scholarly journals Increase in nutrient availability promotes success of invasive plants through increasing growth and decreasing anti-herbivory defenses

2021 ◽  
Author(s):  
Liping Shan ◽  
Ayub M.O. Oduor ◽  
Wei Huang ◽  
Yanjie Liu

Invasive plant species often exhibit greater growth and lower anti-herbivory defense than native plant species. However, it remains unclear how nutrient enrichment of invaded habitats may interact with competition from resident native plants to affect growth and defense of invasive plants. In a greenhouse experiment, we grew five congeneric pairs of invasive and native plant species under two levels of nutrient availability (low vs. high) that were fully crossed with simulated herbivory (clipping vs. no-clipping) and competition (alone vs. competition). Invasive plants produced more gibberellic acid, and grew larger than native species. Nutrient enrichment caused a greater increase in total biomass of invasive plants than of native plants, especially in the absence of competition or without simulated herbivory treatment. Nutrient enrichment decreased leaf flavonoid contents of invasive plants under both simulated herbivory conditions, but increased flavonoid of native plants under simulated herbivory condition. Nutrient enrichment only decreased tannins production of invasive species under competition. For native species, it enhanced their tannins production under competition, but decreased the chemicals when growing alone. The results indicate that the higher biomass production and lower flavonoids production in response to nutrient addition may lead to competitive advantage of invasive species than native species.

2015 ◽  
Vol 112 (14) ◽  
pp. 4387-4392 ◽  
Author(s):  
Chris D. Thomas ◽  
G. Palmer

Plants are commonly listed as invasive species, presuming that they cause harm at both global and regional scales. Approximately 40% of all species listed as invasive within Britain are plants. However, invasive plants are rarely linked to the national or global extinction of native plant species. The possible explanation is that competitive exclusion takes place slowly and that invasive plants will eventually eliminate native species (the “time-to-exclusion hypothesis”). Using the extensive British Countryside Survey Data, we find that changes to plant occurrence and cover between 1990 and 2007 at 479 British sites do not differ between native and non-native plant species. More than 80% of the plant species that are widespread enough to be sampled are native species; hence, total cover changes have been dominated by native species (total cover increases by native species are more than nine times greater than those by non-native species). This implies that factors other than plant “invasions” are the key drivers of vegetation change. We also find that the diversity of native species is increasing in locations where the diversity of non-native species is increasing, suggesting that high diversities of native and non-native plant species are compatible with one another. We reject the time-to-exclusion hypothesis as the reason why extinctions have not been observed and suggest that non-native plant species are not a threat to floral diversity in Britain. Further research is needed in island-like environments, but we question whether it is appropriate that more than three-quarters of taxa listed globally as invasive species are plants.


PLoS ONE ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. e0237894
Author(s):  
Amy E. Kendig ◽  
Vida J. Svahnström ◽  
Ashish Adhikari ◽  
Philip F. Harmon ◽  
S. Luke Flory

Infectious diseases and invasive species can be strong drivers of biological systems that may interact to shift plant community composition. For example, disease can modify resource competition between invasive and native species. Invasive species tend to interact with a diversity of native species, and it is unclear how native species differ in response to disease-mediated competition with invasive species. Here, we quantified the biomass responses of three native North American grass species (Dichanthelium clandestinum, Elymus virginicus, and Eragrostis spectabilis) to disease-mediated competition with the non-native invasive grass Microstegium vimineum. The foliar fungal pathogen Bipolaris gigantea has recently emerged in Microstegium populations, causing a leaf spot disease that reduces Microstegium biomass and seed production. In a greenhouse experiment, we examined the effects of B. gigantea inoculation on two components of competitive ability for each native species: growth in the absence of competition and biomass responses to increasing densities of Microstegium. Bipolaris gigantea inoculation affected each of the three native species in unique ways, by increasing (Dichanthelium), decreasing (Elymus), or not changing (Eragrostis) their growth in the absence of competition relative to mock inoculation. Bipolaris gigantea inoculation did not, however, affect Microstegium biomass or mediate the effect of Microstegium density on native plant biomass. Thus, B. gigantea had species-specific effects on native plant competition with Microstegium through species-specific biomass responses to B. gigantea inoculation, but not through modified responses to Microstegium density. Our results suggest that disease may uniquely modify competitive interactions between invasive and native plants for different native plant species.


Forests ◽  
2019 ◽  
Vol 10 (7) ◽  
pp. 576
Author(s):  
Wang ◽  
Awaya ◽  
Zhu ◽  
Motooka ◽  
Nelson ◽  
...  

Non-native plant species have become serious pests in Hawaii’s delicate island ecosystems. It is necessary to control invasive plants. The herbicides hexazinone and tebuthiuron were evaluated for defoliation efficacy to control several major invasive plants and for non-target effects on native plants at Site I in a rainforest at 1200 m elevation and Site II in a mesic area at 640 m elevation on the island of Kauai, Hawaii. The invasive weed species in the sites included daisy fleabane (Erigeron karvinskianus DC.), faya tree (Myrica faya Ait.), strawberry guava (Psidium cattleyanum Sabine), banana passion fruit (Passiflora mollissima Bailey), vaseygrass (Paspalum urvillei Steud.), and highbush blackberry (Rubus argutus Link. 1822). Native plants included ohia lehua (Metrosideros polymorpha Gaudich.), naupaka (Scaevola cerasifolia Labill.), pilo (Hedyotis mannii), hona (Urera glabra (Hook. & Arn.)), aalii (Dodonaea viscosa Jacq.), and amau (Sadleria sp.). The results showed that broadcast applications of hexazinone granules and tebuthiuron pellets were effective on some of those invasive species. Herbicidal tolerance varied among the native species. For example, D. viscosa showed high tolerance to hexazinone. S. cerasifolia was susceptible to hexazinone, but not to tebuthiuron. The inconsistent defoliation of Sadleria sp. occurred among different applications rates of the two herbicides. M. polymorpha, particularly when it was small, could tolerate hexazinone and tebuthiuron. U. glabra was severely injured by the two herbicides. H. mannii was moderately tolerant to hexazinone, but fairly sensitive to tebuthiuron. The invasive loblolly pine (Pinus taeda L.) was highly tolerant to hexazinone, but was very sensitive to tebuthiuron. M. faya was very sensitive to hexazinone, but very tolerant to tebuthiuron. P. cattleyanum was sensitive to both herbicides. Six and nine months after hexazinone and tebuthiuron treatment, respectively, native plants were transplanted into the Sites to observe injury from residual herbicides. Approximately less than 10% mortality was observed for the out-planted native species three months after planting (MAP), indicating that the native species showed less injury in the early period of transplant. The mortality of the three endangered species Kauai hau kuahiwi (Hibiscadelphis distans), Kauai delissea (Delissea rhytidosperma H.Mann) and kawawaenohu (Alsinidendron lynchnoides), however, increased as the MAP increased. Overall, broadcast treatments of hexazinone and tebuthiuron at rates higher than 1 kg active ingredient per hectare would be problematic. The dissipation half-life values of hexazinone and tebuthiuron in the 1-15 cm layer of soils at the two sites were approximately 7 days and greater than 180 days, respectively.


2006 ◽  
Vol 28 (1) ◽  
pp. 27 ◽  
Author(s):  
A. C. Grice

Most parts of the Australian rangelands are at risk of invasion by one or more species of non-native plants. The severity of current problems varies greatly across the rangelands with more non-native plant species in more intensively settled regions, in climatic zones that have higher and more reliable rainfall, and in wetter and more fertile parts of rangeland landscapes. Although there is quantitative evidence of impacts on either particular taxonomic groups or specific ecological processes in Australian rangelands, a comprehensive picture of responses of rangeland ecosystems to plant invasions is not available. Research has been focused on invasive species that are perceived to have important effects. This is likely to down play the significance of species that have visually less dramatic influences and ignore the possibility that some species could invade and yet have negligible consequences. It is conceivable that most of the overall impact will come from a relatively small proportion of invasive species. Impacts have most commonly been assessed in terms of plant species richness or the abundance of certain groups of vertebrates to the almost complete exclusion of other faunal groups. All scientific studies of the impacts of invasive species in Australian rangelands have focused on the effects of individual invasive species although in many situations native communities are under threat from a complex of interacting weed species. Invasion by non-native species is generally associated with declines in native plant species richness, but faunal responses are more complex and individual invasions may be associated with increase, decrease and no-change scenarios for different faunal groups. Some invasive species may remain minor components of the vegetation that they invade while others completely dominate one stratum or the vegetation overall.


2012 ◽  
Vol 30 (1) ◽  
pp. 51 ◽  
Author(s):  
Senilolia H. Tuiwawa ◽  
Gunnar Keppel

Mahogany (Swietenia macrophylla King) plantations cover a considerable area on the south-eastern parts of Viti Levu, Fiji. The understorey of these plantations often comprise a diverse, but undocumented, assemblage of native plant species. This study investigates the diversity, composition and regeneration potential of native plant species in the Wainiveiota mahogany plantation 40?50 years after establishment. Ten 10 m x 10 m plots were alternately placed at 10 m intervals perpendicular to a 200 m line transect. A total of 491 individual plants with dbh ≥ 1 cm, comprising 69 species, 51 genera and 34 families, were sampled. In addition to the exotic mahogany, there were 68 native (39 endemic, 24 indigenous and 5 identified to genus only) species recorded. Girronniera celtidifolia Gaud., Dillenia biflora (A.Gray) Martelli ex Dur. & Jacks and Barringtonia edulis Seem. had the highest recruitment and Endospermum macrophyllum (Muell.Arg.) Pax & Hoffm. was the dominant native species. Syzygium Gaertn. (Myrtaceae) was the most diverse genus and Myrtaceae the most diverse family. With 98% of the sapling recruitment consisting of native species, there is potential for re-establishment of a lowland rainforest dominated by native species over time.


2012 ◽  
Vol 5 (4) ◽  
pp. 494-505 ◽  
Author(s):  
Nicholas R. Jordan ◽  
Laura Aldrich-Wolfe ◽  
Sheri C. Huerd ◽  
Diane L. Larson ◽  
Gary Muehlbauer

AbstractDiversified grasslands that contain native plant species can produce biofuels, support sustainable grazing systems, and produce other ecosystem services. However, ecosystem service production can be disrupted by invasion of exotic perennial plants, and these plants can have soil-microbial “legacies” that may interfere with establishment and maintenance of diversified grasslands even after effective management of the invasive species. The nature of such legacies is not well understood, but may involve suppression of mutualisms between native species and soil microbes. In this study, we tested the hypotheses that legacy effects of invasive species change colonization rates, diversity, and composition of arbuscular-mycorrhizal fungi (AMF) associated with seedlings of co-occurring invasive and native grassland species. In a glasshouse, experimental soils were conditioned by cultivating three invasive grassland perennials, three native grassland perennials, and a native perennial mixture. Each was grown separately through three cycles of growth, after which we used T-RFLP analysis to characterize AMF associations of seedlings of six native perennial and six invasive perennial species grown in these soils. Legacy effects of soil conditioning by invasive species did not affect AMF richness in seedling roots, but did affect AMF colonization rates and the taxonomic composition of mycorrhizal associations in seedling roots. Moreover, native species were more heavily colonized by AMF and roots of native species had greater AMF richness (number of AMF operational taxonomic units per seedling) than did invasive species. The invasive species used to condition soil in this experiment have been shown to have legacy effects on biomass of native seedlings, reducing their growth in this and a previous similar experiment. Therefore, our results suggest that successful plant invaders can have legacies that affect soil-microbial associations of native plants and that these effects can inhibit growth of native plant species in invaded communities.


Author(s):  
Susan Kalisz ◽  
Stephanie N. Kivlin ◽  
Lalasia Bialic-Murphy

Abstract Invasive species utilize a wide array of trait strategies to establish in novel ecosystems. Among these traits is the capacity to produce allelopathic compounds that can directly inhibit neighboring native plants or indirectly suppress native plants via disruption of beneficial belowground microbial mutualisms, or altered soil resources. Despite the well-known prevalence of allelopathy among plant taxa, the pervasiveness of allelopathy among invasive plants is unknown. Here we demonstrate that the majority of the 524 invasive plant species in our database produce allelochemicals with the potential to negatively affect native plant performance. Moreover, allelopathy is widespread across the plant phylogeny, suggesting that allelopathy could have a large impact on native species across the globe. Allelopathic impacts of invasive species are often thought to be present in only a few plant clades (e.g., Brassicaceae). Yet our analysis shows that allelopathy is present in 72% of the 113 plant families surveyed, suggesting that this ubiquitous mechanism of invasion deserves more attention as invasion rates increase across the globe.


2004 ◽  
Vol 52 (2) ◽  
pp. 141 ◽  
Author(s):  
V. P. Thomson ◽  
M. R. Leishman

Australian soils are naturally low in nutrient concentrations, particularly nitrogen (N) and phosphorus (P). Native plants are well adapted to low-nutrient soils, and can be adversely affected when exposed to higher concentrations of nutrients. The Hawkesbury Sandstone soils in northern Sydney are naturally low in nutrients, but often receive additional nutrient input from urban stormwater run-off. Increases in soil nutrients in urban bushland are associated with the presence of exotic species, and the decline in the diversity of native species. This study tested the hypothesis that high concentrations of nutrients, in particular P, in the disturbed soils of urban bushland, reduce survival of native plants. We examined the survival of native species under five different nutrient concentrations that are typical of nutrient-enriched urban bushland soil, in two glasshouse experiments. The experiments examined both survival of seedlings and survival of 6-month-old plants. We used native species that are adapted to both nutrient-poor and nutrient-rich soils. In general, the survival of native plants decreased with increasing nutrient concentrations. At soil total-P concentrations >200 mg kg–1, most plants died. Seedlings were more sensitive to added nutrients than the 6-month-old plants. Species that were from higher-nutrient soil had consistently higher survival than species from low-nutrient soils, under the nutrient addition treatments. These results suggest that at high soil nutrient concentrations typical of stormwater-affected urban bushland, native plant species of low-nutrient soils will be unable to survive. If ecological restoration works are to be done in such areas, replanting with more mature plants from naturally high-nutrient habitats is likely to be the most successful. However, restoration of these areas may have limited success and they are likely to remain dominated by exotic plant species.


Author(s):  
Fernanda Ribeiro da Silva ◽  
Marco Aurélio Pizo

Abstract Restoration aims to rebuild not only species but also the tangled interactions between species that ensure communities perpetuate by themselves. In tropical forests, restoration of seed dispersal interactions is essential because most plant species depend on animals to spread their seeds. A big challenge in restoring such forests is dealing with invasion by non-native species. Non-native plant species may outcompete and eliminate native species from the community, potentially disrupting or arresting the restoration process. Once established, invasive non-native plants are usually incorporated into the local seed dispersal network, potentially causing loss of biodiversity by competition with native species. This chapter reports on a case study of a 25-year old restored forest invaded by several bird-dispersed plant species. We assessed network metrics at the species level to specifically evaluate the role performed by invasive non-native species in the structure of the bird - seed dispersal network. The removal of invasive non-native plants and the re-establishment of native plant communities should be considered for the restoration of habitats invaded by non-native plants. For this reason, we discuss the impacts of removing such non-native plants and explore the consequences for the structure of the overall network. Because restoration areas are open systems, even after the removal of invasive non-native plant species they can return via seed dispersal. So, both the control and management of invasive non-native species would be more effective if planned with a landscape perspective. We also point out relevant management aspects to avoid the negative influence of invasive non-native plants on the seed dispersal interactions occurring between native plant and bird species in restored tropical forests.


Author(s):  
Fernanda Ribeiro da Silva ◽  
◽  
Marco Aurélio Pizo ◽  

Restoration aims to rebuild not only species but also the tangled interactions between species that ensure communities perpetuate by themselves. In tropical forests, restoration of seed dispersal interactions is essential because most plant species depend on animals to spread their seeds. A big challenge in restoring such forests is dealing with invasion by non-native species. Non-native plant species may outcompete and eliminate native species from the community, potentially disrupting or arresting the restoration process. Once established, invasive non-native plants are usually incorporated into the local seed dispersal network, potentially causing loss of biodiversity by competition with native species. This chapter reports on a case study of a 25-year old restored forest invaded by several bird-dispersed plant species. We assessed network metrics at the species level to specifically evaluate the role performed by invasive non-native species in the structure of the bird - seed dispersal network. The removal of invasive non-native plants and the re-establishment of native plant communities should be considered for the restoration of habitats invaded by non-native plants. For this reason, we discuss the impacts of removing such non-native plants and explore the consequences for the structure of the overall network. Because restoration areas are open systems, even after the removal of invasive non-native plant species they can return via seed dispersal. So, both the control and management of invasive non-native species would be more effective if planned with a landscape perspective. We also point out relevant management aspects to avoid the negative influence of invasive non-native plants on the seed dispersal interactions occurring between native plant and bird species in restored tropical forests.


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