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Lake Urmiah is a large (total surface 4750–6100 km2 in recent times) thalassohaline hypersaline lake (150–180 g l–1 in the period 1994–1996), located in northwestern Iran. It is the habitat of the endemic Artemia urmiana. Over the period July 1994–January 1996 a sampling campaign was organized: 36 fixed sampling stations, distributed over the entire lake's area, were sampled weekly to determine water temperature, salinity and transparency. At each occasion a filter net was dragged over a distance of 400 m in the superficial water layer to assess the density and composition of the Artemia population. A more limited sampling campaign focused on the annual fluctuations in chlorophyll concentration and on the reproductive behaviour of the brine shrimp population. Several stages of brine shrimp survived during winter months (water temperature 3°C) at low densities. Compared to available data for the Great Salt Lake, USA, Lake Urmiah shows a low algal biomass and overall low Artemia density. The increasing grazing pressure of the developing brine shrimp population in spring seems to prevent the phytoplankton from reaching high blooming concentrations, and oviparity is the dominant reproductive mode throughout the reproductive season.  相似文献   
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首次报道了伊朗西北部 Varzeghan 附近发现的大型哺乳动物化石,材料包括三趾马和恐象。根据个体大小和形态特征,将三趾马标本暂时分为一个小至中型类似 Hipparion moldavicum 的种和一个中至大型类似 H. prostylum 或 H. dietrichi 的种。Deinotherium giganteum 也出现于这一地区。依据与其他晚中新世地点哺乳动物化石的对比,这些新化石地点的时代推测为吐洛里期( Turolian) 中期或相当于欧洲哺乳动物带的 MN12。  相似文献   
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The parasitoid community of Anophococcus abaii (Danzig, 1990) – one of the main pests of Haloxylon in Iran – was studied. Four species of Chalcidoidea, belonging to the families Aphelinidae, Encyrtidae, Pteromalidae, and Signiphoridae, were found. Metaphycus anophococcusi Lotfalizadeh, n. sp. is described in the zebratus species group and compared with closely allied species of Metaphycus.  相似文献   
115.
Peach and almond have been considered as model species for the family Rosaceae and other woody plants. Consequently, mapping and characterisation of genes in these species has important implications. High-resolution melting (HRM) analysis is a recent development in the detection of SNPs and other markers, and proved to be an efficient and cost-effective approach. In this study, we aimed to map genes corresponding to known proteins in other species using the HRM approach. Prunus unigenes were searched and compared with known proteins in the public databases. We developed single-nucleotide polymorphism (SNP) markers, polymorphic in a mapping population produced from a cross between the cloned cultivars Nonpareil and Lauranne. A total of 12 SNP-anchored putative genes were genotyped in the population using HRM, and mapped to an existing linkage map. These genes were mapped on six linkage groups, and the predicted proteins were compared to putative orthologs in other species. Amongst those genes, four were abiotic stress-responsive genes, which can provide a starting point for construction of an abiotic resistance map. Two allergy and detoxification related genes, respectively, were also mapped and analysed. Most of the investigated genes had high similarities to sequences from closely related species such as apricot, apple and other eudicots, and these are putatively orthologous. In addition, it was shown that HRM can be an effective means of genotyping populations for the purpose of constructing a linkage map. Our work provides basic genomic information for the 12 genes, which can be used for further genetic and functional studies.  相似文献   
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RAB25, a member of the rat sarcoma (RAS) family of small GTPase, has been implicated in the pathophysiology of ovarian, breast and other cancers. Its role in endosomal transport and recycling of cell-surface receptors and signaling proteins presents a novel paradigm for the disruption of cellular pathways and promotion of tumor development and aggressiveness. Variations in structure and post-translational modifications control the localization of RAS superfamily proteins to specific subcellular compartments and recruitment of downstream effectors, allowing these small GTPases to function as sophisticated modulators of a complex and diverse range of cellular processes. Here, we review the link between RAB25 and tumor development and current knowledge regarding its possible roles in cancer.  相似文献   
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Drug resistance remains a barrier to the effective long term treatment of ovarian cancer. We have established an RNAi-based screen to identify genes which confer resistance to carboplatin or paclitaxel. To validate the screen we showed that siRNA interfering with the apoptosis regulators FLIP and Bcl-XL conferred sensitivity to paclitaxel and carboplatin respectively. The expression of 90 genes which have previously been shown to be over-expressed in drug-resistant ovarian cancer was inhibited using siRNA and the impact on sensitivity to carboplatin and paclitaxel was assessed. ENPP2 was identified as a candidate gene causing drug resistance. ENPP2 encodes autotaxin, a phospholipase involved in the synthesis of the survival factor lysophosphatidic acid. siRNA directed to ENPP2 resulted in earlier apoptosis following treatment with carboplatin. 2-carbacyclic phosphatidic acid (ccPA 16:1), a small molecule inhibitor of autotaxin, also accelerated apoptosis induced by carboplatin. Stable ectopic expression of autotaxin in OVCAR-3 cells led to a delay in apoptosis. When serum was withdrawn to remove exogenous LPA, ccPA caused a pronounced potentiation of apoptosis induced by carboplatin in cells expressing autotaxin. These results indicate that autotaxin delays apoptosis induced by carboplatin in ovarian cancer cells.  相似文献   
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Pre-column derivatization methods for high performance liquid chromatographic assay of specific pharmaceutical agents using 9-fluorenylmethyl chloroformate (FMOC-Cl) have received special attention because highly fluorescent and stable adducts are provided by these methods. However, unlike the post-column on-line techniques, long derivatization time is needed and the reaction cannot be well controlled. A new, sensitive and fast pre-column on-line derivatization technique coupled with high-performance liquid chromatography using FMOC-Cl as labeling agent is described and validated for determination of azithromycin in human serum. After extraction of the drug from serum, the residue was reconstituted in mixture of acetonitrile-phosphate buffer (3:1, v/v; pH 8.5) and directly injected onto the chromatographic system. Continuous on-line derivatization and analysis of the compounds were successfully performed using in-tube elution of FMOC-Cl. The total time needed for derivatization and chromatographic analysis of the drug was 13 min. The assay was reliable and reproducible, with limit of quantification of 10 ng/ml. The described technique may offer significant advantages over existing off-line derivatization methods using FMOC-Cl.  相似文献   
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