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Density effects in a colonial monoculture: experimental studies with a marine bryozoan (Membranipora membranacea L.)

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Summary

Naturally occurring monocultures of plants and animals are not common, despite recent emphasis on the analysis of density effects in artificial plant monocultures. In natural populations, Membranipora membranacea, an encrusting marine bryozoan, usually forms monospecific, nearly even-aged stands on kelp blades. We experimentally manipulated the density of M. membranacea colonies and monitored the responses of individual colonies on settling panels. Colonies undergo a sub-annual cycle of growth, stasis and reproduction, shrinkage, and death. However, crowding by conspecifics accelerates the transition to stasis, triggers early onset of reproduction, and results in increased stage-specific mortality. Unlike many interactions involving colonial invertebrates, overgrowth rarely occurs at boundaries of M. membranacea colonies. Instead, colonies stop growing when they contact conspecifics; therefore more dense assemblages are populated with smaller individual colonies. At the peak in colony size during August, the mean size among colonies grown at high population densities was 300 mm2 less than colonies grown at low densities or approximately 62% smaller. Mortality was concentrated in small size classes; at the end of the season colonies gradually shrank to the smallest size classes and then died. We summarized the demography of M. membranacea colonies on low- and high-density panels using size-classified transition matrices and used loglinear analysis to examine the effects of density and time on the transition patterns. As the amount of free space on panels declined, so did the frequency of upward size-class transitions. Our analysis revealed that free space declined more rapidly on panels in the high density treatment and that the transitional probabilities were sensitive to density of conspecifics and seasonal change, but only for some size classes and during some time periods.

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References

  • Atkins D (1955) The cyphonautes larvae of the Plymouth area and the metamorphosis in Membranipora membranacea (L.). J Mar Biol Assoc UK 34:441–449

    Google Scholar 

  • Bernstein BB, Jung N (1979) Selective pressures and coevolution in a kelp canopy community in southern California. Ecol Monogr 49:335–355

    Google Scholar 

  • Bierzychudek P (1982) The demography of jack-in-the-pulpit, a forest perennial that changes sex. Ecol Monogr 52:335–351

    Google Scholar 

  • Bierzychudek P (1984) Assessing optimal life histories in a fluctuating environment: The evolution of sex-changing by jack-in-the-pulpit. Am Nat 123:829–840

    Google Scholar 

  • Bishop YMM, Fienberg SE, Holland PW (1975) Discrete multivariate analysis: Theory and practice, MIT Press, Cambridge, MA, USA

    Google Scholar 

  • Bushnell JH (1966) Environmental relations of Michigan Ectoprocta, and dynamics of natural populations of Plumatella repens. Ecol Monogr 36:95–123

    Google Scholar 

  • Buss LW (1981) Group living, competition, and the evolution of cooperation in a sessile invertebrate. Science (NY) 213:1012–1014

    Google Scholar 

  • Buss LW (1986) Competition and community organization on hard surfaces in the sea. In: Diamond J, Case TJ (eds) Community ecology. Harper & Row, NY, pp 517–537

    Google Scholar 

  • Caswell H (1982a) Stable population structure and reproductive value for populations with complex life cycles. Ecology 63:1223–1231

    Google Scholar 

  • Caswell H (1982b) Optimal life histories and the maximization of reproductive value: A general theorem for complex life cycles. Ecology 63:1218–1222

    Google Scholar 

  • Caswell H (1985) Evolutionary demography of clonal reproduction. In: Jackson JBC, Buss LW, Cook RE (eds) Population biology and evolution of clonal organisms. Yale Univ Press, New Haven, CT, USA, pp 187–224

    Google Scholar 

  • Caswell H (1986) Life cycle models for plants. Lectures on Mathematics in the Life Sciences 18:171–233

    Google Scholar 

  • Caswell H (1988) Approaching size and age in matrix population models. In: Ebenman B, Persson L (eds) Size-structured populations. Springer, New York, pp 85–105

    Google Scholar 

  • Caswell H (1989) Matrix population models: construction, analysis and interpretation. Sinauer Assoc, Sunderland, MA, USA

    Google Scholar 

  • Comfort A (1979) The biology of senescence. Elsevier, NY

    Google Scholar 

  • Connell JH, Keough M (1985) Succession on marine hard substrata. In: Pickett STA, White PS (eds) The ecology of natural disturbance and patch dynamics. Academic Press, NY

    Google Scholar 

  • Cook RE (1979) Asexual reproduction: A further consideration. Am Nat 113:769–772

    Google Scholar 

  • Dixon WJ (1981) BMDP statistical software. Univ California Press, Berkeley, CA, USA

    Google Scholar 

  • Ellison AM (1987) Effects of competition, disturbance, and herbivory on Salicornia europaea. Ecology 68:576–586

    Google Scholar 

  • Ellison AM, Harvell CD (1989) Size hierarchies in Membranipora membranacea: Do colonial animals follow the same rules as plants? Oikos 55:349–355

    Google Scholar 

  • Elvin DW (1976) Seasonal growth and reproduction of an intertidal sponge, Haliclona permollis. Biol Bull 151:108–125

    Google Scholar 

  • Fingleton B (1984) Models of category counts. Cambridge Univ Press, Cambridge, UK

    Google Scholar 

  • Greene CH, Schoener A, Corets E (1983) Succession on marine hard substrata: The adaptive significance of solitary and colonial strategies in temperate fouling communities. Mar Ecol Proger Ser 13:121–129

    Google Scholar 

  • Grigg RW (1977) Population dynamics of two gorgonian corals. Ecology 58:278–290

    Google Scholar 

  • Grosberg RK (1988) Life history variation within a population of the colonial ascidian Botryllus schlosseri. Evolution 42:900–921

    Google Scholar 

  • Harper JL (1977) Population biology of plants. Academic Press, London

    Google Scholar 

  • Harvell CD (1985) Partial predation, inducible defense and the population biology of a marine bryozoan. Dissertation. Univ Washington, Seattle, WA, USA

  • Harvell CD (1986) The ecology and evolution of inducible defenses in a marine bryozoan: cues, costs and consequences. Am Nat 128:810–823

    Google Scholar 

  • Harvell CD, Greene CH (1984) Foul play: Some consequences of life histories among temperate bryozoans. In: 6th Int Congr Marine Corrosion and Fouling, Athens Greece, pp 261–267

  • Harvell CD, Grosberg RK (1988) The timing of sexual maturity in colonial animals: An empirical study. Ecology 69:1855–1864

    Google Scholar 

  • Holler LC, Abrahamson WG (1979) Seed and vegetative reproduction in relation to density in Fragaria virginiana. Am J Bot 64:1003–1007

    Google Scholar 

  • Hubbell SP, Werner PA (1979) On measuring the intrinsic rate of increase of populations with heterogeneous life histories. Am Nat 113:277–293

    Google Scholar 

  • Hughes TP (1984) Population dynamics based on individual size rather than age: A general model with a reef coral example. Am Nat 123:778–795

    Google Scholar 

  • Hughes TP, Connell J (1987) Population dynamics based on size or age? A reef-coral analysis. Am Nat 129:818–829

    Google Scholar 

  • Hughes TP, Jackson JBC (1980) Do corals lie about their age? Some demographic consequences of partial mortality, fission and fusion. Science (NY) 209:713–715

    Google Scholar 

  • Hughes TP, Jackson JBC (1985) Population dynamics and life histories of foliaceous corals. Ecol Monogr 55:141–166

    Google Scholar 

  • Ivker FB (1972) A hierarchy of histo-incompatibility in Hydractinia echinata. Biol Bull 143:162–174

    Google Scholar 

  • Jackson JBC (1986) Modes of dispersal of clonal benthic invertebrates: Consequences for species distributions and genetic structure of local populations. Bull Mar Sci 39:588–606

    Google Scholar 

  • Jackson JBC, Wertheimer SP (1985) Patterns of reproduction in five common species of Jamaican reef-associated bryozoans. In: Nielsen C, Larwood GP (eds) Bryozoa: Ordovician to Recent. Olsen and Olsen, Fredensborg, Denmark, pp 161–168

    Google Scholar 

  • Keough M (1986) The distribution of a bryozoan on seagrass blades: Settlement, growth and mortality. Ecology 67:846–857

    Google Scholar 

  • Kirkpatrick M (1984) Demographic models based on size, not age, for organisms with indeterminate growth. Ecology 65:1874–1884

    Google Scholar 

  • Lippe E, Smith JT de, Glenn-Lewin DC (1985) Markov models and successions: A test from the heathland in the Netherlands. J Ecol 73:775–793

    Google Scholar 

  • Lovett-Doust L (1981) Population dynamics and local specialization in a clonal perennial (Ranunculus repens). I. The dynamics of ramets in contrasting habitats. J Ecol 69:743–755

    Google Scholar 

  • Mack R (1976) Survivorship of Cerastium atrovirens at Aberffraw, Anglesey. J Ecol 64:309–312

    Google Scholar 

  • McBeth JW (1968) Feeding behavior of Corambella steinbergae. Veliger 11:145–146

    Google Scholar 

  • McFadden CM (1986) Interspecific competition for space between the hydroids Hydractinia echinata and Pococoryne carnea. Biol Bull 171:161–174

    Google Scholar 

  • McFadden CM (1987) Colony fission increases particle capture rates of a soft coral: Advantages of being a small colony. J Exp Mar Biol Ecol 103:1–20

    Google Scholar 

  • Mirmirani M, Oster G (1978) Competition, kin selection and evolutionary stable strategies. Theor Pop Biol 13:304–339

    Google Scholar 

  • Moloney KA (1988) Fine-scale spatial and temporal variation in the demography of a perennial bunchgrass. Ecology 69:1588–1598

    Google Scholar 

  • Okamura B (1984) The effects of ambient flow velocity, colony size and upstream colonies on the feeding success of Bryozoa. I. Bugula stolonifera, an arborescent species. J Exp Mar Biol Ecol 83:179–193

    Google Scholar 

  • Okamura B (1985) The effects of ambient flow velocity, colony size and upstream colonies on the feeding success of Bryozoa. II. Conopeum reticulum, an encrusting species. J Exp Mar Biol Ecol 89:69–80

    Google Scholar 

  • Osburn RC (1950) Bryozoa of the Pacific coast of America, vol. 14, Allan Hancock Pacific Expeditions. Univ Southern California Press, Los Angeles, CA, USA

    Google Scholar 

  • Price M, Waser N (1979) Pollen dispersal and optimal outerossing in Delphinium nelsoni. Nature 277:294–297

    Google Scholar 

  • Roughgarden J, Iwasa Y, Baxter C (1985) Demographic theory for an open marine population with space-limited recruitment. Ecology 66:54–67

    Google Scholar 

  • Ryland JS (1976) Physiology and ecology of marine bryozoans. Adv Mar Biol 14:285–433

    Google Scholar 

  • Schmitt J, Eccleston J, Ehrhardt DW (1987) Density-dependent flowering phenology, outcrossing and reproduction in Impatiens capensis. Oecologia 72:341–348

    Google Scholar 

  • Schoener A, Greene CH (1981) Comparison between destructive and nondestructive sampling of sessile epibenthic organisms. Limnol Oceanogr 26:770–774

    Google Scholar 

  • Sebens K (1982) Competition for space: Growth rate, reproductive output and escape in size. Am Nat 120:189–197

    Google Scholar 

  • Seed R (1976) Observations on the ecology of Membranipora (Broyzoa) and a major predator Doridella steinbergae (Nudibranchiata) along the fronds of Laminaria saccharina at Friday Harbor, Washington. J Exp Mar Biol Ecol 24:1–17

    Google Scholar 

  • Selman M (1970) The population dynamics of Avena fatua in continuous spring barley. Proc Brit Weed Contr Conf 10:1176–1188

    Google Scholar 

  • Sharitz RR, McCormick JF (1972) The population dynamics of two competing annual plant species. Ecology 54:723–740

    Google Scholar 

  • Shaw RG (1985) Response to density in a wild population of the perennial herb Salvia lyrata: Variation among families. Evolution 40:492–506

    Google Scholar 

  • Shields WM (1982) Philopatry, inbreeding and the evolution of sex. State University of New York Press, Albany, NY

    Google Scholar 

  • Silen L (1966) On the fertilization problem in the gymnolaematous Bryozoa. Ophelia 3:113–140

    Google Scholar 

  • Solbrig OT (1980) Demography and evolution in plant populations. Blackwell, Oxford, UK

    Google Scholar 

  • Solbrig OT, Newell SJ, Kincaid DT (1981) The population biology of the genus Viola. The demography of Viola sororia. J Ecol 68:521–546

    Google Scholar 

  • Turner MD, Rabinowitz D (1983) Factors affecting frequency distributions of plant mass: The absence of dominance and suppression in competing monocultures of Festuca paradoxa. Ecology 64:469–475

    Google Scholar 

  • Usher MB (1979) Markovian approaches to ecological succession. J Anim Ecol 48:413–426

    Google Scholar 

  • Wahle CM (1983a) The role of age, size and injury in sexual reproduction among Jamaican gorgonians. [Abstr]. Am Zool 23(4):45

    Google Scholar 

  • Wahle CM (1983b) Regeneration of injuries among Jamaican gorgonians: The roles of colony physiology and environment. Biol Bull 165:778–790

    Google Scholar 

  • Weiner J (1985) Size hierarchies in experimental populations of annual plants. Ecology 66:743–752

    Google Scholar 

  • Weller DE (1987) A reevaluation of the-3/2 power rule of plant self thinning. Ecol Monogr 57:23–43

    Google Scholar 

  • Westoby M (1985) The self-thinning rule. Adv Ecol Res 14:167–225

    Google Scholar 

  • Wethey DS (1983) Intrapopulation variation in growth of sessile organisms: Natural populations of the intertidal barnacle Balanus balanoides. Oikos 40:14–23

    Google Scholar 

  • Winston JE, Jackson JBC (1984) Ecology of cryptic coral reef communities. IV. Development and life histories of encrusting cheilostome bryozoans. J Exp Mar Biol Ecol 76:1–21

    Google Scholar 

  • Yoshioka PM (1973) The population dynamics and ecology of the encrusting ectoproct Membranipora serrilamella. Dissertation. Univ California, San Diego, CA, USA

  • Yoshioka PM (1982a) Predator-induced polymorphism in the bryozoan Membranipora membranacea. J Exp Mar Biol Ecol 61:233–242

    Google Scholar 

  • Yoshioka PM (1982b) Role of planktonic and benthic factors in the population dynamics of the bryozoan Membranipora membranacea. Ecology 63:457–468

    Google Scholar 

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Harvell, C.D., Caswell, H. & Simpson, P. Density effects in a colonial monoculture: experimental studies with a marine bryozoan (Membranipora membranacea L.). Oecologia 82, 227–237 (1990). https://doi.org/10.1007/BF00323539

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