Evidence of autumn overseas migration in the rice planthoppers, Nilaparvata lugens and Sogatella furcifera: analysis of light trap catches and associated weather patterns

ABSTRACT. 1. Daily trap catches of the rice planthoppers, N.lugens Stal and S.furcifera Horvath, and associated synoptic weather patterns were analysed in Kyushu, south-west Japan, in the autumns of 1980–85.
2. Certain weather patterns which seemed to favour overseas immigration, were reflected in trap catches: of eighteen occasions in which back-tracks on 850 mbar wind fields reached central China, marked mass catches in a light trap occurred on six occasions, and peaks in catch curves were found on another seven occasions.
3. These results strongly imply overseas immigration of the planthoppers from China to Kyushu in autumn, identical to invasions by the same species in early summer. However, such autumn migration is apparently non-adaptive because migrants or their progeny are soon killed by cold weather.     

The jaw apparatus of the Cretaceous ammonite Reesidites

Jaws are preserved within the body chambers of three specimens of a collignoniceratid ammonite Reesidites minimus (Hayasaka and Fukada) from the Upper liuoniaq of Hokkaido, Japan. Light microscopic and SEM observations of sections indicate that both upper and lower jaws consist mainly of a thick, double-walled chitinous lamella with a beak-like anterior projection. The outer chitinous lamella of the lower jaw is covered by a thick calcareous layer. The jaw apparatus of this species morphologically resembles aptychus-type jaws of Jurassic ammonites, but is distinguished by the presence of an anterior beak-like projection with serrated ridges and grooves in the lower jaw. These observations strongly suggest a biting ability in this species.     

Involvement of 14-nm Filament-Forming Protein and Tubulin in Gametic Pronuclear Behavior during Conjugation in Tetrahymena

We have studied in detail the immunofluorescence localizations of Tetrahymena 14-nm filament-forming protein (49-kDa protein) in relation to tubulin in conjugating wild-type Tetrahymena thermophila (B strain) pairs and in pairs between B strain and star strains with defective micronuclei. The results suggest that germ nuclear behavior during conjugation may involve the following cytoskeletal structures: (1) during meiosis, microtubule structures are involved in micronuclear elongation and meiotic division; (2) at the postmeiotic stage, 49-kDa protein network structures that are formed independently of the existence of pronuclei are involved in the selection and the survival of one of four meiotic products; (3) during the third prezygotic division, gametic pronuclear transfer, and zygote formation, a cytoskeletal structure in which the 49-kDa protein colocalizes with microtubules and which is dependent on the existence of a normal gametic pronucleus is involved in gametic pronuclear behavior, and (4) during the postzygotic divisions, the microtubules are involved in nuclear behavior.     

Buccal mass structure of the Cretaceous ammonite Gaudryceras

A rhynchaptychus attributed to the lower jaw of Gaudryceras sp. from the Upper Santonian rocks of Hokkaido, Japan, has an interesting impression well-preserved on the inner surface of the outer lamella. The impression is regarded as the imprints of chitin-secreting cells (beccublast cells), because of similarity in the characteristic arrangement of polygonal pits to those of modern coleoids. Each unit cell impression of G. sp. is, however, about five to ten times larger than in modern coleoids known to us. In modern coleoids and Nautilus a layer of tall beccublast cells is intercalated between the buecal muscles and the outer side of the upper jaw and/or the inner side of the lower jaw. The other sides of the jaws are, in contrast, free from jaw muscles, and are covered directly with a thin connecting tissue. Based on these observations a possible buecal mass structure of G. sp. is restored. The beccublast cell impressions of Gaudryceras and modern coleoids markedly differ from that of modern Nautilus in the absence of numerous micropores. This fact suggests weaker mechanical properties of the jaw muscles in Gaudryceras than in Nautilus , as the branching ends of beccublast cells of the latter are inserted in the micropores to keep a firm attachment of the jaw muscles on the jaw plates.     

Role of the pentose phosphate pathway during callus development in explants from potato tuber

Metabolic change during callus formation in explants from potatotuber (Solarium tuberosum L.) was investigated. Under the presentculture conditions, callus starts exponential growth (estimatedby the fresh weight increase) with a 5-day lag period, at whichtime marked production of DNA occurs. In the lag period, respirationis very much resistant to malonate, and the value of the C6/C1ratio and activities of both G6PDH 6PGDH pass their peaks. Onthe basis of these and relevant findings, glucose metabolismthrough the PP pathway is surmised to play a significant rolein the initial DNA multiplication phase of callus development. (Received October 15, 1969; )     

EFFECT OF YEAST SEXUAL HORMONES ON ELONGATION OF AVENA COLEOPTILE

Effect of yeast (Saccharomyces cerevisiae) sexual hormones on the elongation of etiolated Avena coleoptile segments was studied. The elongation was promoted by a hormone excreted by cells of mating type a, but not by α hormone excreted by cells of α type. The effect of the former was as great as that of 5 mg/1 indole-3-acetic acid in the first hour of application. The optimal concentration of a hormone was 10 units/ml. Its growth promoting effect was greatly inhibited by an antiauxin, 2,4,6-trichlorophenoxyacetic acid. a Hormone increased cell wall extensibility just as auxin does. Testosterone, β-estradiol, progesterone and ergosterol showed very little effect on the elongation of coleoptile segments.     

Stress-relaxation properties of plant cell walls with special reference to auxin action

Stress-relaxation analysis was employed to determine changesin cell wall properties of Avena coleoptile and green pea stem.The stress-relaxation curve of the cell wall was simulated bya model consisting of four Maxwell viscoelastic components.Auxin changes only the initial part of the curve, indicatingthat auxin primarily decreases the relaxation time of the model.Significance of the spectrum, representing a generalized Maxwellmodel for cell wall properties, is also discussed in terms ofauxin action. (Received September 1, 1970; )     

AUXIN-INDUCED GROWTH OP TUBER TISSUE OP JERUSALEM ARTICHOKE: III. EFFECT OF ACTINOMYCIN D ON AUXIN-INDUCED EXPANSION GROWTH AND RNA SYNTHESIS

1. The following results were obtained using tissue slices excisedfrom cold-stored Jerusalem artichoke tubers.
2. Actinomycin Dat the concentration of 20 µg/ml given duringthe agingperiod did not affect the subsequent expansion growthcausedby auxin or auxin plus kinetin.
3. Actinomycin D given in thegrowth period, on the other hand,strongly inhibited the expansiongrowth of tissue slices agedin the absence of the antibiotic.
4. In the growth period, auxin or auxin plus kinetin promotedtheincorporation of uracil-2-¹⁴C into RNA fraction.
5. ActinomycinD inhibited the incorporation of ³²P orthophosphateinto ribosomalRNA during the aging period.
6. In the growth period, the incorporationof ³²P into RNA wasenhanced by auxin and was inhibited by actinomycinD, more remarkablyin ribosomal RNA than in lighter RNA.

¹A part of this paper was presented at the Conference on PlantGrowth Regulators held by the New York Academy of Sciences onMay 16, 1966.     

EFFECTS OF ENVIRONMENTAL FACTORS ON MECHANICAL PROPERTIES OF THE CELL WALL IN RICE COLEOPTILES

Cell wall properties determined by the stress-relaxation technique were studied with coleoptiles of rice seedlings grown under different environmental conditions. The cell wall was simulated by a viscoelastic model consisting of either four or an infinite number of Maxwell components. Reciprocal of relaxation time for the first component in the former model (1/τ₁) and minimum and maximum relaxation times (T_o and T_m) in the latter, in addition to the stress/strain ratio, were parameters representing cell wall properties. Parameters changed depending on the ages and regions of the coleoptilles used and 011 the environmental conditions under which rice seedlings were grown. Effects on cell wall properties of aeration during submerged growth, excision of the coleoptile tip, and exposure to small doses of red and/or far-red light were examined. In most cases, high values of 1/τ₁ and of T_m and small values of T_o were consistent with the growth potentiality of cells, while the stress/strain ratio seemed to be a consequence of elongation growth.     

Ubiquitous distribution of fluorescent protein in muscles of four species and two subspecies of eel (genus <Emphasis Type="Italic">Anguilla</Emphasis>)

In this study, the localization of fluorescent protein (FP) was characterized in the muscles of four species and two subspecies of eels Anguilla anguilla, A. australis, A. bicolor bicolor (b.), A. bicolor pacifica (p.) and A. mossambica in addition to the previously reported A. japonica. The open reading frame of each eel FP was 417 bp encoding 139 amino acid residues. The deduced amino acid sequences among the four species and two subspecies exhibited 91.4–100% identity, and belonged to the fatty-acid-binding protein (FABP) family. The gene structure of eel FPs in A. japonica, A. anguilla, A. australis, A. bicolor b., A. bicolor p. and A. mossambica have four exons and three introns, and were common to that of FABP family. The apo eel FPs expressed by Escherichia coli with recombinant eel FP genes were analysed for the fluorescent properties in the presence of bilirubin. The excitation and emission spectra of holo eel FPs had the maximum wavelengths of 490–496 and 527–530 nm, respectively. The holo eel FPs indicated that the fluorescent intensities were stronger in A. japonica and A. bicolor than in A. mossambica, A. australis and A. anguilla. The comparison of amino acid sequences revealed two common substitutions in A. mossambica, A. australis and A. anguilla with weak fluorescent intensity.