Literature DB >> 17874161

Temperatures and locations used by hibernating bats, including Myotis sodalis (Indiana bat), in a limestone mine: implications for conservation and management.

Virgil Brack1.   

Abstract

Understanding temperatures used by hibernating bats will aid conservation and management efforts for many species. A limestone mine with 71 km of passages, used as a hibernaculum by approximately 30,000 bats, was visited four times during a 6-year period. The mine had been surveyed and mapped; therefore, bats could be precisely located and temperatures (T (s)) of the entire hibernaculum ceiling accurately mapped. It was predicted that bats should hibernate between 5 and 10 degrees C to (1) use temperatures that allow a near minimal metabolic rate, (2) maximize the duration of hibernation bouts, (3) avoid more frequent and prolonged arousal at higher temperatures, (4) avoid cold and freezing temperatures that require an increase in metabolism and a decrease in duration of hibernation bouts or that could cause death, and (5) balance benefits of a reduced metabolic rate and costs of metabolic depression. The distribution of each species was not random for location (P < 0.000) or T (s) (P < 0.000). Myotis sodalis (Indiana bat) was most restricted in areas occupied, hibernating in thermally stable yet cold areas (X = 8.4 +/- 1.7 degrees C); 99% associated with cement block walls and sheltered alcoves, which perhaps dampened air movement and temperature fluctuations. Myotis lucifugus (little brown myotis) hibernated in colder, more variable areas (X = 7.2 +/- 2.6 degrees C). Myotis septentrionalis (northern myotis), Pipistrellus subflavus (eastern pipistrelle), and Eptesicus fuscus (big brown bat) typically hibernated in warm, thermally stable areas (X = 9.1 +/- 0.2 degrees C, X = 9.6 +/- 1.9 degrees C, and X = 9.5 +/- 1.5 degrees C, respectively). These data do not indicate that hibernacula for M. sodalis, an endangered species, should be manipulated to cool below 5 degrees C.

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Year:  2007        PMID: 17874161     DOI: 10.1007/s00267-006-0274-y

Source DB:  PubMed          Journal:  Environ Manage        ISSN: 0364-152X            Impact factor:   3.266


  7 in total

Review 1.  Metabolic rate and body temperature reduction during hibernation and daily torpor.

Authors:  Fritz Geiser
Journal:  Annu Rev Physiol       Date:  2004       Impact factor: 19.318

2.  Relationships between body temperature, thermal conductance, Q10 and energy metabolism during daily torpor and hibernation in rodents.

Authors:  G K Snyder; J R Nestler
Journal:  J Comp Physiol B       Date:  1990       Impact factor: 2.200

3.  Reduction of metabolism during hibernation and daily torpor in mammals and birds: temperature effect or physiological inhibition?

Authors:  F Geiser
Journal:  J Comp Physiol B       Date:  1988       Impact factor: 2.200

4.  The effect of temperature on the pattern of torpor in a marsupial hibernator.

Authors:  F Geiser; L S Broome
Journal:  J Comp Physiol B       Date:  1993       Impact factor: 2.200

5.  Torpor, thermal biology, and energetics in Australian long-eared bats (Nyctophilus).

Authors:  F Geiser; R M Brigham
Journal:  J Comp Physiol B       Date:  2000-03       Impact factor: 2.200

Review 6.  The role of energy availability in Mammalian hibernation: a cost-benefit approach.

Authors:  Murray M Humphries; Donald W Thomas; Donald L Kramer
Journal:  Physiol Biochem Zool       Date:  2003 Mar-Apr       Impact factor: 2.247

7.  Effects of temperature on the duration of arousal episodes during hibernation.

Authors:  A R French
Journal:  J Appl Physiol Respir Environ Exerc Physiol       Date:  1982-01
  7 in total
  8 in total

1.  Risk factors associated with mortality from white-nose syndrome among hibernating bat colonies.

Authors:  Aryn P Wilder; Winifred F Frick; Kate E Langwig; Thomas H Kunz
Journal:  Biol Lett       Date:  2011-06-01       Impact factor: 3.703

2.  Drivers of variation in species impacts for a multi-host fungal disease of bats.

Authors:  Kate E Langwig; Winifred F Frick; Joseph R Hoyt; Katy L Parise; Kevin P Drees; Thomas H Kunz; Jeffrey T Foster; A Marm Kilpatrick
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-12-05       Impact factor: 6.237

3.  Improved Analysis of Long-Term Monitoring Data Demonstrates Marked Regional Declines of Bat Populations in the Eastern United States.

Authors:  Thomas E Ingersoll; Brent J Sewall; Sybill K Amelon
Journal:  PLoS One       Date:  2013-06-21       Impact factor: 3.240

4.  Temperature-dependent growth of Geomyces destructans, the fungus that causes bat white-nose syndrome.

Authors:  Michelle L Verant; Justin G Boyles; William Waldrep; Gudrun Wibbelt; David S Blehert
Journal:  PLoS One       Date:  2012-09-28       Impact factor: 3.240

5.  Long-term changes in bat activity in Quebec suggest climatic responses and summer niche partitioning associated with white-nose syndrome.

Authors:  Julie Faure-Lacroix; André Desrochers; Louis Imbeau; Anouk Simard
Journal:  Ecol Evol       Date:  2020-06-02       Impact factor: 2.912

6.  Malassezia vespertilionis sp. nov.: a new cold-tolerant species of yeast isolated from bats.

Authors:  J M Lorch; J M Palmer; K J Vanderwolf; K Z Schmidt; M L Verant; T J Weller; D S Blehert
Journal:  Persoonia       Date:  2018-02-05       Impact factor: 11.051

7.  Body mass and hibernation microclimate may predict bat susceptibility to white-nose syndrome.

Authors:  Catherine G Haase; Nathan W Fuller; Yvonne A Dzal; C Reed Hranac; David T S Hayman; Cori L Lausen; Kirk A Silas; Sarah H Olson; Raina K Plowright
Journal:  Ecol Evol       Date:  2020-12-21       Impact factor: 2.912

8.  The evolution of a bat population with white-nose syndrome (WNS) reveals a shift from an epizootic to an enzootic phase.

Authors:  Craig L Frank; April D Davis; Carl Herzog
Journal:  Front Zool       Date:  2019-12-03       Impact factor: 3.172

  8 in total

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