Population regulation by enemies of the grass Brachypodium sylvaticum: demography in native and invaded ranges.

The enemy-release hypothesis (ERH) states that species become more successful in their introduced range than in their native range because they leave behind natural enemies in their native range and are thus "released" from enemy pressures in their introduced range. The ERH is popularly cited to explain the invasive properties of many species and is the underpinning of biological control. We tested the prediction that plant populations are more strongly regulated by natural enemies (herbivores and pathogens) in their native range than in their introduced range with enemy-removal experiments using pesticides. These experiments were replicated at multiple sites in both the native and invaded ranges of the grass Brachypodium sylvaticum. In support of the ERH, enemies consistently regulated populations in the native range. There were more tillers and more seeds produced in treated vs. untreated plots in the native range, and few seedlings survived in the native range. Contrary to the ERH, total measured leaf damage was similar in both ranges, though the enemies that caused it differed. There was more damage by generalist mollusks and pathogens in the native range, and more damage by generalist insect herbivores in the invaded range. Demographic analysis showed that population growth rates were lower in the native range than in the invaded range, and that sexually produced seedlings constituted a smaller fraction of the total in the native range. Our removal experiment showed that enemies regulate plant populations in their native range and suggest that generalist enemies, not just specialists, are important for population regulation.

[1]  J. Koricheva,et al.  The Ontogeny of Plant Defense and Herbivory: Characterizing General Patterns Using Meta‐Analysis , 2010, The American Naturalist.

[2]  Bart R. Johnson,et al.  Context-dependent pattern and process: the distribution and competitive dynamics of an invasive grass, Brachypodium sylvaticum , 2010, Biological Invasions.

[3]  Vinh Q. Pham,et al.  Cryptic seedling herbivory by nocturnal introduced generalists impacts survival, performance of native and exotic plants. , 2009, Ecology.

[4]  Paul M. Severns,et al.  Selectively eliminating and conserving exotic plants to save an endangered butterfly from local extinction , 2008 .

[5]  M. Cruzan,et al.  Evidence for multiple sources of invasion and intraspecific hybridization in Brachypodium sylvaticum (Hudson) Beauv. in North America , 2008, Molecular ecology.

[6]  M. Ayres,et al.  Role of plant enemies in the forestry of indigenous vs. nonindigenous pines. , 2008, Ecological applications : a publication of the Ecological Society of America.

[7]  J. Burdon,et al.  Pathogen evolution across the agro-ecological interface: implications for disease management , 2008, Evolutionary applications.

[8]  C. Hawkes Are Invaders Moving Targets? The Generality and Persistence of Advantages in Size, Reproduction, and Enemy Release in Invasive Plant Species with Time since Introduction , 2007, The American Naturalist.

[9]  I. Sache,et al.  The fungal dimension of biological invasions. , 2007, Trends in ecology & evolution.

[10]  J. Maron,et al.  What have exotic plant invasions taught us over the past 20 years? , 2006, Trends in ecology & evolution.

[11]  F. Bazzaz,et al.  Geographic patterns of herbivory and resource allocation to defense, growth, and reproduction in an invasive biennial, Alliaria petiolata , 2006, Oecologia.

[12]  Hong Liu,et al.  Testing the enemy release hypothesis: a review and meta-analysis , 2006, Biological Invasions.

[13]  A. Agrawal,et al.  ENEMY RELEASE? AN EXPERIMENT WITH CONGENERIC PLANT PAIRS AND DIVERSE ABOVE- AND BELOWGROUND ENEMIES , 2005 .

[14]  A. Hastings,et al.  Spatial and temporal dynamics of insect outbreaks in a complex multitrophic system: tussock moths, ghost moths, and their natural enemies on bush lupines , 2005 .

[15]  J. Denslow,et al.  NATURAL‐ENEMY RELEASE FACILITATES HABITAT EXPANSION OF THE INVASIVE TROPICAL SHRUB CLIDEMIA HIRTA , 2004 .

[16]  J. Rosenthal,et al.  Tolerating herbivory: does the plant care if the herbivore has a backbone? , 2000, Evolutionary Ecology.

[17]  C. Mitchell,et al.  Release of invasive plants from fungal and viral pathogens , 2003, Nature.

[18]  T. Heinken,et al.  Trägt Schalenwild durch Epizoochorie zur Ausbreitung von Gefäßpflanzen in mitteleuropäischen Wäldern bei? Eine Fallstudie aus Nordostdeutschland , 2002 .

[19]  T. Heinken,et al.  Do Wild Ungulates Contribute to the Dispersal of Vascular Plants in Central European Forests by Epizoochory? A Case Study in NE Germany , 2002, Forstwissenschaftliches Centralblatt vereinigt mit Tharandter forstliches Jahrbuch.

[20]  M. Oesterheld,et al.  Effect of defoliation on grass growth. A quantitative review , 2002 .

[21]  M. Crawley,et al.  Exotic plant invasions and the enemy release hypothesis , 2002 .

[22]  M. Vilà,et al.  When do herbivores affect plant invasion? Evidence for the natural enemies and biotic resistance hypotheses , 2001 .

[23]  Hal Caswell,et al.  Spatial growth and population dynamics of a perennial tussock grass (Achnatherum calamagrostis) in a badland area , 2000 .

[24]  S. Gardner,et al.  Consumer pressure, seed versus safe-site limitation, and plant population dynamics , 2000, Oecologia.

[25]  C. Hæggström,et al.  Flowering and individual survival of a population of the grass Brachypodium sylvaticum in Nåtö, Åland Islands, SW Finland. , 1996 .

[26]  S. Louda,et al.  Effect of Inflorescence‐Feeding Insects on the Demography and Lifetime of a Native Plant , 1995 .

[27]  J. Silvertown,et al.  Tiller dynamics of two grasses: responses to grazing, density and weather , 1994 .

[28]  G. Latch Physiological interactions of endophytic fungi and their hosts. Biotic stress tolerance imparted to grasses by endophytes , 1993 .

[29]  J. Burdon,et al.  Pattern and patchiness in plant-pathogen interactions - causes and consequences , 1989 .

[30]  N. Paul,et al.  On the use of fungicides for experimentation in natural vegetation , 1989 .

[31]  M. Crawley INSECT HERBIVORES AND PLANT POPULATION DYNAMICS , 1989 .