Modelling Temperature Effects in Breaking Rest in Red-osier Dogwood (Cornus sericea L.)

Temperature requirements for bud development after a rest period(breaking rest) from maximum rest to end of rest were determinedto develop an empirical model for predicting rest developmentin terminal vegetative buds of red-osier dogwood (Cornus sericeaL.). One-year-old plants at maximum rest were exposed to temperaturesfrom 5 to 20 °C a 12 h photoperiod (SD) in growth chambers.Depth of rest was measured by days to bud break in either 16h photoperiod (LD) or natural daylength at 20/15 °C/nighttemperature. Developmental stages during rest development wereexpressed by degree growth stage (°GS). Chilling was effective breaking rest after plants attained maximumrest (270 °GS). Development during rest (breaking rest)increased with decreasing temperature. No significant developmentoccurred at 20 °C. Rate of rest development (°GS h^–1)at all temperatures varied during the breaking rest period anddepended on developmental stage (°GS). A °GS model describedand quantified rest development (°GS). Using temperatureand developmental stage, the model predicted end of rest (315°GS)within 3 days and daily rest development (°GS) in both years. Cornus sericea L, Cornus stolonifera Michx, dogwood, bud development, dormancy, temperature effects, chilling, degree growth stage     

Effects of temperature on metabolism, growth and growth efficiency of Thysanoessa longipes (Crustacea: Euphausiacea) in the Japan Sea

Growth (assessed from intermolt period and molt increment) andmetabolism (oxygen consumption) of juvenile and adult Thysanoessalongipes from central Japan Sea were determined at eight differenttemperatures ranging from 0 to 14°C. The intermolt periodshortened progressively as temperature increased from 0 to 14°C.The molt increment was not assessed satisfactorily in the rearingexperiments, and therefore this was estimated from the naturalgrowth curve and habitat temperature, combined with laboratory-obtainedintermolt data. Oxygen consumption rates increased exponentiallyfrom 0 to 8°C and then leveled off. From these results,the growth was expressed as a function of temperature and bodysize and metabolism as a function of temperature. Because ofthe differential effects of temperature on growth and metabolism,the net growth efficiency [NGE: 100 x growth/(growth + metabolism)]changed with temperature. The temperature at which T. longipesattained maximum NGE varied from 0 to 8°C, depending onthe body length of specimens of 5, 10, 15 and 20 mm. The presentresults are compared with our previous data on Euphausia pacificain relation to the body composition and habitat usage of thesetwo trophically important species in the food web of the JapanSea.     

A Comparison of the Effect of High Temperature on Grain Development in Wheat and Rice

Grain weight at maturity of the wheat cultivar Banks was reducedby about 5% for each 1 °C rise in daily mean post-anthesistemperature in the range from 17.7 to 32.7 °C, using grainweight at 17.7 °C as the base. In contrast, the rice cultivarCalrose had a stable grain weight up to 26.7 °C and abovethat showed a 4.4% drop in weight per 1 °C increase in meanpost-anthesis temperatures up to 35.7 °C, using grain weightat 26.7 °C as the base. In both wheat and rice there wasa reduction in the duration of grain growth with increasingtemperature up to a mean of 26.7 °C. In this range rice,but not wheat, showed a compensating increase in the rate ofdry-matter accumulation. Above 26.7 °C the rate of dry-matteraccumulation fell in both species, although this was more stablein rice than in wheat. In wheat the duration of grain growthcontinued to decrease at temperatures above 26.7 °C, butshowed little change in rice up to 35.7°C, the maximum tested.These data are discussed in relation to the physiological, biochemicaland physical constraints that may act to regulate grain developmentin wheat and rice at high temperature. Triticum aestivum, oryza sativa, grain development, high temperature effects     

Temperature-dependent consumption and gut-residence time in the opossum shrimp Mysis relicta

Maximum daily consumption was estimated for Mysis relicta fedad libitum rations of Daphnia pulex at 4,10,15 and 18°C.Gut-residence time was also evaluated for M.relicta fed clado-ceranprey at 4, 10 and 157deg;C. Mean daily consumption (g dry weightof Daphnia g^–1 dry weight of Mysis day^–1) rangedfrom 6% at 4%C to 12% at 10°. At 18°C, Mysis feedingrate declined to 9% day1. Mean, weight-adjusted consumptionrates exhibited a ‘dome-shaped’ response in relationto water temperature. Consumption rate was highest at 10°Cand lowest at 4°C. Estimated Q₁₀ was more sensitive from4 to 10°C (Q₁₀= 3) than from 10 to 15°C (Q₁₀=1.2). Gut-residencetime for Mysis was inversely related to water temperature, implyingthat evacuation rate increases linearly with water temperature.Feeding and gut-evacuation rates become disassociated at watertemperatures >10°C. As water temperature increased above1°C, relative evacuation rate increased, whereas feedingrate declined. It is postulated that at higher water temperatures,disassociated feeding and gut-evacuation rates reduce the scopefor growth of vertically migrating Mysis and impose a physiologicalconstraint that isolates Mysis from warm, epilimnetic waterduring thermal stratification. ¹Present address: Center for Aquatic Ecology, Illinois NaturalHistory Survey, Sam Parr Biological Station, 6401 Meacham Road,Kinmundy, IL 62854, USA     

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     

Vertical distribution of pelagic chaetognaths and feeding of Sagitta enflata in the Central Equatorial Pacific

The vertical distribution and feeding of pelagic chaetognathsat 5°S, 160°W in the Central Equatorial Pacific wereinvestigated using a series of 0–500 m vertical haulswith a VMPS net over a 24 h period between 6 and 7 October 1990.The total number of individuals per haul was between 370 and688. Fourteen species in four genera were found at this station.The most abundant species was Sagitta enflata which comprised32.4–61.1% of the individuals collected from the 0–500m layer. Mesopelagic species made up 9.3–15.1% of thetotal number of individuals. Sagitta enflata and Pterosagittadraco were found in the upper part of the thermocline both byday and at night. The fraction of the population containingfood items (FCF) of S.enflata in the 0–50 m layer variedbetween 4.8 and 12.5% (mean 10.8%) and feeding activity washighest between sunrise and noon. The percentages of Copepoda,Foraminifera, crustacean larvae, Chaetognatha, Pteropoda, Ostracoda,fish and unidentified material in the gut of S.enflata were51.9,6.7,3.8,2.9,1.9,1.9 and 30.9%, respectively. Sagitta enflataconsumed food organisms which were mainly between 0.5 and 1.0mm in length. The daily feeding rate of S.enflata was 1.81 preyper individual, which was equivalent to 8.06 mg C m^–2day^–1. This corresponded to     

Growth, metabolism and growth efficiency of a euphausiid crustacean Euphausia pacifica in the southern Japan Sea, as influenced by temperature

Growth (assessed from intermolt period and molt increment) andmetabolism (oxygen consumption) of the post-larva of Euphausiapacifica from the southern Japan Sea were determined at sevengraded temperatures ranging from 1 to 25°C. The intermoltperiod shortened progressively as temperature increased from1 to 20°C, but an effect of temperature on molt-to-moltgrowth increment was not seen. Oxygen consumption rates wereaccelerated by the increase in temperature up to 20°C. Beyond20°C, E.pacifica exhibited reduced oxygen consumption anddied within 1 day without molting. After removing the effectof body size, the relationships between growth rate and temperature,and between oxygen consumption rate and temperature, were established.The carbon budget was calculated as a function of temperature.Because of differential effects of temperature on growth andmetabolism, the net growth efficiency [K₂ growthx100/(growth+metabolism)]changed with temperature. The optimum temperature at which E.pacificaattained the maximum K₂ was 11.4°C, which was derived fromcalculation of cumulative carbon invested in growth and metabolismin this animal. In an alternative method, the optimum temperaturewas obtained mathematically by solving a set of differentialequations. The biological and ecological significance of theoptimum temperature which leads to the maximum K₂ is discussed.     

Modelling Optimal Temperature Acclimation of the Photosynthetic Apparatus in C3Plants with Respect to Nitrogen Use

A new hypothesis for temperature acclimation by the photosyntheticapparatus is presented. An optimization model is developed toexamined effects of changes in the organization of photosyntheticcomponents on leaf photosynthesis under various growth temperatureswhere the photosynthetic apparatus is not damaged. In this model,photosynthetic rate is limited either by the capacity of ribulosebisphosphate carboxylase (RuBPCase) to consume ribulose bisphosphate(RuBP), or by the capacity of RuBP regeneration. For temperaturedependence of the RuBPCase activity, data fromSpinacia oleraceaL.,which have a temperature optimum of 30 °C, are used. Fortemperature dependence of the capacity of RuBP regeneration,two contrasting curves that have temperature optima of 30 °C(Eucalyptus paucifloraSieb. ex Spreng) and 40 °C (LarreadivaricataCav.) are applied. The temperature dependence of eachprocess is fixed for respective species, but the rate of eachprocess varies with changes in the amounts of components. Thecost of proteins, in terms of nitrogen, required to carry outeach process is calculated when nitrogen is partitioned differentlyamong photosynthetic components. The optimal nitrogen partitioningthat maximizes daily photosynthesis at a given temperature isobtained. The predicted temperature optimum of the photosyntheticrate inLarrea divaricataexhibits large shifts with changes intarget temperature, while shifts are negligible inEucalyptuspauciflora. It is suggested that the shift in temperature optimumof photosynthetic rate is large when the temperature dependencesof the capacities of RuBPCase and RuBP regeneration differ fromeach other.Copyright 1997 Annals of Botany Company Optimization model; nitrogen use efficiency; photosynthetic acclimation; temperature dependence     

Shoot Extension in Picea sitchensis II. Analysis of Weather Influences on Daily Growth Rate

The influence of mean temperature and total solar radiationon the daily increment of shoots of 12-year-old Picea sitchensisis described. Serial auto and cross-correlation analysis isused to show that variation in shoot increment is correlatedwith variations in weather occurring over several previous hours.The relationships between daily increments for the leading andtopmost five whorl shoots and the two controlling variablesof temperature and solar radiation are described for the firsthalf of the growing season by auto-regressive models fittedby time-series methods as described by Box and Jenkins. Thesedynamic system models showed that there was a delay of one dayand two days respectively in the influence of temperature andsolar radiation on shoot increment and that after these delaysthe response continued for more than a single day. The maximumfinal response (or steady state gain) of a typical topmost shootto temperature and solar radiation change was found to be 0.091mm d^–1(°C)^–1 and 0.027 mm d^–1 (MJ m^–2)^–1.For the normal range of these variables experienced this indicatesthat shoot extension was five times more sensitive to changesin temperature than to those in solar radiation. Picea sitchensis, Sitka spruce, shoot growth, weather influences, ARMA model, time-series analysis, Box-Jenkins method     

Growth and development of Neocalanus flemingeri/plumchrus in the northern Gulf of Alaska: validation of the artificial-cohort method in cold waters

In situ growth and development of Neocalanus flemingeri/plumchrusstage C1–C4 copepodites were estimated by both the artificial-cohortand the single-stage incubation methods in March, April andMay of 2001–2005 at 5–6°C. Results from thesetwo methods were comparable and consistent. In the field, C1–C4stage durations ranged from 7 to >100 days, dependent ontemperature and chlorophyll a (Chl a) concentration. Averagestage durations were 12.4–14.1 days, yielding an averageof 56 days to reach C5, but under optimal conditions stage durationswere closer to 10 days, shortening the time to reach C5 (fromC1) to 46 days. Generally, growth rates decreased with increasingstage, ranging from 0.28 day^–1 to close to zero but weretypically between 0.20 and 0.05 day^–1, averaging 0.110± 0.006 day^–1 (mean ± SE) for single-stageand 0.107 ± 0.005 day^–1 (mean ± SE) forartificial-cohort methods. Growth was well described by equationsof Michaelis–Menten form, with maximum growth rates (G_max)of 0.17–0.18 day^–1 and half saturation Chl a concentrations(K_chl) of 0.45–0.46 mg m^–3 for combined C1–3,while G_max dropped to 0.08–0.09 day^–1 but K_chl remainedat 0.38–0.93 mg m^–3 for C4. In this study, in situgrowth of N. flemingeri/plumchrus was frequently food limitedto some degree, particularly during March. A comparison withglobal models of copepod growth rates suggests that these modelsstill require considerable refinement. We suggest that the artificial-cohortmethod is the most practical approach to generating the multispeciesdata required to address these deficiencies.     

Photothermal Time for Flowering in Lentils (Lens culinaris) and the Analysis of Potential Vernalization Responses

Two cultivars of lentils, Laird and Precoz, were subjected to18 potentially vernalizing treatments, comprising constant temperaturesof 1, 5 or 9 °C in factorial combination with photoperiodsof 8 or 16 h for 10, 30 or 60 d. These seeds or seedlings, togetherwith non-vernalized seeds (as controls), were then transferredto four different growing regimes (‘day’/‘night’temperatures of 18/5 °C or 24/13 °C, factorially combinedwith photoperiods of 11 or 16 h). Variation in the number ofdays from sowing to first flower (f) in the growing regimesfor the controls conformed to the equation I/f = a+b+cP, whereis mean temperature (°C), P is photoperiod (h) and a, band c are genotype-specific constants. Accordingly, when theenvironment varies during development, the photothermal timerequired to flower in day-degrees (°C d) is given by 1/babove a base temperature defined as —(a+cP)/b. Most variationin time to flower could be accounted for by the photothermaltime accumulated in the two successive environments. Therefore,there was no evidence of a specific low-temperature vernalizationresponse in either cultivar. Neither was there evidence of ‘short-day’vernalization, i.e. advancement of flowering resulting frompreliminary short-day treatments. A potential error inherentin the predictive model described arises because it ignoresthe presence of a pre-inductive, photoperiod-insensitive phase;but agro-ecological considerations suggest that this error maynot be important in practice. Lens culinaris, lentil, flowering, photoperiodism, vernalization, photothermal time, screening germplasm     

The Effect of Temperature on Growth and Development of Echinochloa Millets

Accumulation of dry weight and leaf plus stem area were measuredin Echinochloa utilis and E. frumentacea grown at temperatureregimes from 15/10°C to 33/28°C (day/night). Tilleringand height were recorded in addition to leaf number which wassubsequently used as a developmental index. In both species shoot dry weight increased with temperatureup to 33/28°C; the increase in relative growth rate (RGR)was negligible above 27/22°C. Below 27/22°C the RGRof E. frumentacea decreased sharply and at 15/10°C it madeno effective growth. At low temperatures the RGR of E. frumentaceawas lower than that of E. utilis due to slow leaf area expansion,and in particular smaller individual leaves. E. frumentaceatillered more than E. utilis. Plant development was retardedat low temperatures but was not as responsive to temperatureas dry weight and leaf area. The different responses to temperatureof the two species were described in equations suitable forinclusion in predictive growth models. Echinochloa spp., millet, growth, development, temperature, relative growth rate     

Effects of temperature and salinity on the growth of the red tide flagellates Heterocapsa circularisquama (Dinophyceae) and Chattonella verruculosa (Raphidophyceae)

Growth responses of the red tide flagellates, Heterocapsa circularisquama(Dinophyceae) and Chattonella verruculosa (Raphidophyceae),were examined with 36 different combinations of temperature(5–30°C) and salinity (10–35 PSU). Heterocapsacircularisquama did not grow at or below a temperature of 10°C.The maximum growth rate of H.circularisquama (1.3 divisionsday^–1) was obtained with a combination of 30°C and30 PSU. In contrast, C. verruculosa did not grow at 10 PSU andat temperatures of 25°C or more. The maximum growth rateof C. verruculosa (1.74 divisions day^–1) was obtainedwith a combination of 15°C and 25 PSU. A significant temperature-salinityinteraction on growth was found by factorial analysis. Basedon the physiological characteristics obtained in the presentstudy, these novel flagellates have a potential for future outbreaksof red tides in pre viously unaffected waters.     

Observations on the vertical distribution of zooplankton, including post-larval teleosts, off Plymouth in the presence of a thermocline and a chlorophyll-dense layer

During 1973 – 1977, when Sagitta elegans was returningto dominance over S. setosa in Plymouth waters, there was often,in summer in stratified conditions, a community characterizedby S. setosa in the warm water above the thermocline, and atypical S. elegans community in the colder layer below the thermocline.This vertical separation persisted at night even though somespecies from the S. elegans community migrated up into the warmlayer. Such vertical migration was not stopped by a temperaturediscontinuity of from 3° to 6°C, but fewer individuals,or a lesser proportion of species, took part at the higher temperaturedifference. Only a small part of the zooplankton, comprisingsmall individuals of Limacina retroversa, the appendicularians,and, possibly, post-larvae of Arnoglossus laterna, showed signsof aggregation at the thermocline or the chlorophyll maximumclose to it.     

The Effects of Temperature on Leaf Growth in Cyperus longus, a Temperate C4 Species

Plants of the C₄ sedge Cyperus longus L. were grown at 10, 20and 30 °C. An asymptotic growth curve, the Richards function,was fitted to growth data for successive leaves. The mean rateof leaf appearance was a linear function of temperature with0.014 leaves appearing per day for every 1 °C increase intemperature. The instantaneous relative rate of leaf extensionshowed a marked ontogenetic drift which was most rapid at 30°C and slowest at 10 °C. The mean absolute extensionrate for foliage had a temperature coefficient of 0.16 cm d^–1° C^–1 in the range from 10 to 30 °C. The durationof leaf growth was independent of leaf number at 10 and 20 °Cbut increased linearly with leaf number at 30 °C. The smalldifferences in relative growth rate at the three temperaturesresulted in large differences in foliage area produced at theend of a 30 d growth period. The final foliage areas at 20 and10 °C were 51 and 9% respectively of that at 30 °C. Cyperus longus, temperature, leaf growth, Richards function, growth analysis     

Comparative Thermal Physiological Ecology of Syntopic Populations of Cacama valvata and Tibicen bifidus (Homoptera: Cicadidae): Modeling Fitness Consequences of Temperature Variation

SYNOPSIS. This paper develops a model based on egg-laying ratesand female oviposition temperature preferences in two speciesof cicada, Cacama valvata and Tibicen bifidus, from a centralNew Mexico desert grassland habitat. Output from the model indicatesthat C. valvata achieves maximal daily egg production (eggsfemale^–1 day^–1) on days when maximum shade ambienttemperatures reach 41°C; the corresponding value for T.bifidus is 33°C. These differences correlate with the thermalregime experienced by each species in its respective typicalhabitat. Simulations of the effects of variation in mean habitatambient temperature on egg production demonstrated that knowndistributional limits for T. bifidus correspond to thermal conditionsthat reduce daily egg production by only about 5–10% relativeto long-term means at the study site. The same is true for C.valvata only in lower-ambient temperature habitats. In higher-temperaturehabitats, C. valvata exhibits an unusual plasticity in the timingof adult activity and reproduction that allows it to occupya much wider geographic range than T. bifidus. Contrary to expectations,frequency distributions of predicted daily egg production rateswere negatively skewed in each species' respective ‘typicalhabitat’, and Gaussian only in thermally marginal habitats.The findings are discussed in the context of attempts to modelpopulation- and community-level effects of climatic change.     

The Effects of Position and Temperature on the Expansion of Leaves of Vicia faba L.

The growth in area of the first eight leaves of broad bean plantswas investigated in growth room experiments. Plants were grownat either 20 or 14 °C or transferred from 20 to 14 °C.Rates of leaf appearance and unfolding increased with temperature.The duration of growth of a leaf increased with leaf numberfor the first five leaves and then remained constant The meangrowth rate declined or remained constant with increasing leafnumber Durations of growth were shorter and growth rates largerat 20 °C than at 14 °C Plants responded immediatelyto the change in temperature Final areas of leaves which expandedafter transfer from 20 to 14 °C were larger than those grownat 20 °C Vicla faba L., broad bean, leaf expansion, temperature responses     

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     

Environmental Control of Flowering in some Northern Carex Species

The environmental control of flowering in some arctic-alpineCarexspecies has been studied in controlled environments.Carex nigra,C. brunnescens, C. atrata, C. norwegica andC. serotina all hada dual induction requirement for flowering. In all exceptC.nigra either low temperature (12 °C or lower) or short days(SD) over a wider range of temperatures were needed for primaryfloral induction and inflorescence formation. InC. nigra primaryfloral induction took place in SD only (9–21 °C),8–10 weeks of exposure being required for a full response.In all these species long days (LD) were required for, or stronglypromoted, culm elongation and inflorescence development (secondaryinduction). Quantitative ecotype differences in both primaryand secondary induction were demonstrated. Unlike the otherspecies,C. bicolor proved to be a regular LD plant which requiredLD only for inflorescence initiation and development. In allspecies leaf growth was strongly promoted by LD, especiallyin the higher temperature range (15–21 °C). In SDand temperatures below 15 °C the leaves became senescentand the plants entered a semi-dormant condition which was immediatelyreversed by LD. The results are discussed in relation to growthform and life history of shoots. Carex ; dual induction; ecotypic diversity; flowering; growth; photoperiod; sedges; temperature