PHOTOPERIODIC ADAPTATION IN DESERT POPULATIONS OF XANTHIUM STRUMARIUM

Reproductive adaptation to photoperiod is diverse among desert populations of Xanthium. Chihuahuan Desert populations require dark periods of 9.5–10.5 hr for reproduction, and Sonoran Desert populations require 9–10.5 hr. Many Chihuahuan populations from western Texas two weeks from sowing need only 10 cycles of 11-hr nights to produce 100% flowering, but Sonoran populations from western Mexico four weeks from sowing need 18 cycles or more. Some Sonoran plants produce buds only at a cooler temperature program, 24–15 C, but Chihuahuan plants produce them more readily under the warmer program, 30–24 C. Chihuahuan plants that were germinated under 11-hr nights and four different temperature programs were induced to flower in each condition. Differences in photoperiod and ripeness-to-flower (maturity) responses were also demonstrated under natural day lengths in central Texas. Although desert populations occurring at approximately the same latitude in either the Chihuahuan or Sonoran Desert are exposed to similar day lengths, each population may be adapted to different photoperiod cues that maximize its utilization of the local growing conditions.     

PHOTOPERIOD IN XANTHIUM POPULATIONS FROM TEXAS AND MEXICO

Photoperiodic responses of Xanthium strumarium L. originating between 19° N in Mexico and 34° N in Texas varied among seedlings grown from seed under controlled conditions. The critical night lengths form a gradient from 9.5 hr in northern Texas to 10.75 hr in southern Texas and northeastern Mexico. Populations with critical night lengths of 9.5 and 9.75 hr showed a longer interval to flower bud formation under cooler temperatures (24 C day/15 C night) than under warmer temperatures (30 C day/24 C night). Three of four populations with a 10.75-hr critical night length showed a shorter interval under the cooler temperature regime. Although the Texas populations demonstrate a strong correlation of photoperiodic response with latitude, the Mexico populations show diverse photoperiodic timing from approximately the same latitude. The study emphasizes that a combination of critical night length and ripeness-to-flower (maturity) response forms the basis for reproductive adaptation in different climatic regimes in Texas and Mexico.     

THE EFFECTS OF LIGHT AND TEMPERATURE ON GROWTH RATES IN BOREAL-SUBARCTIC CRUSTOSE CORALLINES1

A number of boreal-subarctic crustose corallines were kept in natural seawater tanks at temperatures ranging from 0 to 19 C and, using fluorescent lamps at light intensities, ranging from 7 to 750 lux with periods of 8 and 14 hr/day. The resultant growth rates as a function of temperature and light are presented and discussed in relation to the ecology of the plants. All of the Lithothamnieae studied had growth maxima at temperatures from 9 to 15 C. Growth in these species showed little light dependence below 4–6 C, but had a strong light dependence at higher temperatures. The one Lithophyllum species examined gave a flatter growth-temperature curve than the Lithothamnieae and showed little light dependence. The effects of temperature variation, salinity, and current on growth rates were also examined and are discussed. It was found to be especially important in studying growth rates of crustose corallines to allow time for growth stabilization following temperature change. In general, growth was found to exhibit a hysteresis effect, increased rates with the raising of temperatures 5–10 C and decreased rates with lowering temperatures.     

THE EFFECT OF SHORT PERIODS OF HIGH TEMPERATURE DURING DAY AND NIGHT PERIODS ON PEA YIELDS

Karr , E. J. (Ohio State U., Columbus), A. J. Linck , and C. A. Swanson . The effect of short periods of high temperature during day and night periods on pea yields. Amer. Jour. Bot. 46(2) : 91-93. Illus. 1959.—The effect of high temperatures during periods of relatively short duration (3-4 days) at various stages following anthesis at the first bloom node was studied in relation to yield of peas at this node. Except for the periods of differential temperature treatments, the plants were maintained in a standard environment room (24°C., light, 12 hr.; 15°C., darkness, 12 hr.). Three different temperature regimes during the treatment periods were studied: high day temperature—standard night temperature (32°—15°C.) ; standard day temperature—high night temperature (24°—30°C.) ; and high day and night temperatures combined (32°—30°C.). The data reveal the existence of a relatively well-defined thermal-sensitive period, with maximal sensitivity to high day temperatures occurring at about 9-11 days from full bloom, and maximal sensitivity to high night temperatures occurring about 6-9 days from full bloom. High night temperatures proved more critical, resulting in a maximal reduction of 25% in yield, as opposed to about 8% for high day temperatures. The effect of high day and night temperatures combined tended to be roughly additive.     

EXPERIMENTAL CONTROL OF FLOWERING IN LEMNA. II. SOME EFFECTS OF MEDIUM COMPOSITION,CHELATING AGENTS AND HIGH TEMPERATURES ON FLOWERING IN L. PERPUSILLA 6746

Hillman , William S. (Yale U., New Haven, Conn.) Experimental control of flowering in Lemna. II. Some effects of medium composition, chelating agents and high temperatures on flowering in L. perpusilla 6746. Amer. Jour. Bot. 46(7): 489–495. Illus. 1959.—-L. perpusilla 6746 flowers as a short-day plant on Hutner's medium (containing ethylenediaminetetraacetic acid [EDTA]) at constant temperatures from 25 to 30°C., but eventually flowers also in old cultures under 16 or 24 hr. of light. This old-culture flowering is more pronounced in dilute medium. Flowering is rapid under both long and short days at constant temperatures from 25 to 28°C. in media not containing EDTA; the addition of 10^-5 M EDTA or of similar or higher concentrations of numerous other chelating agents suppresses flowering under long days but not under short (8 hr. light). This effect does not depend on promotion or inhibition of vegetative growth. At 29 to 30°C., a short-day requirement is manifested even in media permitting flowering under long days at the lower temperatures. Temperatures above 31°C. completely inhibit flowering under all conditions. Brief periods of high temperature given to plants under short-day conditions inhibit flowering when given during the dark period but not during the light period. The implications of these observations for the further study of flowering are discussed.     

PHOTOCONTROL OF GROWTH AND FLOWERING OF CARYOPTERIS

Piringer , A. A., R. J. Downs , and H. A. Borthwick . (U. S. Dept. of Agriculture, ARS, Belts ville, Md.) Photocontrol of growth and flowering of Caryopteris . Amer. Jour. Bot. 50(1): 86–90. Illus. 1963.—Flower buds were initiated on plants of Caryopteris × clandonensis A. Simmonds (C. incana [Houtt.] Miq. × C. mongholica Bunge) on all photopcriods but developed to anthesis only when daily dark periods exceeded 8 hr. Anthesis occurred in not less than 22 days after the beginning of 11 or more short photoperiods. Treatments with short days could be interrupted by as many as 30 non-inductive long days without significant increase in the minimum number of short days required for anthesis. Anthesis, like floral initiation of many plants, was reversibly controlled by red and far-red radiation acting through phytochrome. The inductive effectiveness of long dark periods was nullified by 1 min of red light or about 1 hr of far red. It was modified by night temperature in the range 45–70.F and filament lengths of stamens were shorter at night temperatures of 60 than at 70 F.     

Differentiation in habitat response in taxodium distichum,taxodium mucronatum,platanus occidentalis,and liquidambar styraciflua from the United States and Mexico

Summary Habitat specialization in populations of three broadly distributed trees includes adaptive differentiation to day length and temperature. Low sensitivity to environmental cues is the adaptive strategy of the southernmost populations (from northeastern Mexico). Early cessation of growth and sensitivity to the environment is adaptive for the northernmost populations (southern Illinois). Intermediate responses characterize trees of Texas. In a comparison under four photoperiod-temperature conditions, the Mexico plants were adapted to the longest growing season. Under out-of-doors conditions in central Texas, these trees from Mexico continue to demonstrate adaptive strategies different from those of Texas or Illinois trees. Stipule production and leaf area inPlatanus showed modifications correlated with latitude. Northernmost trees had the smallest leaves and did not produce stipules under 12-h day lengths and 24–15 °C temperatures. The Mexico trees had stipules under each of the four experimental conditions. The results suggest that populations of deciduous trees in a given climate are selected toward convergence in some responses to that climate. As a result, populations of the three trees resemble each other in behavior in a given ecosystem. Research funds were provided by a grant from the U.S. Forest Service and from National Science Foundation Grant GB-6097. I acknowledge help of David S. May and George J. Williams.     

Developmental strategies of Koenigia islandica, a high-arctic annual plant

Seed germination, growth and flowering of the arctic-alpine annual Koenigia islandica were studied in controlled environment. Intact (unabraded) seeds germinated poorely at temperatures up to 18°C, with an optimum at 24°C (89% in 10 d). Scarified seeds germinated rapidly, and reached 100% germination in 3 d at 21°C, but no >40% germination occurred at 9 and 12°C, The seeds had no light requirement for germination, nor did fluctuating temperatures improve germination
Dry matter production was optimal at 12°C in both short day (SD) and long day (LD) conditions, but was markedly higher in LD than in SD at identical fluences at all temperatures except 21°C where the plants showed symptoms of severe heat stress. The temperature compensation point for net productivity was estimated to 24°C, and negative carbon balance at higher temperatures might be an important physiological mechanism limiting the distribution of K. islandica in Scandinavia.
Flowering was extremely rapid and independent of daylength, even in a high-arctic population from 79°N, In full summer daylight anthesis was reached 24 d after germination and seeds ripened after 36 d at 15°C, Days to anthesis varied little across the temperature range from 6 to 21°C, giving a linear decrease in the heat-sum requirement for the attainment of flowering with decreasing temperature.
It is concluded that conservative seed germination strategy, tininess and rapid development, low temperature optima for growth and reproduction, and daylength indifference of flowering are important adaptations for success of an annual plant in high-arctic and high-alpine environments, Daylength neutrality has facilitated the wide-latitudinal distribution of K. islandica. including the penetration of the species to the southern hemisphere.     

EXPERIMENTS ON THE PHOTOPERIODIC RESPONSE IN PINEAPPLE

Gowing , Donald P. (Pineapple Research Institute of Hawaii, Honolulu.) Experiments on the photoperiodic response in pineapple. Amer. Jour. Bot. 48(1): 16–21. 1961.—The initiation of flowering of ‘Smooth Cayenne’ pineapple plants is neither strictly a response to photoperiod (day lengths of 10 hr. 51 min.–13 hr. 24 min.) nor to a minimum temperature (minima from 50° to 72°F. in different areas) under natural Hawaiian conditions. Depending on the kind of planting material used and the time of planting, natural initiation of flowering may take place any month of the year. Slips planted in the fall generally initiate flowering in December of the following year. However, exposure of an 8-mo.-old slip-planting to a day length of 8 hours for 40 days starting Sept. 8 induced flowering irrespective of night temperatures from about 60 to 80°F. Interruption of the dark period by illumination at 30 ft.-c. from midnight to 1 a.m. suppressed the inductive effect. Lowering the night temperature to 60°F. was, of itself, non-inductive. Field-grown, 11-mo.-old plants treated in place responded similarly, in that 25 periods of 8-hr. day length starting Sept. 5 induced 60% of the plants to flower, and the night illumination suppressed the inductive effect as before. Daily application of 0.12 mg. of the major native pineapple auxin (indole-3-acetic acid) at the beginning of the dark period had no detectable effect on the short-day treatment, and similar application of an antiauxin (4-chlorophenoxyisobutyric acid) did not affect the suppression of flowering by the light-break. Supplemental illumination of field-grown 12-mo. plants to provide a photoperiod of more than 15 hr. daily from Nov. 4 to Jan. 30 did not suppress the natural initiation of flowering which occurred in early December (day length about 10 hr. 50 min.). ‘Smooth Cayenne’ pineapple is therefore a quantitative, but not an obligate, short-day plant.     

Determining critical pre- and post-anthesis periods and physiological processes in Lycopersicon esculentum Mill. exposed to moderately elevated temperatures

To determine the thermosensitive periods and physiological processes in tomato flowers exposed to moderately elevated temperatures, tomato plants (Lycopersicon esculentum Mill., cv. NC 8288) were grown at 28/22 degrees C or 32/26 degrees C day/night temperature regimes and then transferred to the opposite regime for 0-15 d before or 0-24 h after anthesis. For plants initially grown at 28/22 degrees C, moderate temperature stress before anthesis decreased the percentage of fruit set per plant, but did not clarify the thermosensitive period. The same level of stress did not significantly reduce fruit set when applied immediately after anthesis. For plants initially grown at 32/26 degrees C, fruit set was completely prevented unless a relief period of more than 5 d was provided before anthesis. The same level of stress relief for 3-24 h after anthesis also increased fruit set. Plants were most sensitive to 32/26 degrees C temperatures 7-15 d before anthesis. Microscopic investigation of anthers in plants grown continuously at high temperature indicated disruption of development in the pollen, endothecium, epidermis, and stomium. This disruption was reduced, but still observable in plants relieved from high temperature for 10 d before anthesis.     

LENGTH OF THE LIGHT-DARK CYCLE AND PLANT GROWTH

Tukey , H. B., Jr ., and H. J. Ketellapper . (California Inst. Tech., Pasadena.) Length of the light-dark cycle and plant growth. Amer. Jour. Bot. 50(2): 110–115. Illus. 1963.—It has been shown that the length of the light-dark cycle which causes maximal growth of tomato, pea, peanut, and soybean plants is close to 24 hr for cycles consisting of equal periods of light and darkness. The exact optimum for tomato plants was determined by temperature; the optimal cycle length was 20 hr at 30 C and 27–30 hr at 14 C. Such an interaction between temperature and cycle length was not found in pea plants, because peas were less sensitive to cycle length than peanuts, tomatoes, and soybeans and did not respond to changes in cycle length of 2–3 hr. The response to cycle length was not influenced by the conditions in which the seedlings had been raised prior to the treatment. Seedlings raised in a 16-hr light, 8-hr dark regime responded in the same manner as those raised in continuous light. The response to cycle lengths of 18, 24, 36, and 48 hr was not changed qualitatively by the temperature during the growth determination. Small changes in cycle length had no characteristic effects on the rates of photosynthesis, respiration or stem elongation. Stem elongation showed a rapid and initial increase in rate when the light was turned off. It was concluded that plants possess an endogenous time-measuring device with a period of 24 hr. For maximal growth to occur the external periodicity must be synchronized with the endogenous period of the plant. Efforts to obtain direct evidence for this hypothesis were not successful since no overt rhythms could be found in tomato plants.     

THE INFLUENCE OF HEAT ON SOME APHIDS

The thermal death-points of five species of aphids removed from their host plants lay between 38 and 41°C., when tested for 1 hr. at 60% r.h . Many aphids alive after 1 hr. at high temperatures died within the next day; no Myzus persicae recovered and reproduced after 1 hr. above 37.5°C. Third and fourth instars and adult apterae withstood heat better than first and second instars and alatae. More aphids died at 90% r.h . than at 60% r.h , and more at 60% than at 30% r.h . Aphids kept at 15% r.h . for 4 hr. before being heated showed a higher mortality than those kept at 95% r.h . Aphids on plants withstood temperatures higher than their thermal death-point off the plant. Presumably aphids can continue to cool themselves by evaporation while feeding; also lower temperatures on the surface of transpiring plant tissues will aid survival.     

The Control of Growth Habit of Marquillo x Kenya Farmer Wheat Dwarf I by Temperature

The Marquillo × Kenya Farmer 1 “grass-clump” dwarf selection of Triticum aestivum L. was grown under continuous 2000 foot candle light and several regimes of alternating 16° and 26° temperatures combined in total cycle lengths of 6, 12, 24, or 48 hr. Plants at 26° grew as normal wheat. Those exposed to 0.25 to 2 hr of 16° per cycle showed typical “grass-clump” dwarf characteristics which were independent of the cycle length. Treatments with 16° exposures of 4 to 8 hr per 24 hr and 12 to 16 hr per 48 hr exhibited vegetative “grass-clump” dwarfness for 40 days but later displayed extensive reproductive development. Longer 16° treatments killed the plants at a very early stage of vegetative development before floral initiation. The data supported an hypothesis that all 4 growth habits were related to the temperature sensitivity of the vegetative meristem. The cessation of meristem development was possibly due to the accumulation of a stable inhibitory substance produced at low temperatures.     

HEAT INJURY DURING FLORAL DEVELOPMENT IN COWPEA (VIGNA UNGUICULATA,FABACEAE)

High night temperatures during floral development induce male sterility in cowpea (Vigna unguiculata [L.] Walp.). The objectives of this study were to determine: the possible causes of the male sterility; the stage of floral development when damage due to heat stress occurs; and whether specific tissues are damaged during the period of sensitivity to heat. Plants were grown under controlled temperatures in both greenhouses and growth chambers in separate experiments. Floral development was normal under a night temperature of 20 C, whereas flowers developed under high night temperature (30 C) set no pods due to low pollen viability and anther indehiscence. Anthers developed under 33/30 C day/night temperatures did not exhibit endothecial formation, whereas anthers developed under 33/20 C day/night temperatures exhibited normal development of the endothecial layer. Reciprocal transfers of plants between chambers with high or optimum night temperature demonstrated that the stage of floral development most sensitive to heat stress occurs 9 to 7 d before anthesis. Anthers developed under either optimal or high night temperatures were compared cytologically. Development was similar through meiosis, but after tetrad release, which occurred 8 d before anthesis, the tapetal layer degenerated prematurely under high night temperature. Premature degeneration of the tapetal layer and lack of endothecial development may be responsible for the low pollen viability, low anther dehiscence, and low pod set under high night temperatures.     

THE LIFE CYCLE OF BANGIA FUSCOPURPUREA IN CULTURE. I. EFFECTS OF TEMPERATURE AND PHOTOPERIOD ON THE MORPHOLOGY AND REPRODUCTION OF THE BANGIA PHASE12

The Bangia phase of Bangia fuscopurpurea was grown in laboratory culture in a variety of photoperiod and temperature regimes. Plants of the Bangia phase grown from 2 types of asexual spores, monospores and conchospores, exhibited growth differences under similar growing conditions. Plants derived from monospores grew more rapidly and matured earlier than those derived from carpospores. Day length and temperature were found to significantly influence growth rule, maturation, and plant size. Long day lengths resulted in more rapid growth in filament length and diameter and earlier spore formation and spore release. Maximum filament length was observed in a 12/12 hr light-dark cycle at 15 C. Spore formation and release were delayed by decreasing day length or temperature. Temperature and photoperiod were also found to influence the type of spores produced by the Bangia phase. When grown at 22 C, the Bangia phase produced only monospores, which reproduced the Bangia phase. At 9 C, with photoperiods of 11 hr or more of light, the Bangia phase produced carpospores which gave rise to the alternating Conchocelis phase. The conditions under which sporogenesis occurred determined the spore type differentiated.     

EFFECTS OF PHOTOPERIOD AND VERNALIZATION ON THE NUMBER OF LEAVES AT FLOWERING IN 32 ARABIDOPSIS THALIANA (BRASSICACEAE) ECOTYPES

The extent of natural variation among wild type Arabidopsis thaliana L. Heynh for response to environmental stimuli that affect flowering is poorly documented. The effects of photoperiod and vernalization on the number of rosette leaves at the time of anthesis was measured for 32 Arabidopsis ecotypes. All ecotypes were vernalized 24 days at 4 C under continuous illumination. Vernalized and nonvernalized plants were transplanted into 8- (short-day) and 20-hour (long-day) photoperiods in controlled environment growth chambers. Two ecotypes failed to flower after 110 days. Mean leaf number was less for all ecotypes under long day compared to short day. Sixteen ecotypes responded to vernalization; eight had reduced leaf number regardless of photoperiod, and eight had reduced leaf number only under short day. Two ecotypes required vernalization to flower in this study. For three ecotypes, vernalization and short day resulted in a reduction in leaf number whereas vernalization and long day resulted in increased leaf number. Documentation of the effects and interactions of photoperiod and vernalization across many ecotypes provides a broader range of described natural variation for genetic and physiologic study.     

Effects of thermoperiods on diapause induction in the cabbage beetle, Colaphellus bowringi (Coleoptera: Chrysomelidae)

Abstract. The effects of thermoperiods on diapause induction in continuous darkness or under a 12 : 12 h LD photoperiod were investigated in the cabbage beetle, Colaphellus bowringi Baly, a typical short‐day species. The diapause response curves both at different constant temperatures and at the thermocycle of format CT x: (24 ? x) h (16 : 28 °C) under continuously dark rearing conditions showed that the incidence of diapause depended mainly on whether or not the mean temperature was ≤20 °C or >20 °C. If the mean temperature was ≤20 °C, all individuals entered diapause; if >20 °C, the incidence of diapause declined gradually with increasing mean temperatures. The thermocycle (CT 12 : 12 h) with a series of different cryophases (8–22 °C) and thermophases (24–32 °C) under continuous darkness demonstrated a cryophase response threshold temperature of approximately 19 °C and a thermophase response threshold temperature of approximately 31 °C. Thermoperiodic amplitude (temperature difference between cryophase and thermophase) was shown to have a significant influence on diapause induction at the mean temperatures of 22, 23 and 24 °C, but not at ≥25 °C. Thermoperiodic responses under LD 12 : 12 h clearly showed that the incidence of diapause was influenced strongly by the photophase temperature. The thermoperiod under LD 12 : 12 h induced a much lower incidence of diapause than the thermoperiod with the same temperature in continuous darkness. The ecological significance of thermoperiodic induction of diapause in this species is discussed.     

Photoperiodic induction of the pupal diapause in the tobacco hornworm, Manduca sexta

A study was made of photoperiodic induction of the facultative pupal diapause in the tobacco hornworm, Manduca sexta, reared on artificial diet in the laboratory. The species entered a prolonged diapause when the egg and larval feeding stages were reared in daily photoperiods of 13·5 hr or less. Diapause was induced in all insects at photoperiods ranging from 1 to 13 hr, and part of the population entered diapause at only 15 to 30 min of light per day. Photoperiods of 14 hr or more and continous darkness prevented diapause. Duration of diapause varied with the inductive photoperiod in which the hornworms were reared during the sensitive period. Insects reared in longer diapause-inducing photoperiods within a range of 12 to 13·25 hr remained in diapause longer than those reared in shorter photoperiods. There was no difference in the rate of larval development of hornworms reared in diapause-inducing vs diapause-preventing photoperiods. Temperatures of 26 to 30°C were most favourable for the photoperiodic induction of diapause; at 21°C, the critical photoperiod and incidence of diapause were decreased. Diapause induction was suppressed by low (18°C) and higher (33°C) temperatures. The number of inductive 12L:12D (light = 12 hr; dark = 12 hr) cycles required to induce diapause ranged from as few as 5 for some insects to as many as 12 for others when the post-inductive régimen was continuous light, but with insects previously held in continuous dark, as few as 2 12L:12D cycles during the last 2 days of larval feeding induced diapause in 38 per cent of the population. Only 3 to 4 cycles of 15L:9D during the final larval instar reversed inductive effects of 14 to 15 12L:12D cycles. Photoperiodic sensitivity extended from the late embryo to the end of larval feeding but showed considerable fluctuation during development with maximum sensitivity occurring just before egg hatch and during larval growth.Light breaks applied at different times during the dark period of 12L:12D cycles generated different response curves, depending on the number of cycles in which light breaks were repeated. When repeated for 6 cycles, a unimodal response curve was obtained; 10 cycles produced a bimodal curve and light breaks given for 18 cycles throughout the sensitive period averted diapause regardless of time of night applied. It is suggested that diapause is regulated by a photo- and thermolabile substance that accumulates during long nights (11 hr or more) and acts during the early pupal stage to inhibit the translocation and release of development-promoting neurosecretion from the brain.     

Flowering strategies of the high-arctic and high-alpine snow bed grass species Phippsia algida

Flowering requirements of the high-arctic and high-alpine snow bed grass species Phippsia algida (Sol.) R. Br. have been studied in controlled environments. Seedlings flowered rapidly in continuous long days (LD) at temperatures ranging from 9 to 21°C. They also initiated inflorescence primordia at the same temperatures in continuous short days (SD), whereas LD were required for heading and anthesis. The plant thus has the characteristics of a regular long day plant, although the daylength requirement is associated with floral development only. The critical daylength for the LD response was about 17 h at 21°C and 19 h at 9°C. A single LD cycle was enough to trigger inflorescence development, while 5 cycles were required for the full response. Anthesis was reached within a week of LD treatment at 21°C in SD grown plants with preformed inflorescence primordia. The advantages of these versatile flowering responses are discussed in relation to the extreme climatic regime of late snow bed sites.     

Seasonal adaptations of populations of the southwestern corn borer, Diatraea grandiosella, from tropical and temperate regions

Seasonal adaptations of populations of the southwestern corn borer, Diatraea grandiosella, obtained from south-central Mexico (19°N latitude) and southeast Missouri (37°N latitude) were compared. Day length and temperature were found to serve as environmental cues to programme the larval diapause of both populations, but different critical values were observed. The critical day length for diapause induction was about 13 hr light/day for Mexican larvae and about 15 hr light/day for Missouri larvae, and was relatively stable at 20 to 30°C. Mexican larvae displayed a less-intense diapause than did Missouri larvae. Some diapausing Mexican larvae maintained at 25 or 30°C pupated in about 15 days, regardless of the day length to which they were exposed. The rate of diapause development of Mexican larvae was high at day lengths between 14 hr and 16 hr, whereas that of Missouri larvae was accelerated at day lengths of 16 hr at 25 and 30°C. Diapause development of Mexican larvae was virtually unaffected by chilling at 10°C, whereas that of Missouri larvae continued at a low rate at 10°C. Selection of Mexican larvae for diapause showed that only four generations were needed to significantly increase the incidence of diapause.