No abstract

The mixed forests of interior British Columbia, Canada, support a rich community of cavity nesters, accounting for about one-third of forest vertebrate species. For 20 cavity-nesting bird and six cavity-nesting mammal species, representing excavators and secondary cavity nesters, we measured nest-cavity and nest-tree characteristics over 8 years in Interior Douglas-fir (Pseudotsuga menziesii) forest ecosystems. There was overwhelming selection for quaking aspen (Populus tremuloides); 95% of 1692 cavity nests were in aspen, which comprised only 15% of trees available. The full range of live and dead trees were used, but we observed a strong preference for live trees with decay (45% of nests) or dead trees (45% of nests). A cluster analysis based on tree and cavity characteristics divided the community into five groups, including large- and medium-sized woodpeckers and a group comprised mostly of weak excavators. A fourth group included Northern Flickers (Colaptes auratus), the most abundant excavator, and the larger secondary cavity nesters. The final group contained the most aggressive and most abundant secondary cavity nesters. European Starling (Sturnus vulgaris), the most aggressive secondary cavity nester, occupied a narrower nest niche (in less-decayed trees with smaller entrances) relative to their size. Less-competitive excavators and secondary cavity nesters occupied wider nest niches in terms of tree decay class and cavity size. We constructed a nest web for community structure that showed most cavity resource use flowed up the community through aspen trees and cavities excavated by Northern Flickers. Thus, aspen was the critical nesting tree and Northern Flickers were the keystone excavators in this community. Sitios de Nidificación y Redes de Nidos en Comunidades que Nidifican en Cavidades en el Interior de British Columbia, Canadá: Características de los Nidos y Separación de Nichos Resumen. Los bosques mixtos del interior de British Columbia, Canadá, albergan una rica comunidad de animales que nidifican en cavidades, los cuales representan aproximadamente un tercio de las especies de vertebrados de bosque. En este estudio medimos características de las cavidades y de los árboles de nidificación para 20 especies de aves y seis de mamíferos que nidifican en cavidades (incluyendo especies excavadoras y las que utilizan cavidades secundariamente) a lo largo de ocho años en ecosistemas de bosque interior de Pseudotsuga menziesii. Hubo una selección abrumadora de árboles de la especie Populus tremuloides; el 95% de 1692 cavidades de nidificación se encontraron en árboles de esta especie, la cual comprendía sólo el 15% de los árboles disponibles. Todo el espectro de árboles vivos y muertos fue utilizado, pero observamos una preferencia fuerte por árboles vivos con descomposición (45% de los nidos) o árboles muertos (45% de los nidos). Un análisis de agrupamiento basado en características de los árboles y las cavidades dividió la comunidad en cinco grupos, incluyendo carpinteros de tamaño grande y mediano, y un grupo formado principalmente por excavadores débiles. Un cuarto grupo incluyó al carpintero Colaptes auratus (el excavador más abundante) y a las especies de mayor tamaño que nidifican en cavidades secundarias. El último grupo incluyó a las especies más abundantes y agresivas que nidifican en cavidades secundarias. El estornino Sturnus vulgaris, la especie más agresiva que nidifica en cavidades secundarias, ocupó un nicho más estrecho (árboles menos descompuestos con entradas más pequeñas) con relación a su tamaño. Los excavadores menos competitivos y los usuarios de cavidades secundarias ocuparon nichos de nidificación más amplios en términos de la categoría de descomposición de los árboles y el tamaño de la cavidad. Construimos una red de nidos para estudiar la estructura de la comunidad, la cual mostró que la mayor parte del uso de las cavidades como recurso fluye en la comunidad a través de los árboles de P. tremuloides y las cavidades excavadas por C. auratus. Por lo tanto, P. tremuloides fue el árbol de nidificación crítico y C. auratus fue la especie de excavador clave en esta comunidad.

As ground nesting homeotherms, alpine and arctic birds must meet similar physiological requirements for breeding as other birds, but must do so in more extreme conditions. Annual spring snowfall and timing of snow melt can vary by up to 1 month and daily temperatures near the ground surface vary from below freezing to over 45°C in alpine and arctic habitats. Species breeding in these environments have various behavioral, physiological, and morphological adaptations to cope with energetically demanding conditions. We review the ways birds cope with harsh and variable weather, and present data from long term field studies of ptarmigan to examine effects of spring weather on reproduction. In variable but normal spring conditions, timing of breeding was not influenced by snow melt, snow depth or daily temperatures in the alpine, as breeding did not commence until conditions were generally favorable. Arctic ptarmigan tended to vary breeding onset in response to spring conditions. Generally, birds breeding in alpine and arctic habitats suffer a seasonal reproductive disadvantage compared to birds at lower latitudes or elevations because the breeding window is short and in late years, nest failure may be high with little opportunity for renesting. Coping mechanisms may only be effective below a threshold of climactic extremes. Despite strong resilience in fecundity parameters, when snowmelt is extremely delayed breeding success is greatly reduced. Alpine and arctic birds will be further challenged as they attempt to cope with anticipated increases in the frequency and severity of weather events (climate variability), as well as general climate warming.

For animals that are sexually dimorphic in size, the larger sex is expected to be more costly to raise to independence. Manipulating offspring sex ratios may thus be one means by which parents can fine-tune their reproductive effort to resource availability. Parents in poor physical condition or during poor food years should produce more of the cheaper (smaller) sex. We examined the sex ratios of 259 broods of American kestrels (Falco sparverius) between 1988 and 1990 in relation to food abundance (small mammals) and various attributes to the parents. The proportion of males at hatching increased as the food supply declined, and both male and female parents in poor physical condition were more likely to have male-biased broods than those in good condition. The mortality of eggs and young did not appear to be responsible for the biased sex ratios. The sex ratio was independent of the laying date; however, it was correlated with female body size. Small females produced more sons, perhaps because small size is more detrimental for females than males.

I measured structural characteristics of 160 Northern Flicker (Colaptes auratus) nests at Riske Creek, British Columbia, and placed electronic data-loggers in a subsample of 86 nests to record internal temperatures after the flickers completed nesting. Using multiple regression, I found that the best predictors of a variety of nest-cavity temperature variables were tree health, diameter of the tree at cavity height, and orientation of the cavity. Small and dead trees showed the most extreme (maximum and minimum) temperatures during the day, but, on average, were the coldest nests from the perspective of incubation. South-facing cavities reached the highest temperatures during the day, and the orientation of natural cavities was also biased towards the south. I predicted that cold nests would be energetically expensive for adults and nestlings, and found that clutch size was positively correlated with mean cavity temperature. However, there did not appear to be any relationship among nest temperature and hatching or fledging success.