陕西红碱淖遗鸥育雏行为和雏鸟生长

2012年5～7月,应用e-Science信息技术和标记法,对陕西神木县红碱淖(N 38°13′～ 39°27′,E 109°42′～110°54′)遗鸥(Larus relictus)的育雏行为和雏鸟生长发育进行了研究.结果表明,雏鸟由双亲共同承担喂食.育雏前期,亲鸟采取直接喂食、食物呕吐于巢边和在巢中间断性喂食这3种喂食模式;亲鸟昼间平均喂食(0.706±0.036)次/h,夜间平均喂食(0.469±0.024)次/h,双亲在喂食频次上无显著差异(F=32.54,P＞0.05).育雏后期,主要采取双亲直接喂食和亲鸟把食物呕吐于地面上,由雏鸟自己取食的喂食模式;亲鸟昼间平均喂食(0.416±0.021)次/h,夜间平均喂食(0.331±0.018)次/h,亲鸟喂食次数与雏鸟的日龄存在相关性(r =0.074,P＜0.05).随着雏鸟日龄的增长,暖雏次数趋于减少,而在炎热晴天、降雨和大风等天气状况下,暖雏时间和护雏行为都增强.雏鸟20日龄后未再观察到暖雏行为.雏鸟体长及外部器官的形态学参数适合用Gompertz曲线方程拟合.同时,与其近缘种黑嘴鸥(L.saundersi)的育雏行为和雏鸟生长进行了比较.     

黄腹山鹪莺育雏行为和雏鸟生长

2007年3~9月,在广东省肇庆市江溪村对黄腹山鹪莺(Prinia flaviventris)的育雏行为和雏鸟生长进行了研究。通过取食行为观察、育雏食物分析和雏鸟身体量度的测量来研究黄腹山鹪莺亲鸟繁殖投资和雏鸟的生长规律。研究期间,利用隐蔽帐观察窗进行行为观察,观察距离在5 m以内;在雏鸟身体上用无味彩笔标号以区别雏鸟个体:10日龄前,标记于雏鸟背部,10~12日龄,标记在雏鸟跗跖处;对部分数据进行双变量相关分析,利用Logistic曲线拟合雏鸟形态增长,并比较每个回归方程斜率间的差异。结果显示:1)黄腹山鹪莺育雏由雌雄共同承担,育雏期(11.9±0.4)d(n=7巢)。幼雏出壳后亲鸟早晚暖雏,第7天起亲鸟白天不再暖雏;2)随雏鸟的生长,喂食次数和食物种类逐渐增加,雏鸟日龄与喂食次数极显著相关(r=0.995,P0.01);3)育雏期雏鸟食物皆为动物性食物,以蜘蛛目物种所占比例最大(40.95%),其他包括幼虫及直翅目、鳞翅目、鞘翅目、蜻蜓目等节肢动物;4)Logistic曲线方程中,体重的生长率常数k值最大,与其他k值之间存在显著性差异(P0.05);5)黄腹山鹪莺体重、体长、尾长、翼长、嘴峰、嘴裂、第三根初级飞羽(简称为P3)、跗跖及爪各参数间的相关系数均为0.9以上(P0.01),参数之间在一定程度上可相互代替;6)黄腹山鹪莺雏鸟的发育遵循最重要的功能优先发育的原则,符合能量分配假说。黄腹山鹪莺喂食次数、雏鸟生长速率(k值)相对较高,可能与当地丰富的食物资源有关,也可能是对巢址环境多变的适应。     

四川南充市区白腰文鸟的巢址选择与雏鸟的生长发育

20 0 2年 1 1月～ 2 0 0 4年 4月在四川省南充市区内对白腰文鸟 (Lonchurastriata)的繁殖习性进行了研究。结果表明 ,白腰文鸟 2月下旬开始繁殖 ;影响巢址选择的主要因素 9种 ;雌雄参与筑巢 ,营巢期 5～ 6d;雌雄轮流孵卵 ,孵卵期 1 3～ 1 5d ,整个种群的孵卵高峰期在 4～ 6月 ,窝卵数 (5 .61± 0 . 78) (n =1 8)枚 ,孵化率 86 0 7% ;雌雄均参与育雏 ,育雏期 1 8～ 2 1d ,雏离巢率 82 43 % ,繁殖生产力 3. 0 1 ,育雏两个高峰期 :上午 8:0 0～ 1 0 :0 0时和下午 1 6:0 0～ 1 8:0 0时 ,日育雏次数 (1 2 . 77± 6 .0 7) (n =3 4) ,育雏时间间隔(0 . 96± 0 . 42 )h(n =1 61 ) ;雏鸟形态生长曲线呈“S”型。     

乌鸫的繁殖行为与坐巢行为初步观察

于2009年3～7月、2010年3～6月,采用焦点动物观察法和全事件行为记录法对乌鸫(Turdusmerula)的孵卵及育雏行为进行了研究。结果表明,乌鸫是雌鸟孵卵,在孵卵期出现卵损失现象,具补卵行为;孵卵前期与后期的坐巢行为存在差异,且其坐巢时间、频次和坐巢率有随孵卵数递增的趋势。双亲育雏但以雌鸟为主,喂食模式3种:雌鸟喂食、雄鸟喂食、雄鸟将食物递给雌鸟由雌鸟喂食。随着雏鸟日龄的增长,喂食次数增多,暖雏行为减少,至育雏后期未观察到暖雏行为。为权衡孵卵期和育雏前期的能量分配,乌鸫在孵卵期及育雏前期分别采取时间长而频次少和时间短而频次多的坐巢策略。     

四川南充地区白鸰的繁殖习性

2004年2～5月在四川省南充市嘉陵江中上游的河漫滩内对白鹡鸰(Motacilla alba)的繁殖习性进行了研究.结果表明白鹡鸰2月开始繁殖;雌雄参与筑巢,营巢期7～10 d;主要雌鸟孵卵,孵卵期13～14 d,上午800～900时孵卵出现一次高峰;窝卵数(5.00±0.52)(n=16)枚,孵化率42.5%;雌雄参与育雏,育雏期15～16 d,下午1800～1900时育雏出现一次高峰,日育雏次数(112.9±48.6)(n=17),育雏时间间隔(5.60±5.34)min(n=1 584);雏鸟形态生长曲线呈"S"型.     

家燕的繁殖生态及雏鸟生长发育

20 0 4年3～1 0月对南充地区家燕(Hirundorustica)的繁殖生态进行了观察,研究了雏鸟生长发育模式。结果表明,家燕2月中旬迁来,9月中旬迁飞。一般年产卵2窝。4月初已见产卵,卵长径(1 9 1 8±0 90 )mm ,短径(1 4 1 8±0 41 )mm ,卵重(2 5 7±0 3 8)g。孵卵期(1 6±1 )d ,育雏期2 2～2 3d。雏鸟体长及外部器官的形态学参数可以用Logistic曲线方程很好地拟合,体长、翅长及1 3日龄前的体重增长曲线均呈“S”型。     

甘肃莲花山宝兴歌鸫的繁殖记录

2003年5～7月,在甘肃省莲花山自然保护区对中国特产鸟类宝兴歌鸫的繁殖,包括孵卵节律及育雏行为进行了观察。宝兴歌鸫在孵卵期平均每天出巢13．6次(n=7),出巢时间平均为12．0min(n=93),日活动期平均为855．5min(n=7)。亲鸟出巢时间的长度和环境温度呈明显的正相关(r=0．35,P=0．002,n=77)。宝兴歌鸫雌雄共同育雏,两只雏鸟的喂食频次分别为1．33次／h和0．98次／h。     

灰蓝姬鹟的孵卵节律

2 0 0 2年在莲花山自然保护区使用温度自动记录装置对灰蓝姬的孵卵节律进行了研究。研究表明 ,灰蓝姬雌鸟日平均离巢 31.2 5± 7.5 0次 (n =8天 ) ,平均每次离巢持续时间为 7± 2min (n =2 6 4 ) ,平均在巢持续时间 2 1± 9min (n =2 5 6 )。雌鸟在巢率与环境温度间存在显著的负相关关系 (Spearman相关 ,r =- 0 .30 4 ,P <0 .0 1)。进一步的分析表明 ,灰蓝姬雌鸟每次离巢持续时间与环境温度呈显著的正相关 (Spearman相关 ,r =0 .2 6 1,P <0 .0 1) ,每次在巢时间和离巢次数均与环境温度无关 (在巢时间 ,r =0 .0 2 6 ,P =0 .6 82 ;离巢次数 ,r =0 .0 14 ,P =0 .879)。认为灰蓝姬雌鸟主要通过调节离巢时间的长短来控制孵卵节律     

吉林省白城地区干草原栗斑腹的繁殖生态

栗斑腹在吉林省为留鸟 ,一年可繁殖两次 ,其雏鸟为典型的晚成鸟。 4月末开始有求偶追逐和争雌行为 ,5月中旬产卵。雌雄鸟筑巢时间分别是 43 min/d和 3 6min/d(筑巢第 4天 )。平均窝卵数为 5 .0 9± 0 .5 8枚 /巢 (n=3 1 ) ,孵卵前、中、后期雌鸟孵卵占白天活动时间的 3 5 %、74.5 %和 67.6% ,孵化期为 1 2 d,孵化率为 3 6.3 % ,2、8日龄喂雏分别为 4.5次 /h和 9.0次 /h。雏鸟的体重及外部器官的发育除嘴峰外 ,生长曲线均符合 Logistic方程 ,而嘴峰长的生长近似直线 ,栗斑腹雏鸟生长发育体重的生长模型为 :W =1 4.95 /1 +(e- 0 .552 ( t- 3.6 3) ) ,雏鸟 1 1日龄后出飞 ,繁殖成活率为 2 7.7%。     

广西防城发现黄嘴白鹭的繁殖种群

20 0 2年 3～ 8月 ,在广西防城万鹤山首次发现国家Ⅱ级重点保护动物黄嘴白鹭的繁殖种群 ,约 4巢 ,8只成鸟 1 4只雏鸟。黄嘴白鹭于该年 3月底 4月初迁来筑巢繁殖。巢材多为常绿、落叶阔叶树枯枝和松枝。窝卵数 4枚 ,卵为淡蓝青色。雌雄鸟轮流交替孵卵 ,孵化期 2 4 5 0± 1 5 0 ( 2 3～ 2 6)d ,孵化率1 0 0 %。育雏期 41± 2 ( 3 9～ 43 )d ,窝雏数 3 5 0± 0 2 9( 3～ 4)只 ,雏鸟成活率 87 5 0 %。食性主要为鱼( 77 84% )、虾 ( 1 6 76% )和青蛙 ( 5 40 % )。     

Brooding in echinoderms: How can modern experimental techniques add to our historical perspective?

Echinoderms are among the most abundant and ecologically successful groups of marine animals on earth. Their unique adaptations have enabled them to inhabit diverse environments ranging from various substrates in shallow water habitats to the benthos of the deepest seas. Although members of the Echinodermata generally share common characteristics including radial symmetry, a unique water vascular system, and decentralized cephalization, they have evolved a variety of life history strategies that enable them to reproduce successfully across a wide range of habitats. These reproductive strategies range from a complete lack of parental care (broadcasting) to internal and external brooding of the eggs, embryos, and juvenile phases. Although brooding is relatively rare in echinoderms, it is of interest as a “deviant” or “derived” form of reproduction that has been the subject of much study and debate. The aim of the present review is to examine how and why brooding occurs from a historical perspective, and then explore how modern experimental techniques are providing novel approaches to answering fundamental questions related to brooding in this very successful group of benthic marine invertebrates.     

Brood-guarding behaviour in Cory’s Shearwaters Calonectris diomedea

Brood-guarding (or the continual attendance at the nest by one parent) has been relatively little studied in altricial birds. Parental investment in brood-guarding is often highly variable within a species, and the study of such variability may contribute to the understanding of the functions and regulation of this behaviour and of the trade-offs involved in the choice between attending the nest and leaving to forage. In some colonial birds, it has been found that early nesting pairs attend their chick for longer than later nesting counterparts, giving rise to the synchronisation hypothesis that suggests that early pairs prolong brood-guarding in order to reduce the probability of nest predation by a dilution effect. In this paper, for the first time we test the prediction that burrow-nesting colonial birds subject to little predation pressure should not display a seasonal decline in brood-guarding duration. The growth assistance hypothesis suggests that brood-guarding may allow the provision of frequent small meals and the efficient use of energy by chicks with poor homeothermic capabilities, resulting in improved early chick-growth. Finally, the chick-protection hypothesis predicts that chicks in more exposed nests should be brood-guarded for longer. Data collected at two Cory’s Shearwater Calonectris diomedea colonies situated in contrasting environments supported the synchronisation hypothesis, as there was no seasonal trend in brood-guarding duration. Contrary to the growth assistance hypothesis, chicks brood-guarded for longer periods did not have an improved growth (in one colony there was even a negative effect of brood-guarding on early chick development). Finally, we found no difference in brood-guarding between nests with contrasting levels of exposure to potential predators and weather. Despite confirming the prediction of the synchronisation hypothesis, more research is needed to identify the main factors underlying the variability of brood-guarding observed in this and other studies.     

青海祁连山国家公园赤麻鸭早春繁殖记述北大核心CSCD

赤麻鸭(Tadornaferruginea)为雁形目鸭科麻鸭属的大型黄褐色鸭类,繁殖于中国东北、内蒙古、青海、甘肃和西藏等地,越冬于华北、长江流域至西藏、广东等地(郑作新等1979,Roberts1991,Cramp1994)。赤麻鸭在中国与印度等地的种群数量相当丰富,但局部种群存在因过度狩猎和生境破坏导致种群数量下降现象(Vyas 2005,宋亚统等2016)。     

Diversity of brood chambers in calloporid bryozoans (Gymnolaemata,Cheilostomata): comparative anatomy and evolutionary trends

Comparative anatomical studies of 12 species from 10 genera (Callopora, Tegella, Amphiblestrum, Parellisina, Corbulella, Crassimarginatella, Valdemunitella, Bryocalyx, Concertina, Cauloramphus) belonging to one of the largest and most diverse bryozoan taxa, the Calloporidae, and one species from the genus Akatopora belonging to the related taxon Antroporidae, were undertaken to elucidate the morphological diversity of brooding structures and to recognize main trends in their evolution. Most of the species studied possess ovicells (specialized brooding receptacles) formed by the distal and maternal (egg-producing) autozooids. The distal zooid can be an autozooid, a vicarious avicularium or a kenozooid. The calcified protective hood (ooecium) is an outgrowth from the distal zooid. Hyperstomial or prominent ovicells are most common. They were found in species of the genera Callopora, Tegella, Amphiblestrum, Parellisina, Corbulella, Bryocalyx and Concertina. Subimmersed ovicells were found in Valdemunitella, and immersed ovicells in Crassimarginatella and Akatopora. Cauloramphus has an internal brooding sac and a vestigial kenozooidal ooecium, budded by the maternal zooid. Based on the structure of the brooding organs, the following evolutionary trends can be recognized within the group: (1) reduction of the distal (ooecium-producing) zooid, (2) immersion of the brooding cavity correlated with a reduction of the ooecium and ooecial vesicle and with changes in the ovicell closure and the structure of the brood chamber floor, (3) reduction of the calcification of the ectooecium, and (4) transition from bilobate to entire ooecium. The trend towards immersion of the brooding cavity could have evolved repeatedly within the Calloporidae. Transition from bilobate to entire ooecium is characteristic of the related taxon Cribrilinidae, showing a good example of parallel evolution of the ooecium in two closely related clades. Possible causes for the transformations described are discussed.     

Anatomy and reproduction of viviparous Pisidium (Parapisidium) reticulatum Kuiper, 1966: Implications for the phylogeny of Sphaeriidae (Mollusca: Bivalvia: Heterodonta)

The pea clams Sphaeriidae represent a major molluscan freshwater radiation with cosmopolitan distribution in all kinds of lotic and lentic habitats. Their phylogenetic relationships are still controversial, with comprehensive taxonomic sampling and examination of morphological characters still challenging. Here, based on rare and rediscovered original material, we study in detail the anatomy and aspects of brood protection of the African Pisidium reticulatum Kuiper, 1966. Representing the monotypic subgenus Parapisidium Kuiper, 1966, this species is characterized by its peculiar combination of shell and anatomical features of potentially high phylogenetic relevance. While similar to other congeners in several anatomical characters (e.g. reduction of inhalant siphon and descending lamella of outer demibranch, simplified structure of intestine coil and nephridium), P. reticulatum differs from other Pisidium species in retaining both pairs of retractor muscles of the inhalant siphon, and particularly in its peculiar mode of brooding. The yolky eggs are relatively large (160–170 μm in diameter) and are incubated in the gill, albeit in the absence of the formation of brood pouches. During later stages of incubation the larvae are surrounded by large cells similar to nourishing cells in other sphaeriids and probably with similar function. This unique combination of reproductive features is hypothesized to represent an intermediate stage between the typical ovoviviparity of Euperidae and euviviparity (i.e. nourishment by the parent animal) as found exclusively in Sphaeriidae, the latter being characterized by the possession of closed brood pouches. Phylogenetic analyses based on a comprehensive set of morphological characters reveal Parapisidium as the most basal lineage within a clade Pisidium. Evaluating the phylogenetic reconstructions based also on available molecular data for Sphaeriidae, we discuss alternative scenaria of (parallel) evolution of brood pouches and viviparity in this group.     

Dopamine and mesotocin neurotransmission during the transition from incubation to brooding in the turkey

We investigated the neuroendocrine changes involved in the transition from incubating eggs to brooding of the young in turkeys. Numbers of mesotocin (MT; the avian analog of mammalian oxytocin) immunoreactive (ir) neurons were higher in the nucleus paraventricularis magnocellularis (PVN) and nucleus supraopticus, pars ventralis (SOv) of late stage incubating hens compared to the layers. When incubating and laying hens were presented with poults, all incubating hens displayed brooding behavior. c-fos mRNA expression was found in several brain areas in brooding hens. The majority of c-fos mRNA expression by MT-ir neurons was observed in the PVN and SOv while the majority of c-fos mRNA expression in dopaminergic (DAergic) neurons was observed in the ventral part of the nucleus preopticus medialis (POM). Following intracerebroventricular injection of DA or oxytocin (OT) receptor antagonists, hens incubating eggs were introduced to poults. Over 80% of those injected with vehicle or the D1 DA receptor antagonist brooded poults, while over 80% of those receiving the D2 DA receptor antagonist or the OT receptor antagonist failed to brood the poults. The D2 DA/OT antagonist groups also displayed less c-fos mRNA in the dorsal part of POM and the medial part of the bed nucleus of the stria terminalis (BSTM) areas than did the D1 DA/vehicle groups. These data indicate that numerous brain areas are activated when incubating hens initially transition to poult brooding behavior. They also indicate that DAergic, through its D2 receptor, and MTergic systems may play a role in regulating brooding behaviors in birds.     

一窝三趾啄木鸟雏鸟的死亡事件与双亲育幼的关系

三趾啄木鸟的夜间孵卵和抱暖通常由雄性亲鸟承担。我们使用两台数码相机同时对1个三趾啄木鸟巢口和巢室进行了监视,记录了该窝雏鸟的死亡过程。该窝1只雏鸟在孵出的第1天死亡,并在第2天被雌性亲鸟移出巢外。其余两只雏鸟连续两个晚上没有亲鸟的照料,于第9天死亡。在这个巢内,由于雄鸟未归,使得雌鸟不得不连续两个晚上照顾雏鸟;而突发的暴风雨可能是导致雄鸟回巢失败的原因[动物学报52 (2) : 410 -414 , 2006]。     

Gametic, morphometric, and physiological variables influencing clutch size in the Chilean oyster, Ostrea chilensis (Philippi, 1845)

A number of marine bivalve taxa, including species of the genus Ostrea, have adopted brooding of the young in the mantle cavity as a reproductive mechanism. In spite of the importance of brooding in the reproductive success of such species, little is known about the most important variables influencing the process, including those limiting clutch size. This study addresses the regulation of brood size in the hermaphroditic oyster Ostrea chilensis. During spawning, oysters released all their oocytes into the mantle cavity. No residual oocytes remained in the gonad, so a second spawning during the same brooding season was not possible. There was a weak correlation between the number of embryos incubated during the early phase of brooding and the dry tissue weight of the brooding oyster, and between the number incubated and the shell length of the brooding adult during the later phases of brooding. The number of embryos was also correlated with the area of the labial palps of the brooder during the later stages, suggesting that the loss of veligers observed at this time may be at least partially attributable to a limitation of space around the palps, which manipulate the larvae and with which the larvae are closely associated. The oxygen consumption rate of brooders incubating a normal clutch of embryos was not significantly different from that of oysters in which clutch size had been experimentally reduced by 50%. Experimental increase of the normal clutch size by 100% significantly increased the oxygen consumption of the brooder, suggesting that there is a physiological as well as a spatial limit to brood size. Thus the number of embryos brooded by an oyster is initially dependent on its production of oocytes and secondarily by the high metabolic costs of incubating large numbers of embryos. As development proceeds, space available for brooding apparently becomes a limiting factor as the larvae grow. The fate of the excess larvae is not known at present, but any larvae released prematurely cannot be competent to settle, since development is synchronous and there is a complete release of all pediveligers at the end of the brooding period.