Principle Investigator
- Associate Professor Jon Waters, Department of Zoology, University of Otago, New Zealand
Associate Investigators
- Professor Hamish Spencer, Department of Zoology, University of Otago, New Zealand
- Dr Kirsten Donald, Department of Zoology, University of Otago, New Zealand
Postdoctoral Associate
Postgraduate Students
Our recent publications on oceanic rafting
Fraser CI, Nikula R & Waters JM [in press] Oceanic rafting of a coastal community. Proceedings of the Royal Society of London, B. [doi: 10.1098/rspb.2010.1117]
Collins CJ, Fraser CI, Ashcroft A & Waters JM (2010) Asymmetric dispersal of southern bull-kelp (Durvillaea antarctica) adults in coastal New Zealand: testing an oceanographic hypothesis. Molecular Ecology, 19:4572–4580. [doi: 10.1111/j.1365-294X.2010.04842.x]
Nikula R, Fraser CI, Spencer HG, Waters JM (2010) Circumpolar dispersal by rafting in two subantarctic kelp-dwelling crustaceans. Marine Ecology-Progress Series, 405:221-230 [doi: 10.3354/meps08523]
Fraser CI, Nikula R, Spencer HG & Waters JM (2009) Kelp genes reveal effects of subantarctic sea ice during the Last Glacial Maximum. Proceedings of the National Academy of Sciences, USA, 106:3249-3253 [doi: 10.1073/pnas.0810635106]
Background
This new direction in southern marine biology was conceived when two evolutionary research programs at the University of Otago (Department of Zoology) independently revealed dramatic evidence of long-distance rafting in marine invertebrates. First, Jon Waters and Mike Roy's work on the biogeography of sea-stars revealed closely related populations of the sedentary Parvulastra exigua on far-flung continents and oceanic islands of the Southern Hemisphere (Waters & Roy, 2004) (Fig. 1). They concluded that this wide geographic distribution could only have arisen through a number of independent rafting events. Simultaneously, Kirsten Donald and Hamish Spencer's phylogenetic research on trochid gastropods (Fig. 2) indicated that the topshell Diloma nigerrima recently migrated across the Pacific Ocean, from NZ to Chile, probably by rafting on fronds of the buoyant bull-kelp, Durvillaea antarctica (Donald et al 2005).
Fig. 1 Long-distance rafting of the coastal seastar Parvulastra exigua (Waters & Roy 2004, Systematic Biology 53, 18-24)Fig. 2 Trans-Pacific rafting of Diloma nigerrima topshells (Donald et al 2005 Evolution 59:1701-1717)
Biologists have been speculating about the origins of such widely dispersed marine species ever since Darwin noted the broad distribution of giant kelp (Macrocystis). Following the development of plate tectonic theory in the late 1960s, however, the view that species distributions are driven chiefly by geological — rather than biological — processes has held sway among many biogeographers, even today. Now, in light of dramatic new evidence for long-distance rafting (Parvulastra; Diloma: Figs 1-2), the time is right to put biology back into biogeography. We hypothesise that rafting may be a far more common and important biological phenomenon than is currently realised. Only by focusing on a whole community, and one that has an ecological propensity for long-distance dispersal, can we rigorously assess the evolutionary significance of this fundamental process.
Fig. 3 Internal structure of bull-kelp frond
A unique southern system for this work is bull-kelp. Exposed Southern Ocean coastlines are typically characterised by dense bull-kelp 'forests' (Durvillaea). As D. antarctica is both robust and buoyant (Fig. 3), detached plants form natural rafts that may float for vast distances.
Fig. 4 Distribution of buoyant Durvillaea antarctica (dotted lines) versus non-buoyant Durvillaea species (arrows; thick lines) (from Waters 2008)
Fig. 5 Bull-kelp holdfast and associated NZ molluscan species (after Morton and Miller, 1968)
Indeed, the Southern Ocean has an estimated 70 million kelp rafts at any one time (Smith 2002). In addition to the buoyant honeycomb-bladed D. antarctica, which has a circum-subantarctic distribution (NZ, Chile, and subantarctic islands; Fig. 4), the genus includes a number of solid-bladed (non-buoyant) species that are geographically restricted (Fig. 4), allowing a number of natural comparisons to be made, for example, about the respective population structures of buoyant and non-buoyant kelps and their constituent communities. In addition, our recent research indicates that D. antarctica represents a complex of at least two buoyant taxa (Fraser et al, submitted), increasing the scope for multiple independent comparisons.
Durvillaea kelp 'forests' support exceptionally high invertebrate biodiversity. It has been hypothesised that these highly specialised kelp holdfast communities — akin to a host-parasite system — raft together across the far-flung parts of the Southern Ocean.
Fig. 6 Beach-cast Durvillaeaantarctica with holdfast invertebrates (photos courtesy of Ceridwen Fraser)
Fig. 7 Kelp holdfast sampling in southern New Zealand
Research program
This project aims to examine the importance of rafting by focusing on an entire marine community that has rafting potential (Figs 5-7). If one is to attempt to study rare biological events — such as long-distance rafting — one should at least maximise potential success by looking at species that have an ecological propensity for such rafting. In this research program, therefore, we outline a new direction for phylogeography, one that integrates both ecological and historical biogeographic perspectives, and which involves genetic analysis of kelp and its associated rafting invertebrate communities. We will assess the evolutionary importance of rafting using a variety of approaches.
We will compare levels of population genetic structure in buoyant versus non-buoyant sister taxa of kelp (Durvillaea antarctica versus D. willana) together with kelp-associated invertebrates versus their non-rafting sister taxa (e.g. Sypharochiton sinclairi versus S. pelliserpentis). The correlation between buoyancy and geographic range of Durvillaea species is, in itself, circumstantial evidence for rafting as a dispersal mechanism for D. antarctica, but genetic data are required to make this claim robust. We will also use genetic analysis to quantify the frequency and duration of rafting events, and analyse the effect of ocenaography on marine connectivity.