scholarly journals Odour cues influence predation risk at artificial bat roosts in urban bushland

2013 ◽  
Vol 9 (3) ◽  
pp. 20121144 ◽  
Author(s):  
Caragh Threlfall ◽  
Bradley Law ◽  
Peter B. Banks

Odours that accumulate from roosting can attract predators and increase predation risk. Consequently, selection should favour strategies that allow prey to evade detection by predators, including changing roosts. Insectivorous bats that roost in tree hollows regularly switch roosts and roost in different sized groups, strategies that would alter the accumulation of roost odours and are hypothesized to reduce predation risk. We experimentally manipulated the amount and refresh rate of roosting odour cues at 90 artificial bat roosts in Sydney, Australia, to test the hypothesis that odours increase predator visitation. Predators visited roosts with bat faeces significantly more often than untreated control roosts. Roosts with small amounts of faeces mimicking sites used by solitary bats had the greatest rate of visitation. This suggests that bats roosting alone, rather than in groups, have a greater likelihood of disturbance or predation. Roost switching probably decreases the predictability of finding occupied roosts; however, we show that all roosts (those currently or recently occupied) were visited by predators, suggesting generalist urban predators readily investigate potential roosts. This is the first demonstration that bat odours are attractive to predators that use olfactory cues, showing that bats are at risk of predation in visually cryptic roosts.

2006 ◽  
Vol 84 (9) ◽  
pp. 1240-1247 ◽  
Author(s):  
K.R. Abbott

Bees are at risk of predation from flower-dwelling ambush predators. Since these predators tend to be cryptic, bees trying to mitigate predation risk may need to make use of indirect cues of the predator’s presence. For example, they may use cues of past predation events as indirect cues of current predation risk. I conducted a series of experiments that examined how bumblebees (genus Bombus Latreille, 1802) respond to cues of past predation events. In two field experiments, I found that wild rose (genus Rosa L.) flowers containing a freshly killed bumblebee, or the scent of a freshly killed bumblebee, received fewer bumblebee visits than control flowers. To test the possibility that bumblebees in the first two experiments were avoiding cues of competition risk rather than cues of predation risk, captive-reared bumblebees were given a choice between two artificial flowers — one containing a freeze-killed bumblebee (relatively more similar to a live foraging bee) and the other containing a crush-killed bumblebee (relatively more similar to a bee killed by a predator). Most bumblebees chose the flower containing the freeze-killed bee, supporting the hypothesis that the bumblebees in the first two experiments were attempting to avoid predation.


Crustaceana ◽  
2015 ◽  
Vol 88 (7-8) ◽  
pp. 839-856 ◽  
Author(s):  
J. Hesse ◽  
J. A. Stanley ◽  
A. G. Jeffs

Kelp habitats are in decline in many temperate coastal regions of the world due to climate change and expansion of populations of grazing urchins. The loss of kelp habitat may influence the vulnerability to predators of the juveniles of commercially important species. In this study relative predation rates for kelp versus barren reef habitat were measured for early juvenile Australasian spiny lobster, Jasus edwardsii (Hutton, 1875), on the northeastern coast of New Zealand using tethering methods. Variation in assemblages of predators over small spatial scales appeared to be more important for determining the relative predation of lobsters, regardless of habitat type. Therefore, the assessment of relative predation risk to early juvenile lobsters between kelp and barren habitats will require more extensive sampling at a small spatial scale, as well as a specific focus on sampling during crepuscular and nocturnal periods when these lobsters are most at risk of predation.


2010 ◽  
Vol 37 (4) ◽  
pp. 273 ◽  
Author(s):  
Karen Fey ◽  
Peter B. Banks ◽  
Hannu Ylönen ◽  
Erkki Korpimäki

Context. Potential mammalian prey commonly use the odours of their co-evolved predators to manage their risks of predation. But when the risk comes from an unknown source of predation, odours might not be perceived as dangerous, and anti-predator responses may fail, except possibly if the alien predator is of the same archetype as a native predator. Aims. In the present study we examined anti-predator behavioural responses of voles from the outer archipelagos of the Baltic Sea, south-western Finland, where they have had no resident mammalian predators in recent history. Methods. We investigated responses of field voles (Microtus agrestis) to odours of native least weasels (Mustela nivalis) and a recently invading alien predator, the American mink (Mustela vison), in laboratory. We also studied the short-term responses of free-ranging field voles and bank voles (Myodes glareolus) to simulated predation risk by alien mink on small islands in the outer archipelago of the Baltic Sea. Key results. In the laboratory, voles avoided odour cues of native weasel but not of alien mink. It is possible that the response to mink is a context dependent learned response which could not be induced in the laboratory, whereas the response to weasel is innate. In the field, however, voles reduced activity during their normal peak-activity times at night as a response to simulated alien-mink predation risk. No other shifts in space use or activity in safer microhabitats or denser vegetation were apparent. Conclusions. Voles appeared to recognise alien minks as predators from their odours in the wild. However, reduction in activity is likely to be only a short-term immediate response to mink presence, which is augmented by longer-term strategies of habitat shift. Because alien mink still strongly suppresses vole dynamics despite these anti-predator responses, we suggest that behavioural naiveté may be the primary factor in the impact of an alien predator on native prey. Implications. Prey naiveté has long been considered as the root cause of the devastating impacts of alien predators, whereby native prey simply fail to recognise and respond to the novel predation risk. Our results reveal a more complex form of naiveté whereby native prey appeared to recognise alien predators as a threat but their response is ultimately inadequate. Thus, recognition alone is unlikely to afford protection for native prey from alien-predator impacts. Thus, management strategies that, for example, train prey in recognition of novel threats must induce effective responses if they are expected to succeed.


2018 ◽  
Vol 11 (1) ◽  
pp. 100-103
Author(s):  
Aldo Alvarez-Risco ◽  
Jaime Delgado-Zegarra ◽  
Jaime A. Yáñez ◽  
Santiago Diaz-Risco ◽  
Shyla Del-Aguila-Arcentales

Abstract The growth of tourism to Peru and the gastronomic boom with millions of people looking to taste Peruvian food is resulting in a risk of predation of natural sources necessary to make these dishes. The focus in only obtaining these ingredients can generate significant damage to the Peruvian biodiversity, so stakeholders need to develop strategies to avoid predation due to the gastronomic boom. Citizens and visitors need to play a role in protecting the natural resources and contributing to environmental sustainability.


2020 ◽  
Vol 41 (3) ◽  
pp. 373-385 ◽  
Author(s):  
Barbara A. Caspers ◽  
E. Tobias Krause ◽  
Isabelle Hermanski ◽  
Christopher Wiesbrock ◽  
Friedrich-Wilhelm Kastrup ◽  
...  

Abstract Warning colouration reduces predation risk by signalling or mimicking the unpleasantness of prey and therefore increases survival. We tested in two experiments the evolutionary costs and benefits of the yellow colour pattern in fire salamanders (Salamandra salamandra), which display a yellow/black colour pattern usually associated with toxic alkaloids. Our first experiment aimed to test whether the development of colouration is condition dependent and thus related to developmental costs, i.e. influenced by resource availability during the developmental process. Therefore, we reared fire salamander larvae under different nutritional conditions and compared the relative amount of yellow they developed after metamorphosis. Fire salamander larvae reared under limited food conditions had a lower proportion of yellow following metamorphosis than control larvae reared under superior food conditions. In a second experiment we tested whether the proportion of yellow has an impact on the risk of being attacked using artificial models. We tested, in salamander-free and salamander-occupied natural habitats, whether artificial clay models with different proportions of yellow and black receive different attack rates from potential predators (birds, mammals, insects). In clay models the proportion of yellow and the site had a significant effect on predation risk. Models with larger amounts of yellow had fewer bite marks from predators such as carabid beetles and birds, but only in sympatry with salamanders. In conclusion, the early expression of conspicuous colouration seems to be condition dependent and therefore potentially costly. Furthermore, the yellow colouration of fire salamanders act as a signal that potentially reduces their risk of being attacked by predators. Thus, the yellow colouration of fire salamanders seems to represent an adaptive trait that reduces the risk of predation, which can be expressed in higher quantity by individuals of a certain condition.


Behaviour ◽  
2001 ◽  
Vol 138 (5) ◽  
pp. 615-627 ◽  
Author(s):  

AbstractFollowing the theory of parent-offspring conflict parents request from their offspring an honest signal of food requirement to optimally adjust feeding rate. For this purpose, offspring display a highly informative signalling system, begging vocalisation, for which the conspicuousness to predators maintains honesty, since only hungry offspring are willing to take this risk. The risk of predation incurred by begging activities challenges our understanding of how begging vocalisation could evolve towards a high degree of noisiness. A solution to this apparent paradox resides in the possibility that alongside the evolution of begging, birds also evolved strategies that reduce the risk of being depredated. Following the ornithological literature nestlings scream in the presence of a predator to frighten it, induce parents to rescue them and siblings to flee from the nest and hide in the vegetation. I therefore propose the hypothesis that nestling screaming behaviour evolved as a means of reducing the risk of predation incurred by conspicuous begging. Comparative analyses supported the prediction postulating that species in which nestlings scream in the presence of a predator produce begging calls that are more conspicuous to predators than calls of non-screaming species. This suggests that the predation cost of begging lies not only in terms of predation per se but also in the requirement of anti-predator strategies.


2019 ◽  
Vol 30 (5) ◽  
pp. 1265-1272
Author(s):  
Pedro Z de Moraes ◽  
Pedro Diniz ◽  
Esteban Fernandez-Juricic ◽  
Regina H Macedo

AbstractSexual signaling coevolves with the sensory systems of intended receivers; however, predators may be unintended receivers of sexual signals. Conspicuous aerial displays in some species may place males at high risk of predation from eavesdropping predators. There are three different hypotheses to explain how signaling males can deal with increased predation risk: (1) males invest in survival by decreasing signal conspicuousness; (2) males invest in reproduction by increasing signal conspicuousness; and (3) male response is condition-dependent according to his residual reproductive value. Here, we used blue-black grassquits (Volatinia jacarina) to test these hypotheses, asking whether males modify leap displays under different levels of predation risk. Grassquit males develop an iridescent nuptial plumage and spend considerable time emitting a multimodal signal: while leaping from a perch, males clap their wings above their heads and emit a high-pitched short song. We exposed males to predator and nonpredator playbacks while video recording their displays. We found interactions between predation risk and 2 male condition variables (ectoparasite infestation and proportion of nuptial plumage coverage) that influenced display behavior. Less parasitized males and those with higher proportion of nuptial plumage showed no change in display behavior, while more parasitized males and those with lower proportion of nuptial plumage increased the vigor of displays under predation risk. In other words, males with low residual reproductive value increased reproductive effort when there was a high risk of extrinsic death. Our study provides some empirical support for the terminal investment hypothesis.


1995 ◽  
Vol 22 (1) ◽  
pp. 115 ◽  
Author(s):  
D. S. Hik

Like most heavily preyed-upon animals, snowshoe hares (Lepus americanus) have to balance conflicting demands of obtaining food at a high rate and avoiding predators. Adopting foraging behaviours to minimise predation risk may also lead to a decline in condition, and hence fecundity. Predictions of three hypotheses (condition constraint hypothesis, predator-avoidance constraint hypothesis, predation-sensitive foraging (PSF) hypothesis) were tested by comparing changes in the survival and condition of snowshoe hares on four experimental areas in winter during a cyclic peak and decline (1989–1993) near Kluane Lake, Yukon, Canada, where (i) predation risk was reduced by excluding terrestrial predators (FENCE), (ii) food supply was supplemented with rabbit chow ad libitum (FOOD), (iii) these two treatments were combined (FENCE+FOOD), and (iv) an unmanipulated CONTROL was used. Different pattems of survival and changes in body mass were observed in the presence and absence of terrestrial predators. On the CONTROL area, female body mass and fecundity declined, even though sufficient winter forage was apparently available in all years. A similar decrease in body mass was observed on the FOOD treatment, but only during the third year of the population decline. In contrast, female body mass remained high throughout the decline in the absence of terrestrial predators in the FENCE+FOOD and FENCE treatments. Winter survival declined on CONTROL and FENCE areas during the first year of the population decline (1991), but remained higher on FOOD until 1992 and FENCE+FOOD until 1993. These results generally supported the PSF hypothesis where terrestrial predators were present (CONTROL and FOOD grids). Where terrestrial predators were absent (FENCE and FENCE+FOOD), the results supported the alternative condition constraint hypothesis. The evidence suggests that a cascade of sublethal behavioural and physiological effects associated with increased predation risk contribute to the population decline and delayed recovery of cyclic low-phase populations of snowshoe hares.


2008 ◽  
Vol 276 (1657) ◽  
pp. 775-780 ◽  
Author(s):  
Tae Won Kim ◽  
John H Christy ◽  
Stefan Dennenmoser ◽  
Jae C Choe

When females search for mates and their perceived risk of predation increases, they less often express preferences for males that use conspicuous courtship signals, relaxing sexual selection on production of these signals. Here, we report an apparent exception to this general pattern. Courting male fiddler crabs Uca beebei sometimes build pillars of mud at the openings to their burrows in which crabs mate. Females visit several males before they choose a mate by staying and breeding in their burrows, and they preferentially visit males with pillars. Previous studies suggested that this preference is based on a visual orientation behaviour that may reduce females' risk of predation while searching for a mate. We tested this idea by determining whether the female preference for males with pillars increases with perceived predation risk. We attracted avian predators to where crabs were courting and measured the rates that sexually receptive females visited courting males with and without mud pillars. Under elevated risk, females continued to search for mates and they showed a stronger relative preference for males with pillars. Thus, when predation risk is high, females may continue to express preferences that are under natural selection because they help females avoid predation, strengthening sexual selection for use of the preferred signal.


ARCTIC ◽  
2021 ◽  
Vol 74 (1) ◽  
pp. 22-29
Author(s):  
Kevin G. Young ◽  
Lisa V. Kennedy ◽  
Paul A. Smith ◽  
Erica Nol

When monitoring the breeding ecology of birds, the causes and times of nest failure can be difficult to determine. Cameras placed near nests allow for accurate monitoring of nest fate, but their presence may increase the risk of predation by attracting predators, leading to biased results. The relative influence of cameras on nest predation risk may also depend on habitat because predator numbers or behaviour can change in response to the availability or accessibility of nests. We evaluated the impact of camera presence on the predation rate of artificial nests placed within mesic tundra habitats used by Arctic-breeding shorebirds. We deployed 94 artificial nests, half with cameras and half without, during the shorebird-nesting season of 2015 in the East Bay Migratory Bird Sanctuary, Nunavut. Artificial nests were distributed evenly across sedge meadow and supratidal habitats typically used by nesting shorebirds. We used the Cox proportional hazards model to assess differential nest survival in relation to camera presence, habitat type, placement date, and all potential interactions. Artificial nests with cameras did not experience higher predation risk than those without cameras. Predation risk of artificial nests was related to an interaction between habitat type and placement date. Nests deployed in sedge meadows and in supratidal habitats later in the season were subject to a higher risk of predation than those deployed in supratidal habitats early in the season. These differences in predation risk are likely driven by the foraging behaviour of Arctic fox (Vulpes lagopus), a species that accounted for 81% of observed predation events in this study. Arctic fox prey primarily on Arvicoline prey and goose eggs at this site and take shorebird nests opportunistically, perhaps more often later in the season when their preferred prey becomes scarcer. This study demonstrates that, at this site, cameras used for nest monitoring do not influence predation risk. Evaluating the impact of cameras on predation risk is critical prior to their use, as individual study areas may differ in terms of predator species and behaviour.


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