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Australian Journal of Botany Australian Journal of Botany Society
Southern hemisphere botanical ecosystems
INTRODUCTION

Global research on ultramafic (serpentine) ecosystems (8th International Conference on Serpentine Ecology in Sabah, Malaysia)

Antony van der Ent A H , Nishanta Rajakaruna B C , Robert Boyd D , Guillaume Echevarria E , Rimi Repin F and Dick Williams G
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- Author Affiliations

A Centre for Mined Land Rehabilitation, Sustainable Minerals Institute, The University of Queensland, QLD, Australia.

B College of the Atlantic, 105 Eden Street, Bar Harbor, ME 04609, USA.

C Environmental Sciences and Management, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.

D Department of Biological Sciences 101 Rouse Life Sciences Bldg. Auburn University, Alabama 36849, USA.

E Laboratoire Sols et Environnement, UMR 1120, Université de Lorraine – INRA, France.

F Sabah Parks KK Times Square, Coastal Highway, 88100 Kota Kinabalu, Malaysia.

G Australian Journal of Botany, CSIRO Tropical Ecosystems Research Centre, Australia.

H Corresponding author. Email: a.vanderent@uq.edu.au

Australian Journal of Botany 63(4) iii-iv https://doi.org/10.1071/BTv63n4_IN
Published: 25 June 2015

Abstract

Since 1991, researchers from approximately 45 nations have participated in eight International Conferences on Serpentine Ecology (ICSE). The ICSE conferences are coordinated by the International Serpentine Ecology Society (ISES), a formal research society whose members study geological, pedological, biological and applied aspects of ultramafic ecosystems worldwide. These conferences have provided an international forum to discuss and synthesise multidisciplinary research, and have provided opportunities for scientists in distinct fields and from different regions of the world to conduct collaborative and interdisciplinary research. The 8th ICSE was hosted by Sabah Parks in Malaysia, on the island of Borneo, and attracted the largest delegation to date, 174 participants from 31 countries. This was the first time an ICSE was held in Asia, the region that hosts some of the world’s most biodiverse ultramafic ecosystems. The presentations provided a cross-section of the current status of research in all aspects of serpentine-biota relations. In this Special Issue of Australian Journal of Botany, which encompasses two double issues (1–2 and 3–4), we have compiled a selection of papers from among the oral and poster presentations to provide insights into recent advances in geoecological and applied studies of serpentine habitats worldwide.

Introduction

Ultramafic outcrops (also called ‘serpentine’) are widespread but sparse, covering roughly 3% of the Earth’s surface (Guillot and Hattori 2013). The largest outcrops occur in Cuba, New Caledonia, Indonesia, the Philippines and Malaysia, whereas smaller outcrops are found worldwide, mostly along continental margins and orogenic belts (Brooks 1987; Alexander et al. 2007). Soils derived from ultramafic bedrock pose several edaphic challenges for plant growth, including metal toxicity, nutrient imbalances and deficiencies and, in some cases, water stress, with this last feature resulting from the often shallow, rocky, and exposed nature of the outcrops (Proctor 2003; O’Dell and Rajakaruna 2011). Ultramafic ecosystems are renowned for their high levels of plant diversity and endemism, as well as their unique plant–habitat relations (Brooks 1987; Boyd et al. 2004, 2009; Harrison and Rajakaruna 2011). The edaphic challenges associated with these island-like habitats have led to the evolution of unique ecosystems, providing model settings for exploration of biological questions at cellular and organismal levels and for the study of ecosystem-level processes (Harrison and Rajakaruna 2011).



References

Alexander EB, Coleman RB, Keeler-Wolf T, Harrison SP (2007) ‘Serpentine geoecology of western North America.’ (Oxford University Press: New York)

Boyd RS, Baker AJM, Proctor J (Eds) (2004) ‘Ultramafic rocks: their soils, vegetation, and fauna.’ (Science Reviews 2000: St Albans, UK)

Boyd RS, Kruckeberg AR, Rajakaruna N (2009) Biology of ultramafic rocks and soils: research goals for the future. Northeastern Naturalist 16, 422–440.
Biology of ultramafic rocks and soils: research goals for the future.Crossref | GoogleScholarGoogle Scholar |

Brooks RR (1987) ‘Serpentine and its vegetation: a multidisciplinary approach.’ (Dioscorides Press: Portland, OR)

Guillot S, Hattori K (2013) Serpentinites: essential roles in geodynamics, arc volcanism, sustainable development, and the origin of life. Elements 9, 95–98.
Serpentinites: essential roles in geodynamics, arc volcanism, sustainable development, and the origin of life.Crossref | GoogleScholarGoogle Scholar |

Harrison SP, Rajakaruna N (Eds) (2011) ‘Serpentine: evolution and ecology of a model system.’ (University of California Press: Berkeley, CA)

O’Dell RE, Rajakaruna N (2011) Intraspecific variation, adaptation, and evolution. In ‘Serpentine: evolution and ecology of a model system’. (Eds SP Harrison, N Rajakaruna) pp. 97–137. (University of California Press: Berkeley, CA)

Proctor J (2003) Vegetation and soil and plant chemistry on ultramafic rocks in the tropical Far East. Perspectives in Plant Ecology, Evolution and Systematics 6, 105–124.
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