泥鳅几项正常血液指标及其与性别的关系

以60尾泥鳅为材料,测定了红细胞数、白细胞总数、血红蛋白值、白细胞分类记数、红细胞脆性与红细胞大小等正常血液指标,并统计了性别对其血液指标的影响。结果如下:红细胞数为(227 28±43 96)×104个 mm3;白细胞数为(2 56±0 86)×104个 mm3;血红蛋白含量为(12 26±1 89)g 100ml;白细胞分类计数中淋巴细胞占(28 67±8 27)%,血栓细胞占(26 46±5 33)%,中性粒细胞占(43 83±8 37)%;而单核细胞、嗜碱性白细胞以及嗜酸性白细胞观测到的数目很少;红细胞最大抵抗强度为(0 31±0 04)g 100ml;红细胞大小(长径×短径)为:(11 50±1 55)μm×(8 66±1 29)μm;红细胞核大小(长径×短径)为:(5 59±1 04)μm×(3 90±0 89)μm。性别对红细胞数量及红细胞核大小均有显著影响,对其它的血液常数指标则无显著影响。     

达氏鳇外周血细胞的形态学研究

利用光镜和透射电镜技术研究达氏鳇(Kalugaa,Huso dauricus)外周血细胞的显微和超微结构、分类和计数。结果表明,在外周血细胞中可区分出红细胞、单核细胞、大淋巴细胞、小淋巴细胞、粒细胞和血栓细胞。红细胞卵圆形,大小为(11.22±0.56)μm×(7.92±1.01)μm;细胞质内可见到线粒体;单核细胞为圆形,大小为(10.55±1.61)μm×(9.38±2.04)μm;胞质内空泡较多,有的直接与细胞外相通;大淋巴细胞有指状胞凸,大小为(8.09±1.14)μm×(7.22±1.65)μm;小淋巴细胞有伪足样胞凸,大小为(7.22±1.35)μm×(6.31±1.24)μm;血栓细胞圆形,大小为(4.82±0.68)μm×(4.03±0.81)μm;核质比较大,未发现任何细胞器。嗜中性粒细胞的大小为(11.84±1.38)μm×(10.34±1.31)μm,含有多种形态的细胞核及着色和大小不同的颗粒。嗜酸性粒细胞的大小为(11.26±1.35)μm×(10.16±1.29)μm,嗜酸性颗粒数量较多、个体较大。红细胞密度为82.16×104/mm3~106.90×104/mm3,白细胞密度为1.91×104/mm3~4.55×104/mm3。大淋巴细胞、小淋巴细胞、粒细胞和单核细胞所占百分比分别为:0.12%~8.78%、26.35%~107.43%、3.22%~29.42%、0.69%~23.99%;各类血细胞从大到小依次为:粒细胞、单核细胞、红细胞、大淋巴细胞、小淋巴细胞和血栓细胞。     

半滑舌鳎血液指标分析

以20尾半滑舌鳎为材料，测定了红细胞教、白细胞总教、血红蛋白值、白细胞分类计数、红细胞脆性与红细胞及其核大小等正常血液指标，并统计了性别与血液指标的关系，结果如下：红细胞数为（207.88±56.25）×10^4个／mm^3；白细胞数为（9.39±5.54）×10^4个／mm^3；红细胞脆性（0.25±0.02）／g％；血红蛋白含量为（12.36±0.10）g／100mL；白细胞分类记教中单核细胞占1.51‰，中性粒细胞占（98.85±2.51）％，而淋巴细胞、嗜碱性白细胞以及嗜酸性白细胞观测到的数目很少；红细胞大小（长径×短径）为：（7.524±0.58）μm×（6.29±0.72）μm，红细胞核大小（长径×短径）为：（3.14±O.68）μm×（2.54±0.59）μm。红细胞长径、红细胞核长径、短径在雌、雄中有极显著差异，红细胞短径在雌、雄性别中有显著差异，其他的血液指标在雌、雄中则无显著差异。     

繁殖季节大鳍鳠血液学的初步研究

对嘉陵江繁殖季节内的大鳍鳠(Mystus macropterus)11项血液指标值进行了测定。其结果是:红细胞(RBC)的平均值为(1.246±0.208)×1012个/L;白细胞(WBC)的平均值为(2.643±0.696)×1010个/L;血红蛋白(Hb)的平均值为5.905±1.035 mg/100 mL;血球沉降率(ESR)的平均值为2.493±0.718 mm/h;红细胞比积(H t)的平均值为20.567%±4.974%;红细胞的脆性(Eof)在0.362%±0.035%氯化钠溶液中开始溶解,在0.211%±0.028%氯化钠溶液中完全溶解;红细胞的长径(CL)的平均值为12.356±1.579μm、短径(CS)的平均值为8.895±1.155μm;红细胞核的长径(NL)的平均值为4.523±0.607μm、短径(NS)的平均值为3.810±0.485μm;红细胞平均血红蛋白浓度(MCHC)的平均值为15.429%±5.154%;红细胞平均体积(MCV)的平均值为(1.671±0.453)×10-4μm3;红细胞的平均血红蛋白量(MCH)的平均值为(4.842±1.060)×10-8mg,且雌雄之间血液指标无显著性差异。此外,还将繁殖季节内大鳍鳠的血液指标与其它养殖鱼类进行了比较。     

淡水鲳六项血液指标的测定及血细胞结构的显微观察

本文对淡水鲳六项血液指标进行了测定,结果是红细胞(RBC):179×10~4/mm~3;白细胞(WBC):7.22×10~4/mm3,血红蛋白含量(Hb):6.4g/100ml;红细胞脆性(开始溶×完全溶):0.333Nacl％×0.217Nacl％;红细胞大小(长×短):13.69×10.20um~2;红细胞核大小(长×短):5.51×3.39um~2。白细胞的百分式中以淋巴细胞为主,嗜中性细胞次之,嗜碱性、嗜酸性粒细胞和单核细胞数量极少。此外,还对淡水鲳的血液指标与其它养殖鱼类的血液指标进行了比较,并对其数量、形态、生理功能之间的关系进行了探讨。     

二倍体与三倍体虹鳟(Oncorhynchus mykiss)红细胞及部分血液指标的比较

对三倍体和二倍体虹鳟(Oncorhynchus mykiss)的红细胞大小(长、短径值和体积)、形态及部分血液指标(红细胞数、血红蛋白、红细胞压积、红细胞脆性和白细胞数)进行了比较。结果表明:三倍体虹鳟红细胞体积与二倍体比值为1.51∶1,细胞核大小与二倍体比值为1.49∶1,与理论值(1.5∶1)比较均无显著差异(P>0.05)。二倍体红细胞短径/长径比值为0.63,呈现出椭圆形;三倍体红细胞短径/长径比值为0.60,呈现出明显的长椭圆形,并有19%的红细胞有哑铃形或分裂的细胞核,这可作为区别二倍体鱼类的一个重要鉴定标志。三倍体虹鳟的红细胞数、红细胞压积和红细胞脆性明显小于二倍体(P<0.05),而血红蛋白与白细胞数与二倍体比较无明显差异(P>0.05)。     

高原型藏羊七项血液生理指标的测定

对果洛州玛沁县50只高原型藏羊74血液生理指标进行了测定。结果表明:高原型藏羊红细胞数(RBC),[(10.67±1.05)×1012/L];白细胞数(WBC),[(8.04±0.58)×109/L];红细胞压积(PCV),(0.35±0.03)L/L;血红蛋白含量(Hb),(128.48±11.99)g/L;红细胞平均体积(MCV),(32.76±4.60)fL;(MCH),(12.14±1.51)pg,(MCHC),(374.06±45.79)g/L。同时,在性别组间各项生理指标差异不显著(P>0.05)。     

斑鳢与乌鳢血液生理生化指标的比较分析

采用K-4500型血细胞分析仪和OLympus Au400生化分析仪及参照人的血液性状分析法,测得斑鳢的红细胞(3.27±0.54)1012/L比乌鳢(3.71±0.51)1012/L的低,平均红细胞体积(128.5±3.62)fl比乌鳢(124.05±3.06)fl的高。血红蛋白(148.7±9.33)g/L含量比乌鳢(115.0±7.25)g/L高,斑鳢的细胞脆性比乌鳢的小。生化指标中斑鳢除血糖含量比乌鳢大外,血清总蛋白含量(37.30±4.06)g/L、白蛋白含量(21.67±3.39)g/L、血清中甘油三酯的含量(0.53±0.06)mmol/L、胆固醇(4.37±0.68)mmol/L都比乌鳢低。分析表明斑鳢的活动性、抗病力比乌鳢的强。     

青石爬鮡血浆生化指标、血细胞分类与发生

对40尾野生青石爬鮡进行了血液生化指标、血细胞分类与发生研究。测得血浆的总蛋白为(48.35±3.60) g/L，白蛋白为(8.73±0.54) g/L，球蛋白为(39.63±3.10) g/L，血浆白蛋白与球蛋白比为(0.22±0.01)，甘油三酯为(5.05±2.14) mmol/L，总胆固醇为(16.66±3.64) mmol/L，极低密度脂蛋白为(1.01±0.43) mmol/L，葡萄糖为(5.27±2.43) mmol/L。血液生化指标检测结果表明，青石爬鮡血浆中总蛋白与球蛋白、甘油三酯与胆固醇较高，葡萄糖较低，具有活动量较大和冷水性鱼类的特点，主要利用脂肪和蛋白质作为能量。细胞学显示出其外周血液包含红细胞，核影，淋巴细胞，血栓细胞，嗜中性粒细胞和单核细胞。血涂片计数为红细胞96.58％，其中成熟红细胞占65.92％，幼稚红细胞占30.66％。白细胞为3.42％，其中嗜中性粒细胞0.14％、单核细胞0.07％、淋巴细胞2.37％、血栓细胞0.85％。白细胞中淋巴细胞和血栓细胞数量较多。原始血细胞主要在中肾和头肾中，在脾脏中也有部分原始白细胞，而肝脏和外周血液中未见原始血细胞。中肾和头肾是青石爬鮡的主要造血器官，其中红细胞主要由头肾产生，白细胞主要由中肾产生。脾脏亦产生少量白细胞。     

点带石斑鱼血液指标、血细胞分类与发生的观察

对20尾点带石斑鱼进行了血液指标、血细胞分类和发生的研究。血液指标经测定:红细胞密度为(1.89±0.48)×106个/mm3,白细胞密度为(1.65±0.34)×104个/mm3;血红蛋白含量为(7.11±0.67)g/L;红细胞的渗透脆性为(0.54±0.02)%,红细胞比容为(36.7±0.67)%,红细胞沉降率为(2.50±0.25)mm/h。利用Wright’s-Giemsa混染法对点带石斑鱼外周血液以及肝脏、脾脏、头肾和体肾四种造血组织染色观察发现,在外周血涂片上可区分出红细胞(包括未成熟的红细胞)、血栓细胞、淋巴细胞、嗜中性粒细胞和单核细胞,未发现嗜酸性粒细胞和嗜碱性粒细胞。其中大淋巴细胞、小淋巴细胞、嗜中性粒细胞和单核细胞在白细胞中所占的比例分别为(23.13±6.99)%、(48.97±7.42)%、(21.03±4.42)%和(6.87±2.27)%。点带石斑鱼的头肾、体肾和脾脏可以产生各种类型的血细胞,是主要的造血器官;肝脏未观察到原红细胞。     

中华倒刺鲃、白甲鱼和岩原鲤精子的生理特性比较

对中华倒刺鲃(Spinibarbussinensis)、白甲鱼(Onychostomasimus)和岩原鲤(Procyprisrabaudi)3种鱼的鲜精在不同水溶液和不同浓度梯度的NaCl溶液中的活力以及精子形态、密度和精液pH值、浓度等进行了比较研究。结果表明:3种鱼的精液pH值都偏弱碱性,位于7·2~7·7之间;精液浓度依次为71·1%,76·1%和71%;精子头长依次为(3·89±0·53)μm,(2·98±0·08)μm和(6·42±0·59)μm,全长依次为(41·63±3·66)μm,(65·67±2·97)μm和(58·89±5·25)μm;精子密度依次为1·527×1010尾/mL,1·336×1010尾/mL和1·362×1010尾/mL。分析表明,3种鱼的精子大小与密度无相关性。在不同水溶液中,3种鱼的精子活力均以池塘水中最高;在不同浓度NaCl溶液中,3种鱼精子的最适浓度位于0·45%~0·55%之间,有效运动时间以中华倒刺鲃最高,为(85·23±12·02)s,其次是岩原鲤,为(50·45±6·89)s,白甲鱼最短,为(31·44±5·53)s。3种鱼的精子全长与精子活力存在负相关性,即精子越长,活力越低,精子越短,活力越高。     

饥饿对泥鳅某些血液指标的影响

对体长9·7~12·0cm、平均体重8·3g的泥鳅(Misgurnusanguillicaudatus)在正常摄食和饥饿4~16d状态下的血液指标进行了测定。结果表明:随着饥饿时间的延长,红细胞数量呈下降趋势,在饥饿的第4d、8d、12d和16d,红细胞数量分别是正常摄食时数量的67·5%,63·0%、61·3%和60·5%,差异极显著(P<0·01);红细胞的体积变大,饥饿到第16d时,红细胞的长径和短径分别比正常摄食时增加了2·8%和13·0%;白细胞数量呈上升趋势,在饥饿的第4d、8d、12d和16d,白细胞数量分别是正常摄食时数量的114·3%、121·7%、137·1%和139·4%;白细胞的体积逐渐变小,饥饿到第16d时,其长径和短径分别是正常摄食时的88·2%和89·4%,差异显著(P<0·05);血红蛋白含量在前8d的饥饿中是下降的,之后出现上升;红细胞的脆性在饥饿前期有所下降,后期则维持在一定水平;红细胞的沉降率随着饥饿时间的延长而有所加快,差异不显著。     

Changes in the pericellular connective tissue and breaking strength of the three types of muscles of the cultured carp Cyprinus carpio during storage in ice

To elucidate the structural changes in pink (P), white (W), and red (R) muscles during storage in ice, we measured the breaking strength and changes in pericellular connective tissues of cultured carp. The breaking strength just after killing was highest in R muscle (1.00 ± 0.20 N), lowest in W muscle (0.37 ± 0.07 N), and intermediate (0.84 ± 0.12 N) in P muscle. During the storage period, the breaking strength decreased first in R muscle, then in P muscle, followed by W muscle. The diameter of muscle fibers was greater in W muscle (113 ± 15 μm) than in P muscle (72 ± 3 μm) and R muscle (48 ± 2 μm). Destruction of the honeycomb structure of the pericellular connective tissue occurred most rapidly in W muscle and most slowly in R muscle. These results suggest that the interposing of P muscle fibers in the dorsal ordinary muscle contributes to the acceleration of post-mortem tenderization in fish.     

Sperm Motilities in Waigieu Seaperch,Psammoperca waigiensis: Effects of Various Dilutions,pH, Temperature,Osmolality, and Cations

The objectives of this study were to evaluate the effects of varying dilutions, pH, temperature, osmolality, and cations on sperm motility parameters in waigieu seaperch, Psammoperca waigiensis. The maximum velocity of average in path (VAP), percentage of motile cells (MOT), and duration of sperm motility (DSM) were observed when semen was diluted in artificial seawater (ASW) at a ratio of 1:100 (144.9 ± 0.6 µm/sec, 95.6 ± 0.4%, and 230.3 ± 2.3 sec, respectively), at 30 C (142.0 ± 0.6 µm/sec, 93.6 ± 0.4%, and 238.3 ± 0.9 sec, respectively), and pH 8 (144.8 ± 0.6 µm/sec, 93.3 ± 0.4%, and 234.0 ± 1.5 sec, respectively). Maximum VAP, MOT, and DSM were obtained in each solution containing 0.6 M NaCl (143.8 ± 1.0 µm/sec, 91.3 ± 2.0%, and 230.6 ± 4.2 sec, respectively), 0.6 M KCl (135.1 ± 3.1 µm/sec, 91.1 ± 3.1%, and 230.3 ± 3.7sec, respectively), 0.2M CaCl₂ (105.3 ± 4.7μm/sec, 47.9 ± 2.7%, and 120.7 ± 1.3 sec, respectively), 0.2 M MgCl₂ (107.3 ± 3.0 m/s, 42.1 ± 3.3%, and 120.3 ± 4.8 sec, respectively), and osmolality of 400 mOsm/kg (145.1 ± 2.5 µm/sec, 93.0 ± 2.1%, and 346.5 ± 4.4s, respectively). We used these mediums as artificial insemination media for fertilizing matured eggs. The results showed that the fertilization and hatching rates in 0.6 M NaCl (75.3 ± 0.6% and 57.0 ± 2.4%, respectively), ASW (70.8 ± 1.2% and 51.2 ± 1.8%, respectively), or 400 mOsm/kg (72.9 ± 1.8% and 55.3 ± 1.6%, respectively) were higher than that in seawater (63.9 ± 1.2% and 39.2 ± 3.9%, respectively). In conclusion, using 0.6 M NaCl, ASW, or 400 mOsm/kg as an artificial insemination medium is effective for fertilizing of waigieu seaperch.     

日本对虾杆状核病毒性传染病诊断技术

本文提出了分别用暗视野显微技术和透射电子显微技术快速确诊日本对虾杆状核病毒性传染病的方法。在暗视野显微镜下观察到的血淋巴中的病毒粒子大小约为0.5μm;胃表层上皮被病毒感染的细胞核明显地呈白色均质小体,直径10～15μm,球形或椭圆形,坏死细胞被囊化为棕色小块(约20～50μm)。病虾血淋巴和胃经负染制样在透射电子显微镜下观察病毒颗粒大小为400×150nm;核衣壳大小为390×85nm。     

引起池养异育银鲫高死亡率的粘孢子虫新种咽碘泡虫形态和分子分析

对近几年发生在江苏省盐城地区引起池养异育银鲫大批死亡的粘孢子虫进行了形态和分子等方面分析研究,发现该粘孢子虫主要特点是:孢子梨形,部分孢子后部外周包围有透明无色的膜状鞘和壳瓣底部内侧呈现1～6个"V"形缺刻,两个极囊大小不等,孢子前端内侧两个极囊间有一个细长的囊间突起,胚质中无嗜碘泡,孢囊大小10～25 mm,孢子长16.82±0.43(16.03～17.69)μm,孢子宽10.26±0.43(9.12～10.88)μm,孢子厚8.09±0.29(7.50～8.75)μm,孢子长宽比1.64±0.09(1.50～1.93);大极囊长8.66±0.25(8.25～9.16)μm、宽3.65±0.25(3.01～4.19)μm,小极囊长8.35±0.28(7.60～8.85)μm、宽3.58±0.23(3.09～4.11)μm,囊间突起长1.80±0.12(1.59～2.00)μm。特异性地寄生在异育银鲫的口咽腔上颚的咽组织内、具有寄主和寄生在咽部的专一性,PCR扩增得到1 576 bp的18S rDNA序列,GenBank登录号为JQ726700。该粘孢子虫与相近的其它粘孢子虫比较,孢子长分别与白鲟碘泡虫(Myxobolus psephurusi)和扭曲碘泡虫(M.twistus)无显著差异(P>0.05),与M.ampullicapsulatus、M.wulii和鳙碘泡虫(M.aristichthydis)分别有显著差异(P<0.05);孢子宽和厚、极囊长和宽分别与M.ampullicapsulatus、M.wulii、白鲟碘孢虫(M.psephurusi)、鳙碘泡虫(M.twistus)和扭曲碘孢虫(M.aristichthydis)有显著差异(P<0.05);分子系统树分析结果显示,与M.ampullicapsulatus在同一个分支中,亲缘关系最近。从孢子形态学、寄主的特异性、寄生部位的专一性以及18SrDNA序列等特点综合比较分析,表明该粘孢子虫为一新种,命名为咽碘泡虫Myxobolus pharynae n.sp.。     

Thelohanellus testudineus n. sp. (Myxosporea: Bivalvulida) infecting the skin of allogynogenetic gibel carp Carassius auratus gibelio (Bloch) in China

A Thelohanellus species was encountered during a survey on Thelohanellus diversity of Carassius auratus gibelio (Bloch) in China. The infection is characterized by the presence of large cysts of 1.4–3.2 cm in diameter in the skin of host. Mature spores were ampullaceous in frontal view and testudinate in lateral view, measuring 19.7 ± 0.7 (18.6–20.8) μm long, 7.6 ± 0.4 (6.6–8.4) μm wide and 7.3 ± 0.5 (6.6–8.8) μm thick. The single polar capsule was elongated pyriform, with 11.1 ± 0.5 (10.0–11.9) μm long and 5.3 ± 0.3 (4.3–5.8) μm wide. Polar filaments coiled with 7–8 turns. Scanning electron microscopy revealed a smooth spore surface with flat side and convex side. The sutural line was straight or ‘S’ like, running near the middle of the valves. Histologically, the large cysts consisting of numerous small plasmodia developed in the dermis of the skin. The BLAST search indicated that the newly obtained ssrRNA gene sequences did not match any available sequences in GenBank and phylogenetic analysis placed it in the Thelohanellus clade. Based on morphology and molecular differences with reported Thelohanellus spp., this parasite was described as a new species of genus Thelohanellus.     

Changes of sperm morphology,volume, density,and motility parameters in northern pike during the spawning period

Sexually mature males (BW?=?1600?±?150 g and TL?=?235?±?30 mm) of northern pike (Esox lucius L.) were randomly selected from a pond to record changes in their sperm quality parameters (spermatozoa morphology, sperm volume, density, and motility parameters) during the spawning season. The morphological and motility parameters changed significantly during the reproductive season with following trends. Only, head width was not changed during the spawning season. The longest spermatozoa and its flagellar length were found at the middle of spawning period (TL?=?38.24?±?0.37 μm and 35.14?±?0.26 μm) and shortest at the beginning of spawning period (TL?=?34.81?±?0.29 μm and 32.53?±?0.18 μm). Other morphological characters were always the lowest at the beginning of spawning period. Sperm volume was changed from 0.33?±?0.3 ml in February, 0.43?±?0.2 ml in March to 0.24?±?0.1 ml in April, and density from 16.2?±?0.2?×?109 spermatozoa ml^?1 in February, 19.4?±?0.2?×?109 spermatozoa ml^?1 in March to 4.8?±?0.2?×?109 spermatozoa ml^?1 in April. Same sperm velocity was observed in all spawning terms at 10 and 20 s after activation. Higher velocity was found at 30 and 40 s after activation in sperm collected at the middle and the end of spawning period. Significantly, higher percentage of motile sperm was observed at 20, 30, and 40 s after activation in sperm sampled at the end of spawning period. This study supports the hypothesis that longer spermatozoa swim faster.