https://commons.ru.ac.za/vital/access/manager/Index ${session.getAttribute("locale")} 5 Ecological interactions on a rocky shore : the control of macroalgal distribution by intertidal grazers https://commons.ru.ac.za/vital/access/manager/Repository/vital:5665 Wed 21 Jul 2021 13:46:25 SAST ]]> Testing the existence and direction of "spill-over" of mussel recruits beyond the boundaries of marine protected areas https://commons.ru.ac.za/vital/access/manager/Repository/vital:5786 Wed 12 May 2021 22:53:05 SAST ]]> The effects of the invasive mussel mytilus galloprovincialis and human exploitation on the indigenous mussel Perna perna on the South Coast of South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:5684 Wed 12 May 2021 22:44:38 SAST ]]> Growth, feeding and sex change in the sequential protandric shrimp Nauticaris marionis Bate 1888 at the Prince Edward Islands (Southern Ocean) https://commons.ru.ac.za/vital/access/manager/Repository/vital:5704 7mm) were equivalent to ≈10% and ≈5% of body dry weight, respectively. The von Bertalanffy growth curve parameters were empirically identified, by cohort analysis of data collected during 4 years, as K = 0.22239/year, L[subscript]∞ = 14.05789mm, t₀ = -0.05174, L₀ = 0.16083mm. N. marionis can survive up to seven years under natural conditions.]]> Wed 12 May 2021 22:28:01 SAST ]]> Effects of small-scale water movement on the settlement and growth rates of the brown mussel Perna perna, on the south-east coast of South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:5682 Wed 12 May 2021 19:55:48 SAST ]]> Effects of zone and wave exposure on population structure and recruitment of the mussel (Perna perna) in South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:5685 l5mm) were calculated as real densities from randomly placed quads i.e. not from areas of 100% cover. Density decreased up the shore; low, mid and high shore zones were significantly different from each other (ANOVA , p<0.0001; followed by multiple range tests). There was no significant difference between the densities of mussels at exposed and sheltered sites within each zone (ANOVA, p=0.7155). Recruit ( Wed 12 May 2021 19:52:56 SAST ]]> Penguin parenting : assortative mating, nest attendance and sex-specific chick provisioning in the African Penguin (Spheniscus demersus) https://commons.ru.ac.za/vital/access/manager/Repository/vital:5943 Wed 12 May 2021 19:50:45 SAST ]]> The trophic ecology of parrotfish of Zanzibar application of stable isotope analysis https://commons.ru.ac.za/vital/access/manager/Repository/vital:5789 Wed 12 May 2021 19:18:34 SAST ]]> Mesoscale mechanisms of larval transport and settlement in relation to physical factors off the south coast of South Africa: a topographic approach https://commons.ru.ac.za/vital/access/manager/Repository/vital:5947 Wed 12 May 2021 19:05:52 SAST ]]> Population dynamics and growth rates of the brown mussel (Perna perna) on wave exposed and wave sheltered shores of South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:5741 15 mm) were positively correlated with recruit densities (1-5 mm) for both shore types (p15 mm) was significantly lower on exposed (mean of 3 348.m⁻²) than on sheltered shores (mean of 4 796.m⁻²) (pO.05). The effect of exposure on growth rate formed the focal point of this study and was determined using three different approaches. The first technique, mark-recapture, involved filing notches on the growing edges of mussels in the field. After 111 days, mussels were removed and the growth measured. The second approach used internal growth bands to measure growth rates, once the periodicity with which these bands were laid down was established. Thirdly, using Shepherd's length composition analysis (SLCA), growth rates were determined from length frequency distributions in 11 samples taken over 15 months. The general conclusion from all three approaches was that growth rate was twice as fast on the exposed shores as on the sheltered shores (p Wed 12 May 2021 18:40:51 SAST ]]> Interspecific interactions of the sea urchin Parechinus angulosus and the effect of variations in microhabitat availability https://commons.ru.ac.za/vital/access/manager/Repository/vital:5720 Wed 12 May 2021 17:49:53 SAST ]]> Trophic ecology of breeding northern rockhopper penguins, Eudyptes Moseleyi, at Tristan da Cunha, South Atlantic Ocean https://commons.ru.ac.za/vital/access/manager/Repository/vital:5788 90% in the last 130 years), the cause(s)of which are unknown. There is a paucity of data on this species in the South Atlantic Ocean, therefore their trophic ecology at Tristan da Cunha was studied, specifically focusing on diet, using stomach content analysis and stable isotope analysis (SIA), in conjunction with an analysis of diving behaviour, assessed using temperature-depth recorders. In order to evaluate the influence of gender on foraging, a morphometric investigation of sexual dimorphism was confirmed using molecular analysis. Additionally, plasma corticosterone levels were measured to examine breeding stage and presence of blood parasites as potential sources of stress during the breeding season. Northern Rockhopper penguins at Tristan da Cunha displayed a high degree of foraging plasticity, and fed opportunistically on a wide variety of prey, probably reflecting local small-scale changes in prey distribution. Zooplankton dominated (by mass) the diet of guard stage females, whereas small meso-pelagic fish (predominantly Photichthyidae)dominated diet of adults of both sexes in the crèche stage, with cephalopods contributing equally in both stages. Adults consistently fed chicks on lower-trophic level prey (assessed using SIA), probably zooplankton, than they consumed themselves indicating that the increasing demands of growing chicks were not met by adults through provisioning of higher- quality prey. SIA also indicated that adults foraged in different oceanic water masses when feeding for self-maintenance and for chick provisioning, thus temporally segregating the prey consumed for different purposes. It is possible that adults ‘selected’ these higher quality prey for themselves, or this may be a reflection of opportunistic behaviour. At Tristan da Cunha sexual dimorphism was observed in culmen dimensions (length, depth, width), with males having larger beaks and feeding on larger individuals of squid and fish than females. No sexual segregation in terms of foraging habitat (i.e. different water masses, based on ð¹³N or trophic level ð¹⁵N) during the breeding season or pre-moult period was revealed through SIA, and stomach content analysis revealed no sexual differences in prey species targeted. The results of SIA of feathers indicate that during the pre-moult period birds foraged in different water masses than during the breeding period. The fact that throughout the breeding season birds foraged in similar habitats suggests no intra-specific competition, despite both sexes feeding on the same prey.Birds were generally diurnal, daily foragers (12 – 16 hr trips), with extended trips (maximum duration 35.5 hours) and nocturnal diving recorded in a few individuals. Birds dived well within their physiological limits, predominantly utilising the upper 20m of the water column, employing two different strategies to target different prey items. Long, deep (30 – 40 m), energetically costly dives were performed when targeting energy-rich prey (fish), and a greater number of shorter, shallower (5 – 20 m), energy-efficient dives were performed when targeting prey with a lower energy content (zooplankton). More than half of the sampled study population were infected with the intra-cellular blood parasite Babesia, but infection showed no relationship to body mass, corticosterone levels or breeding success. Fasting birds showed no signs of elevated corticosterone levels, suggesting they had acquired sufficient fat reserves prior to breeding. Failed breeders did not exhibit elevated corticosterone levels. Tristan skuas, Catharacta antarctica hamiltoni, were observed to be a significant cause of egg and chick mortality. The absence of sex-based differences in foraging, and the absence of any signs of stress in relation to body mass, presence of Babesia or breeding stage, suggest that there are no obvious signs of high levels of stress or food limitations during breeding at Tristan da Cunha.]]> Wed 12 May 2021 17:44:40 SAST ]]> Population structure, growth and recruitment of two exploited infralittoral molluscs (Haliotis midae and Turbo sarmaticus) along the south east coast, South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:5744 Wed 12 May 2021 17:26:42 SAST ]]> Responses of intertidal macroalgae and associated fauna to interactive processes acting over multiple spatial scales https://commons.ru.ac.za/vital/access/manager/Repository/vital:5890 Wed 12 May 2021 17:16:57 SAST ]]> What limits an invasive biotic and abiotic effects on the distribution of the invasive mussel mytilus galloprovincialis on the South African coastline https://commons.ru.ac.za/vital/access/manager/Repository/vital:5927 Wed 12 May 2021 16:51:18 SAST ]]> A community–wide trophic structure analysis in intertidal ecosystems on the south coast of South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:28392 Thu 13 May 2021 07:14:39 SAST ]]> Ecological engineering on rocky shores: grazing, predation, nutrient availability and their influence on epifaunal communities https://commons.ru.ac.za/vital/access/manager/Repository/vital:20500 Thu 13 May 2021 07:01:36 SAST ]]> Effects of habitat patch size and isolation on the population structure of two siphonarian limpets https://commons.ru.ac.za/vital/access/manager/Repository/vital:5679 Thu 13 May 2021 06:52:07 SAST ]]> Morphometrics and preliminary biology of the caridean shrimp Nauticaris marionis Bate, 1888, at the Prince Edward Islands (South Ocean), 37° 50'E, 46° 45'S https://commons.ru.ac.za/vital/access/manager/Repository/vital:5733 Thu 13 May 2021 06:47:28 SAST ]]> The influence of the physical environment, topography and time on the inshore distribution of invertebrate larvae : a multi-taxon approach https://commons.ru.ac.za/vital/access/manager/Repository/vital:5926 Thu 13 May 2021 06:33:46 SAST ]]> Sand inundation on rocky shores : its effects on species richness and the structure of species assemblages https://commons.ru.ac.za/vital/access/manager/Repository/vital:5814 Thu 13 May 2021 04:51:18 SAST ]]> The trophic ecology of the endangered endemic Barau's Petrel (Pterodroma baraui) from Reunion Island, south-western Indian Ocean https://commons.ru.ac.za/vital/access/manager/Repository/vital:5925 Thu 13 May 2021 04:23:05 SAST ]]> The role of a symbiotic bryozoan in the chemical ecology of a marine benthic predator-prey interaction https://commons.ru.ac.za/vital/access/manager/Repository/vital:5756 Thu 13 May 2021 04:13:04 SAST ]]> Extracellular digestion in two intertidal mussels and the role played by their gut bacteria https://commons.ru.ac.za/vital/access/manager/Repository/vital:5692 Thu 13 May 2021 03:16:35 SAST ]]> Environmental drivers of the composition and distribution of larval fish assemblages off the south coast of South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:29207 Thu 13 May 2021 03:15:17 SAST ]]> Using captive seabirds to assess knowledge gaps in stable isotope analysis of diets https://commons.ru.ac.za/vital/access/manager/Repository/vital:28686 Thu 13 May 2021 03:01:37 SAST ]]> The epibiotic relationship between mussels and barnacles https://commons.ru.ac.za/vital/access/manager/Repository/vital:5847 Thu 13 May 2021 01:12:18 SAST ]]> Mesoscale alongshore and cross-shore transport and settlement of invertebrate larvae on the south east coast of South Africa https://commons.ru.ac.za/vital/access/manager/Repository/vital:31386 Thu 13 May 2021 00:57:15 SAST ]]> The effect of mussel bed structure on the associated infauna in South Africa and the interaction between mussel and epibiotic barnacles https://commons.ru.ac.za/vital/access/manager/Repository/vital:5675 Thu 13 May 2021 00:50:01 SAST ]]> Oxygen limitation and thermal tolerance: a comparison of pulmonate and patellogastropod limpets https://commons.ru.ac.za/vital/access/manager/Repository/vital:21274 slopes> vertical surfaces> tide pools> crevices. The current study found that, while the pulmonate limpets, Siphonaria capensis and S. serrata, preferred rock pools, sloped, vertical and horizontal rock surfaces, the patellogastropod limpets, Cellana capensis and Scutellastra granularis, preferred rock pools and vertical rock surfaces. Furthermore, the pulmonate limpets were only common on horizontal rock surfaces where specific ameliorating conditions would have mitigated thermal stress there. In addition, C. capensis had similar thermal tolerance limits to the pulmonate limpets in air and the pulmonate limpets had similar and/or higher thermal tolerance limits compared to S. granularis in water. This indicates that the pulmonate limpets did not necessarily prefer warmer microhabitats than the patellogastropod limpets and that there were no differences in the collective upper thermal tolerance limits between the two limpet groups in either medium.Consequently, there was no indication from this study that an assumed superior capacity for oxygen supply translates into greater thermal tolerance and that the hypotheses based on the OCLTT were not supported. Although this was an indirect test of the OCLTT theory, I conclude that this study does not support the notion of its general applicability and that mechanisms other than those outlined by the OCLTT theory may help explain the patterns of thermal limitation observed in the current study.]]> Thu 13 May 2021 00:11:29 SAST ]]>