Cacti (Cactaceae) represent a family of highly specialized angiosperm plants with a native range of distribution restricted to the American continents. Columnar cacti of the sub-family Cactoideae evolved in adaptation to their arid or semi-arid habitats characteristics that distinguish them from most other dicot plants, e.g. the stem succulence with a strongly vascularized storage parenchyma and the presence of the spine wearing areoles. Although cacti have been in cultivation since the discovery of America, some studies even suggest the agricultural use in pre-colombian times, and many scientific investigations were carried out on the functional morphology and anatomy with regard to biomechanical adaptations of the found structures, no research focused on the branch-stem attachment. The most conspicuous features of such a ramification are the pronounced constrictions at the branch-stem junctions that are also present in the lignified vascular structures within the succulent cortex. Based on Finite Element Analyses of ramification models it could be demonstrated that these indentations in the region of high flexural and torsional stresses are not regions of structural weakness, e.g. allowing vegetative propagation. On the contrary, they can be regarded as anatomical adaptations to increase the stability by fine-tuning the stress state and stress directions in the junction along prevalent fiber directions. The development of the woody support structure within the succulent cortex of the parental shoot can be traced back to the leaf and bud traces of the dormant axillary buds. Surprisingly, these initials also develop into another woody structure supporting the flowers of the cacti. As these two support structures differ significantly in their macroscopic and microscopic anatomy and as they develop from the same initial state as leaf/bud traces, another objective of this work was to analyze the secondary growth of the two structures with traditional botanic investigation methods. The results of these investigations reveal a wood dimorphism consisting of an early parenchymatous phase followed later by fibrous wood in both kind of support structure. In vegetative branches, the woody support structures have the typical ringlike arrangement as found in the stele of the parental shoot, whereas the flower support structures have a reticular arrangement of interconnected woody strands. This fundamentally different anatomy of the support structures results from the formation of an interfascicular cambium between the leaf/bud traces when a vegetative branch forms or its absence in the case of a flower. After shedding light on the functional morphology and anatomy of the cactus ramification and their development the question arises if the found load adaptation strategies may serve to improve technical fiber composite structures analogue to the design recommendation developed from the biomechanical analyses of tree ramifications. Such a biomimetic transfer from the cactus ramification as biological role model to a technical implementation and the adaptation of the fine-tuned geometric shape and arrangement of lignified strengthening tissues might contribute to the development of alternative concepts for branched fiber-reinforced composite structures within a limited design space.

The thick and woody shell of the fruit of Adansonia species cannot be explained solely by adaptation to zoochory or hydrochory. Since the trunks of Adansonia possess a thick and fire-resistant bark and wildfires occur regularly in its habitat (savannah), we examined with the African Adanonia digitata and the Australian Adansonia gregorii whether the fruit offers protection against high heat typically experienced in wildfires. Heat-resistance tests were conducted by applying a simple heat test based on known temperature and temperature residence times occurring in savannah fires and complemented by tests to reveal the impact of heat on germination since long-term seed dormancy is known for Adansonia. Germination tests with acid treated and heat treated seeds were performed to establish if heat also increased germination rate as effectively as acid treatments have been found to do. Heat was found to increase germination rate, but not as effectively as treatment with acid, therefore fruits exposed to high temperatures experienced in wildfires may have a better chance of germination than fruits that were not exposed to wildfires. The ability of the investigated fruits to protect seeds from high temperatures suggests that wildfires may have played a role in the evolution of the hard-shell structure typically found in Adansonia.

The thick and woody shell of the fruit of Adansonia species cannot be explained solely by adaptation to zoochory or hydrochory. Since the trunks of Adansonia possess a thick and fire-resistant bark and wildfires occur regularly in its habitat (savannah), we examined with the African Adanonia digitata and the Australian Adansonia gregorii whether the fruit offers protection against high heat typically experienced in wildfires. Heat-resistance tests were conducted by applying a simple heat test based on known temperature and temperature residence times occurring in savannah fires and complemented by tests to reveal the impact of heat on germination since long-term seed dormancy is known for Adansonia. Germination tests with acid treated and heat treated seeds were performed to establish if heat also increased germination rate as effectively as acid treatments have been found to do. Heat was found to increase germination rate, but not as effectively as treatment with acid, therefore fruits exposed to high temperatures experienced in wildfires may have a better chance of germination than fruits that were not exposed to wildfires. The ability of the investigated fruits to protect seeds from high temperatures suggests that wildfires may have played a role in the evolution of the hard-shell structure typically found in Adansonia.

Cacti (Cactaceae) represent a family of highly specialized angiosperm plants with a native range of distribution restricted to the American continents. Columnar cacti of the sub-family Cactoideae evolved in adaptation to their arid or semi-arid habitats characteristics that distinguish them from most other dicot plants, e.g. the stem succulence with a strongly vascularized storage parenchyma and the presence of the spine wearing areoles. Although cacti have been in cultivation since the discovery of America, some studies even suggest the agricultural use in pre-colombian times, and many scientific investigations were carried out on the functional morphology and anatomy with regard to biomechanical adaptations of the found structures, no research focused on the branch-stem attachment. The most conspicuous features of such a ramification are the pronounced constrictions at the branch-stem junctions that are also present in the lignified vascular structures within the succulent cortex. Based on Finite Element Analyses of ramification models it could be demonstrated that these indentations in the region of high flexural and torsional stresses are not regions of structural weakness, e.g. allowing vegetative propagation. On the contrary, they can be regarded as anatomical adaptations to increase the stability by fine-tuning the stress state and stress directions in the junction along prevalent fiber directions. The development of the woody support structure within the succulent cortex of the parental shoot can be traced back to the leaf and bud traces of the dormant axillary buds. Surprisingly, these initials also develop into another woody structure supporting the flowers of the cacti. As these two support structures differ significantly in their macroscopic and microscopic anatomy and as they develop from the same initial state as leaf/bud traces, another objective of this work was to analyze the secondary growth of the two structures with traditional botanic investigation methods. The results of these investigations reveal a wood dimorphism consisting of an early parenchymatous phase followed later by fibrous wood in both kind of support structure. In vegetative branches, the woody support structures have the typical ringlike arrangement as found in the stele of the parental shoot, whereas the flower support structures have a reticular arrangement of interconnected woody strands. This fundamentally different anatomy of the support structures results from the formation of an interfascicular cambium between the leaf/bud traces when a vegetative branch forms or its absence in the case of a flower. After shedding light on the functional morphology and anatomy of the cactus ramification and their development the question arises if the found load adaptation strategies may serve to improve technical fiber composite structures analogue to the design recommendation developed from the biomechanical analyses of tree ramifications. Such a biomimetic transfer from the cactus ramification as biological role model to a technical implementation and the adaptation of the fine-tuned geometric shape and arrangement of lignified strengthening tissues might contribute to the development of alternative concepts for branched fiber-reinforced composite structures within a limited design space.