Scatterhoarding rodents favor higher predation risks for cache sites:The potential for predators to influence the seed dispersal process

Scatterhoarding rodents often place caches in the open where pilferage rates are reduced,suggesting that they tradeoff higher risks of predation for more secure cache sites.We tested this hypothesis in two study systems by measuring predation risks inferred from measures of giving-up densities(GUDs)at known cache sites and other sites for comparison.Rodent GUDs were measured with small trays containing 3 L of fine sand mixed with sunflower seeds.In the first experiment,we relied on a 2-year seed dispersal study in a natural forest to identify caches of eastern gray squirrels(Sciurus carolinensis)and then measured GUDs at:(i)these caches;(ii)comparable points along logs and rocks where rodent activity was assumed highest;and(iii)a set of random points.We found that GUDs and,presumably,predation risks,were higher at both cache and random points than those with cover.At the second site,we measured GUDs of eastern gray squirrels in an open park system and found that GUDs were consistently lowest at the base of the tree compared to more open sites,where previous studies show caching by squirrels to be highest and pilferage rates by naïve competitors to be lowest.These results confirm that predation risks can influence scatterhoarding decisions but that they are also highly context dependent,and that the landscape of fear,now so well documented in the literature,could potentially shape the temporal and spatial patterns of seedling establishment and forest regeneration in systems where scatterhoarding is common.

Effects of Predation by Invasive Western Mosquitofish(Gambusia affinis) on Survival of Eggs,Embryos and Tadpoles of Pelophylax nigromaculatus and Duttaphrynus melanostictus in South China

Alien species are one of the most serious threats to the decline and extinction of native amphibian populations. In this study, we examined the predation of invasive Western Mosquitofish Gambusia affinis on the eggs, embryos, and tadpoles of Duttaphrynus melanostictus and Pelophylax nigromaculatus in south China. Our results suggested that the survival of eggs and embryos remaining in the egg capsules of P. nigromaculatus and D. melanostictus was significantly higher than those removed from the egg capsule at 12-h intervals within 72 h in the presence of G. affinis. The survival of P. nigromaculatus eggs and embryos without egg capsules was significantly lower than those of D. melanostictus without egg capsules. The survival of P. nigromaculatus eggs and embryos with egg capsules was significantly higher than those of D. melanostictus with egg capsules from 24 h to 72 h except for 12 h. The survival of D. melanostictus tadpoles was significantly higher than that of P. nigromaculatus tadpoles in the presence of G. affinis. The survival of Gosner stage 26 tadpoles of P. nigromaculatus was significantly higher than that of Gosner stage 30 tadpoles from 12 h to 60 h, but there were no significant differences at 72 h. In contrast, the survival of Gosner stage 26 tadpoles of D. melanostictus was significantly lower than that of Gosner stage 30 tadpoles within 72 h, recording every 12 h. The increasing temperature caused a significant increase in predation by G. affinis on P. nigromaculatus eggs and embryos. The outer jelly capsule surrounding anurans eggs might serve as a mechanical defense against predation by G. affinis due to its large diameter, relatively stationary state and unpalatability. The differences in the vulnerability of P. nigromaculatus and D. melanostictus embryos and tadpoles to G. affinis probably due to differences in the unpalatability, black skin and activity. Based on the magnitude of predation by G. affinis on the eggs, embryos and tadpoles of these two species and the combined impact of temperature, we might speculate that invasive G. affinis and global warming would have more detrimental impacts on population viability of P. nigromaculatus than D. melanostictus in China.

A highly effective incubation strategy enhanced the urban bird hatch success

Urbanization is currently considered one of the most rapid types of global environmental change.Urban habitats are biotically and abiotically different from their rural areas,i.e.,the ambient temperature,predator,and food availability.These novel challenges create new selection pressures,which allow one to investigate ecoevolutionary responses to contemporary environmental change.A total of 118 breeding nests were monitored for nest predation in both urban and rural areas from 2018 to 2020.We used environmental factors from urban and rural areas and behavioral data from 439 Chinese Blackbird(Turdus mandarinus)valid incubation days to understand the impact of urbanization on the incubation behavior of blackbirds and its adaptation mechanism to the urban environment.Cities have warmer ambient temperatures and lower predation pressures than rural areas.Urban blackbirds chose the incubation strategy with shorter and more bouts,while rural blackbirds selected the incubation strategy with longer and fewer bouts.The plasticity of incubation behavior of urban blackbirds was higher than that of rural areas,and the range of egg temperature was also higher than that of rural areas.In addition,incubation temperature and the number of bouts per day were the key factors affecting the day survival rate of blackbirds,and the hatching rate of urban blackbirds was higher than that of rural blackbirds.Our results provide evidence for behavioral shifts in blackbirds during adaptation to urbanization and support the central role of behavioral adaptation in the successful colonization of new environments by wildlife.These help us understand the behavioral characteristics required for wildlife to live in cities and the urban adaptors faced environmental pressures.

Generalization of predator recognition:Velvet geckos display anti-predator behaviours in response to chemicals from non-dangerous elapid snakes

Many prey species detect chemical cues from predators and modify their behaviours in ways that reduce their risk ofpredation. Theory predicts that prey should modify their anti-predator responses according to the degree of threat posed by thepredator. That is, prey should show the strongest responses to chemicals of highly dangerous prey, but should ignore or respondweakly to chemicals from non-dangerous predators. However, if anti-predator behaviours are not costly, and predators are rarelyencountered, prey may exhibit generalised antipredator behaviours to dangerous and non-dangerous predators. In Australia, mostelapid snakes eat lizards, and are therefore potentially dangerous to lizard prey. Recently, we found that the nocturnal velvetgecko Oedura lesueurii responds to chemicals from dangerous and non-dangerous elapid snakes, suggesting that it displays generalisedanti-predator behaviours to chemicals from elapid snakes. To explore the generality of this result, we videotaped the behaviourof velvet geckos in the presence of chemical cues from two small elapid snakes that rarely consume geckos: the nocturnalgolden-crowned snake Cacophis squamulosus and the diurnal marsh snake Hemiaspis signata. We also videotaped geckos in trialsinvolving unscented cards (controls) and cologne-scented cards (pungency controls). In trials involving Cacophis and Hemiaspischemicals, 50% and 63% of geckos spent long time periods (> 3 min) freezing whilst pressed flat against the substrate, respectively.Over half the geckos tested exhibited anti-predator behaviours (tail waving, tail vibration, running) in response to Cacophis(67%) or Hemiaspis (63%) chemicals. These behaviours were not observed in control or pungency control trials. Our resultssupport the idea that the velvet gecko displays generalised anti-predator responses to chemical cues from elapid snakes.Generalised responses to predator chemicals may be common in prey species that co-occur with multiple, ecologically similar,dangerous predators [Current Zoology 56 (3): 337-342, 2010].

An unusual homing behavior found in the Sichuan Partridge during the early brooding period

In this study,we report an unusual homing behavior of the Sichuan Partridge(Arborophila rufipectus)at the Laojunshan National Nature Reserve,Sichuan Province,China.Hen Sichuan Partridges led the chicks back to the nests where they hatched in the evening and roosted there over night.This behavior lasted 6.7±4.3 nights(range=1–15;n=13)after the chicks hatched.At this stage,the hens became very vigilant to predators and human disturbance.If disturbed,they often abandoned the nests immediately and no longer returned thereafter.The ambient temperature at night during the early brooding period of Sichuan Partridge at our study site was^12.4°C.Our findings suggest that hen Sichuan Partridges may make trade-offs between nest predation risks versus the thermoregulatory needs of their young.

On the importance of concomitant conditions: Light and conspecific presence modulate prey response to predation cue

Assessment of individual costs of the anti-predator defence translating into changes in population parameters is meagre.This is because prey responses are likely to be modulated by additional factors,commonly present in the environment,but often neglected in experimental studies.To evaluate the effect of external factors on prey behavior and physiology,we exposed amphipods Dikerogammarus villosus and Gammarus jazdzewskii to the predation cue of Perca fluviatilis in different densities and light conditions.Singletons of both species exposed to the predation cue in light modified their oxygen consumption(D.villosus:reduction,G.jadzewskii:increase)compared to their respiration in predator-free conditions.However,in the presence of conspecifics or in darkness,their respiration became insensitive to the predation cue.On the other hand,the swimming activity of prey was reduced in the presence of the predation cue irrespective of prey density and light conditions,but singletons were consistently more active than groups.Thus,external factors,such as conspecifics and darkness,constantly or periodically occurring in the field,may reduce the costs of predator non-consumptive effects compared to the costs measured under laboratory conditions(in light or absence of conspecifics).Moreover,we showed that behavioral and physiological parameters of prey may change differently in response to predation risk.Thus,conclusions drawn on the basis of single defence mechanisms and/or results obtained in artificial conditions,not reflecting the environmental complexity,strongly depend on the experimental design and endpoint selection and therefore should be treated with care.

Social biology of rodents

Herein, I summarize some basic components of rodent social biology. The material in this paper is summarized andcondensed from a recent book “Rodent Societies: An Ecological and Evolutionary Perspective” edited by J. O.Wolff and P. W. Sherman (2007). I describe the four basic spacing patterns and illustrate how female territoriality isa function of offspring defense and male mating tactics are a function of female defensibility. The vulnerability ofyoung to infanticide shapes female spacing and mating behavior. Food does not appear to be a defensible resourcefor rodents, except for those species that larder hoard nonperishable items such as seeds. Philopatry and theformation of kin groups result in genetic sub-structuring of the population, which in turn affects effectivepopulation size and genetic diversity. Dispersal is male biased and typically involves emigration from the maternalsite to avoid female relatives and to seek unrelated mates. Scent marking is a major form of communication and isused in reproductive competition and to assess prospective mates, but it is also eavesdropped by predators to locateprey. Females do not appear to alter the sex ratio of litters in response to maternal condition but among arvicolinerodents daughters appear to be favored in spring and sons in autumn. Rodents are relatively monomorphic;however, females tend to be larger than males in the smallest species and smaller in the larger species. Predationrisk results from an interaction among foraging time and vulnerability and in turn affects behavioral and life historycharacteristics.