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1.
J Anim Ecol ; 2024 Jul 28.
Artículo en Inglés | MEDLINE | ID: mdl-39073110

RESUMEN

Following a resource pulse, animals may finance reproduction by consuming concurrently available resources (income breeding) or by storing resources for future reproduction (capital breeding). Understanding how these reproductive strategies are used is important for determining the ecological mechanisms that structure timing of reproduction and that drive interannual population fluctuations in animals. We gathered a reproductive dataset for five small mammal species over a 12-year period in Northeastern USA during which six masting events of American beech (Fagus grandifolia) and eastern hemlock (Tsuga canadensis) occurred. Masting created alternate years where seeds were either available late (masting year) or early (cached from the previous year) in the breeding season. The small mammal species differed in reliance on seeds and overwintering strategies. We quantified the diet using stable isotopes and recorded reproduction timing, proportion breeding and litter size in females and testes size in males. Timing of seed availability minimally affected litter size but strongly affected proportion breeding and timing of reproduction. During masting years (late seed availability), a higher proportion of females reproduced, with breeding taking place later in the season (lactation timed with peak seed availability), although the delay was restricted in Napaeozapus insignis, an obligate hibernator. After a fall mast, cached seeds were used as capital in the following spring (early seed availability) to support a litter that, depending on the species, occurred 24-79 days sooner than a mast year. No late-season reproduction occurred in years with early seed availability except for Myodes gapperi which produced a second litter, likely financed by fungal consumption. Males also showed strong responses to seed availability, mirroring female reproduction with testes size staying constant in years with late seed availability and sharply decreasing over the breeding season in years with early seed availability. Our results highlight that although photoperiod and temperature broadly set bounds of the breeding season in temperate environments, resource availability influences the reproductive strategies that species use, which in turn alters reproductive timing and can drive large inter-annual population fluctuations. Differences in overwintering strategies and diet may further modulate reproductive timing and output relative to resource pulses.

2.
Sci Total Environ ; 805: 150223, 2022 Jan 20.
Artículo en Inglés | MEDLINE | ID: mdl-34537710

RESUMEN

Light and noise pollution from human activity are increasing at a dramatic rate. These sensory stimuli can have a wide range of effects on animal behavior, reproductive success, and physiology. However, less is known about the functional and community-level consequences of these sensory pollutants, especially when they co-occur. Using camera traps in a manipulative field experiment, we studied the effects of anthropogenic light and noise, singularly and in tandem, on richness and community turnover at both the taxa and functional group level as well as foraging activity. We showed that both light and noise pollution did alter taxonomic richness and that these effects can differ depending on the scale of observation. Increases in light levels had a negative effect on richness at the camera-level scale, but light-treated sites had the highest pooled (i.e., cumulative) richness of all treatment types. In contrast, noise was found to have a negative effect on cumulative richness; however, when both stimuli were present, the addition of night-lighting mitigated the effects of noise. Artificial light and moonlight had the strongest influence on community turnover, and results remained consistent at both the taxa and functional group level. Additionally, increases in ambient noise and moonlight, but not artificial light, reduced foraging activity. Our study provides evidence that alterations to the sensory environment can alter the richness and composition of communities and that effects can be scale-dependent and also alter foraging behavior. Unexpectedly, the addition of artificial light may have mitigated the negative effects of noise on cumulative taxonomic richness. This highlights the importance of researching the consequences of co-exposure to these globally common pollutants.


Asunto(s)
Iluminación , Ruido , Animales , Conducta Animal , Humanos , Luz , Iluminación/efectos adversos , Ruido/efectos adversos , Reproducción , Vertebrados
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