Laura Warman
University of New South Wales
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Featured researches published by Laura Warman.
Nature | 2014
Amy E. Zanne; David C. Tank; William K. Cornwell; Jonathan M. Eastman; Stephen A. Smith; Richard G. FitzJohn; Daniel J. McGlinn; Brian C. O'Meara; Angela T. Moles; Peter B. Reich; Dana L. Royer; Douglas E. Soltis; Peter F. Stevens; Mark Westoby; Ian J. Wright; Lonnie W. Aarssen; Robert I. Bertin; Andre Calaminus; Rafaël Govaerts; Frank Hemmings; Michelle R. Leishman; Jacek Oleksyn; Pamela S. Soltis; Nathan G. Swenson; Laura Warman; Jeremy M. Beaulieu
Early flowering plants are thought to have been woody species restricted to warm habitats. This lineage has since radiated into almost every climate, with manifold growth forms. As angiosperms spread and climate changed, they evolved mechanisms to cope with episodic freezing. To explore the evolution of traits underpinning the ability to persist in freezing conditions, we assembled a large species-level database of growth habit (woody or herbaceous; 49,064 species), as well as leaf phenology (evergreen or deciduous), diameter of hydraulic conduits (that is, xylem vessels and tracheids) and climate occupancies (exposure to freezing). To model the evolution of species’ traits and climate occupancies, we combined these data with an unparalleled dated molecular phylogeny (32,223 species) for land plants. Here we show that woody clades successfully moved into freezing-prone environments by either possessing transport networks of small safe conduits and/or shutting down hydraulic function by dropping leaves during freezing. Herbaceous species largely avoided freezing periods by senescing cheaply constructed aboveground tissue. Growth habit has long been considered labile, but we find that growth habit was less labile than climate occupancy. Additionally, freezing environments were largely filled by lineages that had already become herbs or, when remaining woody, already had small conduits (that is, the trait evolved before the climate occupancy). By contrast, most deciduous woody lineages had an evolutionary shift to seasonally shedding their leaves only after exposure to freezing (that is, the climate occupancy evolved before the trait). For angiosperms to inhabit novel cold environments they had to gain new structural and functional trait solutions; our results suggest that many of these solutions were probably acquired before their foray into the cold.
Landscape Ecology | 2009
Laura Warman; Angela T. Moles
The vegetation of the Wet Tropics bioregion of Far North Queensland is a complex system whose components (mainly tropical rainforests and fire-prone forests and woodlands) have mostly been studied independently from each other. We suggest that many characteristics of the vegetation are consistent with those of a complex, dynamic, spatially heterogeneous system which exhibits alternative stable states. We propose these states are driven and maintained by the interaction of vegetation-specific positive feedback loops with the regions’ environmental parameters (such as topography, steep humidity gradients and seasonality) and result in the rainforest/fire-prone vegetation mosaic that characterises the area. Given the regions’ magnitude, biodiversity and complexity, we propose the Wet Tropics as an important new example and a good testing ground for alternative stable state and resilience theories in large heterogeneous natural systems. At the same time, thinking in terms of alternative stable states and resilience creates a new context for understanding the regions’ biological dynamics.
Journal of Ecology | 2014
William K. Cornwell; Mark Westoby; Daniel S. Falster; Richard G. FitzJohn; Brian C. O'Meara; Matthew W. Pennell; Daniel J. McGlinn; Jonathan M. Eastman; Angela T. Moles; Peter B. Reich; David C. Tank; Ian J. Wright; Lonnie W. Aarssen; Jeremy M. Beaulieu; Robert M. Kooyman; Michelle R. Leishman; Eliot T. Miller; Ülo Niinemets; Jacek Oleksyn; Alejandro Ordonez; Dana L. Royer; Stephen A. Smith; Peter F. Stevens; Laura Warman; Peter Wilf; Amy E. Zanne
Summary Plant traits vary widely across species and underpin differences in ecological strategy. Despite centuries of interest, the contributions of different evolutionary lineages to modern-day functional diversity remain poorly quantified. Expanding data bases of plant traits plus rapidly improving phylogenies enable for the first time a data-driven global picture of plant functional diversity across the major clades of higher plants. We mapped five key traits relevant to metabolism, resource competition and reproductive strategy onto a phylogeny across 48324 vascular plant species world-wide, along with climate and biogeographic data. Using a novel metric, we test whether major plant lineages are functionally distinctive. We then highlight the trait–lineage combinations that are most functionally distinctive within the present-day spread of ecological strategies. For some trait–clade combinations, knowing the clade of a species conveys little information to neo- and palaeo-ecologists. In other trait–clade combinations, the clade identity can be highly revealing, especially informative clade–trait combinations include Proteaceae, which is highly distinctive, representing the global slow extreme of the leaf economic spectrum. Magnoliidae and Rosidae contribute large leaf sizes and seed masses and have distinctively warm, wet climatic distributions. Synthesis. This analysis provides a shortlist of the most distinctive trait–lineage combinations along with their geographic and climatic context: a global view of extant functional diversity across the tips of the vascular plant phylogeny.
PLOS ONE | 2013
Laura Warman; M. Bradford; Angela T. Moles
Most research on boundaries between vegetation types emphasizes the contrasts and similarities between conditions on either side of a boundary, but does not compare boundary to non-boundary vegetation. That is, most previous studies lack suitable controls, and may therefore overlook underlying aspects of landscape variability at a regional scale and underestimate the effects that the vegetation itself has on the soil. We compared 25 soil chemistry variables in rainforest, sclerophyll vegetation and across rainforest-sclerophyll boundaries in north-eastern Queensland, Australia. Like previous studies, we did find some contrasts in soil chemistry across vegetation boundaries. However we did not find greater variation in chemical parameters across boundary transects than in transects set in either rainforest or woodland. We also found that soil on both sides of the boundary is more similar to “rainforest soil” than to “woodland soil”. Transects in wet sclerophyll forests with increasing degrees of rainforest invasion showed that as rainforest invades wet sclerophyll forest, the soil beneath wet sclerophyll forest becomes increasingly similar to rainforest soil. Our results have implications for understanding regional vegetation dynamics. Considering soil-vegetation feedbacks and the differences between soil at boundaries and in non-boundary sites may hold clues to some of the processes that occur across and between vegetation types in a wide range of ecosystems. Finally, we suggest that including appropriate controls should become standard practice for studies of vegetation boundaries and edge effects worldwide.
Nature | 2014
Amy E. Zanne; David C. Tank; William K. Cornwell; Jonathan M. Eastman; Stephen A. Smith; Richard G. FitzJohn; Daniel J. McGlinn; Brian C. O'Meara; Angela T. Moles; Peter B. Reich; Dana L. Royer; Douglas E. Soltis; Peter F. Stevens; Mark Westoby; Ian J. Wright; Lonnie W. Aarssen; Robert I. Bertin; Andre Calaminus; Rafaël Govaerts; Frank Hemmings; Michelle R. Leishman; Jacek Oleksyn; Pamela S. Soltis; Nathan G. Swenson; Laura Warman; Jeremy M. Beaulieu
This corrects the article DOI: 10.1038/nature12872
Nature | 2014
Amy E. Zanne; David C. Tank; William K. Cornwell; Jonathan M. Eastman; Stephen A. Smith; Richard G. FitzJohn; Daniel J. McGlinn; Brian C. O'Meara; Angela T. Moles; Peter B. Reich; Dana L. Royer; Douglas E. Soltis; Peter F. Stevens; Mark Westoby; Ian J. Wright; Lonnie W. Aarssen; Robert I. Bertin; Andre Calaminus; Rafaël Govaerts; Frank Hemmings; Michelle R. Leishman; Jacek Oleksyn; Pamela S. Soltis; Nathan G. Swenson; Laura Warman; Jeremy M. Beaulieu
This corrects the article DOI: 10.1038/nature12872
Journal of Ecology | 2009
Angela T. Moles; David I. Warton; Laura Warman; Nathan G. Swenson; Shawn W. Laffan; Amy E. Zanne; A. J. Pitman; Frank Hemmings; Michelle R. Leishman
Journal of Ecology | 2012
Angela T. Moles; Habacuc Flores-Moreno; Stephen P. Bonser; David I. Warton; Aveliina Helm; Laura Warman; David J. Eldridge; Enrique Jurado; Frank Hemmings; Peter B. Reich; Jeannine Cavender-Bares; Eric W. Seabloom; Margaret M. Mayfield; Douglas Sheil; Jonathan C Djietror; Pablo Luis Peri; Lucas Enrico; Marcelo Cabido; Samantha A. Setterfield; Caroline E. R. Lehmann; Fiona J. Thomson
Journal of Vegetation Science | 2014
Angela T. Moles; S. E. Perkins; Shawn W. Laffan; Habacuc Flores-Moreno; Monica Awasthy; Marianne L. Tindall; Lawren Sack; A. J. Pitman; Jens Kattge; Lonnie W. Aarssen; Madhur Anand; Michael Bahn; Benjamin Blonder; Jeannine Cavender-Bares; J. Hans C. Cornelissen; William K. Cornwell; Sandra Díaz; John B. Dickie; Grégoire T. Freschet; Joshua G. Griffiths; Alvaro G. Gutiérrez; Frank Hemmings; Thomas Hickler; Timothy D. Hitchcock; Matthew Keighery; Michael Kleyer; Hiroko Kurokawa; Michelle R. Leishman; Kenwin Liu; Ülo Niinemets
Nature Communications | 2013
Robert Lanfear; Simon Y. W. Ho; T. Jonathan Davies; Angela T. Moles; Lonnie W. Aarssen; Nathan G. Swenson; Laura Warman; Amy E. Zanne; Andrew P. Allen