Characterization of the Photoperiodic Response of Post-flowering Development in Maturity Isolines of Soyabean [Glycine max(L.) Merrill] 'Clark'

Plants of all eight isolines of three maturity genes (all combinationsof two alleles at the three lociE₁/e₁,E₂/e₂,E₃/e₃) of soyabean[Glycine max(L.) Merrill] were grown in four different photoperiods(12, 13, 14 or 15 h d^-1) at 30/24 °C from first flower openingto harvest maturity. Photoperiod, isoline, and their interaction,affected significantly (P<0.01) the duration between firstand last flowering, and reproductive duration. The interactionsbetween genotype and photoperiod were sufficiently strong thatconsiderable differences in these durations were detected amongisolines in the least-inductive environment (15 h d^-1) whereasdifferences were negligible in the most-inductive regime (12h d^-1). There was a negative linear relation between photoperiodand both rate of progress from the appearance of the first tothe last flower, and rate of progress from first flowering toharvest maturity; sensitivity to photoperiod varied (P<0.05)six- and five-fold, respectively, among the extreme isolines(e₁e₂e₃andE₁E₂E₃). The three dominant allelesE₁,E₂andE₃, singly,had comparatively little effect on post-flowering traits, butconsiderable epistasis (particularly betweenE₁andE₂) was detectedfor sensitivity to photoperiod in respect of rates of progressfrom the appearance of the first to the last flower, and fromfirst flower to harvest maturity. Thus the large variationsdetected for these traits are the consequence of genexgene (xgene)xenvironmentinteractions.Copyright 1998 Annals of Botany Company. Glycine max(L.) Merrill, soyabean, maturity genes, flowering, photoperiod.     

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 sowingand flowering is comprised of three successive developmentalphases—pre-inductive, inductive and post-inductive—inwhich the rate of development is affected, respectively, bytemperature only, by photoperiod and temperature, and then againby temperature only. A reciprocal-transfer experiment (carriedout at a mean temperature of 25°C) in which cohorts of plantswere transferred successively between short and long photoperiodsand vice-versa showed that eight combinations of three pairsof maturity alleles (E₁/e₁, E₂ /e₂, E₃ /e₃) had their greatesteffect on the duration of the inductive phase in long days.This phase was increased with the increasing photoperiod sensitivityinduced by the different gene combinations, and ranged fromabout 27 to 54 d according to genotype. In a short day regime(11·5 h d^-1), less than the critical photoperiod, theduration of the inductive phase was brief—requiring about11 photoperiodic cycles in the less photoperiod-sensitive genotypesand only about seven cycles in the more sensitive ones. Thematurity genes also affected the duration of the two photoperiod-insensitivephases; these durations were positively correlated with thephotoperiod-sensitivity potential of the gene combinations.The largest effect was on the pre-inductive phase which variedfrom 3 to 11 d, while the post-inductive phase varied from about13 to 18 d. As a consequence of these non-photoperiodic effectsof the maturity genes, even in the most inductive regimes (daylengthsless than the critical photoperiod) the time taken to flowerby the less photoperiod-sensitive combinations of maturity geneswas somewhat less than in the more sensitive combinations—rangingfrom about 28 to 34 d. The genetic and practical implicationsof these findings are discussed.Copyright 1994, 1999 AcademicPress Glycine max (L.) Merrill, soyabean, maturity genes, isolines, flowering, photoperiod     

Effects of Photoperiod and Maturity Genes on Plant Growth, Partitioning, Radiation Use Efficiency, and Yield in Soyabean [Glycine max(L.) Merrill] 'Clark'

Plants of four isolines of soyabean [Glycine max(L.) Merrill]‘Clark’, viz‘L71-920’ (maturity genecomplemente₁e₂e₃ ), ‘L80-5914’ (E₁e₂e₃), ‘Clark’(e₁E₂E₃), and ‘L65-3366’ (E₁E₂E₃), were grown inshort (12.25 h d ^{- 1}natural light) and long days (12.25 h d^{- 1}natural light supplemented with 2.75 h d ^{- 1}low-irradianceartificial light) from first flowering to maturity in a polythenetunnel maintained at 30/24°C (day/night). Whereas therewere few differences among the isolines grown in short days,in long days the dominant alleles increased crop duration, biomassand seed yield substantially. Increases in biological and economicyield were not solely a consequence of longer crop duration:the dominant alleles also increased crop growth rate and radiationuse efficiency in long days (from 1.3 g MJ ^{- 1}total radiationine₁e₂e₃ to 2.8 g MJ ^{- 1}inE₁E₂E₃ ). Greater radiation use efficiencyresulted from a relatively longer leaf area duration, betterdistribution and orientation of a larger mass of leaves withinthe canopy, and smaller partitioning of assimilates to reproductivestructures. The work reveals the substantial effects of thethree lociE₁ / e₁, E₂/ e₂and E₃/e₃ on the response of plantgrowth, as well as development, to environment. Their relevanceto crop adaptation is discussed. Copyright 2000 Annals of BotanyCompany Glycine max(L.) Merrill, soyabean, maturity genes, flowering, phenology, growth, yield     

Linear Relations between Carbon Dioxide Concentration and Rate of Development Towards Flowering in Sorghum, Cowpea and Soyabean

Negative linear relations were detected (P < 0·005)between the rate of progress from sowing to panicle initiationand CO₂ concentration (210-720 µmol CO₂ mol^-1 air) fortwo genotypes of sorghum [Sorghum bicolor (L.) Moench]. Relationsbetween CO₂ concentration and the rate of progress from sowingto first flowering were also negative in soyabean [Glycine max(L.) Merrill] (P < 0·025), but positive in cowpea[Vigna unguiculata (L.) Walp.] (P < 0·025), albeitthat in both grain legumes sensitivity was much less than insorghum. Thus CO₂ elevation does not delay flowering in allshort-day species. The considerable effect of CO₂ concentrationon times to panicle initiation resulted in large differencesamong the sorghum plants at this developmental stage; with increasein CO₂ concentration, plants were taller with slightly moreleaves and more pronounced apical extension. At the same timeafter sowing however, sorghum plants were heavier (P < 0·05)at 210 than at 360 µmol CO₂ mol^-1 air. In contrast, relationsbetween the dry masses of the soyabean and cowpea plants andCO₂ concentration were positive and curvilinear (P < 0·05).It is suggested that the impact of global environmental changecould be severe for sorghum production in the semi-arid tropics.Copyright1995, 1999 Academic Press Sorghum bicolor (L.) Moench., sorghum, Glycine max (L.) Merrill, soyabean, Vigna unguiculata (L.) Walp., cowpea, development, flowering, CO₂, dry matter accumulation, environmental change     

Characterization of Photothermal Flowering Responses in Maturity Isolines of Soyabean [Glycine max (L.) Merrill] cv. Clark

All eight isolines of three maturity genes (E₁/e₁, E₂ /e₂, andE₃ /e₃) of soyabean [Glycine max (L.) Merrill] cv. Clark weregrown in widely different combinations of photoperiod and temperature.Under the more inductive conditions, i.e. in a warm mean temperature(30°C) when daylengths were less than the critical value(i.e. less than about 13 h), the isolines flowered at similartimes (23-24 d). The responses of all isolines to temperaturewere also similar, if not identical. Increase in daylength abovethe critical photoperiod progressively delayed flowering untilthe time taken to flower (f) reached a maximum at the ceilingphotoperiod. The relations between the rate of progress towardsflowering (1/f) and photoperiod (between the critical and ceilingvalues) were linear. The coefficient characterizing the slopeof the response (photoperiod sensitivity) varied amongst theisolines. These responses could be grouped into three categoriesof increasing sensitivity: (1) least sensitive, e₁e₂e₃ , e₁E₂e₃, e₁e₂E₃ ; (2) intermediate, E₁e₂e₃ , e₁E₂E₃ ; and (3) mostsensitive, E₁E₂e₃, E₁e₂E₃ , E₁E₂E₃ . Thus, in the Clark cultivargenetic background, E₁ induces greater photoperiod sensitivitybut neither E₂ nor E₃ on their own have any effect. However,both E₂ and E₃ together induce photoperiod sensitivity comparableto that induced by E₁ alone. Furthermore, in addition to thisepistasis, either E₂ or E₃ has considerable epistatic effecton E₁, further increasing photoperiod sensitivity. The effectsof these genes and their epistasis were also reflected in theextent of the maximum delays to flowering which occur when theceiling photoperiod is exceeded, and also possibly in earlinessin circumstances when photoperiods were below the critical value.Copyright1994, 1999 Academic Press Glycine max (L.) Merrill, soyabean, maturity genes, flowering, photoperiod, temperature     

Durations of the Photoperiod-sensitive and Photoperiod-insensitive Phases of Development to Flowering in Four Cultivars of Soyabean [Glycine max (L.) Merrill]

Four cultivars of soyabean [Glycine max (L.) Merill] of diverseorigin were grown in pots in a plastic-house maintained at day/nighttemperatures of 30/20°C. Plants were transferred at varioustimes after sowing from short (11·5 h d^-1) to long (13·5h d^-1) days and vice versa. The times from sowing to first floweringfor control plants grown continuously in short days varied from38 to 53 d, whereas the flowering of plants grown continuouslyin long days was delayed by about 20 d in each cultivar. Theduration of the initial photoperiod-insensitive phase (oftencalled the juvenile phase) varied three-fold between cultivars,i.e. from 11 to 33 d. As expected, the duration of the photoperiod-sensitivephase was greater in long days, but there was comparativelylittle genetic variation in photoperiod-sensitivity as definedin terms of days delay in time to flowering per hour increasein photoperiod (9-11 d h^-1). Similarly, there was little variationin the photoperiod-insensitive post-inductive phase; it rangedfrom 15 to 20 d. In consequence, the duration of the initialphotoperiod-insensitive phase was a strong determinant of timeto first flowering in these cultivars. The importance of thisso-called juvenile trait is discussed in terms of preventingthe premature flowering of USA-adapted cultivars when grownin short tropical daylengths and thus improving the adaptationof the crop to the lower latitudes.Copyright 1993, 1999 AcademicPress Glycine max (L.) Merill, soyabean, photoperiodism, juvenility, flowering     

Effects of Temperature and Photoperiod on Flowering in Soya bean [Glycine max (L.) Merrill]: a Quantitative Model

Factorial combinations of five photoperiods (8 h 20 min, 10h, 11 h 40 min, 13 h 20 min and 15 h) and three night temperatures(14, 19 and 24 C) combined with a single day temperature (30C) were imposed on nodulated plants of nine soya bean genotypes[Glycine max (L.) Merrill] grown in pots in growth cabinets.The times to first appearance of open flowers were recorded.For a photoperiod-insensitive cultivar, and for the remainingeight photoperiod-sensitive genotypes in photoperiods shorterthan the critical daylength, the rates of progress towards flowering(the reciprocals of the times taken to flower) were linear functionsof mean diurnal temperature. For all photoperiod-sensitive genotypes,times to flowering in photoperiods longer than the criticaldaylength increased as inverse functions of both increasingphotoperiod and decreasing temperature. A consequence of thesetwo relations is that the critical daylength becomes longerwith higher mean temperatures. In the five photoperiod-sensitivegenotypes which flowered in all environments before the experimentwas terminated (after 150 d) the delays in flowering due tolow temperatures or long photoperiods were limited by a maximumperiod to flowering specific for each genotype. These resultsare discussed in relation to the development of a simple techniquefor the large-scale screening of soya bean germplasm to determinephoto-thermal response surfaces for flowering. Glycine max (L.) Merrill, soya bean, flowering, photoperiod, temperature, screening, germplasm     

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.     

Differential Effects of Day and Night Temperature on Development to Flowering in Rice

There are conflicting reports with regard to difference in effectsof day temperature (T_D) and night temperatures (T_N) on plantdevelopment. The objective of this study is to determine whetherthere are different effects ofT_DandT_Non development from sowingto flowering in rice (Oryza sativaL.). Plants of 24 rice cultivars were grown in naturally-lightedgrowth chambers at five diurnally constant (22, 24, 26, 28 and32 °C) and four diurnally fluctuating temperatures (26 /22,30 /22, 22 /26 and 22 /30 °C forT_D/T_Nwith 12hd^-1each) witha constant photoperiod of 12hd^-1. The treatments were selectedto enable the separation of effects ofT_DandT_Non developmentrate (DR). The response of DR to constant temperatures was typically nonlinear.This nonlinearity could not explain the difference in floweringdates between fluctuating temperatures with the same mean dailyvalue but oppositeT_D/T_Ndifferences. Differential effects ofT_DandT_NonDR to flowering were detected in all but one cultivar. In mostcases,T_Dexerted a greater influence thanT_N, in contrast withmany previous reports based on the assumption of a linearitybetween DR and temperature. The data were further analysed bya nonlinear model which separated effects ofT_DandT_N. The estimatedvalue for the optimumT_Nwas generally 25 –29 °C, about2 –4 °C lower than the estimated optimumT_Din mostcultivars. The effects ofT_DandT_Non DR were found to be interactivein some cultivars. These results form a new basis for modellingflowering dates in rice. Oryza sativa; rice; flowering; development; day and night temperature; thermoperiodicity     

Simulation and Prediction of Plant Phenology for Five Crops Based on PhotoperiodxTemperature Interaction

This paper presents a plant phenological model based on genotypextemperaturexphotoperiodinteraction (GPTmodel). In the model, rate of development towardsa specified stage (e.g. flowering) for a given genotype is composedof three components: the genotype's maximum rate of development;any delay due to a non-optimal temperature; and any delay dueto a photoperiod response. It is assumed that development tothe specified stage is an autonomous process established bymost, if not all, genes other than the vernalization genes andthe photoperiod genes; and that this autonomous process is delayedby any activity of the photoperiod genes. Since all physiologicalprocesses are modulated by temperature, any photoperiod responseis inevitably a photoperiodxtemperature interaction. This interactionis simulated by assuming that the photoperiod gene activityoccurs only beyond a critical photoperiod (P_c) and is enlargedby temperature above a base temperature (T_bp) that allows thephotoperiod gene activity. The model is written asR=1/D_b-S_t(T-T_opt)²-S_p(T-T_bp)|P-P_c|, whereRis the expected rate of development to the specifiedstage under any combination of temperature (T) and photoperiod(P). The other model parameters are:S_p, the sensitivity to adelaying photoperiod;T_opt, the optimum temperature for developmentin the absence of the photoperiod response;S_t, the sensitivityto a non-optimum temperature; andD_b, the basic duration to thespecified stage (or intrinsic earliness), the inverse of whichis the maximum rate of development.D_bis observable only ifT=T_optandsimultaneouslyP     

Production of Oikopleura longicauda (Tunicata: Appendicularia) in Toyama Bay, southern Japan Sea

Oikopleura longicauda occurred throughout the year in ToyamaBay, southern Japan Sea, and analysis of its size compositionand maturity revealed that reproduction was continuous overtheyear. Somatic growth production (P_g) varied with season from0.03 to 103 mg carbon (C) m^–2day^–1 (annual P_g 4.5g C m^–2), and house production (P_e) from 0.11 to 266 mgC m^–2 day^–1 (annualP_e 11.3 g C m^–2). The annualP_g/B ratio was 176. Compared with production data of some predominantzooplankton species in Toyama Bay, it is suggested that despitetheir smaller biomass, appendicularians are an important secondaryproducer.     

Photoperiod Sensitivity during Flower Development of Opium Poppy (Papaver somniferum L.)

Photoperiod is a major factor in flower development of the opiumpoppy (Papaver somniferum L. ‘album DC’) which isa long-day plant. Predicting time to flower in field-grown opiumpoppy requires knowledge of which stages of growth are sensitiveto photoperiod and how the rate of flower development is influencedby photoperiod. The objective of this work was to determinewhen poppy plants first become sensitive to photoperiod andhow long photoperiod continues to influence the time to firstflower under consistent temperature conditions. Plants weregrown in artificially-lit growth chambers with either a 16-hphotoperiod (highly flower inductive) or a 9-h photoperiod (non-inductive).Plants were transferred at 1 to 3-d intervals from a 16- toa 9-h photoperiod andvice versa . All chambers were maintainedat a 12-h thermoperiod of 25/20 °C. Poppy plants becamesensitive to photoperiod 4 d after emergence and required aminimum of four inductive cycles (short dark periods) beforethe plant flowered. Additional inductive cycles, up to a maximumof nine, hastened flowering. After 13 inductive cycles, floweringtime was no longer influenced by photoperiod. These resultsindicate that the interval between emergence and first flowercan be divided into four phases: (1) a photoperiod-insensitivejuvenile phase (JP); (2) a photoperiod-sensitive inductive phase(PSP); (3) a photoperiod-sensitive post-inductive phase (PSPP);and (4) a photoperiod-insensitive post-inductive phase (PIPP).The minimum durations of these phases forPapaver somniferum‘album DC’ under the conditions of our experimentwere determined as 4 d, 4 d, 9 d, and 14 d, respectively. Anthesis; days to flowering; flower bud; opium poppy; Papaver somniferum L.; photoperiod; photoperiod sensitivity; predicting time to flowering; transfer     

Influence of group B streptococci on piglet pulmonary artery response to bradykinin

To study whether a sepsis-induced increase indes-Arg⁹-bradykinin(des-Arg⁹-BK) and bradykinin (BK)B₁-receptor activity participatesin the observed increase in pulmonary vascular resistance in neonatal group B streptococcal sepsis (GBS), isometric force bioassays ofpulmonary artery (PA) rings were studied, after 4-h exposure to eitherKrebs or GBS, by using the following protocols:1) BK dose-response curve,2) vascular response to BK withN^G-nitro-L-arginine methyl ester(L-NAME), and3) response todes-Arg⁹-BK (BK metabolite andB₁ agonist). PA rings exposed toBK resulted in contraction in the GBS group and a decrease in restingtension in the Control group (P = 0.034) at a concentration of10⁵ M. GBS-treated PA ringscontracted more to des-Arg⁹-BKthan did Controls (P < 0.001). BK(10⁶ M) relaxedpreconstricted PA rings incubated in GBS less than BK relaxed Controls(P < 0.001), and preincubation withL-NAME decreased relaxation inboth. These results suggest that GBS decreased endothelium-dependent BKrelaxation and increased contractile response todes-Arg⁹-BK. We speculate thatthis occurs secondary to upregulation of B₁ receptors reflected byB₁-agonist-mediated PA contraction.

     

Functional characterization of two S-nitroso-L-cysteine transporters, which mediate movement of NO equivalents into vascular cells

In myogenic C₂C₁₂ cells, 5 mM creatine increased the incorporation of labeled [³⁵S]methionine into sarcoplasmic (+20%, P < 0.05) and myofibrillar proteins (+50%, P < 0.01). Creatine also promoted the fusion of myoblasts assessed by an increased number of nuclei incorporated within myotubes (+40%, P < 0.001). Expression of myosin heavy chain type II (+1,300%, P < 0.001), troponin T (+65%, P < 0.01), and titin (+40%, P < 0.05) was enhanced by creatine. Mannitol, taurine, and -alanine did not mimic the effect of creatine, ruling out an osmolarity-dependent mechanism. The addition of rapamycin, the inhibitor of mammalian target of rapamycin/70-kDa ribosomal S6 protein kinase (mTOR/p70^s6k) pathway, and SB 202190, the inhibitor of p38, completely blocked differentiation in control cells, and creatine did not reverse this inhibition, suggesting that the mTOR/p70^s6k and p38 pathways could be potentially involved in the effect induced by creatine on differentiation. Creatine upregulated phosphorylation of protein kinase B (Akt/PKB; +60%, P < 0.001), glycogen synthase kinase-3 (+70%, P < 0.001), and p70^s6k (+50%, P < 0.001). Creatine also affected the phosphorylation state of p38 (–50% at 24 h and +70% at 96 h, P < 0.05) as well as the nuclear content of its downstream targets myocyte enhancer factor-2 (–55% at 48 h and +170% at 96 h, P < 0.05) and MyoD (+60%, P < 0.01). In conclusion, this study points out the involvement of the p38 and the Akt/PKB-p70^s6k pathways in the enhanced differentiation induced by creatine in C₂C₁₂ cells. protein synthesis; insulin-like growth factor; mitogen-activated protein kinase; extracellular signal-regulated kinase 1/2; 70-kDa ribosomal S6 protein kinase     

The Effect of Temperature on Leaf Appearance in Rice

Temperature is the principal environmental determinant of cropleaf appearance. The objective of this study is to analyse whetherthere are different effects of day temperature (T_D) and nighttemperature (T_N) on main-stem leaf appearance in rice (OryzasativaL.). Plants of 12 rice cultivars were grown at five constant temperatures(22, 24, 26, 28 and 32 °C) and four diurnally fluctuatingtemperatures (T_D/T_N: 26 /22, 30 /22, 22 /26 and 22 /30 °C)with a constant photoperiod of 12hd^-1. The leaf appearance onthe main stem was measured. A constant change in leaf appearance rate was observed duringontogeny. The relation between the number of emerged leavesand days from seedling emergence was described by a power-lawequation with only one cultivar-specific parameter. Values forthis parameter were estimated for the five constant temperaturetreatments, and the relation between this parameter and temperaturewas quantified by a nonlinear model. Leaf appearance for thefour fluctuating temperature treatments could be accuratelypredicted on the basis of these relations in each cultivar.This indicated that there were no specific effects ofT_DandT_Nonleaf appearance in rice, in contrast with phenological developmentto flowering. The optimum temperature for leaf development wasfound to be substantially higher than for development to flowering. The final main-stem leaf number differed with diurnal temperatureconditions. When a diurnal temperature delayed flowering, itincreased the leaf number as well. This might explain whyT_DandT_Nhada different effect on development to flowering but not on leafdevelopment. Oryza sativa; rice; leaf appearance; leaf number; day and night temperature     

Reproductive Allometry in Soybean, Maize and Sunflower

We compared the relationship between grain yield per plant (Y_P)and shoot biomass per plant (S_P) in three annual crops withcontrasting reproductive strategies: sunflower, a determinatespecies with a single inflorescence; maize, a determinate specieswith a limited capacity to adjust the number of ears in responseto resource availability; and indeterminate soybean, a specieswith a large capacity to adjust the number of inflorescences.Our working hypotheses were: H₁—the relationship betweenY_PandS_P is linear; H₂—the intercept of the model is zero,i.e. there is not a threshold plant mass for reproduction. Awide range of Y_Pand S_Pwas generated by manipulation of plantdensity;S_Pvaried between 0.3 and 196 g per plant in soybean,between 6 and 873 g per plant in sunflower and between 23 and697 g per plant in maize. Within these broad ranges of plantsize, both hypotheses were rejected in five out of six experiments,i.e. the relationship between Y_Pand S_Pdeparted from linearityand there was a threshold for S_Pbelow which no grain set occurred.TheS_P threshold for grain set varied widely among species; itwas close to 2 g per plant for soybean, 27 g per plant for sunflowerand 43–71 g per plant for maize. Because of this sizethreshold and non-linearity, harvest index (HI = Y_PS_P^-1) wasstable for mid-size plants, diminished slightly for large plants,and diminished sharply for smaller plants in all three crops.Harvest index stability was highest in soybean, intermediatein sunflower and lowest in maize. Differential stability ofreproductive partitioning partially derived from contrastingpatterns of meristem allocation. Copyright 2000 Annals of BotanyCompany Helianthus annuus L., Zea mays L., Glycine max(L.) Merrill, grain yield, harvest index, plant density, reproductive allocation, meristem allocation, plasticity     

Esophageal temperature threshold for sweating decreases before ovulation in premenopausal women

The purpose ofthis study was to test the hypothesis that regulated body temperatureis decreased in the preovulatory phase in eumenorrheic women. Six womenwere studied in both the preovulatory phase (Preov-2;days 9-12), which was 1-2days before predicted ovulation when 17-estradiol(E₂) was estimated to peak, andin the follicular phase (F; days2-6). The subjects walked on a treadmill (~225W · m²)in a warm chamber (ambient temperature = 30°C; dew-pointtemperature = 11.5°C) while heavily clothed.E₂, esophageal temperature(T_es), local skin temperatures,and local sweating rate were measured. The estimate of when theE₂ surge would occur was correctfor four of six subjects. In these four subjects,E₂ increased(P  0.05) from 42.0 ± 24.5 pg/mlduring F to 123.2 ± 31.3 pg/ml during Preov-2. RestingT_es was 37.02 ± 0.20°Cduring F and 36.76 ± 0.28°C during Preov-2(P  0.05). TheT_es threshold for sweating wasdecreased (P  0.05) from 36.88 ± 0.27°C during F to 36.64 ± 0.35°C during Preov-2. Both meanskin and mean body temperatures were decreased during rest in Preov-2group. The hypothesis that regulated body temperature is decreasedduring the preovulatory phase is supported.

     

Changes in respiratory control during and after 48h of isocapnic and poikilocapnic hypoxia in humans

Ventilatory acclimatization tohypoxia is associated with an increase in ventilation under conditionsof acute hyperoxia(E_hyperoxia) and an increase in acute hypoxic ventilatory response (AHVR). Thisstudy compares 48-h exposures to isocapnic hypoxia( protocol I) with 48-hexposures to poikilocapnic hypoxia ( protocolP) in 10 subjects to assess the importance ofhypocapnic alkalosis in generating the changes observed in ventilatoryacclimatization to hypoxia. During both hypoxic exposures,end-tidal PO₂ was maintained at60 Torr, with end-tidal PCO₂ held at the subject's prehypoxic level( protocol I) or uncontrolled( protocol P).E_hyperoxiaand AHVR were assessed regularly throughout the exposures.E_hyperoxia(P < 0.001, ANOVA) and AHVR(P < 0.001) increased during thehypoxic exposures, with no significant differences betweenprotocols I andP. The increase inE_hyperoxiawas associated with an increase in slope of theventilation-end-tidal PCO₂ response(P < 0.001) with no significantchange in intercept. These results suggest that changes in respiratorycontrol early in ventilatory acclimatization to hypoxiaresult from the effects of hypoxia per se and not the alkalosisnormally accompanying hypoxia.

     

The Interactive Effects of Carbon Dioxide Enrichment and Daylength on Growth and Development inPetunia hybrida

Plants were grown at either 350 or 1000 µl l^-1CO₂and inone of three photoperiod treatments: continuous short days (SD),continuous long days (LD), or short switched to long days atday 41 (SD–LD). All plants received 9 h of light at 450µmol m^-2s^-1and LD plants received an additional 4 h oflight at 8 µmol m^-2s^-1. Growth of SD plants respondedmore positively to elevated CO₂than did LD plants, due largelyto differences in the effect of CO₂on unit leaf rate. High CO₂increasedheight and decreased branching under SD conditions, but hadno effect under LD conditions. Elevated CO₂also increased thenumber of buds and open flowers, the effect for flower numberbeing greater in short than in long days. The specific leafarea of plants grown at 1000 µl l^-1CO₂was reduced regardlessof daylength. High CO₂also decreased leaf and increased reproductiveallocation, the magnitude of these effects being greater underSD conditions. Bud formation and flower opening was advancedunder high CO₂conditions in SD plants but bud formation wasdelayed and there was no effect on flower opening under LD conditions.The effects of CO₂on plants switched from SD to LD conditionswere largely intermediate between the two continuous treatments,but for some parameters, more closely resembled one or the other.The results illustrate that daylength is an important factorcontrolling response of plants to elevated CO₂. Petunia hybridaHort. ex Vilm; carbon dioxide; photoperiod; functional growth analysis; daylength; global change; development; phenology     

Effects of Temperature and Photoperiod on Phenological Development in Three Genotypes of Bambara Groundnut (Vigna subterranea)

Factorial combinations of four photoperiods (10, 11·33,12·66 and 16 h d^-1) and three mean diurnal temperatures(20·2, 24·1 and 28·1°C) were imposedon nodulated plants of three Nigerian bambara groundnut genotypes[Vigna subterranea (L.) Verdc., syn. Voandzeia subterranea (L.)Thouars] grown in glasshouses in The Netherlands. The photothermalresponse of the onset of flowering and the onset of poddingwere determined. The time from sowing to first flower (f) wasdetermined by noting the day on which the first open flowerappeared. The time from sowing to the onset of podding (p) wasestimated from linear regressions of pod dry weight againsttime from sowing. Developmental rates were derived from thereciprocals of f and p. In two genotypes, 'Ankpa 2' and 'Yola',flowering occurred irrespective of photoperiod and 1/f was controlledby temperature only, occurring sooner at 28·1 than at20·2°C. The third genotype, 'Ankpa 4', was sensitiveto temperature and photoperiod and f was increased by coolertemperatures and photoperiods > 12·66 h d^-1 at 20·2°Cand > 11·33 h d^-1 at 24·1 and 28·1°C.In contrast, p was affected by temperature and photoperiod inall three genotypes. In bambara groundnut photoperiod-sensitivitytherefore increases between the onset of flowering and the onsetof podding. The most photoperiod-sensitive genotype with respectto p was 'Ankpa 4', followed by 'Yola' and 'Ankpa 2'. Therewas also variation in temperature-sensitivity between the genotypesinvestigated. Evaluation of bambara groundnut genotypes foradaptation to different photothermal environments will thereforerequire screening for flowering and podding responses.Copyright1994, 1999 Academic Press Vigna subterranea (L.) Verdc., Voandzeia subterranea (L.) Thouars, bambara groundnut, phenology, photoperiod, daylength, temperature, flowering, podding