Effects of the Photoperiod Genes Ppd1 and Ppd2 on Growth and Development of the Shoot Apex in Wheat

Two major genes influencing the photoperiod response in wheat,Ppd1 and Ppd2, have been identified on the group 2 chromosomes.Substitution lines, which had been characterized on the basisof time of ear emergence as carrying either the insensitiveor sensitive alleles of the two Ppd genes, were used to investigatethe effect of these genes on development. They were grown undershort photoperiods, and growth and development of the shootapex was measured. The primary influence of the Ppd genes was on ear growth. Inthe plants carrying the insensitive alleles, Ppd1 and Ppd2,the relative growth rate of the floral apex was faster thanthat of plants with the sensitive alleles, ppd1 and ppd2. Therewere no differences in the rate of spikelet initiation, butthe spikelets of the ppd lines grew and developed more slowly. The Ppd2 material segregated for another gene located on chromosome2B affecting duration of the life cycle. This gene also affectedthe relative growth rate of the ear. It was considered that the major effect of the Ppd1, Ppd2 andthe second genetic factor on chromosome 2B is on floral growthrate. Differences in apex morphology, stem growth and ear emergenceare thought to be due to the differences in floral apex growthand size. Wheat, photoperiod genes, shoot apex development, shoot apex growth     

CO2 balance of boreal, temperate, and tropical forests derived from a global database

Terrestrial ecosystems sequester 2.1 Pg of atmospheric carbon annually. A large amount of the terrestrial sink is realized by forests. However, considerable uncertainties remain regarding the fate of this carbon over both short and long timescales. Relevant data to address these uncertainties are being collected at many sites around the world, but syntheses of these data are still sparse. To facilitate future synthesis activities, we have assembled a comprehensive global database for forest ecosystems, which includes carbon budget variables (fluxes and stocks), ecosystem traits (e.g. leaf area index, age), as well as ancillary site information such as management regime, climate, and soil characteristics. This publicly available database can be used to quantify global, regional or biome‐specific carbon budgets; to re‐examine established relationships; to test emerging hypotheses about ecosystem functioning [e.g. a constant net ecosystem production (NEP) to gross primary production (GPP) ratio]; and as benchmarks for model evaluations. In this paper, we present the first analysis of this database. We discuss the climatic influences on GPP, net primary production (NPP) and NEP and present the CO₂ balances for boreal, temperate, and tropical forest biomes based on micrometeorological, ecophysiological, and biometric flux and inventory estimates. Globally, GPP of forests benefited from higher temperatures and precipitation whereas NPP saturated above either a threshold of 1500 mm precipitation or a mean annual temperature of 10 °C. The global pattern in NEP was insensitive to climate and is hypothesized to be mainly determined by nonclimatic conditions such as successional stage, management, site history, and site disturbance. In all biomes, closing the CO₂ balance required the introduction of substantial biome‐specific closure terms. Nonclosure was taken as an indication that respiratory processes, advection, and non‐CO₂ carbon fluxes are not presently being adequately accounted for.     

Chilling to zero degrees disrupts pollen formation but not meiotic microtubule arrays in Triticum aestivum L.

Throughout the wheat‐growing regions of Australia, chilling temperatures below 2 °C occur periodically on consecutive nights during the period of floral development in spring wheat (Triticum aestivum L.). In this study, wheat plants showed significant reductions in fertility when exposed to prolonged chilling temperatures in controlled environment experiments. Among the cultivars tested, the Australian cultivars Kite and Hartog had among the lowest levels of seed set due to chilling and their responses were investigated further. The developmental stage at exposure, the chilling temperature and length of exposure all influenced the level of sterility. The early period of booting, and specifically the +4 cm auricle distance class, was the most sensitive and corresponded to meiosis within the anthers. The response of microtubules to chilling during meiosis in Hartog was monitored, but there was little difference between chilled and control plants. Other abnormalities, such as plasmolysis and cytomixis increased in frequency, were associated with death of developing pollen cells, and could contribute to loss of fertility. The potential for an above‐zero chilling sensitivity in Australian spring wheat varieties could have implications for exploring the tolerance of wheat flower development to chilling and freezing conditions in the field.     

Reliable estimation of biochemical parameters from C3 leaf photosynthesis–intercellular carbon dioxide response curves

The Farquhar–von Caemmerer–Berry (FvCB) model of photosynthesis is a change‐point model and structurally overparameterized for interpreting the response of leaf net assimilation (A) to intercellular CO₂ concentration (Ci). The use of conventional fitting methods may lead not only to incorrect parameters but also several previously unrecognized consequences. For example, the relationships between key parameters may be fixed computationally and certain fits may be produced in which the estimated parameters result in contradictory identification of the limitation states of the data. Here we describe a new approach that is better suited to the FvCB model characteristics. It consists of four main steps: (1) enumeration of all possible distributions of limitation states; (2) fitting the FvCB model to each limitation state distribution by minimizing a distribution‐wise cost function that has desirable properties for parameter estimation; (3) identification and correction of inadmissible fits; and (4) selection of the best fit from all possible limitation state distributions. The new approach implemented theoretical parameter resolvability with numerical procedures that maximally use the information content of the data. It was tested with model simulations, sampled A/Ci curves, and chlorophyll fluorescence measurements of different tree species. The new approach is accessible through the automated website leafweb.ornl.gov.     

Biotic environments and the maintenance of sex–some evidence from mutualistic symbioses

It has previously been proposed that sex is selected for in organisms living in antagonistic biotic environments. Here, the contrasting case of mutualistic biotic environments is considered. In these environments, it is argued that there should be selection against sex and an accompanying low rate of genetic change. This proposition is tested on mutualistic symbioses with substantial histories of co-evolution in which one partner, the inhabitant, lives partly or wholly inside the other, the exhabitant. This asymmetry between the partners means that inhabitants should exhibit a reduction in sex in comparison to related free-living taxa and a lower rate of genetic change than exhabitants.
The patterns that emerge from an analysis of 10 kinds of mutualistic symbiosis strongly support these predictions. Where adequate information is available, sex is usually reduced in inhabitants in comparison to related free-living taxa, although it remains widespread in exhabitants. Inhabitants are also represented by a much smaller taxonomic diversity than exhabitants. Various alternative reasons for these patterns are considered but it is concluded that they are best explained by the mutualistic environment in which the inhabitants live.     

Steps,challenges and lessons in developing community mental health care

This paper summarises our own accumulated experience from developing community-orientated mental health services in England and Italy over the last 20-30 years. From this we have provisionally concluded that the following issues are central to the development of balanced mental health services: a) services need to reflect the priorities of service users and carers; b) evidence supports the need for both hospital and community services; c) services need to be provided close to home; d) some services need to be mobile rather than static; e) interventions need to address both symptoms and disabilities; and f) treatment has to be specific to individual needs. In this paper we consider ten key challenges that often face those trying to develop community-based mental health services: a) dealing with anxiety and uncertainty; b) compensating for a possible lack of structure in community services; c) learning how to initiate new developments; d) managing opposition to change within the mental health system; e) responding to opposition from neighbours; f) negotiating financial obstacles; g) avoiding system rigidities; h) bridging boundaries and barriers; i) maintaining staff morale; and j) creating locally relevant ser- vices rather than seeking “the right answer” from elsewhere.