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Estuarine gradients and the growth and development of Agapanthia villosoviridescens, (Coleoptera), a stem-borer of the salt marsh halophyte Aster tripolium

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Summary

Phytophagous insects of estuarine salt marshes which live inside their host plants are not directly exposed to estuarine gradients. Host plant quality, however, may change along the estuary as a result of the direct effects of these gradients; as a consequence growth and development of endophagous insects may be influenced. The results of a study of the life cycle of Agapanthia villosoviridescens (Coleoptera, Cerambycidae), a stem-borer of the halophyte Aster tripolium, on three salt marshes along the Westerschelde estuary (the Netherlands) are in line with this hypothesis. It was shown that in upstream direction (1) mean larval weights were consistently higher during the entire period of larval development; (2) the percentage of late instars on a given sampling date generally was higher; (3) the percentage of larvae which underwent successful metamorphosis increased. Furthermore, (4) dry weight of the imagos was highest on the least saline marsh. The effects of estuarine gradients on the Aster host plants was indicated by differences in growth and chloride content between the populations of the three marshes. The non-overlapping geographic distribution of Agapanthia villosoviridescens and its host plant Aster tripolium on the Westerschelde salt marshes may be related to the effects of estuarine gradients on the suitability of the host plant.

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References

  • Åhman I (1985). Larval feeding period and growth of Dasineura brassicae (Diptera) on Brassica host plants. Oikos 44:191–194

    Google Scholar 

  • Austenfeld FA (1974) Untersuchungen zum Ionenhaushalt von Salicornia europaea L. unter besonderer Berücksichtigung des Oxalats in Abhängigkeit von der Substratsalinität. Biochem Physiol Pflanz 165:303–316

    Google Scholar 

  • Ayres MP, MacLean SF (1987) Molt as a component of insect development: Galerucella sagittariae (Chrysomelidae) and Epirrita autumnata (Geometridae). Oikos 48:273–279

    Google Scholar 

  • Baumeister W, Schmidt L (1962) Über die Rolle des Natriums im pflanzlichen Stoffwechsel. Flora 152:24–56

    Google Scholar 

  • Beeftink WG (1957) De buitendijkse terreinen van de Westerschelde en de Zeeschelde. Natuurwetenschappelijke betekenis, bedreiging door het Deltaplan en behoud voor de toekomst. Nat Landschap Tijdchr Contact-Comm Nat Landschapsbescherming 11:33–51

    Google Scholar 

  • Beeftink WG (1976) The coastal salt marshes of Western and Northern Europe: an ecological and phytosociological approach. In: Chapman VJ (ed) Wet coastal ecosystems. Elseviers, Amsterdam London New York, pp 109–155

    Google Scholar 

  • Beeftink WG, Daane MC, Van Liere JM, Nieuwenhuize J (1977) Analysis of estuarine soil gradients in salt marshes of the southwestern Netherlands with special reference to the Scheldt estuary. Hydrobiologia 52:93–106

    Google Scholar 

  • Bultman TL, Faeth SH (1986) Effect of within-leaf density and leaf size on pupal weight of the leaf-mining insect, Cameraria sp. nov. (Lepidoptera: Gracillariidae). Southwestern Nat 46:311–316

    Google Scholar 

  • Cates RG, Henderson CB, Redak RA (1987) Responses of the western spruce budworm to varying levels of nitrogen and terpenes. Oecologia (Berlin) 7:312–316

    Google Scholar 

  • Cavalieri AJ, Huang AHC (1979) Evaluation of proline accumulation in the adaptation of diverse species of marsh halophytes to the saline environment. Am J Bot 66:307–312

    Google Scholar 

  • Cavalieri AJ, Huang AHC (1981) Accumulation of proline and glycinebetaine in Spartina alterniflora Loisel. in response to NaCl and nitrogen in the marsh. Oecologia (Berlin) 49:224–228

    Google Scholar 

  • De Pauw N (1975) Bijdrage tot de kennis van milieu en plankton in het Westerschelde estuarium. Thesis Rijksuniversiteit Gent, Belgium

  • Dyar HG (1890) The number of molts in Lepidopterous larvae. Psyche 5:420–422

    Google Scholar 

  • Flowers TJ, Troke PF, Yeo AR (1977) The mechanism of salt tolerance in halophytes. Annu Rev Plant Physiol 28:89–121

    Google Scholar 

  • Flowers TJ, Hajibagheri MA, Clipson NJW (1986) Halophytes. Q Rev Biol 61:313–337

    Google Scholar 

  • Gillham ME (1957) Vegetation of the Exe estuary in relation to water salinity. J Ecol 45:735–756

    Google Scholar 

  • Heydemann B (1979) Responses of animals to spatial and temporal environmental heterogeneity within salt marshes. In: Jefferies RL, Davy AJ (eds) Ecological processes in coastal environments. Blackwell, Oxford, pp 145–163

    Google Scholar 

  • Horion A (1974) Faunistik der Mitteleuropäischen Käfer, Band XII: Cerambycidae. Überlingen, Bodensee

    Google Scholar 

  • Montfort C, Brandup W (1927) Physiologische und pflanzengeographische Seesalzwirkungen. II. Ökologische Studien über Keimung und erste Entwicklung bei Halophyten. Jahrb Wiss Bot 66:902–946

    Google Scholar 

  • Poljakoff-Mayber A (1975) Morphological and anatomical changes in plants as a response to salinity stress. In: Poljakoff-Mayber A, Gale J (eds) Plants in saline environments. Springer, Berlin Heidelberg New York, pp 97–117

    Google Scholar 

  • Pritchard DW (1967) What is an estuary. Physical viewpoint. Am Ass Adv Sci Publ 83:3–5

    Google Scholar 

  • Pullin AS (1987) Changes in leaf quality following clipping and regrowth of Urtica dioica, and consequences for a specialist insect herbivore, Aglais urticae. Oikos 49:39–45

    Google Scholar 

  • Schroeder LA (1986) Changes in tree leaf quality and growth performance of Lepidopteran larvae. Ecology 67:1628–1636

    Google Scholar 

  • Scriber JM (1984) Host plant suitability. In: Carde RT, Bell WJ (eds) Chemical ecology of insects. Chapman Hall, London, pp 159–202

    Google Scholar 

  • Scriber JM, Slansky F (1981) The nutritional ecology of immature insects. Annu Rev Entomol 26:183–211

    Google Scholar 

  • Shennan C, Hunt R, MacRobbie EAC (1987a) Salt tolerance in Aster tripolium L. I. The effect of salinity on growth. Plant Cell Environ 10:59–65

    Google Scholar 

  • Shennan C, Hunt R, MacRobbie EAC (1987b) Salt tolerance in Aster tripolium L. II. Ionic regulation. Plant Cell Environ 10:67–74

    Google Scholar 

  • Stienstra AW (1986) Nitrate accumulation and growth of Aster trioplium L with a continuous and intermittent nitrogen supply. Plant Cell Environ 9:307–313

    Google Scholar 

  • Storey R, Wyn-Jones RG (1975) Betaine and choline levels in plants and their relationship to sodium chloride stress. Plant Sci Lett 4:161–168

    Google Scholar 

  • Treichel S (1975) Der Einfluß von NaCl auf der Prolin-konzentration verschiedener Halophyten. Z Pflanzenphysiol 76:56–68

    Google Scholar 

  • Van Soelen J, Markussee MM (1983) Notes on the distribution of some insect species living in the stems of Aster tripolium L (Compositae) Entomol Ber 43:124–127

    Google Scholar 

  • Wetteveen J (1986) Marine Littoral Collembola. Thesis, Vrije Universiteit Amsterdam, The Netherlands

    Google Scholar 

  • Yeo AR (1974) Salt tolerance in the halophyte Suaeda maritima L Dum. Thesis, University of Sussex, England

    Google Scholar 

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Hemminga, M.A., van Soelen, J. Estuarine gradients and the growth and development of Agapanthia villosoviridescens, (Coleoptera), a stem-borer of the salt marsh halophyte Aster tripolium . Oecologia 77, 307–312 (1988). https://doi.org/10.1007/BF00378035

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