Eric D. Forsman

Does the presence of barred owls suppress the calling behavior of spotted owls

Abstract ABSTRACT Barred Owls (Strix varia) have expanded their range throughout the ranges of Northern (Strix occidentalis caurina) and California Spotted Owls (S. o. occidentalis). Field observations have suggested that Barred Owls may be behaviorally dominant to Spotted Owls. Therefore, we conducted a test of behavioral dominance by assessing responsiveness of Spotted Owls to conspecific calls when they were in the simulated presence (i.e., imitation of Barred Owl vocalizations) of a Barred Owl. We hypothesized that Spotted Owls would be less likely to respond to conspecific calls in areas where Barred Owls were common. We used a binary 2 × 2 crossover experimental design to examine male Spotted Owl responses at 10 territories randomly selected within two study areas that differed in abundance of Barred Owls. We also conducted a quasi experiment at four study areas using response data from any Spotted Owl (male or female) detected following exposure to Barred Owl calls. We inferred from the crossover experiment that the simulated presence of a Barred Owl might negatively affect Spotted Owl responsiveness. Both subspecies of Spotted Owl responded less to Spotted Owl calls after exposure to Barred Owl calls, Northern Spotted Owls responded less frequently in areas having higher numbers of Barred Owls, and California Spotted Owls responded less frequently than Northern Spotted Owls overall.

Isolation by distance versus landscape resistance: Understanding dominant patterns of genetic structure in Northern Spotted Owls (Strix occidentalis caurina)

Landscape genetics investigations examine how the availability and configuration of habitat influence genetic structure of plants and animals. We used landscape genetics to evaluate the role that forest connectivity plays in determining genetic structure of the federally-threatened Northern Spotted Owl (Strix occidentalis caurina) using genotypes of 339 Northern Spotted Owls obtained for 10 microsatellite loci. Spatial clustering analyses identified a distinct genetic cluster at the southern extent of the region examined. This cluster could not be linked to landscape connectivity patterns and suggested that post-Pleistocene processes were involved with its development rather than contemporary landscape configuration. We also compared matrices of pairwise inter-individual genetic distances with resistance distances derived from a circuit-theory based framework. Resistance distances were obtained for an idealized raster map that reflected continuous unimpeded dispersal habitat across the landscape along with five empirically-derived raster maps reflecting the 1870’s, 1940’s, 1986, 1994, and 2012. Resistance distances from the idealized map served as surrogates for linear geographic distances. Relative to idealized conditions, resistance distances were ~250% higher in the 1940’s and ~200% higher from 1986 onward. Resistance distances from the 1870’s were ~40% higher than idealized conditions. Inter-individual genetic distances were most highly correlated with resistance distances from the idealized map rather than any of the empirical maps. Two hypotheses explain our results. First, our results may reflect temporal lags between the onset of large-scale habitat alterations and their novel effects on genetic structure in long-lived species such as Northern Spotted Owls. Second, because Northern Spotted Owls disperse over long distances, our results may indicate that forest habitat has never been sufficiently fragmented to the point where connectivity was disrupted. The second hypothesis could indicate that forest management practices mandated by the Northwest Forest Plan succeeded with one of its primary goals. However, our results do not represent a complete portrayal of the status of Northern Spotted Owls given detection of significant population declines and bottlenecks in other studies. Future investigations based on computer simulations may help distinguish between hypotheses.

A Field Test of the Northern Goshawk Bioregional Monitoring Design: Is it Cost Effective?

Abstract Monitoring of northern goshawks typically occurs at nest sites, which is an effective approach for obtaining information on nesting activity and reproductive success, but less effective at providing information on goshawk distribution or abundance. In 2002 the United States Department of Agriculture Forest Service began the process of designing a method for monitoring occupancy rates of goshawks over large spatial scales. In 2003 we conducted a field test of the Forest Services bioregional monitoring design in southwestern Colorado. Our goal was to determine how much it would cost to implement. Average costs for surveying each primary sample unit were

Variation in inbreeding rates across the range of Northern Spotted Owls (Strix occidentalis caurina): Insights from over 30 years of monitoring data

1,060.34 and average per station survey-visit costs were

Genetic identification of Spotted owls, Barred owls, and their hybrids: Legal implications of hybrid identity

6.99. It is important to recognize that our primary sample unit survey cost estimate is higher than might be expected on average because our surveys were conducted during a poor nesting year for goshawks. This information will be instrumental to wildlife managers, whether conducting bioregional monitoring or local project level surveys for goshawks (WILDLIFE SOCIETY BULLETIN 34(1):215–217; 2006)

Modeling co-occurrence of northern spotted and barred owls: accounting for detection probability differences.

ABSTRACT Inbreeding has been difficult to quantify in wild populations because of incomplete parentage information. We applied and extended a recently developed framework for addressing this problem to infer inbreeding rates in Northern Spotted Owls (Strix occidentalis caurina) across the Pacific Northwest, USA. Using pedigrees from 14,187 Northern Spotted Owls, we inferred inbreeding rates for 14 types of matings among relatives that produce pedigree inbreeding coefficients of F = 0.25 or F = 0.125. Inbreeding was most common in the Washington Cascades, where an estimated 15% of individuals are inbred. Inbreeding was lowest in western Oregon (3.5%) and northern California (2.7%), and intermediate for the Olympic Peninsula of Washington (6.1%). Estimates from the Olympic Peninsula were likely underestimates because of small sample sizes and the presence of few pedigrees capable of resolving inbreeding events. Most inbreeding resulted from matings between full siblings or half siblings, although a high rate of inbreeding from mother–son pairs was identified in the Olympic Peninsula. Geographic variation in inbreeding rates may reflect population declines and bottlenecks that have been detected in prior investigations. We show that there is strong selection against inbred birds. Only 3 of 44 inbred birds were later identified as parents (6.8%), whereas 2,823 of 10,380 birds that represented a comparable cross section of the data were later seen as reproducing parents (27.2%). Habitat loss and competition with Barred Owls (S. varia) remain primary threats to Northern Spotted Owls. However, given the negative consequences of inbreeding, Spotted Owl populations in Washington with suitable habitat and manageable numbers of Barred Owls may benefit from translocations of individuals from Oregon and California to introduce new genetic variation and reduce future inbreeding events.