ARONSON L R
Zool Sci Contrib N Y Zool Soc. 1949;34(Pt. 3):133-58.
Qualitative descriptions and quantitative measurements of the patterns of reproductive behavior of the African mouthbreeding cichlid fish, Tilapia macrocephala (Bleeker), have been presented. These patterns have been grouped into three categories. The first, namely courtship, includes head-nods, approach-throat-puffs, body-quivers and tail-slaps. Most the females exhibited these courtship items during the observation periods, and at a relatively high frequency. The males performed these courtship acts at a considerably lower frequency. A high percentage of males showed some tail-slaps and body-quivers, and it is believed that if the entire spans of the pre-spawning activity of the pairs could have observed, all of the males would have performed these courtship patterns. On the other hand, it appears that a measurable portion of males do not head-nod or approach-throat-puff prior to the spawning. It is hypothesized that courtship behavior is an expression of the level of excitability of the individual. It may be thought of as a trophallactic process which through mutual stimulation serves to regulate the behavioral activities and physiological processes of the male and female so that well synchronized spawnings result. Nipping, which is closely related to courtship and which also appears to be mutually stimulating, was performed equally by the male female before the spawning, but nipping on the part of the female rises sharply directly after oviposition. Similar post-spawning increases on the part of the female were noted for all of the courtship patterns. It is suggested that the physiological changes following oviposition plus the presence of eggs are the factors responsible for this heightened activity. During the inter-spawning interval, a low level of courtship is in evidence, especially on the part of the females. The second group of reproductive patterns includes those acts which are concerned with the immediate preparation for spawing. Included here are nest-building, nest-passing, spawning-quivers, oviposition movements and the act of fertilization. Considerably more nest-building is exhibited by the female than by the male, but it is likely that all males do some nesting-building before every spawing. With passing-nest and spawning-quivers the frequency is somewhat higher for the males an hour or so before spawning, but at 15 minutes before spawning this relationship is clearly reversed, with the females at the height of their nest-passing and spawning-quivers. A significant correlation between male and female nest-passing during the first pre-spawning interval suggests that this behavior is mutually stimulating. The mean number of oviposition movements of the female did not differ significantly from the mean number of fertilization acts of the male. Moreover these behavior patterns are highly correlated, suggesting that the number of times the male fertilizes the eggs is partly related to and probably dependent upon the number of oviposition movements of the female. In contrast with the courtship patterns, behavioral items in the present category were not observed during the inter-spawning interval. The third category of reproductive acts are those associated with the care of eggs and young. Males start picking up eggs on an average of 1'3" frm the beginning of oviposition. Females, if given the opportunity, took the average 7'59". This is the apportioning mechanism whereby males usually incubate the eggs and females do so only on infrequent or special occasions. Similar quantitative differences were found in other phases of the parental pattern. Thus females gather up the spawn more slowly and are more prone to swallow the eggs. A low order positive correlation was found between the size of the female and the number of eggs laid during a given spawning. Since brood size shows no correlation with the size of the female, it is concluded that a greater mortality occurs in the larger broods. Incubating fish generally carry some gravel intermingled with the spawn, but it was not clear whether this bore any relation to the survival of the embryos. In the majority of vertebrates there are distinct qualitative differences between the patterns of reproductive behavior of the male and female. While both sexes have the neuromuscular mechanism capable of eliciting both the male and female patterns, bisexual of homosexual behavior is limited and generally appears under special conditions. Tilapia are exceptional in this respect insofar as there are not distinct qualitative differences between male and female in their sexual activities. However, there are marked quantitative differences in all of the patterns. Several previous investigators have analyzed cichlid mating behavior in terms of Lorenz's releaser concept. it is felt that even in the expanded and modified form presented by Tinbergen, this concept is still too restricted to form an adequate basis for the analysis of Tilapia reproductive behavior.
本文对非洲口育丽鱼科鱼类——巨头非鲫(Bleeker)的生殖行为模式进行了定性描述和定量测量。这些模式可分为三类。第一类是求偶行为,包括点头、靠近并鼓起喉部、身体颤动和拍尾。在观察期间,大多数雌鱼会表现出这些求偶行为,且频率相对较高。雄鱼表现出这些求偶行为的频率则低得多。高比例的雄鱼会有一些拍尾和身体颤动行为,据信如果能观察到配对产卵前的整个活动过程,所有雄鱼都会表现出这些求偶模式。另一方面,似乎有相当一部分雄鱼在产卵前不会点头或靠近并鼓起喉部。据推测,求偶行为是个体兴奋程度的一种表现。它可被视为一种交换食物的过程,通过相互刺激来调节雄鱼和雌鱼的行为活动及生理过程,从而实现同步产卵。轻咬行为与求偶密切相关,且似乎也具有相互刺激作用,在产卵前雄鱼和雌鱼都会进行轻咬,但产卵后雌鱼的轻咬行为会急剧增加。产卵后雌鱼在所有求偶模式方面都出现了类似的行为增加情况。有人认为产卵后的生理变化以及卵的存在是导致这种活动增强的因素。在产卵间隔期,求偶行为处于较低水平,尤其是雌鱼。第二类生殖模式包括那些与产卵直接准备相关的行为。这里包括筑巢、通过巢穴、产卵颤动、产卵动作和受精行为。雌鱼表现出的筑巢行为比雄鱼多得多,但很可能所有雄鱼在每次产卵前都会进行一些筑巢行为。对于通过巢穴和产卵颤动行为,在产卵前一小时左右雄鱼的频率略高,但在产卵前15分钟这种关系明显反转,此时雌鱼处于通过巢穴和产卵颤动行为的高峰期。在第一个产卵前间隔期,雄鱼和雌鱼通过巢穴行为之间存在显著相关性,表明这种行为具有相互刺激作用。雌鱼产卵动作的平均次数与雄鱼受精行为的平均次数没有显著差异。此外,这些行为模式高度相关,这表明雄鱼使卵受精的次数部分相关且可能取决于雌鱼的产卵动作次数。与求偶模式不同,在产卵间隔期未观察到本类别中的行为项目。第三类生殖行为是与照顾卵和幼鱼相关的行为。雄鱼平均在产卵开始后1分03秒开始捡起卵。雌鱼如果有机会,平均需要7分59秒。这就是分配机制,即通常由雄鱼孵化卵,雌鱼只在很少或特殊情况下才这样做。在亲代行为的其他阶段也发现了类似的数量差异。因此,雌鱼收集鱼卵的速度较慢,且更容易吞食鱼卵。在特定产卵过程中,雌鱼的大小与产卵数量之间存在低度正相关。由于一窝鱼的数量与雌鱼大小无关,因此可以得出结论,较大一窝鱼的死亡率更高。孵化鱼通常会携带一些与鱼卵混在一起的沙砾,但不清楚这是否与胚胎的存活有关。在大多数脊椎动物中,雄鱼和雌鱼的生殖行为模式存在明显的定性差异。虽然两性都具有能够引发雄鱼和雌鱼模式的神经肌肉机制,但双性或同性行为有限,且通常在特殊条件下出现。在这方面,罗非鱼是例外,因为它们在性活动方面雄鱼和雌鱼之间没有明显的定性差异。然而,在所有模式中都存在明显的数量差异。此前有几位研究人员根据洛伦兹的释放者概念分析了丽鱼科的交配行为。有人认为,即使是廷伯根提出的扩展和修改后的形式,这个概念仍然过于局限,不足以作为分析罗非鱼生殖行为的充分基础。