At the rate that new species are being described and distributional records are being found for the first time, we suspect that at least 350 species will be documented in a few decades. The diverse herpetofauna includes 137 species of frogs and toads, 11 caecilians, 4 crocodylians, 4 amphisbaenians, 56 lizards, 97 snakes, and 15 turtles. Endemic species, which occur nowhere else in the world, comprise 15% of the herpetofauna. Most of the endemics are amphibians, comprising 27% of the amphibian fauna. Type localities (where the type specimens or scientific name-bearers of species were found) are located within Guyana for 24% of the herpetofauna, or 36% of the amphibians. This diverse fauna results from the geographic position of Guyana on the Guiana Shield and the isolated highlands or tepuis of the eastern part of the Pantepui Region, which are surrounded by lowland rainforest and savannas. Consequently, there is a mixture of local endemic species and widespread species characteristic of Amazonia and the Guianan Region. Although the size of this volume may mislead some people into thinking that a lot is known about the fauna of Guyana, the work has just begun. Many of the species are known from fewer than five individuals in scientific collections; for many the life history, distribution, ecology, and behavior remain poorly known; few resources in the country are devoted to developing such knowledge; and as far as we are aware, no other group of animals in the fauna of Guyana has been summarized in a volume such as this to document the biological resources. We briefly discuss aspects of biogeography, as reflected in samples collected at seven lowland sites (in rainforest, savanna, and mixed habitats below 500 m elevation) and three isolated highland sites (in montane forest and evergreen high-tepui forest above 1400 m elevation). Comparisons of these sites are preliminary because sampling of the local faunas remains incomplete. Nevertheless, it is certain that areas of about 2.5 km2 of lowland rainforest can support more than 130 species of amphibians and reptiles (perhaps actually more than 150), while many fewer species (fewer than 30 documented so far) occur in a comparable area of isolated highlands, where low temperatures, frequent cloudiness, and poor soils are relatively unfavorable for amphibians and reptiles. Furthermore, insufficient study has been done in upland sites of intermediate elevations, where lowland and highland faunas overlap significantly, although considerable work is being accomplished in Kaieteur National Park by other investigators. Comparisons of the faunas of the lowland and isolated highland sites showed that very few species occur in common in both the lowlands and isolated highlands; that those few are widespread lowland species that tolerate highland environments; that many endemic species (mostly amphibians) occur in the isolated highlands of the Pakaraima Mountains; and that each of the isolated highlands, lowland savannas, and lowland rainforests at these 10 sites have distinctive faunal elements. No two sites were identical in species composition. Much more work is needed to compare a variety of sites, and especially to incorporate upland sites of intermediate elevations in such comparisons. Five species of sea turtles utilize the limited areas of Atlantic coastal beaches to the northwest of Georgetown. All of these are listed by the International Union for the Conservation of Nature as being of global concern for long-term survival, mostly owing to human predation. The categories of Critically Endangered or Endangered are applied to four of the local sea turtles (80%). It is important to protect the few good nesting beaches for the sea turtles of Guyana. We have documented each of the species now known to comprise the herpetofauna of Guyana by citing specimens that exist in scientific collections, many of which were collected and identified by us and colleagues, including students of the University of Guyana (UG). We also re-identified many old museum specimens collected by others in the past (e.g., collections of William Beebe) and we used documented publications and collection records of colleagues, most of whom have been working more recently. We present dichotomous keys for identifying representatives of the species known to occur in Guyana, and we present brief annotated species accounts. The accounts provide the current scientific name, original name (with citation of the original description, which we personally examined in the literature), some outdated names used in the recent past, type specimens, type localities, general geographic distribution, examples of voucher specimens from Guyana, coloration in life (and often a color photograph), and comments pointing out interesting subjects for future research.

Proceedings of the Biological Society of Washingto↗
USGS2012

Distributional records of shrews (Mammalia, Soricomorpha, Soricidae) from Northern Central America with the first record of Sorex from Honduras

Short term surveys for small mammals in Guatemala and Honduras during 1992–2009 provided important new records for 12 taxa of shrews from 24 localities. These locality records expand the known geographic distributions for five species and for the genus Sorex Linnaeus, 1758: the geographic range of Cryptotis goodwini Jackson, 1933, now includes the Sierra de las Minas, Guatemala, and several isolated highlands in western Honduras; the known distribution of Cryptotis mayensis (Merriam, 1901) is increased with the first definite modern record for this shrew from Guatemala; Cryptotis merriami Choate, 1970 , is now known to occur in the Sierra de las Minas and the Sierra del Merendón, Guatemala, as well as the isolated Sierra de Omoa and Montana de La Muralla in Honduras, and its documented elevational range (600–1720 m) is expanded; records of Sorex veraepacis Alston, 1877, expand the known distribution of this species to include the Sierra de Yalijux, Guatemala; and discovery of Sorex salvini Merriam, 1897, at Celaque, Honduras (1825–3110 m), represents a considerable extension of the geographic range of the species, and it is the first record of the genus Sorex from Honduras. In addition, the first record of potential syntopy among C. goodwini, C merriami, and Cryptotis orophilus (J.A. Allen, 1895), is reported at an elevation of 1430 m in the Sierra de Celaque, Honduras. Information associated with these records contributes substantially to knowledge of habitat use, elevational distributions, reproductive patterns, diet, and parasites of the species encountered. General patterns include the first evidence that Neotropical species of soricids have smaller litters than their temperate congeners.

Central America↗
USGS1890

Volume XIII: The tertiary insects of North America

That creatures so minute and fragile as insects, creatures which can so feebly withstand the changing seasons as to live, so to speak, but a moment, are to be found fossil, engraved, as it were, upon the rocks or embedded in their hard mass, will never cease to be a surprise to those unfamiliar with the fact. "So fragile," says Quinet, "so easy to crush, you would readily believe the insect one of the latest beings produced by nature, one of those which has least resisted the action of time; that its type, its genera, its forms, must have been ground to powder a thousand times, annihilated by the revolutions of the globe, and perpetually thrown into the crucible. For where is its defense? Of what value its antennae, its shield, its wings of gauze, against the commotions and the tempests which change the surface of the earth? When the mountains themselves are overthrown and the seas uplifted, when the giants of structure, the mighty quadrupeds, change form and habit under the pressure of circumstances, will the insect withstand them? Is it it which will display most character in nature? Yes! The universe flings itself against a gnat. Where will it find refuge? In its very diminutiveness, its nothingness." The pages and plates of the present volume bear testimony to the fact that our tertiary strata have preserved remnants of an ancient host, so varied in structure, so closely also resembling their brethren of to-day, that nearly or quite every prevalent family-group in the entire range of the insect-world has already been demonstrated to have then existed. While often fragmentary and crushed, sometimes beyond recognition, a not insignificant number are sufficiently preserved for us to repopulate the past; sometimes, too, are they preserved in such a wonderful manner that in tiny creatures with a spread of wings scarcely more than a couple of millimeters one may count under the microscope the hairs fringing the wings. In attempting thus to restore the past world of our insects, two or three general features have been forced upon my attention, which may well be mentioned here. One of them is the rernarkable fact that in hardly a single instance has the same species been found at two distinct localities. These localities, it is true, are in some instances separated by hundreds or even thousands of miles, and analogy with the present distribution of insects would lead us to expect more or less profound changes in passing from one to another. But at other times the distance is not great, or at any rate not great enough to make this a satisfactory reason. It is more probable that the beds in which they occur are not altogether synchronous; and we are led to believe that in the separation of horizons insects will give more precise and definite distinctions than may be gained by the study of the plant remains of the same beds. The data at our disposal are not yet sufficiently varied to enable us to speak with any confidence, but when the other groups of Florissant insects, not considered in the present volume, are worked out, and the new material that is at hand from the other principal localities have been fairly studied, it may be found that we are armed with a new weapon of attack in solving the immediate succession of the Tertiary series of the West in their finer subdivisions. Another point to which attention may be drawn is the very considerable number and quite extraordinary proportion of species which so far are represented by a single specimen. Leaving out of consideration certain marvelously prevalent forms in the beds of Florissant, such as certain Formicidae, Alydina, etc., one working these beds, from which many thousands of insects have already been taken, may confidently expect that every third or fourth specimen will prove something new. A quite similar statement can be made of all, or all but one, of the other localities where insects have been found in our Tertiary deposits: it surely indicates that with all the rich results of the explorations so far undertaken we are only upon the threshold of our possible knowledge. We find a richness of fauna far exceeding anything before supposed possible. The interest of the Tertiary fauna is further enhanced by the discovery that no inconsiderable proportion of the species in this fauna must be referred to genera not now extant. Granted that our knowledge of the subtropical forms of this continent (with which as a whole at least our Florissant fauna seems to be akin) is much too meager to be of great service; granted also that in many cases we are forced to establish new genera upon what would be regarded among recent animals as too slender grounds : it is nevertheless true that an unexpectedly large number of forms can not be forced into modern genera already established; in many cases, throughout whole groups, kindred differences from modern types are found which indicate considerable changes of structure in the intervening epochs along parallel lines. In illustration of this we would call special attention to the differences observed in the genera of plant-lice, and, in several places among other Hemiptera as well as among the Coleoptera, to the decided differences in the relative length of various members of the body. My own belief, which springs from the comparisons instituted in the study of this fauna, is that a much larger proportion of genera should really have been founded, and that, for every type which may turn up in Central American explorations of the near future identical with those now established upon the fossils alone, it will be necessary to separate from the familiar surroundings in which I have placed it some other of the insects from the same beds. It should be stated that the larger part of the plates in this volume were engraved before the insects were studied, except in a cursory manner to separate the species; the insects are therefore not always properly grouped, and the legends upon the plates are in part inaccurate. In the enumeration of the specimens at the end of the specific descriptions the numbers of the obverse and reverse of the same specimen are always connected by "and" without any intervening comma, and this typographical method is employed only for expressing this relation. In the study of these extinct insects much assistance has been received from friends, to whom my cordial thanks are due; for valuable suggestions from the late Dr. J. L. LeConte, from Baron R. von Osten Sacken, Edward Burgess, Esq., and Drs. G. H. Horn and H. A. Hagen; for the open collections of the late G. D. Smith, Esq., and of Messrs. E. P. Austin and Samuel Henshaw; and for important aid in obtaining typical series of modern insects in various groups by Messrs. E. P. Austin, P. R. Uhler, E. P. Van Duzee, Edward Burgess, Dr. A. Forel, and most especially Mr. Samuel Henshaw.

British Columbia, Colorado, Ontario, Utah, Wyoming↗
USGS1992

Outdoors America: recreational opportunites on public lands

What comes to your mind when you think of outdoor recreation? Boating? Camping? Hiking or backpacking? Horse-back riding? Hunting or fishing? Chances are, if you can name an outdoor activity, you can do it on public lands.

General Information Product↗