Some elements of the arthropod fauna of the soil in South Africa
- Authors: Farquhar, M J
- Date: 1947
- Subjects: Uncatalogued
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10962/193691 , vital:45386
- Description: In a paper entitled "Bacteria of the Soil", Dr. Russell of Rothamsted is quoted as saying, ”The top six lashes might almost be called a separate world? 80 great is the number and variety of its inhabitants”• It is with a few forms belonging to this enormous biological complex that the author intends to deal, viz*, representatives of the Orders Pauropoda, Symphyla, Protura, Coleoptera and Hemiptera. Time does not permit the inclusion of a study of the multitude of Arthropod, species that occur in the soil, but a more complete work on these soil groups is intended in the future. McCullogh and Hayes (1922,p.288) state that the soil is an integral factor In the study of biological problems. Hence an understanding of the organic life of the soil, which is of great importance in relation to the other aspects of pedology, is a necessary adjunct to the study of the soil ae a whole. , Thesis (MSc) -- Faculty of Science, Botany, 1947
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- Date Issued: 1947
Thicket expansion in a vachellia karroo-dominated landscape and its effect on herbaceous communities
- Authors: Khoza, Marina Rindzani
- Date: 2022-04-06
- Subjects: Savanna ecology South Africa , Forbs South Africa , Grasslands South Africa , Herbaceous plants South Africa , Vegetation dynamics South Africa , Forest canopies South Africa
- Language: English
- Type: Academic theses , Master's theses , text
- Identifier: http://hdl.handle.net/10962/291015 , vital:56808
- Description: Grass and forb species found in savannas are highly diverse, contributing to the structure and function of the savanna system. Where mean annual rainfall is seasonal and high enough to support closed canopy vegetation such as forests or thickets, savannas can exist as an alternative stable state maintained by disturbances such as fire and browsing. Biotic and abiotic processes act on savanna and forest (or thicket) systems maintaining both their tree and herbaceous cover at levels that ensure their persistence in those states. Studies have shown that many semi-arid rangelands in South Africa have undergone a rapid increase in tree cover (of both native and non-native species) over the past several decades. This process of increasing tree cover in semi-arid savannas, termed bush encroachment, results in a biome shift, changing landscapes that were once grasslands with few trees to ones dominated by broad-leaved trees with fewer sun-adapted forbs and grasses. The aim of this study was to investigate the impact of changing woody cover and its associated changes in tree composition, tree canopy structure, light dynamics in the understory and herbaceous community composition on Endwell farm in the Eastern Cape. Canopy cover changes between the years 1949 and 2019 were analysed at 51 sites on the farm and related to historical rainfall patterns. There had been a general increase in tree cover over the past several decades on the farm, and many sites showed a change from open (0-15%) in 1949 to low (1635%), moderate (36-50%) and high (51-100%) canopy cover in 2019. In earlier years most sites had a canopy cover below 50%, and the higher canopy cover values (>65%) occurred in more recent decades. Canopy cover of ~ 50% was found to be rare in each decade. This suggests that ~50% canopy cover maybe a transient, unstable state. The period with the highest rate of canopy cover increase was 2002-2013, and this increase coincided with a high mean annual rainfall 10 years prior to 2002 and a high mean annual rainfall in most years between the 20022013 period. The period between 2002 and 2013 also had the highest number of sites transitioning from lower to higher tree canopy cover classes, indicating that rainfall may have been a factor driving bush encroachment during the past several decades. An increase in canopy cover (a decrease in light transmittance) was accompanied by changes in woody species composition during thicket formation. The low canopy cover (high light transmittance) sites were dominated by Vachellia karroo and Scutia myrtina trees, while high tree cover sites had fewer V. karroo and S. myrtina trees and were rather characterised by an abundance of thicket tree species. Species proportion, NMDS and dendrogram plots indicated that sites with a light transmittance range between 50-100% had similar tree species compositions, different from sites with light transmittances <50%. An increase in tree density was strongly correlated to an increase in canopy cover (from 2019 satellite imagery), density of trees > 3m, maximum height reached by trees, diversity of trees, total canopy volume, total canopy area and leaf area index (LAI), and a decrease in light transmittance. A structural equation model (SEM) was used to explore the relationships between canopy characteristics (maximum canopy area, canopy volume, tree diversity, density of trees, density of trees >3m, individual trees and maximum canopy height), aerial canopy cover in 2019, and light transmittance. The model explained 73% of the variation in light transmittance, mostly via the direct effect of canopy characteristics. Canopy characteristics had a strong influence on both aerial cover in 2019 and directly on light transmittance, but canopy cover in 2019 had a weak influence on light transmittance. The herbaceous layer was rich and dominated by C4 grasses such as Eragrostis plana, Sporobolus fimbriatus, Themeda triandra and Digitaria eriantha) and forbs including Hibiscus aethiopicus, Helichrysum dregeanum, Helichrysum nudifolium and Gerbera viridifolia at low canopy cover sites with high light transmittance. In contrast, high tree cover sites had fewer herbaceous species in general. Grass and forb species characteristic of these sites high canopy cover sites were Panicum maximum, Loudetia flavida, Pellaea viridis and Cyperus spp. Different sites with low light transmittance (<50%) had similar herbaceous species composition. Basal cover, richness, abundance and diversity of herbaceous plants decreased significantly with an increase in tree density, density of trees >3 m, canopy volume, canopy area, canopy cover, LAI, and increased significantly with increasing light transmittance. Most grasses had their highest densities at LAI <0.5, which was estimated to correspond to ~75% light transmittance and ~38% canopy cover and then started to decline thereafter. Herbaceous species basal cover was also highest at LAI <0.5. An SEM model indicated that herbaceous diversity, basal cover and richness responded both to light availability and to the structure of the woody vegetation directly (R2 = 0.53). While the effect of light transmittance on herbaceous communities was strong (0.41), there was little difference between the effect of light transmittance and canopy characteristics (-0.35) on herbaceous communities. Two possible threshold points, relating to two types of transitions in vegetation structure, could be deduced from this study. The first threshold occurred at canopy cover ~ 40% (LAI < ~ 0.5, light transmittance ~ 75%), at which point many of the common herbaceous species, including the dominant C4 grasses, began to decline in abundance while the composition remained characteristic of the savanna state. A canopy cover of less than ~ 40% at a site provides a suitable state for a high abundance of grass and forb species which help maintain an open system by facilitating fires. The second threshold marked a compositional shift between savanna and closed-canopy vegetation states. Savanna species (trees, grasses and forbs) dominated at high light transmittances (>50%) and were significantly reduced at low light transmittances (< 50%), indicating a possible species composition threshold at ~50% light transmittance at which a savanna state switches to a thicket (LAI ~ 1 and canopy cover ~70%). This point indicated the point where there was a significant difference in both tree and herbaceous plant compositions, with a marked reduction in the occurrence of C4 grasses at light transmittance <50%. Fire is supressed when the C4 grass layer is lost, and further thicket encroachment will take place causing complete canopy closure. Land managers in this system should start becoming concerned about a reduction in grass biomass when canopy cover reaches about 40% and would have to reduce tree cover before the threshold of 50% light transmittance (70% canopy cover from aerial photos) is reached to maintain a savanna system. , Thesis (MSc) -- Faculty of Science, Botany, 2022
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- Date Issued: 2022-04-06
Population dynamics, fire, and reproductive ecology of Oldenburgia grandis (Asteraceae), an unusual fynbos tree endemic to the Eastern Cape
- Authors: Mostert, Emma Charlotte
- Date: 2022-10-14
- Subjects: Uncatalogued
- Language: English
- Type: Academic theses , Master's theses , text
- Identifier: http://hdl.handle.net/10962/365268 , vital:65722
- Description: Thesis embargoed. Possible release date set for early 2024. , Thesis (MSc) -- Faculty of Science, Botany, 2022
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- Date Issued: 2022-10-14
The process of thicket encroachment in semi-arid savanna: community patterns and biotic interactions
- Authors: Nell, Rhys
- Date: 2022-10-14
- Subjects: Scrub encroachment , Savanna ecology , Biotic interaction , Plant nutrients , Plant-water relationships
- Language: English
- Type: Academic theses , Master's theses , text
- Identifier: http://hdl.handle.net/10962/364966 , vital:65666
- Description: Bush encroachment in savannas is widespread in South Africa and is concerning, from both socio-economic and conservation viewpoints, as it affects ecosystem services, functioning and productivity. This phenomenon depends on multiple factors such as history, vegetation, management and environmental conditions, and their interplay. Encroachment into savannas has been relatively well-documented, however understanding of the different roles of tree-tree interactions between species that occur during this process is still limited. This includes the interactions causing spatial patterning, or how interactions and outcomes change over time in terms of encroachment succession from open savanna to closed-canopy thicket. The main objectives of this research are to document thicket establishment in a savanna ecosystem and consider the ecological roles of the key woody species and the abiotic properties of their micro-sites. Determining interactive effects of species co-occurrence is critical to understanding or predicting patterns and changes in biodiversity, nutrient distribution and available water resources. It is also imperative in determining correct and effective land management practices, particularly for reducing bush encroachment and its negative effect on rangelands. All data were collected on Endwell farm, located in the Smaldeel region of the Eastern Cape, South Africa. Endwell farm is a semi-arid savanna with a mean annual rainfall of 730 mm. First, I examine and describe the thicket encroachment process by exploring the associations between species and their size classes in the field. This was done by using plot-based belt transects and looking at changes in species size-class compositions from early to late successional stages. Association rules (market basket) analysis was used to identify the most common species size-class association patterns. The association between the savanna tree Vachellia karroo and the thicket pioneer Scutia myrtina was the most prevalent at all stages, with V. karroo being central to all associations in the first stage of encroachment; during later stages of encroachment, associations shift to incorporating other thicket pioneer species. The demography and clump formation of S. myrtina was strongly linked to associations with V. karroo to initiate bush clump formation. Results suggest that mature V. karroo facilitate the establishment and growth of S. myrtina. These two species were the focus of more detailed investigations to explore the nature and magnitude of their interspecific interactions. I then examined the effects of pairwise tree interactions between V. karroo and S. myrtina on soil and leaf nutrient content. I measureddifferences betweeninter-canopy and sub-canopy soil nutrient content, and the effect of associations on plant leaf nutrients, between pair-size combinations and individual controls. Results confirmed that pair-size tree interactions affected both soil nutrient and leaf nutrient content. All individuals increased soil K, N and organic C in the sub-canopy, while association with V. karrooincreased S. myrtinafoliar N, Pand K. In contrast, association with S. myrtinaloweredV. karroofoliar N, P and K. Small S. myrtina individuals werefound to benefit most from establishing and growing next to a large V. karroo individual, through mechanisms affecting soil and foliar nutrients. Scutia myrtina individuals establishing in association with smaller size classes of V. karroo showed no significant effects. I tested for positive and negative effects of pairwise tree interactions between Vachellia karroo and Scutia myrtina on available soil water and plant water potential (Ψ). This was done by looking at differences betweeninter-canopy and sub-canopy soil moisture and bulk density and associations on plant water stress (pre-dawn and mid-day leaf Ψ), between pair-size combinations and individual controls. I also selectively removed large V. karroo individuals from pairs to confirm the effects of competition andfacilitation. Similar to other studies, results confirmed positive and negative effects of pairwise tree interactions. Small S. myrtina individuals weremost facilitated by establishing and growing up next to a large V. karroo individual, through mechanisms affecting soil water content, bulk density and leaf Ψ. Scutia myrtina establishing in association with other size classes of V. karroo were much less facilitated, showing no significant effects. In contrast, large S. myrtina showed competitive interactions with V. karroo. , Thesis (MSc) -- Faculty of Science, Botany, 2022
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- Date Issued: 2022-10-14
The effects of short-duration overnight kraaling on herbaceous vegetation and soils in mesic grassland
- Authors: Mgwali, Nompendulo
- Date: 2023-10-13
- Subjects: Uncatalogued
- Language: English
- Type: Academic theses , Master's theses , text
- Identifier: http://hdl.handle.net/10962/424721 , vital:72178
- Description: Land degradation is widespread in communal rangelands in the grassland biome of South Africa, and often attributed to overstocking and lack of coordinated management. Excessive pressure on the herbaceous component has contributed to the uncontrolled spread of opportunistic invasive alien woody species e.g. Acacia mearnsii in many degraded areas, resulting in significant loss of ecosystem service capacity, along with soil and land productivity. Short-duration overnight kraaling has been suggested as a tool for restoring degraded rangelands. Recent studies in semi-arid savannas and shrublands have reported increased grass cover, soil nutrients and palatability and concluded that short-duration kraaling is a low-cost and effective way of restoring degraded rangelands using livestock. However, the response of different plant functional types and communities to such intense livestock impact may vary depending on local context. This study used twelve paired kraal and control sites to investigate the effects of short-duration (7-24 days) overnight kraaling of livestock on herbaceous vegetation and soils in a mesic grassland. The study area is generally considered to be overgrazed but has considerable variation in grass composition and basal cover. Sites included relatively intact natural grassland and sites where wattle infestations had been cleared and where mostly bare ground remained. I tested the hypotheses that overnight kraaling would result in (1) increased basal cover due to introduction of grass seed and stimulation of germination through hoof action, (2) increased infiltration due to hoof action, and (3) increased soil nutrients and organic matter due to dung and urine deposition. I also hypothesized that factors such as a site’s initial grass cover, its slope, the occurrence and amount of rainfall before and during kraaling, and the kraaling intensity (number of livestock and duration of the kraaling event) would influence the magnitude and direction of the kraaling effect. The effect of kraaling on vegetation was strongly dependent on initial condition. Kraaling increased basal cover of grasses when sites had low initial basal cover, but decreased basal cover if initial values were over 50%. Infiltration increased if kraaling took place during or after rain but decreased if kraaling took place when soils were dry. Kraaling increased soil P and K. In mesic grasslands, short-duration overnight kraaling is promising as a tool for rehabilitating degraded sites but should be avoided where the grass sward is relatively intact. I recommend that the suitability of kraaling be further evaluated per vegetation type and local context. , Thesis (MSc) -- Faculty of Science, Botany, 2023
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- Date Issued: 2023-10-13