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1.
Proc Natl Acad Sci U S A ; 108(1): 220-5, 2011 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-21173219

RESUMO

Because invasive species threaten the integrity of natural ecosystems, a major goal in ecology is to develop predictive models to determine which species may become widespread and where they may invade. Indeed, considerable progress has been made in understanding the factors that influence the local pattern of spread for specific invaders and the factors that are correlated with the number of introduced species that have become established in a given region. However, few studies have examined the relative importance of multiple drivers of invasion success for widespread species at global scales. Here, we use a dataset of >5,000 presence/absence records to examine the interplay between climatic suitability, biotic resistance by native taxa, human-aided dispersal, and human modification of habitats, in shaping the distribution of one of the world's most notorious invasive species, the Argentine ant (Linepithema humile). Climatic suitability and the extent of human modification of habitats are primarily responsible for the distribution of this global invader. However, we also found some evidence for biotic resistance by native communities. Somewhat surprisingly, and despite the often cited importance of propagule pressure as a crucial driver of invasions, metrics of the magnitude of international traded commodities among countries were not related to global distribution patterns. Together, our analyses on the global-scale distribution of this invasive species provide strong evidence for the interplay of biotic and abiotic determinants of spread and also highlight the challenges of limiting the spread and subsequent impact of highly invasive species.


Assuntos
Formigas/crescimento & desenvolvimento , Clima , Ecologia/métodos , Ecossistema , Espécies Introduzidas/tendências , Modelos Biológicos , Animais , Comércio , Simulação por Computador , Bases de Dados Factuais , Geografia , Atividades Humanas , Humanos , Análise de Regressão
2.
Ecol Appl ; 19(5): 1176-86, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19688925

RESUMO

The characteristics of spread for an invasive species should influence how environmental authorities or government agencies respond to an initial incursion. High-resolution predictions of how, where, and the speed at which a newly established invasive population will spread across the surrounding heterogeneous landscape can greatly assist appropriate and timely risk assessments and control decisions. The Argentine ant (Linepithema humile) is a worldwide invasive species that was inadvertently introduced to New Zealand in 1990. In this study, a spatially explicit stochastic simulation model of species dispersal, integrated with a geographic information system, was used to recreate the historical spread of L. humile in New Zealand. High-resolution probabilistic maps simulating local and human-assisted spread across large geographic regions were used to predict dispersal rates and pinpoint at-risk areas. The spatially explicit simulation model was compared with a uniform radial spread model with respect to predicting the observed spread of the Argentine ant. The uniform spread model was more effective predicting the observed populations early in the invasion process, but the simulation model was more successful later in the simulation. Comparison between the models highlighted that different search strategies may be needed at different stages in an invasion to optimize detection and indicates the influence that landscape suitability can have on the long-term spread of an invasive species. The modeling and predictive mapping methodology used can improve efforts to predict and evaluate species spread, not only in invasion biology, but also in conservation biology, diversity studies, and climate change studies.


Assuntos
Migração Animal , Formigas/fisiologia , Previsões , Modelos Biológicos , Animais , Ecossistema , Geografia , Nova Zelândia , Densidade Demográfica , Dinâmica Populacional , Processos Estocásticos
3.
BMC Genomics ; 9: 49, 2008 Jan 28.
Artigo em Inglês | MEDLINE | ID: mdl-18226240

RESUMO

BACKGROUND: Microsatellites are highly abundant in eukaryotic genomes but their function and evolution are not yet well understood. Their elevated mutation rate makes them ideal markers of genetic difference, but high levels of unexplained heterogeneity in mutation rates among microsatellites at different genomic locations need to be elucidated in order to improve the power and accuracy of the many types of study that use them as genetic markers. Recombination could contribute to this heterogeneity, since while replication errors are thought to be the predominant mechanism for microsatellite mutation, meiotic recombination is involved in some mutation events. There is also evidence suggesting that microsatellites could function as recombination signals. The yeast S. cerevisiae is a useful model organism with which to further explore the link between microsatellites and recombination, since it is very amenable to genetic study, and meiotic recombination hotspots have been mapped throughout its entire genome. RESULTS: We examined in detail the relationship between microsatellites and hotspots of meiotic double-strand breaks, the precursors of meiotic recombination, throughout the S. cerevisiae genome. We included all tandem repeats with motif length (repeat period) between one and six base pairs. Long, short and two-copy arrays were considered separately. We found that long, mono-, di- and trinucleotide microsatellites are around twice as frequent in hot than non-hot intergenic regions. The associations are weak or absent for repeats with less than six copies, and also for microsatellites with 4-6 base pair motifs, but high-copy arrays with motif length greater than three are relatively very rare throughout the genome. We present evidence that the association between high-copy, short-motif microsatellites and recombination hotspots is not driven by effects on microsatellite distribution of other factors previously linked to both recombination and microsatellites, including transcription, GC-content and transposable elements. CONCLUSION: Our findings suggest that a mutation bias relating to recombination hotspots causing repeats to form and grow, and/or regulation of a subset of hotspots by simple sequences, may be significant processes in yeast. Some previous evidence has cast doubt on both of these possibilities, and as a result they have not been explored on a large scale, but the strength of the association we report suggests that they deserve further experimental testing.


Assuntos
DNA Fúngico/genética , Repetições de Microssatélites , Saccharomyces cerevisiae/genética , Sequência de Bases , Quebras de DNA de Cadeia Dupla , DNA Intergênico/genética , Genoma Fúngico , Meiose/genética , Análise de Sequência com Séries de Oligonucleotídeos , Recombinação Genética
4.
Ecol Evol ; 7(20): 8338-8348, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-29075453

RESUMO

Natural and human-induced events are continuously altering the structure of our landscapes and as a result impacting the spatial relationships between individual landscape elements and the species living in the area. Yet, only recently has the influence of the surrounding landscape on invasive species spread started to be considered. The scientific community increasingly recognizes the need for broader modeling framework that focuses on cross-study comparisons at different spatiotemporal scales. Using two illustrative examples, we introduce a general modeling framework that allows for a systematic investigation of the effect of habitat change on invasive species establishment and spread. The essential parts of the framework are (i) a mechanistic spatially explicit model (a modular dispersal framework-MDIG) that allows population dynamics and dispersal to be modeled in a geographical information system (GIS), (ii) a landscape generator that allows replicated landscape patterns with partially controllable spatial properties to be generated, and (iii) landscape metrics that depict the essential aspects of landscape with which dispersal and demographic processes interact. The modeling framework provides functionality for a wide variety of applications ranging from predictions of the spatiotemporal spread of real species and comparison of potential management strategies, to theoretical investigation of the effect of habitat change on population dynamics. Such a framework allows to quantify how small-grain landscape characteristics, such as habitat size and habitat connectivity, interact with life-history traits to determine the dynamics of invasive species spread in fragmented landscape. As such, it will give deeper insights into species traits and landscape features that lead to establishment and spread success and may be key to preventing new incursions and the development of efficient monitoring, surveillance, control or eradication programs.

5.
BMC Genomics ; 7: 179, 2006 Jul 18.
Artigo em Inglês | MEDLINE | ID: mdl-16846522

RESUMO

BACKGROUND: Meiotic recombination events have been found to concentrate in 1-2.5 kilo base regions, but these recombination hot spots do not share a consensus sequence and why they occur at specific sites is not fully understood. Some previous evidence suggests that poly-purine/poly-pyrimidine (poly-pu/py) tracts (PPTs), a class of sequence with distinctive biochemical properties, could be involved in recombination, but no general association of PPTs with meiotic recombination hot spots has previously been reported. RESULTS: We used computational methods to investigate in detail the relationship between PPTs and hot spots. We show statistical associations of PPT frequency with hot spots of meiotic recombination initiating lesions, double-strand breaks, in the genome of the yeast S. cerevisiae and with experimentally well characterized human meiotic recombination hot spots. Supporting a possible role of poly-pu/py-rich sequences in hot spot recombination, we also found that all three single nucleotide polymorphisms previously shown to be associated with human hot spot activity changes occur within sequence contexts of 14 bp or longer that are 85% or more poly-pu/py and at least 70% G/C. These polymorphisms are all close to the hot spot mid points. Comparing the sequences of experimentally characterized human hot spots with the orthologous regions of the chimpanzee genome previously shown not to contain hot spots, we found that in all five cases in which comparisons for the hot spot central regions are possible with publicly available sequence data, there are differences near the human hot spot mid points within sequences 14 bp or longer consisting of more than 80% poly-pu/py and at least 50% G/C. CONCLUSION: Our results, along with previous evidence for the unique biochemical properties and recombination-stimulating potential of poly-pu/py-rich sequences, suggest that the possible functional involvement of this type of sequence in meiotic recombination hot spots deserves further experimental exploration.


Assuntos
Pareamento de Bases , Sequência Rica em GC , Meiose/genética , Purinas/metabolismo , Pirimidinas/metabolismo , Recombinação Genética , Algoritmos , Animais , Quebra Cromossômica , Mapeamento Cromossômico , Humanos , Repetições de Microssatélites , Pan troglodytes/genética , Polimorfismo Genético , Saccharomyces cerevisiae/genética , Análise de Sequência de DNA
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