Skip to main content

Advertisement

Log in

Environmental predictors of shrubby cinquefoil (Dasiphora fruticosa) habitat and quality as host for Maine’s endangered Clayton’s copper butterfly (Lycaena dorcas claytoni)

  • Original Paper
  • Published:
Wetlands Ecology and Management Aims and scope Submit manuscript

Abstract

Population size of habitat-specialized butterflies is limited in part by host plant distribution and abundance. Effective conservation for host-specialist species requires knowledge of host-plant habitat conditions and relationships with the specialist species. Clayton’s copper butterfly (Lycaena dorcas claytoni) is a Maine state-endangered species that relies exclusively on shrubby cinquefoil (Dasiphora fruticosa) as its host. Dasiphora fruticosa occurs in 28 wetlands in Maine, ten of which are occupied by L. d. claytoni. Little is known about environmental conditions that support large, persistent stands of D. fruticosa in Maine. We evaluated the environment (hydrology, pore water and peat nutrients) associated with D. fruticosa distribution, age, and condition in Maine wetlands supporting robust stands of D. fruticosa to compare with L. d. claytoni occurrence. Although dominant water source in D. fruticosa—containing wetlands included both groundwater discharge and surface-flow, D. fruticosa coverage was greater in wetlands with consistent growing season water levels that dropped into or below the root zone by late season, and its distributions within wetlands reflected pore water hydrogen ion and conductivity gradients. Flooding magnitude and duration were greatest during the L.d. claytoni larval feeding period, whereas, mean depth to water table and upwelling increased and were most variable following the L. d. claytoni egg-laying period that precedes D. fruticosa senescence. Oldest sampled shrubs were 37 years, and older shrubs were larger and slower-growing. Encounter rates of L. d. claytoni were greater in wetlands with larger D. fruticosa plants of intermediate age and greater bloom density. Wetland management that combines conditions associated with D. fruticosa abundance (e.g., non-forested, seasonally consistent water levels with high conductivity) and L. d. claytoni occurrence (e.g., drawdown below the root zone following egg-laying, abundant blooms on intermediate-aged D. fruticosa, nearby D. fruticosa-containing wetlands) will aid L. d. claytoni conservation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  • Aikawa S, Hori Y (2006) Effect of a multi-stemmed growth form on matter production of an understory shrub, Stephanandra incise. Plant Spec Biol 21:31–39

    Article  Google Scholar 

  • Anderson DS, Davis RB (1997) The vegetation and its environments in Maine peatlands. Can J Bot 75:1785–1805

    Article  Google Scholar 

  • APHA (1995) American public health association standard methods for the examination of water and wastewater, 19th edn. APHA, Washington, DC

    Google Scholar 

  • Auckland JN, Debinski DM, Clark WR (2004) Survival, movement, and resource use of the butterfly Parnassius clodius. Ecol Entomol 29:139–149

    Article  Google Scholar 

  • Awmack CS, Leather SR (2002) Host plant quality and fecundity in herbivorous insects. An Rev Entomol 47:817–844

    Article  CAS  Google Scholar 

  • Barros HCH, Zucoloto FS (1999) Performance and host preference of Ascia monuste (Lepidoptera, Pieridae). J Insect Physiol 45:7–14

    Article  CAS  PubMed  Google Scholar 

  • Bedford BL, Godwin KS (2003) Fens of the United States: distribution, characteristics, and scientific connection versus legal isolation. Wetlands 23:608–629

    Article  Google Scholar 

  • Bedford BL, Walbridge MR, Aldous A (1999) Patterns in nutrient availability and plant diversity of temperate North America wetlands. Ecology 80:2151–2169

    Article  Google Scholar 

  • Bond BJ (2000) Age-related changes in photosynthesis of woody plants. Trends Plant Sci 5:349–353

    Article  CAS  PubMed  Google Scholar 

  • Boomer KMB, Bedford BL (2008) Groundwater-induced redox-gradients control soil properties and phosphorus availability across four headwater Wetlands, New York, USA. Biogeochemistry 90:259–274

    Article  Google Scholar 

  • Boyer MLH, Wheeler BD (1989) Vegetation patterns in spring-fed calcareous fens: calcite precipitation and constraints on fertility. J Ecol 77:597–609

    Article  CAS  Google Scholar 

  • Bragazza LL, Gerdol RR (2002) Are nutrient availability and acidity-alkalinity gradients related in Sphagnum-dominated peatlands? J Veg Sci 13:473–482

    Article  Google Scholar 

  • Britten HB, Riley L (1994) Nectar Source Diversity as an indicator of Habitat Suitability for the endangered Uncompahgre Fritillary, Boloria acrocnema (Nymphalidae). J Lepid Soc 48:173–179

    Google Scholar 

  • Bryant JP, Chapin FSI, Klein DR (1983) Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 40:357–368

    Article  CAS  Google Scholar 

  • Búrquez A, Corbet SA (1998) Dynamics of production and exploitation of nectar: lessons from Impatiens glandulifera Royle. In: Bahadur B (ed) Nectary biology. Dattsons, Nagpur, pp 130–152

    Google Scholar 

  • Carter V (1986) An overview of the hydrologic concerns related to wetlands in the United States. Can J Bot 64:364–374

    Article  Google Scholar 

  • Dover JW (1997) Conservation headlands: effects on butterfly distribution and behaviour. Agric Ecosyst Environ 63:31–49

    Article  Google Scholar 

  • Drahovzal SA (2013) Environmental assessment of circumneutral wetlands with shrubby cinquefoil (Dasiphora fruticosa), host plant of the endangered Clayton’s Copper butterfly (Lycaena dorcas clatoni). Thesis, University of Maine

  • Eckstein D, Bauch J (1969) Beitrag zur Rationalisierung eines dendrochronologischen Verfahrens und zur Analyse seiner Aus-sagesicherheit. Forstwiss Centralbl 88:230–250

    Article  Google Scholar 

  • Ehrlich PR, Hanski I (2004) On the wings of checkerspots: a model system for population biology. Oxford University Press, Oxford

    Google Scholar 

  • Ehrlich PR, Raven PH (1964) Butterflies and plants: a study in coevolution. Evolution 18:586–608

    Article  Google Scholar 

  • Elkington TT, Woodell SRJ (1963) Potentilla fruticosa L. J Ecol 51:769–781

    Article  Google Scholar 

  • Erhardt A (1991) Nectar sugar and amino acid preferences of Battus philenor (Lepidoptera, Papilionidae). Ecol Entomol 16:425–434

    Article  Google Scholar 

  • Erhardt A (1992) Preferences and non-preferences for nectar constituents in Ornithoptera priamus poseidon (Lepidoptera, Papilionidae). Oecologia 90:581–585

    Article  Google Scholar 

  • Fahrig L (2003) Effects of habitat fragmentation on biodiversity. Annu Rev Ecol Evol S 34:487–515

    Article  Google Scholar 

  • Fahrig L, Merriam G (1985) Habitat patch connectivity and population survival. Ecology 66:1762–1768

    Article  Google Scholar 

  • García-Barros E, Fartmann T (2009) Butterfly oviposition: sites, behavior and modes. In: Settele J, Shreeve TJ, Konvicka M, Van Dyck H (eds) Ecology of butterflies in Europe. Cambridge University Press, Cambridge, pp 29–42

    Google Scholar 

  • Guay R, Gagnon R, Morin H (1992) A new automatic and interactive tree ring measurement system based on a line scan camera. For Chron 68:138–141

    Article  Google Scholar 

  • Hanski I (1998) Metapopulation dynamics. Nature 396:41–49

    Article  CAS  Google Scholar 

  • Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:282–335

    Article  Google Scholar 

  • Hill CJ (1989) The effect of adult diet on the biology of butterflies 2. The common crow butterfly, Euploea core corinna. Oecologia 81:258–266

    Article  Google Scholar 

  • Hill CJ, Pierce NJ (1989) The effect of adult diet on the biology of butterflies: 1. The common imperial blue, Jalmenus evagoras. Oecologia 81:249–257

    Article  Google Scholar 

  • Hughes JB, Daily GC, Ehrlich PR (2000) Conservation of insect diversity: a habitat approach. Conserv Biol 14:1788–1797

    Article  Google Scholar 

  • Ishii H, Takeda H (1997) Effects of the spatial arrangement of aerial stems and current-year shoots on the demography and growth of Hydrangea hirta in a light-limited environment. New Phytol 136:443–453

    Article  Google Scholar 

  • Joy J, Pulllin AS (1999) Field studies on flooding and survival of overwintering large heath butterfly Coenonymha tullia larvae on Fenn’s and Whixall Mosses in Shrophire and Wrexham, U.K. Ecol Entomol 24:426–431

    Article  Google Scholar 

  • Kawamura K, Takeda H (2008) Developmentally programmed and plastic processes of growth in the multistemmed understory shrub Vaccinium hirtum (Ericaceae). Botany 86:268–277

    Article  Google Scholar 

  • Keddy PA (2000) Wetland ecology: principles and conservation. Cambridge University Press, Cambridge

    Google Scholar 

  • Knurek ES (2010) Taxonomic and population status of the Clayton’s Copper butterfly (Lycaena dorcas claytoni). Thesis, University of Maine

  • Kotiaho J, Kaitala V, Komonen A, Päivinen J (2005) Predicting the risk of extinction from shared ecological characteristics. Proc Natl Acad Sci USA 102:1963–1967

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Kotze DJ, Niemelä J, O’Hara RB, Turin H (2003) Testing abundance-range size relationships in European carabid beetles (Coleoptera, Carabidae). Ecography 26:553–566

    Article  Google Scholar 

  • Krauss J, Steffan-Dewnter I, Tscharntke T (2003) Landscape occupancy and local population size depends on host plant distribution in the butterfly Cupido minimus. Biol Conserv 120:355–361

    Article  Google Scholar 

  • Krauss J, Steffan-Dewnter I, Müller CB, Tscharntke T (2005) Relative importance of resource quantity, isolation and habitat quality for landscape distribution of a monophagous butterfly. Ecography 28:465–474

    Article  Google Scholar 

  • LaBaugh JW (1986) Wetland ecosystem studies from a hydrologic perspective. Water Resour Bull 22:1–10

    Article  Google Scholar 

  • Layberry RA, Hall PW, LaFontaine JD (1998) The butterflies of Canada. University of Toronto Press, Toronto

    Google Scholar 

  • Lent M, Reier Ü (1999) Origin, chromosome number and reproduction biology of Potentilla fruticosa (Rosaceae) in Estonia and Latvia. Acta Botanica Fennica 162:191–196

    Google Scholar 

  • León-Cortés JL, Lennon JJ, Thomas CD (2003) Ecological dynamics of extinct species in empty habitat networks. 2. The role of host plant dynamics. Oikos 102:465–477

    Article  Google Scholar 

  • Mattson WJ (1980) Herbivory in relation to plant nitrogen content. Annu Rev Ecol Evol S11:119–161

    Article  Google Scholar 

  • Mattson WJ, Haack RA (1987) The role of drought in outbreaks of plant-eating insects. Bioscience 37:110–118

    Article  Google Scholar 

  • May PG (1985) Foraging selectivity in adult butterflies: morphological, ecological, and physiological factors affecting flower choice. Dissertation, University of Florida

  • McCollough M, Siebenmann M, Swartz BI (2001) Clayton’s copper assessment, maine department of inland fisheries and wildlife. Wildlife Division, Resource Assessment Section, Endangered and Threatened Species Program, Bangor

    Google Scholar 

  • McLean EO (1982) Soil pH and lime requirement. In: Page AL, Miller RH, Keeney DR (eds) Methods of soil analysis. Part 2—Chemical and microbiological properties. (2nd Ed.). Agronomy 9:199–223

    Google Scholar 

  • Meyer GA, Montgomery ME (1987) Relationships between leaf and the food quality of cottonwood foliage for the gypsy moth Lymantria dispar. Oecologia 72:527–532

    Article  Google Scholar 

  • Mitchell WA, Hughes HG (1995) Line intercept: section 6.25, U.S. Army corps of engineers wildlife resources management manual, Technical Report EL-95-22, U.S. Army Engineer waterways Experiment Station, Vicksburg

    Google Scholar 

  • Mitsch WJ, Gosselink JG (2007) Wetlands, 4th edn. Wiley and Sons, Inc., Hoboken

    Google Scholar 

  • Morrant DS, Schumann R, Petit S (2009) Field sampling and storing nectar from flowers with low nectar volumes. Ann Bot 103:533–542

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Nicholls CN, Pullin AS (2003) The effects of flooding on survivorship in overwintering larvae of the large copper butterfly Lycaena dispar batavus (Lepidoptera: Lycaenidae), and its possible implications for restoration management. Eur J Entomol 100:65–72

    Article  Google Scholar 

  • O’Brien DM (1999) Fuel use in flight and its dependence on nectar feeding in the hawkmoth Amphion floridensis. J Exp Biol 202:441–451

    PubMed  Google Scholar 

  • Oñate M, Munné-Bosch S (2010) Loss of flower bud vigour in the Mediterranean shrub, Cistus albidus L. at advanced developmental stages. Plant Biol 12:475–483

    Article  PubMed  Google Scholar 

  • Percival MS (1961) Types of nectar in angiosperms. New Phytol 60:235–281

    Article  Google Scholar 

  • Rusterholtz H, Erhardt A (1997) Preferences for nectar sugars in the peacock butterfly, Inachisio. Ecol Entomol 22:220–224

    Article  Google Scholar 

  • Rydin H, Jeglum J (2006) The biology of peatlands. Oxford University Press, Oxford

    Book  Google Scholar 

  • Schneider C, Dover J, Fry GLA (2003) Movement of two grassland butterflies in the same habitat network: the role of adult resources and size of the study area. Ecol Entomol 28:219–227

    Article  Google Scholar 

  • Schultz CB, Dlugosch KM (1999) Nectar and hostplant scarcity limit populations of an endangered Oregon butterfly. Oecologia 119:231–238

    Article  Google Scholar 

  • Scott JA (1986) The butterflies of North America. Stanford University Press, Stanford

    Google Scholar 

  • Severns PM (2011) Habitat restoration facilitates an ecological trap for a locally rare, wetland-restricted butterfly. Insect Conserv Divers 4:184–191

    Article  Google Scholar 

  • Severns PM, Boldt L, Villegas S (2006) Conserving a wetland butterfly: quantifying early lifestage survival through seasonal flooding, adult nectar, and habitat preference. J Insect Conserv 10:361–370

    Article  Google Scholar 

  • Smolders AJP, Lamers LPM, Lucassen E, Van der Velde G, Roelofs JGM (2006) Internal eutrophication: how it works and what to do about it—a review. Chem Ecol 22:93–111

    Article  CAS  Google Scholar 

  • Thomas JA, Bourn NAD, Clarke RT, Stewart KE, Simcox DJ, Pearman GS, Curtis R, Goodger B (2001) The quality and isolation of habitat patches both determine where butterflies persist in fragmented landscapes. P Roy Soc B Biol Sci 268:1791–1796

    Article  CAS  Google Scholar 

  • VanOverbeke DR, Kleintjes Neff PK, Fettig SM (2007) Potentilla fruiticosa (Rosaceae) as a Nectar Plant for Butterflies. J Lepid Soc 61:222–227

    Google Scholar 

  • Vitt DH (1990) Growth and production dynamics of boreal mosses over climatic, chemical and topographic gradients. Bot J Linn Soc 104:35–59

    Article  Google Scholar 

  • Vitt DH, Bayley SE, Jin TL (1995) Seasonal variation in water chemistry over a bog-rich fen gradient in Continental Western Canada. Can J Fish Aquat Sci 52:587–606

    Article  CAS  Google Scholar 

  • Wassan MJ, Barendregt A, Palczynski A, De Smidt JT, De Mars H (1990) The relationship between fen vegetation gradients, groundwater flow and flooding in an undrained valley mire at Biebrza, Poland. J Ecol 78:1106–1122

    Article  Google Scholar 

  • Weast RC (ed) (1980) CRC handbook of chemistry and physics, 60th edn. CRC Press, Boca Raton

    Google Scholar 

  • Webb MR, Pullin AS (1998) Effects of submergence by winger flooding on diapausing caterpillars of a wetland buttery, Lycaena dispar batavus. Ecol Entomol 23:96–99

    Article  Google Scholar 

  • Webster RP, Swartz BI (2006) Population studies of the Clayton’s copper at Dwinal Pond wildlife management area (Lee/Winn, Penobscot County, Maine). Maine Department of Inland Fisheries and Wildlife, Bangor

    Google Scholar 

  • White J, White J (1980) Demographic factors in populations of plants. In: Solbring OT (ed) Demography and evolution in plant populations. Botanical monographs. Blackwell Scientific Publications, Oxford

    Google Scholar 

  • Wiklund C (1977) Oviposition, feeding and spatial separation of breeding and foraging habitats in a population of Leptidea sinapis (Lepidoptera). Oikos 28:56–68

    Article  Google Scholar 

  • Yoda K, Suzuki M (1993) Quantitative analysis of major axis development in Viburnum dilatatum and V. wrightii (Caprifoliaceae). J Plant Res 106:187–194

    Article  Google Scholar 

Download references

Acknowledgments

Funding was provided by the Maine Agricultural and Forest Experiment Station (MAFES), U.S. Geological Survey, Maine Cooperative Fish and Wildlife Research Unit, Maine Department of Inland Fisheries and Wildlife (MDIFW), Maine Outdoor Heritage Fund, The Nature Conservancy (TNC), U.S. Fish and Wildlife Service (USFWS), and the University of Maine Wildlife, Fisheries, and Conservation Biology Department. We are especially grateful to B. Swartz, N. Sferra, M. McCollough, W. Halteman, A. Reeves, F. Drummond, M. Day, L.B. Perkins, B. Libby, D. Anderson, A.T. Fessenden, and K. Chenard. We thank the landowners for their generosity in allowing access to their land. The manuscript was improved with a review provided by A. Calhoun and 2 anonymous reviewers. Mention of trade names and commercial parts does not constitute endorsement or recommendation for use by the U.S. Government. This is Maine Agricultural and Forest Experiment Station Publication Number H-6-00531-13.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sarah A. Drahovzal.

Additional information

Judith Rhymer: Retired.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 1632 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Drahovzal, S.A., Loftin, C.S. & Rhymer, J. Environmental predictors of shrubby cinquefoil (Dasiphora fruticosa) habitat and quality as host for Maine’s endangered Clayton’s copper butterfly (Lycaena dorcas claytoni). Wetlands Ecol Manage 23, 891–908 (2015). https://doi.org/10.1007/s11273-015-9427-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11273-015-9427-1

Keywords