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Digestion of uncrushed leaf tissues by leaf-snipping larval Lepidoptera

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Summary

Cynodon dactylon (Poaceae) leaf pieces recovered from the frass of final-instar Paratrytone melane larvae (Lepidoptera: Hesperiidae) were composed of 14–22 percent crushed cells and 78–86 percent uncrushed cells, yet approximate digestibilities of soluble carbohydrates and protein averaged 78 and 88 percent, respectively. Therefore, nutrients from uncrushed cells were extracted by P. melane. The ability of P. melane and another leaf-snipping lepidopteran, Pseudaletia unipuncta (Noctuidae), to digest the contents of uncrushed bundle sheath and mesophyll cells in C. dactylon was examined with transmission electron microscopy. Organelles and plasma membranes were digested in the foreguts and midguts of both species. These findings suggest that nutrients in uncrushed leaf cells may be extracted through plasmodesmata and cell wall pores after membranes are digested. The generality of leaf-snipping, vis-a-vis leaf crushing, among larval Lepidoptera was assessed by surveying the mandible morphologies of 202 species. In 82 percent of the species surveyed only incisor regions were present. I conclude that leaf-snipping is a common mode of feeding among phytophagous Lepidoptera and that the digestion of cell contents is efficient despite the fact that few of the cells of ingested plant tissues are crushed.

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References

  • Barbehenn R (1989) The nutritional ecology and mechanisms of digestion of C3 and C4 grass-feeding Lepidoptera. PhD thesis, University of California, Berkeley

    Google Scholar 

  • Baron-Epel O, Gharyal PK, Schindler M (1988) Pectins as mediators of wall porosity in soybean cells. Planta 175:389–395

    Google Scholar 

  • Bennack DE (1981) The effects of mandible morphology and photosynthetic pathway on selective herbiory in grasshoppers. Oecologia 51:281–283

    Google Scholar 

  • Berenbaum M (1980) Adaptive significance of midgut pH in larval lepidoptera. Am Nat 115:138–146

    Google Scholar 

  • Bernays EA, Barbehenn RV (1987) Nutritional ecology of grass foliage-chewing insects. In: Slansky F Jr., Rodriguez JG (eds) Nutritional ecology of insects, mites, spiders, and related invertebrates. John Wiley and Sons, New York, pp 147–176

    Google Scholar 

  • Bernays EA, Janzen DH (1988) Saturniid and sphingid caterpillars: two ways to eat leaves. Ecology 69:1153–1160

    Google Scholar 

  • Berry JA, Downton WJS, Tregunna EB (1970) The photosynthetic carbon metabolism of Zea mays and Gomphrena globosa: the location of CO2 fixation and the carboxyl transfer reactions. Can J Bot 48:777–786

    Google Scholar 

  • Biedermann W (1919) Beiträge zur vergleichenden Physiologie der Verdauung. Arch ges Physiol 174:392–425

    Google Scholar 

  • Bjorkman O, Berry J (1973) High-efficiency photosynthesis. Sci Am 229:80–93

    Google Scholar 

  • Boys M (1981) Food selection by some graminivorous Acrididae. PhD thesis, University of Oxford, U.K.

    Google Scholar 

  • Brown JW (1984) Host records for Paratrytone melane (Edwards) (Hesperiidae). J Lep Soc 38:138

    Google Scholar 

  • Carpita N, Sabularse D, Montezinos D, Delmer DP (1979) Determination of the pore size of cell walls of living plant cells. Science 205:1144–1147

    Google Scholar 

  • Caswell M, Reed FC (1975) Indigestibility of C4 bundle sheath cells by the grasshopper, Melanoplus confusus. Ann Entomol Soc Am 68:686–688

    Google Scholar 

  • Caswell H, Reed FC (1976) Plant-herbivore interactions: the indigestibility of C4 bundle sheath cells by grasshoppers. Oecologia 26:151–156

    Google Scholar 

  • Caswell H, Reed F, Stephenson SN, Werner PA(1973) Photosynthetic pathways and selective herbivory: a hypothesis. Am Nat 107:465–480

    Google Scholar 

  • Chapin FS III, Bloom AJ, Field CB, Waring RH (1987) Plant responses to multiple environmental factors. BioScience 37:49–57

    Google Scholar 

  • Chapman RF (1982) The insects: structure and function. Harvard University Press, Cambridge

    Google Scholar 

  • Chapman MS, Suh SW, Cascio D, Smith WW, Eisenberg D (1987) Sliding-layer conformational change limited by the quaternary structure of plant RuBisCO. Nature 329:354–356

    Google Scholar 

  • Cockfield SD (1988) Relative availability of nitrogen in host plants of invertebrate herbivores: three possible nutritional and physiological definitions. Oecologia 77:91–94

    Google Scholar 

  • Dow JAT (1986) Insect midgut function. Adv Insect Physiol 19:187–328

    Google Scholar 

  • Evans AC (1939) The utilization of food by the larvae of the buff-tip Phalera bucephala (Linn.) (Lepidopt.) Proc Royal Entomol Soc (London) 14:25–30

    Google Scholar 

  • Evert RF, Eschrich W, Heyser W (1977) Distribution and structure of the plasmodesmata in mesophyll and bundle sheath cells of Zea mays L. planta 136:77–89

    Google Scholar 

  • Farrar SC, Farrar JF (1986) Compartmentation and fluxes of sucrose in intact leaf blades of barley. New Phytol 103:645–657

    Google Scholar 

  • Freifelder D (1987) Molecular biology. Jones and Bartlett Publishers, Inc., Boston

    Google Scholar 

  • Harvey GT (1975) Nutritional studies of eastern spruce budworm (Lepidoptera: Tortricidae) II. Starches. Can Entomol 107:717–728

    Google Scholar 

  • Heidorn T, Joern A (1984) Differential herbivory on C3 versus C4 grasses by the grasshopper Ageneotettix deorum (Orthoptera: Acrididae). Oecologia 65:19–25

    Google Scholar 

  • Hocking B, Depner KR (1961) Larval nutrition in Agrotis orthogonia (Lepidoptera: Phalaenidae): digestive enzymes. Ann Entomol Soc Am 54:86–98

    Google Scholar 

  • Horie Y, Nakasome S, Watanabe K, Nakamura M, Suda H (1985) Daily ingestion and utilization of various kinds of nutrients by the silkworm, Bombyx mori (Lepidoptera: Bombycidae). Appl Entomol Zool 20:159–172

    Google Scholar 

  • Jones CG, Hare JD, Compton SJ (1989) Measuring plant protein with the Bradford assay. I. Evaluation and standard method. J Chem Ecol 15:979–992

    Google Scholar 

  • Ku SB, Schmitt MR, Edwards GE (1979) Quantitative determination of RuBP carboxylase-oxygenase in leaves of several C3 and C4 plants. J Exp Bot 30:89–98

    Google Scholar 

  • Martin MM, Martin JS (1984) Surfactants: their role in preventing the precipitation of protein by tannins in insect guts. Oecologia 61:342–345

    Google Scholar 

  • O'Brien TP, McCully ME (1981) The study of plant structure: principles and selected methods. Termarcarphi Pty Ltd., Melbourne

    Google Scholar 

  • Peterson A (1951) Larvae of insects. Part 1: Lepidoptera and plant infesting Hymenoptera. Edwards Bros., Ann Arbor

    Google Scholar 

  • Rintamaki E (1989) Formation of disulphide cross-linked aggregates of large subunit from higher plant ribulose-1,5-bisphosphate carboxylase-oxygenase. J Exp Bot 40:1305–1313

    Google Scholar 

  • Robards AW (1976) Plasmodesmata in higher plants. In: Gunning BES, RobardsAW (eds) Intercellular communication in plants: studies on plasmodesmata. Springer-Verlag, New York, pp 15–57

    Google Scholar 

  • Rybicki M (1957) Mechanism of digestion of leaves of green plants by some lepidopterous caterpillars. Acta Biol Exp (Warsaw) 17:289–316

    Google Scholar 

  • Santos CD, Ferreira C, Terra WR (1983) Consumption of food and spatial organization of digestion in the cassava hornworm, Erinnyis ello. J Insect Physiol 29:707–714

    Google Scholar 

  • Santos CD, Terra WR (1986) Distribution and characterization of oligomeric digestive enzymes from Erinnyis ello larvae and inferences concerning secretory mechanisms and the permeability of the peritrophic membrane. Insect Biochem 16:691–700

    Google Scholar 

  • Schultz JC, Lechowicz MJ(1986) Hostplant, larval age, and feeding behavior influence midgut pH in the gypsy moth (Lymantria dispar). Oecologia 71:133–137

    Google Scholar 

  • Stehr FW (1987) Immature insects. Kendall/Hunt Publishing Co., Dubuque, Iowa

    Google Scholar 

  • Terry BR, Robards AW (1987) Hydrodynamic radius alone governs the mobility of molecules through plasmodesmata. Planta 171:145–157

    Google Scholar 

  • Thomson WW, Moeller CH (1983) Effects of TWEEN-20, polyoxyethylene sorbitan monolaurate on the ultrastructure and organization of chloroplast membranes. Protoplasma 114:173–178

    Google Scholar 

  • Valle EM, Craig S, Hatch MD, Heldt HW (1989) Permeability and ultrastructure of bundle sheath cells isolated from C4 plants: structure-function studies and the role of plasmodesmata. Botanica Acta 102:276–282

    Google Scholar 

  • Vonk HJ, Western JRH (1984) Comparative biochemistry and physiology of enzymatic digestion. Academic Press, New York

    Google Scholar 

  • Wigglesworth VB (1972) The principles of insect physiology. Methuen and Co. London

    Google Scholar 

  • Yemm EW and Willis AJ (1954) The estimation of carbohydrates in plant extracts by anthrone. Biochem J 57:508–514

    Google Scholar 

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Barbehenn, R.V. Digestion of uncrushed leaf tissues by leaf-snipping larval Lepidoptera. Oecologia 89, 229–235 (1992). https://doi.org/10.1007/BF00317222

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