Biological invasions cause ecological and economic impacts across the globe. However, it is unclear whether there are strong patterns in terms of their major effects, how the vulnerability of different ecosystems varies and which ecosystem services are at greatest risk. We present a global meta-analysis of 199 articles reporting 1041 field studies that in total describe the impacts of 135 alien plant taxa on resident species, communities and ecosystems. Across studies, alien plants had a significant effect in 11 of 24 different types of impact assessed. The magnitude and direction of the impact varied both within and between different types of impact. On average, abundance and diversity of the resident species decreased in invaded sites, whereas primary production and several ecosystem processes were enhanced. While alien N-fixing species had greater impacts on N-cycling variables, they did not consistently affect other impact types. The magnitude of the impacts was not significantly different between island and mainland ecosystems. Overall, alien species impacts are heterogeneous and not unidirectional even within particular impact types. Our analysis also reveals that by the time changes in nutrient cycling are detected, major impacts on plant species and communities are likely to have already occurred.
With the growing body of literature assessing the impact of invasive alien plants on resident species and ecosystems, a comprehensive assessment of the relationship between invasive species traits and environmental settings of invasion on the characteristics of impacts is needed. Based on 287 publications with 1551 individual cases that addressed the impact of 167 invasive plant species belonging to 49 families, we present the first global overview of frequencies of significant and non-significant ecological impacts and their directions on 15 outcomes related to the responses of resident populations, species, communities and ecosystems. Species and community outcomes tend to decline following invasions, especially those for plants, but the abundance and richness of the soil biota, as well as concentrations of soil nutrients and water, more often increase than decrease following invasion. Data mining tools revealed that invasive plants exert consistent significant impacts on some outcomes (survival of resident biota, activity of resident animals, resident community productivity, mineral and nutrient content in plant tissues, and fire frequency and intensity), whereas for outcomes at the community level, such as species richness, diversity and soil resources, the significance of impacts is determined by interactions between species traits and the biome invaded. The latter outcomes are most likely to be impacted by annual grasses, and by wind pollinated trees invading mediterranean or tropical biomes. One of the clearest signals in this analysis is that invasive plants are far more likely to cause significant impacts on resident plant and animal richness on islands rather than mainland. This study shows that there is no universal measure of impact and the pattern observed depends on the ecological measure examined. Although impact is strongly context dependent, some species traits, especially life form, stature and pollination syndrome, may provide a means to predict impact, regardless of the particular habitat and geographical region invaded.
Summary1. This account presents information on all aspects of the biology of Ambrosia artemisiifolia L. (Common ragweed) that are relevant to understanding its ecology. The main topics are presented within the standard framework of the Biological Flora of the British Isles: distribution, habitat, communities, responses to biotic factors, responses to environment, structure and physiology, phenology, floral and seed characters, herbivores and disease, and history, conservation, impacts and management. *Nomenclature of vascular plants follows Stace (2010) and, for non-British species, Flora Europaea.
Abstract. Polyploidy is often assumed to increase the spread and thus the success of alien plant species, but few empirical studies exist. We tested this hypothesis with Centaurea maculosa Lam., a species native to Europe and introduced into North America approximately 120 years ago where it became highly invasive. We analyzed the ploidy level of more than 2000 plants from 93 native and 48 invasive C. maculosa populations and found a pronounced shift in the relative frequency of diploid and tetraploid cytotypes. In Europe diploid populations occur in higher frequencies than tetraploids and only four populations had both cytotypes, while in North America diploid plants were found in only one mixed population and thus tetraploids clearly dominated. Our results showed a pronounced shift in the climatic niche between tetraploid populations in the native and introduced range toward drier climate in North America and a similar albeit smaller shift between diploids and tetraploids in the native range. The field data indicate that diploids have a predominately monocarpic life cycle, while tetraploids are often polycarpic. Additionally, the polycarpic life-form seems to be more prevalent among tetraploids in the introduced range than among tetraploids in the native range. Our study suggests that both ploidy types of C. maculosa were introduced into North America, but tetraploids became the dominant cytotype with invasion. We suggest that the invasive success of C. maculosa is partly due to preadaptation of the tetraploid cytotype in Europe to drier climate and possibly further adaptation to these conditions in the introduced range. The potential for earlier and longer seed production associated with the polycarpic life cycle constitutes an additional factor that may have led to the dominance of tetraploids over diploids in the introduced range.
The World's grasslands are under severe threat from on-going degradation, yet they are largely ignored in sustainable development agendas. This degradation is undermining the capacity of grasslands to support biodiversity, ecosystem services, and human wellbeing. In this Perspective, we examine the current state of grasslands worldwide and explore the extent and dominant drivers of global grassland degradation. We identify actions that are critical to the development of socio-ecological solutions to combat degradation and promote restoration of global grasslands. Specifically, we argue that progress can be made by: increasing recognition of grasslands in global policy, developing standardised indicators of grassland degradation, using scientific innovation for effective restoration at regional and landscape scales, and enhancing knowledge transfer and data sharing on restoration experiences. The integration of these strategies into sustainability policy should help to halt grassland degradation and enhance restoration success, and protect the socio-economic, cultural and ecological benefits that grasslands provide.Grasslands, comprising open grassland, grassy shrublands and savannah, cover about 40% of the Earth's surface and some 69% of the world's agricultural land area 1-3 . Not only do they serve as an important global reservoir of biodiversity, including many iconic and endemic species, but also, they provide a wide range of material and non-material benefits to humans and our quality of life. These benefits include a wide range of ecosystem services, such as food production, water supply and regulation, carbon storage and climate mitigation, pollination, and a host of cultural services 1-3 . Despite its importance, grassland degradation is widespread and accelerating in many parts of the world 4-6 with as much as 49% of grassland area worldwide having been degraded to some extent 5,7,8 .Grassland degradation poses an enormous threat to the hundreds of millions of people who rely on grasslands worldwide for food, fuel, fibre and medicinal products, as well as their multiple cultural values 9,10 . In terms of livestock production, the global cost of grassland degradation has been estimated at $6.8 billion 11 , with the impact on human welfare being particularly severe in regions where most the population is below the poverty line Grassland degradation also creates major environmental problems, given that grasslands play a critical role in biodiversity conservation, climate and water regulation, and global biogeochemical cycles 2,4 . For example, the conversion of tropical grassy biomes to arable cropland poses a significant threat to biodiversity given that they have a vertebrate species richness comparable to forests 12 , while the recent expansion of croplands in United States has caused widespread conversion of prairie grasslands, with considerable cost to wildlife 6 . Moreover, the conversion of grasslands to arable cropland and disturbance through overgrazing, fire and invasive species can lead to signif...
Summary1 Plant species may become invasive due to a lack of natural enemies (e.g. herbivores) in their introduced range. Absence of herbivores may result in selection for the loss of costly herbivore-resistance traits, which are expected to show a trade-off with vigour or competitive ability (the evolution of increased competitive ability, or EICA, hypothesis). 2 We conducted a common garden experiment in Switzerland, in which we compared herbivore resistance and vigour of Senecio jacobaea plants exposed to the specialist flea beetle Longitarsus jacobaeae , for four populations originating within the native range (Europe), and four from regions where it had been introduced (New Zealand, USA) and was unaffected by L. jacobaeae . Our predictions were that, compared with plants from the native populations, plants from introduced populations would experience greater herbivory (due to loss of resistance traits), and exhibit more vigorous growth. 3 As expected, we found that introduced S. jacobaea grew larger, and had greater reproductive output, than plants from the native range. Larger plants experienced more feeding damage, and introduced plants were consumed more even when size differences were controlled. Introduced plants also exhibited a greater relative ability to reproduce after damage was sustained, i.e. higher tolerance to herbivory. 4 Contrary to predictions, however, plants from introduced populations had higher total pyrrolizidine alkaloid production (chemical defence against herbivores). 5 Although plants from introduced ranges exhibited life-history traits consistent with EICA predictions, similar phenotypes were common in one of the populations from the native range, suggesting that EICA may not fully explain the invasion success of S. jacobaea . 6 Our results imply that increased competitive ability (vigour) of invasive plants may be associated with changes in resistance as well as tolerance to herbivory, and both types of anti-herbivore defence may need to be examined simultaneously to advance our understanding of invasiveness.
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