Can aerial herbicide application control Grey Willow (Salix cinerea L.) and stimulate native plant recovery in New Zealand wetlands?

2018 ◽  
Vol 19 (1) ◽  
pp. 49-57
Author(s):  
James Griffiths ◽  
Helen Armstrong ◽  
Rachel Innes ◽  
Jon Terry
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>


2008 ◽  
Vol 1 (1) ◽  
pp. 50-58 ◽  
Author(s):  
Bryan A. Endress ◽  
Catherine G. Parks ◽  
Bridgett J. Naylor ◽  
Steven R. Radosevich

AbstractSulfur cinquefoil is an exotic, perennial forb that invades a wide range of ecosystems in western North America. It forms dense populations and often threatens native plant species and communities. In this study, we address the following questions: (1) what herbicides, rates, and application times are most effective at reducing sulfur cinquefoil abundance while having the least impact on native plants; and (2) does postherbicide seeding with native grass species increase native plant abundance? In 2002, we experimentally examined the effects of five herbicides (dicamba + 2,4-D; metsulfuron-methyl; triclopyr; glyphosate; and picloram) at two rates of application (low and high), three application times (early summer, fall, and a combined early summer–fall treatment), and two postherbicide seed addition treatments (seeded or not seeded) on sulfur cinquefoil abundance, plant community composition, and species richness. Experimental plots were monitored through 2005. Picloram was the most effective herbicide at reducing sulfur cinquefoil density, the proportion of remaining adult plants, and seed production. The effects of picloram continued to be evident after 3 yr, with 80% reduction of sulfur cinquefoil in 2005. In addition, seeding of native grass seeds alone (no herbicide application) reduced the proportion of sulfur cinquefoil plants that were reproductively active. Despite reductions in sulfur cinquefoil abundance, all treatments remained dominated by exotic species because treated areas transitioned from exotic forb- to exotic grass-dominated communities. However, a one-time herbicide application controlled sulfur cinquefoil for at least 3 yr, and therefore might provide a foundation to begin ecological restoration. Herbicide applications alone likely are to be insufficient for long-term sulfur cinquefoil control without further modification of sites through native grass or forb seeding. Integrating herbicides with native plant seeding to promote the development of plant communities that are resistant to sulfur cinquefoil invasion is a promising management approach to ecological restoration.


Zootaxa ◽  
2011 ◽  
Vol 2796 (1) ◽  
pp. 67
Author(s):  
NICHOLAS A. MARTIN ◽  
ZHI-QIANG ZHANG

Nameriophyes sapidae Xue & Zhang (Acari: Eriophyidae) was found on transplanted nikau palms, Rhopalostylis sapida (H. Wendl. & Drude) in Auckland, New Zealand and described as a new species (Xue & Zhang 2008). Although R. sapida is a native plant species, it was not known if this mite species was indigenous or adventive because it was collected only from transplanted palms in unnatural gardens in Auckland. A survey was undertaken of R. sapida and the Kermadec Island palm, Rhopalostylis baueri (Hook. f.) Wendl. & Drude in the northern part of the North Island and Chatham Island.


2012 ◽  
Vol 18 (2) ◽  
pp. 77 ◽  
Author(s):  
Heather Parks ◽  
Kyle Clifton ◽  
Lauren Best ◽  
Bridget Johnson

PEST-PROOF (exclusion) fences are designed to prevent non-native, predatory and pest species from repopulating an area set aside to protect vulnerable native plant and animal species. Pest-proof fencing provides security from invasive species, but can isolate the native species enclosed within. On one hand, some rare native species exist on the mainland due to the pest-free status achieved through the use of exclusion fences. On the other hand, these reintroduced populations are now isolated a situation where they would not be found naturally (Jamieson et al. 2006). Exclusion fences must be constantly maintained or the sanctuary risks reinvasion. An important question for conservation biologists and managers to answer is therefore — when is exclusion fencing the best option for protecting native species from introduced pests? We have drawn our examples from New Zealand and Australia where progress has been made with regard to the design and utilization of exclusion fences.


2019 ◽  
Vol 9 (24) ◽  
pp. 13835-13849 ◽  
Author(s):  
Christine B. Rohal ◽  
Chad Cranney ◽  
Eric L. G. Hazelton ◽  
Karin M. Kettenring

2016 ◽  
Author(s):  
Stéphane Boyer ◽  
Young-Nam Kim ◽  
Mike H Bowie ◽  
Marie-Caroline Lefort ◽  
Nicholas M Dickinson

New Zealand has 23 exotic and more than 200 endemic earthworm species. Endemic earthworms disappeared quickly after vegetation clearance and land conversion to agriculture from the early C19th. Environmental changes associated with agronomic practices are believed to have been the main drivers for their disappearance. Exotic earthworms introduced from Europe have since largely replaced endemic earthworms into farming systems and have been intentionally propagated to increase production. Little is known about potential competition between endemic and exotic earthworms in New Zealand, and the capacity of exotic earthworms to extend their range into native habitats. Using two sites in the South Island of New Zealand, we investigated the impact of restoring native vegetation on earthworm communities. The study sites were Quail Island (Banks Peninsula), which has been undergoing native plant restoration for more than 30 years, and the Punakaiki Coastal Restoration Project (West Coast) where 130,000 native trees have been planted in retired pasture in the last seven years. At each site, soil samples (20 x 20 x 20 cm) were collected and hand sorted for earthworms. Sequential restoration plantings revealed that recolonisation by endemic earthworms increases with time after restoration at the two sample sites. With increasing age of the restoration, the biomass of endemic earthworm significantly increased, as did abundance at Punakaiki. However, exotic species did not disappear after restoration of native vegetation, even after 30 years in Quail Island. The persistence of exotic species leads to the cohabitation of the two communities and potential for interspecific competition.


1994 ◽  
Vol 59 (2) ◽  
pp. 121-131
Author(s):  
Ralph E.H. Sims ◽  
Simon B. Berry ◽  
Kerry Harrington

2021 ◽  
Author(s):  
◽  
Emma Anne Earl

<p>Mycobacterium tuberculosis, the causative agent of tuberculosis (TB) has infected approximately 1/3 of the world population, with 9.4 million new TB cases in 2008. In addition to increased cases of drug-resistant strains it is vital that novel antitubercular compounds are discovered in order to treat infections and reduce the time of current TB therapy courses. Natural resources such as plants are now being considered as the focus for discovering new compounds. Plants have long been investigated as a source of antibiotics for the treatment of human disease. New Zealand (NZ) contains a unique and diverse flora; however, to current knowledge no native plants have been examined for antimycobacterial activity. Using ethnobotany as a basis for selection, a total of 58 native plant samples were collected and tested for direct antimycobacterial activity. Samples were extracted with sterile distilled water (SDW), ethanol (EtOH) or methanol (MeOH) and screened for inhibition against the surrogate species, Mycobacterium smegmatis. Active plant samples were then validated for bacteriostatic activity towards M. bovis BCG and M. tuberculosis H37Ra as well as other clinically-important species. Nine extracts from the species Laurelia novae-zelandiae, Lophomyrtus bullata, Metrosideros excelsa, Myoporum laetum, Pittosporum tenuifolium, Pseudopanax crassifolius and Pseudowintera colorata were found to be active against M. smegmatis. Two active extracts were the bark and cambium extracts of Laurelia novae-zelandiae (Pukatea), which were reportedly used by indigenous Māori for the treatment of tubercular lesions. Upon further investigation these extracts also demonstrated bactericidal activity towards M. smegmatis as well as bacteriostatic activity towards the slow-growing species M. bovis BCG and M. tuberculosis. Purification techniques were then performed to improve the efficiency of activity and initial exploration of delivery systems was also examined. The bioactive extracts determined in this research offer a starting point for identifying their chemical basis of antimycobacterial activity with the objective of potentially discovering new anti-tubercular drugs.</p>


2015 ◽  
Vol 68 ◽  
pp. 1-6 ◽  
Author(s):  
T.K. James ◽  
C.A. Dowsett

Tradescantia fluminensis Plectranthus ciliatus Asparagus scandens Hedera helix Lamium galeobdolon and Selaginella kraussiana are all matforming invasive species that limit regeneration of native plants in forest remnants in New Zealand Experiments using potted specimens of these weeds showed that low rates (338675 g/ha) of the herbicide triclopyr gave >90 defoliation of T fluminensis A scandens and L galeobdolon but a higher rate of 1350 g/ha only gave 85 defoliation of H helix Diquat gave 85 defoliation of P ciliatus Aminopyralid was effective against S kraussiana but was very slow acting These experiments have identified herbicides and application rates for effective forest weed management to facilitate native plant regeneration in New Zealand temperate forests


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