African White-backed Vultures were recently uplisted to ‘Critically Endangered’ by IUCN due to declines across their range. Poisoning is widely accepted as the major reason for these declines. Botswana supports a high number of this species (breeding pairs > c.1,200), but as yet no published information exists on their breeding success in the country. However, mass poisonings within Botswana and neighbouring countries have killed thousands of White-backed Vultures in recent years. We therefore expected that nesting numbers may have declined in this region if these poisoning events killed local breeding birds. We used information from aerial surveys conducted between 2006 and 2017 in Khwai and Linyanti, two important breeding areas for this species in north-central Botswana, to determine if there was any change in nesting numbers and breeding success of White-backed Vultures. Results showed an overall 53.5% decline in nesting numbers, with a greater decline in Linyanti than in Khwai. In both areas, breeding success was significantly lower in 2017 than it was 10 ten years earlier. We recommend that similar repeat surveys are continued to provide greater confidence in the trends of both nesting numbers and breeding performance. Population viability analysis suggested that if the productivity levels detected in 2017 were a true indication of current productivity levels for this population, and if recent high poisoning rates continue, this population could be extirpated from the area in the next 13 years.

The germinal layer of sterile 9-month-old murine peritoneal cysts of Echinococcus granulosus equinus shows interrelated variation in depth, tissue integrity, metabolic reserves and the number of autophagic lamellar bodies present. These features are similar in large and medium-sized cysts from the same host, whether occurring singly or within cyst masses. Deep germinal layers (> 16 μm) are lipid- and glycogen-rich and possess numerous autophagic vacuoles with 6 nm period lamellar stacks asymmetrically disposed peripherally; shallow layers (< 12 μm), with indications of degeneration, have depleted metabolic reserves and fewer lamellar bodies. These bodies are formed by smooth endoplasmic reticulum encirclement of small glycogen masses followed by further sequestration, and eventually definition of glycogen particles may be lost. Autophagy of mitochondria and cytoplasmic vesicles also occurs. The presence of lysosomal enzymes within the layer suggests autolysosomal compartmentalization of excess substrate and effete material. Mucopolysaccharide bodies, containing material similar to that exocytosed to form the laminated layer matrix, occur and are formed from fusion and autophagy of Golgi-derived vesicles. These bodies may also develop peripheral 6 nm period lamellar stacks, but of limited depth. Mucopolysaccharide bodies are the dominant feature of the germinal layer of very small cyst-mass cysts in which laminated layer production is considered to be arrested. They thus represent a repository for the unreleased mucopolysaccharide material.

The microfibrillate component of the laminated layer of Echinococcus granulosus equinus contains, except for the zone adjacent to the germinal layer, aggregates of electron-dense bodies displaying a sub-structure of electron-lucent spheres. The tegumentary syncytial cytoplasm contains randomly distributed electron-dense granules, many occurring near the apical plasmalemma, although exocytosis was rarely seen. Granules, similar in size and sub-structure to the bodies of the aggregates, also occur in the internuncial connexions and tegumentary cytons, suggesting that they may be produced in the cytons and released into the laminated layer via the internuncial connexions and tegumentary cytoplasm. Cysts incubated for 0·5–2·5 h in serum- and non-serum-containing media showed differences from non-incubated cysts. The distal half of the syncytium contained a progressive increase in the number of granules (distal:proximal 1·9:1 at 2·5 h; cf. 1:1 in non-incubated cysts), and exocytosis of granules into the laminated layer adjacent to the cyst had occurred. This cannot be attributed wholly to serum proteins. Cysts incubated for 21 h appeared ‘normal’, suggesting re-establishment of an equilibrium. Since the matrix of the laminated layer is considered homologous to the glycocalyx of other cestodes, the possible protective role played by the granules/bodies, characteristic of Echinococcus spp., is discussed.

Peritoneal hydatids of Echinococcus granulosus equinus of 9 months standing in BALB/c mice occurred as free cysts or cysts within cyst masses. Both showed wide variation in size and in host tissue response, and all had a well-developed laminated layer separating the host tissue response from the germinal layer. In the smallest cyst-mass cysts the host tissue response was present as remnants of the initial cellular attack involving eosinophils. Slightly larger cyst-mass cysts possessed a primary macrophage invasion which phagocytosed the remnants of the initial attack and also, though to little effect, the laminated layer material. In the largest cyst-mass cysts a second macrophage invasion, of monocyte origin, had commenced and transformation stages of these cells to macrophages were observed. No fibroblasts surrounded individual cyst-mass cysts but they were present around the cyst mass, encapsulating it and possibly preventing further host cell invasion. Thus, the host tissue response around individual cyst-mass cysts remained ‘preserved’ at an early stage such as existed at the time of encapsulation. Small free cysts showed a primary macrophage invasion and transformation stages of cells of a secondary infiltration of peritoneal origin. Peripheral to the macrophages were fibroblasts demonstrating limited fibrinogenesis, and each cyst was surrounded by a layer of mesothelial cells. Large free cysts, also delimited by a mesothelial layer, possessed peripheral connective tissue, a deep fibrous layer and a monolayer of very compressed macrophages lying adjacent to the laminated layer. It is emphasized that an understanding of the host tissue response in cysts of different sizes and from different locations is an essential pre-requisite for the design of experimental studies.

Cognitive deficits in neurofibromatosis Type 1 (NF-1) have been documented in both the verbal and visuospatial domains. Previous investigations from our laboratory have determined a specific pattern of “spared” (Picture Arrangement, Picture Completion, and Rapid Automatized Naming) and “impaired” (Judgment of Line Orientation, Vocabulary, and Block Design) performance on cognitive measures in this population when compared to sibling-matched controls in pairwise designs. Growth curve analyses were conducted on these repeated measures in 19 patients with NF-1 and their siblings to investigate the longitudinal course and growth pattern of these spared and impaired measures. Results indicated that over time children with NF-1 do not catch up to their siblings on impaired measures, and they continue to perform similarly to their siblings on the spared measures. With respect to growth rates, on average across the 6 cognitive measures there was no significant difference between the groups. However, the variation among families for level of performance was estimated to be larger than variation among siblings within a family for 2 out of 6 cognitive measures (i.e., providing for these 2, Vocabulary and Rapid Automatized Naming, evidence of substantial familial correlation), suggesting that there is need to consider NF-1 associated deficits within a familial context. (JINS, 2002, 8, 838–846.)

From the date of my own A level studies (many moons ago!) I have been dissatisfied with the presentation of the law of elastic restitution. The title Newton’s ‘Experimental’ Law implies that it is a purely empirical phenomenon, yet if there is a wide range of conditions in which it is approximately valid (and it isn’t worth using at all if this isn’t true), then there must be some reason for it. Equally unsatisfactorily, the law implies loss of energy in most circumstances. Even in my school days I could see that the usual argument about conversion into heat, sound etc didn’t really hold water, as this process couldn’t conceivably be instantaneous. A recent article by O’Connor [1] stimulated me to crystallise my thoughts on the subject [2], and I was later able to develop a simple and plausible mechanical model exhibiting restitution, which also conserved energy [3]. My presentation in [3] was mainly focussed on the physical consequences of the model, and solution of the differential equations involved was numerical. Yet, in the simplest case, the model is amenable to fairly elegant exact analytical techniques, which it is the aim of this paper to present. Apart from the interest of the model, the methods used are a nice illustration of the role of normal modes in the solution of simultaneous linear differential equations—a topic approachable by A level students of Further Maths, or by first-year undergraduates.