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At least 199 records · Page 11Linked to original sources
USGS1998

Mourning Dove nesting habitat and nest success in Central Missouri

Previous Mourning Dove (Zenaida macroura) nesting studies conducted in areas containing a mixture of edge and continuous habitats have focused on edge habitats. Consequently, little is known about the potential contribution of continuous habitats to dove production. In this study we evaluated the relative importance of these two extensive habitat types by monitoring the habitat use and nest success of 59 radio-marked doves during 1990-1991 in central Missouri. Of 83 nests initiated by our marked sample, most (81.9%) were located in edge habitats. Although continuous habitats were selected less as nest sites, the proportion of successful nests did not differ significantly from that in edge habitats. Our data indicate that continuous habitats should not be considered marginal nesting habitat. If the intensity of use and nest success that we observed are representative regionally or nationally, continuous habitats could contribute substantially to annual Mourning Dove production because of the high availability of these habitats throughout much of the Mourning Dove breeding range.

Journal of Field Ornithology↗
USGS1999

Loss from harlequin ducks of abdominally implanted radio transmitters equipped with percutaneous antennas

We documented extrusion and loss of abdominally implanted radio transmitters with percutaneous antennas from adult female Harlequin Ducks (Histrionicus histrionicus). Birds were captured during wing molt (late August to mid-September) in 1995-1997. Of 44 Harlequin Ducks implanted with radios and recaptured, 7 (16%) had lost their transmitters and 5 (11%) had radios in the process of extruding. Most (11 of 12) extrusions and losses occurred in birds implanted with radios in 1996 and recaptured in 1997. We suggest that transmitter extrusions and losses were due largely to changes in transmitter design made between 1095 and 1996. Transmitters implanted in 1996 were cylindrical rather than spherical, had a flat end with an abrupt edge, and the lower portion of the antenna was reinforced. Radio losses occurred after the 7-mo monitoring period and caused no apparent harm to the birds. Investigators using implanted radios with percutaneous antennas for long-term projects should be aware of the potential for radio extrusion and should minimize the problem by using transmitters that have no sharp edges and that are wide, rather than narrow.

Journal of Field Ornithology↗
USGS1999

Evaluation of bursal depth as an indicator of age class of harlequin ducks

We contrasted the estimated age class of recaptured Harlequin Ducks (Histrionicus histrionicus) (n = 255) based on bursal depth with expected age class based on bursal depth at first capture and time since first capture. Although neither estimated nor expected ages can be assumed to be correct, rates of discrepancies between the two for within-year recaptures indicate sampling error, while between-year recaptures test assumptions about rates of bursal involution. Within-year, between-year, and overall discrepancy rates were 10%, 24%, and 18%, respectively. Most (86%) between-year discrepancies occurred for birds expected to be after-third-year (ATY) but estimated to be third-year (TY). Of these ATY-TY discrepancies, 22 of 25 (88%) birds had bursal depths of 2 or 3 mm. Further, five of six between-year recaptures that were known to be ATY but estimated to be TY had 2 mm bursas. Reclassifying birds with 2 or 3 mm bursas as ATY resulted in reduction in between-year (24% to 10%) and overall (18% to 11%) discrepancy rates. We conclude that age determination of Harlequin Ducks based on bursal depth, particularly using our modified criteria, is a relatively consistent and reliable technique.

Journal of Field Ornithology↗
USGS1980

Effect of delayed reporting of band recoveries on survival estimates

Brownie et al. (U.S. Fish and Wildl. Serv., Resource Publ. 131, 1978) presented 14 models based on an array of explicit assumptions for the study of survival in avian populations. These methods are replacing the life table methods previously used to estimate survival rates (e.g., Burnham and Anderson, J. Wildl. Manage. , 43: 356-366, 1979). The new methods allow survival or recovery rates, or both, to be constant, time-specific, or time- and age-specific. In studies to estimate survival rates for birds the data are often from recoveries of birds shot or found dead during the hunting season and reported to the Bird Banding Laboratory by sportsmen, conservation agency employees, or the general public. This note examines the bias in estimating annual survival due to a proportion of the recoveries being incorrectly reported a year late. Specifically, a few recoveries each year of, for example, adult male American Widgeon ( Anas americana ) banded in California are reported as being recovered in year i + 1 when in fact they were actually recovered the previous year i. Delayed reporting might typically be caused by people finding a band in their health clothing in the fall of the year and, being embarrassed about their failure to report the band when it was taken, report it a year late not mentioning the actual year of recovery. Heuristically, delayed reporting should bias estimated annual survival rates upwards because it appears from the data that the birds corresponding to the "delayed" recoveries actually lived an additional year.

Journal of Field Ornithology↗
USGS1980

The effect of band loss on estimates of annual survival

Banding has proven to be a useful technique in the study of population dynamics of avian species. However, band loss has long been recognized as a potential problem, (Hickey, 1952; Ludwig, 1967). Recently, Brownie et al. (1978) presented 14 models based on an array of explicit assumptions for the analysis of band recovery data. Various estimation models (assumption sets) allowed survival and/or recovery rates to be (a) constant, (b) time-specific, or (c) time- and age-specific. Optimal inference methods were employed and statistical tests of critical assumptions were developed and emphasized. The methods of Brownie et al. (1978), as with all previously published methods of which we are aware, assume no loss of bands during the study. However, some band loss is certain to occur and this potentially biases the estimates of annual survival rates whatever the analysis method. A few empirical studies have estimated band loss rates (a notable exception is Ludwig, 1967); consequently, for almost all band recovery data, the exact rate of band loss is unknown. In this paper we investigate the bias in estimates of annual survival rates due to varying degrees of hypothesized band loss. Our main results are based on perhaps the most useful model, originally developed by Seber (1970), for estimation of annual survival rate. Inferences are made concerning the bias of estimated survival rates in other models because the structure of these estimators is similar.

Journal of Field Ornithology↗
USGS1985

Determining age and sex of American coots

Reliable techniques for age and sex determination of migrating and wintering American Coots ( Fulica americana ) have not been available. Breeding coots can be ages through age 3 by tarsal color (birds 4 years and older were placed in a 4+ age class) (Crawford 1978), and males and females have sex-specific behaviors and calls while on breeding territories (Gullion 1950, 1952). Externally, juvenile coots differ from adults in having gray (as opposed to white) bills and brown (as opposed to red) eyes to an age of 75 days (Gullion 1954-394). Bill color changes to white by about 120 days. No quantitative data have been available, however, on the proportion of juveniles retaining these traits throughout fall and early winter. Nonbreeding coots can be ages as juvenile or adult by internal examination of the thickness of the wall of the bursa of Fabricius, although bursal depth does not predictably decline with age (Fredrickson 1968). Attempts to sex coots by single external measurements of combinations of measurements have met with mixed success. Eight-five percent of 101 fall migrants in Wisconsin could be sexed by the length of the metatarsus-midtoe including claw by using 139.5 mm as a cutoff point (Burton 1959), whereas 88% of 67 coots in California were correctly sexed by the length of the metatarsus-midtoe without claw using 127.5 mm as the cutoff point (Gullion 1952). Two-hundred-thirty-two of 291 coots collected in Iowa, however, were in the zone of overlap between the sexes for this measurement (Fredrickson 1968). Previous studies attempting to develop aging and sexing techniques for American Coots have been limited to a few study sites or to 1 season or year, often failing to take geographical, annual, and seasonal morphological variation into account (e.g., Visser 1976, Fjeldsa 1977). We designed the present study to refine and quantify external and internal age and sex criteria for postbreeding coots, with the objective of defining techniques applicable for all seasons over a wide geographical area.

Journal of Field Ornithology↗
USGS1993

Growth and survival of Mountain Plovers

Growth and survival rates of Mountain Plovers ( Charadrius montanus ) were monitored using radiotelemetry from hatching until birds left the breeding grounds on the Pawnee National Grassland, Weld County, Colorado. Chick weights increased logarithmically ( r ) = 0.961) and tarsus length linearly ( r = 0.948) with age. Using the average fledgling weight of 69.8 g and an age/weight regression we predicted that the average age at fledging was 36 d. Fourteen Mountain Plover nests each had three effs; an average of 2.6 eggs hatched in seven nests, whereas remaining nests were lost to predation, storms, or trampling by a cow. Twenty-four adult Mountain Plovers were monitored for 275 telemetry days with no mortalities. Twenty flightless chicks had a calculated daily survival rate of 0.979 for 233 telemetry-days. Mortalities of flightless chicks were due to predation or unknown causes. The daily survival rate predicted that 1.2 of the 2.6 chicks hatched per nest lived to fly. Eight fledged chicks were monitored for 74 telemetry-days, with a daily survival rate of 0.974. Mortalities of fledglings were all attributed to predation. The combined survival rates predicted that 0.7 or the 2.6 hatched chicks lived to leave the nesting area. Survival rates of flightless chicks were similar to those reported 20 yr ago, implying that recent declines in Mountain Plover numbers on the continent are not attributable to either longer-term declines in nesting productivity or phenomena occurring at non-breeding locales.

Journal of Field Ornithology↗
USGS1993

Nests and nest sites of the San Miguel Island Song Sparrow

Nests and nest sites of the San Miguel Island ( SMI ) Song Sparrow ( Melospiza melodia micronyx ) are described; nests are compared with those of 16 other races of Song Sparrows. Bush lupins ( Lupinus albifrons ), coyote brush ( Baccharis pilularis ) and golden bush ( Haplopappus venetus ) were the shrubs used most commonly as nest sites by Song Sparrows on SMI. As a result of its location, the nest was effectively concealed from gray foxes ( Urocyon littoralis ), the major predator of this sparrow. Nest and nest site also moderated the combined chilling effects of cool air temperatures and strong northwesterly winds on the eggs and nestlings. Even in the absence of these moderating effects of the nest site, the energetic cost of incubation, estimated at 41-53% of the sparrow's resting metabolic rate, was modest. Twenty-nine percent of the canopy above the nest was open and as much as 73% of the nest cup was in the sun at midday, a time when surface temperatures of foliage, nest and nestlings sometimes exceeded 40 C. Whereas this exposure did not apparently reduce fledging success, it may explain why the incidence of addled eggs was so high in this population of Song Sparrows compared to others. Significant differences existed among races of Song Sparrows in the size, porosity and insulation of the nest. In most cases, these differences were not related to the latitude of the races' nesting areas.

California↗
USGS1997

Evidence of Newell's Shearwater breeding in Puna District, Hawaii

Nocturnal surveys using auditory cues and night-vision equipment were conducted during the seabird breeding season in 1993 to determine use of inland areas in the Puna District, Hawaii by Newell's Shearwater ( Puffinus auricularus newelli ). Two hundred sixty Newell's Shearwater auditory or visual detections were made during 275 survey hours from 23 Jul. 1993 - 20 Sep. 1993. Mean detection rates were 1.26 birds/h at Puulena Crater ( n = 160 Newell's Shearwater detections), 1.05 birds/h at Heiheiahulu ( n = 99) and 0.04 birds/ h at Puu Kaliu ( n = 2). Vocalizing peaked between 50 and 90 min after sunset and 4 h before sunrise. Although night-vision equipment was used on most of the seabird surveys, only 4% of seabirds were detected visually. Two road-killed birds collected in Puna in June 1993, and four burrows located in Puulena Crater after the 1994 breeding season, provided additional evidence of breeding.

Hawaii↗
USGS1998

Nest relocation using PVC "spotters"

A simple device to aid in the rapid relocation of nests, composed on PVC pipe and tie wire, is described. A 16-18 cm length of pipe can be attached to a supporting structure with a section of wire and adjusted to point at the target nest by its discoverer. Used like an lensless spotting scope, the “spotter” allows other observers to quickly and reliably relocate the nest with minimal written or verbal description.

Journal of Field Ornithology↗
USGS1983

The fledging of common and thick-billed murres on Middleton Island, Alaska

Three species of alcids, Common and Thick-billed murres ( Uria aalge and U. lomvia ) and the Razorbill ( Alca torda ), have post-hatching developmental patterns intermediate to precocial and semi-precocial modes (Sealy 1973). The young leave their cliff nest sites at about one quarter of adult weight and complete their growth at sea. At departure, an event here loosely referred to as "fledging," neither primary nor secondary flight feathers are grown, but well-developed wing coverts enable limited, descending flight.

Alaska↗
USGS1988

Factors influencing predation associated with visits to artificial goose nests

Artificial goose nests were used to determine what factors might increase predation after visits to nests of Cackling Canada Geese ( Branta canadensis minima ). We tested whether leaving the nest uncovered, marking the nest location with a flag, or placing the nest on an island or peninsula would increase the rate of predation. Predators destroyed significantly more of the nests with eggs exposed to view (61%) than of the nests with eggs covered with goose down (35%) (P < 0.05). However, the rate of predation was only slightly higher among nests located on peninsulas than on islands and equal proportions of flagged and unflagged nests were destroyed. We also determined that investigators attracted predators to the study area and caused an increase in predation at uncovered nests immediately after the visit. Covering the eggs with down essentially negated the effect of attracting predators when visiting the nest. Among the 46 nests destroyed, 78% were destroyed by birds and 22% by mammals. Results of our study suggested that visibility of exposed eggs rather than nest markers provided important cues to avian predators and that islands probably provided some refuge from mammalian predators. Investigators can take steps to minimize their impact on nesting success and should incorporate a measure of that impact in their studies.

Alaska↗
USGS1992

Breeding chronology of mottled ducks in a Texas coastal marsh

The relationship between breeding chronology of Mottled Ducks ( Anas fulvigula fulvigula ) and wetland conditions at San Bernard National Wildlife Refuge was examined over a 3-yr period. Median nest initiation dates varied by as much as 68 d among years. Initiation occurred earlier in 1985 and 1987 versus 1986 (P < 0.05). Nesting initiation was not associated with winter and spring temperatures, but late nesting occurred in 1986 following low rainfall during fall and winter. Low rainfall caused low water levels in all marsh types. Water levels and wetland availability may influence nesting dates by limiting the food resources available to prenesting and nesting Mottled Ducks.

Texas↗
USGS1992

Intraspecific variation in egg shape among individual emperor geese

Within-clutch variability in shape of 1743 eggs from 301 nests of Emperor Geese ( Chen canagicus ) laid over a 5-yr period was measured. Individual females laid similar shaped eggs in successive years, and eggs among clutches within females could not be distinguished. Cluster analysis correctly identified 69.9% of 136 known conspecific parasitic eggs. Repeatability estimates of elongation (0.73), sphericity (0.72), maximum width (0.69) and radius of the point (0.68) were high and similar to repeatability estimates of egg mass and volume of other species. Although width, volume and area measurements varied inversely with spring population size, shape variables did not. The consistency in shape variables despite changes in egg size suggests that shape variables may be used to separate and identify individuals within and among years despite changes in the population that may result in changes in egg size. Differences in egg shape among eggs within a nest are viable criteria for identifying parasitic eggs, especially when used in conjunction with other methods.

Journal of Field Ornithology↗
USGS1994

Blood sampling in juvenile buff-breasted sandpipers: Movement, weight change and survival

The effect of blood sampling on juvenile Buff-breasted Sandpipers ( Tryngites subruficollis ) was evaluated by comparing movements, mass, and survival of 10 broods (37 chicks) that were bled and eight broods (31 chicks) that were not bled. Blood was sampled from the jugular vein of chicks when they weighed 9.1 ± 0.9 g (x̄ ± SD) on or within 1 d of hatch. Chicks showed few short-term negative effects from blood sampling. Individual chicks suffered little physical injury, and five of eight chicks where injury occurred (i.e., hematomas formed) survived to fledging. Furthermore, bled broods gained mass at a comparable rate during the first 5 d post-hatch, and were resighted at similar frequencies as broods that were not bled. Bled broods moved slightly longer distances than control broods 1 d after hatch, however. This increased activity may have been stress-induced, but was only temporary; bled and control broods made similar long-term movements, and the probability of resighting was similar at fledging. With the proper precautions, it appears that Buff-breasted Sandpiper young can be safely sampled for blood at an early age without causing undue harm.

Alaska↗
USGS1994

Decoy trapping and rocket-netting for northern pintails in spring

Decoy traps and rocket-nets were compared for capturing Northern Pintails ( Anas acuta : hereafter pintails) during May 1991 on the Yukon Flats, Alaska. Males were captured at similar rates using both methods (1.38 vs. 1.07 males/trap d, respectively), but baited rocket-nets were more efficient than decoy traps for capturing females (0.52 vs. 0.12 females/trap d). There were no significant differences in masses of pintails captured by each method.

Alaska↗
USGS1995

A device for simultaneously measuring nest attendance and nest temperature in waterfowl

Previous studies of waterfowl have measured nest attendance and nest temperature separately using a variety of methods. A device was developed that monitors nest attendance and temperature simultaneously. The device consists of an artificial egg with a microswitch that records nest attendance and a thermistor probe that records temperature. Data are stored in a single-channel data logger. The device described measures the length of incubation breaks, and nest cooling and warming rates.

Journal of Field Ornithology↗