Skip to main content
Log in

Digestive enzymes of the saltmarsh periwinkleLittorina irrorata (Mollusca: Gastropoda)

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

The saltmarsh periwinkleLittorina irrorata is well adapted for the digestion of a wide range of polysaccharides. Enzyme extracts attacked cellulose, pectin, xylan, bean gum and mannan (common in cell walls of higher plants), as well as starch and laminarin (representative of major polysaccharide classes in fungal, algal, and animal tissues). Activities were generally highes at a ph of 5 or 6. There was no evidence that chitin was digested, but 19 other enzymes, active toward various carbohydrates, lipids and peptides, were demonstrated. Enzymatic activity toward Azocoll, a general substrate for proteinase activity, was weak compared to that of other aquatic detritivores. The maximum was reached at a pH of 8. Enzymatic activities were generally measured with extracts of the entire visceral hump. Separate stomach or intestine extracts also gave strong activities. The stomach was the most acidic section of the digestive system with an average pH of 5.8; the intestine had an average pH of 7.3.

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

Access this article

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

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Alexander SD (1976) Relationship of macrophyte detritus to the salt marsh periwinkle,Littorina irrorata (Say). Ph. D. Thesis, Louisiana State University, Baton Rouge, Louisiana

    Google Scholar 

  • Alexander SK (1979) Diet of the periwinkleLittorina irrorata in a Louisiana salt marsh. Gulf Res Rep 6:293–295

    Google Scholar 

  • Bärlocher F (1985) The role of fungi in the nutrition of stream invertebrates. Bot J Linn Soc 91:83–94

    Article  Google Scholar 

  • Bärlocher F, Porter CW (1986) Digestive enzymes and feeding strategies of three stream invertebrates. J N Am Benthol Soc 5:58–66

    Article  Google Scholar 

  • Bebout BM (1988) The role of marine fungi in the food selection and nutrition of the salt marsh periwinkleLittorina irrorata Say (Gastropoda). MSc Thesis, Univ of North Carolina, Chapel Hill, NC

    Google Scholar 

  • Bjarnov N (1972) Carbohydrases inChironomus, Gammarus and some Trichoptera larvae. Oikos 23:261–263

    Article  CAS  Google Scholar 

  • Calow P (1974) Some observations on locomotory strategies and their metabolic effects in two species of freshwater gastropods,Ancylus fluviatilis Mull. andPlanorbis contortus Linn. Oecologia 16:149–161

    Article  Google Scholar 

  • Chamier A-C (1985) Cell-wall-degrading enzymes of aquatic hyphomycetes: a review. Bot J Linn Soc 91:67–81

    Article  Google Scholar 

  • Denny M (1983) Molecular biomechanics of molluscan mucous secretions. In: Hochachka PW (ed) The Mollusca. Vol. I. Metabolic biochemistry and molecular biomechanics, Academic Press, New York, pp 431–465

    Google Scholar 

  • Fallon RD, Newell SY, Groene LC (1985) Phylloplane algae of standing deadSpartina alterniflora. Mar Biol 90:121–127

    Article  CAS  Google Scholar 

  • Gessner RV (1980) Degradative enzyme production by salt-marsh fungi. Bot Mar 23:133–139

    Article  CAS  Google Scholar 

  • Goudsmit EM (1972) Carbohydrates and carbohydrate metabolism in Mollusca. In: Florkin M, Scheer BT (eds.) Chemical Zoology, Vol. VII. Academic Press, New York, pp 219–243

    Google Scholar 

  • Hackman RH, Goldberg M (1964) New substrates for use with chitinases. Anal Bioch 8:397–401

    Article  CAS  Google Scholar 

  • Hicks RE, Newell SY (1984) A comparison of glucosamine and biovolume conversion factors for estimating fungal biomass. Oikos 42:355–360

    Article  CAS  Google Scholar 

  • Hamilton PV (1976) Predation onLittorina irrorata (Mollusca: Gastropoda) byCallinectes sapidus (Crustacea: Protunidae). Bull Mar Biol 26:403–409

    Google Scholar 

  • Kohlmeyer J, Bebout B (1986) On the occurrence of marine fungi in the diet ofLittorina angulifera and observations on the behavior of the periwinkle. Mar Ecol 7:333–343

    Article  Google Scholar 

  • Kristensen JH (1972) Carbohydrases of some marine invertebrates with notes on their food and on the natural occurrence of the carbohydrates studied. Mar Biol 14:130–142

    Article  Google Scholar 

  • Livingstone DR, Zwaan A de (1983) Carbohydrate metabolism of gastropods. In: Hochachka PW (ed.) The Mollusca, Vol I. Metabolic biochemistry and molecular biomechanics, Academic Press, New York, pp 177–242

    Google Scholar 

  • Martin MM, Kukor JJ, Martin JS, Lawson DL, Merritt RW (1981a) Digestive enzymes of larvae of three species of caddisflies (Trichoptera). Ins Bioch 11:501–505

    Article  CAS  Google Scholar 

  • Martin MM, Martin JS, Kukor JJ, Merritt RW (1980) The digestion of protein and carbohydrate by the stream detritivore,Tipula abdominalis (Diptera, Tipulidae). Oecologia 46:360–364

    Google Scholar 

  • Martin MM, Martin JS, Kukor JJ, Merritt RW (1981b) The digestive enzymes of detritus-feeding stonefly nymphs. Can J Zool 59:1947–1951

    Article  CAS  Google Scholar 

  • McIntire GL, Dunstan WM (1976) Non-structural carbohydrates inSpartina alterniflora Loisel. Bot Mar 19:93–96

    Article  Google Scholar 

  • Monk DC (1976) The distribution of cellulase in freshwater invertebrates of different feeding habits. Freshw Biol 6:471–475

    Article  CAS  Google Scholar 

  • Monk DC (1977) The digestion of cellulose and other dietary components, and pH of the gut in the amphipodGammarus pulex (L.). Freshw Biol 7:431–440

    Article  CAS  Google Scholar 

  • Nelson DJ, Scott DC (1962) The role of detritus in the production of a rock-outcrop community in a Piedmont stream. Limnol Oceanogr 7:396–413

    Article  Google Scholar 

  • Nelson N (1944) A photometric adaptation of the Somogyi method for the determination of glucose. J Biol Chem 153:375–380

    CAS  Google Scholar 

  • Newell SY, Hicks RE (1982) Direct count estimates of fungal and bacterial biovolume in dead leaves of smooth cordgrass (Spartina alterniflora Loisel.). Estuaries 5:246–260

    Article  Google Scholar 

  • Newell SY, Fallon RD, Rodriguez RMC, Groene LC (1985) Influence of rain, tidal wetting and relative humidity on release of carbon dioxide by standing-dead saltmarsh plants. Oecologia 63:73–79

    Article  Google Scholar 

  • Newell SY, Fallon RD, Miller JD (1986) Measuring fungal biomass dynamics in standing-dead leaves of a saltmarsh vascular plant. In: Moss ST (ed), The biology of marine fungi, Cambridge University Press, Cambridge, pp 19–25

    Google Scholar 

  • Newell SY, Miller JD, Fallon RD (1987) Ergosterol content of salt-marsh fungi: effect of growth conditions and mycelial age. Mycologia 79:688–695

    Article  CAS  Google Scholar 

  • Newell SY, Fallon RD, Miller JD (1989) Decomposition and microbial dynamics for standing, naturally positioned leaves of a salt-marsh grass. Mar Biol (in press)

  • Nielson CO (1962) Carbohydrases in soil and litter invertebrates. Oikos 13:200–215

    Article  Google Scholar 

  • Odum EP, Cruz A de la (1963) Detritus as a major component of ecosystems. AIBS Bull 13:39–40

    Article  Google Scholar 

  • Owen G (1966) Digestion. In: Wilbur KM, Yonge CM (eds), Physiology of Mollusca, Vol. II, Academic Press, New York and London, pp 53–96

    Google Scholar 

  • Sinsabaugh RL, Linkins AE, Benfield EF (1985) Cellulose digestion and assimilation by three leaf-shredding aquatic insects. Ecology 66:1464–1471

    Article  CAS  Google Scholar 

  • Somogyi M (1952) Notes on sugar determination. J Biol Chem 195:19–23

    CAS  Google Scholar 

  • Stiven AE, Kuenzler EJ (1979) The response of two salt marsh mollusks,Littorina irrorata andGeukensia demissa to field manipulations of density andSpartina litter. Ecol Monogr 49:151–171

    Article  Google Scholar 

  • Suberkropp K, Klug MJ (1981) The degradation of leaf litter by aquatic hyphomycetes. In: Wicklow DT, Carroll GC (eds) The fungal community. Marcel Dekker, New York, pp 761–776

    Google Scholar 

  • Teal JM (1962) Energy flow in the salt marsh ecosystems in Georgia. Ecology 43:614–624

    Article  Google Scholar 

  • Torzilli AP, Andrykovitch G (1986) Degradation ofSpartina lignocellulose by individual and mixed cultures of salt-marsh fungi. Can J Bot 64:2211–2215

    Article  CAS  Google Scholar 

  • Vogt PAC (1972) Lipid and sterol componentes and metabolism in Mollusca. In: Florkin M, Scheer BT (eds.) Chemical Zoology, Vol. VII. Academic Press, New York, pp 245–300

    Google Scholar 

  • Weete JD, Weber DJ (1980) Lipid biochemistry of fungi and other organisms. Plenum Publishing Corp. New York

    Book  Google Scholar 

  • Wilson JO (1985) Decomposition of litter ofSpartina alterniflora in a salt marsh ecosystem; biochemical and geochemical studies. PhD Thesis, University of Boston, Boston

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bärlocher, F., Arsuffi, T.L. & Newell, S.Y. Digestive enzymes of the saltmarsh periwinkleLittorina irrorata (Mollusca: Gastropoda). Oecologia 80, 39–43 (1989). https://doi.org/10.1007/BF00789929

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00789929

Key words

Navigation