Seed Germination and Seedling Development in Cyclamen persicum

Cyclamen persicum Mill, seeds germinate in a narrow range oftemperature and germination is strongly inhibited by continuousirradiation with white light. The thermal optimum is approx.15 °C in both darkness and light. Seed germination is alsovery sensitive to oxygen deprivation and this sensitivity ismore pronounced at 20 °C than at the optimum 15 °C.Very immature seeds cannot germinate at any temperature, butgerminability increases during seed maturation Seedling development is unusual since seed reserves are usedimmediately for tuber formation. Tuberization is optimal at15–20 °C in light and in darkness. Supra-optimal temperatures(25–30 °C) or hypoxia inhibit tuber formation andlead to very elongated tubers These results allow the producers to improve the productionof homogeneous populations of cyclamen seedlings Wheat seeds, Triticum aestwum L., acetylcholinesterase, electrophoresis, germination, assay     

Primary Growth and Re-growth of the Tropical Tallgrass Hybrid Pennisetum at Different Temperatures

Dry weight of plant fractions, leaf area, leaf number and tillernumber were recorded throughout primary growth and two subsequentre-growths of hybrid Pennisetum (Pennisetum americanum x P.purpureum) at five temperature regimes from 15/10 °C to33/28 °C (day/night) in summer and winter. Seedling mortality occurred at 15/10 °C, whereas at allhigher temperatures seedlings survived and plants re-grew aftercutting at a height of 10 cm. Shoot weights increased with temperatureup to 33/28 °C when compared at a common chronological agebut showed no differences at a common developmental age. Thetemperature response was associated with increased top/rootratio and rate of leaf appearance; mean individual leaf areaand NAR did not increase beyond 27/22 °C. Shoot weight incrementsin primary growth were the same in winter and summer when expressedper unit of radiation, although leaf area per unit weight wassensitive to changes in radiation associated with differencesin daylength. The rate of shoot weight accumulation in regrowthwas greater than in primary growth because of rapid tilleringfollowing defoliation and an enhanced rate of leaf appearanceper tiller. Pennisetum hybrid, tallgrass, growth, regrowth temperature response     

THE EFFECTS OF STEADY AND CYCLING TEMPERATURES ON THE ACTIVITY OF THE SLUG DEROCERAS RETICULATUM

At constant temperatures, crawling activity in the slug Derocerasreticulatum has an optimum at 13°C in late winter, and 17°Cin early summer. The optimum for feeding remains at 14°C.Activity has anendogenous basis, but daytime activity increaseswith temperature and long daylengths. Cycling temperatures producemore locomotor activity and less feeding in 24 h than constanttemperatures, even when the temperature is higher at night.However, cooling stimulates and warming inhibits activity duringthe period of change and when cooling occurs at dusk, over halfthe 24 h activity occurs in the next three hours. Faster ratesof cooling produce greater responses, but can result in loweroverall activity because the slugs remain longer at low temperatures. (Received 25 May 1984;     

The Influence of Temperature on Seed Germination Rate in Grain Legumes: II. INTRASPECIFIC VARIATION IN CHICKPEA (Cicer arietinum L.) AT CONSTANT TEMPERATURES

Positive linear relationships were shown between constant temperaturesand the rates of progress of germination to different percentiles,G, for single populations of each of five genotypes of chickpea(Cicer anetinum L.). The base temperature, T_b, at which therate of germination is zero, was 0·0°C for all germinationpercentiles of all genotypes. The optimum temperature, T_o(G),at which rate of germination is most rapid, varied between thefive genotypes and also between percentiles within at leastone population. Over the sub-optimal temperature range, i.e.from T_b to T_o(G), the distribution of thermal times within eachpopulation was normal. Consequently a single equation was appliedto describe the influence of sub-optimal temperatures on rateof germination of all seeds within each population of each genotype.The precision with which optimum temperature, T_b(G), could bedefined varied between populations. In each of three genotypesthere was a negative linear relationship between temperatureabove T_b(G) and rate of germination. For all seeds within anyof these three populations thermal time at supra-optimal temperatureswas constant. Variation in the time taken to germinate at supra-optimaltemperatures was a consequence of normal variation in the ceilingtemperature, T_o(G)—the temperature at or above which rateof progress to germination percentile G is zero. A new approachto defining the response of seed germination rate to temperatureis proposed for use in germplasm screening programmes. In two populations final percentage germination was influencedby temperature. The optimum constant temperature for maximumfinal germination was between 10°C and 15°C in thesepopulations; approximately 15°C cooler than the optimumtemperature for rate of germination. It is suggested that laboratorytests of chickpea germination should be carried out at temperaturesbetween 10°C and 15°C. Key words: Chickpea, seed germination rate, temperature     

Effects of Temperature on the In vivo Assay of Nitrate Reductase in some C3 and C4Species

Nitrate reductase (NR) activity was measuredin vivo in differentcrop species at 25–60 °C. Highest NR activity wasobserved at 40 °C in pigeon pea, cowpea, sunflower, sesameand sorghum, 45 °C in maize and 50 °C in bajra. At higherincubation temperatures NR activity declined in all species.In mung bean the optimum incubation temperature varied withthe season. In the summer crop of mung beans, NR activity wasmaximum at 50 °C while in the rainy season crop 30 °Cwas the optimum incubation temperature. NR in sesame was relativelyheat-tolerant. The results indicate that 30 °C is not theoptimum incubation temperature for all crop species. Nitrate reductase, temperature, in vivo assay     

GLOCHIDIA OF THE FRESHWATER MUSSEL LAMPSILIS OVERWINTERING ON FISH HOSTS

Largemouth Bass were infected with glochidia of the freshwatermussel Lampsilis cardium. Three fishes each were held at 4.5,10, and 15.5°C; five fish were held at 21°C. By 64 days,metamorphosed juveniles were found in the 15.5 and 21°Ctrials but not in the 5.5 and 10°C trials, indicating thatthe lower threshold temperature for metamorphosis was between10 and 15.5°C for the duration. In a second experiment,Largemouth Bass were infected with glochidia of L. cardium andheld at 10°C. A sample of fishes was removed monthly andbrought to 21°C. Numbers of glochidia that metamorphosedafter being warmed were compared to the number that metamorphosedwithout warming. The percentage that metamorphosed after warmingdecreased linearly with time. At one month, 100% of the glochidiametamorphosed after warming. This decreased to 80% by two months,to 30% by four months and 3% by six months. Although this post-warmingpercentage decreased with time, the total percentage of metamorphosedjuveniles (at all temperatures) was not correlated with time.Controls kept at 21°C required three weeks to reach peakmetamorphosis, but test subjects subjected to 10°C requiredless than nine days to metamorphose once warmed. Many overwinteringglochidia therefore complete a portion of their developmenton the host at winter temperatures, but stop short of excystment.Some glochidia metamorphosed without being warmed, but thisphenomenon is not understood. This study confirms that glochidiamay overwinter on hosts, with some glochidia persisting formore than six months before metamorphosing when warmer conditionsreturn. (Received 29 September 1998; accepted 18 January 1999)     

A Model for Germination Responses to Alternating Temperatures

When seeds of Chenopodium album are imbibed in 0–01 Mpotassium nitrate solution in the light at constant temperature,percentage germination increases to an optimum at 24 °C,above which it decreases. These relationships are linear ifpercentage germination values are transformed to normal deviates.At supra-optimal temperatures, alternating temperatures havelittle or no effect on this basic relationship. However, atsub-optimal temperatures normal deviate germination increaseslinearly with amplitude at constant mean temperature and theincreases are relatively greater at lower mean temperatures.The effect of amplitude is also greater when more time is spentat the wanner temperature in the diurnal cycle. Seeds of Panicummaximum show very similar responses except that the effect ofamplitude is greater when a shorter time is spent at the warmertemperature in the diurnal cycle. These observations form thebasis of a quantitative model which, at sub- and supra-optimaltemperatures, respectively, accounts for 90 and 75% of the variationin germination of C. album seeds subject to a very wide rangeof thermal environments on a two-dimensional temperature gradientplate. The data presented for P. maximum are less comprehensive,but again the model accounts for 80% of the variation. The relevanceof the same model to two unrelated species from different climatesand of different ecological behaviour suggests that it may begenerally useful in determining optimum temperatures for seedviability testing regimes and ultimately for predicting fieldbehaviour These results allow the producers to improve the productionof homogeneous populations of cyclamen seedlings Chenopodium album L., Panicum maximum Jacq., seed dormancy, germination, alternating temperatures, temperature gradient plate     

Spatial distribution of Euphausia pacifica (Euphausiacea: Crustacea) in the Yellow Sea

Euphausia pacifica were collected in the Yellow Sea in summer(August, 1997) and winter (February, 1998), and their distributionwas investigated in terms of the developmental stages in relationto environmental factors (temperature, salinity and chlorophylla). In summer, the water column was highly stratified with athermocline between 10–30 m depth, whereas the water columnwas well mixed in winter. Seasonal variation in temperaturewas large, ranging between 6.3 and 28.8°C in summer and3.9 and 12.2°C in winter. Chlorophyll a concentration changedlittle seasonally but a high concentration was observed in coastalareas. Salinity in the two seasons varied little spatio-temporally.In the studied area and sampling period, E.pacifica was themost dominant euphausiid species (99.7 and 99.8% in summer andwinter, respectively), and comprised adults and juveniles (74.6%in summer and 41.9% in winter), furcilia (17.5 and 44.9%) andcalyptopis (7.9 and 13.1%). The spatial distribution of theE.pacifica population varied seasonally depending on developmentalstage and appeared to be related primarily to the seawater temperatureand secondly to the chlorophyll a concentration, but not tosalinity. In summer, adults were abundant in areas below 10°C,and furcilia and calyptopis above 9°C. In winter, adultswere confined to areas between 7 and 10°C, and furciliaand calyptopis, to areas between 6 and 8°C. Furcilia andcalyptopis were concentrated in the vicinity, or at the centerof chlorophyll a-rich water masses, whereas adults seemed toavoid those water masses.     

Germination of Stored Cassava Seed at Constant and Alternating Temperatures

Cassava seed is only capable of germinating over a restrictedrange of constant temperatures. During storage the optimum constanttemperature for germination decreases from about 35 to 30 °Cor possibly less. The rate at which the optimum temperaturechanges during dry storage increases with increase in storagetemperature over the range 0 to 40 °C. Some alternating-temperatureregimes (16 h at the lower temperature; 8 h at the higher temperature)can provide conditions as favourable for germination as theoptimum constant temperatures. Furthermore, it has been shownthat temperature alternation itself is stimulatory because whenthe range of the alternation does not include the optimum constanttemperature value, percentage germination is often higher thancould be obtained at any constant temperature within the range,though this stimulatory response declines during storage. Forthese reasons it is provisionally recommended that cassava seedshould be germinated at 25/35 °C which is as stimulatorya treatment as any which has so far been investigated and hasthe advantage of encompassing the range over which the optimumconstant temperature changes during storage. Manihot esculenta Crantz, cassava, germination, dormancy, seed viability, storage of seeds, after-ripening     

Effect of Cultivar, Temperature and Seed Size on the Germination and Emergence of Soya Beans (Glycine max (L.) Merr.)

The rapid and uniform establishment of soya bean [Glycine max(L.) Merr.] stands is conducive to higher yields. This studywas undertaken to determine the effects of cultivar, temperature,and seed size on the rate of germination and emergence. No cultivar effect on the germination rate was observed. However,in an emergence study from a sand-soil-peat mixture, cultivardifferences in emergence rates were noted(‘Chippewa 64’> ‘Wayne’ > ‘Amsoy 71’). In anotheremergence study (sand media) the cvs ‘Calland’ and‘Williams’ emerged faster than the cv. 'Wayne or‘Wells’. Time required for 50 per cent germination decreased (18.8–4.0days) as the temperature increased from 10 to 30 °C (5 °Cincrements). Emergence (50 per cent) from a sand-soil-peat mixturewas more rapid (19.8–6.3 days) as the simulated plantingdate (growth chamber set to simulate field temperatures) wasdelayed from 16 April to 15 June with an intermediate date of16 May. In addition, time required for 50 per cent emergence of thecultivars from sand decreased (793–76 h) as the temperaturewas increased from 10 to 30 °C with no decrease from 30to 35 °C. Seed size effects were apparent, with the very small seed germinatingslower than the three larger seed sizes. In the emergence studieswith both the sand and sand-soil-peat mixture there was a generaltrend toward more rapid emergence with the smaller seeds. However,the absolute differences were small. Significant cultivar x temperature interactions were observedfor the germination and emergence rates. In most cases the cultivarsmerged in terms of germination and emergence rates at temperaturesbetween 10 and 20 °C and at the higher temperatures thecultivar rankings were different from those observed at temperaturesbelow the merging point. Glycine max (L.) Merr, soya bean, seed germination, establishment of seedlings     

Dormancy in Dioscorea: Range, Duration and Timing of High-Temperature Treatment in Germination Inhibition of D. tokoro Seeds

The effects of temperature on induction and release of high-temperatureinhibition in seed germination of Dioscorea tokoro Makino, amonocotyledonous summer perennial of the temperate zone of EastAsia, were investigated. Germination was increasingly inhibitedwith elevation of temperature over 23°C and lengtheningof its duration. The low temperature limit for germination inhibitiondecreased with lengthening of the duration of high temperature.The most sensitive phase for high temperature was 1–2days after the start of imbibition at 20°C. The germination inhibition by high temperature was reversedby chilling at 5°C, which is the optimum temperature forbreaking the natural dormancy (primary dormancy) of this seed.This showed that the high-temperature inhibition of germinationdoes not cause mortal damage but only secondary dormancy (induceddormancy). Seeds from a cold climate (Miyagi Pref.) responded rather quicklyto both high temperature and chilling compared to seeds froma warm climate (Kagoshima Pref.). The responsiveness to hightemperature and chilling of D. tokoro seed may affect the germinationtime under natural conditions. (Received October 22, 1982; Accepted January 14, 1983)     

The Influence of Temperature on Seed Germination Rate in Grain Legumes: III. A COMPARISON OF FIVE FABA BEAN GENOTYPES AT CONSTANT TEMPERATURES USING A NEW SCREENING METHOD

Ellis, R. H., Simon, G. and Covell, S. 1987. The influence oftemperature on seed germination rate in grain legumes. III.A comparison of five faba bean genotypes at constant temperaturesusing a new screening method.—J. exp. Bot. 38: 1033–1043. A screening procedure which requires information on the progressof germination at only four temperatures was able to definethe response of the rate of seed germination to sub- and supra-optimaltemperatures for whole seed populations of each of five fababean (Vicia faba L.) genotypes. In one population of the cultivarSutton the models for sub- and supra-optimal temperatures derivedfrom the screen satisfactorily explained observations from anearlier separate investigation at a wider range of temperatures.Two discrete groups of genotypes were identified. Within eachgroup the base temperature T_b did not differ significantly:for the landraces Lebanese Local Large and Syrian Local Largethe value was estimated to be –7·5°C and forthe landrace Lebanese Local Small and the cultivars Sutton andAquadulce it was –4·0°C. The optimum temperaturefor the 50th percentile [T_o(50), at which temperature the rateof germination is maximal] also varied between these two groupsof genotypes, being 20·5–21·5°C forthe first group and 24·5–26·0°C forthe second. In several temperature regimes some of the viableseeds within a seed population failed to germinate. Nevertheless,even at temperatures where a substantial proportion of the seedsfailed to germinate the models defined by the screening methodpredicted the germination times of those seeds which did germinate. Key words: Faba bean, seed gemination rate, temperature     

Effects of High Temperatures on the Permeability and Germinability of the Hard Seeds of Rhus javanica L.

The effects of temperature, 40–85 °C, on the permeabilityand germinability of the hard seeds of the pioneer tree Rhusjavanica L. with a fire syndrome were studied. The temperatureeffective for removal of the water-impermeable coat dormancyof the seeds was 55 ± 7·4 °C. With increasingtemperature, shorter exposure became sufficient to render theseeds permeable, but at temperatures above 75 °C, heat impairmentof germinability resulted in less than 60% germinability, evenwith long exposure. The most favourable regimes among thosetested were temperatures of 65–75 °C for durationsof 30–120 min, which frequently occur on denuded groundduring the midday hours of clear spring or summer days. Rhus javanica L., water-impermeable coat dormancy, seed germination, high temperature     

Relationship between temperature and cauliflower (<Emphasis Type="Italic">Brassica oleracea</Emphasis> L. <Emphasis Type="Italic">var. botrytis</Emphasis>) growth and development after curd initiation

Two experiments were conducted to assess the response of cauliflower (Brassica oleracea L. var. botrytis) cv. “Nautilus” F1 hybrid to different constant temperatures after curd initiation by keeping the plants in six different temperature-controlled glasshouse compartments with heating set point temperatures of 6, 10, 14, 18, 22, and 26 °C (±4 °C) at the School of Plant Sciences, The University of Reading, UK during winter 1998–1999 and summer 1999. Many of the growth parameters increased with increasing mean growing temperature up to an optimum temperature and then declined with further increases in temperature. Therefore, cauliflower’s growth and development after curd initiation could be resolved into linear or curvilinear function of effective temperatures calculated with optimum temperatures between 19 and 23 °C. It is suggested that future warmer climates will be beneficial for winter cauliflower production rather than summer cauliflower production.     

Acclimation of chlorophyll biosynthetic reactions to temperature stress in cucumber (Cucumis sativus L.)

The adaptive responses of the greening process of plants to temperature stress were studied in cucumber (Cucumis sativus L. cv. Poinsette) seedlings grown at ambient (25 °C), low (7 °C) and high (42 °C) temperatures. Plastids isolated from these seedlings were incubated at different temperatures and the net syntheses of various tetrapyrroles were monitored. In plastids isolated from control seedlings grown at 25 °C, the optimum temperature for synthesis of Mg-protoporphyrin IX monoester or protochlorophyllide was 35 °C. Temperature maxima for Mg-protoporphyrin IX monoester and protochlorophyllide syntheses were shifted to 30 °C in chill-stressed seedlings. The net synthesis of total tetrapyrroles was severely reduced in heat-stressed seedlings and the optimum temperature for Mg-protoporphyrin IX monoester or protochlorophyllide synthesis shifted slightly towards higher temperatures, i.e. a broader peak was observed. To further study the temperature acclimation of seedlings with respect to the greening process, tetrapyrrole biosynthesis was monitored at 25 °C after pre-heating the plastids (28–70 °C) isolated from control, chill- and heat-stressed seedlings. In comparison to 28 °C-pre-heated plastids the percent inhibition of protochlorophyllide synthesis in 40 °C-pre-heated plastids was higher than for the control (25 °C-grown) in chill-stressed seedlings and lower than for the control in heat-stressed seedlings. Maximum synthesis of total tetrapyrroles and protoporphyrin IX was observed when chloroplasts were heated at 50 °C, which was probably due to heat-induced activation of the enzymes involved in protoporphyrin IX synthesis. Prominent shoulders towards lower or higher temperatures were seen in chill-stressed or heat-stressed seedlings, respectively. The shift in optimum temperature for tetrapyrrole biosynthesis in chill- and heat-stressed seedlings was probably due to acclimation of membranes possibly undergoing desaturation or saturation of membrane lipids. Proteins synthesized in response to temperature-stress may also play an important role in conferring stress-tolerance in plants. Received: 8 October 1998 / Accepted: 19 November 1998     

Germination of Tagetes minuta L. I. Temperature Effects

Initial studies have indicated that Tagetes minuta achenes haveboth a temperature and a light requirement for germination.Temperatures tested were 10, 20, 25, 30 and 35 °C. Germinationwas optimal at 25 °C under white light conditions. Underthese conditions 100 per cent of achenes germinated within 7days of imbibition. There was no germination at 10 or 35 °Ceither in the light or in the dark. Achenes imbibed and incubatedat 35 °C for 4 days showed no visible signs of germinationbut on transfer to 25 °C, 100 per cent of these achenesgerminated within 24 h. Furthermore, achenes given this hightemperature (35 °C) treatment could be dried at 25 °C,re-imbibed at 25 °C and again 100 per cent of achenes germinatedwithin 24 h of re-imbibition. This rapid germination responsefollowing removal from the high temperature regime could alsobe induced by transfer to temperatures of 20 °C or 20 °C(16 h) alternating with 10 °C (8 h). Tagetes minuta L., weed seeds, germination, temperature, light     

The effects of temperature, growth medium and darkness on excystment and growth of the toxic dinoflagellate Gymnodinium catenatum from northwest Spain

The chain-forming dinoflagellate Gynmodinium catenatum Grahamcauses recurrent outbreaks of paralytic shellfish poisoning(PSP) in the Galician Rias Bajas (northwest Spain). A sedimentsurvey in Ria de Vigo in April 1986 indicated that the highestconcentrations of cysts of this species were located in themiddle sections of the ria, with maximum abundance of 310 cystscm^–3. The effects of temperature, growth medium compositionand irradiance on the germination of laboratory-produced restingcysts were investigated. Newly formed cysts required very littletime for maturation, as excystment was possible within 2 weeksof encystment. Growth media did not affect germination success.In contrast, the excystment rate was retarded signifiantly indarkness. Germination was also strongly affected by temperature,with {small tilde}75% excystment success at 22–28°Cand little or no germination below 11°C after 1 month ofincubation. In culture, the optimum growth rate of vegetativecells was between 22 and 28°C, the highest rate being 0.53divisions day^–1 at 24°C. Growth did not occur at temperatures< 11°C or >30°C. These results are important withrespect to the different hypotheses proposed to explain theinitiation of G.catenatum blooms in the Galician Rias Bajasand Northern Portugal. The pattern of G.catenatum bloom developmentalong this coast has been related to seasonal upwelling in thearea, with major blooms occurring during the autumn as warmeroffshore surface water is transported towards the coast whenupwelling relaxes. The landward transport of established offshorepopulations of G.catenatum with the warm surface layer remainsa viable explanation for the observed blooms within the rias,but alternatively, our data suggest that cysts within the riascan provide the inoculum population at times conducive to growthand bloom formation. Even though newly formed G.catenatum cystshave a very short maturation time and can germinate in darknessacross a wide temperature range, bloom development will be significantonly during the late summer and early autumn, since in othermonths light levels at the sediment surface and temperaturesthroughout the water column are too low for significant germinationor growth.     

Seed Viability Constants for Lettuce

Seeds of two lettuce cultivars (Lactuca sativa L., cv. Meikoninginand cv. Grand Rapids) were hermetically stored with constantmoisture contents ranging between 3.6 and 17.9 per cent (freshweight basis) at constant temperatures ranging between 5 and75 °C. The decline with time in percentage germination andpercentage normal seedlings was determined for each storagetreatment. The data were fitted to an equation which containsthe constants: K₁, the probit of the initial percentage germinationor normal seedlings; K_E, a species constant; C_W, the constantof a logarithmic moisture term; C_H, the constant of a lineartemperature term and C_Q, the constant of a quadratic temperatureterm. Regression analysis of data from storage periods up to5.5 years at temperatures of 5–75 °C and seed moisturecontents of 3.6–13.6 per cent yielded the following values:K_E= 8.218, C_W=4.797±0.163, C_H=0.0489±0.0050 andC_Q=0.000365±0.000056. Although this equation consistentlyprovided a better fit, simplified equations, assuming eithera log-linear relationship between seed longevity and temperature,or a log-linear relationship between seed longevity and bothmoisture content and temperature, accounted for more than 94per cent of the variation at the restricted temperature rangeof 5–40 °C. Longevity of the same seed lots at sub-zero temperatures (–5,–10 and –20 °C) was studied in separate tests.Freezing damage, resulting in abnormal seedlings in the germinationtest, occurred at –20 °C when the moisture contentof the seeds exceeded 12 per cent. No decline in percentagenormal seedlings was observed after a storage period of 18 monthsor longer at –20 °C, provided the seed moisture contentdid not exceed 9.5 per cent. For seeds stored at –5 and–10 °C with 9.6–12.5 per cent moisture content,the observed rate of decline of percentage normal seedlingswas adequately predicted by the viability equation, using theabove values for the constants. This suggests that for low moisturecontents the viability equation can be applied to estimate longevityat sub-zero temperatures. Lettuce, Lactuca sativa (L.), seed longevity, seed storage, viability constants, storage conditions     

A Mathematical Model to Utilize the Logistic Function in Germination and Seedling Growth

Several models have been proposed to describe germination rates,but most are limited in statistical analysis and biologicalmeaning of indices. Therefore, a mathematical model is proposedto utilize the logistic function. The function was defined asan overall response including time, temperature, and the interactionbetween time and temperature. Cumulative germination percentagesover time were used to develop the model. Germination tests were conducted on indiangrass (Sorghastrumnutans (L.) Nash) strain ‘IG-2C-F1’, at constanttemperatures of 9, 12, 15, 20, 25, and 30 °C. The functionfitted the observed data over six temperatures at r² = 0.99.Time to reach 10% of final germination (Gt₁₀) increased from2.5 d at 30 °C to 44.0 d at 9 °C, and Gt₅₀ (time toreach 50% of final germination) increased from 3.6 d at 30 °Cto 53.8 d at 9 °C. True germination rate (% d^–1) foreach temperature was maximum at Gt₅₀. A linear model of 1/Gt₅₀versus temperature was used to estimate the base temperatureof 8.3 °C for germination. An Arrhenius plot indicated achange occurred between 20 °C and 25 °C for temperatureresponse of germination. Published data on hypocotyl growthof Cucumis melo L. were recalculated using the model. Absolutegrowth rates showed a temperature response similar to the publishedweighted-mean elongation rates. Base temperature for hypocotylgrowth of C. melo was estimated as 8.8 °C. The proposedmodel proved to be useful in calculating and interpreting germinationand growth kinetics. Key words: Indiangrass, Sorghastrum nutans (L.) Nash, Germination rate, Threshold temperature, Arrhenius plot, Growth rate, Cucumis melo L     

Genotypic Differences in the Temperature Responses of Tropical Crops: I. GERMINATION CHARACTERISTICS OF GROUNDNUT (ARACHIS HYPOGAEA L.) AND PEARL MILLET (PENNISETUM TYPHOIDES S. & H.)

Mohamed, H. A., Clark, J. A. and Ong, C. K. 1988. Genotypicdifferences in the temperature responses of tropical crops.I. Germination characteristics of groundnut (Arachis hypogaeaL.) and pearl millet (Pennisetum typhoides S. & H.).—J.exp. Bot. 39: 1121–1128. The germination at constant temperature of several genotypesof groundnut and pearl millet was investigated between 0?C and50?C on a thermal gradient plate. Large differences in bothgermination rate and percentage germination were observed inboth species. Base temperatures vary from 8–11.5?C and 8–13.5?Cin groundnut and millet, respectively and optimum temperaturesfrom about 29–36.5?C in both. Maximum temperatures forgermination ranged from 41–47?C. The results are discussedin terms of adaptation to high soil temperature and crop establishmentin the semi-arid tropics. Key words: Temperature, germination, millet, groundnut