Mammal Community Assembly During Primary Succession on the Pumice Plain at the Mount St. Helens Volcano (1983–2015)

  • Charles M. Crisafulli
  • Robert R. Parmenter
  • Tara E. Blackman
  • James A. MacMahon
Chapter

Abstract

The 1980 eruption of Mount St. Helens created an outstanding opportunity to investigate mammal community assembly during primary succession. From 1983 through 2015, we documented the arrival of 34 of the 45 mammals in the regional species pool and the successful establishment of 25 species. The majority of small mammals that established were likely derived from source populations that survived in isolated refugia in adjacent areas that were less disturbed during the eruption, requiring dispersal distances of a few to several kilometers. In contrast, large mammals arrived from more distant source populations—tens of km away. The next important transition in mammal community assembly will likely occur in three or four decades, as shrub cover and coniferous tree density increases, leading to development of open-forest conditions that provide habitat for forest-associated species not yet established and concomitant decline of early-seral mammal species.

Keywords

Mount St. Helens Volcanic disturbance Long-term studies Primary succession Small mammal Community assembly Rodents Insectivores Dispersal Colonization Biological establishment 

Notes

Acknowledgments

Long-term studies such as ours require the contributions by numerous individuals. We are particularly thankful to the cadre of technicians and graduate students who assisted with the fieldwork. Leslie Carraway at Oregon State University and Jeff Bradley at the Burke Museum aided in identification of voles and shrews. We thank the Burke Museum and Museum of Southwestern Biology for accession of our voucher collections. Kathryn Ronnenberg produced figures and made editorial improvements to this manuscript. Kelly Christiansen assisted with GIS-related figures. Chris Che-Castaldo generously provided mortality rate data for willow stems. This manuscript benefitted from comments provided by Virginia Dale and three anonymous reviewers. We thank the USDA Forest Service and Mount St. Helens National Volcanic Monument for providing access to our study sites. Funding for this research was provided by grants from the National Science Foundation (DEB81-16914, BSR 84-07213 to J.A.M., and LTREB Program DEB-0614538 to C.M.C.), and from the USDA Forest Service Pacific Northwest Research Station.

Glossary

Arrival

A mammal is detected at a site either through capture in a trap or by visual observation.

Blast PDC

In the case of the 1980 Mount St. Helens eruption, failure of the volcano’s north flank unroofed pressurized magma and superheated water. Rapid exsolution of magmatic gases and conversion of superheated water to steam produced a laterally directed blast, which formed a density current that flowed across rugged topography. The current contained fragmented rock debris as well as shattered forest material.

Community development

Process of any number of mammals belonging to a number of different species that co-occur in the same habitat or area and interact through trophic and spatial relationships.

Debris avalanche

A rapid granular flow of an unsaturated or partly saturated mixture of volcanic rock particles (± ice) and water, initiated by the gravitational collapse and disintegration of part of a volcanic edifice. Debris avalanches differ from debris flows in that they are not water saturated. Although debris avalanches commonly occur in association with eruptions, they can also occur during periods when a volcano is dormant.

Dispersal

Movement of a mammal from its point of origin or home site to another.

Establishment/established

A species that is assumed to have a breeding population at a site based on the presence of one or more of the following three criteria: (a) ≥1 adult male and female detected at the same site during the same sampling session, (b) ≥1 pregnant or lactating females detected at a site, or (c) several juveniles of a species detected at a site during a single trapping session.

Lahar

An Indonesian term for a rapid granular flow of a fully saturated mixture of volcanic rock particles (± ice), water, and commonly woody debris. A lahar that has ≥50% solids by volume is termed a debris flow; one that has roughly 10–50% solids by volume is termed a hyperconcentrated flow. Flow type can evolve with time and distance along a flow path as sediment is entrained or deposited.

Microtine rodents

A subfamily of rodents (Arvicolinae) that includes the voles, lemmings, and muskrats. At Mount St. Helens, they include three genera of herbivorous voles (Microtus, Myodes, and Phenacomys).

Pyroclastic flow

Rapid flow of a dry mixture of hot (commonly >700 °C) solid particles, gases, and air that has a ground-hugging flow often directed by topography. Flows are generally gravity driven but may be accelerated initially by impulsive lateral forces of directed volcanic explosions. Flows typically move at high velocity (up to several hundreds of km h−1).

Tephra

Fragmental rock material ejected from a volcano during an eruption and deposited by airfall. It is typically composed of ash (less than 4 mm in diameter), lapilli (4- to 32-mm particles), and blocks (angular stones larger than 32 mm).

References

  1. Adams, A.B., K.E. Hinckley, C. Hinzman, and S.R. Leffler. 1986. Recovery of small mammals in three habitats in the northwest sector of the Mount St. Helens National Volcanic Monument. In Mount St. Helens: Five years later, ed. S.A.C. Keller, 345–358. Cheney: Eastern Washington University Press.Google Scholar
  2. Allen, M.F. 1987. Re-establishment of mycorrhizas on Mount St. Helens: Migration vectors. Transactions of the British Mycological Society 88: 314–417.CrossRefGoogle Scholar
  3. Allen, M.F., and J.A. MacMahon. 1988. Direct VA mycorrhizal inoculation of colonizing plants by pocket gophers (Thomomys talpoides) on Mount St. Helens. Mycologia 80: 413–417.Google Scholar
  4. Allen, M.F., J.A. MacMahon, and D.C. Andersen. 1984. Reestablishment of endogonaceae on Mount St. Helens: Survival of residuals. Mycologia 76: 1031–1038.CrossRefGoogle Scholar
  5. Allen, M.F., C.M. Crisafulli, C.F. Friese, and S.L. Jeakins. 1992. Re-formation of mycorrhizal symbioses on Mount St. Helens, 1980–1990: Interactions of rodents and mycorrhizal fungi. Mycological Research 96: 447–453.CrossRefGoogle Scholar
  6. Allen, M.F., C.M. Crisafulli, S.J. Morris, L.M. Egerton-Warburton, J.A. MacMahon, and J.M. Trappe. 2005. Mycorrhizae and Mount St. Helens: Story of a symbiosis. In Ecological responses to the 1980 eruption of Mount St. Helens, ed. V.H. Dale, F.J. Swanson, and C.M. Crisafulli, 221–231. New York: Springer.CrossRefGoogle Scholar
  7. Andersen, D.C. 1982. Observations on Thomomys talpoides in the region affected by the eruption of Mount St. Helens. Journal of Mammology 63: 652–655.CrossRefGoogle Scholar
  8. Andersen, D.C., and J.A. MacMahon. 1985a. The effects of catastrophic ecosystem disturbance: The residual mammals at Mount St. Helens. Journal of Mammology 66: 581–589.CrossRefGoogle Scholar
  9. ———. 1985b. Plant succession following the Mount St. Helens volcanic eruption: Facilitation by a burrowing rodent, Thomomys talpoides. American Midland Naturalist 114: 62–69.CrossRefGoogle Scholar
  10. Anderson, D.R., K.P. Burnham, G.C. White, and D.L. Otis. 1983. Density estimation of small-mammal populations using a trapping web and distance sampling methods. Ecology 64: 674–680.CrossRefGoogle Scholar
  11. Anderson, K.J. 2007. Temporal patterns in rates of community change during succession. American Naturalist 169: 780–783.CrossRefGoogle Scholar
  12. Bach, C.E. 1990. Plant successional stage and insect herbivory: Flea beetles on sand-dune willow. Ecology 71: 598–609.CrossRefGoogle Scholar
  13. ———. 1994. Effects of a specialist herbivore (Altica subplicata) on Salix cordata and sand dune succession. Ecological Monographs 64: 423–445.CrossRefGoogle Scholar
  14. ———. 2001. Long-term effects of insect herbivory and sand accretion on plant succession on sand dunes. Ecology 82: 1401–1416.CrossRefGoogle Scholar
  15. Banks, S.C., M. Dujardin, L. McBurney, D. Blair, M. Barker, and D.B. Lindenmayer. 2011. Starting points for small mammal population recovery after wildfire: Recolonization or residual populations? Oikos 120: 26–37.CrossRefGoogle Scholar
  16. Bevers, E.J. 1998. Colonization and population biology of pikas (Ochotona princeps) on Mount St. Helens. Doctoral dissertation, New Mexico State University, New Mexico, USA.Google Scholar
  17. Bishop, J.G. 2002. Early primary succession on Mount St. Helens: The impact of insect herbivores on colonizing lupines. Ecology 83: 191–202.CrossRefGoogle Scholar
  18. Bishop, J.G., W.F. Fagan, J.D. Schade, and C.M. Crisafulli. 2005. Causes and consequences of herbivory on prairie lupine (Lupinus lepidus) in early primary succession. In Ecological responses to the 1980 eruption of Mount St. Helens, ed. V.H. Dale, F.J. Swanson, and C.M. Crisafulli, 151–161. New York: Springer.CrossRefGoogle Scholar
  19. Bogdziewicz, M., and R. Zwolak. 2014. Responses of small mammals to clear-cutting in temperate and boreal forests of Europe: A meta-analysis and review. European Journal of Forest Resources 133: 1–11.CrossRefGoogle Scholar
  20. Bryant, J.P., and F.S. Chapin III. 1986. Browsing–woody plant interactions during boreal forest plant succession. In Forest ecosystems in the Alaskan Taiga, ed. K. Van Cleve, F.S. Chapin III, L.A. Viereck, and C.T. Dyrness, 213–225. New York: Springer.CrossRefGoogle Scholar
  21. Burt, W.H. 1961. Some effects of Volcan Paricutin on vertebrates, Occasional Paper No. 620. Ann Arbor: Museum of Zoology, University of Michigan.Google Scholar
  22. Carey, A.B., and C.A. Harrington. 2001. Small mammals in young forests: Implications for management for sustainability. Forest Ecology and Management 154: 289–309.CrossRefGoogle Scholar
  23. Carey, A.B., and M.L. Johnson. 1995. Small mammals in managed, naturally young, and old-growth forests. Ecological Applications 5: 336–352.CrossRefGoogle Scholar
  24. Che-Castaldo, C. 2014. The attack dynamics and ecosystem consequences of stem borer herbivory on Sitka willow at Mount St. Helens. Doctoral dissertation. University of Maryland, College Park, MD, USA.Google Scholar
  25. Clements, F.E. 1916. Plant succession: An analysis of the development of vegetation, Publication No. 242. Washington, DC: Carnegie Institution.CrossRefGoogle Scholar
  26. Connell, J.H., and R.O. Slatyer. 1977. Mechanisms of succession in natural communities and their role in community stability and organizations. American Naturalist 111: 1119–1144.CrossRefGoogle Scholar
  27. Cowles, H.C. 1899. The ecological relations of vegetation on the sand dunes of Lake Michigan. Botanical Gazette 27: 95–117. 167–202, 281–308, 361–391.CrossRefGoogle Scholar
  28. Craig, M.D., E. Giles, St.J. Hardy, J.B. Fontaine, M.J. Garkakalis, A.H. Grigg, C.D. Grant, P.A. Fleming, and R.J. Hobbs. 2012. Identifying unidirectional and dynamic habitat filters to faunal recolonization in restored mine pits. Journal of Applied Ecology 49: 919–928.CrossRefGoogle Scholar
  29. Crisafulli, C.M., J.A. MacMahon, and R.R. Parmenter. 2005. Small mammal survival and colonization on the Mount St. Helens Volcano: 1980–2002. In Ecological responses to the 1980 eruption of Mount St. Helens, ed. V.H. Dale, F.J. Swanson, and C.M. Crisafulli, 199–218. New York: Springer.CrossRefGoogle Scholar
  30. Dale, V.H., F.J. Swanson, and C.M. Crisafulli, eds. 2005. Ecological responses to the 1980 eruption of Mount St. Helens. New York: Springer.Google Scholar
  31. del Moral, R., L.A. Thomason, A.C. Wenke, N. Lazanoff, and M.D. Abata. 2012. Primary succession trajectories on pumice at Mount St. Helens, Washington. Journal of Vegetation Science 23: 73–85.CrossRefGoogle Scholar
  32. Edwards, J.S. 1986. Arthropods as pioneers: Recolonization of the blast zone on Mount St. Helens. Northwest Environmental Journal 2: 263–273.Google Scholar
  33. Edwards, J.S., and P. Sugg. 1993. Arthropod fallout as a resource in the recolonization of Mount St. Helens. Ecology 74: 954–958.CrossRefGoogle Scholar
  34. Fagan, W.F., and J.G. Bishop. 2000. Trophic interaction during primary succession: Herbivores slow a plant reinvasion at Mount St. Helens. American Naturalist 155: 238–251.CrossRefGoogle Scholar
  35. Fisher, J.T., and L. Wilkinson. 2005. The response of mammals to forest fire and timber harvest in the North American boreal forest. Mammal Review 35: 51–81.CrossRefGoogle Scholar
  36. Fox, B.J. 1982. Fire and mammalian secondary succession in an Australian coastal heath. Ecology 63: 1332–1341.CrossRefGoogle Scholar
  37. Franklin, J.F., and C.T. Dyrness. 1973. Natural vegetation of Oregon and Washington, General Technical Report PNW-8. Portland: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station.Google Scholar
  38. Franklin, J.F., J.A. MacMahon, F.J. Swanson, and J.R. Sedell. 1985. Ecosystem responses to the eruption of Mount St. Helens. National Geographic Research 1: 198–216.Google Scholar
  39. Gitzen, R.A., and S.D. West. 2002. Small mammal response to experimental canopy gaps in the southern Washington Cascades. Forest Ecology and Management 168: 187–199.CrossRefGoogle Scholar
  40. Gleason, H.A. 1926. The individualistic concept of the plant association. Bulletin of the Torrey Botanical Club 53: 1–20.CrossRefGoogle Scholar
  41. Irie, K., and S. Tsuyuzaki. 2007. Faunal make-up and abundance of rodents 17 years after volcanic eruptions. Northwest Science 81: 333–336.CrossRefGoogle Scholar
  42. Kielland, K., and J.P. Bryant. 1998. Moose herbivory in taiga: Effects on biogeochemistry and vegetation dynamics in primary succession. Oikos 82: 377–383.CrossRefGoogle Scholar
  43. Kirkland, G.L., Jr. 1990. Patterns of initial small mammal community change after clearcutting of temperate North American forests. Okios 59: 313–330.CrossRefGoogle Scholar
  44. Larkin, J.L., D.S. Maehr, J.J. Krupa, J.J. Cox, K. Alexy, D.E. Unger, and C. Barton. 2008. Small mammal response to vegetation and spoil conditions on a reclaimed surface mine in eastern Kentucky. Southeastern Naturalist 7: 401–412.CrossRefGoogle Scholar
  45. Lipman, P.W., and D.R. Mullineaux. 1981. The 1980 eruptions of Mount St. Helens, Washington, Professional Paper 1250. Washington, DC: U.S. Geological Survey.Google Scholar
  46. MacArthur, R.H., and J.W. MacArthur. 1961. On bird species diversity. Ecology 42: 594–598.CrossRefGoogle Scholar
  47. MacMahon, J.A., R.R. Parmenter, K.A. Johnson, and C.M. Crisafulli. 1989. Small mammal recolonization on the Mount St. Helens volcano: 1980–1987. American Midland Naturalist 122: 365–387.CrossRefGoogle Scholar
  48. Mendonca, A.F., T. Armond, C.L. Camargo, N.F. Carmago, J.F. Ribeiro, P.L. Zangrandi, and E.M. Vieira. 2015. Effects of an extensive fire on arboreal small mammal populations in a neotropical savanna woodland. Journal of Mammalogy 96: 368–379.CrossRefGoogle Scholar
  49. Monamy, V., and B.J. Fox. 2000. Small mammal succession is determined by vegetation density rather than time elapsed since disturbance. Austral Ecology 25: 580–587.CrossRefGoogle Scholar
  50. Nelson, L., Jr., and F.W. Clark. 1973. Correction for sprung traps in catch/effort calculations of trapping results. Journal of Mammalogy 54: 295–298.CrossRefGoogle Scholar
  51. Parmenter, R.R. 2005. Patterns of decomposition and nutrient cycling across a volcanic disturbance gradient: A case study using rodent carcasses. In Ecological responses to the 1980 eruption of Mount St. Helens, ed. V.H. Dale, F.J. Swanson, and C.M. Crisafulli, 233–242. New York: Springer.CrossRefGoogle Scholar
  52. Parmenter, R.R., J.A. MacMahon, M.E. Waaland, M.M. Stuebe, P. Landres, and C.M. Crisafulli. 1985. Reclamation of surface coal mines in western Wyoming for wildlife habitat: A preliminary analysis. Reclamation and Revegetation Research 4: 93–115.Google Scholar
  53. Pearson, O.P. 1994. The impact of an eruption of Volcan Hudson on small mammals in Argentine Patagonia. Mastozoologia Neotropical 1: 103–112.Google Scholar
  54. Pulliam, H.R. 1988. Source, sinks and population regulation. American Naturalist 132: 652–661.CrossRefGoogle Scholar
  55. Pyke, D.A. 1984. Initial effects of volcanic ash from Mount St. Helens on Peromyscus maniculatus and Microtus montanus. Journal of Mammalogy 65: 678–680.CrossRefGoogle Scholar
  56. Saba, S.L., and D.A. de Lamo. 1994. Dynamic responses of mammals to the eruption of Volcan Hudson. Mastozoologia Neotropical 1: 113–122.Google Scholar
  57. Thoreau, H.D. 1887. The succession of forest trees. Cambridge, MA: The Riverside Press, Houghton, Mifflin and Co.Google Scholar
  58. Van Cleve, K., L.A. Viereck, and G.M. Marion. 1993. Introduction and overview of a study dealing with the role of salt-affected soils in primary succession on the Tanana River floodplain, interior Alaska. Canadian Journal of Forest Research 23: 879–888.CrossRefGoogle Scholar
  59. Walker, L.R., and F.S. Chapin III. 1986. Physiological controls over seedling growth in primary succession on an Alaskan floodplain. Ecology 67: 1508–1523.CrossRefGoogle Scholar
  60. Walker, L.R., J.C. Zasada, and F.S. Chapin III. 1986. The role of life history processes in primary succession on an Alaskan floodplain. Ecology 67: 1243–1253.CrossRefGoogle Scholar
  61. West, S.D. 1991. Small mammal communities in the southern Washington Cascade Range. In Wildlife and vegetation of unmanaged Douglas-fir forests, General Technical Report PNW-GTR-285, ed. L.F. Ruggiero, K.B. Aubry, A.B. Carey, and M.H. Huff, 268–283. Portland: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station.Google Scholar
  62. Wilson, D.E., and S. Ruff, eds. 1999. The Smithsonian book of North American mammals. Washington, DC: Smithsonian Institution Press.Google Scholar
  63. Wilson, S.M., and A.B. Carey. 2000. Legacy retention versus thinning: Influences on small mammals. Northwest Science 74: 131–145.Google Scholar
  64. Yurkewycz, R.P., J.G. Bishop, C.M. Crisafulli, J.A. Harrison, and R.A. Gill. 2014. Gopher mounds decrease nutrient cycling rates and increase adjacent vegetation in a volcanic primary succession. Oecologia. https://doi.org/10.1007/s0042-014-3075-7.
  65. Zwolak, R. 2009. A meta-analysis of the effects of wildfire, clearcutting, and partial harvest on the abundance of North American small mammals. Forest Ecology and Management 258: 539–545.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media LLC 2018

Authors and Affiliations

  • Charles M. Crisafulli
    • 1
  • Robert R. Parmenter
    • 2
  • Tara E. Blackman
    • 1
  • James A. MacMahon
    • 3
  1. 1.U.S. Department of Agriculture, Forest Service, Pacific Northwest Research StationMount St. Helens National Volcanic MonumentAmboyUSA
  2. 2.Valles Caldera National PreserveNational Park ServiceJemez SpringsUSA
  3. 3.Department of Biology and the Ecology CenterUtah State UniversityLoganUSA

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