Back |Home |Site Navigation | Tell a Friend

 

 
Update on the Short-tailed bat translocation (31 May 2005 )
 
Introduction
Research has been undertaken to study aspects of the translocation of 20 short-tailed bats from the Tararua Ranges to Kapiti Island. Fieldwork has occurred in two stages: (1) a pre-release assessment of habitat quality and a survey for an existing population of short-tailed bats, and (2) post-release monitoring to confirm that the bats have remained on the island, to monitor their use of the aviary, supplementary food, and use of the natural environment, and to assess their post-release condition.


Pre-release fieldwork - Survey for an existing population of short-tailed bats

Automatic bat monitoring boxes (ABMs) were used to listen for short-tailed bat echolocation calls. These were placed in eight locations throughout the forest in areas considered most likely to be used by bats, and recorded a total of 48 rain free ABM nights, from which no bat passes were recorded.

Habitat quality assessment

  • Roost availability; Trees were randomly sampled in the major tracts of forest on the island, both in a random sample of all trees and in a survey targeting the small proportion of older, larger trees that survived fires that destroyed most forest in the mid 1800s. These latter trees are likely to provide the highest quality roosts for short-tailed bats.
    Trees were characterized according to parameters known to affect roost selection, and all cavities below 2 m height counted and measured.
    Although data have not yet been analysed, Kapiti seems to provide quality roosting habitat, with 6% of all trees having at least one cavity below 2 m, 79% of old trees having at least one cavity below 2 m, and old trees present at a density of 2.4 trees per ha.
  • Food availability; The insect fauna was sampled in the island’s two main tracts of forest to identify taxa known to be eaten by the bats. Pitfall traps and flight intercept traps were used to sample terrestrial and flying insects respectively. Insects were sampled over three two week periods, in November, February and May. These samples are yet to be processed.
  • Five plant taxa are also known components of the bats’ diet: rewarewa, kiekie, Metrosideros, Collospermum, and Leptospermum (Lloyd, 2001). The availability of these plants was assessed by noting presence or absence within 5 m of 108 random sampling points through the forest
    Leptospermum was not found, however all other taxa were abundant, with the least common still present at 18 % of sampling points


Post-release monitoring-
Confirmation the bats remained on the island

  • Telemetry; On the day of release six bats were caught and weighed, and transmitters fitted on the two heaviest individuals. Their presence on the island was confirmed by locating their roosts during the day and by radiotracking around the aviary area at night. Both bats were located for the first four days after release. However, on the fifth day and on four subsequent nights one bat could not be found. It is uncertain whether this represents transmitter failure, mortality, dispersal out of the aviary area, or dispersal off the island.
  • Roost entry / exit counts; A lower limit of the number of bats remaining on the island was achieved using an infra red video camera to record aviary entrances and exits each night. An inability to mark individuals prevented recording the absolute number of individuals using the aviary, however a minimum number was given by the maximum number of bats inside the aviary at one time. Most night’s videos have not been watched, however on the most recently watched video (night of May 24th) at least seven bats used the aviary.
  • Harp trapping In an attempt to more accurately establish a lower limit of the number of bats remaining on the island, harp trapping was undertaken three weeks after release. A harp trap was set up 20 m from the aviary, and captured individuals marked by clipping a patch of fur from their backs. Two bats were caught on the third night of trapping, and when these same individuals were recaught on the sixth night trapping was discontinued to minimise disturbance to the bats. No other bats were caught during the trapping period.

Aviary use, supplementary food use, and use of the natural environment
The aviary remained open to the bats following release, with mealworms and honey water provided ad libitum in the same manner as pre-release. Aviary use was monitored by nightly entry / exit counts, and weights of mealworms and honey water consumed each night were recorded to monitor supplementary food use. Radiotracking at night provided individual level information on aviary use and on movements outside the aviary, while daytime radiotracking was used to locate roosts. Roost boxes placed outside the aviary were monitored for use.
Aviary use
The number of bats day-roosting in the aviary has fluctuated between zero and seven bats since release, although recently there has been a tendency for no bats to use the aviary (figure 1). It is unknown whether only a subset of the same seven bats is using the aviary as a day-roost.

Supplementary food use;Supplementary food consumption has declined since release to roughly one third the pre-release means (figure 2). However since the absolute number of bats using the aviary is unknown it cannot be determined if the amount consumed is a reflection of many bats foraging for wild food and eating a small amount of supplementary food, or if it is a small number of bats relying heavily on supplementary food.
This should be elucidated by analysis of faecal samples collected daily from the aviary, where insect parts will be identified to determine the proportions of different orders present in the faeces. This will indicate the proportion of wild food consumed by the bats.

Nightly movements; Five bats have been fitted with transmitters since release, with the last signal lost 21st May. Four of these bats have been radiotracked at night for 2 – 7 nights each. Due to the rugged terrain and speed of flying bats it was not possible to follow bats throughout their nightly ranges. Radiotracking was confined to the area of flat ground surrounding the aviary. Transmitters placed in known locations suggested bats could be detected up to a distance of ca. 500 m from the aviary.

Three bats commuted quickly into and out of the aviary area, with telemetry signals rapidly being lost when bats left the aviary. Vanishing bearings for individual bats were similar each night, suggesting individuals were visiting the same areas each night, however each bat seemed to commute to a different area.
It is uncertain whether these bats were commuting to foraging areas or to night roosts.

The fourth bat remained in the area of signal reception for most of the time, with the majority of fixes successfully obtained over the seven nights he was followed. Many of these fixes showed fluctuations in signal strength characteristic of the rapid turning of foraging flight.

Day roosts ; Telemetry was also used to follow bats to roosts during the day. Bats roosted out of the aviary on 19 occasions, and were successfully tracked to roost trees on 10 of these. Five individual roost trees were found. These trees are yet to be characterized, but will be compared with trees sampled in the pre-release habitat assessment to identify elements of roost tree selection.

Four roost boxes that had been in the aviary during the captive period were placed on trees ca. 10 – 40 m from the aviary prior to release. No roost boxes have shown any evidence of use since release, although it should be noted that (1) bats did not roost in these particular boxes during captivity, and (2) bird roost boxes are common throughout the forested parts of the island, and these may have been used instead. No bats fitted with transmitters were tracked to roost boxes.

Post release condition

Few bats have been caught and weighed since release to minimise stress, so little information is available on their current condition. Bats that have been caught have either been taken directly from the aviary or harp trapped near the aviary (see above). Weights are summarised in Table 1.
Post-release weights were similar to pre-release, although one bat weighed on April 17th and two on May 11th were lighter than the lightest bat weighed on April 1st, showing some bats have lost weight since release.
In two cases it was possible to track the weight changes of bats fitted with transmitters, as these individuals could be identified by shaved backs. A female weighing 15 g on release night decreased to 14 g on April 17th and 11 g on May 11th. A male weighing 13.5 g on May 11th may have been either a 16g male tagged on release night or a 15.5 g male tagged on April 17th. It seems likely that transmitters contributed to weight loss in these cases. If so, weights taken on May 11th were skewed by this, as two of the three bats had been tagged.

Future plans

The objective from now on is to assess the success of the translocation beyond confirming that the bats remained on the island, by measuring bodyweight changes through time and if possible getting an indication of reproduction.

If the bats continue to visit the aviary throughout the year this will provide an opportunity for capture, either by harp trapping outside the aviary or by taking day roosting bats from the aviary. This will probably occur once every two months until December. If bats do not use the aviary harp trapping or mist netting may be attempted in the forest, however judging by the success of harp trapping so far this is unlikely to be successful.

Captured bats will be weighed and the reproductive condition of the females classified, although short-tailed bats may not breed in their first year. Male reproductive singing may still occur, and may be an indicator of reproductive condition. Singing begins in September (Lloyd, 2001), and will be surveyed for by walking the forest at night.

Lastly, insects will be sampled for a final two week period in August

Top