Role of Horses as Potential Vectors of Non-Native Plant Invasion: An Overview

2020 ◽  
Vol 40 (3) ◽  
Author(s):  
Lauren D. Quinn ◽  
Adda Quinn ◽  
Mietek Kolipinski ◽  
Bonnie Davis ◽  
Connie Berto ◽  
...  
Keyword(s):  
2010 ◽  
Vol 30 (4) ◽  
pp. 408-416 ◽  
Author(s):  
Lauren D. Quinn ◽  
Adda Quinn ◽  
Mietek Kolipinski ◽  
Bonnie Davis ◽  
Connie Berto ◽  
...  
Keyword(s):  

Author(s):  
Anna Traveset ◽  
David M. Richardson

Abstract Diverse biotic interactions between non-native plant species and other species from all taxonomic groups are crucial mediators of the dynamics of plant invasions. This chapter reviews the key hypotheses in invasion ecology that invoke biotic interactions to explain aspects of plant invasion dynamics. We examine the historical context of these hypotheses and assess the evidence for accepting or rejecting their predictions. Most hypotheses invoke antagonistic interactions, mainly competition, predation, herbivory interactions and the role of pathogens. Only in the last two decades have positive (facilitative/mutualistic) interactions been explicitly included in invasion biology theory (as in ecological theory in general). Much information has accumulated in testing hypotheses relating to biotic resistance and Enemy Release Theory, although many of the emerging generalizations are still contentious. There is growing consensus that other drivers of plant invasion success, such as propagule pressure and disturbance, mediate the outcome of biotic interactions, thereby complicating our ability to make predictions, but these have rarely been assessed in both native and adventive ranges of non-native invasive species. It is also widely acknowledged that biogeographic comparisons, more than common garden experiments, are needed to shed light on many of the contradictory results. Contrasting findings have also emerged in exploring the roles of positive interactions. Despite strong evidence that such interactions are crucial in many communities, more work is needed to elucidate the factors that influence the relative importance of positive and negative interactions in different ecosystems. Different types of evidence in support of invasional meltdown have emerged for diverse habitats and across spatial scales. In light of increasing evidence that biotic indirect effects are crucial determinants of the structure, dynamics and evolution of ecological communities, both direct and indirect interactions involving native and non-native species must be considered to determine how they shape plant invasion patterns and the ecological impacts of non-native species on recipient communities. Research that examines both biotic interactions and the factors that mediate their strength and alter interaction outcomes is needed to improve our ability to predict the effects of novel interactions between native and non-native species, and to envisage how existing invaded communities will respond to changing environmental conditions. Many opportunities exist for manipulating biotic interactions as part of integrated control strategies to reduce the extent, density and impacts of non-native plant invasions. These include the introduction of species from the native range of the non-native plant for biological control, diverse manipulations of plant - herbivore interactions and many types of interaction to enhance biotic resistance and steer vegetation recovery following non-native plant control.


2021 ◽  
Author(s):  
◽  
Justyna Giejsztowt

<p>Drivers of global change have direct impacts on the structure of communities and functioning of ecosystems, and interactions between drivers may buffer or exacerbate these direct effects. Interactions among drivers can lead to complex non-linear outcomes for ecosystems, communities and species, but are infrequently quantified. Through a combination of experimental, observational and modelling approaches, I address critical gaps in our understanding of the interactive effects of climate change and plant invasion, using Tongariro National Park (TNP; New Zealand) as a model. TNP is an alpine ecosystem of cultural significance which hosts a unique flora with high rates of endemism. TNP is invaded by the perennial shrub Calluna vulgaris (L.) Hull. My objectives were to: 1) determine whether species-specific phenological shifts have the potential to alter the reproductive capacity of native plants in landscapes affected by invasion; 2) determine whether the effect of invasion intensity on the Species Area Relationship (SAR) of native alpine plant species is influenced by environmental stress; 3) develop a novel modelling framework that would account for density-dependent competitive interactions between native species and C. vulgaris and implement it to determine the combined risk of climate change and plant invasion on the distribution of native plant species; and 4) explore the possible mechanisms leading to a discrepancy in C. vulgaris invasion success on the North and South Islands of New Zealand. I show that species-specific phenological responses to climate warming increase the flowering overlap between a native and an invasive plant. I then show that competition for pollination with the invader decreases the sexual reproduction of the native in some landscapes. I therefore illustrate a previously undescribed interaction between climate warming and plant invasion where the effects of competition for pollination with an invader on the sexual reproduction of the native may be exacerbated by climate warming. Furthermore, I describe a previously unknown pattern of changing invasive plant impact on SAR along an environmental stress gradient. Namely, I demonstrate that interactions between an invasive plant and local native plant species richness become increasingly facilitative along elevational gradients and that the strength of plant interactions is dependent on invader biomass. I then show that the consequences of changing plant interactions at a local scale for the slope of SAR is dependent on the pervasion of the invader. Next, I demonstrate that the inclusion of invasive species density data in distribution models for a native plant leads to greater reductions in predicted native plant distribution and density under future climate change scenarios relative to models based on climate suitability alone. Finally, I find no evidence for large-scale climatic, edaphic, and vegetative limitations to invasion by C. vulgaris on either the North and South Islands of New Zealand. Instead, my results suggest that discrepancies in invasive spread between islands may be driven by human activity: C. vulgaris is associated with the same levels of human disturbance on both islands despite differences in the presence of these conditions between then islands. Altogether, these results show that interactive effects between drivers on biodiversity and ecosystem dynamics are frequently not additive or linear. Therefore, accurate predictions of global change impacts on community structure and ecosystems function require experiments and models which include of interactions among drivers such as climate change and species invasion. These results are pertinent to effective conservation management as most landscapes are concurrently affected by multiple drivers of global environmental change.</p>


2015 ◽  
Vol 8 (1) ◽  
pp. 32-43 ◽  
Author(s):  
Lauren S. Pile ◽  
Geofeng Geoff Wang ◽  
Robert Polomski ◽  
Greg Yarrow ◽  
Claire M. Stuyck

AbstractNonnative invasive plants (NNIP) have far-reaching effects on native ecosystems worldwide. Understanding the role of generalist seed dispersers in spreading NNIP across the landscape is important to the conservation of native ecosystems and to the management of NNIP. We studied white-tailed deer (Odocoileus virginianus) as a seed disperser in a mixed maritime pine (Pinus spp.) forests on Parris Island, SC, with particular interest in the dispersal of Chinese tallowtree [Triadica sebifera (L.) Small], a highly invasive tree species in the southeastern United States, which is a management concern on Parris Island, SC. We collected deer scat pellet groups along transects in two forest types: those that had recently been treated with silvicultural timber harvest (thinned) and those that have not been so treated (unthinned). Using two pellet-treatment methods, directly planting or rinsing and sorting, we determined that, out of 25 species grown under greenhouse conditions, 28% (n = 7) were nonnative, small-seeded, herbaceous species. However, T. sebifera was not identified in either of the two treatment methods. Recent forest thinning significantly affected the number of species determined in deer pellet groups (F = 8.37; df = 1; P < 0.01), with more native plant species identified in unthinned (x̄ = 25 ± 11) than in thinned (x̄ = 3 ± 10) forest stands (F = 5.33; df = 1; P = 0.02). Our results indicate that white-tailed deer are actively dispersing nonnative seeds but not those of T. sebifera or other woody NNIP.


1998 ◽  
Vol 4 (1) ◽  
pp. 21 ◽  
Author(s):  
Max Abensperg-Traun ◽  
Lyn Atkins ◽  
Richard Hobbs ◽  
Dion Steven

Exotic plants are a major threat to native plant diversity in Australia yet a generic model of the invasion of Australian ecosystems by exotic species is lacking because invasion levels differ with vegetation/soil type and environmental conditions. This study compared relative differences in exotic species invasion (percent cover, spp. richness) and the species richness of herbaceous native plants in two structurally very similar vegetation types, Gimlet Eucalyptus salubris and Wandoo E. capillosa woodlands in the Western Australian wheatbelt. For each woodland type, plant variables were measured for relatively undisturbed woodlands, woodlands with >30 years of livestock grazing history, and woodlands in road-verges. Grazed and road-verge Gimlet and Wandoo woodlands had significantly higher cover of exotic species, and lower species richness of native plants, compared with undisturbed Gimlet and Wandoo. Exotic plant invasion was significantly greater in Gimlet woodlands for both grazed (mean 78% cover) and road-verge sites (mean 42% cover) than in comparable sites in Wandoo woodlands (grazed sites 25% cover, road-verge sites 19% cover). There was no significant difference in the species richness of exotic plants between Wandoo and Gimlet sites for any of the three situations. Mean site richness of native plants was not significantly different between undisturbed Wandoo and undisturbed Gimlet woodlands. Undisturbed woodlands were significantly richer in plant species than grazed and road-verge woodlands for both woodland types. Grazed and road-verge Wandoo sites were significantly richer in plant species than communities in grazed and road-verge Gimlet. The percent cover of exotics was negatively correlated with total (native) plant species richness for both woodland types (Wandoo r = ?0.70, Gimlet r = ?0.87). Of the total native species recorded in undisturbed Gimlet, 83% and 61% were not recorded in grazed and road-verge Gimlet, respectively. This compared with 40% and 33% for grazed and road-verge Wandoo, respectively. Grazed Wandoo and grazed Gimlet sites had significantly fewer native plant species than did road-verge Wandoo and road-verge Gimlet sites. Ecosystem implications of differential invasions by exotic species, and the effects of grazing (disturbance) and other factors influencing susceptibility to exotic plant invasion (landscape, competition and allelopathy) on native species decline are discussed. Exclusion of livestock and adequate methods of control and prevention of further invasions by exotic plants are essential requirements for the conservation of these woodland systems.


2020 ◽  

Abstract This book contains 23 chapters divided into seven parts. Part I reviews the key hypotheses in invasion ecology that invoke biotic interactions to explain aspects of plant invasion dynamics; and reviews models, theories and hypotheses on how invasion performance and impact of introduced species in recipient ecosystems can be conjectured according to biotic interactions between native and non-native species. Part II deals with positive and negative interactions in the soil. Part III discusses mutualistic interactions that promote plant invasions. Part IV describes antagonistic interactions that hinder plant invasions, while part V presents the consequences of plant invasions for biotic interactions among native species. In part VI, novel techniques and experimental approaches in the study of plant invasions are shown. In the last part, biotic interactions and the management of ecosystems invaded by non-native plants are discussed.


Agronomy ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 939 ◽  
Author(s):  
Francis A. Drummond

Wild blueberry is a native plant managed as a crop in northeastern North America. Fruit drop in wild blueberry, Vaccinium angustifolium Aiton, was studied over 6 years (1996–1999, 2008 and 2011). Three hypotheses were tested regarding fruit drop mechanisms from plants (clones) sampled in the field: (1) proportional fruit drop; (2) constant or uniform fruit drop; and (3) pollen or resource limitation. In addition, the temporal rate of fruit drop was measured between the end of pollination (petal fall) and fruit maturity just prior to harvest (2008 and 2011). The dynamics of fruit drop were different in the two years. The role of pollination intensity in fruit drop was also assessed. Evidence for both proportional fruit drop and resource limitation at the clone level was found but only proportional drop at the field level. Low levels of seed set are associated with fruit drop. In a four-year study (1996–1999), fruit drop ranged from 23.3 to 49.4% of the total set fruit. Partitioning the variance in fruit drop between years, fields and clones (plant genotypes) showed that the highest variation is between stems within clones (37.4%) and clones (plant genotype) within fields (35.4%), followed by between fields (19.8%) and between years (7.4%).


2008 ◽  
Vol 2 (5) ◽  
pp. 1241-1265 ◽  
Author(s):  
Thomas W. Gillespie ◽  
Jasmine Chu ◽  
Stephanie Pau

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