First Amendment, Newsracks and Public Property after City of Lakewood v. Plain Dealer Publishing Co.

City of Lakewood v. Plain Dealer Publishing Co., 108 S. Ct. 2138 (interim ed. 1988)

Localisation in focal epilepsy: a practical guide

The semiology of epileptic seizures reflects activation, or dysfunction, of areas of brain (often termed the symptomatogenic zone) as a seizure begins and evolves. Specific semiologies in focal epilepsies provide an insight into the location of the seizure onset zone, which is particularly important for presurgical epilepsy assessment. The correct diagnosis of paroxysmal events also depends on the clinician being familiar with the spectrum of semiologies. Here, we summarise the current literature on localisation in focal epilepsies using illustrative cases and discussing possible pitfalls in localisation

Struggling to be Fit: Identity, Integrity, and the Law

This interdisciplinary co-authored Analysis piece introduces identity and integrity, which are argued to sit at the core of the person. It analyses approaches taken to these concepts by legal regimes, particularly in the context of individuals using artificial limbs or digital avatars. The piece concludes that law engages with identity and integrity to a limited and incomplete extent; and that law is thus inadequate in its engagement with the person, and its meaning making in this respect. This piece draws on two interdisciplinary funded projects, funded by the Wellcome Trust and the Arts and Humanities Research Council

Nuptial pad (“breeding gland”) morphology is related to non-random mating in wild male common frogs (<i>Rana temporaria</i>)

Androgen levels are closely linked with breeding in male amphibians. Development of the nuptial pad is driven by androgens and is believed to have importance for determining mating success in anurans, but this has not been tested in wild populations. We investigated the association between nuptial pad morphology (length, colour) and mating (amplexus) success in wild male common frogs (Rana temporaria) in the UK (Devon in Southern England and central Scotland). Once active breeding had been confirmed, pond water (25 L) was placed in 1–6 replicate mesocosms (66 cm diameter circular, black plastic tubs) in situ. Eight male and two female frogs were placed into each mesocosm, and success observed by identifying the male frog(s) in amplexus. The length of nuptial pads for male frogs observed in amplexus was greater than those that did not achieve amplexus. There was no difference in the absolute dark colour of nuptial pads (determined by red/green/blue analysis, Adobe photoshop©) for male frogs observed in amplexus versus those that did not achieve amplexus. However, within each mesocosm, the nuptial pad was relatively darker for winning male frogs compared to losing male frogs. Overall, 91% of winning male frogs from Devon, and 89% winning male frogs from Scotland, possessed either a longer and/or a darker nuptial pad, compared with frogs that did not achieve amplexus. These data suggest that features of nuptial pad morphology are associated with amplexus (and thus mating) success in male common frogs. Given that nuptial pads have been identified in all anuran amphibian species analysed to date, nuptial pad morphology may contribute to non-random mating strategies across a broad range of species

RECIPROCAL RECURRENT SELECTION FOR 21-DAY LITTER WEIGHT OF CROSSBRED GILTS. I. SELECTION APPLIED AND GENETIC CHANGE IN REPRODUCTION OF CROSSBRED GILTS

Six cycles of reciprocal recurrent selection (RRS) between Line 8 (Duroc) and Line 9 (Beltsville No. 1) were completed at the Fort Reno Livestock Research Center, E1 Reno, Oklahoma. A randomly mated control line was maintained. Each cycle of selection required three seasons. Selection of purebred pigs (born in the second season) was based on the mean 21-d litter weight of their maternal and paternal half-sib crossbred gilts that were born in the first season and farrowed in the third season (XB21DLWT). On the average, 5.8 maternal and paternal half-sib gilts contributed to the mean XB21DLWT for each purebred individual. The average potential selection differential for XB21DLWT was 5.64 kg, but only 70.2% of this value was realized in the initial selection (3.95 kg). Disease problems and unsoundness were the primary reasons for this discrepancy. The potential, initial, final and weighted final standardized selection differentials for females averaged 61, 60, 55 and 47%, respectively, of the corresponding differentials for males. Standardized selection differentials were similar for Line 8 and Line 9. The estimate of realized heritability for XB21DLWT was .076 ± .319 for the average of 8 x 9 and 9 x 8 gilts. Environmental trends, estimated from control data, were not significant for any of the traits evaluated. The genetic change in reproductive ability of 8 x 9, 9 x 8 and their unweighted average was estimated by regressing the deviation of the line mean from the control mean on generation number. In general, estimates of genetic change for litter size, litter weight and average pig weight/litter at 0, 21 and 42 d of age were not significant, but all estimates were favorable. The estimated genetic change for 21-d litter weight was 1.04 ± 1.25 kg/cycle of selection. Based on these results and considering the complexity of RRS, the increase in generation interval and the expected decline in purebred performance that theoretically should accompany successful RRS, it seems doubtful that RRS can be more beneficial than selection based on purebred performance as a method to improve productivity of crossbred gilts

RECIPROCAL RECURRENT SELECTION FOR 21-DAY LITTER WEIGHT OF CROSSBRED GILTS. II. REPRODUCTIVE PERFORMANCE OF PUREBRED FEMALES PRODUCING PUREBRED AND TWO-WAY CROSS LITTERS AND PERFORMANCE OF PUREBRED AND CROSSBRED PIGS

This paper reports estimates of correlated genetic change in reproductive performance of purebred gilts producing two-way cross litters and purebred sows producing purebred litters as well as postweaning performance of two-way cross and purebred pigs produced during reciprocal recurrent selection (RRS) between Line 8 (Duroc) and Line 9 (Beltsville No. 1) for 21-d litter weight production of crossbred gilts. A randomly mated control line developed from a crossbred foundation was maintained to monitor environmental change. Data were adjusted for age of dam, inbreeding of dam, inbreeding of litter (or pig) and linear and quadratic effects of day born within season. The traits evaluated were: litter size, litter weight and average pig weight/litter at birth and weaning (42 d); postweaning average daily gain; age at 90.7 kg and backfat thickness at 90.7 kg. Two data sets were analyzed; the first set included seven seasons of data with purebred gilts producing two-way cross litters, and the second set included seven seasons of data with purebred sows producing purebred litters. No estimates of environmental trend were significant in either set of data. In the first data set, only the estimate of genetic change in backfat thickness of two-way cross pigs was significant and it was in the desired direction. All other estimates were small and did not approach significance. In the second data set, estimates of genetic trend were greater in Line 9 than in Line 8. Estimates of genetic trend in Line 9 were significant for average pig weight at birth, age at 90.7 kg and backfat probe at 90.7 kg, and approached significance for litter size at weaning and average daily gain. The estimates were undesirable for preweaning traits and desirable for postweaning traits. The estimates of genetic trend in Line 8 were of the same sign as those in Line 9, but only the estimate for backfat thickness was significant. The decrease in size of purebred litters in Line 9, and to some degree Line 8, suggests an accelerated accumulation of homozygosity beyond that accounted for by adjustment for pedigree inbreeding. The fact that Line 9 showed a greater decrease than Line 8 suggests that most of the increase in level of reproduction of crossbred gilts may have resulted from genetic change in Line 9 rather than Line 8, or that favorable alleles were being fixed in Line 8 and unfavorable alleles in Line 9