992 resultados para H 800 R425r


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India has a long coast line of about 4,800 km along which fish landing centers are scattered. Fish catches are showing an upward trend consequent on rapid mechanization of fishing crafts. Economic utilization of the landed fish is an essential prerequisite for the proper development of Indian fishing and fish processing industries.

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Ⅰ 虎杖聚酮类化合物生物合成相关基因的克隆及功能分析 虎杖 (Polygonum cuspidatum Sieb. et Zucc) 属于蓼科蓼属多年生草本植物,在中国和日本民间曾被广泛用于动脉粥样硬化、高血压、咳嗽、化脓性皮肤炎以及淋病的治疗,具有祛风利湿、散瘀定痛、止咳化痰等功效。而在现代医学上最令人瞩目和具有发展前景的是其在抗肿瘤、心血管保护、抗氧化方面的作用,相关疗效主要来自于虎杖中结构迥异、种类丰富的聚酮化合物及其衍生物资源。这些聚酮类化合物主要包括蒽醌、大黄素、大黄素-甲醚、大黄酚、芪类以及类黄酮化合物等。其中,大部分聚酮类化合物生物合成途径机制尚不明确,但可以肯定的是植物类型III聚酮合酶type III polyketide synthases (PKSs) 在这些聚酮化合物的生物合成起始反应中行使着关键的作用。因此,除了我们所熟悉的类黄酮化合物、芪类化合物之外,进一步分离和分析虎杖中其它重要聚酮类化合物生物合成所涉及的类型III聚酮合酶基因的是非常值得期待的。 目前,已经有14个植物类型III PKS基因被克隆和功能分析。植物类型III PKS的共同特征包括基因结构、序列相似性、保守的活性中心、酶学性质以及共同的催化机制等。显花植物(裸子植物和被子植物)中,植物类型III PKS的基因结构绝对保守,除了一个早期报道的金鱼草(Antirrhinum majus)查尔酮合酶chalcone synthase (CHS) 含有第二个内含子外,迄今为止所有已知的植物类型III PKS基因均含有一个内含子且该内含子位置保守。有趣的是,在本研究中,两个含有3个内含子的类型III PKS基因从虎杖中被分离,且两个基因3个内含子的位置完全保守,这是三内含子类型III PKS基因首次得到分离。除了新奇的基因结构外,体外功能分析显示上述两个基因还具有特殊的酶学性质和功能。 本论文围绕上述2个三内含子基因开展了以下工作: 虎杖中一个由三内含子基因编码的新型类型III聚酮合酶 一个类型III PKS的cDNA及其相应的基因(PcPKS2)从药用植物虎杖中被克隆。序列分析结果表明,PcPKS2的开放阅读框被3个内含子分隔,这是一个出人意料的发现,因为截至到目前为止,除了金鱼草一个CHS基因外,所有已知的类型III PKS基因均在固定位置上含有一个内含子。除了特殊的基因结构外,PcPKS2显示了一些有趣的特性:(i) CHS“守卫”苯丙氨酸——Phe215和Phe265在PcPKS2中双双缺失,它们分别被亮氨酸和半胱氨酸取代;(ii) 体外功能分析结果表明,当酶促反应体系的pH值为6.5-8.5时,大肠杆菌中过表达的重组PcPKS2高效地合成丁烯酮非环化产物——4-香豆酰甘油酸内酯(4-coumaroyltriacetic acid lactone (CTAL))为主产物,而丙烯酮非环化产物bis-noryangonin (BNY) 以及苯亚甲基丙酮为副产物;而当酶促反应体系的pH值为9.0时,PcPKS2高效地合成苯亚甲基丙酮为主产物,而CTAL、BNY为副产物。另外,除了上述3种产物外,在不同的pH条件下,还有痕量的柚皮素查尔酮能被检测到。此外,在4-香豆酰辅酶A(4-coumaroyl-CoA)的类似化合物中,除了4-香豆酰辅酶A外,只有feruloyl-CoA能够被PcPKS2接受作为起始底物。PcPKS2不接受脂肪酰辅酶A——异丁酰基辅酶A(isobutyryl-CoA)、异戊酰基辅酶A(isovaleryl-CoA)以及乙酰辅酶A(acetyl-CoA)作为起始底物。Southern blot杂交结果表明,在虎杖基因组中存在2-4个PcPKS2基因的拷贝。Northern blot杂交结果表明,在根茎和幼叶中,PcPKS2表达量很高,而在根中无表达。叶中的PcPKS2的表达受病原菌诱导,但不受伤诱导。 虎杖中一个编码双功能类型III聚酮合酶的三内含子基因的鉴定 显花植物中,所有已知的类型III PKS 基因均含有一个内含子且位置绝对保守。本研究中,综合运用PCR技术,从富含聚酮类化合物的植物虎杖中克隆得到一个类型III PKS 基因(PcPKS1)及其cDNA。序列分析结果表明,PcPKS1含有3个内含子。系统发育分析结果表明,PcPKS1与其它植物的CHSs归为一类。然而,体外功能分析结果表明,当酶促反应体系pH值为7.0时,大肠杆菌中过表达的重组PcPKS1高效地合成柚皮素查尔酮(naringenin)为单一产物;而当pH值为9.0时,苯亚甲基丙酮(p-hydroxybenzalacetone)几乎为重组PcPKS1的唯一产物。后续的研究表明,与典型的CHSs相比,PcPKS1具有另外一些不同的特点:在pH值为9.0时(PcPKS1的苯亚甲基丙酮合成活性最适pH值),在4-香豆酰辅酶A的类似化合物中,只有feruloyl-CoA能够被PcPKS1接受作为起始底物。与CHSs展现出的对脂肪酰辅酶A宽泛的底物特异性不同,在不同的pH条件下,PcPKS1不接受异丁酰基辅酶A(isobutyryl-CoA)、异戊酰基辅酶A(isovaleryl-CoA)以及乙酰辅酶A(acetyl-CoA)作为起始底物。以上数据指出重组PcPKS1是一个具有查尔酮合酶(CHS)和苯亚甲基丙酮合酶(BAS)活性的双功能酶。Southern blot杂交结果表明,在虎杖基因组中存在2-4个PcPKS1基因的拷贝。Northern blot杂交结果表明,PcPKS1可能在防御病原菌和草食动物方面起着重要作用。PcPKS1和PcPKS2共同从虎杖中被分离的事实极有可能暗示了苯丁烷类化合物(phenylbutanoid)及其衍生物存在于虎杖中。 Ⅱ 高山红景天酪醇生物合成代谢途径机制研究 高山红景天(Rhodiola sachalinensis A. Bor)是景天科(Crassulaceae)红景天属多年生草本植物,作为一种适应原性中草药在中国的应用史已经超过800年。最近红景天提取物作为一种重要的商业药用制剂资源,其应用遍及欧洲、亚洲和美国,其主要治疗范围包括抗变应性和消炎,提高心理机敏性等。目前已经非常明确,红景天甙(salidroside)和甙元酪醇(tyrosol)是红景天属植物的主要功效成分,主要分布于这类植物的根中并且具有抗缺氧、抗疲劳、延缓衰老、预防紫外线辐射伤害等功效。红景天甙为酪醇8-O-β-D葡萄糖甙,是酪醇在葡萄糖基转移酶UDP-glucosyltransferase (UGT) 的催化下糖基化后形成的,可以认为是酪醇在植物体内的贮存形式。酪醇作为一种重要的活性分子,同样存在于橄榄树和葡萄酒中。 虽然已经非常明确酪醇来自于莽草酸代谢途径,然而其具体的生物合成途径及其调控仍不明确。总结以往的报道,在酪醇的生物合成上主要存在两种观点:一是酪醇可能来自于苯丙烷代谢途径产生的4-香豆酸(4-coumaric acid)前体;二是来自于酪氨酸的酪胺(tyramine)可能是酪醇生物合成的直接前体。我们的工作兴趣主要围绕着鉴别高山红景天中的酪醇生物合成途径展开: 高山红景天内源苯丙氨酸解氨酶PALrs1的过表达对红景天甙积累的影响 红景天甙是来自于药用植物高山红景天的一种适应原性新型药物,其生物合成途径可能起始于苯丙氨酸或酪氨酸。由于高山红景天野生植物资源的匮乏和相对含量很低,阐明红景天甙的生物合成途径对于增加红景天甙的供给至关重要。在我们以前的工作中,运用cDNA末端快速扩增技术(RACE),一个编码苯丙氨酸解氨酶phenylalanine ammonia-lyase (PAL)的cDNA从高山红景天中被克隆,命名为PALrs1。在本研究中,PALrs1置于35S启动子+Ω增强子序列的控制下通过农杆菌(Agrobacterium tumefaciens)介导法转化回高山红景天。PCR 和 PCR–Southern blot分析结果表明,PALrs1已经整合到了转基因植物的基因组上。Northern blot杂交结果表明,PALrs1已经获得在转录水平上的高水平表达。与预期的结果相同,高效液相色谱High-performance liquid chromatography (HPLC)测定结果显示PALrs1的过表达引起4-香豆酸含量增长3.3倍。然而,与之相反的是,酪醇和红景天甙含量与对照相比反而分别下降4.7和7.7倍。此外,我们发现PALrs1的过表达造成酪氨酸含量下降2.6倍。这些数据暗示着PALrs1的过表达和4-香豆酸的积累并不能促进酪醇的生物合成。酪醇,作为一种苯乙烷类衍生物并非来自苯丙氨酸,而酪氨酸含量的下降则极有可能是酪醇生物合成和红景天甙积累大规模下降的直接原因。

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Cultured silver carp (Hypopthalmichthys molitrix 800-1000 g) was stored in ice (fish to ice ratio 1:1) in a plywood box insulated with one inch thick expanded polystyrene and subjected to detailed examination of quality by chemical, microbiological and organoleptic evaluation at regular intervals to assess the storage life in good acceptable form. Alpha-amino nitrogen, non-protein nitrogen and pH values showed no positive correlation as spoilage index. Total volatile base nitrogen was not high at the end of the storage period although the fish became unacceptable during the period. There was steep decrease in total bacterial count during initial stages of storage and then increased steadily on further storage. Organoleptic evaluation of raw and cooked meat revealed that fish was in good acceptable form up to 14 days in ice.

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Lhcb2基因是LHCII基因家族中的一个重要成员。目前,对于其特性、结构和功能还不清楚。本文对豌豆Lhcb2基因的克隆、表达、功能及其在大肠杆菌中的表达产物与色素在体外的重组进行了比较系统的探讨,主要的结果如下: 1.采用RT-PCR技术,从豌豆幼叶中克隆了一个约800 bp的Lhcb2 cDNA。以特异探针进行Southern杂交的结果初步证明,Lhcb2基因以单拷贝形式存在于豌豆基因组中,这在文献中尚未见报道。 2.不同光照时间和温度对豌豆幼苗进行处理的RT-PCR,Northem blotting分析表明,Lhcb2基因转录水平上的表达受光照的控制,且明显地表现出对光照时间的依赖性。用400 μmolm-2.s-1的白光照射0~1.5小时Lhcb2基因未见表达,而在光照2小时以上则大量表达,推测该基因的表达可能要求某种(或某些)需光中间物的合成和积累。温度对Lhcb2基因的表达亦有显著的影响,相同的光照处理,4 ℃下Lhcb2基因的表达量比25℃下的表达量低一倍左右。 3.将豌豆Lhcb2基因反向插入植物表达载体pBIl21中,构建CaMV 35S启动子控制下反义Lhcb2基因的植物表达载体pBIantiLhcb2,通过农杆菌LBA4404介导,在Kan浓度为100 mg/L的筛选培养基上,获得120个抗Kan阳性植株。PCR检测表明至少有80个抗性植株为PCR阳性反应。Southern blotting分析表明,外源反义Lhcb2基因已整合到烟草基因组中。转基因植株在表型上主要表现为三大类型:叶色类似于未转基因的绿色植株、叶色发黄的植株、叶色发白甚至枯死的植株。这几类转基因植株光谱特性的分析表明,Lhcb2基因不仅影响光能的捕获,而且还可能参与激发能分配的调节作用。 4.将豌豆的Lhcb2基因亚克隆至原核表达载体pET-3d上,通过定点突变使其在大肠杆菌BL2l(DE3)中得到高效表达,其表达量约占大肠杆菌总蛋白的40%,并经纯化后获得了电泳纯的Lhcb2蛋白。应用改进的液氮/室温冻融重组方法将纯化的蛋白与色素进行体外重组,建立了高效的重组系统。实验结果表明重组后所获得的LHCB2单体与用生化方法从菠菜类囊体膜中分离纯化的天然LHC II单体相比较,其在部分变性胶的电泳行为,低温荧光发射光谱和激发光谱,以及室温吸收光谱和CD光谱的特征等方面都非常相似,说明大量表达的Lhcb2蛋白与色素已成功地重组,并具有与天然的LHCII单体相类似的组成和结构,这在国际上尚属首次。在此基础上又构建了N端和C端氨基酸残基缺失的突变体,并对这些缺失的氨基酸残基在LHCB2中的可能作用进行了初步的研究。结果表明,N端的前12个氨基酸残基、C端的前10个氨基酸残基和第11位的色氨基酸残基对LHCB2单体的形成不是必需的。 此外,从菠菜中纯化了LHCII,并对其多肽和色素组成及其光谱特性进行了比较系统的研究。同时对用不同浓度OGP和Mg2+处理所获得的不同聚集程度的LHCII的光谱特性进行了研究,并对Mg2+在其中的可能作用进行了初步的探讨。

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  "盐渍土是一种分布广泛的土壤类型,盐渍土中生长的植物如何响应夏季较常出现的高温生长环境一直很少受到人们关注,我们以5种不同耐盐类型的植物为材料,研究其盐适应后光合作用的耐热性,并对耐热性原因做了进一步探讨,主要研究结果如下:   1. 用0、100、200、400 mM NaCl处理盐生植物碱蓬、滨藜、大莳萝蒿;用0、50、100、150 mM NaCl处理耐盐的甜土植物小麦和棉花。盐处理后碱蓬的整株干重变化不显著,而其他四种植物随着盐浓度的升高,整株干重逐渐减小,说明5种植物耐盐能力不同。盐处理对所有实验植物的光系统II最大光化学效率(Fv/Fm)、反应中心能量捕获效率(Fv′/Fm′)、实际量子产率(ΦPSII)、光化学猝灭系数(qP)等影响不显著;但对碳同化有明显影响。碱蓬盐处理后虽然气孔导度和胞间CO2浓度稍有下降,但CO2同化速率却高于对照;其他4种植物盐处理后CO2同化速率都明显降低,同时伴随着气孔导度和胞间CO2浓度的显著下降。以上结果表明盐适应植物的PSII并没有受到盐胁迫伤害,盐胁迫抑制这4种植物光合作用的一个重要原因可能是气孔限制。   2. 高温处理(36~48℃)结果显示,在42℃或45℃以上极端高温下,非盐处理植物的CO2同化速率下降至很低甚至为零,而盐适应植物仍保持一定强度的CO2同化能力。高温处理后盐适应植物的Fv/Fm、Fv′/Fm′、qP、ΦPSII下降幅度也都小于非盐处理植物。不同程度的盐胁迫都能诱导5种植物的光合作用对热胁迫产生抗性,说明植物在适应盐胁迫过程中都能启动一些耐逆机制,使得这5种植物的光合作用在获得耐盐性的同时也获得了对热胁迫的抗性。   3. 室温下(30℃)碱蓬盐处理后,过氧化氢酶、单脱氢抗坏血酸还原酶、抗坏血酸过氧化物酶和谷胱甘肽还原酶活性等显著下降,超氧化物岐化酶活性变化不大,只有脱氢抗坏血酸还原酶活性显著增加;抗坏血酸和谷胱甘肽含量也显著下降。42℃高温处理后,碱蓬叶片的抗氧化系统的酶活性和抗氧化小分子物质含量变化与室温时变化类似。而且盐处理碱蓬叶片的膜脂过氧化产物MDA含量无论在室温下还是42℃处理后都显著高于非盐处理。盐处理后,碱蓬的抗氧化能力没有提高,推测盐处理叶片抗氧化能力大小不是决定其光合作用耐热性主要因素。   4. 在菠菜PSII颗粒的保存液中加入不同浓度的甜菜碱、脯氨酸和蔗糖(0~800 mM),测定PSII最大光化学效率(Fv/Fm)结果表明,有机相容性溶质的积累能显著缓解盐(400 mM和800mM NaCl)、热(30℃和40℃)及盐热胁迫共同作用对菠菜PSII颗粒的伤害。而盐处理后碱蓬、滨藜和莳萝蒿叶片中脯氨酸和可溶性糖含量都显著升高,说明盐胁迫诱导的有机相容性溶质的积累可能在盐适应植物光合作用的耐热性中起重要作用。   5. 提取室温下(30℃)或42℃高温处理碱蓬叶片的叶绿体和类囊体膜,用30℃、35℃、40℃、45℃、50℃水浴进行热处理,结果显示:用室温下或42℃高温处理的碱蓬盐适应叶片提取的叶绿体和类囊体经45℃以上水浴温度处理后,其PSII最大光化学效率(Fv/Fm)和放氧活性都显著高于非盐处理碱蓬叶片的叶绿体和类囊体;用42℃高温处理碱蓬叶片提取的叶绿体和类囊体热稳定性显著高于室温下碱蓬的叶绿体和类囊体。表明盐胁迫和热胁迫类似,都能在类囊体水平上诱导某些保护物质,增加植物PSII的耐热性。   6. 分析类囊体膜膜脂组成,结果显示,盐处理后碱蓬的类囊体膜脂中的饱和脂肪酸含量减少,不饱和脂肪酸含量增加;MGDG和DGDG含量变化不明显,而PG含量显著下降;42℃高温处理后碱蓬的类囊体膜脂组成也有类似的变化规律。盐诱导的碱蓬类囊体膜脂成分的变化可能不影响盐适应植物光系统的耐热性。"

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光系统II(PSII)是存在于类囊体膜中的多亚基色素蛋白复合物,是吸收光能、催化光诱导水裂解释放氧气、质子和电子的重要机构。它在体内的基本单位是由外周天线蛋白(LHCII)与PSII核心复合物结合形成的PSII-LHCII超分子复合物,这一结构保证了LHCII吸收的能量能够快速有效的传递到PSII反应中心(RC),进行原初光化学反应。 本论文分为两部分:1、利用捕光色素蛋白复合物(LHCII)与PSII核心复合物在以DGDG、PG、SQDG三种类囊体膜脂形成的脂质体中重组的方法,研究了LHCII与PSII在脂膜上结构与功能的相互作用;2、通过研究光破坏和色素置换对PSII RC的影响,探讨了RC中不同色素的功能。主要结果如下: 1、LHCII与PSII核心复合物的蛋白脂质体研究: 将OECC(粗提核心复合物)、pdOE(纯化核心复合物)、LHCII(大量天线)制剂分别与脂质体重组并研究了其光谱性质。LHCII在与脂质体重组前表现出典型的聚集态光谱特征,重组后吸收和荧光发射峰发生明显蓝移;LHCII、OECC和pdOE三种蛋白脂质体与重组前的样品相比荧光发射强度增加;表明脂环境影响了色素蛋白复合物的聚集状态以及色素和蛋白之间的相互作用。 OECC和pdOE分别与LHCII在脂质体中重组,得到两种重组蛋白(LHCII-OECC和LHCII-pdOE)脂质体,用冰冻蚀刻电镜技术和低温荧光光谱的方法研究其结构和功能特征。LHCII和核心复合物(OECC或pdOE)结合形成PSII-LHCII重组颗粒,并在脂质体中均匀排布,阻止了LHCII晶格状结构的形成。重组蛋白脂质体的吸收光谱既有LHCII的吸收特征,又有核心复合物的特征吸收峰,但低温荧光光谱的主要发射峰是核心复合物的特征峰(684 nm-685 nm),而不是LHCII的特征峰(680 nm);而且激发不同色素得到的荧光发射光谱基本一致,这些结果证明LHCII吸收的能量传递到了核心复合物中,在重组蛋白脂质体中不同色素蛋白复合物在结构和功能上都实现了相互偶联。 通过对OECC或pdOE与LHCII重组形成的蛋白脂质体放氧或DCPIP光还原活性的检测研究了PSII光化学活性特征。LHCII和核心复合物(OECC或pdOE)的重组蛋白脂质体与单独核心脂质体相比,在强光和弱光下光化学活性都明显提高。这从另一个角度证明了核心复合物与LHCII的功能偶联,LHCII的结合使捕光截面积增大,从而使PSII光化学活性增加。 用77K飞秒时间分辨荧光光谱分析了几种蛋白脂质体的能量传递和捕获情况。LHCII、OECC和pdOE三种蛋白脂质体的主要荧光衰减组分分别是670 ps(发射峰在680 nm)、650 ps(发射峰在690 nm)和570 ps(发射峰在685 nm)。LHCII-OECC和LHCII-pdOE脂质体的主要衰减组分分别是940 ps(发射峰在690 nm)和840 ps(发射峰在685 nm),并且出现了一个在核心复合物脂质体和LHCII脂质体中没有的40 ps组分,可以推测,这是LHCII和核心复合物之间达到平衡的时间组分,比激发态衰减的平均寿命要快得多,因此支持了PSII的trap-limited激发能衰减动力学模型。此外,可以看到天线的增大使Chl a荧光衰减的寿命延长,这一特性可能与PSII的光保护机制有关。 LHCII和OECC、LHCII和pdOE在脂质体中都成功的实现了重组,而且在结构和功能上没有明显差异;表明小天线以及23 kDa、17 kDa蛋白可能不是LHCII和核心复合物结合及能量传递所必需的。 2、受体侧光破坏和色素置换对PSII RC的影响: 在800 μmol.m-2 .s-1光照和无外加电子受体、供体的情况下,研究了PSII RC色素的受体侧光破坏情况。Chl a、Pheo和β-Car的光漂白几乎同时发生,其中在680 nm吸收的色素破坏最为显著,670 nm吸收的外周Chl比其他色素更加稳定。荧光发射强度呈先升高后降低的趋势,最大发射峰位逐渐蓝移,表明色素之间的能量传递受到破坏。用β-Car的主要吸收波长488 nm和514.5 nm激发得到两组谱带峰位和强度不同的拉曼光谱,表明在PSII RC中存在两个光谱性质不同的β-Car。光破坏过程中两组谱带的位置和带宽都没有明显变化,表明β-Car的光保护机制不涉及自身构象的变化。 将PSII RC与Cu-Chl a进行色素置换,得到了与Cu-Chl重组的RC(Cu-Chl-RC),含有0.5 Cu-Chl/2Pheo。与对照RC(按同样方式与Chl a置换的RC)和天然RC相比,Cu-Chl含量增加而Chl含量减少,660 nm的吸收增加而670 nm吸收降低,因此推测是外周Chl被替换。色素置换过程对RC的多肽组分及大部分的P680活性没有影响,CD光谱的变化也很小,表明产生CD信号的色素和蛋白环境也没有受到明显影响。但是Cu-Chl-RC的荧光发射强度明显降低,最大发射峰蓝移且峰形发生变化,Cu-Chl可能在重组RC中作为激发态的淬灭剂,阻碍了色素之间的能量传递。

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A simplified process was worked out to prepare crude agar from red seaweeds (Gracilaria sp.). The process required careful preliminary cleaning and bleaching (sun-drying) of the weed. The agar was extracted by boiling with water in a mixture (2%) strong enough to set as a jelly. Freezing the jelly over a 3—day period in an ice-making machine, adjusted to work slowly, separated out ice and agar. The blocks were thawed out and the agar dried in the sun. The efficiency of extraction was over 800/A.

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Reports of cruises carried out off Mozambique between parallels 21 degree 00 and 26 degree 20'S and at depths of 400 and 800 meters including abundance indices, catch composition, geographic and bathymetric distributions of shrimp catches are presented. The main species found were Hymenopenaeus triarthrus and Aristeomorpha foliacea which represent 64 to 72% of total catches.

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本发明涉及杀虫剂领域,具体地说是一种海藻内生真菌二萜生物碱类化合物及其制备和应用。具体结构式如(I)所示,其制备方法为将米曲霉(Aspergillus oryzae)cf-2接种于培养基中静止发酵,发酵液经乙酸乙酯萃取浓缩,菌丝体用有机溶剂提取,再经乙酸乙酯萃取浓缩,合并浓缩物,得到粗提物;粗提物进行硅胶柱层析,用有机溶剂进行梯度洗脱,收集洗脱液,洗脱液经薄层层析检测;将以洗脱液体积比10-15:1梯度的洗脱组分进行凝胶柱层析、硅胶柱层析和薄层层析分离纯化得目标化合物。本发明获得的海藻内生真菌二萜生物碱类化合物,经杀虫活性实验得出化合物在100微克/毫升时对卤虫的致死率为61.9%。

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The mobile water hyacinth, which was produced in growth zones, especially Murchison Bay, was mainly exported to three sheltered storage bays (Thruston, Hannington and Waiya). Between 1996 and May 1998, the mobile form of water hyacinth occupied about 800 ha in Thruston Bay, 750 ha in Hannington Bay and 140 ha in Waiya Bay). Biological control weevils and other factors, including localised nutrient depletion, weakened the weed that was confined to the bays and it sunk around October 1998. The settling to the bottom of such huge quantities of organic matter its subsequent decomposition and the debris from this mass was likely to have environmental impacts on biotic communities (e.g. fish and invertebrate), physico-chemical conditions (water quality), and on socio-economic activities (e.g. at fish landings, water abstraction, and hydro-power generation points). Sunken water. hyacinth debris could also affect nutrient levels in the water column and lead to reduction in the content of dissolved oxygen. The changes in nutrient dynamics and oxygen levels could affect algal productivity, invertebrate composition and fish communities. Socio-economic impacts of dead sunken weed were expected from debris deposited along the shoreline especially at fish landings, water abstraction and hydropower generation points. Therefore, environmental impact assessment studies were carried out between 1998 and 2002 in selected representative zones of Lake Victoria to identify the effects of the sunken water hyacinth biomass

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La difusión de datos de las colecciones biológicas es importante, sin embargo su divulgación es escasa. En esta publicación se informa sobre los huevos depositados en la Sección Ornitología del Museo de La Plata. Los mismos son producto de compras, donaciones o de ejemplares provenientes de cautiverio. El objetivo del presente trabajo es dar a conocer las especies de aves de Eurasia, África, Oceanía y América del Norte representadas en esta colección oológica. Esta colección cuenta con aproximadamente 3.800 huevos, 99 de los cuales pertenecen a aves de las regiones que ocupa este estudio. Se destaca Europa (n= 82), seguido por África (n= 6), Oceanía (n= 5), América del Norte (n=3) y Asia (n= 2). Los huevos de estas regiones representan a 17 órdenes, 37 familias y 72 especies; siendo el Orden Passeriformes el mejor representado con un total de 15 familias. El continente europeo es el mejor representado con un 77,5 % del total de las familias y un 87,7 % del total de las especies; con mayor número de ejemplares en los órdenes Passeriformes (n= 41) y Anseriformes (n= 8). Las colecciones son una valiosa fuente de referencia para diferentes tipos de estudios debiendo ser depositadas en lugares que permitan su correcta preservación y que estén a disponibilidad de quienes lo requieran.

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The Indian muntjac (Muntiacus muntjak vaginalis) has a karyotype of 2n=6 in the female and 7 in the male, the karyotypic evolution of which through extensive tandem fusions and several centric fusions has been well-documented by recent molecular cytogenetic studies. In an attempt to define the fusion orientations of conserved chromosomal segments and the molecular mechanisms underlying the tandem fusions, we have constructed a highly redundant (more than six times of whole genome coverage) bacterial artificial chromosome (BAC) library of Indian muntjac. The BAC library contains 124,800 clones with no chromosome bias and has an average insert DNA size of 120 kb. A total of 223 clones have been mapped by fluorescent in situ hybridization onto the chromosomes of both Indian muntjac and Chinese muntjac and a high-resolution comparative map has been established. Our mapping results demonstrate that all tandem fusions that occurred during the evolution of Indian muntjac karyotype from the acrocentric 2n=70 hypothetical ancestral karyotype are centromere-telomere (head-tail) fusions.

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Sperata aor and S. seenghala are the two important native catfishes of Bangladesh but commercial farming of these species is not possible due to lack of naturally collected or artificially produced seeds for stocking. Attempts were made to develop techniques for seed production by artificial breeding and nursery-rearing of fries of these catfishes. A total of 60 S. seenghala (750-1,500 g) and 10 S. aor (600-1,000 g) broods were collected from the Brahmaputra river-basin and floodplains in Mymensingh region four months prior to their breeding season. The collected brood fishes were reared in separate earthen ponds with supplementary feeds comprising of rice bran (40%), mustard oil cake (29%), fish meal (30%) and vitamin-premix (1 %). Three experiments were conducted to optimize the hormone dose. A total of nine S. seenghala females weighing from 750 to 1,500 g were given an initial and resolving dose of 12-20 and 16-24 mg PG/kg body weight, respectively. The males weighing from 650-950 g were administered a single dose of 18-26 mg PG/kg body weight at the time of the time of administering the resolving dose to the females. The females ovulated partially and the eggs were examined under a compound microscope, but most of them were found to be less ripe or damaged. Collection of milt by stripping the males was not successful. The testes were taken out and sperm were observed to be non-motile and less developed. In view of stimulating natural propagation of S. seenghala, artificial holes (nests) were constructed in the pond bottom. Each hole was 0.7 m in diameter and 0.3 m in depth. A total of 10 holes were made and then 10 pairs of S. seenghala breeders (800-1,200 g) were stocked in the pond. In mid February, 3,000 fry of S. seenghala with a mean length of 4.60 cm and weight of 0.36 g were collected by repeated netting followed by drying of the pond. The fry were then stocked in a nursery pond and fed with commercial feed (SABINCO starter-1). The average length and weight of the fingerlings were 9.01 cm and 3.95 g, respectively and the estimated survival was 60% after two months of rearing. S. aor did not respond to natural spawning. Further study is essential to develop techniques for their successful artificial and natural breeding.

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An experiment was conducted for six months in 6 experimental ponds (each size 80 of m2) to assess the over-wintering performance between mixed sex and monosex tilapia, Oreochromis niloticus. The experiment was carried out with two treatments each with three replicates. In the first treatment (T1), mixed sex tilapia were stocked in 3 ponds with a mean initial of 4.80±0.18 g. In the second treatment (T2), monosex tilapia were stocked in another 3 ponds with a mean initial weight of 4.81 ±0.20 g. Each pond was stocked with 250 fingerlings. Fish were fed at the rate of 6% of fish body weight at the beginning. The feeding rate was gradually reduced to 2% for the third month and finally increased to 3% for rest of the period. Water quality was monitored fortnightly and the ranges were: temperature17.86-29.10°C, dissolved oxygen 4.25-6.10 mg/1, pH 6.97-7.20 and transparency 24.10-36.50 cm. After 6 months of rearing monosex tilapia attained a significantly (phigher mean final weight of 146.26±0.34 g compared to 112.40±0.36 g for mixed sex tilapia. Monosex tilapia also resulted in significantly (Phigher specific growth rate than those of mixed sex tilapia. However, there was no significant (phe mixed sex and monosex tilapia. The production of monosex tilapia (3723.10 kg/ha) was about 32% higher than that of mixed sex tilapia (2776.28 kg/ha). The net profit/ha generated from the 6 months culture period was calculated as Tk. 43,311.45 and. 69,277.32/- for mixed sex and monosex tilapia respectively. The results of the present study suggested that it is possible to successfully culture tilapia during the winter period and the culture of monosex tilapia is more profitable due to its higher growth rate than that of mixesex tilapia.