长江干流圆筒吻(鱼句)的年龄与生长

根据551尾标本研究了生活在长江干流中圆筒吻(鱼句)的年龄与生长,并提出了资源合理利用建议.圆筒吻(鱼句)的鳞片可作为年龄鉴定的依据,年轮形成期主要在2～5月.圆筒吻(鱼句)的体长与鳞长呈直线关系,与体重呈幂指数关系,生长适合Von Bertalanffy生长方程.在1～2龄生长最快,为保护圆筒吻(鱼句)资源,应限捕体长200 mm以下的个体.     

瓦氏黄颡鱼年龄与生长的研究

根据在长江中游嘉鱼至新滩口江段采集的瓦氏黄颡鱼标本,对其年龄与生长进行了研究。以脊椎骨为年龄鉴定材料,胸鳍棘和耳石作为对照材料。透射光下,脊椎骨上较宽的暗带和较窄的亮带相间排列成同心圆环,一个暗带和一个亮带构成一个年轮。2—7月形成新年轮,脊椎骨上不存在幼轮。雌、雄鱼的脊椎骨半径与体长呈显著的正相关,回归方程分别为:L_♀=6.95 131.46R-10.12R~2,L_♂=18.06 113.64R-1.70R~2。体长与体重的关系方程分别为:W_♀=1.85×10~(-5)L~(2.98),W_♂=1.69×10~(-5)L~(2.55)。雌鱼为等速生长,雄鱼为异速生长。雌、雄鱼的生长存在差异,1龄后雄鱼生长明显快于雌鱼。雌、雄鱼适宜的生长方程分别为:♀:L_t=300.88e~(-1.67e~(-0.42t)),W_t=511.77e~(-4.98e~(-0.38t)),♂:L_t=415.15e~(-1.96e~(-0.33t)),W_t=777.53e~(-4.92e~(-0.32t))。雌鱼体长、体重生长的拐点年龄分别为1.22龄和4.22龄,雄鱼分别为2.04龄和4.98龄。     

长江干流圆筒吻鮈的年龄与生长

根据 5 5 1尾标本研究了生活在长江干流中圆筒吻的年龄与生长 ,并提出了资源合理利用建议。圆筒吻的鳞片可作为年龄鉴定的依据 ,年轮形成期主要在 2～ 5月。圆筒吻的体长与鳞长呈直线关系 ,与体重呈幂指数关系 ,生长适合VonBertalanffy生长方程。在 1～ 2龄生长最快 ,为保护圆筒吻资源 ,应限捕体长 2 0 0mm以下的个体     

长江干流圆筒吻鲍的年龄与生长

根据551尾标本研究了生活在长江干流中圆筒吻绚的年龄与生长,并提出了资源合理利用建议。圆筒吻绚的鳞片可作为年龄鉴定的依据,年轮形成期主要在2～5月。圆筒吻绚的体长与鳞长呈直线关系,与体重呈幂指数关系,生长适合Von Benalanffy生长方程。在1～2龄生长最快,为保护圆筒吻绚资源,应限捕体长200mm以下的个体。     

黄山九龙峰保护区尖头的年龄、生长和繁殖

于2011年5月至2012年4月逐月采集标本, 对黄山九龙峰保护区尖头 (Phoxinus oxycephalus)的年龄、生长和繁殖等生活史特征进行了研究. 尖头 雌、雄鱼性比为0.77:1, 与1:1差异显著. 根据体长频率分布来确定年龄组成,结果显示雌鱼和雄鱼的最大寿命分别为3龄和2龄, 均以1龄和2龄为优势年龄组. 1龄时的体长生长速度最大, 至2龄或3龄逐渐变缓. 雌、雄鱼的初次性成熟年龄均为2龄, 对应体长分别为93.0 mm和76.9 mm. 尖头 繁殖时间为4-7月; 绝对繁殖力较低(174-2151卵粒), 且在2、3年龄组间显著差异, 但相对繁殖力无显著的年龄组间差异. 尖头 的上述生活史特征, 可能体现了对局域环境条件(如营养贫乏、环境动荡及水文周期等)的生态适应性. 尖头 在我国东南部的高海拔地区呈零星分布, 种群数量小, 加之繁殖投入低下, 因此该物种在面临人类干扰和环境变化时极易濒危和灭绝.       

养殖美洲鲥的生长特性

通过对各周年生长阶段的养殖美洲鲥(Alosa sapidissima)体长、体重的测量与分析,研究了工厂化养殖美洲鲥的周年生长特性。养殖美洲鲥雌雄鱼的体长与体重关系均呈幂函数增长相关,其方程分别为,雌:W=0.8062×10~(-5) L~(3.1113)(n=122,R~2=0.997 5,P0.01);雄:W=1.0047×10~(-5) L~(3.0574)(n=125,R~2=0.997 5,P0.01),b均接近于3,呈等速生长;雌雄鱼生长均可分快速生长期(0~+龄)、稳定生长期(1~+龄)、生长衰老期(2~+龄)三个时期,雌鱼生长快于雄鱼。拟合出von Bertallanffy生长方程,雌:Lt=467.92(1﹣e~(-0.5748(t+0.1710))),Wt=1637.72(1﹣e~(-0.5748(t+0.1710)))~(3.1113);雄:Lt=389.21(1﹣e~(-0.7374(t+0.1975))),Wt=834.08(1﹣e~(-0.7374(t+0.7189)))~(3.0574)。雌雄鱼体重生长拐点分别位于1.517 8 a和1.224 7 a,属性成熟拐点,拐点前生长较快;拐点后,特别是性成熟后(2龄),2~+龄鱼的生长速度明显降低;同时,2龄鱼繁殖季节过后会出现大量死亡。建议商业化工厂化养殖美洲鲥以2龄前上市为宜。     

卡特拉鱼形态,食性和生长的研究

观测卡特拉鱼的形态特征和1—3龄鱼主要可量性状及其比例的变动。1—3龄鱼除主食商品饲料外,同时也食较大比例的浮游生物。着重对浮游生物的种类和比例进行了分析。肠长与体长呈直线相关。Y=6.38X-89.95。1—4龄鱼体长和体重相对生长率和生长指标都随年龄增加而逐渐下降。体长与体重呈曲线相关。W=0.00002261L~(3.0569)。采用 Von.Bertalanffy 生长方程分析其生长特性。方程参数 L_∞=821.2mm,W_∞=19616.6g,t_0=0.6年,K=0.3。体长生长不具拐点,生长速度随年龄增加而递减;体重生长具拐点,其值4.3年。此时体重生长速度达最大值。4、3龄前是生长旺盛期,此后进入生长缓慢期。     

高体鳑鲏的性选择问题研究

以高体鳑鲏为研究对象,分别设置个体大小不同的雌鱼和雄鱼进行性选择实验并验证性选择理论,对雌鱼的怀卵量和雄鱼的空间学习记忆能力也进行了检测。雄鱼对雌鱼的性选择实验结果表明,雄鱼对大个体雌鱼有明显的选择偏好;雄鱼选择雌鱼的次数及停留时间与雌鱼的体长、体高、产卵管长度等特征呈正相关。推测雄鱼是基于直接收益的角度,即最大限度的获得较多的后代及较高的后代存活率对雌鱼进行选择,因为大个体雌鱼拥有长的产卵管及绝对多的处于Ⅴ时相的成熟卵粒,可以提供较多的后代及较高的后代存活率。雌鱼对雄鱼的性选择结果表明,雌性高体鳑鲏对大个体雄鱼也表现出了明显的偏好;雌鱼选择雄鱼的次数及停留时间与雄鱼的体长、体高呈正相关;大个体雄鱼的空间学习记忆能力比小个体强,能更快捷地找到并占领质量好的河蚌而成为领域鱼。从直接收益的观点看,雌鱼选择大个体的雄鱼可能是因为大个体雄鱼可以更加容易、迅速和便捷地寻找到质量好的河蚌引领雌鱼进行产卵,从而保证子代的存活率。       

泥鳅繁殖和生长的研究

泥鳅的性成熟年龄:雌体为1—2龄,雄体为1龄。其性腺发育和性细胞特征,与鲤科鱼类基本一致。泥鳅属分批产卵类型的鱼类。在天然水域中,4—10月生殖。在一定范围内,泥鳅的生殖力随体长、体重的增长而提高。体长增长以第1—2龄最快,体重年增重率以第2龄为最高。因此,泥鳅的人工养殖周期以两年为佳;收获个体规格宜在体长为11cm以上。     

西藏浪错兰格湖裸鲤的年龄与生长

2017年7月—2018年5月,于西藏自治区昂仁县浪错采集268尾兰格湖裸鲤Gymnocypris chui开展种群年龄结构和生长特征研究。结果显示:雌、雄鱼体长与体质量的关系式分别为W♀=2.03×10-2L2.822(n=134,R2=0.969)、W♂=2.52×10-2L2.738(n=105,R2=0.966)。通过观察微耳石,发现样本由1~23龄组成;采用VonBertalanffy生长方程拟合雌、雄鱼体长、体质量生长方程:Lt♀=34.239[1-e-0.136(t+0.11)]、Wt♀=434.42[1-e-0.136(t+0.11)]2.822;Lt♂=32.201[1-e-0.136(t+0.287)]、Wt♂=338.8[1-e-0.136(t+0.287)]2.738;拐点年龄分别为7.52龄和7.12龄,对应体长分别为22.12cm和20.45cm,体质量分别为126.59g和97.71g。初步研究表明,兰格湖裸鲤生长慢、体型小,种群被破坏后不易恢复,亟待开展资源评估及保护工作。     

哈萨克族学生体质发育状况的10年比较分析

报道新疆阿勒泰地区1995年2589名城镇7—18岁哈萨克族(哈族)中小学生身高、体重、胸围、坐高、肩宽、骨盆宽6项体质发育指标的调查结果。男女生体质发育指标随年龄增加而增长,各项指标的年均增长值皆为男生大于女生。与1985年比较,哈族学生的身高、体重、胸围皆有不同程度增长。哈族男女生的身高突增年龄仍分别为14岁和10岁,但是其身高增长却不伴有相应比例的坐高增长,女生部分年龄组的肩宽和男女生各年龄组的骨盆宽呈现负增长,提示哈族学生的体型与10年前相比已经开始有所改变。     

普通夜鹰的繁殖习性及雏鸟的生长发育

2007年5～6月,对1窝普通夜鹰的繁殖习性及雏鸟的生长发育进行了观察.普通夜鹰育雏期约为18 d.雌、雄性都参与孵卵和育雏.育雏期每天有3个喂食高峰期,分别是晚上20:00～22:00、凌晨0:00~2:00、早上4:00~6:00.育雏过程中,亲鸟的领域性弱,护雏性强.初级飞羽在雏鸟出壳6 d后长出,但生长速度最快.     

圈养条件下仔狍的生长与发育

2003 年4 月至2004 年10 月对12 只狍东北亚种雌性生产的16 只仔狍进行了生长发育观察。记录仔狍出生日期,观察生长过程的毛色变化,定期检查牙齿生长状况,测定体尺和体重,所得数据采用SPSS13. 0 软件处理,绘制生长曲线并建立体长与体重的拟合曲线方程。结果表明,圈养条件下仔狍出生主要集中在5 月中旬至6
月中旬,出生时毛色呈暗棕黄色,身体两侧分布不规则的白斑,翌年换毛后白斑消失;出生仔狍的齿式为(0 03 0 /4 0 3 0)×2 = 20,成年狍的齿式为(0 1 3 3/4 0 3 3)×2 = 34,乳齿6 ～7 月龄开始脱换,8 ～9 月龄完成,脱换的顺序为中央切齿→两侧切齿→隅齿;(上、下颌)后臼齿的第一后臼齿2 月龄萌发、3 ～ 4 月龄生长完成,第
二后臼齿6 ～ 7 月龄萌发,8 ～9 月龄生长完成,第三后臼齿12 ～ 13 月龄萌发,14 ～ 15 月龄生长完成;乳齿的前臼齿从12 月龄开始脱换,14 月龄完成,脱换的顺序是上颌第一前臼齿和下颌第三前臼齿→上、下颌第二前臼齿→上颌第三前臼齿和下颌第一前臼齿;仔狍体尺增长率顺序为体长> 臀高> 肩高> 胸围> 腰围。仔狍体长与体重的拟合曲线方程是Y = 63.1084 - 0.0070x + 1.1e ^{- 6} x² - 3e^{- 11} x³ ,生长发育过程可分为生长快速期、生长缓慢期和雌雄狍生长差异期3 个阶段。     

Polymorphism of somatostatin gene and its association with growth traits in Chinese cattle

Somatostatins play a crucial role in the regulation of growth and development in vertebrates, especially muscle growth. We assessed the association of somatostatin gene polymorphisms with growth traits by PCR-SSCP (polymerase chain reaction-single strand conformation polymorphism) and DNA sequencing methods in 694 individuals from six Chinese cattle breeds. A novel single nucleotide polymorphism, G126A, was detected, and significant associations were found with body length, body height, hip width, heart girth, and hucklebone width index. Polymorphism of the somatostatin gene was found to be highly associated with growth traits in the Qinchuan breed at various ages. Gene frequency analysis showed significant differences among the breeds. Individuals with genotype AA had significantly lower body height, body length, hip width, and hucklebone width values compared to AG at 1.5 years old, and had significantly lower hip width, body length and hucklebone width compared to AG at 2 years old. At 2.5 years old, populations with genotype AA had significantly lower body length, hip width and hucklebone width than AG individuals, with the exception of the Luxi breed, in which two genotypes were found. The Luxi and Ximentaer crossbreed had the lowest frequency of the G allele, while the highest G allele frequencies were found in the Luxi breed.     

IRM-2近交系小鼠的生殖生长特性

目的获取IRM-2近交系小鼠的生殖生长特性的有关资料.方法ICR/JCL为母本,以615小鼠为父本杂交选育的近交系小鼠IRM-2,现已繁育至第38代.经过对其生殖、生长特性的观察和测定来取得相关资料.结果该小鼠出生后45d性成熟;繁殖能力强,平均每窝产仔数为8只以上,最高可达15只;生长发育迅速,出生后60d体重可达28g以上,各脏器重均高于亲代鼠.结论从各项指标来看,IRM-2小鼠是优良的近交品系小鼠.     

湘华鲮的生物学研究

湘华鲮是湖南沅江中上游的一种主要经济鱼类。主要以硅藻为食。1+龄鱼的平均体长为22厘米,平均体重为273.7克;2+龄鱼的平均体长31.3厘米,平均体重704克;3+龄鱼的平均体长为39.2厘米,平均体重1479克。渔获物中的年龄组成,以2+、3+、4+龄为主,渔获物中最大年龄和最大体重为6+龄、3400克。江河生长的湘华鲮,雌性性成熟年龄多为3年,雄性提早成熟一年;达性成熟年龄的雌性以Ⅳ期卵巢越冬;达性成熟年龄的雄性精巢,在冬季发育至Ⅴ期;它的生殖季节为4月底至5月下旬。在江河中有自然产卵场;4—5龄的雌性湘华鲮,成熟卵巢系数为8—17.6%,卵径约2.0—2.2毫米,每克卵粒数为293—321。       

The influence of basic body and hand anthropometry on the results of different throwing tests in young handball and basketball players

The aim of this study was to investigate the relationships between basic body and specific hand anthropometric parameters with some specific and non-specific throw test results in young male handball and basketball players. The subjects included 34 handball and 38 basketball players of the 10-11 years old age group, 39 handball and 22 basketball players of the 12-13 years old age group and 39 handball players of the 14-15 years old age group. Body height and body mass, arms' span, height with outstretched hands and sitting height were the basic anthropometric parameters to be measured. For hand anthropometry, 15 specific hand parameters were measured using the method presented by Visnapuu & Jürim?e (2007). Stepwise multiple regression analysis indicated that medicine ball throw results in the youngest age group are highly dependent on the body height (handball players) and body mass (basketball players). In the middle age group, the most important parameter from the hand anthropometry is TL (handball) or height with outstretched hands (basketball). In the oldest group of handball players, the medicine ball throw results were dependent on the P2 from hand anthropometry and sitting height. Quite different anthropometric parameters appeared to influence the handball or basketball throw results. In the youngest age group, most important were body height (handball) or LFL (basketball). In the middle age group, the most important was height with outstretched hands and in the oldest handball players LFL and sitting height. Handball or basketball pass on speed depended on the combination of body mass and FS5 and body height with height with outstretched hands (even 61.40%, R2 x 100) in the oldest age group. The results of passing the handball or basketball on precision were dependent on body height and P3 or P1 among basketball players in the youngest group. In the middle age group the combination of FS3 and body mass and LFL and height with outstretched hands were the most influential. Anthropometric parameters influence on the passing of the ball on speed or precision is lower in handball players compared with basketball players. Our conclusion is that the basic anthropometric parameters are slightly more important than hand anthropometry that influenced different throw tests results in young handball and basketball players.     

人工驯养下扬子鳄的生长规律

研究结果表明扬子鳄在饲养条件下的生长具有一定的规律性。饲养群体中,5龄以前的鳄生长速率较快,其中在2龄前生长速率最快,在5龄至7龄间生长速率明显减慢;鳄体长与体重之间呈正相关,两者在体长小于50cm时呈直线相关,体长大于50cm时呈曲线相关。不同性别的扬子鳄年生长状况不同,从5龄开始雌雄鳄体重出现显著差异,雄鳄重于雌鳄;从6龄开始雌雄鳄在体长方面的生长速率出现差异,雄鳄生长明显快于雌鳄;达到10龄后,雌雄鳄在体长和体重方面的增长均明显减慢,达到15龄时两者的体形已相差悬殊,雄性大于雌性。由von Berta-lanffy生长模型分析,雌鳄达到25龄而雄鳄达到35龄后,各自的体长几乎停止生长,雌鳄平均最大体长为173cm,雄鳄平均最大体长为219cm。在人工越冬下,除第一次越冬外,扬子鳄在越冬室内的冬眠中体况无明显变化,体能明显消耗出现在户外冬眠过程中。本研究为扬子鳄的科学化饲养提供理论依据。     

Statural growth in known-age African elephants (Loxodonta africana)

The shoulder heights of 224 females and 170 males, and hindfoot length of 236 female and 217 male known-age African elephants ( Loxodonta africana ) were measured, and growth curves constructed for each measure of size. A linear relationship between foot length and shoulder height was confirmed in simultaneous measures of 97 males and 110 females. Growth curves demonstrated the typical sexual dimorphism in both foot length and shoulder height, with males growing more rapidly than females from birth onwards. The size dimorphism in foot length and shoulder height becomes marked by the age of 10 years, with males on average being 60–70 cm taller than females at 65 years. This size dimorphism is produced through faster growth which continues for longer than does that of females. The variance in growth rates is slightly greater for females than for males. It is proposed that female growth after puberty is affected by a trade-off between growth and reproduction, while males who deviate markedly from typical patterns of growth may be subject either to mortality or energetic constraints limiting their potential variance.