We studied prey populations and the use and composition of home ranges of 4 7 Northern Spotted Owls (Strix occidental is caurina) over 12 mo in five landscapes in two forest types in southwestern Oregon. We measured 1-yr home ranges of23 owl pairs, 2-yr home ranges of 13 pairs, and 3-yr home ranges of 3 pairs. The landscapes differed in the degree to which old forest had been fragmented by wildfire and logging. Prey populations were measured at 4 7 sites in southwestern Oregon. Further data on prey populations were gathered on 14 sites on the Olympic Peninsula in northern Washington, where owls use larger ranges than in Oregon.Owls in Washington used ""1700 ha of old forest annually and primarily one prey species; available prey biomass was 61 g!ha. Owls in Oregon Douglas-fir (Pseudotsuga menziesii) forests used 813 ± 133 ha (X ± SE) of old forest annually and concentrated on two prey species that had a combined biomass of 244 glha. Owls in Oregon mixed-conifer forest used 454 ± 84 ha of old forest annually and three primary prey whose availability averaged 338 glha. The amount of old forest used by owls studied for 2 yr was 40% greater in the 2nd yr than that used in the 1st yr. No increase in use of old forest was seen in the 3rd yr in Douglas-fir forest; 50% more old forest was used in 3 yr than in the 1st yr in mixed-conifer forest. The most common prey in Washington and Oregon was the northern flying squirrel ( Glaucomys sabrinus). In areas where the flying squirrel was the primary prey and where predation was intense (as judged by telemetry), flying squirrel populations were depressed. The addition of medium-sized mammal species, especially woodrats (Neotoma spp.), to the prey base appeared to reduce markedly the amount of old forest used for foraging.Owls traversed 85% more Douglas-fir forest and 3 times more mixed-conifer forest in the heavily fragmented areas than in the lightly fragmented areas. Overlap among pairs and separation of birds within pairs in space increased with fragmentation. In the most heavily fragmented landscape, social structure appeared to be abnormal, as judged by the proportion of adult-subadult pairs, instances of adult nomadism, and overlap among the home ranges of pairs. The pattern of fragmentation affected the ability of owls to find concentrations of old forest in the landscapes. Even so, almost all the owls consistently selected old forests for foraging and roosting; only one owl selected a younger type as part of its foraging range. Selection of old forest was significant at three levels: landscape, annual home ranges of pairs, and foraging and roosting sites of individuals. The most important prey species, the northern flying squirrel, was twice as abundant in old forest as in young forest in all areas.Landscape indices (dominance, contagion, variance in density of old forest) had less predictive ability than indices based on owl home ranges because owls selected areas of concentrated old forest and because patterning was complex, reflecting four processes, each operating ...
Estimates of species' vital rates and an understanding of the factors affecting those parameters over time and space can provide crucial information for management and conservation. We used mark-recapture, reproductive output, and territory occupancy data collected during 1985-2013 to evaluate population processes of Northern Spotted Owls (Strix occidentalis caurina) in 11 study areas in Washington, Oregon, and northern California, USA. We estimated apparent survival, fecundity, recruitment, rate of population change, and local extinction and colonization rates, and investigated relationships between these parameters and the amount of suitable habitat, local and regional variation in meteorological conditions, and competition with Barred Owls (Strix varia). Data were analyzed for each area separately and in a meta-analysis of all areas combined, following a strict protocol for data collection, preparation, and analysis. We used mixed effects linear models for analyses of fecundity, Cormack-Jolly-Seber open population models for analyses of apparent annual survival (/), and a reparameterization of the Jolly-Seber capture-recapture model (i.e. reverse Jolly-Seber; RJS) to estimate annual rates of population change (k RJS ) and recruitment. We also modeled territory occupancy dynamics of Northern Spotted Owls and Barred Owls in each study area using 2-species occupancy models. Estimated mean annual rates of population change (k) suggested that Spotted Owl populations declined from 1.2% to 8.4% per year depending on the study area. The weighted mean estimate of k for all study areas was 0.962 (6 0.019 SE; 95% CI: 0.925-0.999), indicating an estimated range-wide decline of 3.8% per year from 1985 to 2013. Variation in recruitment rates across the range of the Spotted Owl was best explained by an interaction between total winter precipitation and mean minimum winter temperature. Thus, recruitment rates were highest when both total precipitation (29 cm) and minimum winter temperature (À9.58C) were lowest. Barred Owl presence was associated with increased local extinction rates of Spotted Owl pairs for all 11 study areas. Habitat covariates were related to extinction rates for Spotted Owl pairs in 8 of 11 study areas, and a greater amount of suitable owl habitat was generally associated with decreased extinction rates. We observed negative effects of Barred Owl presence on colonization rates of Spotted Owl pairs in 5 of 11 study areas. The total amount of suitable Spotted Owl habitat was positively associated with colonization rates in 5 areas, and more habitat disturbance was associated with lower colonization rates in 2 areas. We observed strong declines in derived estimates of occupancy in all study areas. Mean fecundity of females was highest for adults (0.309 6 0.027 SE), intermediate for 2-yr-olds (0.179 6 0.040 SE), and lowest for 1-yr-olds (0.065 6 0.022 SE). The presence of Barred Owls and habitat covariates explained little of the temporal variation in fecundity in most study areas. Climate covariates ...
We analyzed demographic data from northern spotted owls (Strix occidentalis caurina) from 14 study areas in Washington, Oregon, and California for 1985-2003. The purpose of our analyses was to provide an assessment of the status and trends of northern spotted owl populations throughout most of their geographic range. The 14 study areas made up approximately 12% of the range of the subspecies and included federal, tribal, private, and mixed federal and private lands. The study areas also included all the major forest types that the subspecies inhabits. The analyses followed rigorous protocols that were developed a priori and were the result of extensive discussions and consensus among the authors. Our primary objectives were to estimate fecundity, apparent survival (/), and annual rate of population change (k) and to determine if there were any temporal trends in these population parameters. In addition to analyses of data from individual study areas, we conducted 2 meta-analyses on each demographic parameter. One meta-analysis was conducted on all 14 areas, and the other was restricted to the 8 areas that constituted the Effectiveness Monitoring Plan for northern spotted owls under the Northwest Forest Plan. The average number of years of reproductive data per study area was 14 (range ¼ 5-19), and the average number of recapture occasions per study area was 13 (range ¼ 4-18). Only 1 study area had ,12 years of data. Our results were based on 32,054 captures and resightings of 11,432 banded individuals for estimation of survival and 10,902 instances in which we documented the number of young produced by territorial females.The number of young fledged (NYF) per territorial female was analyzed by testing a suite of a priori models that included (1) effects of age, (2) linear or quadratic time trends, (3) presence of barred owls (Strix varia) in spotted owl territories, and (4) an even-odd year effect. The NYF varied among years on most study areas with a biennial cycle of high reproduction in even-numbered years and low reproduction in odd-numbered years. These cyclic fluctuations did not occur on all study areas, and the even-odd year effect waned during the last 5 years of the study. Fecundity was highest for adults (x¼0.372, SE¼0.029), lower for 2-year-olds (x¼0.208, SE¼0.032), and very low for 1-year-olds (x¼0.074, SE¼ 0.029). Fecundity was stable over time for 6 areas (Rainier, Olympic, Warm Springs, H. J. Andrews, Klamath, and Marin), declining for 6 areas (Wenatchee, Cle Elum, Oregon Coast Range, Southern Oregon Cascades, Northwest California, and Simpson), and slightly increasing for 2 areas (Tyee, Hoopa). We found little association between NYF and the proportion of northern spotted owl territories where barred owls were detected, although results were suggestive of a negative effect of barred owls on the Wenatchee and Olympic study areas. The meta-analysis on fecundity indicated substantial annual variability with no increasing or decreasing trends. Fecundity was highest in the mixed-conifer region of eas...
Silvicultural prescriptions to enhance northern flying squirrel (Glaucoinys sabrinus) habitat have been suggested as an aid for recovery of the threatened northern spotted owl (Strix occidentalis caurina). Flying squirrels are hypothesized to be limited by den sites (cavities in trees) and by food (truffles). However, no quantitative information exists on den sites of flying squirrels. Therefore, during 1986-94, we used radiotelemetry to locate 604 different den sites in the southern Coast Range of Oregon, the southern Olympic Peninsula, and the Puget Trough of Washington. Den sites included cavities in live and dead old-growth trees; cavities, stick nests, and moss nests in small (10-50 cm dbh) second-growth trees; dens in cavities in branches of fallen trees; and dens in decayed stumps of oldgrowth trees and suppressed young trees. Two-thirds of all dens located were in live trees. Most dens were located during a study of second-growth forests in the Puget Trough. Females selected cavities for maternal dens. Squirrels used multiple dens; denning partners varied with den. Dens of males were 211 ± 7 m apart; dens of females were 108 ± 4 m apart. Males used 2.2 ± 0.1 dens per month; females 2.3 ± 0.1 dens per month. Dens, except maternal dens, were often occupied simultaneously by several adult squirrels. Many fragile den sites were used by females. Secure cavities are scarce and may limit reproductive success. Management for cavity trees and dens could prove fruitful in owl recovery and habitat restoration efforts.
Concern about the value of old-growth Douglas-fir forests to wildlife in the Pacific Northwest began escalating in the late 1 970s. The available information on wildlife habitat relationships suggested that as many as 75 species including amphibians, birds, and mammals, could be dependent on old-growth forests. The USDA Forest Service chartered the Old-Growth Forest Wildlife Habitat Program to investigate the role old growth plays in maintaining viable populations of wildlife. It was apparent that broad surveys of vertebrate communities would be necessary to determine which species truly were closely associated with old-growth forests. Insufficient guidance on techniques, procedures, and sample sizes was available in the existing literature. We assembled a team of researchers from universities and Federal agencies to conduct pilot studies to develop sampling protocols and to test the basic experimental design for contrasting the wildlife values of young, mature, and old-growth forests. The sampling protocols resulting from the pilot studies were implemented in 1984-86 across broad areas of the Cascade Range in southwestern Washington and Oregon, the Oregon Coast Ranges, and the Klamath Mountains of southwestern Oregon and northern California. Naturally, improvements were made to the protocols as time passed. A tremendous amount of experience in sampling was gained. Our goal in this series is to compile the extensive experiences of our collaborators into a collection of methodology papers providing biologists with pilot study-type information for planning research or monitoring populations. The series will include papers on sampling bats, aquatic amphibians, terrestrial amphibians, forest-floor mammals, small forest birds and arboreal rodents, as well as papers on using telemetry for spotted owls studies and a guide to bird calls.
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