The origin of insect thermoregulatory studies.
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Biomedical subjects
Publications and source records attributed to Bernd Heinrich.
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Like other corvids, food-storing ravens protect their caches from being pilfered by conspecifics by means of aggression and by re-caching. In the wild and in captivity, potential pilferers rarely approach caches until the storers have left the cache vicinity. When storers are experimentally prevented from leaving, pilferers first search at places other than the cache sites. These behaviours raise the possibility that ravens are capable of withholding intentions and providing false information to avoid provoking the storers' aggression for cache protection. Alternatively, birds may refrain from pilfering to avoid conflicts with dominants. Here we examined whether ravens adjust their pilfer tactics according to social context and type of competitors. We allowed birds that had witnessed a conspecific making caches to pilfer those caches either in private, together with the storer, or together with a conspecific bystander that had not created the caches (non-storer) but had seen them being made. Compared to in-private trials, ravens delayed approaching the caches only in the presence of storers. Furthermore, they quickly engaged in searching away from the caches when together with dominant storers but directly approached the caches when together with dominant non-storers. These findings demonstrate that ravens selectively alter their pilfer behaviour with those individuals that are likely to defend the caches (storers) and support the interpretation that they are deceptively manipulating the others' behaviour.
Human social behaviour is influenced by attributing mental states to others. It is debated whether and to what extent such skills might occur in non-human animals. We here test for the possibility of ravens attributing knowledge about the location of food to potential competitors. In our experiments, we capitalize on the mutually antagonistic interactions that occur in these birds between those individuals that store food versus those that try to pilfer these caches. Since ravens' pilfer success depends on memory of observed caches, we manipulated the view of birds at caching, thereby designing competitors who were either knowledgeable or ignorant of cache location and then tested the responses of both storers and pilferers to those competitors at recovery. We show that ravens modify their cache protection and pilfer tactics not simply in response to the immediate behaviour of competitors, but also in relation to whether or not they previously had the opportunity of observing caching. Our results suggest that the birds not only recall whom they had seen during caching, but also know that obstacles can obstruct the view of others and that this affects pilfering.
Differing conclusions have been reached as to how or whether varying heat production has a thermoregulatory function in flying honeybees Apis mellifera. We investigated the effects of air temperature on flight metabolic rate, water loss, wingbeat frequency, body segment temperatures and behavior of honeybees flying in transparent containment outdoors. For periods of voluntary, uninterrupted, self-sustaining flight, metabolic rate was independent of air temperature between 19 and 37 degrees C. Thorax temperatures (T(th)) were very stable, with a slope of thorax temperature on air temperature of 0.18. Evaporative heat loss increased from 51 mW g(-1) at 25 degrees C to 158 mW g(-1) at 37 degrees C and appeared to account for head and abdomen temperature excess falling sharply over the same air temperature range. As air temperature increased from 19 to 37 degrees C, wingbeat frequency showed a slight but significant increase, and metabolic expenditure per wingbeat showed a corresponding slight but significant decrease. Bees spent an average of 52% of the measurement period in flight, with 19 of 78 bees sustaining uninterrupted voluntary flight for periods of >1 min. The fraction of time spent flying declined as air temperature increased. As the fraction of time spent flying decreased, the slope of metabolic rate on air temperature became more steeply negative, and was significant for bees flying less than 80% of the time. In a separate experiment, there was a significant inverse relationship of metabolic rate and air temperature for bees requiring frequent or constant agitation to remain airborne, but no dependence for bees that flew with little or no agitation; bees were less likely to require agitation during outdoor than indoor measurements. A recent hypothesis explaining differences between studies in the slope of flight metabolic rate on air temperature in terms of differences in metabolic capacity and thorax temperature is supported for honeybees in voluntary flight, but not under agitation.
The ability to follow gaze (i.e. head and eye direction) has recently been shown for social mammals, particularly primates. In most studies, individuals could use gaze direction as a behavioural cue without understanding that the view of others may be different from their own. Here, we show that hand-raised ravens not only visually co-orient with the look-ups of a human experimenter but also reposition themselves to follow the experimenter's gaze around a visual barrier. Birds were capable of visual co-orientation already as fledglings but consistently tracked gaze direction behind obstacles not before six months of age. These results raise the possibility that sub-adult and adult ravens can project a line of sight for the other person into the distance. To what extent ravens may attribute mental significance to the visual behaviour of others is discussed.
OBJECTIVE: To develop a procedure using a virtual reality (VR) environment that permitted us to simulate the preoperative fitting of an electronic implantable hearing device (IHD) and assess its implantability. MATERIAL AND METHODS: This was an experimental, prospective study based on VR simulations involving the pre- and postoperative comparison of the implantability of an IHD. The preoperative possibility of implanting an IHD in a VR environment was compared with the postoperative implantability of the device in the temporal bones of human cadavers and patients. Study groups were analyzed according to the criteria "VR implantation" and "real surgery" using contingency tables. RESULTS: A computer simulation method based on CT images was developed for the preoperative planning of the implantation. The VR simulation proved feasible in all cases (15 temporal bones and 24 patients). There was no significant difference between the process of implanting the IHD in patients or in the VR environment. These results indicate that VR-based test fittings of an IHD allow prediction of the implantability of an IHD prior to actual surgery. CONCLUSION: We have described the development of a novel VR procedure for predicting the implantability of hearing devices in otoneurosurgical applications. The VR procedure can be applied universally and may also be used for other parts of the body.