Variation in parental rearing expenditure triggers short‐term physiological effects on offspring in a long‐lived seabird

Parental care in long‐lived bird species involves a trade‐off between the benefits of increasing the effort expended on current offspring and the costs that this represents for future reproductive output. Under regimes of high environmental variability, long‐lived seabirds can adjust their breeding effort to buffer the negative effects of this variability on their offspring. However, the potential impacts of variation in breeding effort on offspring physiology in the short term and on longer‐term survival are poorly understood. In this study, we manipulated brood age through a cross‐fostering experiment to assess whether increasing or decreasing parental reproductive expenditure led to costs in Blue‐footed Booby Sula nebouxii chicks. Specifically, we tested the consequences of altered parental reproductive expenditure on the offspring's physiological condition (plasma metabolites, heterophil to lymphocyte ratio (H/L) and body condition index (BCI)) and survival. Offspring from broods in which parental investment was experimentally increased showed a lower BCI and lower alkaline phosphatase levels and higher H/L ratios than controls. Conversely, offspring showed the opposite pattern when reproductive expenditure was experimentally decreased. We observed no effects of manipulation of parental investment on triglyceride levels or on survival rates. Although our findings suggest that Blue‐footed Booby parents have the ability to adjust their breeding effort according to the demands of their offspring, parental effort could influence the effect of hatching order by suppressing the aggressive tendency of the senior chick.     

Blood parasites and nest defense behaviour of Tengmalm's owls

Infectious diseases are expected to negatively influence essential life history traits of an individual, because investment in immunological response occurs at the expense of reduced investment in other functions. Here we present the first observational evidence that the prevalence of blood parasites is negatively associated with avian nest defense. Because the defense of offspring entails a risk of serious physical harm to the parent, it is also assumed to be a good estimate of parental investment. In both 1994 and 1995, the nest defense intensity of male Tengmalm's owls (Aegolius funereus) against a live American mink (Mustela vison) was strongly curtailed in parents infected by Trypanosoma avium blood parasites. Our data suggests that investment in reproduction can be negatively affected by parasitaemia, and that host-parasite interactions may potentially modify hosts' life-history traits, making it important to consider the costs of parasitism in future studies. Received: 20 October 1997 / Accepted 29 December 1997     

Coadaptation of Offspring Begging and Parental Provisioning - An Evolutionary Ecological Perspective on Avian Family Life

Offspring begging and parental provisioning are the two central social behaviours expressed during the period of parental care. Both behaviours influence each other and it is, therefore, hypothesized that they should ultimately become (genetically) correlated, stabilized by fitness costs to parents and/or offspring. By reciprocally exchanging entire clutches in canaries (Serinus canaria), we tested (1) whether there is covariation between these behaviours and (2) whether a mismatch - as introduced by cross-fostering - entails costs. Begging was scored in a standardized begging test and parental provisioning was measured via (a) the actual feeding rate and (b) using the growth rate of the foster nestlings as a proxy. Costs were established in terms of future reproductive investment in subsequent clutches and offspring growth. We found a positive and significant phenotypic covariation between offspring begging and parental feeding when using the growth rate as a proxy and, to a lesser extent, in case of the parental feeding rate. Female parents suffered no future reproductive costs when feeding foster nestlings that were more demanding than their own nestlings. Neither growth measured amongst all offspring nor the reproductive investment measured amongst the female offspring as adults was influenced by their begging behaviour. However, the reproductive investment of female offspring tended to depend on the parental qualities of their foster parents. Thus, offspring may only be able to extract resources within the limit of generosity of their foster parents. This suggests parental control of feeding, which is also supported by the positive covariation between offspring begging and parental feeding.     

Increased parental care cost for nest-guarding fish in a lake with hyperabundant nest predators

Although parental care increases offspring survival, providingcare is costly, reducing parental growth and survival and, thereby,compromising future reproductive success. To determine if anexotic benthic predator might be affecting parental care bynest-guarding smallmouth bass (Micropterus dolomieu), we comparednest-guarding behavior and energy expenditures in two systems,one with a hyperabundant recently introduced predator, the roundgoby (Neogobious melanostomus). In Lake Erie, USA, smallmouthbass vigorously defended their nests from benthic round gobies.In Lake Opeongo, Canada, smallmouth bass were exposed to fewerand predominantly open-water predators and were less activein their nest defense. From scuba and video observations, wedocumented that nest-guarding smallmouth bass chased predators(99% of which were round gobies) nine times more frequentlyin Lake Erie than in Lake Opeongo. This heightened activityresulted in a significant decline in weight and energetic contentof guarding males in Lake Erie but no change in Lake Opeongomales. Bioenergetic simulations revealed that parental careincreased smallmouth bass standard metabolic rate by 210% inLake Erie but only by 28% in Lake Opeongo. As energy reservesdeclined and offspring became increasingly independent, malesin both lakes consumed more prey and spent more time foragingaway from their nests; however, nest-guarding smallmouth bassconsumed few prey and, in Lake Erie, rarely consumed round gobies.Therefore, increased parental care costs owing to the presenceof round gobies could affect future growth, reproduction, andsurvival if smallmouth bass approach critically low energy reserves.     

Costs of egg-laying and offspring provisioning: multifaceted parental investment in a digger wasp

Nest-building Hymenoptera have been a major testing ground for theories of parental investment and sex allocation. Investment has usually been estimated by the likely costs of offspring provisioning, ignoring other aspects of parental care. Using three experimental treatments, we estimated the costs of egg-laying and provisioning separately under field conditions in a digger wasp Ammophila pubescens. In one treatment, we increased the provisioning effort required per offspring by removing alternate prey items as they were brought to the nest. In two other treatments, we reduced parental effort by either preventing females from provisioning alternate nests or preventing them from both ovipositing and provisioning. Our results indicate that both egg-laying and provisioning represent significant costs of reproduction, expressed as differences in productivity but not survival. A trade-off-based model suggests that other components of parental care such as nest initiation may also represent significant costs. Costs of egg production and nest initiation are probably similar for male and female offspring, so that taking them into account leads to a less male-biased expected sex ratio. Mothers compensated only partially for prey removal in terms of the total provisions they gave to individual offspring.     

Costs of parental care on hunting behaviour of Helobdella papillornata (Euhirudinea: Glossiphoniidae)

Helobdella papillornata, an Australian freshwater leech, feeds primarily on snails and has a high level of parental care involving brooding eggs and young, with direct feeding of young. Parental costs and offspring benefits from these behaviours are poorly understood. A potential cost of parental care may be a change in the time taken to hunt prey. To test this hypothesis, the hunting behaviour of adults without progeny, parents with eggs, and parents with young were compared. We found that parents brooding eggs had a significantly (P = 0.029) longer lag time to begin hunting than parents brooding young, and spent significantly (P = 0.018) less time actively hunting than non-brooding adults. These costs, which may represent lost potential for the parent’s future reproductive success, should be outweighed by the fitness benefits of improved growth and survival of offspring, if parental care is favoured by selection. The hunting costs of care in Helobdella and other benthic, dorsoventrally flattened leeches in the family Glossiphoniidae may be smaller than the costs of brood tending that would be imposed on other freshwater leeches, and this difference may help explain the restriction of care to a single clade of the Euhirudinea.     

Worker ants of <Emphasis Type="Italic">Myrmica rubra</Emphasis>(Hymenoptera,Formicidae) as an unusual prey of the digger wasp <Emphasis Type="Italic">Crossocerus vagabundus</Emphasis> (Hymenoptera,Crabronidae)

The digger wasp Crossocerus vagabundus (Panzer, 1798) (Hymenoptera, Crabronidae, Crabronini) hunting for workers of Myrmica rubra (Linnaeus, 1758) was recorded for the first time. Various dipterans, mostly crane flies (Tipulidae), were the only known prey for this species. The modes of wasp hunting for worker ants are described. The reasons for unusual choice of prey are discussed.     

Estimating expenditure on male and female offspring in a sexually size-dimorphic bird: a comparison of different methods

The parents of sexually size-dimorphic offspring are often assumed to invest more resources producing individuals of the larger sex. A range of different methods have been employed to estimate relative expenditure on the sexes, including quantifying sex-specific offspring growth, food intake, energy expenditure and energy intake, in addition to measures of parental food provisioning and energy expenditure. These methods all have the potential to provide useful estimates of relative investment, but each has particular problems of interpretation, and few studies have compared the estimates derived concurrently from more than two of these measures. In this study we compared these surrogate measures of parental investment in the brown songlark Cinclorhamphus cruralis, which exhibits one of the most extreme cases of sexual size dimorphism among birds. At 10 days of age we found that male chicks, on average, were 49% heavier, received 42% more prey items, expended 44% more energy and ingested 50% more metabolizable energy than their sisters. Furthermore, we created, experimentally, both all-male and all-female broods of 10-day-old chicks and found that mothers delivered 43% more prey items and expended 27% more energy when provisioning all-male broods, providing the first direct evidence for a change in parental energy expenditure in relation to brood sex ratio. These data reveal remarkable agreement between these estimates of investment and suggest that all may provide quantitatively useful information on sex allocation. However, the lower variance associated with estimates of relative mass and energy intake suggest that these methods may be of greater utility, although this may primarily reflect the shorter period over which our provisioning data were collected.     

Differential diet breadths and species coexistence in leafroller-hunting eumenid wasps

There are, at least, three possible ways in which similar species coexist; resource partitioning, interference competition, and exploitation competition. Here, I investigated which way contributed to the coexistence of leafroller-hunting eumenid wasp species. Resource partitioning and, in addition, differential diet breadths proved to promote species coexistence in this case. First, I analyze the prey records and diet overlap of four eumenid species in a local area. The larger two eumenids hunted similar-sized prey items and had similar potential taxonomic prey uses. But the diet breadth of the subsocial eumenid was much wider than that of the solitary one. As a result, the diet overlap between the two large eumenids decreased. This was because the solitary eumenid attend repeatedly to the same hunting site inhabited by one abundant prey species, while the subsocial one made random hunting. On the other hand, the two medium-sized eumenids partitioned resources according to prey size. Secondly, I related these results to prey choice by several other species of eumenid obtained from literature sources. Ten Japanese common eumenids were divided into four groups according to their prey size. In each of the four groups, 2 to 3 wasp species differentiated the habitat (1 group) or coexisted by means of differential diet breadths (parallel with differential sociality, 2 groups).     

Females of the European beewolf preserve their honeybee prey against competing fungi

1. Females of the European beewolf Philanthus triangulum (Hymenoptera, Sphecidae) provision brood cells with paralysed honeybees as larval food. Because brood cells are located in warm, humid locations there is a high risk of microbial decomposition of the provisions. Low incidence of fungus infestation (Aspergillus sp.) in nests in the field suggested the presence of an anti‐fungal adaptation. 2. To test whether the paralysis caused the protection from fungus infestation, the timing of fungus growth on bees that were freeze‐killed, paralysed but not provisioned, and provisioned regularly by beewolf females was determined. Fungus growth was first detected on freeze‐killed bees, followed by paralysed but not provisioned bees. By contrast, fungus growth on provisioned bees was delayed greatly or even absent. Thus, paralysis alone is much less efficient in delaying fungus growth than is regular provisioning. 3. Observations of beewolves in their nests revealed that females lick the body surface of their prey very thoroughly during the period of excavation of the brood cell. 4. To separate the effect of a possible anti‐fungal property of the brood cell and the licking of the bees, a second experiment was conducted. Timing of fungus growth on paralysed bees did not differ between artificial and original brood cells. By contrast, fungus growth on bees that had been provisioned by a female but were transferred to artificial brood cells was delayed significantly. Thus, the treatment of the bees by the female wasp but not the brood cell caused the delay in fungus growth. 5. Beewolf females most probably apply anti‐fungal chemicals to the cuticle of their prey. This is the first demonstration of the mechanism involved in the preservation of provisions in a hunting wasp. Some kind of preservation of prey as a component of parental care is probably widespread among hunting wasps and might have been a prerequisite for the evolution of mass provisioning.     

Dangerous prey and daring predators: a review

How foragers balance risks during foraging is a central focus of optimal foraging studies. While diverse theoretical and empirical work has revealed how foragers should and do manage food and safety from predators, little attention has been given to the risks posed by dangerous prey. This is a potentially important oversight because risk of injury can give rise to foraging costs similar to those arising from the risk of predation, and with similar consequences. Here, we synthesize the literature on how foragers manage risks associated with dangerous prey and adapt previous theory to make the first steps towards a framework for future studies. Though rarely documented, it appears that in some systems predators are frequently injured while hunting and risk of injury can be an important foraging cost. Fitness costs of foraging injuries, which can be fatal, likely vary widely but have rarely been studied and should be the subject of future research. Like other types of risk‐taking behaviour, it appears that there is individual variation in the willingness to take risks, which can be driven by social factors, experience and foraging abilities, or differences in body condition. Because of ongoing modifications to natural communities, including changes in prey availability and relative abundance as well as the introduction of potentially dangerous prey to numerous ecosystems, understanding the prevalence and consequences of hunting dangerous prey should be a priority for behavioural ecologists.     

Specialisation in prey capture drives coexistence among sympatric spider‐hunting wasps

1. Sister taxa that coexist in the same space and time often face competition due to the use of similar resources. However, some closely related species can adopt fine‐grained specialisation in resource use to coexist. This study investigated niche overlap between three sympatric spider‐hunting wasp species of the genus Trypoxylon (Hymenoptera: Crabronidae) known to nest in three of the habitats found in the study area. 2. First, the co‐occurrence of these wasp species in the three habitats was estimated, as a proxy for potential competition. Then, the following hypotheses were tested: (i) niche partitioning is seen more often between species that co‐occur in a habitat, whereas there is niche overlap between species nesting in distinct habitats (prey specialisation hypothesis); and (ii) wasp species capture prey according to their size (physical constraint hypothesis). 3. Two pairs of wasp species were found consistently nesting in the same habitat. Niche partitioning based on prey taxa occurred regardless of the habitat preference. It was also found that differences in the size of wasps reflected distinctions in the size of their prey. 4. These findings were consistent over the years, showing that the significance of specialisation in foraging activities and physical constraints during prey capture can play key roles in the coexistence of sympatric species. The distinctions in the foraging strategies of these wasps are discussed, as well as potential mechanisms driving the evolution in prey specialisation, with insights for future studies.     

Evolutionary Implications of Persistence Hunting: An Examination of Energy Return on Investment for !Kung Hunting

Hominins are smaller, slower, and weaker than most large mammals, yet they have been eating meat from freshly killed large mammals since before the invention of sophisticated weaponry. It is thought that they could have achieved this seemingly impossible feat through persistence hunting, a practice powered by endurance running. Essentially, one or more hunters pursue a prey animal in the heat of the day until it reaches the point of hyperthermia. This allows a hunter to safely kill the weakened animal at close range using methods such as beating, strangling, or spearing. The energy balance of this approach to getting food is controversial and has not been calculated previously. We examined the energy costs and gains of persistence hunting through several energy returned on investment (EROI) calculations based on synthesizing available field and laboratory data on the energy used by the hunters and the energy returned from the greater kudu (Tragelaphus strepsiceros). We estimate that the EROI of these hunter-gatherers hunting a kudu ranged from 26:1 to 69:1. The net energy gained from such an effort would sustain an average sized !Kung family for 6.7 to 11.2 days. The “profit” energy within these ranges would have supported the early human societies that practiced persistence hunting, contributing to the often-noted “leisure” characterizing many foraging societies (Sahlins 1974).     

Parental investment decision rules in tree swallows: parental defense, abandonment, and the so-called Concorde Fallacy

I conducted an experiment to detect the importance of past investmentand expected benefits to reproductive "decision making" by treeswallows (Tachycineta bicolor). Three experimental groups, balancedfor measurable indicators of parental quality, were created:one had its clutch reduced in size near the beginning of incubation,the second had its brood reduced near chickfledging, and thethird had no brood or clutch reduction. All experimental groupswere tested for differences in 19 measures of parental defensebehavior at the same stage in the nesting cycle by exposingthem on successive days to two different predators, a ferretand a rat snake, at the nest box. There were no detectable effectsof experimental treatment on parental defense; however, therewere differences in abandonment frequency related to the severityof experimental clutch reduction. These results suggest thattree swallows respond to differences in expected benefits in"deciding" whether or not to abandon a nesting attempt. Becausepast investment can affect the prospective costs of abandonmentand renesting, the most natural currency for comparing costsand benefits is prospective. Adopting such a currency for parental"decisions" lessens concern over the so-called Concorde Fallacy,but it highlights our relative ignorance of how past reproductiveeffort influences the costs of future reproduction. [Behav Ecol1991,2:133–142]     

Antipredator defense as a limited resource: unequal predation risk in broods of an insect with maternal care

The allocation of parental investment is a potential sourceof conflict within broods whenever offspring are able obtaindifferential access to the parental resource. Unlike the provisioningof food, parental antipredator behavior is usually considereda resource that benefits all offspring simultaneously. In thethornbug treehopper (Umbonia crassicornis), offspring formaggregations in exposed positions on host-plant stems. Theyare subject to intense predation, and maternal defense is theirprimary means of protection. I examined the distribution ofrisk within these offspring groups, using natural variationin the outcome of more than 500 predation attempts (324 recordedon videotape) by vespid wasps (Pseudopolybia compressa) on18 U. crassicornis aggregations. I found three influences onan individual offspring's risk of predation. The first wasthe presence of a defending female: as expected, offspringwere much more likely to survive contact with a wasp if thefemale was present than if the female had disappeared. Thesecond influence was position relative to other offspring: when wasps were successful in removing an individual, they almostalways removed it from the edge of the group. The third influencewas distance from the female: the closer an offspring was tothe female at the time it was contacted by a wasp, the higherits likelihood of survival. The distribution of risk is determinedlargely by the behavior of defending females and the prey-searchingbehavior of wasps. The nature of risk within these aggregations sets the stage for two forms of sibling rivalry: selfish herdbehavior and competition for access to maternal defense. Italso raises the question of how a parent should allocate defenseamong offspring when it is unable to defend them all simultaneously.     

Hunting Behavior in the Ctenizidae

The most primitive way of hunting in Mygalomorph spiders seemsto be the free roaming and catching of encountered prey Theraphosidae.The trap-door spiders Ctenizidae, Actinopodidae and Barychelidawhich are entirely sedentary, lie in wait behind the trap-doorand leap at prey that happens to pass close to the door. Somespecies spin radial silk threads outside the door which functionas stumbleor signal-lines, and some Australian species use grassblades and other litter in the same way. A further evolutionarystep leads to species which do not build a trap-door but crowntheir burrow by a funnel-shaped web. The Dipluridae finallyare real web-builders, which depend on a sheet-web to catchtheir prey. Generally they do not dig a burrow but hide in asmall retreat from which a funnel-web leads to the net. With a few exceptions Ctenizidae are entirely nocturnal. Theirrhythm of activity has been analyzed. The "Zeitgeber" is thedaylight during the last half hour before sunset. Most trapdoorspiders never leave their burrow during their whole life. Theyneed three to four years from hatching to become adults. Adultmales die during or at the end of the restricted mating-season;they take no food when adult. Females, which undergo post-adultmolts, can probably live for 15–20 years. Nemesia caementaria, like most other species, hunts during thewhole night. The mean time of activity is about Si/o hours,consisting of periods of lying in wait and periods of intermediaterests. The spiders make an average of three leaps per nightto catch a prey, but only about 10% of all bounds are successful.A hungry animal, lurking in vain, shows unmotivated leaps. The effects of light, moisture, and temperature on hunting activityare analyzed. Ctenizidae hunt during autumn, winter, and springbut interrupt their activity in summer for an estivation whichlasts usually two months. The females of some species capture the male after mating andeat him; others never attack him. This difference in behaviorlias repercussions on reproduction. Among certain species the young nymphs of the third instar refuseall food until they have made their own burrow and can huntby themselves. The young of other species stay with the motherfor one year and leave her at the fifth or sixth instar to maketheir own burrow. The young of Nemesia caementaria can remainin the burrow of the mother until they are almost adult, i.e.,for two or three years, and feed on the prey the mother hascaught. The behavior of Ctenizidae can be grouped. Some species lurkbehind the closed or almost closed trap-door. Another groupopens the trap-door and puts the pedipalpi and the two anteriorpairs of legs radially out onto the rim of the burrow, whilethe cephalothorax is hidden behind the trap-door. A third groupspins threads of silk radially about the entrance and uses themas signal-lines. A fourth group can come out and pursue theprey, then drags it to the trap-door and into the burrow. The nature of the prey depends on the bio tope. The Ctenizidaefeed almost exclusively on insects, mainly ants and beetles;in the laboratory crickets are accepted as prey. Ctenizidae have no tarsal organ. They have different types oftrichobothria, transversal and longitudinal slit-organs, andlyriform organs. With these three kinds of sense-organs, thefunctions of which are not clearly understood, the trap-doorspiders are able to perceive the approach of prey, to judgeits distance from the trap-door, and to locate it in direction.They seem to have an organ of smell, since certain groups ofinsects are repulsive to them. Sight is not used for hunting.     

Begging, food provisioning, and nestling competition in great tit broods infested with ectoparasites

Ectoparasites are a ubiquitous environmental component of breedingbirds, and it has repeatedly been shown that hematoph-agousectoparasites such as fleas and mites reduce the quality andnumber of offspring of bird hosts, thereby lowering the valueof a current brood. Selection acting on the hosts will favorphysiological and behavioral responses that will reduce theparasites' impact. However, the results of the few bird studiesthat addressed the question of whether parasitism leads to ahigher rate of food provisioning are equivocal, and the beggingresponse to infestation has rarely been quantified. A changein begging activity and parental rate of food provisioning couldbe predicted in either direction: parents could reduce theirinvestment in the brood in order to invest more in future broods,or they could increase their investment in order to compensatefor the parasites' effect on the current brood. Since the nestlingsare weakened by the ectoparasites they may beg less, but onthe other hand they may beg more in order to obtain more food.In this study we show experimentally that (1) hen fleas (Ceratophyllusgallinae) reduce the body mass and size of great tit (Parusmajor) nestlings, (2) nestlings of parasitized broods more thandouble their begging rate, (3) the male parents increase thefrequency of feeding trips by over 50%, (4) the females do notadjust feeding rate to the lowered nutritional state of nestlings,and (5) food competition among siblings of parasitized broodsis increased. Ultimately the difference in the parental feedingresponse may be understood as the result of a sex-related differencein the trade-off of i0vesting in current versus future broods.     

Selection and control of Deborah numbers in plankton ecology

The Deborah number (De) is widely used to characterize processestaking place in deforming continua. De=(the time scale of aprocess)/(the time scale of deformation). When De >>lthe process thus takes place in a functionally fluid medium,but when De <<1 the regime is functionally solid. De hasbeen used to refine concepts in three pelagic processes. Dispersionof dividing cells may be characterized by De, and may be regulatedby means of secretions. Dispersion of microzones by diffusionand shear is characterized. The characteristic time of microzonesis shown to depend on the concentration. Because microzonessmear Out along the shear, to prevent nutrient-seekers and predatorsusing them as scent trails, organisms may convolute their microzonesby swimming, particularly across the shear. In a predator-preymodel, it has been shown that when De, (shear rate) (time takento swim radius of detection sphere), >2.6, not all the perceivedprey is accessible. More economical hunting strategies and thoseallowing access to more of the perceived prey, require bettersensory and navigational abilities. When De >2.6, the predatorwill perceive a greater flux of accessible prey when it swimsacross the shear than when it swims in the other two dimensions.De may help to understand many more biological processes indeforming media.     

Deferred Harvests: The Transition from Hunting to Animal Husbandry

We define animal husbandry as prey conservation. Conservation is rare among extant hunters and only likely to occur when prey are highly valued, private goods. The long-term discounted deferred returns from husbandry must also be greater than the short-term returns from hunting. We compare the returns from hunting and husbanding strategies as a function of prey body size. Returns from husbanding are estimated using a maximum sustainable yield (MSY) model. Following Charnov (1993), allometric analyses show that the MSY is nearly independent of prey body size. The opportunity costs of husbanding are measured as prey standing biomass times the discount rate. Since standing biomass scales positively with body size, the opportunity costs of husbanding are greater for larger animals. An evolutionary discount rate is estimated following Rogers (1994) to be between 2.4% and 6%. Using these values, the prey body size for which hunting and meat-only husbanding provide the same return is approximately 40kg. Animals greater than 40kg are predicted to be hunted, [animal husbandry, evolutionary ecology, allometry, hunting, Neolithic transition]     

Hunted Woolly Monkeys (Lagothrix poeppigii) Show Threat-Sensitive Responses to Human Presence

Responding only to individuals of a predator species which display threatening behaviour allows prey species to minimise energy expenditure and other costs of predator avoidance, such as disruption of feeding. The threat sensitivity hypothesis predicts such behaviour in prey species. If hunted animals are unable to distinguish dangerous humans from non-dangerous humans, human hunting is likely to have a greater effect on prey populations as all human encounters should lead to predator avoidance, increasing stress and creating opportunity costs for exploited populations. We test the threat sensitivity hypothesis in wild Poeppigi''s woolly monkeys (Lagothrix poeppigii) in Yasuní National Park, Ecuador, by presenting human models engaging in one of three behaviours “hunting”, “gathering” or “researching”. These experiments were conducted at two sites with differing hunting pressures. Visibility, movement and vocalisations were recorded and results from two sites showed that groups changed their behaviours after being exposed to humans, and did so in different ways depending on the behaviour of the human model. Results at the site with higher hunting pressure were consistent with predictions based on the threat sensitivity hypothesis. Although results at the site with lower hunting pressure were not consistent with the results at the site with higher hunting pressure, groups at this site also showed differential responses to different human behaviours. These results provide evidence of threat-sensitive predator avoidance in hunted primates, which may allow them to conserve both time and energy when encountering humans which pose no threat.