92 research outputs found

    Changes in mangroves at their southernmost African distribution limit

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    Mangroves in South Africa occur at one of the most southerly locations in the world, which provides a unique opportunity to study their dynamic responses to anthropogenic and natural perturbations. The exposed high-energy South African coastline restricts mangroves to 32 sheltered estuaries of which 18 (56%) are predominantly open to the sea. A large area of mangrove (47% of the country total) occurs in the uMhlathuze Estuary – a novel ecosystem formed by the creation of an artificial mouth. A Drivers-Pressures-State-Impacts-Response (DPSIR) framework was applied to understand factors of change and highlight governance and management responses. The largest mangrove area (440 ha) was lost during the construction of Durban Bay harbour. Mangroves (~7 ha) no longer occur in 10 small KwaZulu-Natal estuaries as a result of catchment and mouth disturbance. In the Eastern Cape, pressures are escalating in the form of harvesting for wood, cattle browsing and changes in mouth condition. Climate related warming and an increase in CO2 are positive conditions for mangroves to expand their distribution to higher latitudes but this will depend on propagule dispersal between estuaries and the availability of suitable habitats

    The benthic regeneration of N and P in the Great Brak estuary, South Africa

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    The Great Brak is a temporarily open/closed estuary (TOCE) located on the south coast of South Africa. The construction of the Wolwedans Dam in 1989 reduced baseflow to the estuary by 56%, decreasing the intensity of flushing events and causing the mouth to breach less often. The aim of this study was to  investigate the flux of inorganic nutrients (NH4 +, TOxN [NO3 - + NO2 -], SRP) as well as total N and P across the  sediment–water interface in the estuary. There have been very few studies on nutrient cycling and benthic  pelagic coupling in South African estuaries. This study showed that the sediment had a net efflux of NH4 +, SRP, TN and TP while TOxN was taken up or converted to other forms of N. The estuary acted as a source of N and P during both summer and winter. If the estuary  remains closed for a prolonged period (12 months), with an increased organic load present on the benthos, the associated rates of efflux of N and P would increase. In order to reduce the organic load to the system better flushing methods or, more importantly, an increase in base flow, is needed to reduce residence times of water in the estuary.Keywords: water quality, nutrient cycling, benthic-pelagic coupling, estuar

    An estuary ecosystem classification that encompasses biogeography and a high diversity of types in support of protection and management

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    For nearly three decades, the Whitfield (1992) characterisation scheme served as a reference framework to type South African estuaries. We outline a revised ecosystem classification scheme that incorporates biogeographical zonation and introduces new types. Coastal outlets were re-categorised as estuaries or micro-systems. For functional estuaries, the Estuarine Lakes, Estuarine Bays and Predominantly Open Estuary types were largely retained. New types are Estuarine Lagoons and Arid Predominantly Closed Estuaries. The numerically dominant, temporarily open/closed category was subdivided into Small and Large Temporarily Closed Estuaries, with a total habitat area of 15 ha, serving as threshold separating these two subdivisions. River mouths were renamed Fluvially Dominated Estuaries and divided into large and small size categories to reflect dissimilar catchment influences. Micro-systems were separated into micro-estuaries, micro-outlets, and waterfalls. South Africa’s 290 estuaries were classified into 22 estuarine ecosystem categories arising from nine estuary types occurring across four biogeographical zones

    Advancing ecosystem accounting in estuaries: Swartkops Estuary case study

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    Rapid degradation of ecosystems and loss of ecosystem services have sparked interest in developing approaches to report and integrate such change with socio-economic information systems, such as the System of National Accounts. Here we describe an approach and application of ecosystem accounting for individual estuaries, building on approaches previously applied at national and bay levels. Using the Swartkops Estuary as a case study, the focus is on physical accounts for ecosystem extent and condition, as well as accounts for two important ecosystem services (carbon sequestration and recreational use). Pressure accounts are also introduced to demonstrate the value of identifying key areas for management and restoration interventions in response to changes in extent and/or condition accounts. Greater resolution in these account reports, achieved through zoning, provides spatially explicit information on ecosystem assets and their services within an estuary to also inform management decision-making at local level. Further, these accounts can also inform local restoration prioritisation, in support of the UN Decade on Ecosystem Restoration (2021–2030), for example offsetting irreversibly degraded areas in one zone with restoration or maintenance of similar habitats in another. Significance: • This study is the first to apply the ecosystem accounting approach at the individual estuary level. • We provide spatially explicit information on ecosystem assets and their services in support of resource management. • Physical accounts include extent and condition, as well as ecosystem service and pressure accounts. • These accounts inform estuary management and restoration at the local governance level

    Reduction in pollution load to an urban estuary using a sustainable drainage system treatment train

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    Rapid urbanisation and industrialisation have placed increased pressure on the ecosystem health of urban estuaries. Sustainable drainage systems (SuDS) are globally accepted practices for managing the water quality of stormwater and effluent discharged into urban systems. The Swartkops Estuary in South Africa is a heavily urbanized estuary that has a long history of pollution, specifically trace metal contamination, originating from industrial sources and urban wastewater. Using a novel SuDS treatment train, the physical characteristics (total suspended solids), macronutrients (orthophosphates, nitrate, ammonium), trace metals (As, Cd, Hg, Fe, Pb, Cu), and E. coli concentrations were measured monthly for one year, both before and after the treatment train. The treatment train consisted of five interconnected 500 L plastic tanks for sedimentation, filtration (sand and stone), biodegradation and floating wetlands. Results indicate that the SuDS treatment train provided an efficient method in reducing the pollution load to this urban estuary, by reducing macronutrient concentrations by 76 %, trace elements concentrations by 74 % and faecal bacteria counts (E. coli) by 80 %

    Dispersal and coastal geomorphology limit potential for mangrove range expansion under climate change

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    Latitudinal range limits for mangroves on high-energy, wave-dominated coasts are controlled by geomorphological features and estuarine dynamics. Mangroves reach a southern global range limit along the South African coastline, but the distribution is patchy, with stands occurring in only 16% of the estuaries in the region. Yet, the persistence of forests planted \u3e50 years ago beyond the natural distribution limit suggests that additional estuaries could support mangroves. Understanding regional drivers is necessary to inform global-scale estimates for how this important ecosystem is predicted to respond to climate change. Here, we combine species distribution modelling (MaxEnt), Lagrangian particle tracking using an eddy- and tide-resolving numerical ocean model, and connectivity matrices, to identify suitable mangrove habitats along the South African coastline at present, as well as under the IPCC RCP4.5 and RCP8.5 climate scenarios. Within the current South African distribution range (±900 km), eight more estuaries were identified to be suitable under contemporary conditions. When considering potential range extension (±110 km), an additional 14 suitable estuaries were identified. Connectivity matrices suggest limited long-distance dispersal, stranding mostly at or near the release location, and a decreased probability of connectivity towards the range limit. Under both future climate scenarios, 30% of estuaries currently supporting mangroves are predicted to become unsuitable, while an additional six estuaries beyond the current distribution are predicted to become suitable. However, there is limited connectivity between these new sites and established forests. Synthesis. This study shows that dispersal substantially limits mangrove distribution at the southern African range limit and highlights the importance of including this process in species distribution models. Ultimately, our results provide new insight into mangrove conservation and management at range limits that are not controlled predominantly by temperature, as it has been assumed that mangroves will largely expand to higher latitudes under climate change

    Teratology Primer-2nd Edition (7/9/2010)

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    Foreword: What is Teratology? “What a piece of work is an embryo!” as Hamlet might have said. “In form and moving how express and admirable! In complexity how infinite!” It starts as a single cell, which by repeated divisions gives rise to many genetically identical cells. These cells receive signals from their surroundings and from one another as to where they are in this ball of cells —front or back, right or left, headwards or tailwards, and what they are destined to become. Each cell commits itself to being one of many types; the cells migrate, combine into tissues, or get out of the way by dying at predetermined times and places. The tissues signal one another to take their own pathways; they bend, twist, and form organs. An organism emerges. This wondrous transformation from single celled simplicity to myriad-celled complexity is programmed by genes that, in the greatest mystery of all, are turned on and off at specified times and places to coordinate the process. It is a wonder that this marvelously emergent operation, where there are so many opportunities for mistakes, ever produces a well-formed and functional organism. And sometimes it doesn’t. Mistakes occur. Defective genes may disturb development in ways that lead to death or to malformations. Extrinsic factors may do the same. “Teratogenic” refers to factors that cause malformations, whether they be genes or environmental agents. The word comes from the Greek “teras,” for “monster,” a term applied in ancient times to babies with severe malformations, which were considered portents or, in the Latin, “monstra.” Malformations can happen in many ways. For example, when the neural plate rolls up to form the neural tube, it may not close completely, resulting in a neural tube defect—anencephaly if the opening is in the head region, or spina bifida if it is lower down. The embryonic processes that form the face may fail to fuse, resulting in a cleft lip. Later, the shelves that will form the palate may fail to move from the vertical to the horizontal, where they should meet in the midline and fuse, resulting in a cleft palate. Or they may meet, but fail to fuse, with the same result. The forebrain may fail to induce the overlying tissue to form the eye, so there is no eye (anophthalmia). The tissues between the toes may fail to break down as they should, and the toes remain webbed. Experimental teratology flourished in the 19th century, and embryologists knew well that the development of bird and frog embryos could be deranged by environmental “insults,” such as lack of oxygen (hypoxia). But the mammalian uterus was thought to be an impregnable barrier that would protect the embryo from such threats. By exclusion, mammalian malformations must be genetic, it was thought. In the early 1940s, several events changed this view. In Australia an astute ophthalmologist, Norman Gregg, established a connection between maternal rubella (German measles) and the triad of cataracts, heart malformations, and deafness. In Cincinnati Josef Warkany, an Austrian pediatrician showed that depriving female rats of vitamin B (riboflavin) could cause malformations in their offspring— one of the early experimental demonstrations of a teratogen. Warkany was trying to produce congenital cretinism by putting the rats on an iodine deficient diet. The diet did indeed cause malformations, but not because of the iodine deficiency; depleting the diet of iodine had also depleted it of riboflavin! Several other teratogens were found in experimental animals, including nitrogen mustard (an anti cancer drug), trypan blue (a dye), and hypoxia (lack of oxygen). The pendulum was swinging back; it seemed that malformations were not genetically, but environmentally caused. In Montreal, in the early 1950s, Clarke Fraser’s group wanted to bring genetics back into the picture. They had found that treating pregnant mice with cortisone caused cleft palate in the offspring, and showed that the frequency was high in some strains and low in others. The only difference was in the genes. So began “teratogenetics,” the study of how genes influence the embryo’s susceptibility to teratogens. The McGill group went on to develop the idea that an embryo’s genetically determined, normal, pattern of development could influence its susceptibility to a teratogen— the multifactorial threshold concept. For instance, an embryo must move its palate shelves from vertical to horizontal before a certain critical point or they will not meet and fuse. A teratogen that causes cleft palate by delaying shelf movement beyond this point is more likely to do so in an embryo whose genes normally move its shelves late. As studies of the basis for abnormal development progressed, patterns began to appear, and the principles of teratology were developed. These stated, in summary, that the probability of a malformation being produced by a teratogen depends on the dose of the agent, the stage at which the embryo is exposed, and the genotype of the embryo and mother. The number of mammalian teratogens grew, and those who worked with them began to meet from time to time, to talk about what they were finding, leading, in 1960, to the formation of the Teratology Society. There were, of course, concerns about whether these experimental teratogens would be a threat to human embryos, but it was thought, by me at least, that they were all “sledgehammer blows,” that would be teratogenic in people only at doses far above those to which human embryos would be exposed. So not to worry, or so we thought. Then came thalidomide, a totally unexpected catastrophe. The discovery that ordinary doses of this supposedly “harmless” sleeping pill and anti-nauseant could cause severe malformations in human babies galvanized this new field of teratology. Scientists who had been quietly working in their laboratories suddenly found themselves spending much of their time in conferences and workshops, sitting on advisory committees, acting as consultants for pharmaceutical companies, regulatory agencies, and lawyers, as well as redesigning their research plans. The field of teratology and developmental toxicology expanded rapidly. The following pages will show how far we have come, and how many important questions still remain to be answered. A lot of effort has gone into developing ways to predict how much of a hazard a particular experimental teratogen would be to the human embryo (chapters 9–19). It was recognized that animal studies might not prove a drug was “safe” for the human embryo (in spite of great pressure from legislators and the public to do so), since species can vary in their responses to teratogenic exposures. A number of human teratogens have been identified, and some, suspected of teratogenicity, have been exonerated—at least of a detectable risk (chapters 21–32). Regulations for testing drugs before market release have greatly improved (chapter 14). Other chapters deal with how much such things as population studies (chapter 11), post-marketing surveillance (chapter 13), and systems biology (chapter 16) add to our understanding. And, in a major advance, the maternal role of folate in preventing neural tube defects and other birth defects is being exploited (chapter 32). Encouraging women to take folic acid supplements and adding folate to flour have produced dramatic falls in the frequency of neural tube defects in many parts of the world. Progress has been made not only in the use of animal studies to predict human risks, but also to illumine how, and under what circumstances, teratogens act to produce malformations (chapters 2–8). These studies have contributed greatly to our knowledge of abnormal and also normal development. Now we are beginning to see exactly when and where the genes turn on and off in the embryo, to appreciate how they guide development and to gain exciting new insights into how genes and teratogens interact. The prospects for progress in the war on birth defects were never brighter. F. Clarke Fraser McGill University (Emeritus) Montreal, Quebec, Canad

    Supporting Spartina: Interdisciplinary perspective shows Spartina as a distinct solid genus

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    In 2014 a DNA-based phylogenetic study confirming the paraphyly of the grass subtribe Sporobolinae proposed the creation of a large monophyletic genus Sporobolus, including (among others) species previously included in the genera Spartina, Calamovilfa, and Sporobolus. Spartina species have contributed substantially (and continue contributing) to our knowledge in multiple disciplines, including ecology, evolutionary biology, molecular biology, biogeography, experimental ecology, environmental management, restoration ecology, history, economics, and sociology. There is no rationale so compelling to subsume the name Spartina as a subgenus that could rival the striking, global iconic history and use of the name Spartina for over 200 years. We do not agree with the arguments underlying the proposal to change Spartina to Sporobolus. We understand the importance of taxonomy and of formalized nomenclature and hope that by opening this debate we will encourage positive feedback that will strengthen taxonomic decisions with an interdisciplinary perspective. We consider the strongly distinct, monophyletic clade Spartina should simply and efficiently be treated as the genus Spartina
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