The response of an Eastern Amazonian rain forest to drought stress: results and modelling analyses from a throughfall exclusion experiment

Warmer and drier climates over Eastern Amazonia have been predicted as a component of climate change during the next 50–100 years. It remains unclear what effect such changes will have on forest–atmosphere exchange of carbon dioxide (CO₂) and water, but the cumulative effect is anticipated to produce climatic feedback at both regional and global scales. To allow more detailed study of forest responses to soil drying, a simulated soil drought or 'throughfall exclusion' (TFE) experiment was established at a rain forest site in Eastern Amazonia, Brazil, for which time-series sap flow and soil moisture data were obtained. The experiment excluded 50% of the throughfall from the soil. Sap flow data from the forest plot experiencing normal rainfall showed no limitation of transpiration throughout the two monitored dry seasons. Conversely, data from the TFE showed large dry season declines in transpiration, with tree water use restricted to 20% of that in the control plot at the peak of both dry seasons. The results were examined to evaluate the paradigm that the restriction on transpiration in the dry season was caused by limitation of soil-to-root water transport, driven by low soil water potential and high soil-to-root hydraulic resistance. This paradigm, embedded in the soil–plant–atmosphere (SPA) model and driven using on-site measurements, provided a good explanation ( R ² > 0.69) of the magnitude and timing of changes in sap flow and soil moisture. This model-data correspondence represents a substantial improvement compared with other ecosystem models of drought stress tested in Amazonia. Inclusion of deeper rooting should lead to lower sensitivity to drought than the majority of existing models. Modelled annual GPP declined by 13–14% in response to the treatment, compared with estimated declines in transpiration of 30–40%.     

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.