Additive apportioning of lepidopteran and coleopteran species diversity across spatial and temporal scales in a cool–temperate deciduous forest in Japan

Abstract.  1. Forest entomofauna retain high diversity, and examining beta diversity, or species turnover, among assemblages in a forest community is vital to elucidate the source of this diversity.
2. Under the DIVERSITAS in Western Pacific and Asia–International Biodiversity Observation Year (DIWPA–IBOY) project for simultaneously documenting biodiversity throughout the Western Pacific and Asian Region, 892 lepidopteran species (51 742 specimens) and 355 coleopteran species (11 633 specimens) were collected in 2001 by light traps in a cool–temperate forest in northern Japan.
3. This study evaluated the beta diversity of lepidopteran and coleopteran communities by ecological categories (i.e. trap location, forest strata, sampling days, and months), and assessed the habitat preferences of lepidopteran and coleopteran species.
4.  anova -like additive apportioning models were used to quantify the beta diversity among the categories. The models simultaneously provide assessments of whether species distributions are biased in favour of particular habitats.
5. Significantly high beta diversity was observed among months for both Lepidoptera and Coleoptera. The category of months corresponded fairly well to the number of specialist species detected in the category, although a remarkably large number of significant specialists in Coleoptera were observed on strata.
6. The high beta diversity and number of specialist species among strata in both communities indicate that stratification between canopy and ground, and seasonal variation, played major roles in species composition and the rich entomofauna in the forest. Highly mobile adults were influenced by the vertical spatial scale, as previously suggested for larvae.     

Development and characterization of simple sequence repeat DNA markers for Zelkova serrata

We developed 14 microsatellite loci from an enriched genomic DNA library of a broad‐leaved deciduous tree, Zelkova serrata. Of 198 clones from the library, 112 contained microsatellite repeat regions. The M13‐tailed primer method was used for economy. Sequence‐specific primer pairs were designed for 58 of 76 candidate clones. Fourteen of these primer pairs successfully amplified polymorphic single loci among 34 individuals collected from the Kanto breeding region in Japan. The expected heterozygosity for the 14 microsatellite markers ranged from 0.378 to 0.876, suggesting that these will prove valuable for breeding and ecological studies on Z. serrata.     

Comparison of lepidopteran larval communities among tree species in a temperate deciduous forest, Japan

Abstract.  1. The enormous diversity of phytophagous insects in forest canopies is hypothesised to be supported by the number of herbivorous species per host tree species or host specificity. It is therefore necessary to examine the effect of host plant species on compositional changes in the herbivore communities.
2. The lepidopteran larval communities were examined in the canopies of 10 tree species in a temperate deciduous forest of Japan. The phylogeny and leaf flush phenology of host plant species were taken into account as factors affecting the herbivore community assembly.
3. Examination of seasonal changes in the larval community structures on each tree species showed that larval species richness, abundance, and evenness decreased significantly from spring to summer. Larval species richness and abundance were characterised by family-level phylogenetic differences among tree species, whereas evenness was determined at a higher taxonomic level.
4. Compositional changes in the larval communities among tree species showed a remarkable pattern, with a phylogenetic effect at a high taxonomic level in spring, similar to evenness, but a phenological effect in summer. This suggests that host specificity could support the lepidopteran larval diversity in spring.
5. These results suggest that the differences in host utilisation of the herbivore, which reflects the phylogenetic effect of the host plants, can be important as a factor affecting the diversity of lepidopteran larval communities in temperate forests.     

OFF-RESPONSE OF GUSTATORY NERVE FOLLOWING TERMINATION OF QUININE STIMULI APPLIED TO THE FROG TONGUE

After a Ringer-adapted frog tongue was stimulated with 0.001M quinine-HCl(Q-HCl) in deionized water, the Ringer rinse ofthe tongue elicited a large gustatory nerve response. Sincethe Ringer-adapted tongue did not respond to Ringer solution,this nerve response after Q-HC1 is termed an off-response. Itwas revealed that the off-response of gustatory nerve to theRinger rinse resulted from the enhancing effect of Q-HCl adaptationupon the response to 111.2 mM NaCl component of Ringer whichwas ineffective for Ringer-adapted tongue. Weaker enhancementof the response to NaCl of Ringer was also produced by adaptingthe tongue to water. Therefore, the enhancing effect of Q-HClin deionized water is the summed effect of Q-HCl solute andwater solvent. Microelectrode study revealed that during theadaptation to Q-HCl the membrance potential of some NaCl-sensitivetaste cells was more hyperpolarized than that of Ringer-adaptedstate. The larger membrane potential maintained under Q-HCladaptation was markedly depolarized by the NaCl component ofthe Ringer. This sufficient depolarization response of the tastecells might be associated with generation of the off-responsein the gustatory nerve.     

Surface Architecture of Sperm Tail Entry into the Hamster Oocyte

At various times after artificial insemination in vivo , fertilized eggs were flushed from the ampulla of the oviduct of the hamster. The processes of sperm tail entry into the oocyte were studied with phase-contrast and electron microscopes. At 6–7 hr after insemination, the sperm head was incorporated completely into the ooplasm, but the entire length of the sperm tail still projected freely over the oocyte surface. The region on the oocyte surface where the second polar body was extruded was different from where the first polar body emerged. At 8–9 hr after insemination, the sperm tail was attached in a wave-like fashion to the oocyte surface. Where some portions of the tail were attached, they were trapped by the microvilli of the oocyte and had begun to sink into the ooplasm. Thus, the entire length of the sperm tail was incorporated into the ooplasm successively but almost synchronously. From the present observations, we have proposed a model for the mechanism of sperm tail entry into the vitellus in vivo .