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Article

Tree Girdling for Potential Bat Roost Creation in Northwestern West Virginia

AllStar Ecology LLC, 1582 Meadowdale Road, Fairmont, WV 26554, USA
*
Author to whom correspondence should be addressed.
Submission received: 22 November 2021 / Revised: 27 January 2022 / Accepted: 5 February 2022 / Published: 8 February 2022

Abstract

:
Cavity/crevice tree-roosting bats in North America face an uncertain future with many factors impacting their populations. To benefit crevice/cavity roosting bat species, forests are often enhanced with the use of tree girdling. In October 2015, 20 maples, 22 oaks, and 18 hickories were girdled using a method with fell cut and herbicide (frilling) or double-girdling with a chainsaw. From 2016–2021, targeted trees were observed and the tree’s decay state was collected. The average time for trees to display suitable roosting characteristics for frilling trees was 3.23 years while it was 4.46 years for double girdling. The average time frilling trees contained suitable roosting characteristics was 3.20 years while it was 1.63 years for double girdling. The frilling method resulted in a quicker kill of trees than double girdling and frilling trees had suitable roosting characteristics for a longer duration. Frilling was effective killing all three types of trees, while the double girdling was less effective, especially on oaks. When grouping species and treatment in analysis, only average decay states between maple frill and oak double girdling and hickory frill and oak double girdling were significantly different. This evaluation demonstrates that roost tree creation relating to tree species and girdling methodology has a temporal component that should be considered when managing for crevice/cavity bat roosts and multiple habitat creation methods should be used in conjunction with snag creation to provide sustainable bat habitat over longer time periods.

1. Introduction

Crevice/cavity roosting bats rely on trees for roosting, either under loose bark or within cavities [1,2,3,4,5,6,7]. Many tree-roosting bats in eastern North America (including the Indiana (Myotis sodalis Miller and Allen) and northern long-eared bat (Myotis septentrionalis Trouessart) only use caves during hibernation (approximately October–April) with the rest of the year being spent in forests. These same bat species rely on crevice/cavity tree roosts to rear their young during the summer. The maternity roosts provide a thermal advantage to allow their young to grow at faster rates [8] which gives them advantages such as reduced competition and early access to foraging resources. Roosts also provide other advantages such as protection from adverse weather conditions and predators [7].
Although Indiana bats and northern long-eared bats are both cavity/crevice roosters, they differ somewhat in their roost use and selection. Indiana bats prefer roosting underneath exfoliating bark while northern long-eared bats prefer cavities [9,10]. Indiana bats prefer roosts that are larger in diameter and taller than the surrounding stand with greater solar exposure [9,11,12]. Northern bats prefer more heavily shaded roosts in interior forest [13].
Most crevice/cavity roosting bats rely on trees that have progressed to a snag [2,5,6] for desirable roost characteristics to form with live hickory species being an exception [2,7,14]. Once a tree has died, the tree may start to have its bark fall off and/or the tree may start to decay and produce cavities as roosting opportunities. Only a select subset of trees in a particular forest contain these desirable characteristics for bat roosts and these resources are ephemeral [15]. At times, a forest may fall below the desired “optimal” roost density of 14 roosts/acre [16]. Snag creation can aide in keeping desired roost densities.
Snag creation methodology began in the 1970s [17] and was tested mostly in the northwestern United States (Oregon, Washington, Idaho, Montana) with a few studies in the Midwest and Southeast (Michigan, Wisconsin, Florida, Texas, Kentucky) [17,18,19,20,21,22,23,24,25,26,27,28]. Various snag creation techniques have been used including: girdling [19,20,25], fungal inoculation [25,29,30], explosives [25,29], and saw topping [25,31,32].
Girdling is an effective snag creation method. It can create a dead tree having an intact top (in comparison to saw-topping) [17]. Girdling can be used in tandem with other techniques (fungal inoculation and limbing). The safest and most cost effective snag-creation method is girdling [17].
A major gap in snag creation research, especially girdling, concerning cavity/crevice roosting bats is how quickly these targeted trees develop desirable roost characteristics (sloughing bark, cavities) and how long they retain these desirable bat roost characteristics. Very little published research exists on snag creation in West Virginia or in the Northeastern United States in general. Gathering additional data on tree decay states over many years on trees targeted for snag creation would help inform land managers on proper treatment options to aid cavity/crevice tree roosting bat populations in the Northeastern United States.
As populations of cavity/crevice tree roosting bat species in North America continue to decline due to disease and habitat destruction, forest managers and natural resource agencies will be considering these bats in development and management plans moving forward [1]. Decision making entities will need bat conservation measures at their disposal in order to balance economic and wildlife resources. Therefore, documenting and studying potential bat conservation measures should be a priority as information regarding longevity and effectiveness is lacking [7]. Using roost tree decay state data collected at an established bat conservation site in West Virginia, we assessed the effectiveness of two tree girdling methods on three different genera of trees. Our study objectives were: (1) To determine the temporal loss associated with tree girdling methodologies as they relate to replacing bat cavity/crevice roosts; (2) to determine the length of time the girdled trees display desirable cavity/crevice roosting characteristics; and (3) to identify how tree species and treatment methods affect potential roost tree creation.

2. Materials and Methods

2.1. Study Site

The North Fork Hughes River (NFHR) Bat Conservation Site is a 23.6 hectares (20.0 hectares forested) property on a predominately west facing hillside located in Ritchie County, West Virginia (Figure 1). The bats in the state have been hit hard with White Nose Syndrome with dramatic declines in little brown (Myotis lucifugus Le Conte), Indiana, northern long-eared, and tri-colored bats (Perimyotis subflavus Cuvier) and the area provides much needed permanent habitat for the species [33]. The site along with the adjoining acreage is mostly forested with hay fields present in large bottomlands adjacent to the property. NFHR and a perennial tributary Goose Run runs within and adjacent to the property that places it upon a connecting corridor to other landscape features. The site is composed of moderately xeric, deciduous forest (Quercus spp. Linnaeus, Carya spp. Nutt., Pinus spp. Linnaeus, and Liriodendron tulipifera Linnaeus) with elevations ranging from 220–299 m. Bottomlands contained boxelder (Acer negundo Linnaeus) and American sycamore (Platanus occidentalis Linnaeus). NFHR is of moderate slope with approximately 60% of the site’s hillsides ranging from 0–35°. Resident bats species include: northern long-eared bat, silver-haired bat (Lasionycteris noctivagans Le Conte), Indiana bat, little brown bat, big brown bat (Eptesicus fuscus Palisot de Beauvois), eastern red bat (Lasiurus borealis Müller), eastern small-footed bat (Myotis leibii Audubon and Bachman), hoary bat (Lasiurus cinereus Palisot de Beauvois), and tricolored bat. The study area on average receives 113.7 cm of rain and averages 11°Celcius (C) [34].

2.2. Tree Girdling

Trees selected for girdling were based on two factors: (1) species and (2) diameter at breast height (DBH). Targeted trees were ≥20.32 cm DBH [35]. Black oak (Quercus velutina Lam.), red oak (Quercus rubra Linnaeus), white oak (Quercus alba Linnaeus), chestnut oak (Quercus prinus Willd.), pignut hickory (Carya glabra Mill.), mockernut hickory (Carya tomentosa Lam. Ex Pior.), shagbark hickory (Carya ovata Mill.), and red maple (Acer rubrum Linnaeus) trees were species chosen to be girdled. Ten groups of six trees (sixty trees total) were selected for girdling (Table 1). Half of the trees of each genus chosen were randomly selected for one of two girdling treatments: frilling or double chainsaw (Figure 2).

2.2.1. Frilling

This girdling technique involves applying herbicide after a single line of hatchet cuts has been made around the trunk of the tree [36,37] (Figure 2). A 50:50 mix of 41% glyphosate was used as the herbicide.

2.2.2. Double Chainsaw Girdling

To create a snag using double chainsaw (DC) girdling, one uses a chainsaw to cut parallel, horizontal grooves through the bark several inches apart [37] (Figure 2).
After treatment in October 2015, we visited trees once in fall of the following years (2016–2021) and we categorized trees into a roost decay state [35] that ranged from 1–9 (Figure 3).

2.3. Decay States

Trees were considered to have roosting potential if they contained cavities or sloughing bark (roost decay states 4–6). The United States Fish and Wildlife Service’s Indiana Bat Survey Guidelines contains roost decay states and are utilized for classifying Indiana bat roost trees that are found via radio telemetry and for identifying potential Indiana bat habitat [35].

2.4. Data Analysis

Trees were categorized into their respective genus in data analysis due to sample size. Categories in data analysis included: maples treated via DC, maples treated via frilling, hickories treated via DC, hickories treated via frilling, oaks treated via DC, and oaks treated via frilling. We assessed differences between years, species, and treatments relating to decay states with Kruskal–Wallis test and then followed with a post-hoc Games–Howell test for evaluation of treatments and species groups. Descriptive statistics were run on decay state. Statistical significance was accepted at α = 0.05.

3. Results

Decay states declined during the years (H = 183.993, d.f. = 5, p value < 0.001; Table 2; Table S1). Mean decay states started at 2.5 in 2016 and ended at 5.9 in 2021. No trees reached the sloughing bark state (4) until 2017 with a maximum number of trees (42) reaching this state in 2019.
Decay states differed between treatments from 2016–2021 (H = 17.457, d.f. = 1, p value < 0.001). The mean decay state of double chainsaw trees was 3.71 compared to frilled trees with a mean decay state of 4.01. All frilled trees were in at least the declining state by 2017 while some double chainsaw trees were still in the live stage.
Between the six groups of treatments/species from 2016–2021, decay states differed (H = 19.738, d.f. = 5, p value = 0.001). However, only average decay state between two treatments/genera groups (1-maple frill and oak DC 2-hickory frill and oak DC) had close to one average decay stage of difference (Table 3 and Table 4). These were only treatments/species groups (1. maple frill and oak DC 2. hickory frill and oak DC) that had significant differences in average decay stages.
Tree species decay states varied between treatments within maples and oaks (maple: H = 5.624, d.f. = 1, p value = 0.018; oak: H = 9.643, d.f. = 1, p = 0.002). There was no significant difference in treatment types and roost decay state in hickories (hickory: H = 2.264, d.f. = 1, p value = 0.132). Across all species, decay state was greater in frilled trees than DC trees from 2016–2019. However, in 2020–2021 DC treatment trees exceeded frilled trees in average decay state (Figure 4).
The average length of time both treatments contained suitable bat roost characteristics (sloughing bark, cavities, decay state 4–6) was 3.2 years for frilling and 1.63 years for DC.

4. Discussion

Based on our results, frilled trees decayed at a faster rate initially than DC trees (Table 2). This is in agreement with previous studies on snag decay methods [25,26,38]. Most frilled trees died within the first year after treatment while it took some DC trees almost five years to reach the same decay state. However, the mean decay state in DC trees in 2020–2021 exceeded that of frilled trees due mostly to these trees falling over and rapidly increasing their decay state.
When data collection took place in October 2021, 43% of the trees had already fallen or had significant pieces fall off (decay states 7–9) and desirable roosting characteristics only lasted on average 1.63–3.2 years between both treatments. This is in contrast to a study on Douglas-fir snags that can remain standing for ≥25 years [18]. It appears these species of hardwoods in West Virginia do not remain standing long once killed and are much more ephemeral in nature than Douglas-fir snags. Perhaps selection of larger diameter trees would help the longevity of the snag [27]. Snag retention was similar to a study done in California conifers where most snags fell after 8 years [39]. Based on our current average decay state over time for experimental trees, forest managers in the Northeastern United States may need to continue supplementation of forests with newly created snags to keep roost trees at appropriate availability levels.
It took approximately four years after treatment for most trees to become potential bat roosts (decay states 4–6, sloughing bark, cavities). This should be considered by forest managers and agency regulators especially if trees are being girdled as a conservation measure for bats to offset tree clearing activities are needed immediately. Artificial roosts can serve as immediate replacements for lost natural roosts and have been proven to be an effective conservation tool and can be used as a temporal stop-gap until girdled trees become suitable habitat [40,41,42,43,44,45]. However, care needs to be taken in order for the artificial roosts to be appropriately chosen and deployed [46].
Oaks were the most resilient species when girdled (Average Decay State: Oak = 4.5; Maple = 6.55; Hickory = 7). Other studies [22,47] found decay states over time were species specific. Oaks took the longest to progress through decay stages. This should be considered by forest managers in the region as oaks are a common tree species. A mixture of faster decaying tree species (Acer spp.) and slower decaying trees species (Quercus spp.) will help cover a larger temporal space where roosts will be available.
Our study is in line with previous research that cites 84% [22] of girdled trees within 4.5 years in Wisconsin died and 31 out of 75 snags (43%) being downed after 4 years in Texas [48]. Our study found 97% of DC trees to die within 5 years (in line with the Wisconsin study) and 33% of total treated trees to be down within 5 years (similar to the Texas study). Both Wisconsin and Texas studies used similar DBH selection criteria as ours (≥25.4 cm).
Knowing that DC treated trees took longer to decay and that oaks were the slowest to decay can help increase snag retention in oak-maple-hickory dominated forests which can be found in the Northeast and Midwest United States.
All treated trees produced desirable bat roost tree characteristics such as sloughing bark and/or cavities which are necessary for eastern United States cavity/crevice tree roosting bats (such as the Indiana and northern long-eared bat) during the summer reproductive period [1,2,6,7,11,13,14,15,16,49]. These girdling methods can be used across the range of any cavity/crevice tree roosting bats to increase roosting availability. Using these techniques can help provide much needed roosting habitat for cavity/crevice tree roosting species as development continues to decrease available forested habitat.

5. Conclusions

When creating snags as potential bat roosts, it would be advisable for land managers to use both girdling treatments and various tree species as it will leave more snags on the landscape for a longer period of time. It appears snags will need to be replenished in deciduous Northeastern United States forests approximately every eight years, as it takes on average four years for native trees to display desirable roosting characteristics for cavity/crevice roosting bats, and then they only last in this state for 1–4 years.

Supplementary Materials

The following supporting information can be downloaded at: www.mdpi.com/article/10.3390/f13020274/s1, Table S1: NFHR PRT Creation Evaluation Results_20211122_ForSubmission.xlsx.

Author Contributions

E.S.S. drafted the first version of the manuscript. R.L.W. conceptualized the study and created the methodology; data analysis, E.S.S.; data collection, R.L.W. and E.S.S.; writing—review and editing, E.S.S. and R.L.W.; supervision, R.L.W.; project administration, R.L.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding. It was funded by AllStar Ecology LLC to improve its work and practices in the Mid-Atlantic Region.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

We thank all the employees at AllStar Ecology LLC that helped create our experimental snag areas and assisted in data collection.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Silvis, A.; Perry, R.; Ford, W.M. Relationships of Three Species of Bats Impacted by White-Nose Syndrome to Forest Condition and Management; U.S. Department of Agriculture, Forest Service, Southern Research Station: Asheville, NC, USA, 2016; p. SRS-GTR-214.
  2. Timpone, J.C.; Boyles, J.G.; Murray, K.L.; Aubrey, D.P.; Robbins, L.W. Overlap in Roosting Habits of Indiana Bats (Myotis sodalis) and Northern Bats (Myotis septentrionalis). Am. Midl. Nat. 2010, 163, 115–123. [Google Scholar] [CrossRef]
  3. Rabe, M.J.; Morrell, T.E.; Green, H.; deVos, J.C.; Miller, C.R. Characteristics of Ponderosa Pine Snag Roosts Used by Reproductive Bats in Northern Arizona. J. Wildl. Manag. 1998, 62, 612. [Google Scholar] [CrossRef]
  4. Perry, R.W.; Thill, R.E. Roost selection by male and female northern long-eared bats in a pine-dominated landscape. For. Ecol. Manag. 2007, 247, 220–226. [Google Scholar] [CrossRef]
  5. Cryan, P.M.; Bogan, M.A.; Yanega, G.M. Roosting habits of four bat species in the Black Hills of South Dakota. Acta Chiropterologica 2001, 3, 43–52. [Google Scholar]
  6. Waldien, D.L.; Hayes, J.P.; Arnett, E.B. Day-Roosts of Female Long-Eared Myotis in Western Oregon. J. Wildl. Manag. 2000, 64, 785. [Google Scholar] [CrossRef]
  7. Humphrey, S.R.; Richter, A.R.; Cope, J.B. Summer Habitat and Ecology of the Endangered Indiana Bat, Myotis sodalis. J. Mammal. 1977, 58, 334–346. [Google Scholar] [CrossRef]
  8. Racey, P.A. Ecology of Bat Reproduction. In Ecology of Bats; Springer: Boston, MA, USA, 1982; pp. 57–104. ISBN 978-0-306-40950-9. [Google Scholar]
  9. Carter, T.C.; Feldhamer, G.A. Roost tree use by maternity colonies of Indiana bats and northern long-eared bats in southern Illinois. For. Ecol. Manag. 2005, 219, 259–268. [Google Scholar] [CrossRef]
  10. Callahan, E.V.; Drobney, R.D.; Clawson, R.L. Selection of summer roosting sites by Indiana bats (Myotis sodalis) in Missouri. J. Mammal. 1997, 78, 818–825. [Google Scholar] [CrossRef]
  11. Watrous, K.S.; Donovan, T.M.; Mickey, R.M.; Darling, S.R.; Hicks, A.C.; Oettingen, S.L.V. Predicting Minimum Habitat Characteristics for the Indiana Bat in the Champlain Valley. J. Wildl. Manag. 2006, 70, 1228–1237. [Google Scholar] [CrossRef]
  12. Kurta, A.; Kennedy, J. The Indiana Bat: Biology and Management of an Endanagered Species; Bat Conservation International: Austin, TX, USA, 2002. [Google Scholar]
  13. Foster, R.W.; Kurta, A. Roosting Ecology of the Northern Bat (Myotis septentrionalis) and comparisions with the endangered Indiana bat (Myotis sodalis). J. Mammal. 1999, 80, 659–672. [Google Scholar] [CrossRef]
  14. Schroder, E.S.; Ekanayake, D.B.; Romano, S.P. Indiana bat maternity roost habitat preference within Midwestern United States upland Oak-Hickory (Quercus-Carya) forests. For. Ecol. Manag. 2017, 404, 65–74. [Google Scholar] [CrossRef]
  15. Gardner, J.E.; Garner, J.D.; Hofman, J.E. Summer Roost Selection and Roosting Behavior of Myotis sodalis, Indiana Bat, in Illinois; Illinois Natural History Survey: Champaign, IL, USA, 1991; p. 56. [Google Scholar]
  16. Carter, T.C. Summer habitat use of roost trees by the endangered Indiana bat (Myotis sodalis) in the Shawnee National Forest of Southern Illinois. Ph.D. Thesis, Southern Illinois University, Carbondale, IL, USA, 2003. [Google Scholar]
  17. Lewis, J.C. Creating Snags and Wildlife Trees in Commercial Forest Landscapes. West. J. Appl. For. 1998, 13, 97–101. [Google Scholar] [CrossRef] [Green Version]
  18. Barry, A.M.; Hagar, J.C.; Rivers, J.W. Long-term dynamics and characteristics of snags created for wildlife habitat. For. Ecol. Manag. 2017, 403, 145–151. [Google Scholar] [CrossRef]
  19. Conner, R.N.; Dickson, J.G.; Locke, B.A. Herbicide-Killed Trees Infected by Fungi: Potential Cavity Sites for Woodpeckers. Wildl. Soc. Bull. 2006, 9, 308–310. [Google Scholar]
  20. McComb, W.C.; Rumsey, R.L. Characteristics and Cavity-Nesting Bird Use of Picloram-Created Snags in the Central Appalachians. South. J. Appl. For. 1983, 7, 34–37. [Google Scholar] [CrossRef]
  21. Rose, C.L.; Marcot, B.G.; Mellen, T.K.; Ohmann, J.L.; Waddell, K.L.; Lindley, D.L.; Schreiber, B. Decaying Wood in Pacific Northwest Forests: Concepts and Tools for Habitat Management. In Wildlife-Habiat Relationships in Oregon and Washington; Oregon State University Press: Corvallis, OR, USA, 2001; pp. 580–621. ISBN 0-87071-488-0. [Google Scholar]
  22. Fassnacht, K.S.; Steele, T.W. Snag dynamics in northern hardwood forests under different management scenarios. For. Ecol. Manag. 2016, 363, 267–276. [Google Scholar] [CrossRef] [Green Version]
  23. Weiss, S.A.; Corace, R.G.; Toman, E.L.; Herms, D.A.; Goebel, P.C. Wildlife implications across snag treatment types in jack pine stands of Upper Michigan. For. Ecol. Manag. 2018, 409, 407–416. [Google Scholar] [CrossRef]
  24. Thomas, J.W. Wildlife Habitats in Managed Forests the Blue Mountains of Oregon and Washington; Forest Service: Portland, OR, USA, 1979; p. 512.
  25. Bull, E.L.; Partridge, A.D. Methods of Killing Trees for Use by Cavity Nesters. Wildl. Soc. Bull. 1986, 14, 5. [Google Scholar]
  26. Hallett, J.G.; Lopez, T.; O’Connell, M.A.; Borysewicz, M.A. Decay Dynamics and Avian Use of Artificially Created Snags. Northwest Sci. 2001, 75, 9. [Google Scholar]
  27. Russell, R.E.; Saab, V.A.; Dudley, J.G.; Rotella, J.J. Snag longevity in relation to wildfire and postfire salvage logging. For. Ecol. Manag. 2006, 232, 179–187. [Google Scholar] [CrossRef]
  28. Arno, S.F.; Harrington, M.G.; Fiedler, C.E.; Carlson, C.E. Restoring Fire-Dependent Ponderosa Pine Forests in Western Montana. Ecol. Restor. 1995, 13, 32–36. [Google Scholar] [CrossRef]
  29. Bull, E.; Patridge, A.; Williams, W. Creating Snags with Explosives; USDA Forest Service: LaGrande, OR, USA, 1991; p. 4.
  30. Carey, A.B.; Sanderson, H.R. Routing to Accelerate Tree-Cavity Formation. Wildl. Soc. Bull. 2006, 9, 14–21. [Google Scholar]
  31. Bull, E.L.; Partridge, A.D. Trees and Logs Important to Wildlife in the Interior Columbia River Basin; USDA Forest Service: LaGrande, OR, USA, 1997; p. 55.
  32. Chambers, C.L.; Carrigan, T.; Sabin, T.E.; Tappeiner, J.; McComb, W.C. Use of Artificially Created Douglas-Fir Snags by Cavity-Nesting Birds. West. J. Appl. For. 1997, 12, 93–97. [Google Scholar] [CrossRef] [Green Version]
  33. Stihler, C. State Update: West Virginia; The Northeast Bat Working Group: State College, PA, USA, 2019. [Google Scholar]
  34. US Climate Data Climate Harrisville-West Virginia. Available online: https://www.usclimatedata.com/climate/harrisville/west-virginia/united-states/uswv1-0 (accessed on 21 November 2021).
  35. United States Fish and Wildlife Service Range-Wide Indiana Bat Survey Guidelines. Available online: https://www.fws.gov/midwest/endangered/mammals/inba/surveys/pdf/FINAL%20Range-wide%20IBat%20Survey%20Guidelines%203.23.20.pdf (accessed on 1 November 2021).
  36. Neitro, W.A.; Binkley, V.W.; Cline, S.P.; Mannan, R.W.; Marcot, B.G.; Taylor, D.; Wagner, F.F. Snags (wildlife trees). In Management of Wildlife and Fish Habitats in Forests of Western Oregon and Washington; USDA Forest Service Pulication: Portland, OR, USA, 1985; pp. 129–169. [Google Scholar]
  37. Kilroy, B.; Windell, K. Tree Girdling Tools; USDA Forest Service: Missoula, MT, USA, 1999; pp. 1–4.
  38. Parks, C.G.; Conklin, D.A.; Bednar, L.; Maffei, H. Woodpecker Use and Fall Rates of Snags Created by Killing Ponderosa Pine Infected with Dwarf Mistletoe; United States Department of Agriculture, Forest Service, Pacific Northwest Research Station: Portland, OR, USA, 1999; p. 11.
  39. Ritchie, M.W.; Knapp, E.E.; Skinner, C.N. Snag longevity and surface fuel accumulation following post-fire logging in a ponderosa pine dominated forest. For. Ecol. Manag. 2013, 287, 113–122. [Google Scholar] [CrossRef]
  40. Cruz, J.L.D.L.; Ward, R.L.; Schroder, E.S. Landscape Characteristics Related to Use of Artificial Roosts by Northern Long-Eared Bats in North-Central West Virginia. Northeast. Nat. 2018, 25, 487–501. [Google Scholar] [CrossRef]
  41. Mering, E.D.; Chambers, C.L. Artificial roosts for tree-roosting bats in northern Arizona. Wildl. Soc. Bull. 2012, 36, 765–772. [Google Scholar] [CrossRef]
  42. Ritzi, C.M.; Everson, B.L.; Whitaker, J.O. Use of Bat Boxes by a Maternity Colony of Indiana Myotis (Myotis sodalis). Northeast. Nat. 2005, 12, 217–220. [Google Scholar] [CrossRef]
  43. Adams, J.; Gumbert, M.; Sewell, P.; Roby, P.; Schwierjohann, J. BrandenBarkTM: Artificial Bark Designed for Roost Use by Indiana Bats (Myotis sodalis). J. Am. Soc. Min. Reclam. 2013, 4, 15. [Google Scholar]
  44. Hoeh, J.P.S.; Bakken, G.S.; Mitchell, W.A.; O’Keefe, J.M. In artificial roost comparison, bats show preference for rocket box style. PLoS ONE 2018, 13, e0205701. [Google Scholar] [CrossRef]
  45. Brittingham, M.C.; Williams, L.M. Bat Boxes as Alternative Roosts for Displaced Bat Maternity Colonies. Wildl. Soc. Bull. 2000, 28, 197–207. [Google Scholar]
  46. Crawford, R.D.; O’Keefe, J.M. Avoiding a conservation pitfall: Considering the risks of unsuitably hot bat boxes. Conserv. Sci. Pract. 2021, 3, 1–8. [Google Scholar] [CrossRef]
  47. Corace, R.G.; Stout, A.T.; Goebel, P.C.; Hix, D.M. Snag Benchmarks and Treatment Options for Mixed-Pine Forest Restoration in Eastern Upper Michigan: Snags and Mixed-Pine Restoration. Restor. Ecol. 2013, 21, 608–616. [Google Scholar] [CrossRef]
  48. Dickson, J.G.; Conner, R.N.; Williamson, J.H. Snag Retention Increases Bird Use of a Clear-Cut. J. Wildl. Manag. 1983, 47, 799. [Google Scholar] [CrossRef]
  49. Lacki, M.J.; Hayes, J.P.; Kurta, A. Bats in Forests; The John Hopkins University Press: Baltimore, MD, USA, 2007. [Google Scholar]
Figure 1. A view of North Fork Hughes River Bat Conservation Site.
Figure 1. A view of North Fork Hughes River Bat Conservation Site.
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Figure 2. A view of tree girdling techniques after application: (a) Frilling (b) DC.
Figure 2. A view of tree girdling techniques after application: (a) Frilling (b) DC.
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Figure 3. Roost decay states and their corresponding numbers and representative condition [35].
Figure 3. Roost decay states and their corresponding numbers and representative condition [35].
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Figure 4. Average decay state of both treatment types over time. The rectangle encompasses the time period where trees are in a decay state that could produce potential bat roosts.
Figure 4. Average decay state of both treatment types over time. The rectangle encompasses the time period where trees are in a decay state that could produce potential bat roosts.
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Table 1. Treatment types and tree species.
Table 1. Treatment types and tree species.
Genus/Treatment TypeNumber of Trees
Maple DC10
Maple Frill10
Hickory DC9
Hickory Frill9
Oak DC11
Oak Frill11
Table 2. Percent kill * of each treatment/species group.
Table 2. Percent kill * of each treatment/species group.
Treatments* 2016* 2017* 2018* 2019* 2020* 2021
Maple DC0%0%0%63%100%100%
Maple Frill80%90%90%90%100%100%
Hickory DC11%56%67%89%100%100%
Hickory Frill89%89%100%100%100%100%
Oak DC27%45%91%91%91%91%
Oak Frill91%91%100%100%100%100%
* kill is indicated by decay state 3 or greater.
Table 3. Games Howell Test output on species/treatment.
Table 3. Games Howell Test output on species/treatment.
Group 1Group 2MeanStandard Errorq-Statdfq-CritLowerUpperp-ValueMean-Crit
Maple frillOak frill0.550.183.0984.34.12−0.181.270.250.73
Maple frillHickory frill0.020.230.09111.54.10−0.910.9510.93
Maple frillMaple DC0.110.290.39101.114.10−1.091.320.991.21
Maple frillOak DC0.940.204.72111.104.100.121.750.010.81
Maple frillHickory DC0.370.281.2995.834.11−0.791.520.941.16
Oak frillHickory frill0.570.183.2075.784.13−0.161.300.220.73
Oak frillMaple DC0.430.261.6769.994.14−0.631.500.841.07
Oak frillOak DC0.390.142.80110.324.10−0.180.970.350.57
Oak frillHickory DC0.180.240.7464.204.15−0.831.190.991.01
Hickory frillMaple DC0.140.300.4799.874.10−1.071.350.991.21
Hickory frillOak DC0.960.204.81101.484.100.141.780.010.82
Hickory frillHickory DC0.390.281.3794.494.11−0.771.550.921.16
Maple DCOak DC0.830.273.0185.184.12−0.301.950.281.13
Maple DCHickory DC0.250.340.73111.994.10−1.141.640.991.39
Oak DCHickory DC0.580.262.2079.754.12−0.501.650.621.07
Table 4. Descriptive statistics per treatment/genera from 2016–2021.
Table 4. Descriptive statistics per treatment/genera from 2016–2021.
GroupMeanSizeVariance
Maple Frill4.20603.08
Oak Frill3.65660.75
Hickory Frill4.22542.82
Maple DC4.08607.33
Oak DC3.26661.86
Hickory DC3.83545.84
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Schroder, E.S.; Ward, R.L. Tree Girdling for Potential Bat Roost Creation in Northwestern West Virginia. Forests 2022, 13, 274. https://0-doi-org.brum.beds.ac.uk/10.3390/f13020274

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Schroder ES, Ward RL. Tree Girdling for Potential Bat Roost Creation in Northwestern West Virginia. Forests. 2022; 13(2):274. https://0-doi-org.brum.beds.ac.uk/10.3390/f13020274

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Schroder, Eric S., and Ryan L. Ward. 2022. "Tree Girdling for Potential Bat Roost Creation in Northwestern West Virginia" Forests 13, no. 2: 274. https://0-doi-org.brum.beds.ac.uk/10.3390/f13020274

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