Feeding activity of the northern bat Eptesicus nilssoni during pregnancy and lactation

Summary Female northern bats emerged at dusk to feed when aerial insect density was 0.1 m^-3 or higher. A model suggests that this is the threshold level above which foraging may be energetically profitable. Insect density was determined mainly by air temperature, and reached the threshold level at 6–10°C. Mean temperature during early summer in six years was correlated with the date of parturition. This suggests that periods when foraging was not energetically profitable were spent in torpor.     

Food habits of northern (Eptesicus nilssoni) and brown long-eared (Plecotus auritus) bats in Sweden

Food habits of sympatric northern and brown long-eared bats were examined by analysis of droppings collected in six maternity roosts of each species. Relatively large, nocturnal flying insects such as moths (Lepidoptera), June-beetles (Coleoptera: Scarabaeidae), crane-flies (Diptera: Tipulidae) and caddis-flies (Trichoptera), were eaten by both bat species, representing 47% (by volume) of the northern and 57% of the long-eared bat's diet. Small dipterans were important food items for the northern bat (47% of the diet) but not for the long-eared bat, which instead consumed large amounts of diurnal or predominantly non-flying taxa such as blow-flies (Diptera: Calliphoridae), earwigs (Dermaptera), spiders (Araneae) and harvestmen (Opiliones) (40% of the diet). The difference in food selection by the two species is probably due to the different foraging strategies used.     

Seasonal use of illuminated areas by foraging northern bats Eptesicus nilssoni

Foraging northern bats Eptesicus nilssoni were monitored from a car along a 27 km line transect in southern Sweden every week during a 14 month period by means of a bat detector. The number of bats observed along the transect was highly correlated with air temperature, and no bats were observed at temperatures < 6°C. Hence, feeding was infrequent in April and May as well as in September and October and did not occur at all from November to March. In summer, the bats were observed in forest and farmland, but in spring and autumn most bats were detected along rows of street-lights. By attracting insects, artificial lights apparently provide local patches of food for some species of bats during periods which may be critical for their survival and reproduction.     

Foraging behaviour and habitat use of the serotine bat (Eptesicus serotinus) in southern England

Radio-tracking was useed to dertermine the foraging behaviour and habitat use of the serotine bat, Eptesicus serotinus , at two roosts in southren England. The basts communted an average of 6.5 km to and from distinct foraging sites and used up ot five sites per night. Serotine foraged in a wide range of habitats and were able to locate and exploit temporary feeding site such as recently mown grass. They foraged regulary arround white streelamps and in alte summer over cattle pasture on which fresh dung was present. Reproductively active females were strongly philopatric to their day-roost. In contrast, reproductively inactive females, from the same roosts. moved to new day-roosts up to 10 km from the site of capture. Serotines used thre distinct foraging strategies, short filight, ground feeding, and, predominantly, aerial hawking. Foraging bouts were interpresed with resting phases, with individuals roosting alone on walls of houses or in trees close to foraging sites. It is concluded that serotines are well adapted to an anthropogenic envioronment. They are strongly philopartric to roosts in human habitations, in close proximity to a range of feeding sites wehre they can take advantage of favourarble land amangement practices.     

Feeding Territoriality in Female Northern Bats,Eptesicus nilssoni

A nursing colony of 26 Northern bats was studied in South-Central Sweden. The foraging behaviour is described with emphasis on social interactions on feeding grounds. The bats foraged in small feeding territories used night after night. The reproducing females defended feeding territories against other colony members as well as non-members by means of aggressive chases and vocalizations. A linear dominance order occurred among the females that regularly visited a feeding site. Intrusions into already occupied feeding sites resulted in territorial conflicts (47 %), passive departure by one or both opponents (43%) or mutual acceptance (11%). Conflicts occurred throughout the summer, but became less frequent in July when insect abundance increased.     

Influence of night length on home range size in the northern bat Eptesicus nilssonii

The northern bat Eptesicus nilssonii is widespread in Fennoscandia, with breeding populations well above the Arctic Circle. I studied this species at its extreme northern limit, at 69°N in Norway. I radio-tracked 17 bats from 2 maternity roosts during 2003–2006 to study the influence of the midnight sun and increasing lengths of darkness on activity (time spent out of roost) and home range size. Activity and home range was highly correlated with night length (light intensity); both increasing progressively with season. Bats were classified into 3 groups based on the time of the season they were tracked (basically July, August and September–October); short activity (average 1.57 h) and small home range (average 0.91 km²), medium activity (3.69 h) and medium-sized home range (4.58 km²), and long activity (4.80 h) and large home range (17.2 km²). Bats visited roosts several times during the night, and the duration of roost visits increased significantly by group. The number of periods out of roost increased from the first to the second group (1.45 vs. 2.36 flight periods per night), but insignificantly to the third group (2.37 flights). The most significant increase in activity and home range was associated with the first flight of juveniles in early August. These bats appeared to have a threshold level of around 1700 lux for activity out of roost, with little difference between light levels at emergence and return (the second group returned in significantly poorer light than they emerged in). Although the northern bat at this extreme latitude had adapted to the ambient light conditions, the bright nights under the midnight sun and the short season strongly reduced their window of opportunity for activity and may possibly reduce survival and reproductive success.     

The diet of the parti-coloured bat Vespertilio murinus in Sweden

Food habits of the parti-coloured bat in southern Sweden were investigated by analysis of fecal samples collected from three maternity roosts used in summer and, in addition, one roost used by a male during the mating season m autumn Small (c 3-10 mm) dipterans dominated all samples, representing 64-82% by volume, but larger flying insects like moths, caddis-flies and dung beetles were also eaten, together representing 14-33% At the family level, midges (Chironomidae) were by far the most common prey items, compnsing 12-67% of the diet The dominance of small prey items in the diet of the parti-coloured bat in Sweden contrasts with other bat species of similar size and foraging habits, but agrees with observations on parti-coloured bats in Ukrama and Poland     

Behavioural Variation in Echolocation Pulses of the Northern Bat,Eptesicus nilssoni

17 northern bats, comprising a maternity colony, were observed and recorded in their natural feeding habitat in southern Sweden. They searched for insects in more or less open habitats, 2–50 m above ground, and usually established individual feeding territories, which were patrolled in straight or slightly curved flight paths at rather constant altitudes. Duration, bandwidth, amplitude, repetition rate and, to a lesser extent, terminal frequency of the echolocation pulses varied according to feeding habitat and situation. In general, long (13.0–17.7 ms), loud, shallow frequency-modulated (FM) signals were used during search flight near treetop level (15 m) or above. At lower altitudes, steep FM-components were added, and the terminal shallow-sweep portions were shortened. These pulses were 6.3–13.4 ms long. Steep FM-signals of short (0.4–8.4 ms) duration and relatively low amplitude were used in the vicinity of obstacles or targets.     

Target-detection by the echolocating bat,Eptesicus fuscus

Summary The long-range echo-detection capabilities of echolocating bats (Eptesicus fuscus) were studied in a two-choice psychophysical procedure.E. fuscus can detect 4.8 mm diameter spheres at a distance of 2.9 m, and 19.1 mm diameter spheres at a distance of 5.1 m. The threshold of echo-detection corresponds to the distance at which a target returns an echo amplitude in the region of 0 dB SPL. The results demonstrate that the maximum effective range of bat sonar is greater than previously indicated by obstacleavoidance and target-interception tasks.     

Vole diet on experimentally managed reforestation areas in northern Sweden

In northern Sweden two field experiments with the reforestation techniques soil scarification, ploughing, burning and grass herbicidal treatment were performed. Small rodents were trapped regularly on the managed plots and their stomachs were examined microscopically for diet composition. Both bank voles Clethrionomys glareolus and field voles Microtus agrestis were common on the reforestation areas while only a small number of grey-sided voles Clethrionomys rufocanus were taken. All three species underwent a population cycle during the studies. The management techniques generally resulted in small and irregular effects on the food selection. The most pronounced changes were lower intake of grasses by M. agrestis after herbicidal treatment and of filamentous tree lichens by C. glareolus after most treatments.
Both bank voles and field voles ate predominantly forbs in the summer half of the year, whereas the field voles took also a considerable amount of grass. As a complement to green vegetable-matter bank voles ate berries and fungi in summer-autumn and tree lichens at other times of the year, but seeds and animals food only in very small amounts. Ail three species consumed large quantities of dwarf-shrubs in autumn and especially in winter. Considerable amounts of bark were eaten by field voles and a smaller proportion by bank voles in autumn-winter.
Both for bank and field voles there were indications of worsening food conditions as the population cycle went on, There were, for example, an increase in grass and bark intake in field voles and a decrease in seeds and berries for the hank vole.     

Retinofugal projections of the big brown bat, Eptesicus fuscus and the neotropical fruit bat, Artibeus jamaicensis

Retinal connections were studied in Eptesicus fuscus and Artibeus jamaicensis using anterograde axonal degeneration and autoradiographic techniques following unilateral enucleations and uniocular injections of radioactive amino acids. Although each retina projected bilaterally to the brainstem, the number of silver grains in the emulsion of autoradiographs indicated that nearly all fibers in the optic nerve entered the contralateral optic tract. Ipsilaterally, a major portion of the projection ended in the suprachiasmatic nucleus; caudal to the suprachiasmatic nucleus, the amount of label was so small that individual silver grains were counted to determine the location and quantity of label in other ipsilateral nuclei. In both species the retinal projection terminated bilaterally in the suprachiasmatic, dorsal lateral geniculate, ventral lateral geniculate, and pretectal olivary nuclei and contralaterally in the posterior pretectal nucleus, superficial gray layers of the superior colliculus, and nuclei of the accessory optic system. In Eptesicus the projection to the nucleus of the optic tract ended contralaterally, and in Artibeus it ended in this nucleus bilaterally. The results of this study revealed a basic theme in the optic projection of the two ecologically different microchiropterans. The results differed, however, in that the projection was larger and visually related nuclei were better developed in Artibeus. Such variations are presumed to relate to eye size and the relative use of vision by the two chiropterans.     

Detection of jitter in intertarget spacing by the big brown bat Eptesicus fuscus

We trained bats to detect intertarget jitter, i.e., relative motion between two virtual (electronically synthesized) targets. Both targets were themselves moving with respect to nearby objects (e.g., the microphone and speaker used to create the virtual targets) so that the only reliable cue available to the bats was variation in intertarget spacing. Given a target at 80 cm and another at 95, 110 or 125 cm, the threshold for intertarget jitter (ITJ) of the two bats tested was <10 μs, corresponding to <1.7 mm of range. When, for one bat, we increased the range instability of the targets by adding varying amounts of random range shift to the target complex (while preserving the correct intertarget spacing), ITJ threshold worsened. When we presented three targets, one of which was jittering, the bat's threshold improved to 0.9 μs (equivalent to 0.16 mm). If no second target was presented, i.e., if the task was to detect jitter added to a single moving target, then bats' jitter threshold was very high (>200 μs). Eptesicus fuscus appears to be very good at detecting changes in intertarget spacing, which might prove valuable for detecting targets moving relative to the background or for constructing a spatial image of a complex environment. Accepted: 7 April 1997     

Thermoregulatory responses to preoptic-anterior hypothalamic heating and cooling in the bat,Eptesicus fuscus

Summary The central nervous control of temperature regulation in the bat, Eptesicus fuscus, was evaluated by heating the preoptic-anterior hypothalamus (PO/AH) of active, unanaesthetized bats. Because bats are metabolically very variable, change in body temperature was used as the criterion of change in heat balance in response to change in brain temperature and change in wing temperature as an indicator of vasomotor changes.Heating the preoptic-anterior hypothalamic area (PO/AH) of the bat Eptesicus fuscus caused an average increase in wing temperature due to vasodilation of 1.0° C and an average increase in body temperature of 0.4° C. Conversely, cooling the PO/AH led to an average decline in wing temperature due to vasoconstriction of 0.9° C and an average decline in body temperature of 0.4° C.Bats were heat-stressed to augment the responsiveness of the PO/AH. Heat-stress alone causes a rise in body temperature and wing temperature. Release from heat stress causes a fall in body temperature and a fall in wing temperature. When the PO/AH is heated following a period of high heat-stress, the body temperature continues to fall but wing temperature reverses its direction of change and rises. When bats are given a low heat-stress and simultaneous heating of the PO/AH, wing temperature rises in response to PO/AH temperature and the body temperature stabilizes. When the PO/AH is cooled in bats under high heat-stress, body temperature stabilizes and wing temperature falls. When bats are cold-stressed, body temperature and wing temperature fall regardless of heating of the PO/AH.These responses are related to the life habits of the bat.It is concluded that the PO/AH of the bat Eptesicus fuscus may be less thermally sensitive than the PO/AH in other vertebrates studied, and that other central nervous structures have acquired an increased thermoregulatory function.We thank Mrs. Ruth Chalmers for her excellent histological preparstions.This work was supported, in part, by National science Foundation grant GB 6303 and GB 13797.     

Ultrastructure of the atrioventricular node of the big brown bat, Eptesicus fucus

This investigation describes the ultrastructure of the atrioventricular node of Eptesicus fuscus. Two conducting cells types (nodal and transitional) are indentified which differ in location, myofibrillar content, and types of intercellular junctions. Centrally located nodal cells display variable staining intensity and contain disorganized myofibrils which rarely form sarcomeres. Desmosomes and nexus-like junctions connect the nodal cells. Transitional cells, situated peripherally, exhibit distinct sarcomeres and are attached to the adjacent cells through desmosomes and underdeveloped intercalated discs. Longitudinal arrangement of the mitochondrial cristae is frequently seen in both cells types. In the connective tissue stroma, numerous capillaries (with micropinocytotic vesicles), axons, and possibly axonal terminals, some filled with vesicles, are observed. A large ganglionated nerve trunk is present on the nodal periphery. True nexuses and neuromuscular junctions are not observed. It is suggested that nodal cell types previously reported in different vertebrates under various names are merely simple variations of the two basic types of conducting cell--nodal and transitional. No interspecific differences are observed between these cells of the big brown bat compared with those in other vertebrates.