Wheat seed weight and quality differ temporally in sensitivity to warm or cool conditions during seed development and maturation.

Background and aims: Short periods of extreme temperature may affect wheat (Triticum aestivum) seed weight, but also quality. Temporal sensitivity to extreme temperature during seed development and maturation was investigated. Methods: Plants of 'Tybalt' grown at ambient temperature were moved to growth cabinets at 29/20°C or 34/20°C (2010), or 15/10°C or 34/20°C (2011), for successive 7-d periods from 7 DAA (days after anthesis) onwards, and also 7-65 DAA in 2011. Seed samples were harvested serially and moisture content, weight, ability to germinate, subsequent longevity in air-dry storage and bread-making quality were determined. Key Results: High temperature (34/20°C) reduced final seed weight, with greatest temporal sensitivity at 7-14 or 14-21 DAA. Several aspects of bread-making quality were also most sensitive to high temperature then, but whereas protein quality decreased protein and sulphur concentrations improved. Early exposure to high temperature provided earlier development of ability to germinate and tolerate desiccation, but had little effect on maximum germination capacity. All treatments at 15/10°C resulted in ability to germinate declining between 58 and 65 DAA. Early exposure to high temperature hastened improvement in seed storage longevity, but the subsequent decline in late maturation preceded that in the control. Long (7-65 DAA) exposure to 15/10°C disrupted the development of seed longevity, with no improvement after seed filling ended. Longevity improved during maturation drying in other treatments. Early (7-14 DAA) exposure to high temperature reduced and low temperature increased subsequent longevity at harvest maturity, whereas late (35 or 42-49 DAA) exposure to high temperature increased and low temperature reduced it. Conclusions: Temporal sensitivity to extreme temperature was detected. It varied considerably amongst the contrasting seed variables investigated. Subsequent seed longevity at harvest maturity responded negatively to temperature early in development, but positively later in development and throughout maturation.

Increases in the longevity of desiccation-phase developing rice seeds: response to high-temperature drying depends on harvest moisture content.

BACKGROUND AND AIMS: Previous studies have suggested that the drying conditions routinely used by genebanks may not be optimal for subsequent seed longevity. The aim of this study was to compare the effect of hot-air drying and low-temperature drying on subsequent seed longevity for 20 diverse rice accessions and to consider how factors related to seed production history might influence the results. METHODS: Seeds of rice, Oryza sativa, were produced according to normal regeneration procedures at IRRI. They were harvested at different times [harvest date and days after anthesis (DAA), once for each accession] and dried either in a drying room (DR; 15 % relative humidity, 15 °C) or in a flat-bed heated-air batch dryer (BD; 45 °C, 8 h d(-1)) for up to six daily cycles followed by drying in the DR. Relative longevity was assessed by storage at 10·9 % moisture content and 45 °C. KEY RESULTS: Initial drying in the BD resulted in significantly greater longevity compared with the DR for 14 accessions (seed lots): the period of time for viability to fall to 50 % for seeds dried in the BD as a percentage of that for seeds dried throughout in the DR varied between 1.3 and 372·2 % for these accessions. The seed lots that responded the most were those that were harvested earlier in the season and at higher moisture content. Drying in the BD did not reduce subsequent longevity compared with DR drying for any of the remaining accessions. CONCLUSIONS: Seeds harvested at a moisture content where, according to the moisture desorption isotherm, they could still be metabolically active (>16·2 %) may be in the first stage of the post-mass maturity, desiccation phase of seed development and thus able to increase longevity in response to hot-air drying. The genebank standards regarding seed drying for rice and, perhaps, for other tropical species should therefore be reconsidered.

Developmental changes in the germinability, desiccation tolerance, hardseededness, and longevity of individual seeds of Trifolium ambiguum.

BACKGROUND AND AIMS: Using two parental clones of outcrossing Trifolium ambiguum as a potential model system, we examined how during seed development the maternal parent, number of seeds per pod, seed position within the pod, and pod position within the inflorescence influenced individual seed fresh weight, dry weight, water content, germinability, desiccation tolerance, hardseededness, and subsequent longevity of individual seeds. METHODS: Near simultaneous, manual reciprocal crosses were carried out between clonal lines for two experiments. Infructescences were harvested at intervals during seed development. Each individual seed was weighed and then used to determine dry weight or one of the physiological behaviour traits. KEY RESULTS: Whilst population mass maturity was reached at 33-36 days after pollination (DAP), seed-to-seed variation in maximum seed dry weight, when it was achieved, and when maturation drying commenced, was considerable. Individual seeds acquired germinability between 14 and 44 DAP, desiccation tolerance between 30 and 40 DAP, and the capability to become hardseeded between 30 and 47 DAP. The time for viability to fall to 50 % (p(50)) at 60 % relative humidity and 45 degrees C increased between 36 and 56 DAP, when the seed coats of most individuals had become dark orange, but declined thereafter. Individual seed f. wt at harvest did not correlate with air-dry storage survival period. Analysing survival data for cohorts of seeds reduced the standard deviation of the normal distribution of seed deaths in time, but no sub-population showed complete uniformity of survival period. CONCLUSIONS: Variation in individual seed behaviours within a developing population is inherent and inevitable. In this outbreeder, there is significant variation in seed longevity which appears dependent on embryo genotype with little effect of maternal genotype or architectural factors.

Priming and re-drying improve the survival of mature seeds of Digitalis purpurea during storage.

BACKGROUND AND AIMS: Most priming studies have been conducted on commercial seed lots of unspecified uniformity and maturity, and subsequent seed longevity has been reported to both increase and decrease. Here a seed lot of Digitalis purpurea L. with relatively uniform maturity and known history was used to analyse the effects of priming on seed longevity in air-dry storage. METHODS: Seeds collected close to natural dispersal and dried at 15% relative humidity (RH), 15 degrees C, were placed into experimental storage (60% RH, 45 degrees C) for 14 or 28 d, primed for 48 h at 0, -1, -2, -5, -10 or -15 MPa, re-equilibrated (47% RH, 20 degrees C) and then returned to storage. Further seed samples were primed for 2 or 48 h at -1 MPa and either dried at 15% RH, 15 degrees C or immediately re-equilibrated for experimental storage. Finally, some seeds were given up to three cycles of experimental storage and priming (48 h at -1 MPa). KEY RESULTS: Priming at -1 MPa had a variable effect on subsequent survival during experimental storage. The shortest lived seeds in the control population showed slightly increased life spans; the longer lived seeds showed reduced life spans. In contrast, seeds first stored for 14 or 28 d before priming had substantially increased life spans. The increase tended to be greatest in the shortest lived fraction of the seed population. Both the period of rehydration and the subsequent drying conditions had significant effects on longevity. Interrupting air-dry storage with additional cycles of priming also increased longevity. CONCLUSIONS: The extent of prior deterioration and the post-priming desiccation environment affect the benefits of priming to the subsequent survival of mature seeds. Rehydration-dehydration treatments may have potential as an adjunct or alternative to the regeneration of seed accessions maintained in gene banks for plant biodiversity conservation or plant breeding.

Post-abscission, pre-dispersal seeds of Digitalis purpurea remain in a developmental state that is not terminated by desiccation ex planta.

BACKGROUND AND AIMS: Seed quality may be compromised if seeds are harvested before natural dispersal (shedding). It has been shown previously that slow or delayed drying can increase potential quality compared with immediate rapid drying. This study set out to investigate whether or not there is a critical moisture content, below which drying terminates maturation events for seeds harvested after mass maturity but before dispersal. METHODS: Seeds of foxglove (Digitalis purpurea) in the post-abscission pre-dispersal phase were held at between 15 and 95 % RH for 4 or 8 d, with or without re-hydration to 95 % RH for a further 4 d, before drying to equilibrium at 15 % RH. In addition, dry seeds were primed for 48 h at -1 MPa. Subsequent seed longevity was assessed at 60 % RH and 45 degrees C. KEY RESULTS: Rate of germination and longevity were improved by holding seeds at a wide range of humidities after harvest. Longevity was further improved by re-hydration at 95 % RH. Priming improved the longevity of the seeds dried immediately after harvest, but not of those first held at 95 % RH for 8 d prior to drying. CONCLUSIONS: Maturation continued ex planta in these post-abscission, pre-dispersal seeds of D. purpurea dried at 15-80 % RH at a rate correlated positively with RH (cf. ageing of mature seeds). Subsequent re-hydration at 95 % RH enabled a further improvement in quality. Priming seeds initially stored air-dry for 3 months also allowed maturation events to resume. However, once individual seeds within the population had reached maximum longevity, priming had a negative impact on their subsequent survival.

Temperature sensitivity of the low-moisture-content limit to negative seed longevity--moisture content relationships in hermetic storage.

UNLABELLED: BACKGROUND AND AIMS The negative logarithmic relationship between orthodox seed longevity and moisture content in hermetic storage is subject to a low-moisture-content limit (m(c)), but is m(c) affected by temperature? METHODS: Red clover (Trifolium pratense) and alfalfa (Medicago sativa) seeds were stored hermetically at 12 moisture contents (2-15 %) and five temperatures (-20, 30, 40, 50 and 65 degrees C) for up to 14.5 years, and loss in viability was estimated. KEY RESULTS: Viability did not change during 14.5 years hermetic storage at -20 degrees C with moisture contents from 2.2 to 14.9 % for red clover, or 2.0 to 12.0 % for alfalfa. Negative logarithmic relationships between longevity and moisture contents >m(c) were detected at 30-65 degrees C, with discontinuities at low moisture contents; m(c) varied between 4.0 and 5.4 % (red clover) or 4.2 and 5.5 % (alfalfa), depending upon storage temperature. Within the ranges investigated, a reduction in moisture content below m(c) at any one temperature had no effect on longevity. Estimates of m(c) were greater the cooler the temperature, the relationship (P < 0.01) being curvilinear. Above m(c), the estimates of C(H) and C(Q) (i.e. the temperature term of the seed viability equation) did not differ (P > 0.10) between species, whereas those of K(E) and C(W) did (P < 0.001). CONCLUSIONS: The low-moisture-content limit to negative logarithmic relationships between seed longevity and moisture content in hermetic storage increased the cooler the storage temperature, by approx. 1.5 % over 35 degrees C (4.0-4.2 % at 65 degrees C to 5.4-5.5 % at 30-40 degrees C) in these species. Further reduction in moisture content was not damaging. The variation in m(c) implies greater sensitivity of longevity to temperature above, compared with below, m(c). This was confirmed (P < 0.005).

Mutant alleles at the rugosus loci in pea affect seed moisture sorption isotherms and the relations between seed longevity and moisture content.

Pea (Pisum sativum L.) mutant near-isogenic lines (RRrbrb, rrRbRb, rrrbrb) with lower starch but higher lipid contents, brought about by lesions in the starch biosynthetic pathway, had seed moisture sorption isotherms displaced below that of the wild type (RRRbRb). The negative logarithmic relationship between seed longevity and seed storage moisture content (%, f.wt basis), determined in hermetic storage at 65 degrees C, also differed: longevity in the mutant near-isogenic lines was poorer and less sensitive to moisture content than in the wild type (i.e. C(W) was lower). The low-moisture-content limit (m(c)) to this relation also differed, being lower in the mutant near-isogenic lines (5.4-5.9%) than in the wild type (6.1%). In contrast, all four near-isogenic lines showed no difference (P >0.25) in the negative semi-logarithmic relationship between equilibrium relative humidity (ERH) and seed longevity. It is concluded that the effect of these alleles at the r and rb loci on seed longevity was largely indirect; a consequence of their effect on seed composition and hence on moisture sorption isotherms. However, this explanation could not be invoked at moisture contents below m(c) where differences in longevity remained substantial (RRRbRb double that of rrrbrb). Hence, these mutant alleles affected seed longevity directly at very low moisture contents.

Use of field observations to characterise genotypic flowering responses to photoperiod and temperature: a soyabean exemplar.

Thirty-nine accessions of soyabean [Glycine max (L.) Merrill] and 1 of wild annual soyabean (Glycine soja L.) were sown at two sites in Taiwan in 1989 and 1990 and on six occasions during 1990 at one site in Queensland, Australia. On two of the occasions in Australia additional treatments extended natural daylengths by 0.5 h and 2 h. The number of days from sowing for the first flower to appear on 50% of the plants in each treatment was recorded (f), and from these values the rate of progress towards flowering (1/f) was related to temperature and photoperiod. In photoperiod-insensitive accessions it was confirmed that the rate is linearly related to temperature at least up to about 29°C. In photoperiod-sensitive genotypes this is also the case in shorter daylengths but when the critical photoperiod (P c) is exceeded flowering is delayed. This delay increases with photoperiod until a ceiling photoperiod (P ce) is reached. Between P c and P ce, 1/f is linearly related to both temperature (positive) and photoperiod (negative), but in photoperiods longer than P ce there is no further response to either factor. The resulting triple-intersecting-plane response surface can be defined by six genetically-determined coefficients, the values of which are environment-independent but predict time to flower in any environment, and thus quantify the genotype x environment interaction. By this means the field data were used to characterise the photothermal responses of all 40 accessions. The outcome of this characterisation in conjunction with an analysis of the world-wide range of photothermal environments in which soyabean crops are grown lead to the following conclusions: (1) photoperiod-insensitivity is essential in soyabean crops in temperate latitudes, but such genotypes flower too rapidly for satisfactory yields in the tropics; (2) photoperiod-sensitivity appears to be essential to delay flowering sufficiently to allow adequate biomass accumulation in the warm climates of the tropics; (3) contrary to a widely held view, some degree of photoperiod-sensitivity is also needed in the tropics if crop-duration homeostasis is required where there is variation in sowing dates (this is achieved through a photoperiod-controlled delay in flowering which counteracts the seasonal increase in temperature that is correlated with increase in day-length); and (4) a greater degree of photoperiod-sensitivity is necessary to provide maturity-date homeostasis for variable sowing dates - a valuable attribute in regions of uncertain rainfall. Since the triple-intersecting-plane response model used here also applies to other species, the use of field data to characterise the photothermal responses of other crops is discussed briefly.

Characterization of photothermal flowering responses in maturity isolines of soyabean [Glycine max (L.) Merrill] cv. Clark.

All eight isolines of three maturity genes (E(1)/e(1), E(2)/e(2), and E(3)/e(3)) of soyabean [Glycine max (L.) Merrill] cv. Clark were grown in widely different combinations of photoperiod and temperature. Under the more inductive conditions, i.e. in a warm mean temperature (30 degrees C) when daylengths were less than the critical value (i.e. less than about 13 h), the isolines flowered at similar times (23-24 d). The responses of all isolines to temperature were also similar, if not identical. Increase in daylength above the critical photoperiod progressively delayed flowering until the time taken to flower (f) reached a maximum at the ceiling photoperiod. The relations between the rate of progress towards flowering (1/f) and photoperiod (between the critical and ceiling values) were linear. The coefficient characterizing the slope of the response (photoperiod sensitivity) varied amongst the isolines. These responses could be grouped into three categories of increasing sensitivity: (1) least sensitive, e(1)e(2)e(3), e(1)E(2)e(3), e(1)e(2)E(3); (2) intermediate, E(1)e(2)e(3), e(1)E(2)E(3), and (3) most sensitive, E(1)E(2)e(3), E(1)e(2)E(3), E(1)E(2)E(3). Thus, in the Clark cultivar genetic background, E(1) induces greater photoperiod sensitivity but neither E(2) nor E(3) on their own have any effect. However, both E(2) and E(3) together induce photoperiod sensitivity comparable to that induced by E(1) alone. Furthermore, in addition to this epistasis, either E(2) or E(3) has considerable epistatic effect on E(1), further increasing photoperiod sensitivity. The effects of these genes and their epistasis were also reflected in the extent of the maximum delays to flowering which occur when the ceiling photoperiod is exceeded, and also possibly in earliness in circumstances when photoperiods were below the critical value.

Variation in the durations of the photoperiod-sensitive and photoperiod-insensitive phases of development to flowering among eight maturity isolines of soyabean [Glycine max (L.) Merrill].

In soyabean [Glycine max (L.) Merrill] the period between sowing and flowering is comprised of three successive developmental phases--pre-inductive, inductive and post-inductive--in which the rate of development is affected, respectively, by temperature only, by photoperiod and temperature, and then again by temperature only. A reciprocal-transfer experiment (carried out at a mean temperature of 25 degrees C) in which cohorts of plants were transferred successively between short and long photoperiods and vice-versa showed that eight combinations of three pairs of maturity alleles (E(1)/e(1), E(2)/e(2), E(3)/e(3)) had their greatest effect on the duration of the inductive phase in long days. This phase was increased with the increasing photoperiod sensitivity induced by the different gene combinations, and ranged from about 27 to 54 d according to genotype. In a short day regime (11.5 h d(-1)), less than the critical photoperiod, the duration of the inductive phase was brief-requiring about 11 photoperiodic cycles in the less photoperiod-sensitive genotypes and only about seven cycles in the more sensitive ones. The maturity genes also affected the duration of the two photoperiod-insensitive phases; these durations were positively correlated with the photoperiod-sensitivity potential of the gene combinations. The largest effect was on the pre-inductive phase which varied from 3 to 11 d, while the post-inductive phase varied from about 13 to 18 d. As a consequence of these nonphotoperiodic effects of the maturity genes, even in the most inductive regimes (daylengths less than the critical photoperiod) the time taken to flower by the less photoperiod-sensitive combinations of maturity genes was somewhat less than in the more sensitive combinations-ranging from about 28 to 34 d. The genetic and practical implications of these findings are discussed.

Field evaluation of a model of photothermal flowering responses in a world lentil collection.

A model to predict flowering time in diverse lentil genotypes grown under widely different photothermal conditions was developed in controlled environments. The present study evaluated that model with a world germ plasm collection of 369 accessions using two field environments in Syria and two in Pakistan. Photoperiod alone accounted for 69% of the variance in 1/f, the reciprocal of time (d) from sowing to flower. In contrast, temperature alone did not account for a significant proportion of variation in flowering time due to the exposure of plants to supra-optimal temperatures in the late-sown Syrian trial. With the model mean pre-flowering values of photoperiod and temperature combined additively to account for 90.3% of the variance of 1/f over accessions. The correlation of field-derived estimates of temperature sensitivity of accessions to glass-house-derived estimates was significant at P = 0.05, but the equivalent correlation for estimates of photoperiodic sensitivity was higher at P < 0.01. Flowering in the field was better measured as time from sowing to 50% plants in flower rather than time to first bloom or its node number. Dissemination of the lentil crop following domestication in West Asia to the lower latitudes such as Ethiopia and India has depended on selection for intrinsic earliness and reduced sensitivity to photoperiod. Movement from West Asia to the higher latitudes accompanied by spring sowing has resulted in a modest reduction in photoperiod sensitivity and an increase in temperature sensitivity.

Uses of an empirically derived client typology based on level of functioning: twelve years of the CCAR.

The Colorado Client Assessment Record (CCAR) is a problem checklist and level of functioning rating instrument used to describe admission to a public mental health system. A brief, non-technical summary of recent research and administrative applications involving this instrument is presented. A stable factor structure, generalizable to several diverse client populations, is reported. Scaling procedures for measuring these procedures and a client typology based on this scaling are described. The client typology is differentially related to the types of services received and the costs of treatment episodes. The typology is also used to understand differences in case mixes and lengths of stay at two state hospitals.

Characterization of responses to temperature and photoperiod for time to flowering in a world lentil collection.

The times from sowing to first flowering (f) of 231 accessions of lentil (Lens culinaris Medik.), comprising germ plasm from eight countries and breeding lines from ICARDA in Syria, were recorded in four glasshouse environments; two photoperiods (16 and 13 h/day) combined with warmer (24°/13°C) and cooler (18°/9°C) day/night temperatures. The linear model 1/f=a+bT + cP (where T is mean diurnal temperature and P is photoperiod) provided an average fit over the 231 accessions of r (2)=0.852. Since there is no interaction term in this linear model, the flowering responses of an accession to temperature and photoperiod are independent. The values of the constants b and c indicate relative responsiveness of rate of progress towards flowering (1/f) to temperature and photoperiod, respectively. Comparison among the 231 accessions showed a weak, but significant, negative correlation between the values of b and c (r=-0.291, P<0.01). Since the proportion of the variance of b not attributed to its linear regression on c was >0.91, we conclude that these phenological responses are under separate control and that there is considerable scope for selection of any combination of sensitivities to temperature and photoperiod in lentil. Just as a large proportion of the variation among accessions in mean time to first flowering was attributed to country of origin, so also was variability in the values of the constants a, b, and c. In particular, sensitivity to photoperiod (i.e., the value of constant c) was dependent upon latitude of origin. Breeding lines from ICARDA were equally variable in a, b, and c as were germ plasm accessions from elsewhere, while the mean values were similar to those of accessions from neighboring Jordan. A single accession of wild lentil (L. culinaris subsp. orientalis) from Turkey showed flowering responses to T and P similar to the mean value of accessions of cultivated lentil from that country. Results from diverse environments for the Argentinian cv Precoz show that the use of this linear model facilitates predictions of time to flowering in any environment (within wide limits) of known mean temperature and photoperiod. The model, then, minimizes the need for multisite evaluations of phenology, since predictions of pre-flowering duration in any environment, and characterization of flowering responses to photoperiod and temperature, can now be achieved by screening germ plasm in a few, carefully selected locations.

Planning a continuum of residential/service settings for the chronically mentally ill: the Colorado experience.

Thinking regarding the needs of the chronically mentally ill has changed substantially in the post-deinstitutionalization period. Increasingly, the heterogeneity existing within this population has been recognized along with the need for an integrated continuum of residences and services. At a state level, this realization has stimulated the development of planning models which are used to predict the number and types of residential/service slots needed by the chronically mentally ill. In Colorado, a model was developed which uses data-based client profiles to predict needs along a continuum of services ranging from inpatient treatment to independent living with mental health support. In this paper, we discuss the development of the model and present the results of implementing it for a sample of 5,017 chronically mentally ill clients. The practical and heuristic value of the model is featured as well as its implications for further research.

Insensitivity of erythrocyte 2,3-bisphosphoglycerate to changes in extracellular phosphate concentration in vitro.

Erythrocytes maintained in vitro under controlled conditions at pH 7.40 were unable to respond to changes in extracellular phosphate concentrations with changes in intracellular 2,3-bisphosphoglycerate content over an 8 h incubation period. Increased extracellular phosphate concentrations did not retard the rate at which 2,3-bisphosphoglycerate concentrations fell when erythrocytes were incubated at pH 7.10. Elevated extracellular phosphate concentrations did not increase the rate of recovery of intracellular 2,3-bisphosphoglycerate concentrations when erythrocytes were returned to pH 7.40 having been incubated at pH 7.10. The rate at which 2,3-bisphosphoglycerate concentrations increased under these latter conditions was too slow to counterbalance any effect that adjustment of blood pH may have on the position of the haemoglobin-oxygen dissociation curve during treatment of diabetic ketoacidosis.