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- Sjöling, Sara, et al.
(author)
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Benthic bacterial diversity and nutrient processes in mangroves : impact of deforestation
- 2005
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In: Estuarine, Coastal and Shelf Science. - United Kingdom : Academic Press. - 0272-7714 .- 1096-0015. ; 63:3, s. 397-406
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Journal article (peer-reviewed)abstract
- The bacterial diversity and nutrient dynamics of mangrove sediments in Kisakasaka, Tanzania, was investigated in order to evaluate potential changes associated with deforestation of mangroves. Study sites included relatively undisturbed, recently protected mangroves and clear-cut mangrove areas that were sampled during both the wet and dry seasons. Physicochemical parameters, nitrogenase activity, pore water nutrient concentrations and bacterial diversity were measured in sediment depth profiles using both molecular and chemical techniques. Results show that there are significant differences in sediment pore water nutrient concentrations and bacterial diversity in sediments of mangrove areas which have been deforested compared to those which have been protected. Average measured values for protected and deforested areas, respectively, were: sulphide (S-2-),S- < 42 +/- 10 mu M and > 1.9 +/- 0.5 mM at 30 cm depth; ammonium (NH4+), 58 +/- 2 mu M and 113 +/- 12 mu M at 4-5 cm depth; soluble reactive phosphate, 40.2 +/- 11 mu M and 18.4 +/- 1.2 at 4-5 cm depth. Nitrogen fixation rates were lower in deforested areas during day and night, organic content was higher in protected areas (20 +/- 5%) compared to deforested areas (12 +/- 3%). The bacterial diversity was lower in deforested areas as determined by Shannon index using 16S rRNA gene analysis with terminal restriction fragment length polymorphism.
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| 2. |
- Eklöf, J.S., et al.
(author)
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Sea urchin overgrazing of seagrasses: A review of current knowledge on causes, consequences and management
- 2008
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In: Estuarine, Coastal and Shelf Science. - : Elsevier BV. - 0272-7714 .- 1096-0015. ; 79:4, s. 569-580
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Journal article (peer-reviewed)abstract
- Sea urchins are one of the most common seagrass macro-grazers in contemporary seagrass systems. Occasionally their grazing rates exceed seagrass growth rates, a phenomenon sometimes referred to as overgrazing. Because of a reported increasing frequency of overgrazing events, concomitant with loss of seagrass-associated ecosystem services, it has been suggested that overgrazing is one of the key threats to tropical and subtropical seagrasses. In light of this, we review the current knowledge on causes, consequences. and management of sea urchin overgrazing of seagrasses. Initially we argue that the definition of overgrazing must include scale and impairment of ecosystem services, since this is the de facto definition used in the literature, and will highlight the potential societal costs of seagrass overgrazing. A review of 16 identified cases suggests that urchin overgrazing is a global phenomenon, ranging from temperate to tropical coastal waters and involving at least 11 seagrass and 7 urchin species. Even though most overgrazing events Seem to affect areas of <0.5 km(2), and recovery often occurs within a few years, overgrazing can have a range of large, long-term indirect effects such as loss of associated fauna and decreased sediment stabilization. A range of drivers behind overgrazing have been suggested, including bottom-up (nutrient enrichment). top-down (reduced predation control due to e.g. overfishing), "side-in" mechanisms (e.g. changes in water temperature) and natural population fluctuations. Based on recent studies, there seems to be fairly strong support for the top-down and bottom-up hypotheses. However, many potential drivers often co-occur and interact, especially in areas with high anthropogenic pressure, suggesting that multiple disturbances-by simultaneously reducing predation control, increasing urchin recruitment and reducing the resistance of seagrasses-could pave the way for overgrazing. In management, the most common response to overgrazing has been to remove urchins, but limited knowledge of direct and indirect effects makes it difficult to assess the applicability and sustainability of this method. Based on the wide knowledge gaps, which severely limits management, we suggest that future research should focus on (1) identification and quantification of ecosystem and societal scale effects of overgrazing; (2) assessment of the relative importance and interactions of different drivers; and (3) development of a holistic proactive and reactive long-term management agenda.
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| 4. |
- Lyimo, Liberatus D., et al.
(author)
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Shading and simulated grazing increase the sulphide pool and methane emission in a tropical seagrass meadow
- 2018
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In: Marine Pollution Bulletin. - : Elsevier BV. - 0025-326X .- 1879-3363. ; 134, s. 89-93
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Journal article (peer-reviewed)abstract
- Though seagrass meadows are among the most productive habitats in the world, contributing substantially to long-term carbon storage, studies of the effects of critical disturbances on the fate of carbon sequestered in the sediment and biomass of these meadows are scarce. In a manipulative in situ experiment, we studied the effects of successive loss of seagrass biomass as a result of shading and simulated grazing at two intensity levels on sulphide (H2S) content and methane (CH4) emission in a tropical seagrass meadow in Zanzibar (Tanzania). In all disturbed treatments, we found a several-fold increase in both the sulphide concentration of the sediment pore-water and the methane emissions from the sediment surface (except for CH4 emissions in the low-shading treatment). This could be due to the ongoing degradation of belowground biomass shed by the seagrass plants, supporting the production of both sulphate-reducing bacteria and methanogens, possibly exacerbated by the loss of downwards oxygen transport via seagrass plants. The worldwide rapid loss of seagrass areas due to anthropogenic activities may therefore have significant effects on carbon sink-source relationships within coastal seas.
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| 8. |
- Dalusi, Lucy, et al.
(author)
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Toxigenic Vibrio cholerae identified in estuaries of Tanzania using PCR techniques
- 2015
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In: FEMS Microbiology Letters. - : Oxford University Press (OUP). - 0378-1097 .- 1574-6968. ; 362:5
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Journal article (peer-reviewed)abstract
- The current study assessed the occurrence of the Vibrio cholerae serogroups O1 and O139 in environmental samples along salinity gradients in three selected estuaries of Tanzania both through culture independent methods and by cultured bacteria. Occurrence of V. cholerae was determined by PCR targeting the V. cholerae outer membrane protein gene ompW. Furthermore, the presence of toxigenic strains and serogroups O1 and O139 was determined using multiplex PCR with specific primers targeting the cholera toxin gene subunit A, ctxA, and serotype specific primers, O1-rfb and O139-rfb, respectively. Results showed that V. cholerae occurred in approximately 10% (n = 185) of both the environmental samples and isolated bacteria. Eight of the bacteria isolates (n = 43) were confirmed as serogroup O1 while one belonged to serogroup O139, the first reported identification of this epidemic strain in East African coastal waters. All samples identified as serogroup O1 or O139 and a number of non-O1/O139 strains were ctxA positive. This study provides in situ evidence of the presence of pathogenic V. cholerae O1 and O139 and a number of V. cholerae non-O1/O139 that carry the cholera toxin gene in estuaries along the coast of Tanzania.
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| 9. |
- George, Rushingisha, et al.
(author)
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Methane emission and sulfide levels increase in tropical seagrass sediments during temperature stress: A mesocosm experiment
- 2020
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In: Ecology and Evolution. - : Wiley. - 2045-7758. ; 10:4, s. 1917-1928
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Journal article (peer-reviewed)abstract
- Climate change-induced ocean warming is expected to greatly affect carbon dynamics and sequestration in vegetated shallow waters, especially in the upper subtidal where water temperatures may fluctuate considerably and can reach high levels at low tides. This might alter the greenhouse gas balance and significantly reduce the carbon sink potential of tropical seagrass meadows. In order to assess such consequences, we simulated temperature stress during low tide exposures by subjecting seagrass plants (Thalassia hemprichii) and associated sediments to elevated midday temperature spikes (31, 35, 37, 40, and 45°C) for seven consecutive days in an outdoor mesocosm setup. During the experiment, methane release from the sediment surface was estimated using gas chromatography. Sulfide concentration in the sediment pore water was determined spectrophotometrically, and the plant's photosynthetic capacity as electron transport rate (ETR), and maximum quantum yield (Fv/Fm) was assessed using pulse amplitude modulated (PAM) fluorometry. The highest temperature treatments (40 and 45°C) had a clear positive effect on methane emission and the level of sulfide in the sediment and, at the same time, clear negative effects on the photosynthetic performance of seagrass plants. The effects observed by temperature stress were immediate (within hours) and seen in all response variables, including ETR, Fv/Fm, methane emission, and sulfide levels. In addition, both the methane emission and the size of the sulfide pool were already negatively correlated with changes in the photosynthetic rate (ETR) during the first day, and with time, the correlations became stronger. These findings show that increased temperature will reduce primary productivity and increase methane and sulfide levels. Future increases in the frequency and severity of extreme temperature events could hence reduce the climate mitigation capacity of tropical seagrass meadows by reducing CO2 sequestration, increase damage from sulfide toxicity, and induce the release of larger amounts of methane. © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.
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| 10. |
- Gullström, Martin, et al.
(author)
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Seagrass Meadows in Chwaka Bay : Socio-ecological and Management Aspects
- 2012
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In: People, Nature and Research in Chwaka Bay, Zanzibar, Tanzania. - Zanzibar : Western Indian Ocean Marine Science Associoation (WIOMSA). - 9789987955916 ; , s. 89-110
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Book chapter (peer-reviewed)abstract
- The shallow-water seascape of Chwaka Bay consists of diverse habitats including coral reefs, sand/mud flats, algal belts and mangrove forests, but the embayment is primarily characterized by its widespread and highly productive seagrass beds. The Bay is a unique seagrass diversity “hotspot”, with eleven species observed, from small, fast-growing and thin-leaved “pioneer” species like Halophila ovalis and H. stipulacea to large, slower-growing “climax species” with thick and long leaves like Thalassodendron ciliatum and Enhalus acoroides. Consequently, it is not surprising that the small-scale subsistence fishery of Chwaka Bay can be seen as a seagrass fishery, with catches consisting primarily of species intimately associated with the seagrass meadows (de la Torre-Castro and Rönnbäck 2004; de la Torre-Castro 2006).Seagrasses are a polyphyletic group of marine vascular, rhizomal plants (den Hartog 1970, 12-13), which form stands of varying sizes usually called “beds” or “meadows” in intertidal and subtidal coastal waters across the globe. Seagrass meadows typically occur on nearshore soft bottoms (although some species are found on rocky bottoms) in single- or mixed-species assemblages, with the typical wide range from tropical to boreal margins of coastal waters (Green and Short 2003, 21-22). They form one of the most productive aquatic ecosystems on Earth (Duarte and Chiscano 1999) and in most areas occur intermixed with other large primary producers like macroalgae. Seagrass ecosystems support multiple ecological functions, including nursery grounds, food and refuge for many benthic,
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