School of Agriculture, Food and Ecosystem Sciences - Research Publications

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    AusTraits, a curated plant trait database for the Australian flora
    Falster, D ; Gallagher, R ; Wenk, EH ; Wright, IJ ; Indiarto, D ; Andrew, SC ; Baxter, C ; Lawson, J ; Allen, S ; Fuchs, A ; Monro, A ; Kar, F ; Adams, MA ; Ahrens, CW ; Alfonzetti, M ; Angevin, T ; Apgaua, DMG ; Arndt, S ; Atkin, OK ; Atkinson, J ; Auld, T ; Baker, A ; von Balthazar, M ; Bean, A ; Blackman, CJ ; Bloomfeld, K ; Bowman, DMJS ; Bragg, J ; Brodribb, TJ ; Buckton, G ; Burrows, G ; Caldwell, E ; Camac, J ; Carpenter, R ; Catford, J ; Cawthray, GR ; Cernusak, LA ; Chandler, G ; Chapman, AR ; Cheal, D ; Cheesman, AW ; Chen, S-C ; Choat, B ; Clinton, B ; Clode, PL ; Coleman, H ; Cornwell, WK ; Cosgrove, M ; Crisp, M ; Cross, E ; Crous, KY ; Cunningham, S ; Curran, T ; Curtis, E ; Daws, M ; DeGabriel, JL ; Denton, MD ; Dong, N ; Du, P ; Duan, H ; Duncan, DH ; Duncan, RP ; Duretto, M ; Dwyer, JM ; Edwards, C ; Esperon-Rodriguez, M ; Evans, JR ; Everingham, SE ; Farrell, C ; Firn, J ; Fonseca, CR ; French, BJ ; Frood, D ; Funk, JL ; Geange, SR ; Ghannoum, O ; Gleason, SM ; Gosper, CR ; Gray, E ; Groom, PK ; Grootemaat, S ; Gross, C ; Guerin, G ; Guja, L ; Hahs, AK ; Harrison, MT ; Hayes, PE ; Henery, M ; Hochuli, D ; Howell, J ; Huang, G ; Hughes, L ; Huisman, J ; Ilic, J ; Jagdish, A ; Jin, D ; Jordan, G ; Jurado, E ; Kanowski, J ; Kasel, S ; Kellermann, J ; Kenny, B ; Kohout, M ; Kooyman, RM ; Kotowska, MM ; Lai, HR ; Laliberte, E ; Lambers, H ; Lamont, BB ; Lanfear, R ; van Langevelde, F ; Laughlin, DC ; Laugier-kitchener, B-A ; Laurance, S ; Lehmann, CER ; Leigh, A ; Leishman, MR ; Lenz, T ; Lepschi, B ; Lewis, JD ; Lim, F ; Liu, U ; Lord, J ; Lusk, CH ; Macinnis-Ng, C ; McPherson, H ; Magallon, S ; Manea, A ; Lopez-Martinez, A ; Mayfeld, M ; McCarthy, JK ; Meers, T ; van der Merwe, M ; Metcalfe, DJ ; Milberg, P ; Mokany, K ; Moles, AT ; Moore, BD ; Moore, N ; Morgan, JW ; Morris, W ; Muir, A ; Munroe, S ; Nicholson, A ; Nicolle, D ; Nicotra, AB ; Niinemets, U ; North, T ; O'Reilly-Nugent, A ; O'Sullivan, OS ; Oberle, B ; Onoda, Y ; Ooi, MKJ ; Osborne, CP ; Paczkowska, G ; Pekin, B ; Pereira, CG ; Pickering, C ; Pickup, M ; Pollock, LJ ; Poot, P ; Powell, JR ; Power, S ; Prentice, IC ; Prior, L ; Prober, SM ; Read, J ; Reynolds, V ; Richards, AE ; Richardson, B ; Roderick, ML ; Rosell, JA ; Rossetto, M ; Rye, B ; Rymer, PD ; Sams, M ; Sanson, G ; Sauquet, H ; Schmidt, S ; Schoenenberger, J ; Schulze, E-D ; Sendall, K ; Sinclair, S ; Smith, B ; Smith, R ; Soper, F ; Sparrow, B ; Standish, RJ ; Staples, TL ; Stephens, R ; Szota, C ; Taseski, G ; Tasker, E ; Thomas, F ; Tissue, DT ; Tjoelker, MG ; Tng, DYP ; de Tombeur, F ; Tomlinson, K ; Turner, NC ; Veneklaas, EJ ; Venn, S ; Vesk, P ; Vlasveld, C ; Vorontsova, MS ; Warren, CA ; Warwick, N ; Weerasinghe, LK ; Wells, J ; Westoby, M ; White, M ; Williams, NSG ; Wills, J ; Wilson, PG ; Yates, C ; Zanne, AE ; Zemunik, G ; Zieminska, K (NATURE PORTFOLIO, 2021-09-30)
    We introduce the AusTraits database - a compilation of values of plant traits for taxa in the Australian flora (hereafter AusTraits). AusTraits synthesises data on 448 traits across 28,640 taxa from field campaigns, published literature, taxonomic monographs, and individual taxon descriptions. Traits vary in scope from physiological measures of performance (e.g. photosynthetic gas exchange, water-use efficiency) to morphological attributes (e.g. leaf area, seed mass, plant height) which link to aspects of ecological variation. AusTraits contains curated and harmonised individual- and species-level measurements coupled to, where available, contextual information on site properties and experimental conditions. This article provides information on version 3.0.2 of AusTraits which contains data for 997,808 trait-by-taxon combinations. We envision AusTraits as an ongoing collaborative initiative for easily archiving and sharing trait data, which also provides a template for other national or regional initiatives globally to fill persistent gaps in trait knowledge.
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    Vulnerability of Human Populations to Contamination from Petroleum Exploitation in the Napo River Basin: An Approach for Spatially Explicit Risk Assessment
    Espinosa, CI ; Reyes-Bueno, F ; Ramirez, MI ; Arevalo, AP ; Bailon-Moscoso, N ; Duncan, DH (MDPI, 2021-08)
    Background: contamination of aquatic ecosystems by oil spills associated with petroleum exploitation represents a serious problem of environmental contamination that can affect human health. We developed a spatial model of contamination risk in the Ecuadorian Amazon, and evaluated the model using independent datasets on environmental contamination and clinical indicators of human health risk factors. Methods: the spatial risk of contamination for the Napo River basin was based on the calculation of a friction surface and the accessibility of possible oil contamination. Human health was evaluated using peripheral blood samples from 256 individuals. We used monitoring data on contamination to validate the spatial model of contamination risk and analyzed whether the estimated risk explained the incidence of human health risk factors. Results: our risk model showed a significant association with actual contamination detected in the study area. According to our risk model, around 30% of the territory has some level of contamination. Risk of contamination was associated with an increasing mean incidence in risk factors for human health in resident populations, but elevated contamination risk was not a significant predictor of the incidence of selected health indicators; only the incidence of inflammation was significantly increased. Conclusions: a large proportion of the populations in the Napo River basin has high vulnerability to contamination from petroleum exploitation, and this contamination risk may be traced in some indicators of health risk. Closer examination of health risk factors is warranted, and our spatial model of contamination risk can inform the design and analysis of such studies, as well as risk mitigation and management. Our approach to building the model of contamination risk could be applied in other catchments where petroleum exploitation is contemplated.
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    Intraspecific interactions affect the spatial pattern of a dominant shrub in a semiarid shrubland: A prospective approach
    Espinosa, CI ; Velez-Mora, DP ; Ramon, P ; Gusman-Montalvan, E ; Duncan, DH ; Quintana-Ascencio, PF (WILEY, 2019-04)
    Dispersal, physical conditions and biotic interactions contribute to determine the spatial distribution of individuals in plant populations. Much of what we know has been learned from studies that retrospectively posit mechanisms presumed to have generated the observed spatial patterns. Here we present a prospective approach. We start by measuring spatial demographic effects and evaluate if they can generate observed spatial patterns. We evaluated the influence of interactions among conspecifics on vital rates, demography and spatial distribution of Croton aff. wagneri, a dominant shrub in dry Andean ecosystems. Recruitment, survival and growth varied in relation with distance to conspecifics neighbours and with their summed cover. We built a spatial individual‐based model and simulated its population dynamics in 30 × 30 m plots for a 30‐year period. We compared the predicted spatial pattern from these demographic models with that observed among plants in 16 independent plots with the same area. Simulated populations mimicked observed spatial patterns, although in plots at high elevations the simulated populations did not reproduce the observed inhibition at small scales. Observed and simulated patterns indicated differences between elevations in maximum aggregation and location of the distances with higher aggregation. We discuss how consideration of critical seed and juvenile stages and interspecific interactions could further improve our understanding of spatial pattern and recommend that these factors be considered in future models.
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    Misinformation, internet honey trading and beekeepers drive a plant invasion
    Lenda, M ; Skorka, P ; Kuszewska, K ; Moron, D ; Belcik, M ; Baczek Kwinta, R ; Janowiak, F ; Duncan, DH ; Vesk, PA ; Possingham, HP ; Knops, JMH ; Thrall, P (WILEY, 2020-11-17)
    Biological invasions are a major human induced global change that is threatening global biodiver-sity by homogenizing the world’s fauna and flora. Species spread because humans have movedspecies across geographical boundaries and have changed ecological factors that structure ecosys-tems, such as nitrogen deposition, disturbance, etc. Many biological invasions are caused acciden-tally, as a byproduct of human travel and commerce driven product shipping. However, humansalso have spread many species intentionally because of perceived benefits. Of interest is the role ofthe recent exponential growth in information exchange via internet social media in driving biologi-cal invasions. To date, this has not been examined. Here, we show that for one such invasive spe-cies, goldenrod, social networks spread misleading and incomplete information that is enhancingthe spread of goldenrod invasions into new environments. We show that the notion of goldenrodhoney as a “superfood” with unsupported healing properties is driving a demand that leads bee-keepers to produce goldenrod honey. Social networks provide a forum for such informationexchange and this is leading to further spread of goldenrod in many countries where goldenrod isnot native, such as Poland. However, this informal social information exchange ignores laws thatfocus on preventing the further spread of invasive species and the strong negative effects thatgoldenrod has on native ecosystems, including floral resources that negatively impact honeybeeperformance. Thus, scientifically unsupported information on “superfoods” such as goldenrodhoney that is disseminated through social internet networks has real world consequences such asincreased goldenrod invasions into novel geographical regions which decreases native biodiversity.
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    Environmental drivers of femaleness of an inter-Andean monoecious shrub
    Velez-Mora, D ; Ramon, P ; Vallejo, C ; Romero, A ; Duncan, D ; Quintana-Ascencio, PF (WILEY, 2021-01-01)
    Hetero‐and conspecific interactions, nutrient availability, climate, habitat heterogeneity, and disturbances can generate variation and spatial patterns of femaleness in plants. We assessed whether year, site, plant size, plant density, and canopy area of conspecific neighbors influenced the expression and spatial aggregation of femaleness in Croton aff. wagneri, a monoecious shrub from dry shrublands of the inter‐Andean valleys in Ecuador. We georeferenced in two sites (1,700 and 1,400 m.a.s.l) in five 10 × 10 m plots, within each site, the position of each Croton reproductive plant during first part of flowering season in two years, and measured their height, length, and width. The femaleness index of each plant was determined by the number of female and male buds and flowers. Plant density was determined for each plot, along with the number of neighbors and the summed canopy area of conspecific neighbors (at 1.0, 2.0, and 2.5 m radius, and the five closest plants) from each focal plant. Croton´s femaleness at the lower elevation site was greater than at the higher elevation site and increased with plant size and with canopy of the closest five neighbors. Soil at the lower elevation site had higher temperatures and lower water content. Aggregate patterns of femaleness were found in more plots at the lower elevation site. Our results indicate that location, plant size, and canopies of conspecific neighbors of Croton can affect femaleness and its aggregation and support the hypothesis that femaleness can be influenced by facilitative interactions.
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    Beyond the blame game: a restoration pathway reconciles ecologists' and local leaders' divergent models of seasonally dry tropical forest degradation
    Jara-Guerrero, AK ; Maldonado-Riofrio, D ; Espinosa, CI ; Duncan, DH (The Resilience Alliance, 2019-12-01)
    An understanding of ecosystem dynamics under different scenarios of degradation is required to reverse ecological degradation and identify restoration priorities. Such knowledge can be the result of scientific investigation, but important insight can also reside in observant local land managers. In seasonally dry tropical forests in southern Ecuador, recent decades have seen important advances in the knowledge of the biodiversity values of these forests, but the available data have not yet been integrated and translated into tools that support managers in deciding restoration measures. One powerful framework to organize and communicate information about ecosystem degradation and recovery dynamics is the state-transition model. We generated such a model by combining ecologist and local knowledge obtained through an adaptation of the Stanford/SRI expert elicitation protocol. Through this information, we identified five forest states with specific attributes of vegetation, human pressures, and restoration needs. Ecologists and locals agreed on the restoration actions but partially disagreed on the causes of degradation. Whereas ecologists considered that grazing management, often introduced with or after logging, was the catalyst for a transition to degraded states, locals attributed those transitions to the effects of logging alone. Importantly, however, both ecologists and locals considered that exclusion of livestock grazing was a necessary action to promote ecological recovery. A forward-looking strategy focusing on objectives for ecosystem recovery and ecosystem management for biodiversity and human well-being might be more successful than strategies that emphasize or seek to attribute responsibility for degradation.
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    Towards open, reliable, and transparent ecology and evolutionary biology
    O'Dea, RE ; Parker, TH ; Chee, YE ; Culina, A ; Drobniak, SM ; Duncan, DH ; Fidler, F ; Gould, E ; Ihle, M ; Kelly, CD ; Lagisz, M ; Roche, DG ; Sanchez-Tojar, A ; Wilkinson, DP ; Wintle, BC ; Nakagawa, S (BMC, 2021-04-09)
    Unreliable research programmes waste funds, time, and even the lives of the organisms we seek to help and understand. Reducing this waste and increasing the value of scientific evidence require changing the actions of both individual researchers and the institutions they depend on for employment and promotion. While ecologists and evolutionary biologists have somewhat improved research transparency over the past decade (e.g. more data sharing), major obstacles remain. In this commentary, we lift our gaze to the horizon to imagine how researchers and institutions can clear the path towards more credible and effective research programmes.
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    Indigenous plants promote insect biodiversity in urban greenspaces
    Mata, L ; Andersen, AN ; Moran-Ordonez, A ; Hahs, AK ; Backstrom, A ; Ives, CD ; Bickel, D ; Duncan, D ; Palma, E ; Thomas, F ; Cranney, K ; Walker, K ; Shears, I ; Semeraro, L ; Malipatil, M ; Moir, ML ; Plein, M ; Porch, N ; Vesk, PA ; Smith, TR ; Lynch, Y (WILEY, 2021-06)
    The contribution of urban greenspaces to support biodiversity and provide benefits for people is increasingly recognized. However, ongoing management practices favor vegetation oversimplification, often limiting greenspaces to lawns and tree canopy rather than multi-layered vegetation that includes under- and midstorey, and the use of nonnative species. These practices hinder the potential of greenspaces to sustain indigenous biodiversity, particularly for taxa like insects that rely on plants for food and habitat. Yet, little is known about which plant species may maximize positive outcomes for taxonomically and functionally diverse insect communities in greenspaces. Additionally, while cities are expected to experience high rates of introductions, quantitative assessments of the relative occupancy of indigenous vs. introduced insect species in greenspace are rare, hindering understanding of how management may promote indigenous biodiversity while limiting the establishment of introduced insects. Using a hierarchically replicated study design across 15 public parks, we recorded occurrence data from 552 insect species on 133 plant species, differing in planting design element (lawn, midstorey, and tree canopy), midstorey growth form (forbs, lilioids, graminoids, and shrubs) and origin (nonnative, native, and indigenous), to assess (1) the relative contributions of indigenous and introduced insect species and (2) which plant species sustained the highest number of indigenous insects. We found that the insect community was overwhelmingly composed of indigenous rather than introduced species. Our findings further highlight the core role of multi-layered vegetation in sustaining high insect biodiversity in urban areas, with indigenous midstorey and canopy representing key elements to maintain rich and functionally diverse indigenous insect communities. Intriguingly, graminoids supported the highest indigenous insect richness across all studied growth forms by plant origin groups. Our work highlights the opportunity presented by indigenous understory and midstorey plants, particularly indigenous graminoids, in our study area to promote indigenous insect biodiversity in urban greenspaces. Our study provides a blueprint and stimulus for architects, engineers, developers, designers, and planners to incorporate into their practice plant species palettes that foster a larger presence of indigenous over regionally native or nonnative plant species, while incorporating a broader mixture of midstorey growth forms.
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    The vegetation structure and condition of contracting lowland habitat for Leadbeater's possum (Gymnobelideus leadbeateri)
    Greet, J ; Harley, D ; Ashman, K ; Watchorn, D ; Duncan, D (CSIRO PUBLISHING, 2021)
    Lowland Leadbeater’s possums are on a trajectory to extinction, with fewer than 40 individuals surviving in the wild. Quantification of the vegetation characteristics of their occupied habitat is urgently needed to inform strategies to conserve this genetically distinct population. We surveyed the canopy and midstorey vegetation at all remaining (nine) occupied territories and eleven abandoned territories in lowland swamp forest at the Yellingbo Nature Conservation Reserve. For each territory we quantified canopy and midstorey stem density, basal area (total and live) and vegetation condition (percentage live basal area, tree crown vigour and plant area index) within a 50-m radius of known den locations. The canopy at all locations was dominated by mountain swamp gum (Eucalyptus camphora), with most occupied sites supporting dense midstorey dominated by paperbarks, either Melaleuca squarrosa or Melaleuca ericifolia. Occupied territories had higher stem densities and better vegetation condition than abandoned territories. Stem density alone was able to predict occupancy vis-à-vis abandoned sites with a high (80%) degree of accuracy. Lowland Leadbeater’s possums occupy swamp forests characterised by high stem density, particularly in the midstorey, structural complexity and healthy vegetation. These findings can help guide habitat restoration and translocation projects currently underway to expand the area of lowland habitat for this critically endangered species.