蓬莱玉参早期发育的形态学观察

本研究对仿刺参(Apostichopus japonicus)的一个特殊品系蓬莱玉参产卵、受精及胚胎和幼体发育过程进行显微观察,并与普通仿刺参进行比较。在19~21℃水温下,蓬莱玉参受精卵分别在受精12 min和24 min后释放第一、二极体,1 h后卵裂成2细胞期,之后每30 min左右完成一次卵裂,6 h后进入囊胚期,19 h后发育成原肠胚;40 h后进入耳状幼体阶段,在其后侧臂的一端出现一个不规则形的石灰质骨片,并发现其位置与水体腔处于同一侧这一规律;5 d和8 d后发育为中耳状幼体和大耳状幼体,10 d后变态发育为樽形幼体,骨片由不规则状发育为齿轮状,并出现第二个石灰质骨片;12 d后发育为五触手,14 d后发育成稚参,40 d后发育为幼参。蓬莱玉参胚胎和幼体发育时序与当前已报道的仿刺参无显著差异,但从幼参开始蓬莱玉参通体始终为白色,而普通仿刺参在45日龄时体表局部出现色素,疣足处较为明显,60日龄幼体一半以上全身布满色素。蓬莱玉参因通体纯白色而受到了众多养殖企业和研究领域的关注,本文的结果为其今后的研究奠定了可靠的理论基础。     

多肠目薄背涡虫的胚胎发育

薄背涡虫(Notoplana humilis)的产卵高峰期在春末夏初。胚胎发育为螺旋式卵裂、外包法形成原肠胚,以大卵裂球储存卵黄。14~16℃下约20d左右幼虫由卵膜中孵化,但不是典型的牟勒氏幼虫。幼虫经历一周左右的浮游生活和两周左右的底栖生活后,逐渐发育为涡虫幼体。     

深圳宋卡湖根管虫(多毛纲:龙介虫科)个体发育的初步观察

对分布于中国深圳的宋卡湖根管虫Ficopomatus talehsapensis Pillai,2008进行了实验观察.结果表明:1)雌雄异体,精子或卵从鳃冠基部喷射至水中,体外受精,繁殖力强,受精后约0.8h开始卵裂,生活史经历早期胚胎发育、担轮幼虫、后担轮幼虫、游毛幼虫、后游毛幼虫、刚节幼体及成虫;2)鳃丝具呼吸、感觉、滤食功能,以单细胞藻类和有机碎屑为食;3)担轮幼虫至成体均具眼点,但视觉功能退化;4)对水环境的适应能力极强.讨论了根管虫对生境水质的影响.     

甲状腺激素对蝌蚪变态发育的影响

蝌蚪是青蛙的幼体,它是由青蛙的受精卵经4～5d的发育而形成的。蝌蚪在水中生活,主要吃植物性食物。蝌蚪生长到一定程度,即开始变态。在变态期,内、外部各器官由适应水栖转变为适应陆栖生活。在外观上．尾部逐渐萎缩,最后趋于消失,成对的附肢代替了鳍。由孵化出蝌蚪到变态完成,形成成体幼蛙,大约需时3个月左右。幼体蝌蚪变为成体青蛙的变态过程包括了许多重要的生理和基因调控的变化。     

富营养化对白洋淀底栖-浮游耦合食物网结构和功能的影响

国际湖沼学的长期研究发现,一个完整的湖泊生态系统应包括底栖食物网和浮游食物网,而营养条件变化会显著改变浅水湖泊中底栖-浮游食物网的结构和功能。为了明晰富营养化对浅水湖泊底栖-浮游耦合食物网结构和功能的影响,以浅水草型湖泊——白洋淀为研究区,运用野外监测和ECOSIM与ECOPATH(Ew E)模型相结合方法,构建白洋淀底栖-浮游耦合食物网的概念模型,模拟1982—2011年间富营养化对白洋淀底栖路径和浮游路径的结构和功能影响:(1)野外监测的结果表明,从1999年至今白洋淀一直处于富营养化状态;(2)Ew E模型模拟结果表明1982—2006年,总生物量呈下降趋势,下降比例达66.38%;能流路径从以底栖路径为主转变为以浮游路径为主;(3)运用Pearson相关分析,结果表明:浮游植物与TN(r=0.67,P0.01)和TP(r=0.37,P0.05)呈显著正相关,而底栖藻类和大型沉水植物与TN(r=0.77,P0.01;r=0.67,P0.01)和TP(r=0.54,P0.01;r=0.36,P0.05)呈显著负相关。富营养化是白洋淀底栖初级和次级生产力向浮游初级和次级生产力转变的主要驱动力。采用科学的方法准确评估富营养化对湖泊底栖-浮游耦合食物网结构和功能的影响,可为湖泊生态系统管理提供技术和方法支持。     

海南岛近岸沉积物中的有孔虫特征与分布

对位于海南岛近岸7-170 m水深、180个站位沉积物表层样的有孔虫分析表明,研究区浮游有孔虫类型较少、共发现浮游有孔虫19种,单个站位最多含有浮游有孔虫16种,而且浮游有孔虫含量(丰度)亦较低.底栖有孔虫则较为丰富,仅在较粗砂中底栖有孔虫丰度相对较低.常见近40多个底栖有孔虫属种,多数样品中以含有螺旋式与平旋式玻璃质底栖有孔虫为主,少数样品以胶结壳、列式玻璃质壳或大型底栖有孔虫为优势特征.本研究在详细阐述了底栖有孔虫主要特征属种的基础上进行了有孔虫分区,从而揭示其所包含的环境意义.     

巴布亚硝水母无性生殖过程及形态变化北大核心CSCD

以巴布亚硝水母(Mastigias papua)为研究对象,观察了水螅体无性生殖产生类浮浪幼虫胞芽、类浮浪幼虫胞芽变态发育为水螅体、水螅体横裂产生碟状体以及碟状体发育为水母体的过程和形态变化。25℃时类浮浪幼虫胞芽经过93 h后变态发育为水螅体。换用带有虫黄藻的天然海水并将培养温度从25℃升至27℃后,水螅体开始横裂,萼部触手环下方产生缢痕。水螅体横裂开始47 h后,缢痕更加明显,其上方部分发育为碟状幼体,后期碟状体搏动越来越频繁,最后释放。释放后的碟状体在实验室培养条件下21 d后可发育为水母幼体。巴布亚硝水母虽然只有产生类浮浪幼虫胞芽一种无性生殖方式,但繁殖速度较快,27℃时1个水螅体平均1 d可产生1.7个类浮浪幼虫胞芽,类浮浪幼虫胞芽可在3或4 d的短时间内附着变态。     

三疣梭子蟹胚胎发育过程中肝胰腺的发生与卵黄物质利用的关系

通过对三疣梭子蟹胚胎进行连续采样和组织切片,系统研究了三疣梭子蟹胚胎发育过程中卵黄囊和肝胰腺的发生与卵黄物质利用的关系。结果表明:(1)三疣梭子蟹胚胎的卵黄岛和卵黄囊结构分别出现在原肠期和无节幼体期,胚胎从原肠期至卵内第一期溞状幼体期,始终存在卵黄岛结构,且卵黄岛中的卵黄物质不断被分解和利用. (2)卵内第二期溞状幼体后,卵黄囊分为两个区域,卵黄囊壁中出现肝胰腺细胞(柱状上皮细胞),此时肝胰腺前体已开始形成,卵黄岛开始融合. (3)卵内第三期溞状幼体阶段,卵黄囊发育成一双肝胰腺,由于肝胰腺中的卵黄物质互相融合,卵黄岛结构消失。此阶段胚胎对卵黄物质的利用加快, 卵黄物质中存在许多空泡状结构;(4)胚胎发育进入孵化前期后,肝胰腺腔内的卵黄物质极少,而初孵溞状幼体肝胰腺腔内卵黄物质已完全消失,肝胰腺为一对囊状结构。这些结果表明在三疣梭子蟹胚胎发育从原肠期到孵化前的过程中,卵黄岛和肝胰腺细胞对于卵黄物质分解和利用起着十分重要的作用。     

绢丝丽蚌寄生变态发育的研究

绢丝丽蚌钩介幼虫在雌蚌外鳃中发育成熟后于冬季排放到体外,而后寄生到宿主鱼的鳃丝进行变态发育,寄生期历时近4个月.寄生后3d,内、外足丝消失;35d后,肉足形成;90d后,肠、闭壳肌、肾脏和鳃原基等生成;壳面加厚且外凸.次年春季,钩介幼虫变态发育成大小为253.37×273.26×179.96μm的稚蚌,脱离鱼鳃营独立生活     

南草蜥胚胎生长及物质和能量动用

用3种水热条件下(3温度×1湿度)孵化南草蜥(Takydomus sexlineatusDaudiin)卵以观测孵化卵质量变化、卵大小、孵化期、胚胎发育及孵出幼体特征。孵化过程中, 每5 d测定卵质量和大小。初生幼体称重后冰冻处死, 解剖分离为躯干、剩余卵黄和腹脂肪体, 65 ℃恒温干燥后称重。不同孵化温度对孵化期的长短有明显影响, 孵化期随孵化温度升高而缩短, 24 ℃平均41.8 d、27 ℃平均35.4 d、30 ℃平均34.0 d。卵孵化到14 d肉眼可见胚胎, 此后胚胎发育变化明显加速。孵化温度显著影响孵出幼体的质量、大小。本实验的受精卵在24 ℃、27 ℃中孵出的幼体质量较大。24 ℃、27 ℃发育的胚胎对卵黄的利用最充分, 剩余卵黄少。     

AChE及M1 受体在柄袋沙蠋胚胎和 幼虫中的免疫组化定位

采用免疫组织化学S-ABC法和兔抗鼠抗体研究了乙酰胆碱酯酶(AChE)及M1受体在柄袋沙蠋(Arenicola brasiliensis)胚胎和幼虫的分布.结果表明,ACNE及M1受体在柄袋沙蠋胚胎和幼虫中分布非常广泛,从未受精卵开始,直至研究的5刚毛节幼虫均有分布,但不同发育阶段分布的情况不同.卵裂期主要分布于细胞膜...     

Feeding biology of the pelagic larvae of Marenzelleria cf. viridis (Polychaeta: Spionidae) from the Baltic Sea

Phytoplankton < 20 µm was a principal dietary component of the larvae of Marenzelleria cf. viridis. Maximum ingested particle size increased as animal size increased, reaching a maximum diameter of 80 µm for larvae with 6 to 10 setigers. The larvae started ingesting particulate matter at the 1-setiger stage and were able selectively to ingest phytoplankton and polystyrene particles of various sizes. Larvae in the 6 to 10-setiger size group did not differ from those in the 11 to 17-setiger size group in respect of size selectivity for polystyrene particles. The gut passage time for Chlorella vulgaris was 20 min. The ingestion rate was limited by food concentrations even at concentrations much higher than those encountered in the natural biotope, saturation being reached at a concentration of 28.5 times 10⁶ cells ml^-1 (117.7 mg C l^-1. The low maximum filtration rate of only 1.19 µl ind.^-1 h^-1 indicates that the filtering capacity of the larvae is low. The larvae are still capable of food uptake at 1 °C. Further experiments demonstrated that larval growth and survival were strongly dependent on both food concentration and quality. Larval growth was food-limited under biotope conditions of the Darss–Zingst Boddens and even more so under Baltic Sea conditions. The results indicate that Marenzelleria cf. viridis is a species adapted to eutrophic conditions prevailing in brackish waters.     

Effects of the desiccation on Biomphalaria tenagophila (Orbigny, 1835) (Mollusca) infected by Schistosoma mansoni Sambon, 1907

Specimens of Biomphalaria tenagophila exposed to miracidia of Schistosoma mansoni were submitted to different desiccation periods as follows: group I: 24 h after exposure, desiccated for 28 days; group II: after cercariae elimination, desiccated for 7 days; group III: 21 days after exposure, desiccated for 7 days; group IV: 14 days after exposure, desiccated for 14 days; group V: 7 days after exposure, desiccated for 21 days. From the obtained data it was verified that desiccation was not capable of interrupting the development of larvae of S. mansoni in mollusks. A delay in the development of S. mansoni larvae in groups I, III, IV and V was observed. A pause was verified in the development of S. mansoni larvae in groups II, III, IV and V. Some larvae, in groups I, III, IV and V, did not suffer as a result of desiccation and continued their development. Larvae in the cercariae stage were shown to be more sensitive to desiccation. It was possible to obtain clearing of mollusks infected by sporocysts II and cercariae using a period of 7 days of desiccation.     

Development of the sand dollar <Emphasis Type="Italic">Scaphechinus mirabilis</Emphasis>

Under laboratory conditions, the development of larvae of the sand dollar Scaphechinus mirabilis (Agassiz) took 28.5–29 days from fertilization to settling and the end of metamorphosis at a temperature 20°C and salinity 32.2–32.6‰ The cleavage divisions were completed in 12 hours after fertilization (AF) by the release of free swimming ciliary blastula from the egg membrane. The larvae attained pluteus I stage with one pair of arms at an age of 40 hours. In 4.5–5 days the pluteus II stage with three pairs of arms, and in 9 days the pluteus III stage with four pairs of arms were formed. On the 20–21st day AF the larvae developed a vestibule, in which the adult skeleton rudiments, spicules, plates and pedicellariae were formed on the 26–27th day AF. The size of the larvae at an age of 22.5 days was 1064.3 ± 44.7 μm. The settling of larvae was recorded on the 28–29th day of development. Most of the larvae completed their metamorphosis in 4.5–5 hours after settling.     

Development of the starfish <Emphasis Type="Italic">Asterias amurensis</Emphasis> under laboratory conditions

Under laboratory conditions the development of the starfish Asterias amurensis Lütken from Vostok Bay (Sea of Japan) was studied at 14 and 17°C. At 14°C and a salinity of 31.6–32.6, ciliated coeloblastulae hatched from egg envelopes 19 h after fertilization. At this temperature the development proceeded slowly and stopped at the stage of bipinnaria. At 17°C and normal salinity of seawater, the development of A. amurensis was successful. The swimming blastula appeared in 14 h. It took 30.5 h for the embryos to reach the gastrula stage. The larvae began swimming in a horizontal position with the apical tip ahead. The dipleurula appeared at 60 h. These larvae began feeding. At 71 h after the beginning of development, the early bipinnaria has developed. In the larva, the edged ciliated band, the preoral plate, and the anal plate were already formed. At the age of 4.2 days, the larvae reached the stage of bipinnaria and the brachiolaria stage developed by 26–28 days after fertilization. The larvae had three identical brachiolar arms with attachment papillae on their tips and an attachment disk. In 37–44 days (at 17°C) the pelagic phase of A. amurensis development was completed by the attachment of larvae to the bottom plates and termination of metamorphosis. Most likely, the specificity to a substrate is not expressed in the brachiolaria of A. amurensis. They can settle on almost any hard substrate which is coated with a bacterial film. The newly settled juvenile starfish had five well-developed arms and moved using their ambulacral podia.Original Russian Text Copyright © 2005 by Biologiya Morya, Kashenko.     

The Larval Development of the Chiton <Emphasis Type="Italic">Deshayesiella curvata</Emphasis> (Carpenter in Dall, 1879) (Mollusca: Polyplacophora)

Chronological study of the larval development of the chiton Deshayesiella curvata with sketching of the first stages of egg division and embryos up to the seven-valved shell stage is presented for the first time. D. curvata exhibits pelagic development with lecithotrophic larvae. Larval eyes form at the age of 3 days; at the age of 6 days, a Schwabe organ appears near the eyes in the form of two pigmented spots. Chitons at the stage of seven-valved shell have larval eyes, as well as the Schwabe organ.     

DEVELOPMENTAL MODE AND SPECIES GEOGRAPHIC RANGE IN REGULAR SEA URCHINS (ECHINODERMATA: ECHINOIDEA)

Among marine benthic organisms, the ability to disperse, primarily during the larval stage, is widely thought to influence the extent of species geographic range. Because related species often differ in their modes of larval development (pelagic, feeding larvae; pelagic, nonfeeding larvae; or brooded development), and these can have dramatically different planktonic intervals, the mode of development may influence geographic range. A global survey of 215 regular echinoids shows that species with pelagic, feeding larvae have significantly larger ranges than those with pelagic, nonfeeding larvae, but there is no difference in ranges between species with pelagic, nonfeeding larvae and those with brooded development. These patterns are maintained within the Cidaroida and the Temnopleuroida, which account for the great majority of species with pelagic, nonfeeding development and brooded development. This limited effect of developmental mode on geographic range is found among species occurring predominantly in waters shallower than 100 m. For species occurring deeper than 100 m, there is no significant difference in geographic range related to type of development. The relationship between developmental mode and species range was examined more closely for circa 30 species for which the developmental period was known from laboratory observations. Adjusting the developmental times to a common temperature, 20°C, using realistic values for Q₁₀ from 2.0 to 3.6, showed a highly significant, negative correlation between egg volume and developmental time, indicating the potential for developmental mode to influence the planktonic interval. However, there was no relationship between time in the plankton, estimated from unadjusted developmental times, and extent of species geographic range. These results suggest that developmental mode may influence extent of species geographic ranges indirectly through the consequences of dispersal for gene flow or recovery from disturbance.     

Influence of salinity and temperature on growth and survival of the planktonic larvae of Marenzelleria viridis (Polychaeta, Spionidae)

In a series of experiments, the planktonic larvae of Marenzelleriaviridis (Verrill, 1873) were exposed to various combinationsof salinity (S = 0.6, 2.5, 5.0, 10 and 20) and temperature (T= 5, 10 and 20C) from the 1-setiger stage to the onset of metamorphosis(16- to 17-setiger stage). One-setiger larvae were unable tocomplete their development to metamorphosis at salinities below5. Metamorphosis was successful at salinities of 10 and 20,when the animals adopted a benthic life mode. Larval developmentwas more rapid at 10 than at 20, and was positively affectedby higher temperatures. Larvae exposed to a salinity of 3.5at the 4- to 5-setiger stage developed and completed metamorphosisto benthic juveniles despite the low salinity. These larvaedeveloped most rapidly at a temperature of 10C. The salinitytolerances (LC₅₀) of M. viridis larvae (t = 48 h), juvenilesand adults (t = 72 h in each case) were determined at 10C.The results showed that all development stages can toleratesalmities <1 The importance of constraints on developmentand tolerance to low salinities for the successful colonizationof oligohaline regions is shown and discussed in connectionwith other brackish-water organisms.     

Laboratory studies on larval growth ofPolydora ligni,Polydora ciliata,andPygospio elegans (Polychaeta,Spionidae)

The spionid polychaete speciesPolydora ligni, P. ciliata, andPygospio elegans were cultivated in the laboratory over several successive generations. A flow-through cultivation system forPolydora spp. is described. Duration of life cycles (time from hatching of the larva to first reproduction) and life spans (hatching to death) of these species were not significantly influenced by the degree of inbreeding nor by individual age of the parents. Minimum time from metamorphosis (15-setiger stage) to first hatching of offspring larvae (in the 3-setiger stage) at 18°C was 33 days inPolydora spp. and 81 days inPygospio elegans. Larval growth patterns are described in terms of number of setigers, body length, and biomass (dry weight, carbon, nitrogen, hydrogen), in relation to time after hatching. Regression models are proposed which link these measures of larval growth and, thus, may be used for conversions. Rates of development and growth show a high degree of variability in all three species, not only caused by variation in environmental factors such as temperature or food, but also among and within single hatches of larvae reared under identical conditions. Larvae were reared at constant temperatures (6°, 12°, and 18°C). Temperature affected larval growth inPolydora ligni more than inP. ciliata, and least of all inPygospio elegans. Only the latter species was able to develop at 6°C from hatching to metamorphosis. This differential response may be explained by differences in the natural spawning season of these species. Eleven phytoplankton species were tested as to their food values. A relative index of growth is proposed which compares the slopes of two growth curves (one standard and one test condition). The flagellateDunaliella tertiolecta was used as a standard food in these experiments. Most algal species were less suitable, and only the diatomThalassiosira rotula was consistently better food for spionid larvae thanD. tertiolecta.