http://vital.seals.ac.za:8080/vital/access/manager/Index ${session.getAttribute("locale")} 5 http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53880 Wed 27 Jul 2022 11:35:40 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51448 Wed 25 May 2022 12:59:02 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51441 Wed 25 May 2022 12:14:55 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58953 Wed 23 Nov 2022 15:34:31 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58924 Wed 23 Nov 2022 14:34:54 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58888 Wed 23 Nov 2022 11:42:27 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:52344 Wed 22 Jun 2022 12:41:15 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:50008 Wed 20 Jul 2022 12:45:32 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51913 Wed 19 Oct 2022 09:27:41 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54939 Wed 17 Aug 2022 14:39:15 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54946 Wed 17 Aug 2022 14:34:11 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54941 Wed 17 Aug 2022 13:03:29 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60229 Wed 14 Dec 2022 11:59:40 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60218 Wed 14 Dec 2022 09:29:08 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58248 Wed 13 Mar 2024 14:33:10 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:57870 Wed 13 Mar 2024 14:09:53 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58189 Wed 13 Mar 2024 09:44:06 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:65718 Wed 12 Jul 2023 09:09:50 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54560 Wed 10 Aug 2022 18:28:20 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54559 Wed 10 Aug 2022 17:47:17 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54558 Wed 10 Aug 2022 16:59:25 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54554 50 y), global environmental datasets and innovative meta-analyses, building deep knowledge of regional bio-physical dynamics and responses to specific perturbed states remains an essential component of the collective effort. Algoa Bay, situated on the warmtemperate south-east coast of South Africa presents a unique opportunity to study key elements of plankton ecology relevant to climate change problems in the regional sense. The embayment is locally subjected to frequent wind-driven upwelling and regionally, to periodic mesoscale oceanographic forcing (e.g., large solitary meanders, Agulhas Current intrusions), all of which culminate in a complex physical and biogeochemical environment. Using zooplankton as the focal component and drawing from a multi-year monthly dataset incorporating a bay-scale sampling framework, the present study addressed three key hypotheses pertaining to 1) drivers of spatio-temporal variability, 2) biomass rate of change over temporal scales using time-series analyses, and 3) community responses to a bay-scale biological perturbation event. Zooplankton biomass exhibited prominent seasonal patterns with bimodal peaks corresponding with near-consistent year-to-year autumn and spring blooms. Overall, the spatial trend showed no heterogeneity, though statistical significance between-station variability was noted per season. An analytical framework involving generalised additive models revealed zooplankton spatial heterogeneity in Algoa Bay to be a function of seasonal variation in a suite of physicochemical variables, including the combined effects of temperature, salinity, dissolved oxygen, total nitrogen and silicate, but not ammonium, phosphate or chlorophyll-a (as proxy for phytoplankton). Fronts (including river plumes), warm water intrusion from the Agulhas Current, and wind-driven upwelling were postulated to be key driving forces. Structural breaks analysis performed on station-specific time series revealed significant incremental increases in zooplankton biomass over time, which in turn, corresponded with a gradual decrease in thermocline depth. The most pronounced increasing effect was associated with a period (2013– 14) of amplified land-derived nutrient input and increasing harmful algal bloom (HAB) activity.]]> Wed 10 Aug 2022 15:58:07 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58280 Wed 09 Nov 2022 13:52:34 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58279 Wed 09 Nov 2022 12:17:41 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58275 Wed 09 Nov 2022 11:17:34 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58273 Wed 09 Nov 2022 11:03:22 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58267 Wed 09 Nov 2022 09:09:59 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58265 Wed 09 Nov 2022 08:33:02 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51916 Wed 08 Jun 2022 12:18:05 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51915 Wed 08 Jun 2022 11:29:12 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51914 Wed 08 Jun 2022 10:33:05 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:72805 Tue 28 May 2024 12:33:16 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:52594 Tue 28 Jun 2022 13:27:44 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:62032 Tue 28 Feb 2023 15:43:36 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:65790 Tue 25 Jul 2023 16:09:04 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58186 Tue 22 Nov 2022 16:08:32 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58217 Tue 22 Nov 2022 16:01:03 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53407 Tue 19 Jul 2022 22:34:00 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53404 Tue 19 Jul 2022 17:36:59 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:50002 Tue 19 Jul 2022 15:47:40 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53383 Tue 19 Jul 2022 14:26:06 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60126 Tue 13 Dec 2022 10:57:08 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58254 Tue 08 Nov 2022 15:26:06 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58232 Tue 08 Nov 2022 14:13:24 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58231 Tue 08 Nov 2022 12:01:46 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58228 Tue 08 Nov 2022 09:19:39 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58227 Tue 08 Nov 2022 08:41:34 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:56013 Tue 06 Sep 2022 14:34:13 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:55973 Tue 06 Sep 2022 12:46:23 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:55956 Tue 06 Sep 2022 12:08:04 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:52755 Tue 05 Jul 2022 15:13:11 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58187 Thu 29 Jun 2023 11:01:03 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:57758 Thu 27 Oct 2022 15:47:39 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58996 Thu 24 Nov 2022 15:16:25 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58984 Thu 24 Nov 2022 14:04:34 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58975 Thu 24 Nov 2022 12:17:22 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58970 Thu 24 Nov 2022 09:44:32 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60246 Thu 15 Dec 2022 11:40:39 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60245 85% HRpeak compared to the 52% and 78% spent at >85% HRpeak during the INTER test and the Dynamic Yo-Yo test respectively. The INTER test produced a greater number of statistically significant correlations with the combined matches compared to the Dynamic Yo-Yo test. When identifying the differences between the variables measured in the INTER test and the Dynamic Yo-Yo test, it was identified that there were many significant differences. Conclusions: Both the Dynamic Yo-Yo and the INTER test can be used by hockey coaches. However, the researcher would recommend the utilisation of the INTER test, because it displayed stronger, more significant correlations to match-play. The set-up of the INTER test is also more convenient as it can be conducted on the astro turf. While, both tests did have some correlations to match-play, additional tests would need to be included in a testing battery to provide coaches with complete profiles of the players in order to assist in team selections.]]> Thu 15 Dec 2022 10:57:51 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60244 Thu 15 Dec 2022 10:12:13 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:49991 Thu 14 Jul 2022 16:50:43 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:64756 Thu 11 Jan 2024 18:00:54 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51988 40) individually, using logistic regression. A strong linear relationship between dNBR and stem fire severity (r2 = 0.69, p < 0.001) confirmed the accuracy of dNBR as a measure of fire severity in Afrotemperate forest. In the fire investigated, 4 628 ha of Afrotemperate forest burnt of which 67% burnt at low severity, 21% at medium severity and 12% at high severity. The dNBR values associated with fire severity categories were comparable between Afrotemperate and North American forests, suggesting that dNBR values are relatively standard across forest types. Information on the distribution of fire severity facilitates investigation of further questions regarding past and future fire regimes and the fire ecology of Afrotemperate forest. The post-fire survival rate of Afrotemperate forest trees was 45% which is comparable to that in coniferous forests of North America but lower than that in temperate forests of Australia and Portugal and the neighbouring dune thicket which shares several species with Afrotemperate forest. Fire severity had a significant negative effect on survival and tree size a significant positive effect. Total variance explained by the model (for species collectively) was 40.8%, of which fire severity and tree size combined explained 13.2%, and species as random factor, 27.6%. Respective tree species showed differential survival responses – four species showed high survival (> 60% of individuals), while five species showed low survival (< 40%). This study was the first post-fire assessment of the resprouting ability of Afrotemperate forest trees and a third of the trees surveyed (for species collectively) resprouted from the stem. This suggested that resprouting from the stem is a primary means of post-fire recovery in Afrotemperate forest trees, in contrast with previous assertions that several common canopy species, including Podocarpus latifolius, Afrocarpus falcatus, Scutia myrtina, Scolopia mundii and Rapanea melanophloeos, are unable to resprout. Varying resilience to fire among species supports previous suggestions that fire affects species’ composition and diversity in these forests and calls for careful management of fire regimes in the face of global change.]]> Thu 09 Jun 2022 16:02:39 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:59929 Thu 08 Dec 2022 11:38:02 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58075 Thu 03 Nov 2022 15:47:07 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58073 Thu 03 Nov 2022 15:26:47 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58064 Thu 03 Nov 2022 13:41:48 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58059 Thu 03 Nov 2022 12:17:47 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:70246 Sun 21 Jan 2024 14:10:03 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54399 Sat 06 Aug 2022 22:47:34 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54398 1000 cell m L-1 ) of H. akashiwo was present during all but the winter months in the poly- to mesohaline zone, yet it peaked in warmer spring/summer months with a density of ca. 70 000 cell m L-1 corresponding to 800 µg Chl-a L -1 . This species significantly altered the estuary's water quality, causing supersaturated surface- and hypoxic bottom-water during severe HABs or referred to as hypereutrophic bloom phases (> 60 µg Chl-a L -1 ). Despite these changes, the common copepod, Pseudodiaptomus hessei, occurred at similar densities among HAB phases and responded to similar triggers to the HAB. However, a shift in predator-prey interactions within the zooplankton community was evident, with scavenger or opportunist species such as the isopod, Cirolana fluviatilis, and the polychaete, Perinereis falsovariegata, occurring at higher densities during hypereutrophic bloom phases. The overall abundance of juvenile and small adult fishes were high during HABs, but the diversity decreased during HABs. Some species, notably the Mugilidae occurred at lower densities during HABs. Mugilidae also had pronounced histological gill alterations and a lowered proportion of secondary lamellae available for gas exchange during an in situ cage experiment where fishes were isolated inside and outside the HAB. Deformities such as tumorous growths were also found for the first time in a South African Estuary. This indicated a stressed population of Mugilidae in the Sundays Estuary. The ubiquitous mugilid, Mugil cephalus, actively avoided HABs during an acoustic telemetry study, despite having a home range that overlapped the HAB area. Tagged individuals mostly occupied areas directly above the HAB in the upper mesohaline to lower oligohaline zones and only iv briefly transitioned through the HAB area to utilise the lower reaches of the estuary. Since the formation of HABs is reliant on various factors, including specific species responses, environmental variables, nutrient enrichment, and flow characteristics, the impacts of HABs on estuarine communities may vary between estuarine systems or affected species. Therefore, more research that focuses on the impacts of HABs on estuaries is needed to limit the potential loss of ecosystem services. Particularly in light of further unsustainable development, upstream freshwater abstraction and climate change, will cause more frequent and severe HABs, that may result in fish population declines in the long-term. Better management and mitigation strategies are needed to reduce HAB formation such as reducing nutrient enrichment and restoring natural freshwater flow and flooding events to the Sundays Estuary.]]> Sat 06 Aug 2022 22:03:17 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:71963 Sat 06 Apr 2024 14:59:11 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:49971 Sat 01 Jul 2023 15:28:05 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:57635 40) individually, using logistic regression. A strong linear relationship between dNBR and stem fire severity (r2 = 0.69, p < 0.001) confirmed the accuracy of dNBR as a measure of fire severity in Afrotemperate forest. In the fire investigated, 4 628 ha of Afrotemperate forest burnt of which 67% burnt at low severity, 21% at medium severity and 12% at high severity. The dNBR values associated with fire severity categories were comparable between Afrotemperate and North American forests, suggesting that dNBR values are relatively standard across forest types. Information on the distribution of fire severity vi facilitates investigation of further questions regarding past and future fire regimes and the fire ecology of Afrotemperate forest. The post-fire survival rate of Afrotemperate forest trees was 45% which is comparable to that in coniferous forests of North America but lower than that in temperate forests of Australia and Portugal and the neighbouring dune thicket which shares several species with Afrotemperate forest. Fire severity had a significant negative effect on survival and tree size a significant positive effect. Total variance explained by the model (for species collectively) was 40.8%, of which fire severity and tree size combined explained 13.2%, and species as random factor, 27.6%. Respective tree species showed differential survival responses – four species showed high survival (> 60% of individuals), while five species showed low survival (< 40%). This study was the first post-fire assessment of the resprouting ability of Afrotemperate forest trees and a third of the trees surveyed (for species collectively) resprouted from the stem. This suggested that resprouting from the stem is a primary means of post-fire recovery in Afrotemperate forest trees, in contrast with previous assertions that several common canopy species, including Podocarpus latifolius, Afrocarpus falcatus, Scutia myrtina, Scolopia mundii and Rapanea melanophloeos, are unable to resprout. Varying resilience to fire among species supports previous suggestions that fire affects species’ composition and diversity in these forests and calls for careful management of fire regimes in the face of global change.]]> Mon 31 Oct 2022 14:43:48 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:59066 Mon 28 Nov 2022 11:13:57 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:59052 Mon 28 Nov 2022 10:22:45 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:59003 Mon 28 Nov 2022 09:20:46 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53334 Mon 18 Jul 2022 14:17:35 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53331 Mon 18 Jul 2022 13:27:35 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:52017 Mon 13 Jun 2022 12:24:52 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60121 Mon 12 Dec 2022 14:51:48 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60097 Mon 12 Dec 2022 11:56:48 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:60084 Mon 12 Dec 2022 10:58:12 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:65373 Mon 08 Jan 2024 12:35:40 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58218 0.05). The dietary effects of PPPM supplementation on growth performance, digestibility, carcass, and organ weight indices of Cobb 500 birds were determined. The POSCON diet enhanced (p < 0.05) feed conversion ratio (FCR) at week 3. The average final body weight and average daily weight gain were highest (p < 0.05) in birds fed PPPM2 and PPPM4 diets, whereas birds fed PPPM2 diet had enhanced (p < 0.05) FCR and protein efficiency ratio when compared with birds on POSCON. Thigh and breast weights were highest (p < 0.05) in birds on PPPM4 and PPPM8 diets, whereas birds fed PPPM4 diet had enhanced (p < 0.05) nutrient digestibility compared with those on POSCON. The antioxidant status and breast meat quality of Cobb 500 broiler birds fed diets supplemented with PPPM were determined. Meat from birds fed PPPM8 diet had the highest (p < 0.05) thawing loss, while cooking loss was lowest (p < 0.05) in the PPPM2 group. The highest (p < 0.05) ability to scavenge ABTS [(2, 2-azinobis (3ethylbenzothiazoline-6 sulfonic acid))] radical cation (ABTS+) was recorded in the PPPM2 and PPPM4 meat while PPPM8 meat had increased (p < 0.05) catalase activity. The fatty acid composition, oxidative status, and drip loss in breast meat of Cobb 500 broiler birds fed graded levels of PPPM was determined. Meat from birds fed PPPM4 diet had the lowest (p < 0.05) margaric (C17:0) and arachidic (C20:0) acids, while meat from birds fed PPPM8 diet had higher (p < 0.05) levels of eicosadenoic (C20:2, n-6) and arachidonic (AA, 20:4) acids. The POSCON had higher (p < 0.05) ability to reduce TBARS levels in meat on day-1 and day-16 of storage than the NEGCON and PPPM diets, whereas TBARS levels were lowest (p < 0.05) in PPPM6 meat on day-16. The gut pH, histology, haematology, serum-biochemical indices, and bone quality parameters of Cobb 500 broiler birds fed diets supplemented with PPPM was determined. Birds fed POSCON, PPM2 and PPPM4 diets had the lowest (p < 0.05) pH in the duodenum, jejunum, and caecum, whereas duodenal pH values were lowest (p < 0.05) in birds fed PPPM2 and PPPM4 diets compared with birds on NEGCON. Birds fed PPPM4 diet had the highest (p < 0.01) duodenal, jejunal and ileal villi height (VH), and the highest (p < 0.01) VH to crypt depth (CD) ratio in the duodenum, jejunum, and ileum. The lowest (p < 0.05) CD in the duodenum, jejunum and ileum was also recorded in birds fed PPPM4 diet. Birds fed PPPM8 diet had higher (p < 0.05) values for white blood cell count, red blood cell count, haemoglobin concentration and packed cell volume, whereas the lowest (p < 0.05) concentration of serum aspartate transaminase was recorded in birds fed PPPM4 diet. Birds on PPM4 diet had longer (p < 0.05) bones. Bone weight and bone breaking strength were highest (p < 0.05) in birds fed PPPM8 diet. Tibia zinc and iron concentrations increased as the inclusion levels of pomegranate peel powder meal increased. It was concluded that broiler birds require 4 g/kg pomegranate peel powder for enhanced growth performance, nutrient digestibility, gut histology, quality, and antioxidant enzyme activity of meat, whereas 8 g/kg pomegranate peel powder meal supplementation is required for enhanced heamato-biochemical indices, bone quality, fatty acid composition and lipid peroxidative parameters in broiler birds.]]> Mon 07 Nov 2022 15:47:45 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58223 Mon 07 Nov 2022 15:26:26 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58200 Mon 07 Nov 2022 14:17:57 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58195 Mon 07 Nov 2022 12:51:52 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58193 Mon 07 Nov 2022 11:40:14 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58191 Mon 07 Nov 2022 11:07:45 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58188 Mon 07 Nov 2022 09:58:44 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58054 Mon 07 Nov 2022 09:29:41 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58094 Mon 07 Nov 2022 08:27:46 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58180 Mon 07 Nov 2022 08:24:03 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:59002 Fri 25 Nov 2022 09:23:34 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:54395 Fri 15 Mar 2024 12:10:52 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:53410 Fri 15 Mar 2024 12:05:51 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:51996 Fri 10 Jun 2022 11:50:14 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:59979 Fri 09 Dec 2022 10:50:52 SAST ]]> http://vital.seals.ac.za:8080/vital/access/manager/Repository/vital:58102 Fri 04 Nov 2022 10:46:37 SAST ]]>