1,081 results — topic: Wildlife Behavior

Dataset

Data from: Atypical flowers can be as profitable as typical hummingbird flowers

In western North America, hummingbirds can be observed systematically visiting flowers that lack the typical reddish color, tubular morphology, and dilute nectar of "hummingbird flowers". Curious about this behavior, we asked whether these atypical flowers are energetically profitable for hummingbir

Waser, Nickolas M., CaraDonna, Paul J., Price, Mary V.2018DOI: 10.5061/dryad.cd4h7f1Cited 1 times
Dataset

Data from: Progressive sensitivity of trophic levels to warming underlies an elevational gradient in ant-aphid mutualism strength

Although species interactions are often proposed to be stronger at lower latitudes and elevations, few studies have evaluated the mechanisms driving such patterns. In this study, we assessed whether, and by which mechanisms, abiotic changes associated with elevation altered the outcome of an ant-aph

Nelson, Annika S., Pratt, Riley T., Pratt, Jessica D.2018DOI: 10.5061/dryad.kf2553jCited 1 times
Student Paper

Do beaver, <i>Castor canadensis</i>, follow optimal foraging in Gothic, Colorado

Lautenschlager K.1998
Student Paper

The effect of trout on the diversity, richness and abundance of the mayfly species

Lautenschlager K.1998
Student Paper

Time allocation to behavior in marmots: a comparison of adults and juveniles

Kocis A.1998
Student Paper

Does insect abundance affect bat activity in three subalpine habitats?

Doerr N.1998
Student Paper

Phoretic mite distributions among the burying beetle, <i>Nicrophorus investigator</i>

Dinnel J.1998
Student Paper

Is the foraging behavior of <i>Castor canadensis</i> optimal?

Allen E., Bonilla M.1998
Student Paper

Does insect abundance affect bat activity?

Allen E.1998
Article

Trapline foraging by bumble bees: III. Temporal patterning of visits

Williams N., Thomson J. D.1998Behavioral Ecology
Article

Hummingbird foraging at experimental patches of flowers: evidence for weak risk-aversion

Hummingbirds foraging for nectar in mountains of the western USA encounter spatially-variable rewards under energetically-demanding environmental conditions. Previous workers have found that hummingbirds respond quickly to the average quantity and quality of reward; in addition, one might expect a r

Waser N. M., McRobert J. A.1998Journal of Avian BiologyDOI: 10.2307/3677113Cited 16 times
Article

Pollination, angiosperm speciation, and the nature of species boundaries

Despite much recent research on pollination, we have amassed relatively little hard information about how animal pollinators contribute to angiosperm speciation and species distinctiveness. We usually assume that pollinators make important contributions by specializing on plant species and providing

Waser N. M.1998OikosDOI: 10.2307/3546930Cited 135 times
Article

A 32-year demography of yellow-bellied marmots (<i>Marmota flaviventris</i>)

Yellow-bellied marmots Marmota ¯aviventris in the East River Valley of Colorado were live-trapped and individually marked annually from 1962 through 1993. These pooled data were used to produce a demography and life table for these years. Females had signi®cantly better survivorship than males beyon

Schwartz O. A., Armitage K. B., Van Vuren D. H.1998J Zool LondonDOI: 10.1111/j.1469-7998.1998.tb00163.xCited 94 times
Article

Empirical considerations on the stable age distribution

Schwartz O. A., Armitage K. B.1998Oecologia Montana
Article

Fitness and community consequences of avoiding multiple predators

This study demonstrates the importance of considering multiple predators when measuring direct sublethal effects of predators on prey fitness and indirect effects on lower trophic levels, and attributes the non-additivity of effects of fish and stoneflies on mayfly growth to an interaction modificat

Peckarsky B. L., McIntosh A. R.1998OecologiaDOI: 10.1007/s004420050410Cited 205 times
Article

Life histories and the strengths of species interactions: combining mortality, growth, and fecundity effects

Interactive effects of one species on another may simultaneously influence mortality, growth, and fecundity. To quantify the strength of an interaction between two species, we must therefore use techniques that integrate these various responses into estimates of overall effect. Demographic models of

McPeek M. A., Peckarsky B. L.1998EcologyDOI: 10.1890/0012-9658(1998)079[0867:lhatso]2.0.co;2Cited 238 times
Article

A trade-off between the frequency and duration of bumblebee visits to flowers

The potential for a trade-offs between these two components of pollinator service exists when visit duration depends on reward quantity; whether the trade-off is realized will depend on variation in nectar production and on whether pollinators forage systematically.

Jones K. N., Reithel J., Irwin R.1998OecologiaDOI: 10.1007/s004420050644Cited 31 times
Article

Nectar Robbing in <i>Ipomopsis aggregata</i>: Effects on Pollinator Behavior and Plant Fitness

Irwin R. E., Brody A. K.1998Oecologia
Article

A test of the acoustic adaptation hypothesis in four species of marmots

The evidence did not support the acoustic adaptation hypothesis for these marmot species, and factors other than maximizing long-distance transmission through the environment may be important in the evolution of species-specific marmot alarm calls.

Daniel J. C., Blumstein D. T.1998Animal BehaviorDOI: 10.1006/anbe.1998.0929Cited 85 times