Invading Species (invading + species)

Distribution by Scientific Domains


Selected Abstracts


Rapid evolution in introduced species, ,invasive traits' and recipient communities: challenges for predicting invasive potential

DIVERSITY AND DISTRIBUTIONS, Issue 4 2008
Kenneth D. Whitney
ABSTRACT The damaging effects of invasive organisms have triggered the development of Invasive Species Predictive Schemes (ISPS). These schemes evaluate biological and historical characteristics of species and prioritize those that should be the focus of exclusion, quarantine, and/or control. However, it is not clear how commonly these schemes take microevolutionary considerations into account. We review the recent literature and find that rapid evolutionary changes are common during invasions. These evolutionary changes include rapid adaptation of invaders to new environments, effects of hybridization, and evolution in recipient communities. Strikingly, we document 38 species in which the specific traits commonly associated with invasive potential (e.g. growth rate, dispersal ability, generation time) have themselves undergone evolutionary change following introduction, in some cases over very short (, 10 year) timescales. In contrast, our review of 29 ISPS spanning plant, animal, and microbial taxa shows that the majority (76%) envision invading species and recipient communities as static entities. Those that incorporate evolutionary considerations do so in a limited way. Evolutionary change not only affects the predictive power of these schemes, but also complicates their evaluation. We argue that including the evolutionary potential of species and communities in ISPS is overdue, present several metrics related to evolutionary potential that could be incorporated in ISPS, and provide suggestions for further research on these metrics and their performance. Finally, we argue that the fact of evolutionary change during invasions begs for added caution during risk assessment. [source]


Developing an approach to defining the potential distributions of invasive plant species: a case study of Hakea species in South Africa

GLOBAL ECOLOGY, Issue 5 2008
David C. Le Maitre
ABSTRACT Aim, Models of the potential distributions of invading species have to deal with a number of issues. The key one is the high likelihood that the absence of an invading species in an area is a false absence because it may not have invaded that area yet, or that it may not have been detected. This paper develops an approach for screening pseudo-absences in a way that is logical and defensible. Innovation, The step-wise approach involves: (1) screening environmental variables to identify those most likely to indicate conditions where the species cannot invade; (2) identifying and selecting the most likely limiting variables; (3) using these to define the limits of its invasion potential; and (4) selecting points outside these limits as true absence records for input into species distribution models. This approach was adopted and used for the study of three prominent Hakea species in South Africa. Models with and without the false absence records were compared. Two rainfall variables and the mean minimum temperature of the coldest month were the strongest predictors of potential distributions. Models which excluded false absences predicted that more of the potential distribution would have a high invasion potential than those which included them. Main conclusions, The approach of applying a priori knowledge can be useful in refining the potential distribution of a species by excluding pseudo-absence records which are likely to be due to the species not having invaded an area yet or being undetected. The differences between the potential distributions predicted by the different models convey more information than making a single prediction, albeit a consensus model. The robustness of this approach depends strongly on an adequate knowledge of the ecology, invasion history and current distribution of that species. [source]


Invasive alien plants infiltrate bird-mediated shrub nucleation processes in arid savanna

JOURNAL OF ECOLOGY, Issue 4 2007
S. J. MILTON
Summary 1,The cultivation and dissemination of alien ornamental plants increases their potential to invade. More specifically, species with bird-dispersed seeds can potentially infiltrate natural nucleation processes in savannas. 2To test (i) whether invasion depends on facilitation by host trees, (ii) whether propagule pressure determines invasion probability, and (iii) whether alien host plants are better facilitators of alien fleshy-fruited species than indigenous species, we mapped the distribution of alien fleshy-fruited species planted inside a military base, and compared this with the distribution of alien and native fleshy-fruited species established in the surrounding natural vegetation. 3Abundance and diversity of fleshy-fruited plant species was much greater beneath tree canopies than in open grassland and, although some native fleshy-fruited plants were found both beneath host trees and in the open, alien fleshy-fruited plants were found only beneath trees. 4Abundance of fleshy-fruited alien species in the natural savanna was positively correlated with the number of individuals of those species planted in the grounds of the military base, while the species richness of alien fleshy-fruited taxa decreased with distance from the military base, supporting the notion that propagule pressure is a fundamental driver of invasions. 5There were more fleshy-fruited species beneath native Acacia tortilis than beneath alien Prosopis sp. trees of the equivalent size. Although there were significant differences in native plant assemblages beneath these hosts, the proportion of alien to native fleshy-fruited species did not differ with host. 6Synthesis. Birds facilitate invasion of a semi-arid African savanna by alien fleshy-fruited plants, and this process does not require disturbance. Instead, propagule pressure and a few simple biological observations define the probability that a plant will invade, with alien species planted in gardens being a major source of propagules. Some invading species have the potential to transform this savanna by overtopping native trees, leading to ecosystem-level impacts. Likewise, the invasion of the open savanna by alien host trees (such as Prosopis sp.) may change the diversity, abundance and species composition of the fleshy-fruited understorey. These results illustrate the complex interplay between propagule pressure, facilitation, and a range of other factors in biological invasions. [source]


Breeding system, branching processes, hybrid swarm theory, and the humped-back diversity relationship as additional explanations for apparent monophyly in the Macaronesian island flora

JOURNAL OF ECOLOGY, Issue 4 2005
N. ELIZABETH SAUNDERS
Summary 1Niche pre-emption and competitive exclusion is unsatisfactory as a sole explanation for the apparent paradox of a large number of monophyletic taxa in the Macaronesian island flora. 2Undetected hybridizations have been proposed as an additional plausible explanation. In addition, hybrid swarm theory predicts that hybridizations between invading species would promote adaptive radiation. 3We suggest that branching processes and coalescence offer yet another plausible explanation allowing for multiple colonizations of closely related taxa, which, because of their later local extinction or hybridization, would lead to apparent monophyly in the molecular record. 4The cause of such widespread radiation of a few taxa has not been explained, but may involve intermediate conditions of disturbance or productivity. This proposition has, to date, only been tested in a microbial model system, but it offers a reasonable explanation for the patterns observed in the Macaronesian flora, and perhaps in other island floras worldwide. [source]


Blowfly succession from possum (Trichosurus vulpecula) carrion in a sheep-farming zone

MEDICAL AND VETERINARY ENTOMOLOGY, Issue 4 2006
M. D. LANG
Abstract The significance of brushtail possum, Trichosurus vulpecula Kerr (Diprotodontia: Phalangeridae) carcasses to the succession and production of Diptera species and its relevance to fly strike management in Tasmania, Australia was examined. Calliphora stygia (Fabricius), Lucilia sericata (Meigen) and Calliphora vicina Robineau,Desvoidy (Diptera: Calliphoridae) were found to be the most abundant and Lucilia cuprina (Wiedemann) (Diptera: Calliphoridae) always the least abundant (< 1%) of the putative primary fly invading species to emerge. Carcasses that were left for up to 15 days in the field before being exposed to flies for 2 days also acted as breeding sites for large numbers of all primary fly species, with the exception of L. cuprina. Ordination analysis revealed no relationship between possum carcasses according to their length of exposure but did show significant negative associations between the number of putative secondary invaders (Chrysomya rufifacies (Macquart) (Diptera: Calliphoridae), Chrysomya varipes (Macquart) (Diptera: Calliphoridae) and putative tertiary flies (Hydrotaea rostrata Robineau,Desvoidy (Diptera: Muscidae)) to the number of C. vicina or C. stygia to emerge. There was enormous variability in the numbers of secondary/tertiary fly species to emerge from carcasses (0,11 450) that negatively correlated with the proportion of all flies to emerge that were primary, and with the mean size of adult L. sericata. Although carcass temperatures, especially those with a large larval population, were elevated, this did not appear to result in significant pre-adult fly mortality. The most important primary fly strike species L. cuprina was only found in insignificant numbers, whereas three other members of the fly strike fauna C. stygia, L. sericata and Ch. rufifacies did use possum carrion as an important breeding resource, but left implications for fly strike management inconclusive. [source]


Reciprocal hybrid formation of Spartina in San Francisco Bay

MOLECULAR ECOLOGY, Issue 6 2000
C. K. Anttila
Abstract Diversity in the tRNALEU1 intron of the chloroplast genome of Spartina was used to study hybridization of native California cordgrass, Spartina foliosa, with S. alterniflora, introduced to San Francisco Bay , 25 years ago. We sequenced 544 bases of the tRNALEU1 intron and found three polymorphic sites, a pyrimidine transition at site 126 and transversions at sites 382 and 430. Spartina from outside of San Francisco Bay, where hybridization between these species is impossible, gave cpDNA genotypes of the parental species. S. foliosa had a single chloroplast haplotype, CCT, and this was unique to California cordgrass. S. alterniflora from the native range along the Atlantic coast of North America had three chloroplast haplotypes, CAT, TAA, and TAT. Hybrids were discriminated by random amplified polymorphic DNA (RAPD) phenotypes developed in a previous study. We found one hybrid that contained a cpDNA haplotype unknown in either parental species (TCT). The most significant finding was that hybridization proceeds in both directions, assuming maternal inheritance of cpDNA; 26 of the 36 hybrid Spartina plants from San Francisco Bay contained the S. foliosa haplotype, nine contained haplotypes of the invading S. alterniflora, and one had the cpDNA of unknown origin. Furthermore, cpDNA of both parental species was distributed throughout the broad range of RAPD phenotypes, suggesting ongoing contributions to the hybrid swarm from both. The preponderance of S. foliosa cpDNA has entered the hybrid swarm indirectly, we propose, from F1s that backcross to S. foliosa. Flowering of the native precedes by several weeks that of the invading species, with little overlap between the two. Thus, F1 hybrids would be rare and sired by the last S. foliosa pollen upon the first S. alterniflora stigmas. The native species produces little pollen and this has low viability. An intermediate flowering time of hybrids as well as pollen that is more vigourous and abundant than that of the native species would predispose F1s to high fitness in a vast sea of native ovules. Thus, spread of hybrids to other S. foliosa marshes could be an even greater threat to the native species than introductions of alien S. alterniflora. [source]


Alpine flora dynamics , a critical review of responses to climate change in the Swedish Scandes since the early 1950s

NORDIC JOURNAL OF BOTANY, Issue 4 2010
Leif Kullman
Reports about changes of alpine plant species richness over the past 60 years in the Swedish Scandes are reviewed, synthesized and updated with data from recent reinventories. Methodologically, this endeavour is based on resurveys of the floristic composition on the uppermost 20 m of four high-mountain summits. The key finding is that the species pool has increased by 60,170% since the 1950s and later. Some of the invading species are new to the alpine tundra, with more silvine and thermophilic properties than the extant alpine flora. Not a single species of the original flora has disappeared from any of the summits. This circumstance is discussed in perspective of widespread expectations of pending temperature-driven extinction of alpine species in an alleged future warmer climate. These progressive changes coincided with distinct warming (summer and winter) since the late 1980s. During a short cooler period (1974,1994), the species numbers decreased and the upper elevational limits of some ground cover species descended. Thus, discernible responses, concurrent with both warming and cooling intervals, sustain a strong causal link between climate variability and alpine plant species richness. Methodologically, plot-less revisitation studies of the present kind are beset with substantial uncertainties, which may overstate floristic changes over time. However, it is argued here that carefully executed and critically interpreted, no other method can equally effectively sense the earliest phases of plant invasions into alpine vegetation. [source]


Invasibility of grassland and heath communities exposed to extreme weather events , additive effects of diversity resistance and fluctuating physical environment

OIKOS, Issue 10 2008
Juergen Kreyling
Understanding the resistance of plant communities to invasion is urgent in times of changes in the physical environment due to climate change and changes in the resident communities due to biodiversity loss. Here, we test the interaction between repeated drought or heavy rainfall events and functional diversity of grassland and heath communities on invasibility, measured as the number of plant individuals invading from the matrix vegetation. Invasibility of experimental plant communities was influenced by extreme weather events, although no change in above-ground productivity of the resident communities was observed. Drought decreased invasibility while heavy rainfall increased invasibility, a pattern that is consistent with the fluctuating resource hypothesis. Higher community diversity generally decreased invasibility, which can be explained by a combination of the fluctuating resource hypothesis and niche theory. The effects of the physical environment (extreme weather events) and diversity resistance (community composition) were additive, as they were independent from each other. Differences in the composition of invading species sets were found, and Indicator Species Analysis revealed several invading species with significant affinity to one particular extreme weather event or community composition. This finding supports niche theory and contradicts neutral species assembly. Our data supports theories which predict decreased resistance of plant communities due to both increased climate variability and biodiversity loss. The effects of these two factors, however, appear to be independent from each other. [source]


When does ecosystem engineering cause invasion and species replacement?

OIKOS, Issue 8 2008
Andrew Gonzalez
Introduced exotic species can dominate communities and replace native species that should be better adapted to their local environment, a paradox that is usually explained by the absence of natural enemies and by habitat alteration resulting from anthropogenic disturbance. Additionally, introduced species can enhance their invasion success and impact on native species by modifying selection pressures in their new environment through ecosystem engineering. We analyse a simple dynamic model of indirect competition for habitat between a non-engineering resident species and an engineering exotic species. The conditions for invasion and competitive exclusion of the resident by the exotic species and the range of dynamic outcomes suggested by the model are determined by the form of density dependence. We give simple criteria for the success of the invading species on dimensionless quantities involving rates of ecosystem engineering and of habitat degradation. The model's predictions offer an additional explanation for a range of invasion dynamics reported in the literature, including lag times between introduction and establishment. One intriguing result is that a series of failed invasions may successively reduce environmental resistance to subsequent invasion, through a cumulative effect of habitat transformation. More work is needed to determine the frequency and conditions in which engineering is required for successful establishment, and whether highly-successful (or high-impact) invaders are more likely to possess ecosystem engineering traits. [source]


Are invasive plant species better competitors than native plant species?

OIKOS, Issue 2 2004
evidence from pair-wise experiments
Invasive plants often appear to be more competitive than native species, but there have been few tests of this hypothesis. We reviewed published pair-wise experiments between invading and native plant species. Although the designs that have been used allow only limited inferences, the available data suggest that the effect of invasive species on native species is usually stronger than vice versa. Furthermore, mixtures of invasive and native species are generally less productive than monocultures of the native species, but not less than monocultures of the invasive species. However, the selection of invaders and natives for study has not been random, and the data could be biased towards highly competitive invaders and natives that are weaker than average competitors. We attempt to clarify confusion surrounding the concept of competitive superiority in the context of plant invasions, and we discuss the limitations of the methods that have been used to investigate competition between invasive and native species. To rigorously test the generality of the hypothesis that invaders are better competitors than natives we need to compare the effects of closely related native and invasive species on each other. We suggest that the influence of an invading species on total plant community biomass is an important clue in understanding the role of competition in a plant invasion. The role of competition in the establishment and naturalization stages of the invasion process may be very different from its role in the "outbreak" stage. [source]