Nicholas H. Wolff
University of Queensland
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Featured researches published by Nicholas H. Wolff.
PLOS ONE | 2010
Daphne G. Fautin; Penelope Dalton; Lewis S. Incze; Jo-Ann C. Leong; Clarence Pautzke; Andrew A. Rosenberg; Paul A. Sandifer; George R. Sedberry; John W. Tunnell; Isabella A. Abbott; Russell E. Brainard; Melissa Brodeur; Lucius G. Eldredge; Michael Feldman; Fabio Moretzsohn; Peter S. Vroom; Michelle Wainstein; Nicholas H. Wolff
Marine biodiversity of the United States (U.S.) is extensively documented, but data assembled by the United States National Committee for the Census of Marine Life demonstrate that even the most complete taxonomic inventories are based on records scattered in space and time. The best-known taxa are those of commercial importance. Body size is directly correlated with knowledge of a species, and knowledge also diminishes with distance from shore and depth. Measures of biodiversity other than species diversity, such as ecosystem and genetic diversity, are poorly documented. Threats to marine biodiversity in the U.S. are the same as those for most of the world: overexploitation of living resources; reduced water quality; coastal development; shipping; invasive species; rising temperature and concentrations of carbon dioxide in the surface ocean, and other changes that may be consequences of global change, including shifting currents; increased number and size of hypoxic or anoxic areas; and increased number and duration of harmful algal blooms. More information must be obtained through field and laboratory research and monitoring that involve innovative sampling techniques (such as genetics and acoustics), but data that already exist must be made accessible. And all data must have a temporal component so trends can be identified. As data are compiled, techniques must be developed to make certain that scales are compatible, to combine and reconcile data collected for various purposes with disparate gear, and to automate taxonomic changes. Information on biotic and abiotic elements of the environment must be interactively linked. Impediments to assembling existing data and collecting new data on marine biodiversity include logistical problems as well as shortages in finances and taxonomic expertise.
Journal of Applied Ecology | 2012
C. Roland Pitcher; Peter Lawton; Nick Ellis; Stephen J. Smith; Lewis S. Incze; Chih-Lin Wei; Michelle E. Greenlaw; Nicholas H. Wolff; Jessica A. Sameoto; Paul V. R. Snelgrove
Summary 1. Environmental variables are often used as indirect surrogates for mapping biodiversity because species survey data are scant at regional scales, especially in the marine realm. However, environmental variables are measured on arbitrary scales unlikely to have simple, direct relationships with biological patterns. Instead, biodiversity may respond nonlinearly and to interactions between environmental variables. 2. To investigate the role of the environment in driving patterns of biodiversity composition in large marine regions, we collated multiple biological survey and environmental data sets from tropical NE Australia, the deep Gulf of Mexico and the temperate Gulf of Maine. We then quantified the shape and magnitude of multispecies responses along >30 environmental gradients and the extent to which these variables predicted regional distributions. To do this, we applied a new statistical approach, Gradient Forest, an extension of Random Forest, capable of modelling nonlinear and threshold responses. 3. The regional‐scale environmental variables predicted an average of 13–35% (up to 50–85% for individual species) of the variation in species abundance distributions. Important predictors differed among regions and biota and included depth, salinity, temperature, sediment composition and current stress. The shapes of responses along gradients also differed and were nonlinear, often with thresholds indicative of step changes in composition. These differing regional responses were partly due to differing environmental indicators of bioregional boundaries and, given the results to date, may indicate limited scope for extrapolating bio‐physical relationships beyond the region of source data sets. 4. Synthesis and applications. Gradient Forest offers a new capability for exploring relationships between biodiversity and environmental gradients, generating new information on multispecies responses at a detail not available previously. Importantly, given the scarcity of data, Gradient Forest enables the combined use of information from disparate data sets. The gradient response curves provide biologically informed transformations of environmental layers to predict and map expected patterns of biodiversity composition that represent sampled composition better than uninformed variables. The approach can be applied to support marine spatial planning and management and has similar applicability in terrestrial realms.
Global Change Biology | 2015
Alice Rogers; Alastair R. Harborne; Christopher J. Brown; Yves Marie Bozec; Carolina Castro; Iliana Chollett; Karlo Hock; Cheryl Knowland; Alyssa Marshell; Juan Carlos Ortiz; Tries Razak; George Roff; Jimena Samper-Villarreal; Megan I. Saunders; Nicholas H. Wolff; Peter J. Mumby
Under projections of global climate change and other stressors, significant changes in the ecology, structure and function of coral reefs are predicted. Current management strategies tend to look to the past to set goals, focusing on halting declines and restoring baseline conditions. Here, we explore a complementary approach to decision making that is based on the anticipation of future changes in ecosystem state, function and services. Reviewing the existing literature and utilizing a scenario planning approach, we explore how the structure of coral reef communities might change in the future in response to global climate change and overfishing. We incorporate uncertainties in our predictions by considering heterogeneity in reef types in relation to structural complexity and primary productivity. We examine 14 ecosystem services provided by reefs, and rate their sensitivity to a range of future scenarios and management options. Our predictions suggest that the efficacy of management is highly dependent on biophysical characteristics and reef state. Reserves are currently widely used and are predicted to remain effective for reefs with high structural complexity. However, when complexity is lost, maximizing service provision requires a broader portfolio of management approaches, including the provision of artificial complexity, coral restoration, fish aggregation devices and herbivore management. Increased use of such management tools will require capacity building and technique refinement and we therefore conclude that diversification of our management toolbox should be considered urgently to prepare for the challenges of managing reefs into the 21st century.
Nature Communications | 2015
Maria Beger; Jennifer McGowan; Eric A. Treml; Alison Green; Alan T. White; Nicholas H. Wolff; Peter J. Mumby; Hugh P. Possingham
Multinational conservation initiatives that prioritize investment across a region invariably navigate trade-offs among multiple objectives. It seems logical to focus where several objectives can be achieved efficiently, but such multi-objective hotspots may be ecologically inappropriate, or politically inequitable. Here we devise a framework to facilitate a regionally cohesive set of marine-protected areas driven by national preferences and supported by quantitative conservation prioritization analyses, and illustrate it using the Coral Triangle Initiative. We identify areas important for achieving six objectives to address ecosystem representation, threatened fauna, connectivity and climate change. We expose trade-offs between areas that contribute substantially to several objectives and those meeting one or two objectives extremely well. Hence there are two strategies to guide countries choosing to implement regional goals nationally: multi-objective hotspots and complementary sets of single-objective priorities. This novel framework is applicable to any multilateral or global initiative seeking to apply quantitative information in decision making.
Journal of Applied Ecology | 2014
Karlo Hock; Nicholas H. Wolff; Scott A. Condie; Kenneth R. N. Anthony; Peter J. Mumby
Many ecosystems suffer systemwide outbreaks of damaging species propagating from primary outbreak sites. Connectivity patterns can identify parts of the ecosystem that help turn local outbreaks into a systemwide contagion through a series of transmission events. Here, we show that patterns of larval connectivity among reefs can help explain periodic crown-of-thorns starfish (COTS) epidemics across the Great Barrier Reef (GBR). We simulated potential dispersal of COTS larvae to obtain a connectivity network of coral reefs across the entire GBR. Network analysis revealed areas of high local connectivity where any outbreaks could be amplified locally, as well as those areas with potential to cause large-scale epidemics with ecosystem-wide impacts. We find that the regions where COTS epidemics are known to originate are predictable from their high local and systemwide connectivity. Extensive larval exchanges among reef clusters in these regions can start a chain reaction of COTS population build-up. The same regions also have high potential to reach and affect other parts of the GBR, thereby maximizing the likelihood that any outbreaks would eventually propagate throughout the ecosystem. Hydrodynamic properties and geography of the GBR make it vulnerable to COTS epidemics. Using network analysis to identify regions with high-risk high-impact sources could help control these devastating events in future. Synthesis and applications. The observed centre of origin for COTS epidemics (the Cooktown-Cairns region) can be predicted from its elevated short- and long-range levels of larval connectivity. Connectivity analysis of per-reef risks provides spatially explicit targets to guide surveillance and control measures that might help curtail COTS epidemics through prioritization of highly connected reefs. The analytical approach developed here for COTS connectivity can also be applied to identify well-connected patches and regions in other interconnected ecological systems. The observed centre of origin for COTS epidemics (the Cooktown-Cairns region) can be predicted from its elevated short- and long-range levels of larval connectivity. Connectivity analysis of per-reef risks provides spatially explicit targets to guide surveillance and control measures that might help curtail COTS epidemics through prioritization of highly connected reefs. The analytical approach developed here for COTS connectivity can also be applied to identify well-connected patches and regions in other interconnected ecological systems.
Journal of Crustacean Biology | 2006
Lewis S. Incze; Richard A. Wahle; Nicholas H. Wolff; Carl Wilson; Robert S. Steneck; E. Annis; Peter Lawton; Huijie Xue; Yong Chen
Abstract Beginning in the late 1980s, lobster (Homarus americanus) landings for the state of Maine and the Bay of Fundy increased to levels more than three times their previous 20-year means. Reduced predation may have permitted the expansion of lobsters into previously inhospitable territory, but we argue that in this region the spatial patterns of recruitment and the abundance of lobsters are substantially driven by events governing the earliest life history stages, including the abundance and distribution of planktonic stages and their initial settlement as Young-of-Year (YOY) lobsters. Settlement densities appear to be strongly driven by abundance of the pelagic postlarvae. Postlarvae and YOY show large-scale spatial patterns commensurate with coastal circulation, but also multi-year trends in abundance and abrupt shifts in abundance and spatial patterns that signal strong environmental forcing. The extent of the coastal shelf that defines the initial settlement grounds for lobsters is important to future population modeling. We address one part of this definition by examining patterns of settlement with depth, and discuss a modeling framework for the full life history of lobsters in the Gulf of Maine.
Journal of Crustacean Biology | 2007
Eric R. Annis; Lewis S. Incze; Nicholas H. Wolff; Robert S. Steneck
Abstract Larval development time is a critical factor in assessing the potential for larval transport, mortality, and subsequently, the connectivity of marine populations through larval exchange. Most estimates of larval duration are based on laboratory studies and may not reflect development times in nature. For larvae of the American lobster (Homarus americanus), temperature-dependent development times have been established in previous laboratory studies. Here, we used the timing of seasonal abundance curves for newly hatched larvae (stage I) and the final plankonic instar (postlarva), coupled with a model of temperature-dependent development to assess development time in the field. We were unable to reproduce the timing of the seasonal abundance curves using laboratory development rates in our model. Our results suggest that larval development in situ may be twice as fast as reported laboratory rates. This will result in reduced estimates of larval transport potential, and increased estimates of instantaneous mortality rate and production.
Global Change Biology | 2015
Nicholas H. Wolff; Simon D. Donner; Long Cao; Roberto Iglesias-Prieto; Peter F. Sale; Peter J. Mumby
For many ecosystem services, it remains uncertain whether the impacts of climate change will be mostly negative or positive and how these changes will be geographically distributed. These unknowns hamper the identification of regional winners and losers, which can influence debate over climate policy. Here, we use coral reefs to explore the spatial variability of climate stress by modelling the ecological impacts of rising sea temperatures and ocean acidification, two important coral stressors associated with increasing greenhouse gas (GHG) emissions. We then combine these results with national per capita emissions to quantify inequities arising from the distribution of cause (CO2 emissions) and effect (stress upon reefs) among coral reef countries. We find pollution and coral stress are spatially decoupled, creating substantial inequity of impacts as a function of emissions. We then consider the implications of such inequity for international climate policy. Targets for GHG reductions are likely to be tied to a countrys emissions. Yet within a given level of GHG emissions, our analysis reveals that some countries experience relatively high levels of impact and will likely experience greater financial cost in terms of lost ecosystem productivity and more extensive adaptation measures. We suggest countries so disadvantaged be given access to international adaptation funds proportionate with impacts to their ecosystem. We raise the idea that funds could be more equitably allocated by formally including a metric of equity within a vulnerability framework.
PLOS Biology | 2017
Karlo Hock; Nicholas H. Wolff; Juan Carlos Ortiz; Scott A. Condie; Kenneth R. N. Anthony; Paul G. Blackwell; Peter J. Mumby
Australia’s iconic Great Barrier Reef (GBR) continues to suffer from repeated impacts of cyclones, coral bleaching, and outbreaks of the coral-eating crown-of-thorns starfish (COTS), losing much of its coral cover in the process. This raises the question of the ecosystem’s systemic resilience and its ability to rebound after large-scale population loss. Here, we reveal that around 100 reefs of the GBR, or around 3%, have the ideal properties to facilitate recovery of disturbed areas, thereby imparting a level of systemic resilience and aiding its continued recovery. These reefs (1) are highly connected by ocean currents to the wider reef network, (2) have a relatively low risk of exposure to disturbances so that they are likely to provide replenishment when other reefs are depleted, and (3) have an ability to promote recovery of desirable species but are unlikely to either experience or spread COTS outbreaks. The great replenishment potential of these ‘robust source reefs’, which may supply 47% of the ecosystem in a single dispersal event, emerges from the interaction between oceanographic conditions and geographic location, a process that is likely to be repeated in other reef systems. Such natural resilience of reef systems will become increasingly important as the frequency of disturbances accelerates under climate change.
PLOS ONE | 2011
William K. W. Li; Robert A. Andersen; Dian J. Gifford; Lewis S. Incze; Jennifer L. Martin; Cynthia H. Pilskaln; Juliette N. Rooney-Varga; Michael E. Sieracki; William H. Wilson; Nicholas H. Wolff
In the Gulf of Maine area (GoMA), as elsewhere in the ocean, the organisms of greatest numerical abundance are microbes. Viruses in GoMA are largely cyanophages and bacteriophages, including podoviruses which lack tails. There is also evidence of Mimivirus and Chlorovirus in the metagenome. Bacteria in GoMA comprise the dominant SAR11 phylotype cluster, and other abundant phylotypes such as SAR86-like cluster, SAR116-like cluster, Roseobacter, Rhodospirillaceae, Acidomicrobidae, Flavobacteriales, Cytophaga, and unclassified Alphaproteobacteria and Gammaproteobacteria clusters. Bacterial epibionts of the dinoflagellate Alexandrium fundyense include Rhodobacteraceae, Flavobacteriaceae, Cytophaga spp., Sulfitobacter spp., Sphingomonas spp., and unclassified Bacteroidetes. Phototrophic prokaryotes in GoMA include cyanobacteria that contain chlorophyll (mainly Synechococcus), aerobic anoxygenic phototrophs that contain bacteriochlorophyll, and bacteria that contain proteorhodopsin. Eukaryotic microalgae in GoMA include Bacillariophyceae, Dinophyceae, Prymnesiophyceae, Prasinophyceae, Trebouxiophyceae, Cryptophyceae, Dictyochophyceae, Chrysophyceae, Eustigmatophyceae, Pelagophyceae, Synurophyceae, and Xanthophyceae. There are no records of Bolidophyceae, Aurearenophyceae, Raphidophyceae, and Synchromophyceae in GoMA. In total, there are records for 665 names and 229 genera of microalgae. Heterotrophic eukaryotic protists in GoMA include Dinophyceae, Alveolata, Apicomplexa, amoeboid organisms, Labrynthulida, and heterotrophic marine stramenopiles (MAST). Ciliates include Strombidium, Lohmaniella, Tontonia, Strobilidium, Strombidinopsis and the mixotrophs Laboea strobila and Myrionecta rubrum (ex Mesodinium rubra). An inventory of selected microbial groups in each of 14 physiographic regions in GoMA is made by combining information on the depth-dependent variation of cell density and the depth-dependent variation of water volume. Across the entire GoMA, an estimate for the minimum abundance of cell-based microbes is 1.7×1025 organisms. By one account, this number of microbes implies a richness of 105 to 106 taxa in the entire water volume of GoMA. Morphological diversity in microplankton is well-described but the true extent of taxonomic diversity, especially in the femtoplankton, picoplankton and nanoplankton – whether autotrophic, heterotrophic, or mixotrophic, is unknown.