The American house dust mite, Dermatophagoides farinae Hughes, 1961 (Acari: Pyroglyphidae), is recognized as an important source of allergens in the domestic environment. An assessment was made of the toxicity of constituents from essential oil of cade, Juniperus oxycedrus L. (Cupressaceae), and related compounds as well as four experimental spray formulations containing the oil (10–40 g/liter sprays) to adult D. farinae. In a contact + fumigant mortality bioassay, methyleugenol (24-h LC50,5.82 μg/cm2) and guaiacol (8.24 μg/cm2) were the most toxic constituents to the mites and the toxicity of these constituents and benzyl benzoate did not differ significantly.

This study was conducted to determine the toxicity to adult Myzus persicae (Sulzer) and Aphis gossypii Glover of 88 plant essential oils and six experimental spray formulations containing bitter orange or marjoram oil was examined using the vapor-phase mortality and spray bioassays. Results were compared with those of two conventional insecticides deltamethrin and dichlorvos. As judged by 24 h LC50 values, bitter orange oil (0.0212 and 0.0192 mg/cm3) was the most active material, followed by marjoram, celeryseed, and cypress oils (0.0239-0.0508 and 0.0209-0.0542 mg/cm3). These essential oils were significantly less toxic than dichlorvos, respectively. These essential oils were consistently more toxic to adult M. persicae in closed versus open containers, indicating that toxicity was achieved mainly through the action of vapor. Bitter orange oil and marjoram oil applied as 1% spray provided complete mortality toward two aphid species adults. Reasonable aphid control in greenhouses can be achieved by a spray formulation containing the 1% oil as potential contact-action fumigant.

Inhibition of acetylcholinesterase (AChE) is one of the important modes of action available for the control of insects. An assessment was made of the electric eel AChE inhibitory activity of 55 endophytic fungi isolated from the leaves of Huperzia serrata collected in Eunshi, Hubei Province, China. Of 55 mycelial extracts and 55 ethyl acetate-soluble fractions from liquid culture of the fungi, the ethyl acetate-soluble fraction of strain ES056 exhibited strong AChE inhibitory activity (88%) at a concentration of 100 μg/mL. Based on morphological characteristics and nuclear ribosomal DNA ITS sequence analysis, this fungus showed greatest similarity to members of the order Eurotiales and was shown to be most closely related to members of the Aspergillus aculeatus group. It was designated Aspergillus sp. MY056. This strain merits further study as a potential anti-AChE product.

일반적인 중국어 독자는 약 3000개의 독특한 문자를 기억해야지만, 일상적인 글 읽기에 대처할 수 있는데, 이 때 사용되는 대부분의 글자들은 본인의 대량의 필사를 통하여 학습해 얻은 것이다. 이 때 학습자가 학습하는 필순은 이미 수천 년의 역사를 가지고 있다. 이론상으로 말하면, 독자는 글자를 식별하는 것만 필요 하고, 정확한 필순을 공부하는 것은 불필요하다. 뇌에 어떤 형상이 형성되는 과정 에 대한 연구에서는, 중문의 독해 능력은 업무를 수행하는 기억 속의 시각 공간 처리와 관계가 있다는 것을 보여준다. 때문에, 본 연구는 중문 독해와 관계있는 여러 요소와 시각 공간 기억의 관계를 연구하여 밝히는 것이며, 아울러 중문 독해 중 필순에 대한 인식이 필요한지 아닌지를 연구 토론해 보고자 한다. 본 연구의 대상은 북경의 한 초등학교에서 공부하는 1학년 학생 40명으로, 연구 과정 중에서 비언어 지능 지수, 독해의 표현, 필획과 부건에 대한 단기 기억과 그 들이 익숙하거나 생소한 한자에 대한 필순의 정확성을 측정하였다. 결과는 필획의 기억과 독해 능력 표현은 확실한 관련성이 있고, 필순과도 관련 있다는 것을 보여준다. 부건에 대한 단기 기억과 독해 능력은 무관하였으나, 생소 한 어휘의 필순의 정확성을 판별하는데 대해서는 오히려 관련성이 있었다. 또한, 필순과 독해 능력 표현은 강한 상관성이 있었다. 총체적으로 필순에 대하여 정확 성은 독해 능력 표현의 중요한 지표가 되었다. 익숙한 어휘의 필순 정확성은 또한 생소한 어휘의 필순 정확성의 지표가 되기도 하였다. 요컨대, 필획에 대한 단기 기억이 부건에 대한 단기 기억보다 더욱 중요하였음을 보여주고 있으며, 정확한 필순의 인식은 중국어 속의 독해 능력에 아주 중요한 영향을 끼치고 있음을 알 수 있다.

The early diagnosis of bovine pregnancy is an essential component of successful reproductive planning on farms, because lack of bovine pregnancy over the long term results in reproductive failure and low milk yield‐the latter of which is a special concern on dairy farms. This study was designed to identify early pregnancy‐specific whey proteins in bovine, by comparing milk samples collected from cattle during pregnancy (Days 30 and 50) and from non‐pregnant cattle. In this study, differentially expressed proteins in five pregnant and five non‐pregnant Holstein dairy cattle were investigated and compared, using proteomics analysis. The first dimension was applied to a pH 3.0～10.0 strip, by loading a 2‐mg milk protein sample. After the second‐dimension separation was performed, the gels were stained with colloidal Coomassie brilliant blue. The stained gels were scanned and the images were analyzed, to detect variations in protein spots between non‐pregnant and pregnant cattle milk protein spots, using ImageMaster; this was followed by analysis with MALDI TOF‐MS. Analysis of the 2‐DE gel image resulted in a total of approximately 500～600 protein spots, of which 12 spots were differentially expressed, six spots were up‐regulated, and four spots were downregulated; two spots were identified as pregnancy‐specific proteins. These proteins were identified as lactoferrin, NADH dehydrogenase subunit 2, albumin, serum albumin precursor and transferrin. Our results via 2‐D PAGE analysis revealed composite profiles of several milk proteins related to early bovine pregnancy, implying the possible use of these milk proteins in the early detection of bovine pregnancy.

Interspecies somatic cell nuclear transfer (iSCNT) is a valuable tool for studying the interactions between an oocyte and somatic nucleus. The object of this study was to investigate the developmental competence of in vitro‐matured porcine oocytes after transfer of the somatic cell nuclei of 2 different species (goat and rabbit). Porcine cumulus oocytes were obtained from the follicles of ovaries and matured in TCM‐199. The reconstructed embryos were electrically fused with 2 DC pulses of 1.1 kV/cm for 30 μs in 0.3 M mannitol medium. The activated cloned embryos were cultured in porcine zygote medium‐3 (PZM‐3), mSOF or RDH medium for 7 days. The blastocyst formation rate of the embryos reconstructed from goat or rabbit fetal fibroblasts was significantly lower than that of the embryos reconstructed from porcine fetal fibroblast cells. However, a significantly higher number of embryos reconstructed from goat or rabbit fetal fibroblasts cultured in mSOF or RDH, respectively, developed to the morular stage than those cultured in PZM‐3. These results suggest that goat and bovine fetal fibroblasts were less efficacious than porcine‐porcine cloned embryos and that culture condition could be an important factor in iSCNT. The lower developmental potential of goat‐porcine and porcine‐bovine cloned embryos may be due to incompatibility between the porcine oocyte cytoplasm and goat and bovine somatic nuclei.

Insulin, transferrin and selenium (ITS) complex is reported to improve in vitro development of oocytes and embryos. This study was carried out to investigate the effects of ITS during in vitro culture (IVC) of porcine parthenogenetic and nuclear transfer (NT) embryos on subsequent developmental capacity in vitro. The electrically activated oocytes were cultured in Porcine Zygote Medium (PZM-3) with various concentrations (0, 0.1, 0.5, and 1.0%) of ITS for 7 days. Also, the electrically activated reconstructed embryos were cultured in PZM-3 with various concentrations (0, 0.1, 0.5, and 1.0%) of ITS for 6 days. Addition of ITS to culture medium did not affect development of porcine parthenogenetic embryos in vitro. To test the effect of ITS on the in vitro development of porcine NT embryos, factorial experiments were also performed for in vitro maturation (IVM) medium (TCM-199) with or without 1% ITS and culture medium (PZM-3) with or without 0.5% ITS. Addition of 0.5% ITS to culture medium increased (p<0.05) the proportion of NT blastocysts compared with non-treated group. In contrast, addition of 1% ITS to culture medium was ineffective or had a detrimental effect. Also, addition of ITS only to maturation medium increased (p<0.05) the percentage of NT blastocysts formation compared with the control group. In conclusion, addition of ITS to IVM or IVC medium could improve subsequent blastocyst development of porcine NT embryos.

To examine the differential protein expression pattern in the 11.5 day post-coitus (dpc) and 18.5 dpc placenta of mouse, we have used the global proteomics approach by 2-D gel electrophoresis (2-DE) and MALDI-TOF-MS. The differential protein patterns of 3 placentae at the 11.5 dpc and 18.5 dpc from nature mating mice were analyzed. Proteins within isoelectric point range of 3.0~10.0, separately were analyzed in 2DE with 3 replications of each sample. A total of approximately 1,600 spots were detected in placental 2-D gel stained with Coomassie-blue. In the comparison of 11.5 dpc and 18.5 dpc placentae, a total of 108 spots were identified as differentially expressed proteins, of which 51 spots were up-regulated proteins such as alpha-fetoprotein, mKIAA0635 protein and transferrin, annexin A5, while 48 spots were down-regulated proteins such as Pre-B-cell colony-enhancing factor 1(PBEF), aldolase 1, A isoform, while 4 spots were 11.5 dpc specific proteins such as chaperonin and Acidic ribosomal phosphoprotein P0, while 3 spots were 18.5 dpc specific proteins such as aldo-keto reductase family 1, member B7 and CAST1/ERC2 splicing variant-1. Most identified proteins in this analysis appeared to be related with catabolism, cell growth, metabolism and regulation. Our results revealed composite profiles of key proteins involved in mouse placenta during pregnancy.