Equal Protection for Illegitimate Children Conceived by Artificial Insemination

This Comment explores the equal protection rights of illegitimate children born to artificially inseminated women in light of the Uniform Parentage Act (UPA), which guarantees equal treatment under the law for all children, and California\u27s adoption of a modified version of the UPA. The author considers the conflict between those rights and the right of unmarried women to procreate and concludes that the California modifications of UPA section 5(b) are unconstitutional because they violate the equal protection rights of illegitimate children born to artificially inseminated women, and that they actually contradict the purpose of the Act. The author suggests that the California law be amended to conform to UPA section 5(b)

Specific leaf area responses to environmental gradients through space and time

Plant communities can respond to environmental changes by altering their species composition and by individuals (within species) adjusting their physiology. These responses can be captured by measuring key functional traits among and within species along important environmental gradients. Some anthropogenic changes (such as fertilizer runoff) are known to induce distinct community responses, but rarely have responses across natural and anthropogenic gradients been compared in the same system. In this study, we used comprehensive specific leaf area (SLA) data from a diverse Australian annual plant system to examine how individual species and whole communities respond to natural and anthropogenic gradients, and to climatically different growing seasons. We also investigated the influence of different leaf-sampling strategies on community-level results. Many species had similar mean SLA values but differed in SLA responses to spatial and temporal environmental variation. At the community scale, we identified distinct SLA responses to natural and anthropogenic gradients. Along anthropogenic gradients, increased mean SLA, coupled with SLA convergence, revealed evidence of competitive exclusion. This was further supported by the dominance of species turnover (vs. intraspecific variation) along these gradients. We also revealed strong temporal changes in SLA distributions in response to increasing growing-season precipitation. These climate-driven changes highlight differences among co-occurring species in their adaptive capacity to exploit abundant water resources during favorable seasons, differences that are likely to be important for species coexistence in this system. In relation to leaf-sampling strategies, we found that using leaves from a climatically different growing season can lead to misleading conclusions at the community scale

Charged Higgs bosons from the 3-3-1 models and the R(D(∗))\mathcal{R}(D^{(*)}) anomalies

Several anomalies in the semileptonic B-meson decays such as $\mathcal{R}(D^{(*)})$ have been reported by $BABAR$, Belle, and LHCb collaborations recently. In this paper, we investigate the contributions of the charged Higgs bosons from the 3-3-1 models to the $\mathcal{R}(D^{(*)})$ anomalies. We find that, in a wide range of parameter space, the 3-3-1 models might give reasonable explanations to the $\mathcal{R}(D^{(*)})$ anomalies and other analogous anomalies of the B meson's semileptonic decays.Comment: Accpeted by Physical Review

Adaptive paternal effects? Experimental evidence that the paternal environment affects offspring performance

The ability of females to adaptively influence offspring phenotype via maternal effects is widely acknowledged, but corresponding nongenetic paternal effects remain unexplored. Males can adjust sperm phenotype in response to local conditions, but the transgenerational consequences of this plasticity are unknown. We manipulated paternal density of a broadcast spawner (Styela plicata, a solitary ascidean) using methods shown previously to alter sperm phenotype in the field, then conducted in vitro fertilizations that excluded maternal effects and estimated offspring performance under natural conditions. Offspring sired by males from low-density experimental populations developed faster and had a higher hatching success than offspring sired by males living in high densities. In the field, offspring survived relatively better when their environment matched their father's, raising the possibility that fathers can adaptively influence the phenotype of their offspring according to local conditions. As the only difference between offspring is whether they were artificially fertilized by sperm from males kept in high- vs. low-density cages, we can unequivocally attribute any differences in offspring performance to an environmentally induced paternal effect. Males of many species manipulate the phenotype of their sperm in response to sperm competition: our results show this plasticity can influence offspring fitness, potentially in adaptive ways, raising the possibility that adaptive nongenetic paternal effects may be more common than previously thought

Requirements for the spatial storage effect are weakly evident for common species in natural annual plant assemblages

Coexistence in spatially varying environments is theorised to be promoted by a variety of mechanisms including the spatial storage effect. The spatial storage effect promotes coexistence when: (i) species have unique vital rate responses to their spatial environment and, when abundant, (ii) experience stronger competition in the environmental patches where they perform better. In a naturally occurring southwest Western Australian annual plant system we conducted a neighbour removal experiment involving eleven focal species growing in high-abundance populations. Specifically, we measured species' fecundity across a variety of environmental gradients in both the presence and absence of neighbours. For the environmental variables that we measured, there was only limited evidence for species-specific responses to the environment, with a composite variable describing overstory cover and leaf litter cover being the best predictor of fecundity for a subset of focal species. In addition, although we found strong evidence for intra-specific competition, positive environment-competition covariance was only detected for one species. Thus, positive environment-competition covariance may not be as common as expected in populations of species growing at high abundance, at least when tested in natural assemblages. Our findings highlight the inherent limitations of using natural assemblages to study spatial coexistence mechanisms, and we urge empirical ecologists to take these limitations into account when designing future experiments