scholarly journals Mesopredator suppression by an apex predator alleviates the risk of predation perceived by small prey

2015 ◽  
Vol 282 (1802) ◽  
pp. 20142870 ◽  
Author(s):  
Christopher E. Gordon ◽  
Anna Feit ◽  
Jennifer Grüber ◽  
Mike Letnic

Predators can impact their prey via consumptive effects that occur through direct killing, and via non-consumptive effects that arise when the behaviour and phenotypes of prey shift in response to the risk of predation. Although predators' consumptive effects can have cascading population-level effects on species at lower trophic levels there is less evidence that predators' non-consumptive effects propagate through ecosystems. Here we provide evidence that suppression of abundance and activity of a mesopredator (the feral cat) by an apex predator (the dingo) has positive effects on both abundance and foraging efficiency of a desert rodent. Then by manipulating predators' access to food patches we further the idea that apex predators provide small prey with refuge from predation by showing that rodents increased their habitat breadth and use of ‘risky′ food patches where an apex predator was common but mesopredators rare. Our study suggests that apex predators' suppressive effects on mesopredators extend to alleviate both mesopredators' consumptive and non-consumptive effects on prey.

2015 ◽  
Vol 282 (1810) ◽  
pp. 20150124 ◽  
Author(s):  
Tracey Hollings ◽  
Hamish McCallum ◽  
Kaely Kreger ◽  
Nick Mooney ◽  
Menna Jones

Apex predators structure ecosystems through lethal and non-lethal interactions with prey, and their global decline is causing loss of ecological function. Behavioural changes of prey are some of the most rapid responses to predator decline and may act as an early indicator of cascading effects. The Tasmanian devil ( Sarcophilus harrisii ), an apex predator, is undergoing progressive and extensive population decline, of more than 90% in long-diseased areas, caused by a novel disease. Time since local disease outbreak correlates with devil population declines and thus predation risk. We used hair traps and giving-up densities (GUDs) in food patches to test whether a major prey species of devils, the arboreal common brushtail possum ( Trichosurus vulpecula ), is responsive to the changing risk of predation when they forage on the ground. Possums spend more time on the ground, discover food patches faster and forage more to a lower GUD with increasing years since disease outbreak and greater devil population decline. Loss of top–down effects of devils with respect to predation risk was evident at 90% devil population decline, with possum behaviour indistinguishable from a devil-free island. Alternative predators may help to maintain risk-sensitive anti-predator behaviours in possums while devil populations remain low.


2017 ◽  
Vol 284 (1854) ◽  
pp. 20170111 ◽  
Author(s):  
Timothy Morris ◽  
Mike Letnic

It is widely assumed that organisms at low trophic levels, particularly microbes and plants, are essential to basic services in ecosystems, such as nutrient cycling. In theory, apex predators' effects on ecosystems could extend to nutrient cycling and the soil nutrient pool by influencing the intensity and spatial organization of herbivory. Here, we take advantage of a long-term manipulation of dingo abundance across Australia's dingo-proof fence in the Strzelecki Desert to investigate the effects that removal of an apex predator has on herbivore abundance, vegetation and the soil nutrient pool. Results showed that kangaroos were more abundant where dingoes were rare, and effects of kangaroo exclusion on vegetation, and total carbon, total nitrogen and available phosphorus in the soil were marked where dingoes were rare, but negligible where dingoes were common. By showing that a trophic cascade resulting from an apex predator's lethal effects on herbivores extends to the soil nutrient pool, we demonstrate a hitherto unappreciated pathway via which predators can influence nutrient dynamics. A key implication of our study is the vast spatial scale across which apex predators' effects on herbivore populations operate and, in turn, effects on the soil nutrient pool and ecosystem productivity could become manifest.


2007 ◽  
Vol 85 (11) ◽  
pp. 1091-1116 ◽  
Author(s):  
L.S. Weilgart

Ocean noise pollution is of special concern for cetaceans, as they are highly dependent on sound as their principal sense. Sound travels very efficiently underwater, so the potential area impacted can be thousands of square kilometres or more. The principal anthropogenic noise sources are underwater explosions (nuclear and otherwise), shipping, seismic exploration by mainly the oil and gas industries, and naval sonar operations. Strandings and mortalities of especially beaked whales (family Ziphiidae) have in many cases been conclusively linked to noise events such as naval maneuvers involving tactical sonars or seismic surveys, though other cetacean species may also be involved. The mechanisms behind this mortality are still unknown, but are most likely related to gas and fat emboli at least partially mediated by a behavioral response, such as a change in diving pattern. Estimated received sound levels in these events are typically not high enough to cause hearing damage, implying that the auditory system may not always be the best indicator for noise impacts. Beaked whales are found in small, possibly genetically isolated, local populations that are resident year-round. Thus, even transient and localized acoustic impacts can have prolonged and serious population consequences, as may have occurred following at least one stranding. Populations may also be threatened by noise through reactions such as increased stress levels, abandonment of important habitat, and “masking” or the obscuring of natural sounds. Documented changes in vocal behavior may lead to reductions in foraging efficiency or mating opportunities. Responses are highly variable between species, age classes, behavioral states, etc., making extrapolations problematic. Also, short-term responses may not be good proxies of long-term population-level impacts. There are many examples of apparent tolerance of noise by cetaceans, however. Noise can also affect cetaceans indirectly through their prey. Fish show permanent and temporary hearing loss, reduced catch rates, stress, and behavioral reactions to noise. Management implications of noise impacts include difficulties in establishing “safe” exposure levels, shortcomings of some mitigation tools, the need for precaution in the form of reducing noise levels and distancing noise from biologically important areas, and the role of marine protected areas and monitoring in safeguarding cetaceans especially from cumulative and synergistic effects.


2021 ◽  
Vol 118 (21) ◽  
pp. e2023709118
Author(s):  
André M. de Roos

Natural ecological communities are diverse, complex, and often surprisingly stable, but the mechanisms underlying their stability remain a theoretical enigma. Interactions such as competition and predation presumably structure communities, yet theory predicts that complex communities are stable only when species growth rates are mostly limited by intraspecific self-regulation rather than by interactions with resources, competitors, and predators. Current theory, however, considers only the network topology of population-level interactions between species and ignores within-population differences, such as between juvenile and adult individuals. Here, using model simulations and analysis, I show that including commonly observed differences in vulnerability to predation and foraging efficiency between juvenile and adult individuals results in up to 10 times larger, more complex communities than observed in simulations without population stage structure. These diverse communities are stable or fluctuate with limited amplitude, although in the model only a single basal species is self-regulated, and the population-level interaction network is highly connected. Analysis of the species interaction matrix predicts the simulated communities to be unstable but for the interaction with the population-structure subsystem, which completely cancels out these instabilities through dynamic changes in population stage structure. Common differences between juveniles and adults and fluctuations in their relative abundance may hence have a decisive influence on the stability of complex natural communities and their vulnerability when environmental conditions change. To explain community persistence, it may not be sufficient to consider only the network of interactions between the constituting species.


2018 ◽  
Vol 285 (1877) ◽  
pp. 20180303 ◽  
Author(s):  
Jonathan M. Parrett ◽  
Robert J. Knell

Strong sexual selection has been reported to both enhance and hinder the adaptive capacity and persistence of populations when exposed to novel environments. Consequently, how sexual selection influences population adaption and persistence under stress remains widely debated. Here, we present two empirical investigations of the fitness consequences of sexual selection on populations of the Indian meal moth, Plodia interpunctella, exposed to stable or gradually increasing temperatures. When faced with increasing temperatures, strong sexual selection was associated with both increased fecundity and offspring survival compared with populations experiencing weak sexual selection, suggesting sexual selection acts to drive adaptive evolution by favouring beneficial alleles. Strong sexual selection did not, however, delay extinction when the temperature became excessively high. By manipulating individuals' mating opportunities during fitness assays, we were able to assess the effect of multiple mating independently from the effect of population-level sexual selection, and found that polyandry has a positive effect on both fecundity and offspring survival under increasing temperatures in those populations evolving with weak sexual selection. Within stable temperatures, there were some benefits from strong sexual selection but these were not consistent across the entire experiment, possibly reflecting changing costs and benefits of sexual selection under stabilizing and directional selection. These results indicate that sexual selection can provide a buffer against climate change and increase adaptation rates within a continuously changing environment. These positive effects of sexual selection may, however, be too small to protect populations and delay extinction when environmental changes are relatively rapid.


2019 ◽  
Vol 112 (5) ◽  
pp. 2094-2102 ◽  
Author(s):  
Ruth Kahuthia-Gathu ◽  
Stephen T O Othim

AbstractThe diamondback moth (DBM), Plutella xylostella L., is the most destructive pest affecting vegetable production in Kenya and around the world. Parasitoids have shown promising results in lowering the pest populations and damage caused by DBM. However, variations in host plant quality have been reported to have bottom-up effects up to the third and fourth trophic levels. We assessed the effects of two cultivated Brassica varieties (cabbage, Brassica oleracea var. capitata L. cultivar ‘Gloria F1’ and kale, B. oleracea var. acephala L. cultivar ‘Thousand headed’) on the development and performance of the specialist pest P. xylostella and two exotic parasitoids Diadegma semiclausum (Hellen) and Cotesia vestalis (Haliday). The exposed larval period of DBM took about 1.5 d longer on kale than cabbage and the total immature development time of both females and males was significantly longer on kale than cabbage. Higher pupal weight and higher fecundity were recorded on DBM fed on kale. Development time of D. semiclausum and C. vestalis was not affected by the host crop as was the parasitism rate of D. semiclausum. Heavier male pupae and larger adults of D. semiclausum, as well as more fecund adults of C. vestalis, were obtained from hosts fed on cabbage. Larger adults of C. vestalis were obtained from herbivores fed on kale. These results show potentially positive effects of host plant allelochemicals that are detrimental to herbivores while promoting parasitoid development and performance, which can be harnessed for the control of DBM.


The Condor ◽  
2000 ◽  
Vol 102 (4) ◽  
pp. 723-737 ◽  
Author(s):  
David B. Irons ◽  
Steven J. Kendall ◽  
Wallace P. Erickson ◽  
Lyman L. McDonald ◽  
Brian K. Lance

Abstract We compared post Exxon Valdez oil-spill densities of marine birds in Prince William Sound from 1989–1991, 1993, 1996, and 1998 to pre-spill densities from 1984–1985. Post-spill densities of several species of marine birds were lower than expected in the oiled area of Prince William Sound when compared to densities in the unoiled area. These negative effects continued through 1998 for five taxa: cormorants, goldeneyes, mergansers, Pigeon Guillemot (Cepphus columba), and murres. Black Oystercatchers (Haematopus bachmani) and Harlequin Ducks (Histrionicus histrionicus) exhibited negative effects in 1990 and 1991. Loons showed a weak negative effect in 1993. Black-legged Kittiwakes (Rissa tridactyla) showed relative decreases in 1989, 1996, and 1998 which may have been caused by shifts in foraging distribution rather than declines in populations. Glaucous-winged Gulls (Larus glaucescens) showed positive effects in most post-spill years. Murrelets and terns showed relative increases in 1993, 1996, and 1998. Generally, taxa that dive for their food were negatively affected, whereas taxa that feed at the surface were not. Effects for some taxa were dependent upon the spatial scale at which they were analyzed. Movements of birds and the mosaic pattern of oiling reduced our ability to detect oil-spill effects, therefore our results may be conservative. Several marine bird species were negatively affected at the population level and have not recovered to pre-spill levels nine years after the oil spill. The reason for lack of recovery may be related to persistent oil remaining in the environment and reduced forage fish abundance.


2020 ◽  
Vol 287 (1938) ◽  
pp. 20202202
Author(s):  
L. Mark Elbroch ◽  
Jake M. Ferguson ◽  
Howard Quigley ◽  
Derek Craighead ◽  
Daniel J. Thompson ◽  
...  

Top-down effects of apex predators are modulated by human impacts on community composition and species abundances. Consequently, research supporting top-down effects of apex predators occurs almost entirely within protected areas rather than the multi-use landscapes dominating modern ecosystems. Here, we developed an integrated population model to disentangle the concurrent contributions of a reintroduced apex predator, the grey wolf, human hunting and prey abundances on vital rates and abundance of a subordinate apex predator, the puma. Increasing wolf numbers had strong negative effects on puma fecundity, and subadult and adult survival. Puma survival was also influenced by density dependence. Overall, puma dynamics in our multi-use landscape were more strongly influenced by top-down forces exhibited by a reintroduced apex predator, than by human hunting or bottom-up forces (prey abundance) subsidized by humans. Quantitatively, the average annual impact of human hunting on equilibrium puma abundance was equivalent to the effects of 20 wolves. Historically, wolves may have limited pumas across North America and dictated puma scarcity in systems lacking sufficient refugia to mitigate the effects of competition.


2015 ◽  
Vol 36 (2) ◽  
pp. 155-163 ◽  
Author(s):  
Ori Segev ◽  
Ariel Rodríguez ◽  
Susanne Hauswaldt ◽  
Karen Hugemann ◽  
Miguel Vences

Amphibians vary in the degree of pre-metamorphic developmental plasticity in response to risk of predation. Changes in hatching time and development rate can increase egg or tadpole survival respectively by shortening the duration of the more vulnerable stages. The intensity of predator induced developmental response and its direction, i.e. delayed, accelerated, or none, varies considerably between amphibian and predator species. We surveyed freshly deposited clutches of the European common frog Rana temporaria in a population in Braunschweig, Germany and found that 62% (N = 20) of the clutches contained planarians (Schmidtea nova), with an average of 3.94 ± 0.79 and a maximum of 13 planarians per clutch. A laboratory predation experiment confirmed that this planaria preys on R. temporaria eggs and early embryos. We further exposed freshly laid egg masses to either free, caged, or no planarians treatments using floating containers within a breeding pond where the two species co-occur. After 10 days exposure, embryos showed developmental stages 14-25 along the Gosner scale with statistically significant positive effects of both predator treatments. The observed effect was rather slight as predator-exposed individuals showed an increase by a single Gosner stage relative to those raised without planarians. The detected trend suggests that direct and indirect cues from flatworms, rarely considered as anuran predators, might induce a developmental response in R. temporaria early developmental stages.


Paleobiology ◽  
1979 ◽  
Vol 5 (2) ◽  
pp. 107-125 ◽  
Author(s):  
Jennifer A. Kitchell

The foraging paradigm of trace fossil theory has historically accorded random behavior to non-food-limited deposit-feeders and non-random behavior to food-limited feeders. A series of randomness measures derived from empirical modeling, simulation modeling, stochastic modeling and probability theory applied to foraging patterns observed in deep-sea bottom photographs from the Arctic and Antarctic yielded a behavioral continuum of increasing non-randomness. A linear regression of trace positions along the continuum to bathymetric data did not substantiate the optimal foraging efficiency-depth dependence model of trace fossil theory, except that all traces exhibited a greater optimization than that of simulated random foraging. It is hypothesized that optimization as evidenced by non-random foraging strategies represents maximization of the cost/benefit ratio of resource exploitation to risk of predation and that individual foraging patterns reflect an exploration response to the morphometry of a patchily distributed food resource. Differential predation and competition may account for the co-occurrence of random and non-random strategies within the same bathymetric zone.


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