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库氏索沙蚕(韦伯斯特)(多毛纲:沙蚕科)的幼体发育及习性

LARVAL DEVELOPMENT AND HABITS OF LAEONEREIS CULVERI (WEBSTER) (POLYCHAETA: NEREIDAE).

作者信息

Mazurkiewicz Michael

出版信息

Biol Bull. 1975 Aug;149(1):186-204. doi: 10.2307/1540489.

Abstract

The nereid polychaete Laeonereis culveri (Webster) reproduces in the atokal condition in the Mystic River Estuary, Connecticut. Females spawn demersal eggs, 135-162 µ in diameter, that do not extrude a jelly layer upon fertilization and that give rise to unciliated embryos. Embryogenesis leads directly to a 3-setigen larva in four days (at 22 ± 3° C; 30‰). The trochophore is suppressed due to the retarded development of locomotory cilia which do not appear until the 3-setiger larva has formed. Although provided with ciliary tracts and capable of swimming, L. culveri larvae are normally benthic in habit. They reside in burrows within the upper 2 cm of fine, flocculent sediments where they feed chiefly on benthic diatoms until developing past the 5-setiger stage after which they become non-selective deposit feeders. The primary function of the larval ciliature is to pass water currents through the burrow. In the laboratory, 3-to 5-setiger larvae alternately swim and crawl in the absence of sediments on in the presence of coarse sediments (particle diameters > 250 µ); but they readily burrow into and remain within fine sediments (particle diameters < 250 µ) even if the latter are relatively free of organic matter. Swim-crawl behavior also appears to be elicited under conditions of unfavorable water quality. When the sixth setiger forms, the larva is no longer capable of swimming by means of its cilia. Development beyond the 3-setger stage approximates that of other species except that L. culveri larvae are apparently unique in ultimately developing eight nototrochs (one per each of the first eight trunk segments). The nototrochs are retained and function in burrow ventilation until the 16-to 18-setiger stages when body undulations commence creating ventilation currents. Larval development is completed with addition of the eighth trunk segment. At this stage, the tentacular segment (first trunk segment) is incorporated into the peristomium and the first pair of parapodia are modified to form the posterodorsal tentacular cirri. Sigmoid growth curves resulted when either length or segment-formation was used as an indicator of growth among laboratory-reared worms. Sexually mature, laboratory-reared worms were only about one-half the length of sexually mature worms in a natural population. Thirty-two individuals (17 females, 15 males) of an F generation were reared to maturity and spawned after 168-198 days of development. F generation larvae were identical in morphology to those of the F generation.

摘要

多毛纲沙蚕科的库氏阔沙蚕(韦氏阔沙蚕)在康涅狄格州神秘河河口以无节幼体状态进行繁殖。雌虫产出沉性卵,直径为135 - 162微米,受精时不会排出胶膜,发育出无纤毛的胚胎。胚胎发育在四天内(22±3℃;盐度30‰)直接形成具3刚节的幼虫。由于运动纤毛发育迟缓,担轮幼虫阶段缺失,直到具3刚节幼虫形成时纤毛才出现。尽管具纤毛束且能游泳,但库氏阔沙蚕幼虫通常营底栖生活。它们栖息在细粒絮凝沉积物上部2厘米内的洞穴中,主要以底栖硅藻为食,直至发育到5刚节阶段之后,便成为非选择性的沉积物摄食者。幼虫纤毛的主要功能是使水流通过洞穴。在实验室中,具3至5刚节的幼虫在没有沉积物时或者在有粗沉积物(粒径>250微米)时会交替游泳和爬行;但它们很容易钻入细沉积物(粒径<250微米)并留在其中,即使后者相对缺乏有机物。在水质不利的条件下也会引发游泳 - 爬行行为。当第六刚节形成时,幼虫就不再能够通过纤毛游泳。除了库氏阔沙蚕幼虫最终发育出八个背纤毛束(前八个躯干节段各一个)这一点明显独特外,其超过3刚节阶段的发育过程与其他物种相近。背纤毛束一直保留并在洞穴通风中发挥作用,直到16至18刚节阶段身体开始波动产生通风水流。随着第八个躯干节段的增加,幼虫发育完成。在此阶段,触手节(第一个躯干节段)并入口前叶,第一对 parapodia 经过改造形成后背面触手须。当使用长度或节段形成作为实验室饲养蠕虫生长指标时,得到了S形生长曲线。实验室饲养的性成熟蠕虫长度仅约为自然种群中性成熟蠕虫的一半。F1代的32个个体(17只雌性,15只雄性)饲养至成熟,并在发育168 - 198天后产卵。F1代幼虫在形态上与F0代幼虫相同。

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