Advertisement

Biological Invasions

, Volume 20, Issue 12, pp 3475–3490 | Cite as

Biogeographic differences between native and non-native populations of crayfish alter species coexistence and trophic interactions in mesocosms

  • M. G. Glon
  • L. S. Reisinger
  • L. M. Pintor
Original Paper

Abstract

Biogeographical comparisons of native and non-native populations allow researchers to understand the degree to which traits contributing to invasion success are intrinsic or change during the invasion process. Here, we investigate whether traits underlying interspecific competition change following invasion and whether these alter the impacts of two crayfish congeners that have invaded into each other’s native ranges. Specifically, we compared native and non-native populations of rusty (Faxonius rusticus) and virile crayfish (F. virilis). We compared native and non-native populations of each species using laboratory assays to examine aggression and large mesocosms with the congeners in sympatry to examine growth and survival as well as impacts on lower trophic levels. We found that non-native virile crayfish were more aggressive in response to a threat than native virile crayfish and exhibited greater growth and survival in sympatry with rusty crayfish. These intraspecific differences were large enough to alter coexistence between species in the mesocosm experiment, which is consistent with patterns of coexistence between these species in the field. We did not observe differences in traits between native and non-native rusty crayfish, but rusty crayfish were consistently competitively dominant over virile crayfish in paired laboratory assays. Non-native populations of both species had greater impacts on lower trophic levels than native populations. Taken together, these findings provide new evidence that trait changes during invasions may enhance ecological impacts of invasive animals and their ability to compete with closely related native species.

Keywords

Invasive species Phenotypic plasticity Evolution Interspecific competition Ecological impacts Behavior 

Notes

Acknowledgements

We thank the 2016 Central Michigan University (CMU) Great Lakes Summer Research Program students, students in the Pintor Lab at The Ohio State University (OSU), the University of Wisconsin-Madison’s Trout Lake Station Staff, Ying Guy and Rongyi Zhu for help with crayfish collection and husbandry, the CMU Biological Station staff for assistance with mesocosm setup and maintenance, Ray Clark of CMU for assistance with fabrication of experimental equipment, and two anonymous reviewers for their help in preparing this manuscript for publication. Funding provided to LMP and MGG by OSU’s School of Environment and Natural Resources and the Ohio Agricultural Research and Development Center and to LSR by CMU’s Institute for Great Lakes Research. This is contribution 100 of the Central Michigan University Institute for Great Lakes Research.

Supplementary material

10530_2018_1788_MOESM1_ESM.jpg (1.1 mb)
Supplementary material 1 (JPEG 1125 kb)

References

  1. Bates D, Mächler M, Bolker B, Walker S (2014) Fitting linear mixed-effects models using lme4. arXiv 1406.5823Google Scholar
  2. Berger-Tal O, Embar K, Kotler BP, Saltz D (2015) Everybody loses: intraspecific competition induces tragedy of the commons in Allenby’s gerbils. Ecology 96:54–61.  https://doi.org/10.1890/14-0130.1 CrossRefPubMedGoogle Scholar
  3. Bergman D, Moore PA (2003) Field observations of intraspecific agonistic behavior of two crayfish species, Orconectes rusticus and Orconectes virilis, in different habitats. Biol Bull 205:26–35.  https://doi.org/10.2307/1543442 CrossRefPubMedGoogle Scholar
  4. Bergman DA, Kozlowski CP, McIntyre JC, Huber R, Daws AG, Moore PA (2003) Temporal dynamics and communication of winner-effects in the crayfish, Orconectes rusticus. Behaviour 140(6): 805–825CrossRefGoogle Scholar
  5. Bergman DA, Redman CN, Fero KC, Simon JL, Moore PA (2006) The impacts of flow on chemical communication strategies and fight dynamics of crayfish. Mar Freshw Behav Physiol 39:245–258.  https://doi.org/10.1080/10236240600980608 CrossRefGoogle Scholar
  6. Blackburn TM, Pyšek P, Bacher S, Carlton JT, Duncan RP, Jarošík V, Wilson JR, Richardson DM (2011) A proposed unified framework for biological invasions. Trends Ecol Evol 26:333–339.  https://doi.org/10.1016/j.tree.2011.03.023 CrossRefGoogle Scholar
  7. Bossdorf O, Auge H, Lafuma L, Rogers WE, Siemann E, Prati D (2005) Phenotypic and genetic differentiation between native and introduced plant populations. Oecologia 144:1–11.  https://doi.org/10.1007/s00442-005-0070-z CrossRefPubMedGoogle Scholar
  8. Bruski CA, Dunham DW (1987) The importance of vision in agonistic communication of the crayfish Orconectes rusticus. I: an analysis of bout dynamics. Behaviour 103:83–107.  https://doi.org/10.1163/156853987X00288 CrossRefGoogle Scholar
  9. Byers JE (2000) Competition between two estuarine snails: implications for invasions of exotic species. Ecology 81:1225–1239.  https://doi.org/10.1890/0012-9658(2000)081[1225:CBTESI]2.0.CO;2 CrossRefGoogle Scholar
  10. Capelli G, Munjal BL (1982) Aggressive interactions and resource competition in relation to species displacement among crayfish of the genus Orconectes. J Crustac Biol 2:486–492.  https://doi.org/10.1163/1937240X82X00176 CrossRefGoogle Scholar
  11. Charlebois PM, Lamberti GA (1996) Invading crayfish in a Michigan stream: direct and indirect effects on periphyton and macroinvertebrates. J N Am Benthol Soc 15:551–563.  https://doi.org/10.2307/1467806 CrossRefGoogle Scholar
  12. Crandall KA, De Grave S (2017) An updated classification of the freshwater crayfishes (Decapoda: Astacidea) of the world, with a complete species list. J Crustac Biol 37:615–653.  https://doi.org/10.1093/jcbiol/rux070 CrossRefGoogle Scholar
  13. Englund G, Krupa JJ (2000) Habitat use by crayfish in stream pools: influence of predators, depth and body size. Freshw Biol 43:75–83.  https://doi.org/10.1046/j.1365-2427.2000.00524.x CrossRefGoogle Scholar
  14. Garvey JE, Stein RA (1993) Evaluating how chela size influences the invasion potential of an introduced crayfish (Orconectes rusticus). Am Midl Nat 129:172–181.  https://doi.org/10.2307/2426446 CrossRefGoogle Scholar
  15. Garvey JE, Stein RA, Thomas HM (1994) Assessing how fish predation and interspecific prey competition influence a crayfish assemblage. Ecology 75:532–547.  https://doi.org/10.2307/1939556 CrossRefGoogle Scholar
  16. Gherardi F, Barbaresi S, Raddi A (1999) The agonistic behaviour in the red swamp crayfish, Procambarus clarkii: functions of the chelae. Freshw Crayfish 12:233–243Google Scholar
  17. Gioria M, Osborne BA (2014) Resource competition in plant invasions: emerging patterns and research needs. Front Plant Sci 5:1–21.  https://doi.org/10.3389/fpls.2014.00501 CrossRefGoogle Scholar
  18. Glon MG, Larson ER, Reisinger LS, Pangle KL (2017) Invasive dreissenid mussels benefit invasive crayfish but not native crayfish in the Laurentian Great Lakes. J Great Lakes Res 43:289–297.  https://doi.org/10.1016/j.jglr.2017.01.011 CrossRefGoogle Scholar
  19. Green PT, Lake PS, O’dowd DJ (2004) Resistance of island rainforest to invasion by alien plants: influence of microhabitat and herbivory on seedling performance. Biol Invasions 6:1–9.  https://doi.org/10.1023/B:BINV.0000010144.12808.cb CrossRefGoogle Scholar
  20. Grosholz ED, Ruiz GM (2003) Biological invasions drive size increases in marine and estuarine invertebrates. Ecol Lett 6:700–705.  https://doi.org/10.1046/j.1461-0248.2003.00495.x CrossRefGoogle Scholar
  21. Hierro JL, Maron JL, Callaway RM (2005) A biogeographical approach to plant invasions: the importance of studying exotics in their introduced and native range. J Ecol 93:5–15.  https://doi.org/10.1111/j.0022-0477.2004.00953.x CrossRefGoogle Scholar
  22. Hill AM, Lodge DM (1999) Replacement of resident crayfishes by an exotic crayfish: the roles of competition and predation. Ecol Appl 9:678–690.  https://doi.org/10.1890/1051-0761(1999)009[0678:RORCBA]2.0.CO;2 CrossRefGoogle Scholar
  23. Hill AM, Sinars DM, Lodge DM (1993) Invasion of an occupied niche by the crayfish Orconectes rusticus: potential importance of growth and mortality. Oecologia 94:303–306.  https://doi.org/10.1007/BF00317102 CrossRefPubMedGoogle Scholar
  24. Holway DA, Suarez AV (1999) Animal behavior: an essential component of invasion biology. Trends Ecol Evol 14:328–330.  https://doi.org/10.1016/S0169-5347(99)01636-5 CrossRefGoogle Scholar
  25. Hulme PE, Bacher S, Kenis M, Klotz S, Kühn I, Minchin D, Nentwig W, Olenin S, Panov V, Pergl J, Pyšek P, Roques A, Sol D, Solarz W, Vilà M (2008) Grasping at the routes of biological invasions: a framework for integrating pathways into policy. J Appl Ecol 45:403–414.  https://doi.org/10.1111/j.1365-2664.2007.01442.x CrossRefGoogle Scholar
  26. Human KG, Gordon DM (1996) Exploitation and interference competition between the invasive Argentine ant, Linepithema humile, and native ant species. Oecologia 105:405–412.  https://doi.org/10.1007/BF00328744 CrossRefPubMedGoogle Scholar
  27. Human KG, Gordon DM (1999) Behavioral interactions of the invasive Argentine ant with native ant species. Insectes Soc 46:159–163.  https://doi.org/10.1007/s000400050 CrossRefGoogle Scholar
  28. Joshi J, Vrieling K (2005) The enemy release and EICA hypothesis revisited: incorporating the fundamental difference between specialist and generalist herbivores. Ecol Lett 8:704–714.  https://doi.org/10.1111/j.1461-0248.2005.00769.x CrossRefGoogle Scholar
  29. Kilian JV, Becker AJ, Stranko SA, Ashton M, Klauda RJ, Gerber J, Hurd M (2010) The status and distribution of Maryland crayfishes. Southeast Nat 9:11–32.  https://doi.org/10.1656/058.009.s302 CrossRefGoogle Scholar
  30. Kolar CS, Lodge DM (2001) Progress in invasion biology: predicting invaders. Trends Ecol Evol 16:199–204.  https://doi.org/10.1016/S0169-5347(01)02101-2 CrossRefPubMedGoogle Scholar
  31. Kuznetsova A, Brockhoff PB, Christensen RHB (2016) lmerTest: tests in linear mixed effects models. R package version 2.0-33Google Scholar
  32. Lee CE (2002) Evolutionary genetics of invasive species. Trends Ecol Evol 17:386–391.  https://doi.org/10.1016/S0169-5347(02)02554-5 CrossRefGoogle Scholar
  33. Lenth RV (2016) Least-squares means: the R package lsmeans. J Stat Softw 69:1–33CrossRefGoogle Scholar
  34. Levine JM, Adler PB, Yelenik SG (2004) A meta-analysis of biotic resistance to exotic plant invasions. Ecol Lett 7:975–989.  https://doi.org/10.1111/j.1461-0248.2004.00657.x CrossRefGoogle Scholar
  35. Lodge DM, Kratz TK, Capelli GM (1986) Long-term dynamics of three crayfish species in Trout Lake, Wisconsin. Can J Fish Aquat Sci 43:993–998.  https://doi.org/10.1139/f86-122 CrossRefGoogle Scholar
  36. Lodge DM, Williams S, MacIsaac HJ, Hayes KR, Leung B, Reichard S, Mack RN, Moyle PB, Smith M, Andow DA, Carlton JT, McMichael A (2006) Biological invasions: recommendations for US policy and management. Ecol Appl 16:2035–2054.  https://doi.org/10.1890/1051-0761(2006)016[2035:BIRFUP]2.0.CO;2 CrossRefPubMedGoogle Scholar
  37. Mccarthy JM, Hein CL, Olden JD, Jake Vander Zanden M (2006) Coupling long-term studies with meta-analysis to investigate impacts of non-native crayfish on zoobenthic communities. Freshw Biol 51:224–235.  https://doi.org/10.1111/j.1365-2427.2005.01485.x CrossRefGoogle Scholar
  38. Moore PA (2007) Agonistic behavior in freshwater crayfish: the influence of intrinsic and extrinsic factors on aggressive behavior and dominance. In: Emmett DJ, Thiel M (eds) Evolutionary ecology of social and sexual systems: crustacea as model organisms. Oxford University Press, Oxford, pp 90–114CrossRefGoogle Scholar
  39. Moore PA, Bergman DA (2005) The smell of success and failure: the role of intrinsic and extrinsic chemical signals on the social behavior of crayfish. Integr Comp Biol 45:650–657.  https://doi.org/10.1093/icb/45.4.650 CrossRefPubMedGoogle Scholar
  40. Olden JD, McCarthy JM, Maxted JT, Fetzer WW, Vander Zanden MJ (2006) The rapid spread of rusty crayfish (Orconectes rusticus) with observations on native crayfish declines in Wisconsin (USA) over the past 130 years. Biol Invasions 8:1621–1628.  https://doi.org/10.1007/s10530-005-7854-2 CrossRefGoogle Scholar
  41. Olsen TM, Lodge DM, Capelli GM, Houlihan RJ (1991) Mechanisms of impact of an introduced crayfish (Orconectes rusticus) on littoral congeners, snails, and macrophytes. Can J Fish Aquat Sci 48:1853–1861.  https://doi.org/10.1139/f91-219 CrossRefGoogle Scholar
  42. Perry WL, Lodge DM, Lamberti GA (2000) Crayfish (Orconectes rusticus) impacts on zebra mussel (Dreissena polymorpha) recruitment, other macroinvertebrates and algal biomass in a lake-outlet stream. Am Midl Nat 144:308–316.  https://doi.org/10.1674/0003-0031(2000)144[0308:CORIOZ]2.0.CO;2 CrossRefGoogle Scholar
  43. Peters JA, Lodge DM (2013) Habitat, predation, and coexistence between invasive and native crayfishes: prioritizing lakes for invasion prevention. Biol Invasions 15:2489–2502.  https://doi.org/10.1007/s10530-013-0468-1 CrossRefGoogle Scholar
  44. Phillips BL, Brown GP, Shine R (2010) Life-history evolution in range-shifting populations. Ecology 91:1617–1627.  https://doi.org/10.1890/09-0910.1 CrossRefPubMedGoogle Scholar
  45. Pintor LM, Sih A (2009) Differences in growth and foraging behavior of native and introduced populations of an invasive crayfish. Biol Invasions 11:1895–1902.  https://doi.org/10.1007/s10530-008-9367-2 CrossRefGoogle Scholar
  46. Pintor LM, Sih A, Bauer ML (2008) Differences in aggression, activity and boldness between native and introduced populations of an invasive crayfish. Oikos 117:1629–1636.  https://doi.org/10.1111/j.1600-0706.2008.16578.x CrossRefGoogle Scholar
  47. Pyšek P, Křivánek M, Jarošík V (2009) Planting intensity, residence time, and species traits determine invasion success of alien woody species. Ecology 90:2734–2744.  https://doi.org/10.1890/08-0857.1 CrossRefPubMedGoogle Scholar
  48. R Core Team (2016) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/. Accessed 1 May 2016
  49. Rehage JS, Sih A (2004) Dispersal behavior, boldness, and the link to invasiveness: a comparison of four Gambusia species. Biol Invasions 6:379–391.  https://doi.org/10.1023/B:BINV.0000034618.93140.a5 CrossRefGoogle Scholar
  50. Reisinger LS, Elgin AK, Towle KM, Chan DJ, Lodge DM (2017) The influence of evolution and plasticity on the behavior of an invasive crayfish. Biol Invasions 19:815–830.  https://doi.org/10.1007/s10530-016-1346-4 CrossRefGoogle Scholar
  51. Rubenstein DI, Hazlett BA (1974) Examination of the agonistic behaviour of the crayfish Orconectes virilis by character analysis. Behaviour 50:193–215.  https://doi.org/10.1163/156853974X00453 CrossRefGoogle Scholar
  52. Rutherford PL, Dunham DW, Allison V (1995) Winning agonistic encounters by male crayfish Orconectes rusticus (Girard) (Decapoda, Cambaridae): chela size matters but chela symmetry does not. Crustaceana 68:526–529CrossRefGoogle Scholar
  53. Sakai AK, Allendorf FW, Holt JS, Lodge DM, Molofsky J, With KA, Baughman S, Cabin RJ, Cohen JE, Ellstrand NC, McCauley DE, O’Neil P, Parker IM, Thompson JN, Weller SG (2001) The population biology of invasive species. Annu Rev Ecol Evol Syst 32:305–332.  https://doi.org/10.1146/annurev.ecolsys.32.081501.114037 CrossRefGoogle Scholar
  54. Sanders NJ, Gotelli NJ, Heller NE, Gordon DM (2003) Community disassembly by an invasive species. Proc Natl Acad Sci USA 100:2474–2477.  https://doi.org/10.1073/pnas.0437913100 CrossRefPubMedGoogle Scholar
  55. Sargent LW, Lodge DM (2014) Evolution of invasive traits in nonindigenous species: increased survival and faster growth in invasive populations of rusty crayfish (Orconectes rusticus). Evol Appl 7:949–961.  https://doi.org/10.1111/eva.12198 CrossRefPubMedPubMedCentralGoogle Scholar
  56. Schneider RAZ, Huber R, Moore PA (2001) Individual and status recognition in the crayfish, Orconectes rusticus: the effects of urine release on fight dynamics. Behaviour 138:137–153.  https://doi.org/10.1163/15685390151074348 CrossRefGoogle Scholar
  57. Seebacher F, Wilson RS (2007) Individual recognition in crayfish (Cherax dispar): the roles of strength and experience in deciding aggressive encounters. Biol Lett 3:471–474.  https://doi.org/10.1098/rsbl.2007.0289 CrossRefPubMedPubMedCentralGoogle Scholar
  58. Shea K, Chesson P (2002) Community ecology theory as a framework for biological invasions. Trends Ecol Evol 17:170–176.  https://doi.org/10.1016/S0169-5347(02)02495-3 CrossRefGoogle Scholar
  59. Stein RA (1976) Sexual dimorphism in crayfish chelae: functional significance linked to reproductive activities. Can J Zool 54:220–227.  https://doi.org/10.1139/z76-024 CrossRefGoogle Scholar
  60. Suarez AV, Tsutsui ND, Holway DA, Case TJ (1999) Behavioral and genetic differentiation between native and introduced populations of the Argentine ant. Biol Invasions 1:43–53.  https://doi.org/10.1023/A:1010038413690 CrossRefGoogle Scholar
  61. Swecker CD, Jones TG, Donahue K II, McKinney D, Smith GD (2010) The extirpation of Orconectes limosus (Spinycheek crayfish) populations in West Virginia. Southeast Nat 9:155–164.  https://doi.org/10.1656/058.009.s306 CrossRefGoogle Scholar
  62. Torchin ME, Lafferty KD, Kuris AM (2001) Release from parasites as natural enemies: increased performance of a globally introduced marine crab. Biol Invasions 3:333–345.  https://doi.org/10.1023/A:1015855019360 CrossRefGoogle Scholar
  63. Tsutsui ND, Suarez AV, Holway DA, Case TJ (2000) Reduced genetic variation and the success of an invasive species. Proc Natl Acad Sci USA 97:5948–5953.  https://doi.org/10.1073/pnas.100110397 CrossRefPubMedGoogle Scholar
  64. Usio N, Azuma N, Larson ER, Abbott CL, Olden JD, Akanuma H, Takamura K, Takamura N (2016) Phylogeographic insights into the invasion history and secondary spread of the signal crayfish in Japan. Ecol Evol 6:5366–5382.  https://doi.org/10.1002/ece3.2286 CrossRefPubMedPubMedCentralGoogle Scholar
  65. Van Kleunen M, Weber E, Fischer M (2010) A meta-analysis of trait differences between invasive and non-invasive plant species. Ecol Lett 13:235–245.  https://doi.org/10.1111/j.1461-0248.2009.01418.x CrossRefGoogle Scholar
  66. Venables WN, Ripley BD (2002) Modern applied statistics with S, 4th edn. Springer, New YorkCrossRefGoogle Scholar
  67. Warton DI, Hui FKC (2011) The arcsine is asinine: the analysis of proportions in ecology. Ecology 92:3–10.  https://doi.org/10.1890/10-0340.1 CrossRefPubMedGoogle Scholar
  68. Wetzel RG, Likens GE (2000) Limnological analysis, 3rd edn. Springer, New YorkCrossRefGoogle Scholar
  69. Wickham H (2009) Ggplot2: elegant graphics for data analysis. Springer, New YorkCrossRefGoogle Scholar

Copyright information

© Springer International Publishing AG, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Evolution, Ecology and Organismal BiologyThe Ohio State UniversityColumbusUSA
  2. 2.Institute for Great Lakes ResearchCentral Michigan UniversityMount PleasantUSA
  3. 3.School of Forest Resources and ConservationUniversity of FloridaGainesvilleUSA
  4. 4.School of Environment and Natural ResourcesThe Ohio State UniversityColumbusUSA

Personalised recommendations