Talling P.J.,UK National Oceanography Center
Marine Geology | Year: 2014
Turbidity currents, and other types of underwater sediment density flow, are arguably the most important flow process for moving sediment across our planet. Direct monitoring provides the most reliable information on the varied ways in which these flows are triggered, and thus forms the basis for this contribution. Recent advances in flow monitoring make this contribution timely, although monitoring is biased towards more frequent flow types. Submarine deltas fed by bedload dominated rivers can be very active with tens of events each year. Larger events are generated by delta-lip failures, whilst smaller events can be associated with motion of up-slope migrating bedforms. River-fed submarine canyons are flushed every few years by powerful long run-out flows. Flows in river-fed delta and canyon systems tend to occur during months of elevated river discharge. However, many flows do not coincide with flood peaks, or occur where rivers do not reach hyperpycnal concentrations, and are most likely triggered by failure of rapidly deposited sediment. Plunging of hyperpycnal river floodwater commonly triggers dilute and slow moving flows in lakes and reservoirs, and has been shown to produce mm-thick fine-grained deposits. It is proposed here that such thin and fine deposits are typical of flows triggered by hyperpycnal river floods, rather than thicker sand layers with traction structure or displaying inverse-to-normal grading. Oceanographic canyons are detached from river mouths and fed by oceanographic processes (wave and tide resuspension, longshore drift, etc.). Most events in these canyons are associated with large wave heights. Up-slope migrating crescentic bedforms are seen, similar to those observed in river-fed deltas. Oceanographic processes tend to infill canyons, which are flushed episodically by much more powerful flows, inferred to result from slope failure. This filling and flushing model is less applicable to river-fed canyons in which flushing events are much more frequent. Oceanographic canyons may result from rapid sea level rise that detaches river mouths from canyon heads, and they can remain active during sea level highstands. Deep-water basin plains are often dominated by infrequent but very large flows triggered by failure of the continental slope. Recurrence intervals of these flows appear almost random, and only weakly (if at all) correlated with sea level change. Turbidites can potentially provide a valuable long-term record of major earthquakes, but widespread slope failure is the only reliable criteria for inferring seismic triggering. However, not all major earthquakes trigger widespread slope failure, so that the record is incomplete in some locations. © 2014 Elsevier B.V.
Bett B.J.,UK National Oceanography Center
Marine Ecology Progress Series | Year: 2014
Warwick (2014; Mar Ecol Prog Ser 505:295-298) suggests that my claim that the biology of marine metazoan benthos may scale continuously with body mass (Bett 2013; Mar Ecol Prog Ser 487:1-6) is an overstatement. His alternative hypothesis is that there is a 'step-change' in allometric relationships between the meio- and macrobenthos. I continue to propose that simple null hypotheses for standing stock size spectra and species size spectra of the metazoan benthos, consistent with metabolic theory and macroecology, offer parsimonious solutions. For standing stock and species size spectra I present field data that conform to these null hypotheses. Data from other studies, such as those suggested by Warwick (2014), may be difficult to place in the macroeco - logical context, as those studies are constructed or presented in a different manner (e.g. they lack data on the number of individuals identified). I suggest that it may be useful to consider 'evolutionary species size spectra' separately from 'macroecological species size spectra'. Both are valid testable hypotheses, and are not necessarily contradictory. © 2014 Inter-Research.
Thatje S.,UK National Oceanography Center
Integrative and Comparative Biology | Year: 2012
The likelihood of marine invertebrates to maintain large geographic ranges is widely dependent on the ability of their early ontogenetic stages to disperse over long distances. Marine benthic invertebrates inhabiting the cold-stenothermal environment of the Southern Ocean are known for their overall reduced number of pelagic larvae, or drifting stages of any kind, when compared with organisms elsewhere in the sea. The diversity of organisms thriving in Antarctic waters is the result of evolution in situ and of the intrusion of species from surrounding seas. The reasons for a high level of endemism and a stunning diversity of benthic invertebrates found today are frequently discussed in the literature, but the mechanisms whereby diversity has been controlled over time remain largely theoretical. Here, I suggest that, indeed, early life-history patterns play a key role in defining the radiation and the speciation potential of Antarctic benthic invertebrates. In arguing this case, I synthesize the growing body of molecular studies on population connectivity in Antarctic benthic invertebrates, and compare this information with knowledge of their life histories and biogeography. I conclude that differences in early life-history patterns are key to the resilience potential of species in response to late Cenozoic glacial periods and propose that there is a direct relationship between rate of speciation and the ability of taxa to disperse. © 2012 The Author. Published by Oxford University Press on behalf of the Society for Integrative and Comparative Biology. All rights reserved.
Statham P.J.,UK National Oceanography Center
Science of the Total Environment | Year: 2012
The fate and cycling of macronutrients introduced into estuaries depend upon a range of interlinked processes. Hydrodynamics and morphology in combination with freshwater inflow control the freshwater flushing time, and the timescale for biogeochemical processes to operate that include microbial activity, particle-dissolved phase interactions, and benthic exchanges. In some systems atmospheric inputs and exchanges with coastal waters can also be important. Climate change will affect nutrient inputs and behaviour through modifications to temperature, wind patterns, the hydrological cycle, and sea level rise. Resulting impacts include: 1) inundation of freshwater systems 2) changes in stratification, flushing times and phytoplankton productivity 3) increased coastal storm activity 4) changes in species and ecosystem function. A combination of continuing high inputs of nutrients through human activity and climate change is anticipated to lead to enhanced eutrophication in the future. The most obvious impacts of increasing global temperature will be in sub-arctic systems where permafrost zones will be reduced in combination with enhanced inputs from glacial systems.Improved process understanding in several key areas including cycling of organic N and P, benthic exchanges, resuspension, impact of bio-irrigation, particle interactions, submarine groundwater discharges, and rates and magnitude of bacterially-driven recycling processes, is needed. Development of high frequency in situ nutrient analysis systems will provide data to improve predictive models that need to incorporate a wider variety of key factors, although the complexity of estuarine systems makes such modelling a challenge. However, overall a more holistic approach is needed to effectively understand, predict and manage the impact of macronutrients on estuaries. © 2011 Elsevier B.V.
Benn A.R.,UK National Oceanography Center
PloS one | Year: 2010
Environmental impacts of human activities on the deep seafloor are of increasing concern. While activities within waters shallower than 200 m have been the focus of previous assessments of anthropogenic impacts, no study has quantified the extent of individual activities or determined the relative severity of each type of impact in the deep sea. The OSPAR maritime area of the North East Atlantic was chosen for the study because it is considered to be one of the most heavily impacted by human activities. In addition, it was assumed data would be accessible and comprehensive. Using the available data we map and estimate the spatial extent of five major human activities in the North East Atlantic that impact the deep seafloor: submarine communication cables, marine scientific research, oil and gas industry, bottom trawling and the historical dumping of radioactive waste, munitions and chemical weapons. It was not possible to map military activities. The extent of each activity has been quantified for a single year, 2005. Human activities on the deep seafloor of the OSPAR area of the North Atlantic are significant but their footprints vary. Some activities have an immediate impact after which seafloor communities could re-establish, while others can continue to make an impact for many years and the impact could extend far beyond the physical disturbance. The spatial extent of waste disposal, telecommunication cables, the hydrocarbon industry and marine research activities is relatively small. The extent of bottom trawling is very significant and, even on the lowest possible estimates, is an order of magnitude greater than the total extent of all the other activities. To meet future ecosystem-based management and governance objectives for the deep sea significant improvements are required in data collection and availability as well as a greater awareness of the relative impact of each human activity.
Talling P.J.,UK National Oceanography Center
Geosphere | Year: 2013
Hybrid flows comprising both turbidity current and submarine debris flow are a significant departure from many previous influential models for submarine sediment density flows. Hybrid beds containing cohesive debrite and turbiditeare common in distal depositional environments, as shown by detailed observations from more than 20 modern and ancient systems worldwide.Hybrid flows, and cohesive debris flows more generally, are best classified in terms of a continuum of decreasing cohesive debris flow strength. High-strength cohesive debris flows tend to be clast rich and relatively thick, and their deposit extends back to near the siteof original slope failure. They are typically confined to higher gradient continental slopes, but may occasionally form megabeds on basin plains, in both cases overlain by a thin turbidite. Intermediate-strength cohesive debris flows typically contain clasts, but their deposits may be <1 or 2 m thick onlow-gradient fan fringes, and are encased in turbidite sand and mud. Clasts may be fartraveled, and meter-sized clasts can be rafted long distances across very low gradients if they are less dense than surrounding flow. Low-strength cohesive debris flows generally lack mud clasts, and as cohesive strength decreases further there is a transition into fluidmud layers that do not support sand. Intermediate- and low-strength cohesive debrites are consistently absent in more proximal parts of submarine systems, where faster moving sediment-charged flows are more likely to be turbulent. Intermediatestrength debris flows can run out for long distances on low gradients without hydroplaning. Very low strength cohesive debris flows most likely form through late-stage transformations near the site of debrite deposition, and emplaced gently to avoid mixing with surrounding seawater. The location and geometry of cohesive debrites in hybrid beds are controlled strongly by seafloor morphology and small changes in gradient. Debrites occur as fringes around raised channel-lev e ridges, or in the central and lowest parts of basin plains lacking such ridges. Small variations in mud fraction produce profound changes in cohesive strength, flow viscosity, permeability, and the time taken for excess pore pressuresto dissipate that span multiple orders of magnitude. Reduction in flow speed can also cause substantial increases in viscosity and yield strength in shear thinning muddy fluids. Small amounts of sedimnt can dampen or extinguish turbulence, especially as flow decelerates, affecting how sediment is supported or deposited. This ensures that cohesive debris flows and hybrid flows have a rich variety of behaviors. © 2013 Geological Society of America.
Tyrrell T.,UK National Oceanography Center
Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences | Year: 2011
Human activities are altering the ocean in many different ways. The surface ocean is warming and, as a result, it is becoming more stratified and sea level is rising. There is no clear evidence yet of a slowing in ocean circulation, although this is predicted for the future. As anthropogenic CO2 permeates into the ocean, it is making sea water more acidic, to the detriment of surface corals and probably many other calcifiers. Once acidification reaches the deep ocean, it will become more corrosive to CaCO3, leading to a considerable reduction in the amount of CaCO3 accumulating on the deep seafloor. There will be a several thousand-year-long interruption to CaCO3 sedimentation at many points on the seafloor. A curious feedback in the ocean, carbonate compensation, makes it more likely that global warming and sea-level rise will continue for many millennia after CO2 emissions cease. © 2011 The Royal Society.
Lucas C.H.,UK National Oceanography Center
Advances in marine biology | Year: 2012
Large population fluctuations of jellyfish occur over a variety of temporal scales, from weekly to seasonal, inter-annual and even decadal, with some regions of the world reported to be experiencing persistent seasonal bloom events. Recent jellyfish research has focussed on understanding the causes and consequences of these population changes, with the vast majority of studies considering the effect of changing environmental variables only on the pelagic medusa. But many of the bloom-forming species are members of the Scyphozoa with complex metagenic life cycles consisting of a sexually reproducing pelagic medusa and asexually reproducing benthic polyp. Recruitment success during the juvenile (planula, polyp and ephyrae) stages of the life cycle can have a major effect on the abundance of the adult (medusa) population, but until very recently, little was known about the ecology of the polyp or scyphistoma phase of the scyphozoan life cycle. The aim of this review is to synthesise the current state of knowledge of polyp ecology by examining (1) the recruitment and metamorphosis of planulae larvae into polyps, (2) survival and longevity of polyps, (3) expansion of polyp populations via asexual propagation and (4) strobilation and recruitment of ephyrae (juvenile medusae). Where possible, comparisons are made with the life histories of other bentho-pelagic marine invertebrates so that further inferences can be made. Differences between tropical and temperate species are highlighted and related to climate change, and populations of the same species (in particular Aurelia aurita) inhabiting different habitats within its geographic range are compared. The roles that polyps play in ensuring the long-term survival of jellyfish populations as well as in the formation of bloom populations are considered, and recommendations for future research are presented. Copyright © 2012 Elsevier Ltd. All rights reserved.
Hauton C.,UK National Oceanography Center
Journal of Invertebrate Pathology | Year: 2012
The culture or wild capture of marine and freshwater shellfish, including crustaceans, is without doubt a key source of protein for a burgeoning world population. Historically the expansion of aquaculture has, however, been accompanied by the increased incidence of economically significant diseases, most notably of viral and bacterial origin. Since the late 1970s great progress has been made in our understanding of the generalized protostome innate immune system. Distinct pathways, pathogen receptor proteins and effector molecules have since been identified that are not ancestral or homologous to those of the deuterostomes, including vertebrates. Within the past decade progress has accelerated with the rapid characterisation of new classes of recognition proteins, immune effectors and regulatory pathways. This paper provides a broad overview of our current understanding of invertebrate immunology, taking the crustacean decapod immune system as its focus. Recent developments in the field are described briefly and their implications and potential considered. These advances offer fundamental new insights in our efforts to understand disease in cultured populations and also to develop knowledge of environmental effects on host/pathogen interactions within a fishery context. Of course, challenges do remain, including the lack of an immortal cell line and the limited publically-available genomic resources. These are considered in this review as priorities for future research effort. With the continued application of more insightful technologies, coupled with associated investment, it is expected that the speed at which some of these issues are resolved will accelerate. © 2012 Elsevier Inc.
Brown A.,UK National Oceanography Center |
Thatje S.,UK National Oceanography Center
Biological Reviews | Year: 2014
Bathymetric biodiversity patterns of marine benthic invertebrates and demersal fishes have been identified in the extant fauna of the deep continental margins. Depth zonation is widespread and evident through a transition between shelf and slope fauna from the shelf break to 1000m, and a transition between slope and abyssal fauna from 2000 to 3000m; these transitions are characterised by high species turnover. A unimodal pattern of diversity with depth peaks between 1000 and 3000m, despite the relatively low area represented by these depths. Zonation is thought to result from the colonisation of the deep sea by shallow-water organisms following multiple mass extinction events throughout the Phanerozoic. The effects of low temperature and high pressure act across hierarchical levels of biological organisation and appear sufficient to limit the distributions of such shallow-water species. Hydrostatic pressures of bathyal depths have consistently been identified experimentally as the maximum tolerated by shallow-water and upper bathyal benthic invertebrates at in situ temperatures, and adaptation appears required for passage to deeper water in both benthic invertebrates and demersal fishes. Together, this suggests that a hyperbaric and thermal physiological bottleneck at bathyal depths contributes to bathymetric zonation. The peak of the unimodal diversity-depth pattern typically occurs at these depths even though the area represented by these depths is relatively low. Although it is recognised that, over long evolutionary time scales, shallow-water diversity patterns are driven by speciation, little consideration has been given to the potential implications for species distribution patterns with depth. Molecular and morphological evidence indicates that cool bathyal waters are the primary site of adaptive radiation in the deep sea, and we hypothesise that bathymetric variation in speciation rates could drive the unimodal diversity-depth pattern over time. Thermal effects on metabolic-rate-dependent mutation and on generation times have been proposed to drive differences in speciation rates, which result in modern latitudinal biodiversity patterns over time. Clearly, this thermal mechanism alone cannot explain bathymetric patterns since temperature generally decreases with depth. We hypothesise that demonstrated physiological effects of high hydrostatic pressure and low temperature at bathyal depths, acting on shallow-water taxa invading the deep sea, may invoke a stress-evolution mechanism by increasing mutagenic activity in germ cells, by inactivating canalisation during embryonic or larval development, by releasing hidden variation or mutagenic activity, or by activating or releasing transposable elements in larvae or adults. In this scenario, increased variation at a physiological bottleneck at bathyal depths results in elevated speciation rate. Adaptation that increases tolerance to high hydrostatic pressure and low temperature allows colonisation of abyssal depths and reduces the stress-evolution response, consequently returning speciation of deeper taxa to the background rate. Over time this mechanism could contribute to the unimodal diversity-depth pattern. © 2013 Natural Environment Research Council. Biological Reviews published by John Wiley & Sons Ltd on behalf of Cambridge Philosophical Society.