LINKING BIOGEOGRAPHY AND COMMUNITY ECOLOGY: LATITUDINAL VARIATION IN PLANT–HERBIVORE INTERACTION STRENGTH

Ecological interactions may vary geographically as a function of diversity, density, or per capita interaction strengths, but we know little about the relative importance of these three mechanisms. We examined variation in species richness, abundance, and interactions among leaf-chewing herbivores and the dominant salt-marsh plant Spartina alterniflora along the Atlantic Coast of the United States. High-latitude S. alterniflora plants are more palatable to herbivores than are low-latitude plants. Within this range of latitude, diversity and density of the dominant leaf-chewing consumers, snails and grasshoppers, in Spartina-dominated portions of the marsh varied little. Low-latitude plants, however, experienced much greater levels of leaf damage from consumers than did high-latitude plants. Per capita feeding rates of low-latitude snails (Littoraria irrorata) and grasshoppers (Orchelimum fidicinum) in the laboratory were greater than feeding rates of high-latitude snails (Melampus bidentatus) and grasshoppers (Conocephalus spartinae). In field experiments, low-latitude snails strongly suppressed S. alterniflora growth, but high-latitude snails had no effect on primary production. Thus, latitudinal differences in the effect of herbivores on plants (i.e., interaction strength), driven by differences in per capita effects among species, rather than differences in diversity or density, may contribute to selection for latitudinal differences in plant palatability. Because geographical differences in interaction strength can occur in the absence of differences in diversity or density, linking biogeography with community ecology will require experimental studies that explicitly measure interaction strength at multiple geographic locations.

[1]  Eric Post,et al.  LARGE‐SCALE SPATIAL GRADIENTS IN HERBIVORE POPULATION DYNAMICS , 2005 .

[2]  S. Pennings,et al.  LATITUDINAL VARIATION IN PALATABILITY OF SALT-MARSH PLANTS: ARE DIFFERENCES CONSTITUTIVE? , 2005 .

[3]  S. Pennings,et al.  Habitat range and phenotypic variation in salt marsh plants , 2005, Plant Ecology.

[4]  P. Reich,et al.  Global patterns of plant leaf N and P in relation to temperature and latitude. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[5]  S. Pennings,et al.  Environmental gradients and herbivore feeding preferences in coastal salt marshes , 2004, Oecologia.

[6]  Sean C. Thomas,et al.  The worldwide leaf economics spectrum , 2004, Nature.

[7]  Helmut Hillebrand,et al.  On the Generality of the Latitudinal Diversity Gradient , 2004, The American Naturalist.

[8]  G. Cronin,et al.  Are Tropical Herbivores More Resistant Than Temperate Herbivores to Seaweed Chemical Defenses? Diterpenoid Metobolites from Dictyota acutiloba as Feeding Deterrents for Tropical Versus Temperate Fishes and Urchins , 1997, Journal of Chemical Ecology.

[9]  N. Targett,et al.  Biogeographic comparisons of marine algal polyphenolics: evidence against a latitudinal trend , 1992, Oecologia.

[10]  Mark D. Bertness,et al.  Population dynamics of the ribbed mussel, Geukensia demissa: The costs and benefits of an aggregated distribution , 1985, Oecologia.

[11]  A. Ellison,et al.  Consumer pressure and seed set in a salt marsh perennial plant community , 2004, Oecologia.

[12]  B. Silliman,et al.  Fungal farming in a snail , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[13]  B. Silliman,et al.  Underestimation of Spartina productivity in western Atlantic marshes: marsh invertebrates eat more than just detritus , 2003 .

[14]  M. Bertness,et al.  GEOGRAPHIC VARIATION IN POSITIVE AND NEGATIVE INTERACTIONS AMONG SALT MARSH PLANTS , 2003 .

[15]  G. C. Johns,et al.  Local Selection and Latitudinal Variation in a Marine Predator-Prey Interaction , 2003, Science.

[16]  B. Menge 2. The Overriding Importance of Environmental Context in Determining the Outcome of Species-Deletion Experiments , 2003 .

[17]  S. Pennings,et al.  LATITUDINAL VARIATION IN PALATABILITY OF SALT-MARSH PLANTS: WHICH TRAITS ARE RESPONSIBLE? , 2002 .

[18]  M. Hay,et al.  Geographic variation among herbivore populations in tolerance for a chemically rich seaweed , 2002 .

[19]  Mark D. Bertness,et al.  Latitudinal and climate-driven variation in the strength and nature of biological interactions in New England salt marshes , 2002, Oecologia.

[20]  M. Bertness,et al.  A trophic cascade regulates salt marsh primary production , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[21]  C. Lortie,et al.  Positive interactions among alpine plants increase with stress , 2002, Nature.

[22]  J. Thompson,et al.  Geographic structure and dynamics of coevolutionary selection , 2002, Nature.

[23]  C. Edward Proffitt,et al.  A Comparative Assessment of Genetic Diversity among Differently‐Aged Populations of Spartina alternif lora on Restored Versus Natural Wetlands , 2002 .

[24]  David M. Burdick,et al.  The regulation of ecosystem functions by ecotypic variation in the dominant plant: a Spartina alterniflora salt‐marsh case study , 2002 .

[25]  B. Silliman,et al.  TOP‐DOWN CONTROL OF SPARTINA ALTERNIFLORA PRODUCTION BY PERIWINKLE GRAZING IN A VIRGINIA SALT MARSH , 2001 .

[26]  J. Roughgarden,et al.  A LATITUDINAL GRADIENT IN RECRUITMENT OF INTERTIDAL INVERTEBRATES IN THE NORTHEAST PACIFIC OCEAN , 2001 .

[27]  M. Bertness,et al.  LATITUDINAL DIFFERENCES IN PLANT PALATABILITY IN ATLANTIC COAST SALT MARSHES , 2001 .

[28]  K. Gaston,et al.  Pattern and Process in Macroecology , 2000 .

[29]  E. Aschehoug,et al.  Invasive plants versus their new and old neighbors: a mechanism for exotic invasion. , 2000, Science.

[30]  J. Stachowicz,et al.  Geographic Variation in Camouflage Specialization by a Decorator Crab , 2000, The American Naturalist.

[31]  J. Cebrian Patterns in the Fate of Production in Plant Communities , 1999, The American Naturalist.

[32]  F. Barlocher,et al.  SPARTINA ALTERNIFLORA IN TWO NEW BRUNSWICK SALT MARSHES. II. POTENTIAL USEBY LITTORINA SAXATALIS , 1999 .

[33]  J. Thompson,et al.  Specific Hypotheses on the Geographic Mosaic of Coevolution , 1999, The American Naturalist.

[34]  Sanford,et al.  Regulation of keystone predation by small changes in ocean temperature , 1999, Science.

[35]  A. Ives,et al.  Reptile Extinctions on Land‐Bridge Islands: Life‐History Attributes and Vulnerability to Extinction , 1999, The American Naturalist.

[36]  S. Pennings,et al.  Effects of Wrack Burial in Salt-Stressed Habitats: Batis Maritima in a Southwest Atlantic Salt Marsh , 1998 .

[37]  J. Roughgarden,et al.  A Latitudinal Gradient in Northeast Pacific Intertidal Community Structure: Evidence for an Oceanographically Based Synthesis of Marine Community Theory , 1998, The American Naturalist.

[38]  D. Bigger,et al.  How different would a world without herbivory be?: A search for generality in ecology , 1998 .

[39]  A. C. James,et al.  Genetic and environmental responses to temperature of Drosophila melanogaster from a latitudinal cline. , 1997, Genetics.

[40]  D. Strong,et al.  Reduced herbivore resistance in introduced smooth cordgrass (Spartina alterniflora) after a century of herbivore-free growth , 1997, Oecologia.

[41]  M. Hay,et al.  Are Tropical Plants Better Defended? Palatability and Defenses of Temperate vs. Tropical Seaweeds , 1996 .

[42]  J. Travis The Significance of Geographical Variation in Species Interactions , 1996, The American Naturalist.

[43]  B. Cole,et al.  Mobile Cellular Automata Models of Ant Behavior: Movement Activity of Leptothorax allardycei , 1996, The American Naturalist.

[44]  D. Srivastava,et al.  A POSITIVE FEEDBACK : HERBIVORY, PLANT GROWTH, SALINITY, AND THE DESERTIFICATION OF AN ARCTIC SALT-MARSH , 1996 .

[45]  J. Thompson,et al.  The Coevolutionary Process , 1994 .

[46]  R. Swihart,et al.  Latitudinal patterns in consumption of woody plants by snowshoe hares in the eastern United States , 1994 .

[47]  M. Bertness,et al.  Positive interactions in communities. , 1994, Trends in ecology & evolution.

[48]  A. E. Stiven,et al.  Population processes in the ribbed mussel Geukensia demissa (Dillwyn) in a North Carolina salt marsh tidal gradient: spatial pattern, predation, growth and mortality , 1992 .

[49]  M. Bertness,et al.  CONSUMER DRIVEN POLLEN LIMITATION OF SEED PRODUCTION IN MARSH GRASSES , 1992 .

[50]  R. Paine,et al.  Food-web analysis through field measurement of per capita interaction strength , 1992, Nature.

[51]  J. Travis,et al.  The Role of Abiotic Factors in Community Organization , 1991, The American Naturalist.

[52]  R. Jefferies,et al.  Destruction of wetland habitats by lesser snow geese: a keystone species on the west coast of Hudson Bay. , 1990 .

[53]  James H. Brown,et al.  Macroecology: The Division of Food and Space Among Species on Continents , 1989, Science.

[54]  M. Horn Biology of marine herbivorous fishes , 1989 .

[55]  C. Langdon,et al.  Comparative utilization of detritus and bacteria as food sources by two bivalve suspension-feeders, the Crassostrea virginica and the mussel, Geukensia demissa , 1989 .

[56]  J. Lin Influence of location in a salt marsh on survivorship of ribbed mussels , 1989 .

[57]  I. Valiela,et al.  DETRITAL CHEMISTRY, GROWTH, AND FOOD CHOICE IN THE SALT-MARSH SNAIL (MELAMPUS BIDENTATUS) , 1988 .

[58]  J. Thompson,et al.  VARIATION IN INTERSPECIFIC INTERACTIONS , 1988 .

[59]  C. Langdon,et al.  Utilization of refractory cellulosic carbon derived from Spartina alterniflora by the ribbed mussel Geukensia demissa , 1988 .

[60]  G. Vermeij Evolution and Escalation: An Ecological History of Life , 1987 .

[61]  Aaron M. Ellison,et al.  Determinants of Pattern in a New England Salt Marsh Plant Community , 1987 .

[62]  M. N. Hardwick-Witman Biological consequences of ice rafting in a New England salt marsh community , 1985 .

[63]  M. Fawcett Local and Latitudinal Variation in Predation on an Herbivorous Marine Snail , 1984 .

[64]  M. Bertness Habitat and Community Modification by An Introduced Herbivorous Snail , 1984 .

[65]  L. S. Thompson Comparison of the diets of the tidal marsh snail, Melampus bidentatus and the amphipod, Orchestia grillus , 1984 .

[66]  D. Strong,et al.  Weak Competition among Spartina Stem Borers, by Means of Murder , 1983 .

[67]  J. Lubchenco,et al.  A UNIFIED APPROACH TO MARINE PLANT-HERBIVORE INTERACTIONS. II. BIOGEOGRAPHY , 1982 .

[68]  F. Daiber Animals of the Tidal Marsh , 1981 .

[69]  M. Bertness,et al.  PREDATION PRESSURE AND GASTROPOD FORAGING: A TROPICAL‐TEMPERATE COMPARISON , 1981, Evolution; international journal of organic evolution.

[70]  J. Lubchenco,et al.  Community Organization in Temperate and Tropical Rocky Intertidal Habitats: Prey Refuges in Relation to Consumer Pressure Gradients , 1981 .

[71]  R. Paine Food webs : linkage, interaction strength and community infrastructure , 1980 .

[72]  R. Paine,et al.  FOOD WEBS: LINKAGE, INTERACTION STRENGTH AND , 1980 .

[73]  R. Jeanne,et al.  A Latitudinal Gradient in Rates of Ant Predation , 1979 .

[74]  E. Kuenzler,et al.  The Response of Two Salt Marsh Molluscs, Littorina irrorata and Geukensia demissa, to Field Manipulations of Density and Spartina Litter , 1979 .

[75]  J. Teal,et al.  The Nature of Growth Forms in the Salt Marsh Grass Spartina alterniflora , 1978, The American Naturalist.

[76]  R. Denno Comparison of the Assemblages of Sap-Feeding Insects (Homoptera-Hemiptera) Inhabiting Two Structurally Different Salt Marsh Grasses in the Genus Spartina , 1977 .

[77]  R. Macarthur Mathematical Ecology and Its Place among the Sciences. (Book Reviews: Geographical Ecology. Patterns in the Distribution of Species) , 1974 .

[78]  Alfred C. Redfield,et al.  Development of a New England Salt Marsh , 1972 .

[79]  A. Smalley Energy Flow of a Salt Marsh Grasshopper Population , 1960 .

[80]  S. A. Hausman A Contribution to the Ecology of the Salt Marsh Snail, Melampus bidentatus Say , 1932, The American Naturalist.