Regional moose (Alces alces) responses to forestry cutblocks are driven by landscape-scale patterns of vegetation composition and regrowth

https://doi.org/10.1016/j.foreco.2020.118763Get rights and content

Highlights

  • The influence of forestry cutblocks on moose (Alces alces) differs across systems.

  • Moose use and selection of cutblocks is influenced by successional stage.

  • Vegetation composition and regrowth drive regional moose responses to cutblocks.

  • Moose populations might tolerate more intense logging in more productive areas.

  • Managers should consider vegetation composition and regrowth in forestry planning.

Abstract

Forestry activities are globally widespread and can have a large positive or negative influence on wildlife. Wildlife responses to forestry cutblocks (defined areas where trees were harvested) vary as a function of forest succession, which differs across systems. Across their distribution, moose (Alces alces) and forestry are often closely associated. Moose are predicted to select for cutblocks because of greater browse quantity in early successional vegetation, but moose responses to cutblocks are inconsistent across studies. Our objective was to compare moose spatial responses to cutblocks as a function of year since cut between study areas (Prince George South [PGS] and Bonaparte [BP]) while considering differences in vegetation composition and regrowth to better inform forestry planning in British Columbia, Canada. We characterized cutblocks by dominant tree species as a proxy for vegetation composition and estimated the normalized burn ratio (NBR) from multispectral satellite imagery as an index of vegetation regrowth (i.e., structure). We then examined the use of cutblocks by moose dependent upon vegetation composition and NBR using generalized additive mixed effects models. Next, we used locations of collared moose and nearby available locations to examine moose responses as a function of year since cut and used those responses to group cutblocks into age classes, which were incorporated into resource selection functions (RSF) to compare moose responses between study areas. Vegetation composition differed between study areas, and although cutblocks in both study areas followed similar regrowth trajectories, NBRs for cutblocks > 13 years post-logging in PGS exceeded those in BP. Moose demonstrated greater use of locations within cutblocks with intermediate NBRs and dominanted by spruce (Picea engelmannii × glauca) versus Douglas fir (Pseudotsuga menziesii var. glauca). Moose responses as a function of year since cut varied seasonally, but across seasons, moose tended to avoid new cutblocks (1–8 years), select for regenerating cutblocks (9–24 years), and avoid older cutblocks (25–40 years). In both study areas, RSFs revealed that moose avoided new cutblocks, but moose in PGS were more likely to select for regenerating cutblocks in comparison to BP. Our analyses suggest that the use of cutblocks by moose is a function of year since cut, vegetation composition, and vegetation regrowth, likely resulting from differences in browse quantity and lateral cover. To maintain stable moose populations, managers should consider vegetation composition and regrowth during forestry planning, and future research should focus on identifying region-specific forestry thresholds for moose.

Introduction

Among landscape disturbances, forestry cutblocks (defined areas where trees were harvested) are widespread globally and are estimated to account for ~26% of the total global loss in forests over the last 15 years (Curtis et al., 2018). Although lawfully harvested forests are often managed to ensure vegetation regrowth, changes in forest-successional stage can affect the behaviour and space-use of many species, with cascading effects on populations and communities. Amphibians experienced higher dispersal and lower survival rates in regenerating pine plantations in the southeastern USA (Haggerty et al., 2019). Stark differences were also observed in the composition of bird species as a function of time since cut in Missouri, USA (George et al., 2019) and northern Alberta, Canada (Leston et al., 2018). In Brazil, regenerating tropical forests demonstrated a shift in small mammal communities from generalists to specialists as forests aged post-logging (Pinotti et al., 2015).

These studies suggest that the effects of forestry on wildlife vary greatly and change as forest succession ensues, but differences in the progression of vegetation regrowth among similarly aged cutblocks contributes additional variability. In Sweden, differences in slope among re-growing cutblocks predicted the occurrence of bilberry (Vaccinum myrtillus), which in turn drove the selection of cutblocks by grizzly bears (Ursus arctos) (Domevščik, 2018). In Canada, differences in vegetation regrowth affected the use of regenerating cutblocks by grizzly bears (Kearney et al., 2019) and American marten (Martes americana) (Potvin et al., 2000). Gaining a better understanding of the complexities underlying wildlife responses to cutblocks is paramount for managers to strategically plan in order to limit negative and maximize positive effects of forestry activities on individual populations and their interconnected communities.

Among species linked to forestry cutblocks, moose (Alces alces) are thought to benefit from the creation of early successional vegetation via logging (Fisher and Wilkinson, 2005). Past studies on moose demonstrated greater use of younger cutblocks in comparison to other forest patches (Heikkilä and Härkönen, 1993, Bjørneraas et al., 2011) and logging has been associated with increases in moose abundance (Forbes and Théberge, 1993). Other studies, however, suggest a decline in moose abundance and a more complex relationship between moose and logging. In Québec, Canada, for example, logging reduced moose abundance by nearly 50% in resource-poor, black spruce (Picea mariana) forests (Potvin and Courtois, 2004). More recent research in Québec—examining the potential for logging to exacerbate apparent competition between moose and woodland caribou (Rangifer tarandus caribou)—demonstrated a decrease in the strength of selection by moose for cutblocks along a 400-km latitudinal gradient as a function of lower amounts of deciduous shrub regrowth at higher latitudes (Gagné et al., 2016).

Our objective was to examine differences in spatial responses by moose to cutblocks as a function of year since cut, while also considering vegetation composition and regrowth, to better inform forestry planning in order to maintain stable moose populations. Because forests are often managed at the landscape scale, we compared moose spatial responses to cutblocks between two regions in British Columbia (BC), Canada that differed in vegetation composition and regrowth. In BC, moose populations are declining in abundance across the majority of the province (Kuzyk et al., 2018a), following mountain pine beetle (Dendroctonus ponderosae) outbreaks and extensive salvage logging. The decline, however, is not consistent as populations in several regions are stable or increasing and the magnitude of the decline varies across regions with similar amounts of disturbance (Kuzyk et al., 2018a). We hypothesized that (i) moose avoid younger cutblocks, but (ii) select for regenerating cutblocks that likely contain more structure, thus providing greater browse and lateral cover, which provides concealment from predators. We also hypothesized that (iii) selection for regenerating cutblocks is greater in areas demonstrating more vegetation regrowth (i.e., structure) and (iv) as a function of an individual’s reproductive status (calf presence or absence), potentially resulting from the avoidance of more open areas with higher predation risk for calves. Our mechanistic approach allowed us to estimate thresholds for moose in response to forest succession and provided a greater understanding for why moose often demonstrate variable responses to forestry cutblocks across studies.

Section snippets

Study areas, animal capture, and monitoring

Our study areas, Prince George South (PGS) and Bonaparte (BP), spanned 9942 km2 and 6009 km2, respectively and were located on the interior plateau of BC (Fig. 1). The interior plateau is characterized by a humid continental climate with dry, warm summers and moderately dry, cold winters. Lodgepole pine (Pinus contorta var. latifolia) was the dominant tree species, while other common coniferous tree species included spruce (Picea engelmannii × glauca), subalpine fir (Abies lasiocarpa), and

Study area differences

Prince George South had a larger proportion of broadleaf-, lodgepole pine-, and spruce-dominant stands and a smaller proportion of Douglas fir-dominant stands in comparison to BP (Table 1). The proportions of fir-dominant, open, shrub, and wet vegetation classes were similar between study areas (Table 1). A greater proportion of BP burned within the last 40 years in comparison to PGS as a result of one large fire in 2017 (Elephant Hill Fire, ~1896 km2 total area burned both within and outside

Moose responses to vegetation composition and regrowth

Not all cutblocks are the same, nor should all cutblocks be considered high quality habitat for moose. Previous research demonstrated that moose responses to forestry cutblocks vary dependent upon successional stage (Bjørneraas et al., 2011). Our research suggests that succession can vary across seemingly similar regions in relation to vegetation composition and regrowth (i.e., structure), which are likely related to landscape productivity (Beets et al., 2019) and directly influence the

Conclusion

Dissimilar moose responses to forestry cutblocks across regions are a reflection of the underlying complexity exhibited by cutblocks of differing ages with disparate patterns of vegetation composition and regrowth. This study highlights this complexity and provides a better understanding for why not all cutblocks are equivalent with regards to habitat quality for moose. Moose demonstrated more positive spatial responses to cutblocks in a study area with higher proportions of lodgepole pine and

CRediT authorship contribution statement

Matthew A. Mumma: Conceptualization, Investigation, Formal analysis, Data curation, Writing - original draft, Writing - review & editing, Visualization, Supervision. Michael P. Gillingham: Conceptualization, Writing - review & editing, Supervision, Funding acquisition. Shelley Marshall: Investigation, Resources, Data curation, Writing - review & editing, Supervision. Christopher Procter: Investigation, Resources, Data curation, Writing - review & editing, Supervision. Alexandre R. Bevington:

Declaration of Competing Interest

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: SM, CP, ARB, and MS are employed by the Province of British Columbia.

Acknowledgments

We would like to thank the Habitat Conservation Trust Foundation and Fulbright Canada for funding our analyses. We also thank British Columbia’s Ministry of Forestry, Natural Resource Operations, and Rural Development, along with Gerry Kuzyk, Francis Iredale, Doug Jury, Helen Schwantje, Mike Klaczek, Morgan Anderson, Adrian Batho, Doug Heard, and Glen Watts for financial, field and logistical support. We thank Doug Beattie for his insightful review of the manuscript. We also appreciate the

Data accessibility

Data is under the ownership and control of British Columbia’s Ministry of Forestry, Natural Resource Operations, and Rural Development.

Funding

This work has been funded by the Habitat Conservation Trust Foundation, Fulbright Canada, and through British Columbia’s Ministry of Forests, Lands, Natural Resource Operations, and Rural Development.

References (57)

  • Barton, K., 2015. MuMIn: Multi-model Inference, R Package Version...
  • Basille, M., 2015. Hab: Functions related to habitat quality and movement analyses, R Package Version...
  • Baskin, L.M., 2009. Status of regional moose populations in European and Asiatic Russia. Alces 45,...
  • D. Bates et al.

    Fitting linear mixed-effects models using lme4

    J. Stat. Softw.

    (2015)
  • K. Bjørneraas et al.

    Moose Alces alces habitat use at multiple temporal scales in a human-altered landscape

    Wildlife Biol.

    (2011)
  • K.P. Burnham et al.

    Model Selection and Multimodel Inference: A Practical Information-theoretic Approach

    (2002)
  • P.G. Curtis et al.

    Classifying drivers of global forest loss

    Science

    (2018)
  • C.A. DeMars et al.

    Moose, caribou, and fire: have we got it right yet?

    Can. J. Zool.

    (2019)
  • M. Dickie et al.

    Faster and farther: wolf movement on linear features and implications for hunting behaviour

    J. Appl. Ecol.

    (2017)
  • Domevščik, M., 2018. Resource distribution in disturbed landscapes – the effect of clearcutting on berry abundance and...
  • M.L. Drew et al.

    Reproduction of winter tick, Dermacentor albipictus, under field conditions in Alberta, Canada

    Can. J. Zool.

    (1986)
  • C. Dussault et al.

    Behavioural responses of moose to thermal conditions in the boreal forest

    Ecoscience

    (2004)
  • S. Escuin et al.

    Fire severity assessment by using NBR (Normalized Burn Ratio) and NDVI (Normalized Difference Vegetation Index) derived from LANDSAT TM/ETM images

    Int. J. Remote Sens.

    (2008)
  • M. Festa-Bianchet et al.

    Conservation of caribou (Rangifer tarandus) in Canada: an uncertain future

    Can. J. Zool.

    (2011)
  • J.T. Fisher et al.

    The response of mammals to forest fire and timber harvest in the North American boreal forest

    Mammal Rev.

    (2005)
  • G.J. Forbes et al.

    Multiple landscape scales and winter distribution of moose, Alces alces, in a forest ecotone

    Can. Field-Naturalist

    (1993)
  • A.D. George et al.

    Response of shrubland birds to regenerating clearcut area and shape

    J. Wildl. Manage.

    (2019)
  • C.J.E. Haggerty et al.

    Effects of forestry-driven changes to groundcover and soil moisture on amphibian desiccation, dispersal, and survival

    Ecol. Appl.

    (2019)
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