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Species Grow (species + grow)
Selected AbstractsDetection of an invasive gall-inducing pest, Quadrastichus erythrinae (Hymenoptera: Eulophidae), causing damage to Erythrina variegata L. (Fabaceae) in Okinawa Prefecture, JapanENTOMOLOGICAL SCIENCE, Issue 2 2007Nami UECHI Abstract In 2005, Quadrastichus erythrinae Kim, 2004 (Hymenoptera: Eulophidae), which induces stem, petiole, and leaf galls on Erythrina variegata L. (Fabaceae), was found on the following six islands in Okinawa Prefecture, Japan: Okinawa, Kume, Miyako, Ishigaki, Iriomote, and Hateruma. Galls were also found in Vietnam. In Japan, no further infestation records have been reported from any of Japan's other south-western prefectures where Erythrina species grow. Because no Erythrina galls were observed in Okinawa Prefecture before 2005, Q. erythrinae seems to have invaded quite recently. [source] THE PHYLOGENY OF THE PENTASCHISTIS CLADE (DANTHONIOIDEAE, POACEAE) BASED ON CHLOROPLAST DNA, AND THE EVOLUTION AND LOSS OF COMPLEX CHARACTERSEVOLUTION, Issue 4 2007C. Galley We construct a species-level phylogeny for the Pentaschistis clade based on chloroplast DNA, from the following regions: trnL-F, trnT-L, atpB-rbcL, rpL16, and trnD-psbA. The clade comprises 82 species in three genera, Pentaschistis, Pentameris, and Prionanthium. We demonstrate that Prionanthium is nested in Pentaschistis and that this clade is sister to a clade of Pentameris plus Pentaschistis tysonii. Forty-three of the species in the Pentaschistis clade have multicellular glands and we use ancestral character state reconstruction to show that they have been gained twice or possibly once, and lost several times. We suggest that the maintenance, absence, loss, and gain of glands are correlated with leaf anatomy type, and additionally that there is a difference in the degree of diversification of lineages that have these different character combinations. We propose that both glands and sclerophyllous leaves act as defense systems against herbivory, and build a cost/benefit model in which multicellular glands or sclerophyllous leaves are lost when the alternative defense system evolves. We also investigate the association between leaf anatomy type and soil nutrient type on which species grow. There is little phylogenetic constraint in soil nutrient type on members of the Pentaschistis clade, with numerous transitions between oligotrophic and eutrophic soils. However, only orthophyllous-leaved species diversify on eutrophic soils. We suggest that the presence of these glands enables the persistence of orthophyllous lineages and therefore diversification of the Pentaschistis clade on eutrophic as well as oligotrophic soils. [source] THE FALL LINE: A PHYSIOGRAPHIC-FOREST VEGETATION BOUNDARY,GEOGRAPHICAL REVIEW, Issue 4 2007David Shankman ABSTRACT. The range boundaries for many tree species in the southeastern United States correspond to the Fall Line that separates the Coastal Plain from the Appalachian Highlands. Trees in the Coastal Plain with northern range boundaries corresponding to the Fall Line occur exclusively in alluvial valleys created by lateral channel migration. These species grow mostly on lower bottomland sites characterized by a high water table, soils that are often saturated, and low annual water fluctuation. In contrast to the Coastal Plain, the southern Appalachian Highlands are occupied mostly by bedrock streams that have few sites suitable for the regeneration of these species. The Fall Line is also an approximate southern boundary for trees common in the southern Appalachians that typically occur on either dry, rocky ridgetops or in narrow stream valleys, habitats that are uncommon on the relatively flat Coastal Plain. The ranges for many trees in eastern North America are controlled by large-scale climatic patterns. Tree species with range boundaries corresponding to the Fall Line, however, are not approaching their physiological limits caused by progressively harsher climatic conditions or by competition. Instead, the Fall Line represents the approximate boundary of habitats suitable for regeneration. [source] River corridor plants (Stromtalpflanzen) in Central European lowland: a review of a poorly understood plant distribution patternGLOBAL ECOLOGY, Issue 5 2001Michael Burkart Abstract Aim and location In Central European lowlands certain plant species grow mainly or exclusively in the corridors of large rivers. In German-speaking plant geography, they are known as ,Stromtalpflanzen'. The aim of this paper is to review the literature about definitions, explanations and species characteristics and to suggest future directions in research concerning this species group. Results A preliminary list contains 129 ecologically heterogeneous plant species. The mechanisms generating the peculiar distribution pattern may include hydrochory along river corridors, high levels of disturbance by water, variable water availability including inundation and summer drought, warm summers and high nutrient supply on alluvial soils. There is evidence from observational studies for all above mechanisms. However, none of them has been tested experimentally. Demographic data of river corridor plants are limited to very few species, including mainly invasive annuals (Artemisia annua, Bidens frondosa, Cuscuta campestris, Xanthium albinum) and annual (hemi)parasites (Cuscuta campestris, Melampyrum cristatum). Metapopulation studies do not exist to date for European species. Apart from their habitat requirements, river corridor plants were grouped according to their similarities in overall distribution pattern or their distribution within particular river corridors. Main conclusions River corridor plants include a high proportion of threatened plant species. In order to preserve them, and in order to understand the mechanisms generating the peculiar distribution pattern, much more has to be known about their population biology and metapopulation dynamics. [source] Contrasting phylogeographies inferred for the two alpine sister species Cardamine resedifolia and C. alpina (Brassicaceae)JOURNAL OF BIOGEOGRAPHY, Issue 1 2009Judita Lihová Abstract Aim, We use Cardamine alpina and C. resedifolia as models to address the detailed history of disjunctions in the European alpine system. These species grow on siliceous bedrock: C. alpina in the Alps and Pyrenees, and C. resedifolia in several mountain ranges from the Sierra Nevada to the Balkans. We explore differentiation among their disjunct populations as well as within the contiguous Alpine and Pyrenean ranges, and compare the phylogeographical histories of these diploid sister species. We also include samples of the closely related, arctic diploid C. bellidifolia in order to explore its origin and post-glacial establishment. Location, European alpine system, Norway and Iceland. Methods, We employed amplified fragment length polymorphisms (AFLPs). AFLP data were analysed using principal coordinates analysis, neighbour joining and Bayesian clustering, and measures of diversity and differentiation were computed. Results, For the snow-bed species C. alpina (27 populations, 203 plants) we resolved two strongly divergent lineages, corresponding to the Alps and the Pyrenees. Although multiple glacial refugia were invoked in the Pyrenees, we inferred only a single one in the Maritime Alps , from which rapid post-glacial colonization of the entire Alps occurred, accompanied by a strong founder effect. For C. resedifolia (33 populations, 247 plants), which has a broader ecological amplitude and a wider distribution, the genetic structuring was rather weak and did not correspond to the main geographical disjunctions. This species consists of two widespread and largely sympatric main genetic groups (one of them subdivided into four geographically more restricted groups), and frequent secondary contacts exist between them. Main conclusions, The conspicuously different histories of these two sister species are likely to be associated with their different ecologies. The more abundant habitats available for C. resedifolia may have increased the probability of its gradual migration during colder periods and also of successful establishment after long-distance dispersal, whereas C. alpina has been restricted by its dependence on snow-beds. Surprisingly, the arctic C. bellidifolia formed a very divergent lineage with little variation, contradicting a scenario of recent, post-glacial migration from the Alps or Pyrenees. [source] | |||||||||||||