scholarly journals Evidence of Qualitative Differences between Soil-Occupancy Effects of Invasive vs. Native Grassland Plant Species

2011 ◽  
Vol 4 (1) ◽  
pp. 11-21 ◽  
Author(s):  
Nicholas R. Jordan ◽  
Diane L. Larson ◽  
Sheri C. Huerd

AbstractDiversified grasslands that contain native plant species are being recognized as important elements of agricultural landscapes and for production of biofuel feedstocks as well as a variety of other ecosystem services. Unfortunately, establishment of such grasslands is often difficult, unpredictable, and highly vulnerable to interference and invasion by weeds. Evidence suggests that soil-microbial “legacies” of invasive perennial species can inhibit growth of native grassland species. However, previous assessments of legacy effects of soil occupancy by invasive species that invade grasslands have focused on single invasive species and on responses to invasive soil occupancy in only a few species. In this study, we tested the hypothesis that legacy effects of invasive species differ qualitatively from those of native grassland species. In a glasshouse, three invasive and three native grassland perennials and a native perennial mixture were grown separately through three cycles of growth and soil conditioning in soils with and without arbuscular mycorrhizal fungi (AMF), after which we assessed seedling growth in these soils. Native species differed categorically from invasives in their response to soil conditioning by native or invasive species, but these differences depended on the presence of AMF. When AMF were present, native species largely had facilitative effects on invasive species, relative to effects of invasives on other invasives. Invasive species did not facilitate native growth; neutral effects were predominant, but strong soil-mediated inhibitory effects on certain native species occurred. Our results support the hypothesis that successful plant invaders create biological legacies in soil that inhibit native growth, but suggest also this mechanism of invasion will have nuanced effects on community dynamics, as some natives may be unaffected by such legacies. Such native species may be valuable as nurse plants that provide cost-effective restoration of soil conditions needed for efficient establishment of diversified grasslands.

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.


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.


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.


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.


2017 ◽  
Vol 9 (4) ◽  
pp. 86 ◽  
Author(s):  
Cristina A. Gómez-Moya ◽  
Talita P. S. Lima ◽  
Elisângela G. F. Morais ◽  
Manoel G. C. Gondim Jr. ◽  
Gilberto J. De Moraes

The expansion of red palm mite (RPM), Raoiella indica (Acari: Tenuipalpidae) in Brazil could impact negatively the native plant species, especially of the family Arecaceae. To determine which species could be at risk, we investigated the development and reproductive potential of R. indica on 19 plant species including 13 native species to the Brazilian Amazon (12 Arecaceae and one Heliconiaceae), and six exotic species, four Arecaceae, a Musaceae and a Zingiberaceae. Values of the instantaneous rate of increase (ri) were initially estimated at 7, 14, 21 and 28 days after infestation of each species. Higher values of ri (> 0.05) were determined on the Arecaceae Adonidia merrillii, Astrocaryum jauari, Cocos nucifera, Bactris simplicifrons, Mauritia flexuosa, Phoenix dactylifera and Socratea exorrhiza, and on the Heliconiaceae Heliconia psittacorum Sassy; these were classified as “potential primary hosts”. Lower, but still positive values of ri (0-0.05) were determined on the Arecaceae Bactris maraja, Oenocarpus bacaba, Oenocarpus bataua and on the Musaceae Musa × paradisiaca (Prata variety); these were classified as “potential secondary hosts”. Negative values of ri were determined for the remaining plants, i.e., the Arecaceae Astrocaryum aculeatum, Attalea maripa, Bactris gasipaes, Elaeis guineensis, Euterpe oleracea, Euterpe precatoria, and the Zingiberaceae Alpinia rosea; these were considered “non-hosts”. Species with ri < 0.05 were considered not to be threatened by the RPM. Biological parameters of RPM were evaluated on the plant species with positive ri (except B. maraja) and two native species with negative ri (E. oleracea and E. precatoria). Mean developmental time ranged from 14.7 days on C. nucifera to 21.4 days on Musa × paradisiaca, showing a significant influence of the plant substrate. Immature viability, oviposition rate, net reproductive rate (R0) and intrinsic rate of increase (rm) were affected by the plant species.


2021 ◽  
Author(s):  
Ingmar Staude ◽  
Josiane Segar ◽  
Corey Thomas Callaghan ◽  
Emma Ladouceur ◽  
Jasper Meya ◽  
...  

Global commitments to species conservation have failed to halt systematic widespread declines in plant species. Current policy interventions, such as protected areas and legal species legislation, remain insufficient, and there is an urgent need to engage novel approaches and actors in conservation. Here, we propose that urban conservation gardening, namely the cultivation of declining native plant species in public and private green spaces, can be one such approach. Conservation gardening can address key (a)biotic drivers of species decline, act as a critical dispersal pathway and increase the occupancy of declining native species. We identify policy mechanisms to upscale conservation gardening to a mainstream activity by reforming the existing horticultural market into an innovative nature protection instrument. This involves incentivizing the integration of the native seed sector, leveraging existing certification and labelling schemes, promoting consumer access, as well as building citizen-science projects to foster public engagement. Mainstreamed conservation gardening can be an economically viable, sustainable, and participatory measure that complements traditional approaches to plant conservation.


Author(s):  
Elizabeth M. Wandrag ◽  
◽  
Jane A. Catford ◽  
◽  
◽  
...  

The introduction of species to new locations leads to novel competitive interactions between resident native and newly-arriving non-native species. The nature of these competitive interactions can influence the suitability of the environment for the survival, reproduction and spread of non-native plant species, and the impact those species have on native plant communities. Indeed, the large literature on competition among plants reflects its importance in shaping the composition of plant communities, including the invasion success of non-native species. While competition and invasion theory have historically developed in parallel, the increasing recognition of the synergism between the two themes has led to new insights into how non-native plant species invade native plant communities, and the impacts they have on those plant communities. This chapter provides an entry point into the aspects of competition theory that can help explain the success, dominance and impacts of invasive species. It focuses on resource competition, which arises wherever the resources necessary for establishment, survival, reproduction and spread are in limited supply. It highlights key hypotheses developed in invasion biology that relate to ideas of competition, outlines biotic and abiotic factors that influence the strength of competition and species' relative competitive abilities, and describes when and how competition between non-native and native plant species can influence invasion outcomes. Understanding the processes that influence the strength of competition between non-native and native plant species is a necessary step towards understanding the causes and consequences of biological invasions.


2010 ◽  
Vol 19 (4) ◽  
pp. 490 ◽  
Author(s):  
Erich K. Dodson ◽  
David W. Peterson ◽  
Richy J. Harrod

Slope stabilisation treatments like mulching and seeding are used to increase soil cover and reduce runoff and erosion following severe wildfires, but may also retard native vegetation recovery. We evaluated the effects of seeding and fertilisation on the cover and richness of native and exotic plants and on individual plant species following the 2004 Pot Peak wildfire in Washington State, USA. We applied four seeding and three fertilisation treatments to experimental plots at eight burned sites in spring 2005 and surveyed vegetation during the first two growing seasons after fire. Seeding significantly reduced native non-seeded species richness and cover by the second year. Fertilisation increased native plant cover in both years, but did not affect plant species richness. Seeding and fertilisation significantly increased exotic cover, especially when applied in combination. However, exotic cover and richness were low and treatment effects were greatest in the first year. Seeding suppressed several native plant species, especially disturbance-adapted forbs. Fertilisation, in contrast, favoured several native understorey plant species but reduced tree regeneration. Seeding, even with native species, appears to interfere with the natural recovery of native vegetation whereas fertilisation increases total plant cover, primarily by facilitating native vegetation recovery.


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