Effects of photoperiod and temperature on the cholinesterase activity in the ganglia of Schistocerca gregaria

The presence of acetyl cholinesterases, cholinesterases, and non-specific esterases in four different ganglia of Schistocerca gregaria was demonstrated using various substrates, as well as by means of inhibition with physostigmine salicylate and BW 284 C51. The contribution of these enzymes to the total esterase activity in each ganglion was also determined quantitatively.In animals kept under a L:D = 12:12 regime with concurrent changes of temperature (about 30°C during the light period and 20°C during the dark period), the activity of the AChE displays a maximum at about the time of light change or 1 to 2 hr later. The activity peak lasts for about 2 hr. If average enzyme activities are calculated, no statistically significant differences between ‘day’ and ‘night’ animals are apparent.An elevation of the environmental temperature from 20°C to 30°C during the light period led to a significant rise in enzyme activity in all ganglia after 1 to 3 hr. Lowering the environmental temperature from 30°C to 20°C during the light period led to a significant decrease in enzyme activity only in the suboesophageal ganglion after 2 hr. Artificial stimulation of the animals in a wind tunnel decreases the acetyl cholinesterase activity in the suboesophageal ganglion, whereas in the other ganglia no significant change in enzyme activity was observed. Further, no correlation was found between the enzyme activity and O₂ consumption of the experimental animals.     

Seasonal adaptations of different geographical populations of the sunflower moth, Homoeosoma electellum

A photothermogram constructed for a central Missouri population (ca. 39°N latitude) of the sunflower moth, Homoeosoma electellum (Hulst) predicted that this population has a seasonal life cycle of 2 complete and a partial third generation per year, and that daylengths of less than 13 h 30 min light/day and mean temperatures of less than 20°C induce the mature larval diapause. A test of the predicted life cycle revealed that larvae entered diapause when they were exposed from their first instar onwards to natural conditions in central Missouri beginning September 15, 1982. Sunflower moths obtained from northwest Texas (ca. 35°N latitude) and northeast South Dakota (ca. 45°N latitude) displayed shorter critical photoperiods for diapause induction at 20°C (12 h 30 min light/day and 12 h 15 min light/day, respectively) than did those from Missouri. The population of the sunflower moth obtained from South Dakota does not, therefore, appear to be adapted to local conditions, and moths might disperse from lower latitudes to establish transiet populations each year.     

Effect of freezing and thawing on the microcirculation and capillary endothelium of the hamster cheek pouch

Golden Syrian hamster cheek pouches were prepared in vivo for observation of microvasculature under the light microscope. On an apparatus designed especially for this purpose, pouches were cooled from plus 10 °C to minus 30 °C at 1 °C/min, held at minus 30 °C for 1 min and warmed at 1 °C/min to plus 10 °C whence spontaneous rewarming to ambient was permitted. Pouches were observed under the light microscope throughout freezing and for 1 hr after thaw. At 0, 1, 5, 15, 30, and 60 min after thaw pouch tissue was taken for electron microscopy. After thaw hemostasis evolved in a biphasic pattern. In the early phase in which the degree of stasis reached its peak at about 20 min after thaw, cessation of circulation was caused by obstructive embolic platelet aggregates and a second uncharacterized factor, possibly humoral in nature. After 30 min, blood flow spontaneously resumed in at least one portion of each pouch. In 6 specimens, by 45–50 min, blood flow had returned to normal in about 90% of the microvasculature. After 50 min hemostasis began again and by 60 min blood flow had ceased in virtually all areas of the pouch, this time in the absence of vascular obstruction by platelet aggregates. Ultrastructural damage to endothelial cells occurring immediately at thaw and progressing through 1 hr thereafter included the rupture of cell membranes, early thinning, and later condensation of ground substance, decrease in the number and concentration of pinocytotic vesicles, swelling of rough endoplasmic reticulum, and the swelling and loss of cristal structure of mitochondria. This endothelial destruction can account for the permanent hemostasis of frostbite.     

Studies on the vegetative life cycle of Chlamydomonas reinhardi Dangeard in synchronous culture IV. Effects of 6-methyl purine on the revolution of the cell cycle

Cells of Chlamydomonas reinhardi Dangeard were synchronouslygrown under a 12 hr light-12 hr dark regime. The algal cellcycle under these conditions starts with a light-induced reaction(s)at the beginning of the light period and ends, after a definiteperiod of time (23–24 hr at 25°C), in zoospore liberation.When cells were exposed to 6-methyl purine for short periods(0.5–2.5 hr) at different times during the early and intermediatephases of the cell cycle, it exerted, as an analogue of adenine,two different effects on the revolution of the cell cycle: onea "lengthening" effect seen at its low concentrations in whichthe length of the cell cycle was somewhat prolonged, the othera "return to start" effect at higher concentrations. In thelatter a short exposure of cells to 6-methyl purine broughtthem to the starting point of the cell cycle concurrent withthe abortion of the cycle in process. When 6-methyl purine wasapplied during the later phase of about 1/4 the length of thecell cycle, it casued no effect. Control of the revolution ofthe algal cell cycle by an "adenine-involving reaction(s)" disturbedby this adenine analogue is discussed. (Received September 1, 1975; )     

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.     

Superovulation in immature and mature Chinese hamsters

Mature female Chinese hamsters ovulate an average of 8.8 ± 1.0 (mean ± SD) eggs per female in each estrous cycle. Superovulation can be induced in both immature and mature females by subcutaneous or intraperitoneal injections of pregnant mare serum gonadotropin (PMSG) and either human chorionic gonadotropin (hCG) or pituitary luteinizing hormone (PLH). The best superovulation in immature females was induced by the administration of 15 IU of PMSG followed 72 hr later by injection of 15 IU of hCG (about 25 eggs per female) or 0.2 mg (200 IU) PLH (about 46 eggs per female). Ovulation started about 13–15 hr after administration of hCG (or PLH) and was completed during the next 5–6 hr. Superovulation in mature females could be induced by injecting PMSG any day of the estrous cycle, but the best superovulation (about 39 eggs per female) was induced by injecting 15 IU of PMSG on day 1 (day of ovulation) followed by the injection of 0.4 mg of PLH 72 hr later. When immature females treated with the best superovulatory protocol were mated on the evening of PLH injection, only 5% of the eggs were found fertilized 50 hr after PLH administration. On the other hand, about 60% of the eggs were found fertilized in mature females mated following treatment with the best superovulatory protocol. The majority (83–85%) of superovulated eggs obtained from both immature and mature females were normally fertilized in vitro.     

Field performance of Solanum sisymbriifolium, a trap crop for potato cyst nematodes. I. Dry matter accumulation in relation to sowing time, location, season and plant density

Solanum sisymbriifolium is an interesting trap crop to control potato cyst nematodes. A series of field experiments was carried out in the Netherlands between 2001 and 2003 to test its performance under field conditions. Experimental factors included sowing time, sowing density and site. Rate of germination, plant establishment and change over time in light interception were monitored. Growth analysis was performed at 7 and 14 weeks after emergence, and dry weight of component plant parts was determined. Time to 50% emergence was 36–38 days for planting at early April and declined to minimum values of ca 8–11 days when planting took place in June, July or the first week of August. When planted later, time to 50% germination increased again. Time to 50% light interception showed a similar trend with sowing time; minimum time was 35–40 days for planting between June and half of July. Planting before May did not advance crop growth. Crop performance was very variable across years and sites when planted later than the end of July to beginning of August. Dry matter accumulation up to 400 g m^?2 was found at 7 weeks after emergence and up to 1040 g m^?2 after 14 weeks. At 7 weeks after emergence, dry matter production increased with planting density (range 50–400 m^?2), but no statistically significant differences were found after 14 weeks. A seed rate of 100 m^?2 seems generally sufficient. Radiation use efficiency was 1.69 g MJ^?1 PAR (SE = 0.0208). Dry matter accumulation (2002–2003) was somewhat higher in Wageningen (51°58’N) on light sandy soil than in Flevoland (52°31′N) on clay soil and in Drenthe (52°51′N) on reclaimed peat soil. It is concluded that above‐ground growth of S. sisymbriifolium in the Netherlands is adequate if planted between early May and the end of July.     

T-lymphocyte mediated cytolysis: Temperature dependence of killer cell dependent and independent phases and lack of recovery from the lethal hit at low temperatures

Using alloantiserum and complement to inactivate cytolytic T-lymphocytes after they had administered the “lethal hit” to target cells, the rate of killer-cell independent lysis (KCIL) as measured by radiochromium release was followed at various temperatures. Under usual conditions, KCIL was half-completed on the average after 1.7 hr at 37 °C. The average Q₁₀ of KCIL is about 1.6 during the first few hours after cooling, but near 0 °, lysis slows down at later times. Thus, the extent of KCIL after 6–8 hr at 0 ° is frequently less than one-tenth of that at 37 °C. The Q₁₀ of the whole killing process is 2.5 near 37 °C but exceeds 6 near 22 °C.Evidence has been presented elsewhere suggesting that recovery from complement mediated damage may occur under appropriate conditions. Since KCIL can largely be arrested at low temperatures, we tested for possible recovery from or repair of the T-cell administered “lethal hit” during incubations at low temperature following (i) inactivation of killer cells by antiserum and complement or (ii) detachment of killer cells with EDTA and prevention of subsequent killer-target cell contact with dextran. No evidence for recovery from the “lethal hit” was found during incubations from 0.3 to 5 hr at 20 °, 15 °, or 0 °C. The temperature dependence of KCIL raises the possibility that metabolic events are of importance during KCIL. However, the previous finding that lysis following damage mediated by antiserum and complement is equally temperature sensitive leaves no basis for postulating such metabolic events. Hence, although unequivocal direct evidence has been difficult to obtain, colloid osmotic lysis is at present the simplest and most plausible explanation of killer-cell independent lysis.     

GROWTH PATTERNS IN NUTATING AND NONNUTATING SUNFLOWER (HELIANTHUS ANNUUS) HYPOCOTYLS

Dark-grown sunflower (Helianthus annuus L.) seedling hypocotyls (15–30 mm) were marked with two rows of lanolin-coated resin beads, and the events of the following 24 hr, in physiological darkness, were recorded on time-lapse video. Nutational movement of the hypocotyl, followed for 20–24 hr for each of 21 seedlings, was found to have a mean period of 153 ± 26 min (ca. 24 C). Displacement of each bead, with time, was measured with a microcomputer-controlled video analyzer, and relative elemental elongation rate and relative growth rate analyses were carried out to determine the spatial and temporal distribution of growth. Relative elemental elongation rates were plotted against distance and time to produce “growth landscapes.” A strongly nutating seedling showed periodic fluctuations in local growth rates that alternated between values of 0.0 hr^−-1 and >0.12 hr^−-1 near the hypocotyl hook. Nearer the base, maximum growth rates were lower but local periodic changes still were evident. Seedlings, in which nutation appeared during the time period analyzed, showed non-synchronous pulses of growth along the axis. With nutational development, these local growth fluctuations became synchronized along each side and phased (usually 180° out of phase) with the coordinated growth fluctuations along the opposite side. In some seedlings the changes from low to high local growth rates occur nearly simultaneously over two-thirds of the active region. In others, basipetally traveling waves of growth are suggested by the growth landscapes.     

In vitro germination and origin of thallus in Griffithella hookeriana (Podostemaceae)

Griffithella hookeriana (Tul.) Warm. (Podostemaceae) is a thalloid plant with no true leaves, stem or root. The seeds are extremely small (1000 seeds weigh 0.809 mg) and can be germinated on moist filter paper, but the resulting seedlings fail to survive beyond 5–6 days. A technique of germinating seeds in vitro on thermocole cubes floated in Murashige and Skoog's liquid medium (MS 1/5 strength with 0.5% sucrose) in continuous light (500–1000 lux) at 27±2°C has been developed. During germination, the radicular pole emerges from the seed coat and elongation of the two cotyledons follows. Rhizoids arise from the radicular pole and secrete a sticky substance that helps the seedling to adhere firmly to the substratum. The plumular apex ceases to funciton after producing 2 or 3 pairs of leaf-like outgrowths. A lateral protuberance is formed from the primary axis below the level of cotyledons and develops into a flat, green and oval, round or tubular (branched or unbranched) thallus (up to 0.5–0.8 cm in diameter) within 65–70 days. There is a high mortality of seedlings and plants at various stages of development: about 20% senesce before the initiation of the plumule, 15–20% after the formation of the leaf-like structures and 2–4% during the thallus stage. Seeds retain 83% viability for more than a year when stored dry at 10–15°C.     

Light-induced nuclear translocation of endogenous pea phytochrome A visualized by immunocytochemical procedures

Although the physiological functions of phytochrome A (PhyA) are now known, the distribution of endogenous PhyA has not been examined. We have visualized endogenous PhyA apoprotein (PHYA) by immunolabeling cryosections of pea tissue, using PHYA-deficient mutants as negative controls. By this method, we examined the distribution of PHYA in different tissues and changes in its intracellular distribution in response to light. In apical hook cells of etiolated seedlings, PHYA immunolabeling was distributed diffusely in the cytosol. Exposure to continuous far-red (cFR) light caused a redistribution of the immunolabeling to the nucleus, first detectable after 1.5 hr and greatest at 4.5 hr. During this time, the amounts of spectrally active phytochrome and PHYA did not decline substantially. Exposure to continuous red (cR) light or to a brief pulse of red light also resulted in redistribution of immunolabeling to the nucleus, but this occurred much more rapidly and with a different pattern of intranuclear distribution than it did in response to cFR light. Exposures to cR light resulted in loss of immunolabeling, which was associated with PHYA degradation. These results indicate that the light-induced intracellular location of PHYA is wavelength dependent and imply that this is important for PhyA activity.     

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.     

Light-induced changes of enzyme activities in parsley cell suspension cultures: Increased rate of synthesis of phenylalanine ammonia-lyase

When dark-grown cell suspension cultures of parsley (Petroselinum hortense) were illuminated for increasing periods of time, increasing amounts of phenylalanine ammonialyase activity were obtained 5 hr after the onset of light.Pulses of [³⁵S]methionine of varying duration from 1 to 150 min were given to cell cultures in the dark period subsequent to a light period of 2.5 hr. The cells were harvested 5 hr after the onset of light. Analysis of the soluble proteins by polyacrylamide gel electrophoresis revealed a distinct peak of radioactivity coinciding with the activity of phenylalanine ammonia-lyase. The results of experiments in which radioactive methionine was administered for 10 min to dark-grown or light-induced cells at different times after the light period were compared. An efficient incorporation of radioactivity into the fractions possessing the enzyme activity was observed 5 hr after induction, while no significant labeling was detected either after 1.5 or 25 hr, or in extracts from nonilluminated cells. The radioactive fractions containing the enzyme activity were further analyzed by sodium dodecyl sulfate-disc gel electrophoresis. Significant amounts of radioactivity at the molecular weight of the subunits of phenylalanine ammonia-lyase (84,000) were found only in the extracts from cells which had been labeled 5 hr after induction. These results suggest that the light-induced increase in phenylalanine ammonia-lyase activity is due to de novo synthesis, but not to an activation of preformed, inactive enzyme.     

Reversible uncoupling of energy transfer between phycobilins and chlorophyll in Anacystis nidulans. Light stimulation of cold-induced phycobilisome detachment

Phycobilin fluorescence of Anacystis nidulans grown at 28°C increases substantially upon cooling below 10°C. A maximal increase is found around ?5°C and amounts to 300%, with almost complete reversibility upon re-warming. Illumination with actinic light leads to considerable stimulation of the cold-induced phycobilin fluorescence increase. Analysis of the light stimulation phenomenon reveals: (1) Actinic illumination shifts the fluorescence-temperature characteristic by about 3°C upwards on the T-axis. At temperatures below 5°C the light stimulating effect becomes smaller again and fluorescence-temperature characteristics measured at high and low light intensity converge around ?5°C. (2) In the 13-8°C region a large (up to 100%) light-induced phycobilin fluorescence increase is observed, while only negligible changes occur in the dark. (3) 3-(3,4-Dichlorophenyl)-1,1-dimethyl urea (DCMU) as well as uncouplers inhibit the light stimulation, which hence depends on coupled electron transport.In agreement with previous work (Schreiber, U. (1979) FEBS Lett. 107, 4–9) it is concluded that illumination enhances cold-induced phycobilisome detachment by increasing the net negative charge at the outer surface of the thylakoid membrane. The possible role of a fluid → ordered transition of membrane lipids (Murata, N. and Fork, D.C. (1975) Plant Physiol. 56, 791–796) is discussed.     

CONTROL OF GERMINATION OF ALEXANDRIUM TAMARENSE (DINOPHYCEAE) CYSTS FROM THE LOWER ST. LAWRENCE ESTUARY (CANADA)

Cysts of the toxic dinoflagellate Alexandrium tamarense (Lebour) Balech 1992 from the lower St. Lawrence estuary were used in a test of the following hypotheses: (1) cyst germination is triggered by a change in temperature, and (2) germination rate varies throughout the year and is controlled by a circannual internal biological clock. Results show that cyst germination was not affected significantly by temperature of incubation over the range 1°–16° C, and light showed no significant stimulation of germination. This is supported by the lack of effect of cyst incubation conditions during evaluation of the seasonal changes in germination rate (two temperatures: 4° and 15° C, and two light conditions: darkness and 150 μmol photons·m^?2·s^?1). Thus, direct environmental control through short-term increases in temperature and exposure to light has no effect on the germination of the cysts tested. The rate of germination, observed monthly over a 16-month period, showed low germination (<20%) over most of the period tested, except for a maximum reaching more than 50% germination in August to October of the second year of the experiment. This pattern was observed for cysts both from monthly field collections and from laboratory-stored cysts kept under constant environmental conditions (4° C, in the dark). The peak in germination observed under constant environmental conditions (in the laboratory), the almost coincidental increase in cyst germination observed for the field-collected cysts, and the absence of effects of temperature and light during incubation could be explained either by a temperature-controlled cyst maturation period (the time-temperature hypothesis of Huber and Nipkow 1923) or by the presence of an internal biological clock. However, the large decline in the rate of germination 2 months after the maximum provides strong support for the biological clock hypothesis. The ca. 12-month maturation (dormancy) period observed for the laboratory-stored cysts is the longest reported for this species to our knowledge; this might be related to the low storage temperature (4° C), which is close to bottom temperatures generally encountered in this environment (0° to 6° C). Similar field and laboratory storage temperatures could explain the coincidental increase in germination rate in the fall of the second year if cyst maturation is controlled by temperature. A fraction of the laboratory-stored cysts did not follow a rhythmic pattern: A rather constant germination rate of about 20% was observed throughout the year. This continuous germination of likely mature cysts may supplement the local blooms of this toxic dinoflagellate, as these often occur earlier than peak germination observed in late summer. It seems that two cyst germination strategies are present in the St. Lawrence: continuous germination after cyst maturation, with temperature controlling the length of the maturation period, and germination controlled by a circannual internal rhythm.     

Reduced temperature prevents transfer of a membrane glycoprotein to the cell surface but does not prevent terminal glycosylation

The transport kinetics of the influenza virus hemagglutinin from its site of synthesis to the apical plasma membrane of Madin-Darby canine kidney cells, a polarized epithelial cell line, were studied by a sensitive tryptic assay. Hemagglutinin acquired terminal sugars, as judged by sensitivity to endo-β-N-acetylglucosaminidase H, 10–15 min after synthesis, and first appeared on the apical domain 15 min later. None of the pulse-labeled hemagglutinin accumulated on the basolateral domain. At 20°C, terminal glycosylation continued, but no hemagglutinin was detected on the cell surface within 2 hr. If the incubation temperature was raised from 20°C to 37°C, hemagglutinin was quickly externalized, demonstrating that the inhibition at low temperature was reversible.     

The role of ecdysteroids in the determination of gut-purge timing in the saturniid, Samia cynthia ricini

Under a 12-hr light and 12-hr dark photoperiod, haemolymph ecdysteroid titre of the last(5th)-instar larva of Samia cynthia ricini begins to rise in the early scotophase preceding gut purge, which marks the larval-prepupal transition, to reach a peak titre of 7.6 ng/ml ca. 4.5 hr before gut purge. This profile of ecdysteroid increment is phase-shifted in response to phase shifts of the scotophase immediately before gut purge, in parallel with gut-purge phase shifts, suggesting that ecdysone release is under the control of a circadian clock dictating gut-purge timing. Ecdysone and 20-hydroxyecdysone (10–20 μg), injected no later than 18 hr before the normal gate of gut purge induced well-defined peaks of precocious gut purge ca. 8 hr after injection. Earlier injections caused acceleration of gut purge but the degree of acceleration was unpredictable. These results suggest that the timed surge of ecdysteroids is responsible for the gated occurrence of gut purge and that 18 hr before gut purge larvae acquire the competence to undergo gut purge in a gated fashion provided that they are exposed to a sufficient surge of ecdysteroids.     

Length–weight relationships of three fish species from Kerala waters,south‐west coast of India

Length–weight relationships (LWRs) of three fish species: Scomberomorus commerson, Alepes vari, and A. kleinii were estimated from Kerala waters, south‐west coast of India. Fish were captured between June 2016 and June 2017 by various gears such as ring seine (8–26 mm mesh size), trawl (30–40 mm cod end mesh size), hook and line (hook number VI–XII), smaller mesh sized drift gill net (26–90 mm) and larger one (120–170 mm) for bigger size fishes. Fish were collected on weekly basis from Cochin Fisheries Harbour (Lat. 09°56′327″N, Long. 76°15′764″E), Munambam Fisheries Harbour (Lat. 10°10′965″N, Long. 76°10′258″E), Kalamukku (Lat. 09°59′924″N, Long. 76°14′564″E) and Chellanam (Lat. 09°47′950″N, Long. 76°16′551″E). All LWRs were significant with r² values ranged from 0.944 to 0.996 and b values ranged from 2.722 to 3.021 (p < .001). In addition, this study provides the information on LWRs and new maximum size for Alepes vari and A. kleinii.     

Control of the Hypocotyl Hook Angle in Phaseolus mungo L.: the Role of Parts of the Seedling

Phaseolus mungo L. seedlings were grown in the dark for 5 d.They were either kept in the dark or exposed to 5 min red light.The location of the light-sensitive region (the hook) and theanatomy of light-induced opening are described. The responsewas phytochrome-mediated. The time course of light-induced openingand its far-red reversal are described and the implicationsfor the mechanism of light-induced opening discussed. The lagphase between irradiation and the start of opening was >8h, for 3 h of which the response remained completely photoreversible.This implies that some critical level of a factor is requiredbefore hook opening can be initiated. The terminal parts (leavesand cotyledons) kept the hooks shut in the dark, but did notdirectly affect the light response. The necessity for distinguishingbetween treatment effects on hook angle and on light-inducedopening is noted. We hypothesize that the terminal parts produceda hook-maintaining factor whose level declined after their removal.This factor was dispersed or inactivated following irradiation,or the hook cells were rendered less sensitive to it. Differencesbetween the responses of P. mungo and those reported for otherspecies are discussed.     

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.