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The Coneybury ‘Anomaly’ is an Early Neolithic pit located just south-east of Stonehenge, Wiltshire. Excavations recovered a faunal assemblage unique in its composition, consisting of both wild and domestic species, as well as large quantities of ceramics and stone tools, including a substantial proportion of blades/bladelets. We present a suite of new isotope analyses of the faunal material, together with ancient DNA sex determination, and reconsider the published faunal data to ask: What took place at Coneybury, and who was involved? We argue on the basis of multiple lines of evidence that Coneybury represents the material remains of a gathering organised by a regional community, with participants coming from different areas. One group of attendees provided deer instead of, or in addition to, cattle. We conclude that the most likely scenario is that this group comprised local hunter-gatherers who survived alongside local farmers.
The Coneybury ‘Anomaly’ is an Early Neolithic pit located just south-east of Stonehenge, Wiltshire. Excavations recovered a faunal assemblage unique in its composition, consisting of both wild and domestic species, as well as large quantities of ceramics and stone tools, including a substantial proportion of blades/bladelets. We present a suite of new isotope analyses of the faunal material, together with ancient DNA sex determination, and reconsider the published faunal data to ask: What took place at Coneybury, and who was involved? We argue on the basis of multiple lines of evidence that Coneybury represents the material remains of a gathering organised by a regional community, with participants coming from different areas. One group of attendees provided deer instead of, or in addition to, cattle. We conclude that the most likely scenario is that this group comprised local hunter-gatherers who survived alongside local farmers.
A study was conducted to examine the relationship between fibre shedding and staple strength in Merino weaners genetically different in staple strength and fed different levels of nutrition. Fibre shedding at the point of break along the staple was estimated using 3 different techniques: (i) a subjective scoring system of wool follicle activity, based on their morphology in transverse skin sections; (ii) the number of fibres with club-ends after differential staining to identify remnants of the shed-follicle bulb; and (iii) changes in the number of fibres in the cross-section along individual staples. Irrespective of the technique used, the estimated proportion of shed fibres did not differ significantly between the sheep bred for sound and tender wool, but increased significantly (P < 0·05) in response to adverse nutritional conditions. Across all treatments, there was a significant (r2 = 0·63; P < 0·001) correlation between the proportion of shutdown follicles and the percentage decrease in the number of fibres in the staple cross-section, although the average difference between the techniques was 11·5%. Both techniques indicated that, on average, about 30% of the total follicle population became inactive and shed their fibre under the most adverse nutritional conditions, and that this was as high as 50–60% for some individual sheep. Neither of these techniques was closely correlated to the proportion of fibres with club-ends (r2 = 0·15 and 0·20, respectively; P < 0·01). The proportion of shutdown follicles and the percentage decrease in the number of fibres in the staple cross-section explained 54% and 52% of the variance in staple strength, respectively, compared with only 19% explained by the percentage of fibres with club-ends at the point of break. However, as fibre shedding failed to remove any variance in staple strength additional to that already attributed to along- and between-fibre changes in diameter, it is concluded that fibre shedding per se does not contribute significantly to nutritional-induced differences in staple strength.
The pathomechanism of furuncle has not been fully elucidated and should be investigated using an appropriate animal model. We observed the invasion of Staphylococcus aureus cells into hair follicles in mice, using a strain of S. aureus isolated from human furunculosis. Light microscopical examination revealed that S. aureus cells attached to corneocytes at 6 h after inoculation, proliferated around the ostium of the hair follicle and invaded the hair follicle at 12 h after inoculation. Electron microscopically, S. aureus cells attached to the horny layer of hair follicle with long, thick, string-like structures. At 12 h after inoculation, S. aureus cells invaded in a file between the inner root sheath and outer root sheath. We could not induce direct invasion from the follicle ostium. Our findings suggest that there are some regions of the hair follicle through which S. aureus cells can relatively easily invade deeper into the follicle. The most important question is what confines the invasion and inflammation of S. aureus to the hair follicle. We suggest that there is some locus minoris for invasion into hair follicles by S. aureus, such as an interface between the two sheaths.
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