An alien Sennertia mite (Acari: Chaetodactylidae) associated with an introduced Oriental bamboo‐nesting large carpenter bee (Hymenoptera: Apidae: Xylocopa) invading the central Honshu Island,Japan

Since 2006, an introduced Oriental bamboo‐nesting large carpenter bee, Xylocopa tranquebarorum, has been recorded from the central Honshu Island, Japan, which is inhabited only by the endemic subspecies, Xylocopa appendiculata circumvolans. Carpenter bees (tribes Xylocopini and Ceratinini) have ecological associations with specific Sennertia spp. in all geographic regions of their distribution, thus it is worried that the introduced carpenter bee has brought non‐indigenous mites into Japan. In their native ranges, X. a. circumvolans and X. tranquebarorum each has specific Sennertia mite faunas: the four Japanese Alloxylocopa bees including X. a. circumvolans have associations with S. alfkeni, while X. tranquebarorum has association with S. potanini in China (except Taiwan) and with S. horrida in South to East Asia including Taiwan. In the present study, we examined phoretic mite fauna on the introduced X. tranquebarorum, and determined whether the mites are indigenous or not based on morphological character and two gene sequences (mitochondrial cytochrome oxidase subunit I gene and nuclear ribosomal internal transcribed spacer). It was found from the result of this study that the non‐indigenous Sennertia mite has invaded Japan with the introduced X. tranquebarorum. We discuss geographic origin of the introduced X. tranquebarorum based on associated mite fauna and potential ecological risk caused by the introduced Xylocopa‐Sennertia association.     

Leaf toughness changes the effectiveness of larval aggregation in the butterfly Byasa alcinous bradanus (Lepidoptera: Papilionidae)

Two subspecies of the papilionid butterfly Byasa alcinous , B. a. bradanus and B. a. alcinous , have varying degrees of larval aggregation. Early instar larvae of ssp. bradanus always occur in aggregations. To determine the functions of larval aggregation in this subspecies, we examined the effects of leaf toughness on larval performance when caterpillars were reared alone and in aggregations. Newly hatched larvae were reared either individually or in groups of 10 and were fed either tough or tender leaves of Aristolochia debilis . When fed tough leaves, more gregarious larvae survived the first instar. This difference between solitary and aggregated larvae did not occur when caterpillars were fed soft leaves. The effects of aggregation on larval weight and duration were not significant between leaf-toughness treatments. Larval aggregation of B. a. bradanus improves larval survivorship in early instars that use host plants with tough leaves.     

Nitrogen assimilation in citrus trees

Assimilation of ¹⁵N-ammonium and ¹⁵N-nitrate was examined in 3-year-old satsuma mandarin (Citrus unshiu Marcovitch) trees. Experiments were designed to establish the time course of incorporation of nitrogen just taken up into amino compounds. In fine roots, absorbed ¹⁵N-ammonium was actively incorporated into glutamine and then into glutamic acid and asparagine. When feeding ¹⁵N-nitrate, glutamic acid and asparagine were actively synthesized, but glutamine synthesis was comparatively low as compared with that in ammonium feeding. In current leaves and fruits, a clear difference in the labelling patterns of amino acids was found between the ammonium and nitrate feedings. The amino acid most markedly labelled was asparagine in the ammonium feeding and glutamine in the nitrate feeding. Considering the most heavily labelled component in leaves and fruits, the main form of the nitrogen components transported upward in the xylem was discussed.     

日本北海道地区细石叶技术研究概述

细石叶技术是晚更新世晚期东北亚和西北美新的变革性剥坯技术和适应手段。北海道地区拥有丰富、多样的细石器遗存,相关材料最早可以追溯到距今约2.5万年前,持续了约1.2万年。以北海道具有明显技术复杂性和多样性特点的细石器为材料,学者们基于技术式“阅读”和拼合研究划分出一系列细石核工艺类型和剥坯技法;岛内以楔形细石核为代表的细石器工业传统在不断延续的同时,也表现出明显的阶段性变化,并在一定程度上显示出与气候环境变化较强的相关性。本文对北海道地区晚更新世末次盛冰期以来的气候、环境背景以及细石器的发现与研究历程进行介绍。在此基础上,厘清北海道细石核工艺类型的划分,并对细石器群的阶段性演变进行系统梳理,以期对我国相关研究有所裨益。     

Generation of multivirus-specific T cells by a single stimulation of peripheral blood mononuclear cells with a peptide mixture using serum-free medium

Background: Restoration of virus-specific immunity by virus specific T cells (VSTs) offers an attractive alternative to conventional drugs, and can be highly effective in immunocompromised patients, including hematopoietic stem cell transplant (HSCT) recipients. However, conventional VSTs manufacture requires preparation of specialized antigen-presenting cells (APCs), prolonged ex vivo culture in serum-containing medium and antigen re-stimulation with viruses or viral vectors to provide viral antigens for presentation on APCs. Methods: To simplify this complex process, we developed a method to generate multiple VSTs by direct stimulation of peripheral blood mononuclear cells (PBMCs) with overlapping peptide libraries in serum-free medium. Results: We generated VSTs that targeted seven viruses (cytomegalovirus [CMV], Epstein-Barr virus [EBV], adenovirus [AdV], human herpesvirus 6 [HHV-6], BK virus [BKV], JC virus [JCV] and Varicella Zoster virus [VZV]) in a single line. The phenotype, growth and specificity of multiple VSTs produced in serum-free medium were equivalent to those generated in conventional serum-containing medium. Discussion: The use of serum-free medium allows this approach to be readily introduced to clinical practice with lower cost, greater reproducibility due to the absence of batch-to-batch variability in serum and without concerns for infectious agents in the serum used. This simplified approach will now be tested in recipients of Human Leukocyte Antigen (HLA)–matched sibling HSCT.     

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.     

Viable Chimeras between Embryonal Carcinoma Cells and Mouse Embryos: Comparison of Aggregation and Injection Methods

An embryonal carcinoma (EC) cell line having the ability to form chimeric mice was isolated from embryo-derived teratocarcinomas experimentally induced in BALB/cCrSlc mice. This EC cell line, B242 g, was one of the 5 EC cell lines pre-selected based on the ability to incorporate into blastocysts by means of aggregating with 8-cell mouse embryos.
Using the B242g EC cells, the effectiveness of producing chimeras was compared between two currently available techniques, aggregation and injection, by examining chimerism of the midgestationally recovered conceptuses and live-born mice. The present result revealed that EC cells studied here were able to form chimeras more efficiently by injection as compared to aggregation method.     

{alpha}-Amylase synthesis by a cell free system and plant growth substances

A microsomal preparation from the aleurone layer pre-treatedwith GA or H-ol had the ability to synthesize -amylase whenit was incubated with an appropriate medium. -Amylase synthesiswas inhibited by the addition of p-fluorophenylalanine or bypre-treatment with RNase. The synthesized -amylase was separatedinto three isozymes by disc-electrophoresis (Received July 25, 1970; )