446 resultados para OYSTER


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Relation of weight to height, length and breadth in the Indian backwater oyster Crassostrea madrasensis (Preston) is reported. The relative importance of the variables on weight was found to be height, length and breadth in their order of preference. The multiple regression V = -0.4017 + 0.46743 X + 0.8278 Y + 0.1130 Z can be used to estimate the meat weight (logarithm) for given dimensions of length, height and breadth (all in logarithms). An exponential relation between weight and height is also observed.

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Preliminary findings from a spatfall forecasting programme initiated in April 1981 at Himamaylan River, Negros Occidental are presented. Two main activities are involved: 1) monitoring of daily counts of oyster larvae in the plankton; and 2) monitoring of actual setting of oysters on standardized collectors put in the vicinity of oyster farm sites. Findings indicate that when the count of mature larvae exceeds 5 per 100 ml sample and persists for at least 3 days, spat may be expected to occur shortly afterwards.

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An experiment was carried out in farmers' gher (shrimp farm) at Bagerhat sadar upazilla, Bagerhat to ascertain the effects of three different types of feeds on the production and economics of brackishwater shrimp, Penaeus monodon for a period of 120 days. There were three treatments such as T1 (BFRI dough feed containing of 30% fish meal, 10% protein conc., 10% soya meal, 15% mustard oil cake, 18% rice bran, 5% maize, 10% wheat flour, 1% oyster shell powder and 1% vitamin premix), T2 (Commercial diet Saudi-Bangla grower) and T3 (Saudi-Bangla special feed). Each treatment had two replicates and the stocking of shrimp in each gher was 3 nos/m². Water quality parameters did not differ significantly among the treatments except water depth. Average production and net return of shrimp in different treatments varied from 404.0 to 509.0 kg/ha and Tk. 56,493.99-Tk. 84,209.60, respectively. T2 showed significantly (p<0.05) the highest production and economic return. The result of the study implied that T2 is more suitable and economically viable than that of other treatments for shrimp farming.

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Genetic diversity of Saccostrea cucullata in the northern coast lines of the Persian Gulf and the Sea of Oman were determined using DNA extraction and RAPD - PCR. A total of 300 samples were collected from 6 station along the coastline. Two out of six primers showed positive results namely GCG - ATC - CCC - A (Primer 1) and GTC - CAC - ACG - C (Primer 5) which were in accordance with morphometric analysis. The number of bands in the two above - mentioned primers in Khor - Tang and Chabahar station (Province of Sistan and Balouchestan) was significantly different from the number of produced bands in Dayer and Bushehr station (Province of Bushehr) as well as Gheshm and Bandar - Lengeh station (Province of Hormozgan). The cluster analisys was used to confirm the above variations. The results showed that the oyster population can be divided into two separate clusters. The first cluster included Bushehr Dayer Gheshm and Bandar - Lengeh species. The second cluster included Khor - Tang and Chabahar species. The analysis also showed that the first cluster can be divided into two Sub — cluster. Bushehr and Dayer belong to one Sub - cluster whereas Gheshm and Bandar - Lengeh form the other Sub — cluster. The formation of different vluster can be related to Physico - Chemical properties of water and climatic variations in different habitats along the Persion Gulf and the Sea of Oman. Key words: Molecular genetics, Population, RAND, PCR' Saccostrea cucullata

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Annual cycle of gonad development and spawning in pearl oyster, Pinctada ficata (Gould) in Nakhiloo, Northeast Persian Gulf, was investigated over two years from August 1994 to June 1996. Gonadal condition was assessed by staging criteria to describe gametogenic development from histological preparations of randomly collected individuals of all sizes. A bimodal gametogenic pattern with summer and autumn spawning periods was evident throughout the study. Gametogensis commenced in November-December which proceeded by major gonadal maturation during February-April. Summer spawning was observed from April to July with major spawning at the latter end. During spawning peak in July, low level of gametogensis was noticed. Gametogenic activity was picked up again in August-September which proceeded by autumn spawning from September to December. Towards the end of spawning season, incidence of gonadal inactivation increased. Minimum level of gonadal activity was observed in November. Temperature regime appears to have influential role in regulation of gametogenic and spawning processes. Gonadal development and spawning trends were similar in both sexes. P. radiaata was found to be protandrous hermaphrodite which matured as a male at shell height greater than 20 mm. Biseivality was uncommon and the sex ratio was about 1:1. Ultrastructure of gametes were investigated in the Pictada fucata (Gould). "Auxiliary cells" closely accociated with developing oocytes were observed. Each oocyte seems to be associated with only one secretory cell. which is characterized by an abundant rough endoplasmic reticulum at the onset of vitellogenesis. Contact between this cell and a developing oocytes is maintained by a desmosome-like junction which can be observed when the vitelline coat is formed. these "auxiliary or nursing cells" seem to play a tropic role in vitellogenesis, and may be involved in the formation of the vitelline coat of the oocytes. Oocytic degeneration is observed in this species, it is a continuous phenomenon of varing intensity throughout the year. The ultrastructural changes resulting in lysis of the oocyte are described. Mature spermatozoa consist of a broad, cap-shaped acrosomal vesicle, subacrosomal material, a round nucleus, two triplet substructure centrioles surrounded by four spherical mitochondria, and a flagellum anchored to the distal centriole and plasma membrane. Spermatozoa of Plucata closley resemble to those of other investigated Pteriidae. Changes in proximate composition of soft tissue and gonadal cycle of Pinctada fucata was studied. Mobilization and utilization of stored reserves are apparent during gametogenesis and gonadal maturation. Protein reserves are utilized during spermatogenesis while reserved carbohydrates form the main energy donor in oogenesis. The role of lipid as am.: energy reserve is second to that of carbohydrate.

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Studies on mixed mass cultivation of Anabaena spp. on a large scale (5170 m2) were conducted continuously for 3 years. Under the continental monsoon climate in northern subtropics (30-degrees-N, 115-degrees-E), 7-11 g dry weight m-2 day-1 of microalgal biomass on average was harvested in simple plastic greenhouses in the effective growth days during the warmer seasons. The maximum productivity was 22 g m-2 day-1 in the middle of summer. Observations on the productive properties of strains of Anabaena spp. indicated that they were different from and could compensate for each other in their productivities and adaptations to the seasonal changes. With different lining materials (PVC sheets, concrete, sand and soil) in the culture ponds, no significant variation of productivity was found, but bubbling with biogas in the middle of the day and the application of some growth regulating substances (2,4-D, NaHSO3 and extracts of oyster mushroom spawn) was able to improve the production. The cost of microalgal biomass in this way was around 0.75-1.0 US dollar(s) per kilogram.

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Karyotype and chromosomal location of the major ribosomal RNA genes (rDNA) were studied using fluorescence in situ hybridization (FISH) in five species of Crassostrea: three Asian-Pacific species (C. gigas, C. plicatula, and C. ariakensis) and two Atlantic species (C. virginica and C. rhizophorae). FISH probes were made by PCR amplification of the intergenic transcribed spacer between the 18S and 5.8S rRNA genes, and labeled with digoxigenin-11-dUTP. All five species had a haploid number of 10 chromosomes. The Atlantic species had 1-2 submetacentric chromosomes, while the three Pacific species had none. FISH with metaphase chromosomes detected a single telomeric locus for rDNA in all five species without any variation. In all three Pacific species, rDNA was located on the long arm of Chromosome 10 (10q)-the smallest chromosome. In the two Atlantic species, rDNA was located on the short arm of Chromosome 2 (2p)-the second longest chromosome. A review of other studies reveals the same distribution of NOR sites (putative rDNA loci) in three other species: on 10q in C. sikamea and C. angulata from the Pacific Ocean and on 2p in C. gasar from the western Atlantic. All data support the conclusion that differences in size and shape of the rDNA-bearing chromosome represent a major divide between Asian-Pacific and Atlantic species of Crassostrea. This finding suggests that chromosomal divergence can occur under seemingly conserved karyotypes and may play a role in reproductive isolation and speciation.

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Cu, Zn superoxide dismutases (SODs) are rnetalloenzymes that represent one important line of defence against reactive oxygen species (ROS). A cytoplasmic Cu. Zn SOD cDNA sequence was cloned from scallop Chlamys farreri by the homology-based cloning technique. The full-length cDNA of scallop cytoplasmic Cu, Zn SOD (designated CfSOD) was 1022 bp with a 459 bp open reading frame encoding a polypeptide of 153 amino acids. The predicted amino acid sequence of CfSOD shared high identity with cytoplasmic Cu. Zn SOD in molluscs, insects, mammals and other animals, such as cytoplasmic Cu, Zn SOD in oyster Crassostrea sostrea gigas (CAD42722), mosquito Aedes aegypti (ABF18094), and cow Bos taurus (XP_584414). A quantitative reverse transcriptase real-time PCR (qRT-PCR) assay was developed to assess the mRNA expression of CfSOD in different tissues and the temporal expression of CfSOD in scallop challenged with Listonella anguillarum, Micrococcus luteus and Candida lipolytica respectively. Higher-level mRNA expression of CfSOD was detected in the tissues of haemocytes, gill filaments and kidney. The expression of CfSOD dropped in the first 8-16 h and then recovered after challenge with L. anguillarum and M. litteus, but no change was induced by the C. lipolytica challenge. The results indicated that CfSOD was a constitutive and inducible acute-phase protein, and could play an important role in the immune responses against L. anguillarum and M. luteus infection. (C) 2007 Elsevier Ltd. All rights reserved.

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Crassostrea ariakensis is an important aquacultured oyster species in Asia, its native region. During the past decade, consideration was given to introducing C. ariakensis into Chesapeake Bay, in the United States, to help revive the declining native oyster industry and bolster the local ecosystem. Little is known about the ecology and biology of this species in Asia due to confusion with nomenclature and difficulty in accurately identifying the species of wild populations in their natural environment. Even less research has been done on the population genetics of native populations of C. ariakensis in Asia. We examined the magnitude and pattern of genetic differentiation among 10 wild populations of C. ariakensis from its confirmed distribution range using eight polymorphic microsatellite markers. Results showed a small but significant global theta (ST) (0.018), indicating genetic heterogeneity among populations. Eight genetically distinct populations were further distinguished based on population pairwise theta (ST) comparisons, including one in Japan, four in China, and three populations along the coast of South Korea. A significant positive association was detected between genetic and geographic distances among populations, suggesting a genetic pattern of isolation by distance. This research represents a novel observation on wild genetic population structuring in a coastal bivalve species along the coast of the northwest Pacific.

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本研究应用显带技术和荧光原位杂交(Fluorescence in situ hybridization,FISH)技术,鉴定了牡蛎的染色体;应用FISH方法定位了一系列的重复序列和大分子的P1克隆DNA;制备了染色体特异性探针。应用FISH特异性探针成功地鉴定了长牡蛎的三体10。结果如下:1.分析了G带和C带在美洲牡蛎染色体上的分布。G带在每一条染色体上的带型不同,某些染色体间(如第1对和第4对染色体,第7对和第9对染色体)的带型差别不是很明显。G带型容易受染色体收缩程度的影响。C带型重复性较好,染色体带型较清楚,分布在染色体的端粒区域和着丝粒区域。G带和C带带型能够用来鉴定牡蛎的染色体,但是重复性低和带型差异不显著,并不适合常规的染色体鉴定。2.早期胚胎和担轮幼虫制备的染色体适合于FISH分析。染色体制备方法重复性好,可适用于其它贝类的染色体制备。3.研究了重复序列基因--rDNA的定位:1)18S-5.8S rDNA在研究的五种巨蛎属Crassostrea牡蛎均只有一个位 点。太平洋种(C.gigas,C. ariakensis和C. plicatula)中,杂交信号位于最短的染色体一第10对染色体长臂的端粒区域,在大西洋种(C. virginica和C. rhizophorae)中,同一序列定位在第2对染色体短臂的端粒区域。2)18S-28S rDNA在两种蛤中有两个位点。rDNA探针定位在侏儒蛤(Mulinis Lateralis)的第15对和第19对染色体的端粒区域,同一序列定位在硬壳蛤(Mercenaria mercenaria)的第10对染色体的长臂和第12对染色体短臂的端粒区域。信号强度在两对染色体之间有差异。 3)5s rDNA位于美洲牡蛎的第5对染色体的短臂上靠近着丝粒区域和第6 对染色体的短臂的中间区域。信号强度在两对染色体之间没有显著差异。5S rDNA探针可以作为鉴定和识别第5对和第6对染色体的特异性探针。4.研究了一些重复序列的定位1)两个短的重复序列1G8,1P2均产生很强的荧光信号分布在美洲牡蛎所有的染色体上。在低严谨条件下,这些序列均产生很强的信号散布在所有的染色体上。在高严谨条件下,信号强度大大减弱,但是信号仍散布在所有的染色体上。这些重复序列散布在美洲牡蛎的整个基因组中。2)高度重复序列Cgl70产生的信号分布在长牡蛎的7对染色体的着丝粒区域,没有发现间区信号。在第1对,第2对,第4对和第7对染色体上的荧光信号强且稳定。在第5对,第8对和第10对染色体上的信号相对弱且不稳定。在剩余的染色体上(第3对,第6对和第9对染色体)没有检测到荧光信号。结果表明此卫星序列是一个着丝粒卫星序列。在美洲牡蛎的染色体上没有检测到荧光信号,表明了这个着丝粒卫星序列在这两种牡蛎中的分布存在着显著的差异。3)脊椎动物端粒序列(TTAGGG)n的FISH信号局限在四种双壳贝类(美洲牡蛎,the mangrove oyster,硬壳蛤,侏儒蛤)所有染色体的端粒区域,没有发现间区信号的存在。研究结果与已报道的研究结果表明脊椎动物端粒序列或许存在于所有双壳贝类的染色体末端。双壳贝类是目前研究过的唯一含有脊椎动物端粒序列DNA的无脊椎动物。4)研究了RAPD探针在美洲牡蛎染色体上的定位。大多数RAPD探针产生了多个信号散布在间期细胞核和所有的染色体上。引物OPX-03,OPX-04,OPX—06,OPG-02,OPM—04,OPM-11,0PS-02制备的探针在适宜的条件下产生特异性荧光 信号,分布在牡蛎的特定的染色体上。PCR特异性带产生的探针OPX—06—310和0PG-02—300产生了特异性的荧光信号:OPX—06—310产生的信号位于第5对染色体的短臂的近端粒区域,0PG—02—300探针定位到第3对染色体的短臂上。这两个探针是鉴定美洲牡蛎单条染色体的特异性探针。5.研究了大分子Pl克隆DNA(插入片断为80~100 kb)在美洲牡蛎染色体上的定位。Pl克隆DNA通过切口平移方法标记digoxigenin—11-dUTP用作FISH的探针。Cot-1 DNA作为竞争剂有效地抑制了Pl克隆序列中的重复序列产生的信号。杂交信号用fluorescein标记的anti—digoxigenin抗体来检测,用两层抗体rabbit-anti-sheep抗体和FITC anti—rabbit抗体来扩增信号。9个P1探针成功地定位在特定的染色体上。46—1探针杂交到第1对染色体的长臂靠近着丝粒区域;47-10探针定位到第2对染色体的长臂近端粒区域;Cvpl和48-13两探针定位到第3对染色体上:Cvpl位于短臂的端粒区域,48-13探针位于长臂的近着丝粒区域;48—10探针杂交到第4对染色体的长臂上;48-1探针杂交到第5对染色体长臂的近着丝粒区域;49-11探针位于第7对染色体长臂上;探针49-10和44-11位于第8对染色体长臂上。同时我们成功地将2个P1探针杂交到同一染色体分裂相中,进一步确定了Pl探针在美洲牡蛎染色体 上的定位。6.应用18S-28S rDNA探针成功地鉴定出长牡蛎非整倍体中的三体10。经鉴定AF-35,AF-39和AF-3三体家系属于三体10家系。rDNA探针分布在三条染色体上,即多出的一条染色体为染色体10。相应地在间期细胞核上有三个信号出现。AF-34和AF-36家系不属于三体10家系。rDNA探针分布在两条染色体上,相应地在间期细胞核上有两个信号出现。FISH和染色体特异性探针为非整倍体的鉴定提供了一个快速准确可靠的方法和途径。

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长牡蛎是重要的经济养殖贝类,良种化、抗逆性状及快速生长个体的培育是长牡蛎养殖业得以持续发展的基础。目前飞速发展的分子标记辅助育种技术为优良品种的快速培育提供了理论基础和实践经验。本研究以长牡蛎为主要研究材料,探讨了长牡蛎SNP标记的筛选和多态性评价。 本研究利用已有长牡蛎EST库中的序列进行单核苷酸多态(SNP)标记开发。通过对长牡蛎(Crassostrea gigas)已有的EST序列数据库检索,经过序列聚类和拼接得到EST簇4548个,含有不少于4条EST序列的簇共1079个,经过进一步设置筛选条件,整理出可供利用的EST簇313个,得到候选SNP位点共计1140个。目前根据候选SNP位点共设计引物82组,通过片段长度差异等位基因特异性PCR(fragment length discrepant allele specific PCR,FLDAS-PCR)的分型方法,在一野生群体中进行检测和验证,结果共有17个SNP候选位点显示多态性,期望杂合度分布区间为0.088至0.506,观测杂合度分布区间为0.091至0.667;通过哈代-温伯格(HW) 平衡、连锁不平衡检验,结果显示除3个SNP位点的差异显著(P值<0.05),不符合HW平衡之外,其他14个位点没有明显的连锁不平衡。对含有17个SNP的EST的共同序列进行BlastX分析,推测其功能并确定开放阅读框,从而预测17个SNP的性质。 本研究表明对于目前基因组学研究尚处在初级阶段的海洋生物物种,通过基于EST数据库的SNP开发是一条重要途径,可以有效弥补海洋生物基因组学滞后影响SNP标记开发的现状。

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附着生物又称污损生物,是附生在海洋设施和生物体表面的动物、植物和微生物等生物的总称(Azis et al., 2001)。附生在养殖器材和生物体表面的数量巨大的附着生物,对贝类养殖和海湾生态系统内的物质和营养盐循环等多个方面产生影响。本研究以北方重要的养殖海湾----桑沟湾为研究对象,对贝藻养殖区附着生物的群落演替及其生态效应进行了研究。主要研究结果如下: ① 2007年5月至2008年5月,采用挂网的方法对桑沟湾栉孔扇贝和海带混养区的附着生物的季节变化进行了研究。结果显示挂网上的附着生物具有显著的季节变化特征,网片上的附着生物湿重与水温的变化相一致,生物量为3~1210 g•m-2。2月份附着生物的生物量最低,8月份最高。2007年9月至11月,对栉孔扇贝养殖笼上和贝壳上的附着生物种类和数量进行了研究。结果显示9月份养殖笼上附着生物的湿重约为1.94 kg,10月份降至0.99 kg,11月份又稍有增加,为1.03 kg。扇贝壳上的附着生物变化趋势与养殖笼上的相同,9~11月份壳上附着生物的数量约0.49~2.09 g。扇贝养殖笼上可鉴定的大型附着生物约23种,包括藻类、海鞘类、苔藓虫类、环节动物、腔肠动物、软体动物、甲壳动物和海绵动物等。玻璃海鞘、柄海鞘、紫贻贝和苔藓虫等是附着生物群落中的优势种。 ② 通过在栉孔扇贝和虾夷扇贝上壳上添加不同重量的“模拟附着生物”(速凝水泥)的方法,研究了贝壳上附着生物的重量对这两种扇贝生长和存活的影响。结果显示水泥重量是上壳重0.5-3倍的各组实验组扇贝的生长和存活与对照组(未添加水泥的扇贝)之间没有显著差异。说明贝壳上附着生物重量为上壳的3倍重时,也不会显著影响扇贝生长存活。9-11月份贝壳上的自然附着生物的重量约为1.47-2.09 g,为上壳重的28.16 (±38.6)%—31.29 ± (31.63)%。因此,贝壳上附着的生物重量不太可能对扇贝的生长存活造成显著的负面影响。 ③ 在桑沟湾现场测定了玻璃海鞘和柄海鞘的生物沉积速率。9月份(水温约24℃)玻璃海鞘和柄海鞘的生物沉积速率分别为32.14和90.06 mg•ind-1•d-1或(858.99 和467.76 mg•gdw-1•d-1),据此计算,养殖笼上的两种海鞘的生物沉积速率约为84.29 mg•m-2•d-1。海区的自然沉积速率为41.49 mg•m-2•d-1;玻璃海鞘和柄海鞘沉积物中有机质含量分别为14.34%和13.77%,对照组海区自然的有机质含量为14.36%;以上三者有机碳的含量分别为24.72%,23.74%和24.76%;氮的含量分别为0.27%和0.25%,自然沉积物中的氮含量为0.30%。9月份扇贝养殖笼上附着的海鞘将产生2588.16吨的沉积物,即向底部沉积363.77吨的有机物、6.99吨的氮和1.79吨的磷。 ④ 通过测定扇贝养殖笼上优势种附着生物--玻璃海鞘、柄海鞘和贻贝的摄食、呼吸和排泄,研究了这些优势种类对贝类养殖和海湾环境的影响。9月份(水温约24.5℃)玻璃海鞘和柄海鞘对颗粒有机物(POM)的摄食率分别为14.30 和17.01 mg• h-1•ind-1。根据实验结果计算这两种海鞘摄取的颗粒有机物相当于312个扇贝的摄取量,大于笼内养殖的扇贝的摄取量;玻璃海鞘和柄海鞘的耗氧率分别约为0.32和0.18 mg•h-1•ind-1,养殖笼上的这两种海鞘消耗的溶解氧约等于75个扇贝消耗的溶解氧。栉孔扇贝、玻璃海鞘、柄海鞘和贻贝的排氨率分别为33.66 ±11.34,117.90±23.46,35.91±6.22,28.08±3.41 ug NH4-N•gdw-1•h-1。以此估算,9月份玻璃海鞘、柄海鞘和贻贝每天排泄的氨氮约为654.08 kg,相当于16467吨栉孔扇贝(鲜重)排泄的氨氮。海鞘和贻贝排泄的氨氮可提供浮游植物等所需的2.75%的氮,可以提供1204吨海带的生长所需的氮。 ⑤ 一个养殖笼内的栉孔扇贝和全部附着生物(Scallop Culture Unit, SCU)在夏季(6-9月)对颗粒有机物的摄食速率约为43.13-98.94 mg/h,平均74.05 mg/h,期间桑沟湾养殖的栉孔扇贝及附着生物摄取的POM约为1279.58吨;同期,SCU对氨氮和磷(PO4-P)的排泄速率分别为125.59-1432.23 μmol•h-1和76.2-252.89μmol•h-1,期间桑沟湾养殖扇贝及附着生物排泄的氮磷分别为211.09 吨和83.79 吨。一串牡蛎及吊绳和牡蛎壳上的附着生物(Oyster Culture Unit, OCU),夏季摄食率为5-41.43μmol•h-1,耗氧率为16.54-41.76μmol•h-1,对氨氮和磷(PO4-P)的排泄速率分别为35.56-489.34μmol•h-1 和9.92-16.68μmol•h-1。以此估算,夏季OCU可摄取POM535.68吨,消耗溶解氧955.58吨,排泄氮磷分别为62.37 吨和15.50 吨。

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中国牡蛎种类丰富,但是由于贝壳可塑性强,表型变化大,分类学及系统发生学研究进展缓慢,存在诸多争议。本文在全国部分海区采集牡蛎样品,并通过表型和分子生物学方法进行鉴定,重点调查潮下带牡蛎的分布情况。选取江苏南通小庙洪牡蛎礁作为典型海域,研究亲缘关系接近的巨蛎属牡蛎之间在繁殖上如何维持相互之间的关系。本研究的目的在于摸索牡蛎物种鉴定的实用方法,并阐明熊本牡蛎和近江牡蛎生殖隔离是如何维持的。研究结果对牡蛎等海洋贝类的分类及系统发生学研究具有一定的借鉴作用,为牡蛎礁的生态保护提供生物学参考依据。 在辽宁营口、海洋岛,河北秦皇岛,山东西霞口、潍坊、青岛,江苏南通,浙江舟山、奉化,福建莆田,广东汕头等地区采集牡蛎样品,重点采集潮下带的牡蛎,通过地理分布、表型、DNA含量测定和COI种特异性探针鉴定对各地区的牡蛎物种组成进行分析。选取了南通小庙洪牡蛎礁作为研究牡蛎物种间相互关系的最佳地点。该地区牡蛎由主要分布在潮间带的熊本牡蛎和主要分布在潮下带的近江牡蛎组成。 对南通小庙洪牡蛎礁上两种巨蛎属牡蛎在空间上的分布进行调查;定期取样,制作性腺切片,观察两种牡蛎的性腺发育情况;同时,定期在海区挂板,采用半人工采苗的方式采集海区牡蛎幼体,通过ITS1基因鉴定采集的稚贝所属物种。通过调查发现二者的分布存在重叠区域;两种牡蛎在2007年6月中旬至9月中旬存在两个明显的繁殖高峰期,在每个繁殖期内两种牡蛎同时发生大量繁殖行为的可能性极高。结果表明,两种牡蛎不存在明显的生态隔离和季节隔离等交配前生殖隔离机制。 在室内对两种牡蛎进行2×2完全双列杂交,并通过ITS1基因的克隆测序验证杂种后代。双列杂交受精实验采用多亲本混合交配的方式(即每个物种的卵子或精子均来自多个个体),共进行7次重复。结果表明,熊本牡蛎的卵子能够被近江牡蛎的精子以较低的受精率(24.6%)受精,且形成的后代确实为两个物种杂交产生,而反方向不能受精。 幼虫和稚贝生长存活的双列杂交实验共进行3次重复。估测受精率、受精卵的孵化率,第1至29日每两天测量一次D形幼虫的壳高和密度。结果表明杂交幼虫(熊本牡蛎♀与近江牡蛎♂的杂交,SA)的受精率(12.5%)显著低于(P < 0.05)熊本牡蛎(75.4%)和近江牡蛎(84.5%)纯种对照组;而孵化率与对照组无显著差异(P > 0.05);自受精至29日龄,杂交幼虫壳高的生长速度明显低于纯种对照组(P < 0.05);但是存活率与熊本牡蛎无显著差异(P > 0.05)。杂交幼虫附着变态期间死亡率高;93日龄,熊本牡蛎有10.08%的匍匐期面盘幼虫存活至稚贝,显著大于(P < 0.05)近江牡蛎(2.18%)和杂交幼虫(0.76%);杂交稚贝壳高显著小于(P < 0.05)纯种对照组。稚贝在海区挂养3个月。与挂养前相比,杂交稚贝在潮下带的存活率为19.2%,125个稚贝仅存24个,壳高平均增加2.15 mm。熊本牡蛎在潮间带的存活率达到65%,壳高平均增加3.99 mm。近江牡蛎在潮下带的存活率达到85.7%,壳高平均增加5.22 mm,在潮间带的存活率仅10.9%,壳高平均增加3.28 mm。受精6个月后,所有杂交稚贝仅剩3枚,运回实验室暂养一段时间后全部死亡。 设置20、25、30、35共4个盐度梯度,估算双列杂交组合在不同盐度下的受精率、孵化率、7日内的存活率和壳高生长,实验共进行3个重复。结果表明,杂交组合在4个盐度下的受精率(平均为11.2%)均显著低于(P < 0.05)熊本牡蛎(75.0%)和近江牡蛎(77.5%)纯种对照组;而孵化率与对照组无显著差异(P > 0.05);杂交组合在盐度35时的孵化率(85.0%)显著大于20(49.6%)、25(51.3%)和30(55.4%)三个盐度梯度。7日龄杂交幼虫(10.5%)和近江牡蛎(11.4%)的存活率显著小于(P < 0.05)熊本牡蛎(30.3%);杂交幼虫的壳高(75.7 μm)显著小于(P < 0.05)熊本牡蛎(81.5 μm)和近江牡蛎(85.6 μm)对照组。两因素方差分析表明,杂交组合方式对受精率、孵化率、7日龄存活率和7日龄壳高均有显著影响,盐度对7日龄壳高的影响显著。 实验结果表明,江苏小庙洪牡蛎礁上的熊本牡蛎和近江牡蛎之间在分布空间上存在重叠区域,繁殖时间也存在重叠,并未产生明显的生态隔离和季节隔离。二者之间存在不对称性杂交,熊本牡蛎的卵子能够与近江牡蛎的精子以较低的受精率受精,而反方向完全不亲和。杂交幼虫在受精率上存在显著劣势;但是受精卵的孵化率与纯种受精卵无显著差异;杂交幼虫在生长上也存在显著劣势;而存活率与熊本牡蛎无显著差异;杂交幼虫附着变态期间大量死亡,存活下来的稚贝生长缓慢,死亡率高。表明熊本牡蛎和近江牡蛎之间即存在交配前的配子不亲和性隔离,又存在交配后隔离,主要表现为杂种不活。

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TO understand possible reproductive interaction between Crassostrea ariakensis (Fujita, 1913) and C. sikamea (Amemiya, 1928), which coexist ill estuaries of China and Japan, we conducted 2 X 2 factorial crosses between the two species. Asymmetry in fertilization success was observed where C. sikamea eggs can be fertilized be C. ariakensis the receprocal cross resulted in no fertilization. Fertilization Success ill C.sikamea female X C. ariakemvis male (SA) crosses was lower than that in the two intraspecific crosses and produced larvae that had similar growth the rate as their maternal species during the first nine days because of maternal effects. After that, genome incompatibility casted negative effects on the growth and survival of the hybrid larvae. Most hybrid larvae died during metamorphosis. but a small number of spat survived. Genetic analysis revealed that the survived SA spat contained DNA from both species and were the hybried. This study demonstrates that hybridization between C. ariakensis and C. sikamea is possible in one direction.

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Food Sources of three filter-feeding bivalves from two habitats (intertidal oyster Crassostrea gigas, mussel Mytilus galloprovincialis. and subtidal cultured scallop Chlamys farreri) of Jiaozhou Bay (Qingdao,China) were determined by fatty acid and stable isotope in analysis. Cultured scallop was characterized by significant diatom markets such as 16:1/16:0 close to 1 and high ratio of 20:5(n - 3)/22:6(n - 3), hence we assume that the scallop mainly feeds on diatoms. Fatty acid biomarkers specific to bacteria and terrestrial materials were also found in considerable amounts in scallop tissue, which suggested that there were Substantial bacterial and terrestrial input into the food of the species. Intertidal oyster and mussel, however, exhibited significant flagellate marker. 22:6(n - 3). and lower level of diatom markers. which indicated that flagellates are also part of intertidal bivalves' Planktonic food Sources: meanwhile, high level of Chlorophyta fatty acid marker, Sigma 18:2(n - 6) + 18:3(n - 3), suggested that Ulva pertusa (Chlorophyta) seaweed bed supplied important food sources to intertidal bivalves. Additionally, result of stable isotope analysis showed that phytoplankton contributed 86.2 to 89.0% to intertidal bivalves' carbon budget; macroalga U. pertusa origin source had a contribution of MIX, to 11.0%, which indicated its role Lis in important supplemental food source to intertidal bivalves. From this study. it is concluded that the dietary difference of three bivalves probably relates to the different potential food sources in the scallop farm and intertidal zone in Jiaozhou Bay.