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Geology topics

S.G. Fancy

Publications and source records attributed to S.G. Fancy.

13 recordsLinked to original sources

Statistical approaches to the analysis of point count data: A little extra information can go a long way

Point counts are a standard sampling procedure for many bird species, but lingering concerns still exist about the quality of information produced from the method. It is well known that variation in observer ability and environmental conditions can influence the detection probability of birds in point counts, but many biologists have been reluctant to abandon point counts in favor of more intensive approaches to counting. However, over the past few years a variety of statistical and methodological developments have begun to provide practical ways of overcoming some of the problems with point counts. We describe some of these approaches, and show how they can be integrated into standard point count protocols to greatly enhance the quality of the information. Several tools now exist for estimation of detection probability of birds during counts, including distance sampling, double observer methods, time-depletion (removal) methods, and hybrid methods that combine these approaches. Many counts are conducted in habitats that make auditory detection of birds much more likely than visual detection. As a framework for understanding detection probability during such counts, we propose separating two components of the probability a bird is detected during a count into (1) the probability a bird vocalizes during the count and (2) the probability this vocalization is detected by an observer. In addition, we propose that some measure of the area sampled during a count is necessary for valid inferences about bird populations. This can be done by employing fixed-radius counts or more sophisticated distance-sampling models. We recommend any studies employing point counts be designed to estimate detection probability and to include a measure of the area sampled.

Book chapter

Temporal variation in bird counts within a Hawaiian rainforest

We studied monthly and annual variation in density estimates of nine forest bird species along an elevational gradient in an east Maui rainforest. We conducted monthly variable circular-plot counts for 36 consecutive months along transects running downhill from timberline. Density estimates were compared by month, year, and station for all resident bird species with sizeable populations, including four native nectarivores, two native insectivores, a non-native insectivore, and two non-native generalists. We compared densities among three elevational strata and between breeding and nonbreeding seasons. All species showed significant differences in density estimates among months and years. Three native nectarivores had higher density estimates within their breeding season (December-May) and showed decreases during periods of low nectar production following the breeding season. All insectivore and generalist species except one had higher density estimates within their March-August breeding season. Density estimates also varied with elevation for all species, and for four species a seasonal shift in population was indicated. Our data show that the best time to conduct counts for native forest birds on Maui is January-February, when birds are breeding or preparing to breed, counts are typically high, variability in density estimates is low, and the likelihood for fair weather is best. Temporal variations in density estimates documented in our study site emphasize the need for consistent, well-researched survey regimens and for caution when drawing conclusions from, or basing management decisions on, survey data.

Hawaii

Demography of an introduced red-billed Leiothrix population in Hawaii

Relative abundance, timing of breeding and molting, annual survival, and philopatry of an introduced population of Red-billed Leiothrix ( Leiothrix lutea ) were studied at four sites on the island of Hawaii. Numbers of leiothrix on our study areas showed a regular cyclical pattern, with highest numbers during the breeding season. Peak breeding occurred May-August, followed by peak molting of flight and body feathers in August-October. Flocking behavior increased post-breeding, and many leiothrix left the study areas during the fall and winter months. Populations on two intensive study areas were stable, with high annual survival (x ± SE = 0.581 ± 0.115 for hatching-year birds and 0.786 ± 0.047 for adults). Leiothrix seem to be relatively unaffected by avian diseases that have decimated some Hawaiian bird populations, and yet reasons for their large historical population fluctuations remain unexplained.

Hawaii

A new approach for analyzing bird densities from variable circular-plot counts

An approach for calculating bird densities from variable circular-plot counts is described. The approach differs from previous methods in that data from several surveys are pooled and detection distances are adjusted as if all distances were recorded by a single observer under a given set of field conditions. Adjustments for covariates that affect detection distances such as observer, weather, time of day, and vegetation type are made using coefficients calculated by multiple linear regression. The effective area surveyed under standard conditions is calculated from the pooled data set and then used to determine the effective area surveyed at each sampling station under the actual conditions when the station was sampled. The method was validated in two field studies where the density of birds could be determined by independent methods. Computer software for entering and analyzing data by this method is described.

Pacific Science

Timing of breeding and molting in six species of Hawaiian honeycreepers

The timing of breeding and molting was studied in six species of Hawaiian honeycreepers with differing food habits on the Island of Hawaii. The availability of nectar was highly seasonal, whereas insect abundance was relatively constant throughout the year. All six species of honeycreeper had extended breeding and molting periods with peak breeding between April and July and peak molting in August. Breeding and molting periods for Apapane (Himatione sanguinea) and Iiwi (Vestiaria coccinea), two nectarivorous species, were shorter than those for the more insectivorous Common Amakihi (Hemignathus virens), Hawaii Creeper (Oreomystis mana), Akepa (Loxops coccineus), and Akiapolaau (Hemignathus munroi). Missing or growing flight feathers and either a brood patch or enlarged cloacal protuberance occurred simultaneously in only 3.2% of 2.786 adult birds examined. Although overlap of breeding and molting was rare, some individuals may have been able to allocate energy resources to both activities because of low clutch size, extended brooding of young, and a low rate of molting.

Condor

Demography and movements of the omao (Myadestes obscurus)

Density, age-specific survival, timing of breeding and molting, and movements of the Omao or Hawaiian Thrush (Myadestes obscurus) were studied at four sites on the island of Hawaii. Mean monthly density (birds/ha) was 3.23 +- 0.57, 1.07 +- 0.33, 3.23 +- 0. 16, and 3.74 +- 0.36 at Kau Forest, Hamakua. Keauhou Ranch, and Kilauea Forest study areas, respectively. Annual survival of juvenile Omao (0.40 +- 0.09) was lower than that of adults (0.66 +- 0.08). Emigration and mortality was greatest during November through May. Breeding and molting occurred throughout the year, with peak breeding in May through July. Omao showed strong site fidelity and were highly sedentary. Mean home range size (n = 39) was 2.20 t 0.26 ha and did not differ between sexes or study sites.

Condor

Identifying sex and age of akiapolaau

Methods for identifying the sex and age of the Akiapolaau (Hemignathus munroi), an endangered honeycreeper found only on the island of Hawaii, were developed by examination and measurement of 73 museum specimens and 24 live birds captured in mist nests. Akiapolaau probably undergo a single annual molt, with most birds molting between February and July. The mottled juvenal plumage is replaced by a first basic plumage characterized by yellowish-gray or yellowish-green underparts and often by retained wingbars. Male Akiapolaau may not attain adult plumage until their third molt. In adult females, only the throat and upper breast become yellow, whereas in adult males the superciliaries, cheeks, and entire underparts are yellow. Adult males have greater exposed culmen, gonys, wing chord, tail, and tarsus lengths than do females. Akiapolaau in first prebasic molt or older can be identified as to sex by culmen length, that of males being >23.4 mm.

The Wilson Bulletin

Demography and movements of the endangered akepa and Hawaii creeper

We studied populations of the endangered Akepa (Loxops coccineus coccineus) and Hawaii Creeper (Oreomystis mana) at four sites on the island of Hawaii. Mean monthly density (? SL) of Akepa was 5.74 t 0.87, 1.3? 0.41, 0.96 -? 0.13, and 0.76 ? 0.12 Akepa/ha at Kau Forest, Hamakua, Keauhou Ranch, and Kilauea Forest study areas, respectively. Hawaii Creepers were found at densities of 1.68 ? 0.53, 1.79 ? 0.42, 0.48 ? 0.06, and 0.54 2 ? 0.08 birds/ha, respectively, at the four study areas. Highest capture rates and numbers of birds counted from stations occurred from August through November and February through March. Hatching-year birds were captured from May through December for Akepa and April through December for Hawaii Creeper. Annual survival for adults at Keauhou Ranch was 0.70 ? 0.27 SE for 61 Akepa and 0.73 ? 0.12 SE for 49 Hawaii Creepers. Lowest rates of mortality and emigration occurred between May and August. Both species appeared to defend Type-B territories typical of cardueline finches, retained mates for more than one year, and showed strong philopatry. Home ranges for Hawaii Creepers (X = 7.48 ha) were larger than those for Akepa (X = 3.94 No difference was found between home range sizes of males and females for either species.

The Wilson Bulletin

Identifying sex and age of apapane and iiwi on Hawaii

Methods to determine the sex and age of Apapane (Himatione sanguinea) and Iiwi (Vestiaria coccinea) were developed on the basis of 189 museum specimens and 91 live birds captured in mist nets on the Island of Hawaii (USA). Both species retain all juvenal primaries and some juvenal secondaries and body feathers after the first prebasic molt and attain full adult plumage after the second prebasic molt. Apapane in their first basic plumage retain some buff-edged juvenal secondaries (particularly secondaries five and six) and sometimes retain a few gray-brown feathers on the head. The first basic plumage of Iiwi is characterized by secondaries 6-9 being longer and darker than secondaries 1-4 and the presence of a few yellowish juvenal body feathers with black spots at the tips. Adult male Apapane and Iiwi have longer wing, tail, exposed culmen, culmen and tarso-metatarsus lengths than females. Linear discriminant functions are presented to sex adult Apapane and Iiwi from lengths of their wing chord and exposed culmen.

Journal of Field Ornithology

Site tenacity of the endangered palila

Strong site tenacity might prevent Palila (Loxioides bailleui), an endangered Hawaiian honeycreeper, from repopulating favorable habitats in their former range. We used radio telemetry during the nonbreeding and breeding seasons to study movements and dispersal rates of 57 Palila. All Palila remained in the study area, and home range sizes and movement distances were small relative to the potential mobility of the species. Banding and nesting studies revealed that Palila show strong site tenacity. An inverse correlation between movements and elevation was related to an elevational gradient in food supply. Translocations of Palila into presently unoccupied areas in their range might speed the recovery of this endangered species.

The Wilson Bulletin

Sex and age identification of palila

Methods to sex and age Palila (Loxioides bailleui), an endangered Hawaiian finch restricted to subalpine woodlands on Hawai'i, were identified on the basis of measurements and plumage characteristics of 17 museum specimens and 96 known-age, live Palila. Palila undergo a single annual molt during September-December following the breeding season. Presence of a complete or partial wingbar distinguishes hatch-year and second-year Palila from after-second-year birds. Adult male Palila are distinguished from females by a distinct napeline and lt 30% gray feathers intermixed with yellow feathers on the head. The black or gray feathers of the lores and chin of males are darker than those on the back, whereas the lores and chin of females are lighter or of the same shade as back feathers.

Journal of Field Ornithology