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The adaptive significance of alpine melanism in the butterfly Parnassius phoebus F. (Lepidoptera: Papilionidae)

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Summary

The adaptive significance of alpine melanism, the tendancy for insects to become darker with increased elevation and latitude, was investigated using the butterfly Parnassius phoebus. The effects on temperature dependent activity of five components of overall wing melanism, as well as size, were examined. The components of wing melanism examined were the transparency of the basal hindwing and distal fore-wing areas, the width of the black patch in the basal hind-wing area and the proportion of black to white scales in that area, and the proportion of the distal fore-wing covered by predominantly black scaling.

The body temperature of dead specimens was correlated with air temperature, solar radiation, the width of the black patch at the base of the wings, and the proportion of black to white scales at the base of the wings. The minimum air temperatures and solar radiation levels required for initiation of flight did not vary with wing melanism of P. phoebus, in contrast to the results found for Colias butterflies by Roland (1982). However, under environmental conditions suitable for flight initiation, males with a higher proportion of black to white scales in the basal area of the hind-wing, and wider basal black patches, spent a greater proportion of time in flight at low air temperatures and low insolation. Increased basal wing melanism was also associated with increased movement of males within a population. In contrast, melanism in the distal area of the wings has no effect on activities which are dependant on body temperature. The amount of time spent feeding did not vary with differences in wing melanism. I suggest that in dorsal basking, slow-flying butterflies (Parnassius) basal wing color affects body temperature primarily during flight (rather than while basking), such that butterflies with darker wing bases cool down less rapidly because they absorb more solar radiation during flight.

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References

  • Baker RR (1968) A possible method of evolution of the migratory habit in butterflies. Phil Trans Roy Soc Lond B 253:309–341

    Google Scholar 

  • Baker RR (1969) The evolution of the migratory habit in butterflies. J Anim Ecol 38:703–746

    Google Scholar 

  • Beall G, Williams CB (1945) Geographic variation in the wing length of Danaus plexippus (Lep. Rhopalocera). Proc R Ent Soc Lond A 20:65–76

    Google Scholar 

  • Benham BR, Lonsdale D, Muggleton J (1974) Is polymorphism in two-spot ladybird an example of non-industrial melanism? Nature 249:179–180

    Google Scholar 

  • Bernstein C (1980) Density-dependent changes in sex ratio in Colias lesbia (Lepidoptera: Pieridae) Ecol Ent 5:105–110

    Google Scholar 

  • Brussard PF, Ehrlich PR (1970) The population structure of Erebia epipsodea (Lepidoptera: Satyrinae). Ecology 51:119–129

    Google Scholar 

  • Chaplin SB, Wells PH (1982) Energy reserves and metabolic expenditures of Monarch butterflies overwintering in southern California. Ecol Entomol 7:249–256

    Google Scholar 

  • Clench HK (1966) Behavioral thermoregulation in butterflies. Ecology 4766:1021–1034

    Google Scholar 

  • Clifford TJ (1981) A comparative study of three Colorado populations of Parnassius phoebus F. (Papilionidae). Univ Wyoming MSc thesis, p 105

  • Cook LM, Brower LP, Croze HJ (1967) The accuracy of a population estimation from multiple recapture data. J Anim Ecol 57–60

  • Douglas MM (1978) The behavioral and biophysical strategies of thermoregulation in temperate butterflies. Univ Kansas PhD thesis, p 323

  • Douglas MM, Grula JW (1978) Thermoregulatory adaptations allowing ecological range expansion by the Pierid butterfly Nathalis iole Boisduval. Evolution 32:776–783

    Google Scholar 

  • Douwes P (1976) Activity in Heodes virgaurae (Lep., Lycaenidae) in relation to air temperature, solar radiation, and time of day. Oecologia (Berlin) 22:287–298

    Google Scholar 

  • Downes JA (1964) Arctic insects and their environment. Can Ent 96:279–307

    Google Scholar 

  • Downes JA (1965) Adaptations of insects in the arctic. Ann Rev Entomol 10:257–274

    Google Scholar 

  • Ehrlich PR, Launer AE, Murphy DD (1984) Can sex ratio be defined or determined? The case of a population of checkerspot butterflies. Amer Nat 124:527–539

    Google Scholar 

  • Ehrlich PR, White RR, Singer MC, McKecknie SW, Gilbert LE (1975) Checkerspot butterflies: A historical perspective. Science 188:221–228

    Google Scholar 

  • Ferris CD (1976) A proposed revision of non-arctic Parnassius phoebus Fabricius in North America (Papilionidae). J Res Lepid 15:1–22

    Google Scholar 

  • Freeman TN (1958) The distribution of arctic and subarctic butterflies. Proc 10th Internat Congr Ent 1:659–672

    Google Scholar 

  • Gilbert LE, Singer MC (1975) Butterfly ecology. Ann Rev Ecol System 6:365–395

    Google Scholar 

  • Guppy CS (1984) Alpine melanism in the butterfly Parnassius phoebus F. (Lepidoptera: Papilionidae). Univ British Columbia MSc thesis, p 159

  • Guppy CS (1986) Geographic variation in wing melanism of the butterfly Parnassius phoebus F. (Lepidoptera: Papilionidae). Can J Zool 64:956–962

    Google Scholar 

  • Harrison RG (1980) Dispersal polymorphisms in insects. Ann Rev Ecol Syst 11:95–118

    Google Scholar 

  • Heinrich B (1981) Insect Thermoregulation. John Whiley and Sons, New York

    Google Scholar 

  • Hovanitz W (1941) Parallel ecogenotypical color variation in butterflies. Ecology 22:259–284

    Google Scholar 

  • Hovanitz W (1950) The biology of Colias butterflies. I. The distribution of the North American species. Wasman J Biology 8:49–75

    Google Scholar 

  • Jones RE, Hart JR, Bull GD (1982) Temperature, size, and egg production in the cabbage butterfly, Pieris rapae L.. Aust J Zool 30:223–232

    Google Scholar 

  • Kammer AE (1970) Thoracic temperature, shivering, and flight in the Monarch butterfly, Danaus plexippus (L.). Z Vergl Physiologie 68:334–344

    Google Scholar 

  • Kettlewell B (1973) The evolution of melanism. the study of a recurring necessity. Clarendon Press, Oxford

    Google Scholar 

  • Kevan PG, Shorthouse JD (1970) Behavioural thermoregulation by high artic butterflies. Arctic 23:268–279

    Google Scholar 

  • Kingsolver JG (1983a) Thermoregulation and flight in Colias butterflies: Elevational patterns and mechanistic limitations. Ecology 64:534–545

    Google Scholar 

  • Kingsolver JG (1983b) Ecological significance of flight activity in Colias butterflies: Implications for reproductive strategy and population structure. Ecology 64:546–551

    Google Scholar 

  • Kingsolver JG, Koehl MAR (1985) Aerodynamics, thermoregulation, and the evolution of insect wings: Differential scaling and evolutionary change. Evolution 39:488–504

    Google Scholar 

  • Kingsolver JG, Moffat RJ (1982) Thermoregulation and the determinates of heat transfer in Colias butterflies. Oecologia (Berlin) 53:27–33

    Google Scholar 

  • Kingsolver JG, Watt WB (1983) Thermoregulatory strategies in Colias butterflies: Thermal stress and the limits to adaptation in temporally varying environments. Am Nat 121:32–55

    Google Scholar 

  • Mani MS (1962) Introduction to high altitude entomology. Insect life above the timberline in the north-west Himalaya. Methuen and Co Ltd, London

    Google Scholar 

  • Mani MS (1968) Ecology and biogeography of high altitude insects. Dr W Junk NV Publishers, The Hague

    Google Scholar 

  • Murphy DD, Launer AE, Ehrlich PR (1983) The role of adult feeding in egg production and population dynamics of the checkerspot butterfly Euphydryas editha. Oecologia (Berlin) 56:257–263

    Google Scholar 

  • Murphy DD, Menninger MS, Ehrlich PR (1984) Nectar source distribution as a determinant of oviposition host species in Euphydryas chalcedona. Oecologia (Berlin) 62:269–271

    Google Scholar 

  • Neville AC, Weis-Fogh T (1963) The effect of temperature on locust flight muscle. J Exp biol 40:111–121

    Google Scholar 

  • Nielsen ET, Nielsen HT (1959) Temperatures preferred by the Pierid Ascia monuste L.. Ecology 40:181–185

    Google Scholar 

  • Rainey RC (1974) Biometeorology and insect flight: Some aspects of energy exchange. Ann Rev Ent 19:407–439

    Google Scholar 

  • Roff D (1977) Dispersal in Dipterans: Its costs and consequences. J Anim Ecol 46:443–456

    Google Scholar 

  • Roland J (1978) Variation in spectral reflectance of alpine and arctic Colias (Lepidoptera: Pieridae). Can J Zool 56:1447–1453

    Google Scholar 

  • Roland J (1982) Melanism and diel activity of alpine Colias (Lepidoptera: Pieridae). Oecologia (Berlin) 53:214–221

    Google Scholar 

  • Shapiro AM (1970) The role of sexual behavior in density-related dispersal of Pierid butterflies. Amer Nat 104:367–372

    Google Scholar 

  • Southwood TRE (1962) Migration of terrestrial arthropods in relation to habitat. Biol Rev 37:171–214

    Google Scholar 

  • Vielmetter W (1958) Physiologie des Verhaltens zur Sonnenstrahlung bei dem Tagfalter Argynnis paphia L.-I. Untersuchungen im Freiland. J Insect Physiol 2:13–37

    Google Scholar 

  • Watt WB (1968) Adaptive significance of pigment polymorphisms in Colias butterflies. I. Variation of melanin pigment in relation to thermoregulation. Evolution 22:437–458

    Google Scholar 

  • Watt WB (1985) Bioenergetics and evolutionary genetics: Opportunities for new synthesis. Am Nat 125:118–143

    Google Scholar 

  • Young AM (1982) Population biology of tropical insects. Plenum Press, N.Y.

    Google Scholar 

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Guppy, C.S. The adaptive significance of alpine melanism in the butterfly Parnassius phoebus F. (Lepidoptera: Papilionidae). Oecologia 70, 205–213 (1986). https://doi.org/10.1007/BF00379241

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