F. Dane Panetta
National Administrative Department of Statistics
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Featured researches published by F. Dane Panetta.
Invasive Plant Science and Management | 2009
F. Dane Panetta
Abstract There has been recent interest in determining the upper limits to the feasibility of weed eradication. Although a number of disparate factors determine the success of an eradication program, ultimately eradication feasibility must be viewed in the context of the amount of investment that can be made. The latter should reflect the hazard posed by an invasion, with greater investment justified by greater threats. In simplest terms, the effort (and hence investment) to achieve weed eradication comprises the detection effort required to delimit an invasion plus the search and control effort required to prevent reproduction until extirpation occurs over the entire infested area. The difficulty of estimating the required investment at the commencement of a weed eradication program (as well as during periodic reviews) is a serious problem. Bioeconomics show promise in determining the optimal approach to managing weed invasions, notwithstanding ongoing difficulties in estimating the costs and benefits of eradication and alternative invasion management strategies. A flexible approach to the management of weed invasions is needed, allowing for the adoption of another strategy when it becomes clear that the probability of eradication is low, owing to resourcing or intractable technical issues. Whether the considerable progress that has been achieved towards eradication of the once massive witchweed invasion can be duplicated for other weeds of agricultural systems will depend to a large extent upon investment (>
Weed Science | 2007
F. Dane Panetta; Roger Lawes
250 million over 50 yr in this instance). Weeds of natural ecosystems seem destined to remain more difficult eradication targets for a variety of reasons, including higher impedance to eradication, more difficulty in valuing the benefits arising from eradication, and possibly less willingness to pay from society at large. Nomenclature: Witchweed, Striga asiatica (L.) Kuntze.
Invasive Plant Science and Management | 2009
Gabrielle Vivian-Smith; F. Dane Panetta
Abstract Because weed eradication programs commonly take 10 or more years to complete, there is a need to evaluate progress toward the eradication objective. We present a simple model, based on information that is readily obtainable, that assesses conformity to the delimitation and extirpation criteria for eradication. It is applied to the program currently targeting the annual parasitic weed, branched broomrape, in South Australia. The model consists of delimitation and extirpation (E) measures plotted against each other to form an ‘eradograph.’ Deviations from the ‘ideal’ eradograph plot can inform tactical responses, e.g., increases in survey and/or control effort. Infestations progress from the active phase to the monitoring phase when no plants have been detected for at least 12 mo. They revert to the active phase upon further detection of plants. We summarize this process for the invasion as a whole in a state-and-transition model. Using this model we demonstrate that the invasion is unlikely to be delimited unless the amount of newly detected infested area decreases, on average, by at least 50% per annum. As a result of control activities implemented, on average approximately 70% (range, 44 to 86%) of active infestations progressed to the monitoring phase in the year following their detection. Simulations suggest that increasing this rate of transition will not increase E to a significant extent. The rate of reversion of infestations from the monitoring phase to the active phase decreased logarithmically with time since last detection, but it is likely that lower rates of reversion would accelerate the trend toward extirpation. Program performance with respect to the delimitation criterion has been variable; performance with respect to the extirpation criterion would be improved considerably by the development and application of cost-effective methods for eliminating branched broomrape soil seed populations. Nomenclature: branched broomrape, Orobanche ramosa L. ORARA
Invasive Plant Science and Management | 2016
Doria R. Gordon; S. Luke Flory; Deah Lieurance; Philip E. Hulme; Chris Buddenhagen; Barney P. Caton; Paul D. Champion; Theresa M. Culley; Curt Daehler; Franz Essl; Jeffrey E. Hill; Reuben P. Keller; Lisa Kohl; Anthony L. Koop; Sabrina Kumschick; David M. Lodge; Richard N. Mack; Laura A. Meyerson; Godshen R. Pallipparambil; F. Dane Panetta; Read Porter; Petr Pyšek; Lauren D. Quinn; Daniel Simberloff; Montserrat Vilà
Abstract Seed persistence is poorly quantified for invasive plants of subtropical and tropical environments and Lantana camara, one of the worlds worst weeds, is no exception. We investigated germination, seedling emergence, and seed survival of two lantana biotypes (Pink and pink-edged red [PER]) in southeastern Queensland, Australia. Controlled experiments were undertaken in 2002 and repeated in 2004, with treatments comprising two differing environmental regimes (irrigated and natural rainfall) and sowing depths (0 and 2 cm). Seed survival and seedling emergence were significantly affected by all factors (time, biotype, environment, sowing depth, and cohort) (P < 0.001). Seed dormancy varied with treatment (environment, sowing depth, biotype, and cohort) (P < 0.001), but declined rapidly after 6 mo. Significant differential responses by the two biotypes to sowing depth and environment were detected for both seed survival and seedling emergence (P < 0.001). Seed mass was consistently lower in the PER biotype at the population level (P < 0.001), but this variation did not adequately explain the differential responses. Moreover, under natural rainfall the magnitude of the biotype effect was unlikely to result in ecologically significant differences. Seed survival after 36 mo under natural rainfall ranged from 6.8 to 21.3%. Best fit regression analysis of the decline in seed survival over time yielded a five-parameter exponential decay model with a lower asymptote approaching −0.38 (% seed survival = [( 55 − (−0.38)) · e (k · t)] + −0.38; R2 = 88.5%; 9 df). Environmental conditions and burial affected the slope parameter or k value significantly (P < 0.01). Seed survival projections from the model were greatest for buried seeds under natural rainfall (11 yr) and least under irrigation (3 yr). Experimental data and model projections suggest that lantana has a persistent seed bank and this should be considered in management programs, particularly those aimed at eradication. Nomenclature: Lantana, Lantana camara L.
Diversity and Distributions | 2000
Petr Pyšek; Marcel Rejmánek; Michael G. Barbour; F. Dane Panetta; Carol J. West
Doria R. Gordon, S. Luke Flory, Deah Lieurance, Philip E. Hulme, Chris Buddenhagen, Barney Caton, Paul D. Champion, Theresa M. Culley, Curt Daehler, Franz Essl, Jeffrey E. Hill, Reuben P. Keller, Lisa Kohl, Anthony L. Koop, Sabrina Kumschick, David M. Lodge, Richard N. Mack, Laura A. Meyerson, Godshen R. Pallipparambil, F. Dane Panetta, Read Porter, Petr Pysek, Lauren D. Quinn, David M. Richardson, Daniel Simberloff, and Montserrat Vila*
Ecology Letters | 2006
Tracey J. Regan; Michael A. McCarthy; P. W. J. Baxter; F. Dane Panetta; Hugh P. Possingham
Diversity and Distributions | 2005
F. Dane Panetta; Roger Lawes
Diversity and Distributions | 2006
F. Dane Panetta
Journal of Applied Ecology | 2011
F. Dane Panetta; Oscar J. Cacho; Susie Hester; Nikki Sims-Chilton; Simon Brooks
Diversity and Distributions | 2013
Susan M. Hester; Oscar J. Cacho; F. Dane Panetta; Cindy E. Hauser
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Commonwealth Scientific and Industrial Research Organisation
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