Physiological implications of the bone histology of Syntarsus rhodesiensis (Saurischia: Theropoda)

Femora of Syntarsus rhodesiensis specimens of differing ontogenetic stages were sectioned and prepared for histological study. Features such as the structure of the cortical bone tissue, the degree of vascularisation and haversian substitution, and the general pattern of bone deposition through ontogeny, are described. The question of the bearing of bone histology on interpretation of the probable physiology of Syntarsus is also discussed

Assessing the biology of fossil vertebrates through bone histology

Main articleSoon after death and burial of an animal, the organic components of bone generally decay. The closely associated inorganic components (mainly apatite) are more resilient and even after millions of years of burial, preserve the spatial organisation of the collagen fibres and hence the structure of the bone. In the past fossil bone histology has been the subject of substantial research. Such studies have included a wide array of extinct vertebrates including fishes, amphibians, pelycosaurs, therapsids, ichthyosaurs, pterosaurs, and dinosaurs. The relative rate ofbone formation is indicated by the texture of the fibrillar matrix, while the overall nature of the primary compact bone provides a direct assessment of whether bone deposition was continuous or interrupted. The amount of secondary bone formation depicts the extent of primary bone resorption and subsequent redeposition. In addition, the internal organisation of bone indicates remodelling and relocation processes of growth, including functional adaptations of the bone morphology. Thus, osteohistology reflects ontogeny, growth dynamics, biomechanical adaptations, as well as various events that punctuate the life history of an animal.the Foundation for Research and Development (SA), and by the National Science Foundation (USA)

Growth and life habits of the Triassic cynodont Trirachodon, inferred from bone histology

Growth pattern and lifestyle habits of the Triassic non−mammalian cynodont Trirachodon are deduced from bone histol−ogy and cross−sectional geometry. Several skeletal elements of Trirachodon were examined in order to document histological changes during ontogeny, as well as histovariability in the skeleton. The bone histology of all the elements consists of a moderately vascularized, periodically interrupted, fibro−lamellar bone tissue. This suggests that the overall growth of Trirachodon was probably rapid during the favourable season, but decreased or ceased during the unfavourable season. As the environment is thought to have been semi−arid with seasonal rainfall, it is possible that Trirachodon was sensitive to such environmental fluctuations. Some inter−elemental histovariability was noted where the number and prominence of growth rings varied. Limb bone cross−sectional geometry revealed a relatively thick bone wall and sup−ports earlier proposals that Trirachodon was fossorial

Preparation of fossil bone for histological examination

Palaeo-histology is the branch of palaeontology concerned with the microscopic structure of fossil bone. Researchers entering the field for the first time become aware of a need for a concise description of a technique to prepare thin sections from fossil bone. This note aims to fill that need by describing the procedure used in a recent palaeohistological study (Chinsamy 1988, 1990, 1991, 1992). The technique described has been successfully applied to the bones of dinosaurs and mammal-like reptiles, as well as to archaeological samples ofhuman bone and also to defatted bone of recent taxa. There is no one 'correct' method of making sections of hard tissues like bones, but all existing techniques share a number of core processes in common (Enlow 1954; Enlow and Brown 1956; Honjo and Fischer 1965; Peabody 1961 ; Macfall and Wollin 1972; Buffrenil, Ricqles, Ray and Domning 1990). Although the method described here is specifically intended for use on bone, thin sections of fossilised wood have also been obtained using the same method

Osteohistology and palaeobiology of giraffids from the Mio-Pliocene Langebaanweg (South Africa)

The reconstruction of life history traits, such as growth rate, age at maturity and age at death can be estimated from the histological analysis of long bones. Here, we studied 20 long bones (metapodials, tibia and femora) of Sivatherium hendeyi and Giraffa cf. Giraffa jumae recovered from the Miocene–Pliocene locality of Langebaanweg on the West Coast of South Africa. We analysed the long bone histology and growth marks of juvenile and adult specimens of these taxa. Our results show that bone tissue types and vascular canal orientation varies during ontogeny, as well as between the different skeletal elements, and also across single cross sections of bones. Majority of our specimens appear to be still growing, with only an adult metacarpal of S. hendeyi being skeletally mature as indicated by the presence of an outer circumferential layer. We propose that the growth marks preserved in the cortices of the bones studied are most likely related to multiple catastrophic events as opposed to being annual/seasonal.Fil: Jannello, Juan Marcos. Universidad Tecnológica Nacional. Facultad Regional San Rafael. Instituto de Evolución, Ecología Histórica y Ambiente. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Evolución, Ecología Histórica y Ambiente; ArgentinaFil: Chinsamy, Anusuya. University of Cape Town; Sudáfric

Dicynodont (Therapsida) bone histology: phylogenetic and physiological implications

The bone histology of humeri of a number of taxonomically well established and easily definable dicynodont genera is described and compared. The bone of Aulacephalodon, Cistecephalus, Dicynodon, Endothiodon, Lystrosaurus, Kannemeyeria and Oudenodon consists of alternating fibro-lamellar and lamellated bone tissue, while that of Diictodon consists only of fibro-lamellar tissue. The presence of fibro-lamellar bone in all the genera studied, indicates that the bone was deposited rapidly, but the occurrence of lamellated bone tissue suggests that all the genera except Diictodon, also had intermittent periods of slow growth. This is the first time that a comparative study of bone histology of different dicynodont genera has been attempted by using one particular bone element to standardise intergeneric comparisons

Pathologies in the Early Pliocene phocid seals from Langebaanweg, South Africa

Abundant vertebrate fossils have been recorded from the Early Pliocene locality, Langebaanweg, South Africa. This study documents the pathologies evident in the 5 million-year-old fossil phocid seal assemblage. Careful anatomical assessment of the remains revealed that 0.73% showed evidence of disease and/or trauma. The majority of the ailments were forms of osteoarthritis, although periodontitis and osteomyelitis were also evident. Some bones also showed healed fractures, suggesting that the individuals survived the traumatic event. Two cases of dental pathologies were also noted

Taxonomic and palaeobiological implications of a large, pathological sabretooth (Carnivora, Felidae, Machairodontinae) from the Lower Pliocene of South Africa

Abstract:We describe the most complete postcranialremains of a pathological, large-bodied sabretooth from theLower Pliocene site of Langebaanweg ‘E’ Quarry (SouthAfrica). The skeleton consists of hind limb and vertebral ele-ments that exhibit distinctive exostoses, osteophytes andeburnation. We performed a quantitative morphologicalcomparison of the new postcranial remains found in Lange-baanweg, with other Neogene and Quaternary sabretoothand non-sabretooth felids, consisting of the generaAmphi-machairodus,Machairodus,Lokotunjailurus,Dinofelis,Pan-thera,HomotheriumandSmilodonfrom several sites inAfrica, Europe and North America, using principal compo-nent analysis and Mosimann transformations. Although thepathological deformation of the remains distorted some ofthe linear measurements, most of the analysed variables donot contain pathological features, and strongly indicate thatthe Langebaanweg sabretooth is morphologically closer toMachairodus aphanistusandLokotunjailurus emageritusthanit is toAmphimachairodus giganteus. This indicates that theremains could belong to an undetermined sabretooth speciesfrom the Langebaanweg locality. The observed pathologies inthe foot and lumbar spine are consistent with diagnostic cri-teria for severe osteoarthritis (due to maturity), which wouldhave limited limb mobility with severe consequences forhunting success

South African medicinal orchids : a pharmacological and phytochemical evaluation.

Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2012.The Orchidaceae makes up the largest and most diverse family of flowering plants. Orchids are popular, often expensive ornamentals, with a broad range of ethnobotanical applications. There is very limited documented information on South African medicinal orchid species; no formal pharmacopoeia outlining ethnobotanical uses; and ethnobotanical and distribution records are either scarce or inconsistent and plant populations are becoming gradually smaller. There have been significant developments in medicinal orchid research worldwide with medicinal use and corresponding pharmacological and phytochemical properties being extensively investigated. It is evident from the literature that there is no pharmacological research on South African medicinal orchids; hence the need to explore biological activity and chemical composition of South African medicinal orchid species. The ethnobotanical approach used to select the orchid species for pharmacological and phytochemical research elsewhere, yielded valuable biological compounds. Thus, a similar approach was applied to South African medicinal orchids. There are approximately 20 000 species and 796 genera of orchids distributed across the world. In southern Africa, orchids are widely represented with 55 genera and 494 species. Approximately 75% are endemic to this region. As part of the current investigation a review of available ethnobotanical literature on South African medicinal orchids was prepared. The review revealed that an estimated 49 indigenous orchid species from 20 orchid genera are currently being informally traded and used in South African traditional medicine. They are used primarily for medicinal and cultural purposes, especially by the Zulu community in South Africa. Medicinal uses of orchid species include: treatment of inflammatory, intestinal, neurological and reproductive disorders and emetics are used to cause emesis. Non-medicinal uses of orchid species include: love, fertility, protective and lethal charms. Based on their ethnobotanical uses and endemism, South African orchids were considered to be one of the untapped sources of bioactive compounds that needed to be researched. The current investigation addressed the broader aims of medicinal plant research by determining the efficacy, safety and chemical profile of seven indigenous orchid species used in South African traditional medicine and practices. The biological and toxic effects of orchid plant extracts were assessed using established pharmacological bioassays. The phytochemical evaluation of the seven orchid plant extracts provided insight into the classes of chemical compounds present and their possible role in the observed biological activities. The potential of plant extracts from seven orchid species used in South African traditional medicine, as sources of natural bioactive products, are discussed. The current investigation determined the biological activity and chemical profile of seven orchid species commonly traded in KwaZulu-Natal herbal markets: Ansellia africana Lindl., Bulbophyllum scaberulum (Rolfe) Bolus, Cyrtorchis arcuata (Lindl.) Schltr., Eulophia hereroensis Schltr., Eulophia petersii (Rchb.f.) Rchb.f., Polystachya pubescens (Lindl.) Rchb.f. and Tridactyle tridentata (Harv.) Schltr. Well established in vitro micro-dilution bioassays were used to determine the antibacterial, antifungal, anthelmintic activities of crude orchid extracts. A minimum inhibitory and/or lethal effect of organic and aqueous crude orchid extracts was observed against Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, Candida albicans and Caenorhabditis elegans. Tridactyle tridentata aqueous root extract produced the most effective antibacterial activity against S. aureus (0.049 mg/ml). All T. tridentata organic root extracts produced significant inhibitory activities against B. subtilis and S. aureus. Eulophia petersii DCM pseudobulb extracts significantly inhibited all bacterial strains tested (0.39 mg/ml against S. aureus and 0.78 mg/ml against B. subtilis, E. coli, and K. pneumoniae). Eulophia hereroensis 80% EtOH root extract was the only other extract to exhibit significant inhibitory effects against K. pneumoniae (0.65 mg/ml). After 48 h C. albicans was most susceptible to P. pubescens aqueous pseudobulb extract (0.0816 mg/ml). Eulophia petersii DCM pseudobulb extract however, exhibited significant activity against C. albicans (0.65 mg/ml) over 72 h. Cyrtorchis arcuata leaf and root extracts were the most effective anthelmintic extracts with MLCs of 0.041 mg/ml for 80% EtOH leaf and root extracts; 0.049 mg/ml for aqueous leaf extracts and 0.78 mg/ml for aqueous and DCM root extracts. Caenorhabditis elegans was most susceptible to all A. africana and T. tridentata organic root extracts. A similar significant effect was observed for all E. petersii organic pseudobulb extracts, DCM extracts and organic root extracts of B. scaberulum. Only the DCM tuber and root extracts of E. hereroensis exhibited lethal effects on C. elegans. All of the P. pubescens extracts showed poor anthelmintic activity. Similarly, in vitro enzyme based cyclooxygenase (COX) 1 and 2 and acetylcholinesterase (AChE) inhibitory bioassays, revealed significant inhibition of COX-1, COX-2 and AChE enzymes by crude organic and certain aqueous orchid extracts. Out of a total of 53 evaluated extracts, 21 and 13 extracts exhibited significant anti-inflammatory activity in the COX-1 and COX-2 assays respectively. The DCM tuber extract of E. hereroensis was the only extract to significantly inhibit both COX enzymes, 100.02±0.11% and 87.97±8.38% respectively. All B. scaberulum root extracts (DCM, EtOH and water) exhibited COX-2 selective inhibitory activity (100.06±0.01, 93.31±2.33 and 58.09±3.25%). Overall, the DCM root extract of A. africana was found to be the most potent extract (EC50 0.25±0.10 mg/ml). The 80% EtOH root extract of B. scaberulum was the most potent in the COX-2 assay (EC50 0.44±0.32 mg/ml). Generally the root extracts exhibited greater AChE inhibitory activity; where the most active extract was B. scaberulum DCM root extract (EC50 0.02±0.00 mg/ml). All aqueous extracts, except that of A. africana roots and B. scaberulum pseudobulbs, showed poor or no COX-1 and COX-2 inhibition. The antioxidant capacity of crude orchid extracts was determined using: hydrogen atom transfer (HAT) (β-carotene/linoleic acid assay) and single electron transfer (SET) (2,2‟-diphenylpicrylhydrazyl (DPPH) free radical scavenging assay and ferric reducing antioxidant power (FRAP) assay) reaction-based assays. Potent antioxidant effects were observed for certain crude methanolic orchid extracts. Generally, there was a dose-dependent change in radical scavenging activities of crude extracts from which EC50 values were determined. The root extracts of all species, except that of E. petersii, had consistently more effective radical scavenging activity than that of other plant parts within each species. The pseudobulb extract of E. petersii, was the most potent extract (EC50 1.32±0.86 mg/ml). In the β-carotene-linoleic acid assay, based on the oxidation rate ratio (ORR), the leaf extract of T. tridentata and the root extracts of C. arcuata and E. hereroensis exhibited the best antioxidant effects (0.02, 0.023 and -0.15 respectively). Similarly, the average antioxidant activity (%ANT) of these samples was greater than that of BHT (95.88±6.90%) and all other samples. Bulbophyllum scaberulum leaf, pseudobulb and root extracts, E. petersii pseudobulb extract and T. tridentata root extract also exhibited a greater capacity to prevent β-carotene oxidation when compared to BHT. All crude orchid extracts tested demonstrated a general dose-dependent response in the ferric reducing power assay. The reducing power of ascorbic acid (0.08 mM) and BHT (0.05 mM), as measured as absorbance, was 1.12±0.12 and 0.73±0.08 respectively. At 6.25 mg/ml, A. africana root and E. petersii pseudobulb extracts were the most effective in reducing power activity. The short-term bacterial reverse mutation Ames Salmonella/microsome mutagenicity (ASMM) assay, which makes use of mutant histidine-dependent Salmonella typhimurium strains, was used to determine the mutagenicity and toxicity of crude orchid extracts. In the presence of a mutagen S. typhimurium TA98 strain detects frameshift events while the TA100 and TA102 strains detect base-pair substitutions. In the absence of metabolic activation, mutagenic extracts were observed against the TA98 strain only. All A. africana DCM leaf and stem extracts tested, the DCM root extract (0.5, 0.05 mg/ml) and EtOH leaf, stem and root extracts at 5 mg/ml exhibited mutagenic effects. The EtOH root extracts (5, 0.5 mg/ml) of B. scaberulum exhibited mutagenic indices (MI) comparable to that of 4NQO (17.00 and 13.00, respectively). Eulophia petersii PE pseudobulb extract demonstrated mutagenic potential at 5 mg/ml. The ethanolic root extracts of T. tridentata showed mutagenic effects at 5 and 0.5 mg/ml. The mutagenicity index (MI) with metabolic activation (S9) was determined using only the TA98 strain; where no mutagenic effects were observed. In the phytochemical evaluation of crude methanol orchid extracts, the Folin-Ciocalteu assay for total phenolics, butanol-HCl assay for condensed tannins, rhodanine assay for gallotannins and vanillin assay for flavonoids revealed a quantitative chemical profile of the tested samples. The correlation between observed biological effects and chemical compounds present was found to be generally significant. The significant antimicrobial, anthelmintic, anti-inflammatory and antioxidant activity of E. petersii pseudobulb extracts and E. hereroensis tuber and root extracts may be attributed to their high total phenolic content. Alternatively, the significant levels of gallotannin content in E. hereroensis may have contributed to the bioactivity. The flavonoid content of B. scaberulum and T. tridentata may explain the potent activity observed in the anti-inflammatory, antioxidant and acetylcholinesterase inhibitory assays; while the flavonoid content C. arcuata may have contributed to the potent anthelmintic and antioxidant activities. The significantly higher levels of gallotannin content may explain the significant anti-inflammatory and anthelmintic activity of A. africana. A number of biologically active compounds have been isolated from certain Orchidaceae species around the world on the basis of their traditional medicinal uses. The traditional uses of these orchid species were scientifically validated. No pharmacological research has been previously conducted on South African medicinal orchids; therefore the current investigation has produced novel findings on the efficacy and safety of these orchid species and promotes the continued research of medicinal orchids in South Africa