Cereal production,crop protection and plant breeding*

Trends in British agriculture which have led to the eclipse of rotations, to the concentration of cereal production on wheat and barley, and to a changeover to winter cereals, have increased the vulnerability of cereal crops to disease. Epidemics have been prevented by the deployment of effective resistances and, more recently, of a wide range of crop protection chemicals. Ecological protection by means of variety mixtures and field diversification has now added a new and effective element for the defence of cereals. The problem of durability of resistances and of the continuing effectiveness of chemicals remains, and new problems of susceptibility of crop varieties to herbicides have arisen. It is possible through the combined use of genetical, chemical and ecological defence mechanisms, to maximise the period of effectiveness of resistance genes and of fungicides and insecticides. The experience of the past half-century has shown that dependence on a single protective mechanism provides only a transient solution to controlling disease.     

Pollen tube growth and the pollen‐tube pathway of Nymphaea odorata (Nymphaeaceae)

An important aspect of the evolution of carpel closure, or angiospermy, is the relationship between pollen tube growth patterns and internalization of the pollen‐tube pathway. True carpel closure, involving postgenital fusion of inner carpel margins, is inferred to have arisen once within the ancient order Nymphaeales, in the common ancestor of Nymphaeaceae. We studied pollen tube development, from pollination to fertilization, in a natural population of Nymphaea odorata, using hand pollinations and timed flower collections. Pollen germinates in stigmatic secretions within 15 min and pollen tubes enter subdermal transmitting tissue within an hour, following wide intercellular spaces towards the zone of postgenital fusion. At the zone of fusion they turn downwards to grow in narrow spaces between interlocked cells and then wander freely to ovules within ovarian secretions. The pollen‐tube pathway is 2–6 mm long and upper ovules are first penetrated 2.5 h after pollination. Pollen tubes grow at rates of approximately 1 mm/h whether in stigmatic fluid, transmitting tissues or ovarian secretions. Pollen‐tube pathways are structurally diverse across Nymphaeales, yet their pollen tubes have similar morphologies and rapid growth rates. This pattern suggests pollen tube growth innovations preceded and were essential for the evolution of complete carpel closure. © 2010 The Linnean Society of London, Botanical Journal of the Linnean Society, 2010, 162 , 581–593.     

Sexual maturation and moult in juvenile Starlings Sturnus vulgaris in response to different daylengths

Starlings, like most other species, show no gonadal development until spring of the year after they hatch, even though they hatch and attain full body size during long days. This could be because they develop in a physiological state analogous to that of photorefractory adults and so need to experience short days in order to activate the reproductive system. To test this possibility, young were hand-reared under different photoperiodic regimes. Young raised under constant long days showed no gonadal development, nor did birds initially raised under short days and then transferred to long days at 3 weeks of age. However, birds transferred from short to long days at 10 weeks of age did show gonadal development, followed by gonadal regression, while birds raised under constant short days showed slow continual gonadal development. This last group, unlike the other three groups, did not moult into adult plumage. Since 4 weeks of long days are required to terminate photorefractoriness in adult Starlings, these results demonstrate that the reproductive system of young birds is in a similar state to that of photorefractory adults, and hence that puberty is analogous to the termination of photofractoriness.