Depth distribution of three Typha species, Typha orientalis Presl, Typha angustifolia L. and Typha latifolia L., in an artificial pond

The depth distribution of the aquatic macrophyte Typha orientalis Presl was examined in comparison with two other Typha species: Typha angustifolia L. and Typha latifolia L. Vegetation surveys mapping the depth distributions were conducted at Ushigafuchi Pond, Tokyo, Japan, in autumn 2004 and 2005. All vegetation had been cleared from this artificial pond in spring 2003. In 2004 T. orientalis was distributed in shallow to deep water habitats between T. latifolia (shallow water regions) and T. angustifolia (shallow to deep water regions). However, by 2005 T. orientalis had almost disappeared from the pond. It had been replaced by Leersia japonica Makino at depths of 0–30 cm, by Schoenoplectus validus (Vahl) at depths of 30–60 cm and by T. angustifolia at depths of 60–100 cm. It appears that T. orientalis is not a strong competitor, particularly with taller species, but rather a pioneer species.     

PERITHECIAL FORMATION IN GELASINOSPORA RETICULISPORA. I. EFFECTS OF LIGHT AT TWO DIFFERENT GROWTH STATES

Hyphae of Gelasinospora reticulispora were cultured on corn meal agar in a growth tube at 25 ± 0.4°C under different light conditions. While the hyphal tip was growing, perithecia were not formed under continuous white light (ca. 2000 ergs cm^?2 sec^?1), but some perithecia were initiated in total darkness. However, when white light was given after a dark period, perithecial formation was greatly promoted. In these cases, perithecial formation occurred in older portion of the culture (the portion nearest the point of inoculation) at first, and then gradually spread to the younger portion. Immediately after the tip of hyphae reached the other end of the growth tube, perithecia were induced in the youngest portion of the hyphae irrespective of the photoconditions; then formation proceeded toward the older portion. This induction was not age-dependent, because in growth tubes with different lengths, perithecia always became visible ca. 24 hr after the tip of hyphae reached the other end of growth tube. The photoinhibitory effect was no longer observed thereafter, but photopromotive effect was still evident.     

Denervation Effects on Limb Regeneration in Postmetamorphic Xenopus laevis

The effects of denervation on limb regeneration of postmetamorphic Xenopus laevis in the early to late stages of regeneration were studied. Limbs that were denervated immediately after amputation did not show any signs of regeneration. Moreover regenerating limbs denervated 20, 30, 40 and 60 days after amputation showed significant regression of regenerates. After this regression of regenerates, the regenerative capacity was not restored during a long observation period. Denervation reduced both protein synthesis (³H leucine autoradiography) and mitotic activity of regenerating limbs even in later stages of regeneration. These results on the role of the nerve in limb regeneration of Xenopus were compared with results in Xenopus and urodeles reported previously.     

Effects of photoperiod and temperature on the rhythm and free‐running of adult eclosion in the Indian meal moth Plodia interpunctella

The rhythm of adult eclosion in the Indian meal moth Plodia interpunctella Hübner (Lepidoptera: Pyralidae) is investigated under various photoperiods and temperatures aiming to determine the nature of the temperature compensation and the free‐running period. Insects that are committed to a nondiapause larval development show diel rhythms of adult eclosion at 30, 25 and 20 °C. At 30 °C, the eclosion peak (i.e. the mean time of eclosion) occurs approximately 20 h after lights off under an LD 4 : 20 h photocycle, and at approximately 15 h under an LD 20 : 4 h photocycle. At 25 °C, the peak of eclosion occurs approximately 19 h after lights off under an LD 2 : 20 h photocycle and at approximately 16 h under an LD 20 : 4 h photocycle. At 20 °C, the eclosion peak is significantly advanced under long days of >12 h (i.e. approximately 20 h after lights off under an LD 4 : 20 h photocycle and approximately 9 h under an LD 20 : 4 h photocycle), indicating an effect of both lights‐off and lights‐on signals on the timing of the adult eclosion. To determine the involvement of a self‐sustained oscillator, the rhythm of adult eclosion is examined under darkness at different temperatures (30 to 21 °C). The mean free‐running periods are 22.4, 22.8, 22.0 and 22.5 h at 30, 24, 23 and 22 °C, respectively, indicating that the eclosion rhythm is temperature‐compensated. However, this rhythm does not free‐run under constant darkness at 21 °C. Because a clear diel rhythm is observed under 24‐h photocycles at 20 °C, the oscillator might be damped out within 24 h at the lower temperature.     

Analysis of Rice Mutants by Low Temperature-Derivative Spectrophotometry in Relation to Pigment Compositions and Photochemical Activities

The chloroplasts of five rice (Oryza sativa) mutants examined in the present study possessed the following pigment and activity characteristics as compared with those of normal strain (Nohrin No. 8); a) less chlorophylls (especially, chlorophyll b, the molar ratio of a to b= 6 ～ 41) and less carotenoids but higher ratios of β-carotene to chlorophylls; b) only photosystem 1 particles were obtained by density gradient centrifugation of digitonin-treated mutant chloroplasts while both photosystem 1 and 2 particles were obtained from normal strain chloroplasts; c) the photosystem 2 activities of mutant chloroplasts were lower (48 ～ 81 %) than that of normal chloroplasts while their photosystem 1 activities were 1.9 ～ 2.4 times higher. The derivative absorption spectrum of the normal chloroplasts (a/b= 4) measured at liquid nitrogen temperature showed many small but distinct maxima and minima in the red region in addition to those observable for chlorophylls in solution. These band structures including the French inflection were lost partially in the derivative spectra of three mutants with a/b= 6, 8 and 11 and almost completely in those of the remaining two mutants with a/b= 18 and 41. The lack of such band structures reflecting specific states of chlorophylls in vivo was attributed to the absence of some conformational structures such as those expected in photosystem-2 particles, which are formed by the presence of chlorophyll b and are resistant to the digitonin treatment. Chlorophylls in specific states in such structures were thought to exhibit a higher photosystem 2 activity.