Preventing Ultimate Harm as the Justification for Biomoral Modification

Most advocates of biogenetic modification hope to amplify existing human traits in humans in order to increase the value of such traits as intelligence and resistance to disease. These advocates defend such enhancements as beneficial for the affected parties. By contrast, some commentators recommend certain biogenetic modifications to serve social goals. As Ingmar Persson and Julian Savulescu see things, human moral psychology is deficient relative to the most important risks facing humanity as a whole, including the prospect of Ultimate Harm, the point at which worthwhile life is forever impossible on the planet. These risks can be mitigated, they say, by enhancing moral psychology in novel ways. Persson and Savulescu argue that some parents should modify the underlying biogenetics of their children's moral psychology, if such measures were safe and effective, but they admit these interventions may not decouple humanity from Ultimate Harm. Neither are these modifications the only options, they concede, for addressing risks to humanity. Even with these concessions, saving humanity from itself is a fairly poor reason to modify the moral psychology of children. In most ways, adults would be better candidates, morally speaking, for modifications of psychology. Even then, there is no direct link between morally enhanced human beings and the hoped‐for effect of better protection from Ultimate Harm. Asserting a general duty of all to contribute to the avoidance of Ultimate Harm is a better moral strategy than intervening in the moral psychology of some, even though meeting that duty may involve substantial interference with the free exercise of one's interests.     

Dose-related upwind anemotaxis and movement up odour gradients in still air in the presence of methyl eugenol by the wild tobacco fly, Bactrocera cacuminata

The behaviour of Bactrocera cacuminata (Hering) in wind varied according to the concentration of methyl eugenol (0, 95, 327 and 500 μg m^?3, respectively). General locomotor activity (as measured by mean distance moved in 5 min, regardless of direction) was not significantly different in the first two treatments but was significantly lower in the others. Most flies in the fourth treatment did not move more than one body length. In the first two treatments, the rate and pattern of movement of most flies was basically similar, with walking in tortuous paths interspersed with short flights and usually no obvious bias in direction. However, 32% of flies in the second treatment did move in a biased direction, achieving upwind anemotaxis of at least 400 mm, but only 2–8% did so in the other conditions. Flies moved up a concentration gradient to a source of methyl eugenol in still air when released at a distance of 100, 150 or 200 mm. With one exception, no more than 40% did this within 3 min of release (whether or not the olfactory stimulus was augmented by a visual one). However, 77% responded when released 100 mm from a combined olfactory and visual stimulus. Visual augmentation of an olfactory stimulus may also be responsible for far fewer flies flying out of the vicinity at distances up to 150 mm, but not 200 mm.     

Early life environment determines the development of adult phobic‐like fear responses in BALB/cAnN mice

Environmental factors may unleash genetically determined susceptibility to psychopathology. Great effort has been spent in identifying both the genetic basis and environmental sources of exaggerated fear in animal models of anxiety disorders. Here, we show that the origin of inbred mice, probably via subtle differences in breeding and rearing conditions, may have large consequences specifically on acquisition and retention of fear memories, while leaving anxiety‐related behaviours unaffected. These effects could be seen in BALB/cAnN (BALB), but not in C57BL/6N (C57BL/6) mice, thus suggesting their dependency on the genetic background. Increased susceptibility for developing exaggerated fear responses was accompanied by decreased long‐term depression and increased surface trafficking of the AMPA receptor GluR1 subunit at the level of the basolateral amygdala complex. Together, these data raise a novel caveat in the debate about the origins of variation in behavioural studies with experimental animals. Considering that there are currently no animal models which explicitly consider conceptual analogy to the specific gene–environment interactions observed in the aetiology of phobias, our study might suggest a novel approach and direction for further preclinical studies focusing on such aspects of phobic‐like fears.     

The influence of environmental factors on the spatial distribution of saxicolous lichens in a Norwegian coastal community

Abstract. The effects of vegetation cover, radiation, micro‐habitat variables and maritime influence on the floristic composition of a saxicolous community in Vingen, western Norway were studied. Particular emphasis is put on the local distribution of Fuscidea cyathoides, Ochrolechia tartarea, Ophioparma ventosa and Pertusaria corallina. Very little of the variation in the lichen community composition is directly related to measured micro‐environmental variables but variance partitioning shows that vegetation cover explains more of the floristic variation than radiation, maritime influence and microhabitat variables. Logistic regression analyses nevertheless indicate that the micro‐environment influences the spatial distribution of the four species. The high fraction of unexplained floristic variation, 91%, is suggested to result from (1) lack of fit of data to the response model; (2) some influential environmental variables that have not been recorded; (3) local historical factors that affect present day distribution and/or (4) apparent randomness in colonization. The results also agree with the view that the four lichen species in this study are able to co‐exist in the long‐term because of different spatial distributions resulting from different strategies with respect to ecology, dispersion and interaction.     

Understanding plant reproductive diversity

Flowering plants display spectacular floral diversity and a bewildering array of reproductive adaptations that promote mating, particularly outbreeding. A striking feature of this diversity is that related species often differ in pollination and mating systems, and intraspecific variation in sexual traits is not unusual, especially among herbaceous plants. This variation provides opportunities for evolutionary biologists to link micro-evolutionary processes to the macro-evolutionary patterns that are evident within lineages. Here, I provide some personal reflections on recent progress in our understanding of the ecology and evolution of plant reproductive diversity. I begin with a brief historical sketch of the major developments in this field and then focus on three of the most significant evolutionary transitions in the reproductive biology of flowering plants: the pathway from outcrossing to predominant self-fertilization, the origin of separate sexes (females and males) from hermaphroditism and the shift from animal pollination to wind pollination. For each evolutionary transition, I consider what we have discovered and some of the problems that still remain unsolved. I conclude by discussing how new approaches might influence future research in plant reproductive biology.     

Modelling the effect of size on the aerial dispersal of microorganisms

Aim We investigate the long‐standing question of whether the small size of microbes allows most microbial species to colonize all suitable sites around the globe or whether their ranges are limited by opportunities for dispersal. In this study we use a modelling approach to investigate the effect of size on the probability of between‐continent dispersal using virtual microorganisms in a global model of the Earth’s atmosphere. Location Global. Methods We use a computer model of global atmospheric circulation to investigate the effect of microbe size (effective diameters of 9, 20, 40 and 60 μm) on the probability of aerial dispersal. Results We found that for smaller microbes, once airborne, dispersal is remarkably successful over a 1‐year period. The most striking results are the extensive within‐hemisphere distribution of virtual microbes of 9 and 20 μm diameter and the lack of dispersal between the Northern and Southern Hemispheres during the year‐long time‐scale of our simulations. Main conclusions Above a diameter of 20 μm wind dispersal of virtual microbes between continents becomes increasingly unlikely, and it does not occur at all (within our simulated 1‐year period) for those of 60 μm diameter. Within our simulation, the success of small microbes in long‐distance dispersal is due both to their greater abundance and to their longer time in the atmosphere – once airborne – compared with larger microbes.