Drastic changes in host preference in a gall‐parasitic flea weevil,Orchestes hustachei,during the last decade

1. Factors affecting host preference in herbivorous insects are actively discussed. Larval performance, competition and predation on each host, and host abundance are reportedly factors affecting the host preference of ovipositing females. In the present study, chronological changes in female host preference were examined by employing a flea weevil species that uses the original host and a newly introduced host simultaneously. 2. Orchestes hustachei Klima (Coleoptera: Curclionidae) is an aphidophagous flea weevil that oviposits on aphid galls, and the larvae feed on aphids inside. The weevil's native hosts are galls of the Tetraneura species on Ulmus davidiana, while the novel hosts are galls of an introduced species, Paracolopha morrisoni on Zelkova serrata, an introduced hardwood. Choice experiments were conducted using Tetraneura galls and Paracolopha galls and the results were compared with experiments conducted 10 years ago. 3. More than 90% of ovipositing females selected Paracolopha galls. This result is in marked contrast with the result of the 2002 experiment, in which 66.3% of females selected Paracolopha galls. To explore driving forces of the preference change, mortality factors, pupal mass on the two hosts, and temporal changes in the abundance of the host galls were examined. 4. Abundance of Tetraneura galls decreased gradually throughout the last 26 years. By contrast, weevil survival and performance did not vary significantly between the two hosts. Therefore, it is concluded that temporal changes in the relative abundance of two hosts are main factors of the change in host preference.     

Light and Electron Microscopic Studies on Fertilization of Pelmatohydra Robusta I. Sperm Entry to a Specialized Region of the Egg

Fertilization of a fresh water polyp, Pelmatohydra robusta , was studied by light and electron microscopy. A small depression was observed in the animal pole of the unfertilized egg. The egg pronucleus was always situated in close contact with the bottom of the depression. Microvilli which were covered with an egg coat consisting of filamentous components were observed on the egg surface. Microvilli and the egg coat were not detected on the surface of the depression. Sperm were associated with the egg plasma membrane and entered the egg only at the bottom of the depression. Excess sperm aggregated around the depression of inseminated eggs. After fertilization, the egg made a protrusion in the region where the egg pronucleus and sperm were in close contact with each other. A new egg coat was formed on the entire surface of the fertilized egg. The restriction of sperm-egg interactions to a specialized region of the hydra egg is discussed in connection with the micropyle of Pisces eggs and the animal dimple of Discoglossus (Anura) eggs.     

Vessel element formation in cultured carrot-root phloem slices

The effects of light, auxin and cytokinin on vessel elementformation in phloem slices of carrot root were examined. When slices of carrot cultivars, ‘Nakamura-senko-futo’and ‘Yamada-hyakunichisenk6- naga’, preculturedin the dark on modified Murashige and Skoog's medium for twodays were cultured on a medium containing 5x10^–6 M 2,4-Din the dark, no vessel element formation occurred. When preculturedslices were cultured in the light with 5x10^–6M 2,4-D,vessel element formation was remarkable. But when 5x10^–7Mkinetin, benzyladenine or zeatin was added, vessel elementswere readily formed even in the dark. When slices were cultured in the light, a cytokinin-like substance(s)that causes vessel element formation was produced in the slices,then was released to the medium. The substance(s) was fairlystable to heat. In slices of carrot cultivars, kuroda-gosun, ‘Kintoki’and ‘Kokubu-senk6-6naga’, a different result forvessel element formation was obtained. When slices of thesecultivars were cultured on a medium containing 5x10^–6M2,4-D in the dark, vessel element formation was remarkable.It seemed, therefore, that these cultivars contain enough ofa cytokinin-like substance(s) to form vessel elements. In fact,vessel element forming activity was found in the alcohol extractof carrot root phloem from these cultivars. (Received June 8, 1971; )     

Plastic Response of Crown Architecture to Crowding in Understorey Trees of Two Co-dominating Conifers

Crown architecture and growth rate of trunk height, trunk diameterand lateral branches of understorey trees (5–10m tall)were compared between two co-dominating conifers,Abies sachalinensisandPiceaglehnii, in relation to the index of local crowding intensity,W,represented as a function of density, distance and basal areaof taller neighbours. For the two conifers, the growth of trunkheight and diameter was decreased and crowns became flat withincreasingW, keeping crown projection area. Self-pruning oflower branches was more intense inAbiesthan inPiceain crowdedconditions, while both conifers showed similar crown forms inless crowded conditions. These results suggest that the growthin lateral branches exceeded that in height in crowded conditions,especially inAbies. Tree age of both conifers increased withincreasingW, resulting from the low growth rate in crowded conditions.The age of the longest and lowest branch ofPicea, up to 150years, was positively correlated with the tree age ranging from70 to 250 years, whereas that ofAbieswas constant at around30 years irrespective of tree age varying from 40 to 140 years.This result agrees with the observation that agedAbieshad moreflat-shaped crowns than in agedPiceain crowded conditions. Theseresults suggest that each conifer adapted to crowding in differentways: high elongation of branches with high turnover rate forAbiesandviceversaforPicea. Abies; crown form; neighbourhood interference; Picea; plasticity     

ON THE DE NOVO FORMATION OF THE CENTRIOLE IN THE ACTIVATED SEA URCHIN EGG

Eggs of Pseudocentrotus depressus were activated artificially by Loeb's "double treatment method". 50 min after activation, a number of asters were produced in the eggs. It was confirmed by electron microscopy that centrioles with a typical fine structure were present in artificially induced asters.
An unfertilized egg of Hemicentrotus pulcherrimus was divided into 2 halves, nucleated and non-nucleated, by centrifugation on a sucrose bed. Each half was activated by the same method as mentioned above. Several asters were produced in both halves after a certain period of incubation. The presence of bodies considered to be centrioles were demonstrated in the asters in both nucleated and non-nucleated halves.
The results add probability to the view that the centrioles are produced de novo in artificially activated eggs and fragments.     

Fusion of Spermatozoa with Embryonic Cells and Somatic Cells in the Sea Urchin

Spermatozoa can enter the separated blastomeres of 8- and 16-cell stage embryos, the cells of blastulae and even somatic cells of the oesophagus wall of an adult sea urchin, under certain conditions. In the presence of egg jelly solution, the rate of entrance of spermatozoa is remarkably increased. In the case of the blastomere of 8-cell stage embryos, characteristic cytoplasmic protrusions are formed at the sites of sperm entry, in succession to the formation of the cytoplasmic bulge. These protrusions elongate until 4 min after insemination, and then they retract gradually. The nucleus of penetrated sperm swells and decondenses to form a pronucleus. In most cases, the pronucleus seems to fuse with the preexisting diploid nucleus of the blastomere. When the dissociated oesophagus cells were inseminated, a certain type of the cells was found to fuse with spermatozoa, although the percentage of fused cells was very low.     

Disappearance of Mating Reactivity in Paramecium caudatum upon Repeated Washing

SYNOPSIS The appearance of mating reactivity of Paramecium caudatum was retarded by repeated washing of the cells in the logarithmic growth phase with Dryl's and other solutions. Highly reactive cells in the stationary phase also lost reactivity during the same treatment. Dryl's solution, sodium and potassium phosphate buffers, Miyake's physiologic balanced solution and exhausted culture medium were effective but deionized water saturated with CaCO₃ was ineffective. The addition of supernatant fluid from stationary phase cultures restored reactivity in 2 hr but was unable to do so when applied to extremely starved cells. These findings may be useful for study of the synthesis of mating-type substances.     

RELATION BETWEEN THE ACROSOME REACTION AND FERTILIZATION IN THE SEA URCHIN. II. FERTILIZATION IN ACIDIFIED SEA WATER WITH EGG-WATER-TREATED SPERMATOZOA*

Fertilization of sea urchin eggs fails to occur at a pH lower than 6.5. Analytical studies on this problem were made with Hemicentrotus pulcherrimus, Anthocidaris crassispina and Pseudocentrotus depressus. If the spermatozoa have been pretreated with egg water, eggs can be fertilized even at pH 6.5 and 6.0. The acrosome reaction is inhibited at a pH lower than 6.5. Intact spermatozoa fail to adhere to the fixed eggs in acidified sea water, whereas egg-water-treated spermatozoa adhere even at pH 6.5 and 6.0. From these results we infer that the failure of fertilization at pH 6.5–6.0 is caused by non-occurrence of the acrosome reaction, and that fertilization reactions other than the acrosome reaction, such as the binding and fusion of the gametes, are not inhibited in this range of pH. At pH 5.5, the spermatozoa become inert and fertilization is inhibited or suppressed, even though egg-water-treated spermatozoa are employed.     

The relationship between aryl hydrocarbon hydroxylase activity and DNA adducts measured by 32P-postlabelling assay in lymphocytes of lung cancer patients

We have investigated the correlation between DNA adduct levels and aryl hydrocarbon hydroxylase (AHH) activity in peripheral lymphocyte samples obtained from 42 lung cancer patients. DNA adducts and AHH activity were determined by the ³²P-postlabelling technique and the fluorometric method, respectively. The mean +/- SD of DNA adduct level was 0.88 +/- 0.37 (ranged from 0.22 to 1.90) per 10⁸ nucleotides. The geometric means of non-induced and 3-methylcholanthrene (MC)-induced AHH activity, as well as AHH inducibility (MC-induced AHH activity/non-induced AHH activity) were 0.029, 0.228 pmol min^-1 10^-6 cells, and 7.776, respectively. There was no statistically significant correlation between DNA adduct levels and non-induced or MC-induced AHH activity. A tendency of positive correlation was found between DNA adduct levels and AHH inducibility for the all subjects (n = 42, r = 0.25, p = 0.11). Such a positive correlation reached statistical significance in the subjects with squamous cell carcinoma (n = 13, r = 0.70, p < 0.01). In addition, similar correlation of DNA adducts with AHH inducibility was also observed in the GSTM1 present genotype (n = 17, r = 0.44, p = 0.07) and GSTP1-AA genotype (n = 29, r = 0.37, p = 0.05) individuals. These findings suggest that DNA adduct levels are mediated by CYP1A1 enzyme, and AHH inducibility may be a more relevant indicator than specific AHH activity for explaining the variation of DNA adduct levels in lymphocytes.