小杜鹃对强脚树莺的巢寄生及其卵色模拟

于1999-2009年的鸟类繁殖季(4-8月)对贵州宽阔水自然保护区内的强脚树莺(Cettia fortipes)的繁殖进行监测,并采用光纤光谱仪,通过主成分分析、反射光谱、罗宾逊投射等方法对强脚树莺的卵色与小杜鹃(Cuculus poliocephalus)对其寄生的卵色模拟程度进行分析。研究结果表明,强脚树莺的繁殖成效在不同年份间均无显著差异,但其巢被捕食率和巢被寄生率都较高,分别为49.26%和9.18%。通过反射光谱分析,表明小杜鹃卵在色调和色度上高度模拟强脚树莺的卵,但其亮度高于宿主卵,而且在人眼无法探测的紫外光部分存在差异。     

小杜鹃对强脚树莺的巢寄生及其卯色模拟

于1999-2009年的鸟类繁殖季(4-8月)对贵州宽阔水自然保护区内的强脚树莺(Cettia fortipes)的繁殖进行监测,并采用光纤光谱仪,通过_芏成分分析、反射光谱、罗宾逊投射等方法对强脚树莺的卵色与小杜鹃(Cuculuspoliocephalus)对其寄生的卵色模拟程度进行分析.研究结果表明,强脚树莺的繁殖成效在不同年份间均尤显著差异,但其巢被捕食率和巢被寄生率都较高,分别为49.26%和9.18%.通过反射光谱分析,表明小杜鹃卵在色调和色度上高度模拟强脚树莺的卵,但其亮度高于宿主卵,而且在人眼无法探测的紫外光部分存在差异.     

鹰鹃对白腹短翅鸲的巢寄生

2015年4~8月,在贵州宽阔水国家级自然保护区,记录到1巢白腹短翅鸲(Hodgsonius phaenicuroides)被鹰鹃(Cuculus sparverioides)寄生,寄生率为1/16(n=16)。发现时白腹短翅鸲巢内有1枚白色的寄生卵和2枚蓝色的寄主卵,且卵已凉,疑为亲鸟弃巢。鹰鹃卵重6.09 g,卵大小20.20 mm×27.73 mm;两枚白腹短翅鸲的卵重分别为2.34 g和2.40 g,大小分别为20.05 mm×14.94 mm和19.95 mm×15.09 mm。鹰鹃的卵重量(6.09 g)和大小(27.73 mm×20.20 mm)均明显大于白腹短翅鸲的卵。卵色光谱测量结果表明,鹰鹃和白腹短翅鸲卵色的反射光谱图差别明显,鹰鹃卵在色度和色调上明显低于白腹短翅鸲,但卵色亮度却明显比白腹短翅鸲卵高,为典型的非模拟寄生卵。     

海南临高和澄迈池鹭种群的卵色光谱分析

2009年4-7月,利用光纤光谱仪和鸟类视觉模型对海南临高和澄迈2个池鹭(Ardeola bacchus)种群的卵色进行量化分析.结果表明:池鹭卵的反射光谱波峰位于中波区域,最高峰位于绿色光区域,卵色为以绿色为主的蓝绿色,这种卵色可能是对捕食、营巢生境或雄鸟性选择的适应.基于鸟类视觉模型的分析表明,2个种群池鹭的卵在色度、亮度和色调UV上无显著差异,但在色调RGB上存在极显著差异.罗宾逊(Robinson)投射分析表明,澄迈种群的池鹭,其卵的色调RGB变异明显大于临高种群,这种变异可能与2个种群的巢寄生压力或营巢生境的差异有关.     

贵州宽阔水自然保护区小杜鹃对小鳞胸鹪鹛的巢寄生

2015年4—8月,在贵州宽阔水国家级自然保护区记录到小杜鹃Cuculus poliocephalus在小鳞胸鹪鹛Pnoepyga pusilla巢中寄生繁殖。发现时小鳞胸鹪鹛已处于孵卵后期,巢内有1枚红棕色的小杜鹃寄生卵和3枚小鳞胸鹪鹛的白色卵。小杜鹃卵质量为2.55 g,体积2.72 cm~3,小鳞胸鹪鹛卵质量(1.64±0.16)g(n=7),体积(1.65±0.08)cm~3(n=7),两者的卵在颜色和大小上差别明显。光纤光谱仪对卵色的测量和分析结果表明,小鳞胸鹪鹛的卵色亮度显著高于小杜鹃,小杜鹃的卵为高度非模拟寄生卵。这是小鳞胸鹪鹛被小杜鹃寄生的第二例报道,说明其可能是小杜鹃的适宜寄主。     

辽宁鸟类分布新记录5种:小鸦鹃、雪鹀、 红翅凤头鹃、宝兴歌鸫和黄眉姬鹟

近年来,随着观鸟活动和鸟类科研工作在辽宁的持续开展(Baietal.2015,汤姆·滨客2016),辽宁各地不断发现鸟种分布新记录种(白清泉等2019)。2012至2020年间,在丹东、大连、抚顺等市先后发现小鸦鹃(Centropus bengalensis)、雪鹀(Plectrophenax nivalis)、红翅凤头鹃(Clamator coromandus)、宝兴歌鸫(Turdus mupinensis)和黄眉姬鹟(Ficedula narcissina)5种,经查阅相关资料(邱英杰等2006,郑光美2017),确定为辽宁省鸟类分布新记录种。     

辽宁鸟类分布新记录5种:小鸦鹃、雪鹀、 红翅凤头鹃、宝兴歌鸫和黄眉姬鹟北大核心CSCD

近年来,随着观鸟活动和鸟类科研工作在辽宁的持续开展(Baietal.2015,汤姆·滨客2016),辽宁各地不断发现鸟种分布新记录种(白清泉等2019)。2012至2020年间,在丹东、大连、抚顺等市先后发现小鸦鹃(Centropus bengalensis)、雪鹀(Plectrophenax nivalis)、红翅凤头鹃(Clamator coromandus)、宝兴歌鸫(Turdus mupinensis)和黄眉姬鹟(Ficedula narcissina)5种,经查阅相关资料(邱英杰等2006,郑光美2017),确定为辽宁省鸟类分布新记录种。     

利用光纤光谱仪量化和分析鸟类的卵色

在国内首次利用光纤光谱仪对鸟卵的颜色进行量化和分析。通过对灰林鵖（Saxicola ferrea）和矛纹草鹛（Babax lanceolatus）2种鸟的卵色300～700 nm的光谱测量,表明这2种鸟除蓝色色度外,二者卵色在亮度、绿色、黄色以及红色色度上均存在显著差异。灰林鵖和矛纹草鹛卵色的可见光反射光谱反射比值呈现很相似的平行关系,拥有共同的高峰和低峰;而其卵色的紫外光部分呈现从差异大到差异小的变化。用主成分分析光谱的反射和形状,结果对于灰林鵖和矛纹草鹛,前3个主成分分别解释了99.9%和99.8%的光谱变量,其中代表鸟卵亮度的第1主成分分别解释了93.7%和89.3%的变量,代表卵色饱和度的第2主成分分别占总变量的5.5%和9.1%。利用光纤光谱仪对鸟卵的颜色进行定量分析,可为鸟类的区系分类、系统进化和行为生态学等方面的研究提供更客观和科学的数据,同时也拓展了新的研究领域和视角。     

以鸟类视觉模型揭示中杜鹃对冠纹柳莺的卵色模拟(英文)

于2009年4—7月,采用光谱仪量化卵色和建立鸟类视觉模型的方法,在贵州宽阔水自然保护区对中杜鹃(Cuculus saturatus)寄生冠纹柳莺(Phylloscopus reguloides)的卵色模拟进行了研究。中杜鹃产白色卵带极少数而微小的棕色斑,明显大于宿主卵,重2.06g,体积1.91cm3。从人眼看,中杜鹃卵对宿主卵在很大程度上是模拟的,但视觉模型表明,两者的卵色在色调和色度上都完全分离,揭示了人眼探测不到的卵色模拟情况。该文首次对中杜鹃的雏鸟特征进行描述,在4日龄以后雏鸟嘴裂中出现三角形黑斑,并随着日龄的增长而更加明显,这种特征在霍氏中杜鹃(C.optatus)的雏鸟中也存在,但未见于其他种类的杜鹃雏鸟。     

大杜鹃在荒漠伯劳巢中寄生繁殖

2010年5～7月在安西极旱荒漠国家级自然保护区发现3巢荒漠伯劳被大杜鹃寄生,寄生率10.34%.荒漠伯劳产白色和粉红色两种颜色的卵,大杜鹃产白色寄生卵于卵色为白色的宿主巢中.寄生卵均产于6月,当月寄生率达42.86%.大杜鹃雏鸟19日龄离巢,离巢时体重66.24 g.     

Egg Coloration and Recognition of Conspecific Brood Parasitism in Eastern Bluebirds

Individual eastern bluebird (Sialia sialis) females produce clutches of eggs with unique coloration and older females and females in better body condition lay more pigmented blue‐green eggs. Conspecific brood parasitism in this species is not uncommon and bluebirds occasionally reject what appear to be normal eggs by moving them to the periphery of the nest. I used UV‐visual reflectance spectrometry to objectively measure coloration of eggs and nest material. To estimate the conspicuousness of the trait, I calculated the contrast between eggs and background nest material. I found high achromatic and chromatic contrast between the coloration of eggs and of the nests, suggesting that bluebird eggs are highly conspicuous. To test the hypothesis that expression of blue‐green coloration eggs facilitates recognition of eggs laid by conspecific brood parasites, I cross‐fostered individual eggs into host nests during egg laying and monitored the fate of those eggs. I found no support, however, for the hypothesis that egg coloration facilitates discrimination of parasitic eggs from host eggs.     

大杜鹃对家燕的巢寄生

了解杜鹃(Cuculus spp.)对不同宿主鸟类的巢寄生,是研究杜鹃与其宿主之间协同进化的重要基础资料。大杜鹃(Cuculus canorus)和家燕(Hirundo rustica)分布遍及全国,且为同域分布,但两者之间的寄生现象尚未有过系统调查。2012年和2014年4~8月,对繁殖于吉林市昌邑区桦皮厂镇(34°58′44.18″N,126°13′26.83″E,海拔184 m)和海南岛的家燕种群进行调查,结果表明,吉林市昌邑区桦皮厂镇家燕种群的寄生率为2.4%(1/42),而在海南岛所调查的1 719个家燕巢未发现杜鹃寄生现象。同时在网络上搜集家燕巢寄生的报道案例,共记录到13巢家燕被大杜鹃寄生繁殖,均发生在北方的家燕种群。     

大杜鹃在白腹短翅鸲巢中寄生繁殖

2009年至2012年期间,在甘肃莲花山自然保护区共发现91个白腹短翅鸲(Hodgsonius phaenicuroides)巢,其中15巢被大杜鹃(Cuculus canorus)寄生,寄生率为16.48%。根据对13枚寄生的大杜鹃卵的观察,其中12枚卵色为浅蓝色,与白腹短翅鸲的深蓝绿色卵差异明显,仅1枚与白腹短翅鸲卵色一致。大杜鹃与白腹短翅鸲的卵重(t =11.208, df=38, P<0.001)和卵短径(t=0.970,df=38, P<0.001)差异极显著。白腹短翅鸲具有识别大杜鹃卵的能力,15巢中只有4巢接受寄生卵并继续孵化,7巢成功识别,剩余4巢无法确定是否识别。白腹短翅鸲为雌鸟单独孵卵,推测识别大杜鹃卵可能只与雌鸟有关。     

画眉消化系统形态的初步观察

对8只(4♀,4♂)画眉消化系统的形态学作了初步的观察与研究,画眉的舌成细长三角形,前端有刺毛状结构,雌鸟的刺毛数目多且较细,雄鸟的刺毛则数量少,但是相对较粗大.舌后端有1～2排尖端后指的栉状突.雌雄鸟在舌前端正中央还有一"V"形的凹缺,雌鸟深约1.22 mm,雄鸟深约1.87 mm.食管管径较细,整体宽窄不等,无明显可见的嗉囊.腺胃乳突短而小,分布均匀,肌胃发达,具角质膜.肠道长与体长基本相等,小肠较发达,雌鸟小肠长178.53 mm,占肠道总长87.43%;雄鸟小肠长186.62 mm,占肠道总长89.01%.具有不发达的双侧盲肠,盲肠有未倒置现象.肝为体内最大的消化腺,分左右两叶,右叶又分一小叶.胰位于十二指肠袢内,细长形,分两小叶.并与同科的蓝翅希鹛、灰胸薮鹛进行了比较.     

鹰鹃在橙翅噪鹛巢中寄生繁殖

2011年和2012年每年的5月到8月,在甘肃莲花山地区共发现了5例鹰鹃(Hierococcyx sparverioides)在橙翅噪鹛(Garrulax elliotii)巢中寄生繁殖的案例.鹰鹃卵为椭圆形,浅蓝色,卵壳上没有斑点.测量了其中2枚卵,卵重分别为6.9g和7.2g,长径×短径分别为29.76 mm×20.40 mm和28.40mm×21.68 mm.鹰鹃幼鸟在出壳后的第20天离巢.     

神农架川金丝猴捕食矛纹草鹛雏鸟简报

目前,捕食脊椎动物的现象在非人灵长类动物中多有报道,如卷尾猴(Cebus capucinus,Rose,1996)、东非狒狒(Papio anubis,Harding,1973;Strum,1975)、猕猴(Macaca arctoides,Estrada and Estrada,1977;Macaca sylvanus,Young et al.,2012)、西黑冠长臂猿(Nomascus concolor jingdongensis,Fan and Jiang,2009)、苏门答腊猩猩(Pongo abelii, Hardus et al.,2012)和黑握握^抓加尽-lodytes, Gilby et al., 2006;Newton-Fisher, 2014)等。     

Brood Parasitism and Nest Takeover in Common Eiders

Conspecific brood parasitism (CBP) is an alternative breeding tactic that occurs in many brood‐tending animals and can have important fitness effects for both host and parasite. We use protein fingerprinting of egg albumen to distinguish the eggs from different females and to estimate the frequency, pattern and tactics of CBP and other forms of mixed maternity in a Hudson Bay population of common eiders (Somateria mollissima sedentaria). Mixed clutches, containing eggs from more than one female, occurred in 31% of the 86 nests studied that progressed to clutch completion. Other females than the host laid 8% of the eggs. In 11 (41%) of the mixed clutches another female laid before the host started laying, corroborating the hypothesis that takeover of nests started by other females accounts for many of the mixed clutches in this population. Our results also indicate that traditional non‐molecular methods of identifying foreign eggs may considerably underestimate the frequency of mixed clutches.     

Consistency in Egg Rejection Behaviour: Responses to Repeated Brood Parasitism in the Blackcap (Sylvia atricapilla)

To evaluate host responses towards repeated brood parasitism we experimentally parasitized and continuously videotaped blackcap nests in two consecutive trials. The ejection of a foreign egg was the most common response (94.5%) in both trials, but desertion (4.1%) and acceptance (1.4%) also occurred. The general method of ejection was puncturing. In 9.8% of identified ejections, already punctured eggs stuck to the abdominal feathers of the incubating bird and were carried out of the nest. Females were responsible for the majority of ejections in both trials and their response time was significantly shorter than that of males. Blackcaps exhibited consistency in the sex responsible for egg ejection over the two trials; but in five (20.8%) experiments individuals changed their behaviour. Repeatability for host responses within the nest was very high. In ejections accomplished by the same bird, the response was significantly quicker in the second trial, indicating the presence of certain learning abilities. Our results suggest that cuckoo hosts are quite consistent in their responses towards parasitic eggs when parasitized repeatedly within one breeding attempt.     

Large Hawk‐Cuckoo Hierococcyx sparverioides parasitism on the Chinese Babax Babax lanceolatus may be an evolutionarily recent host–parasite system

We documented brood parasitism by the poorly studied Large Hawk‐Cuckoo on a previously unknown host species, the Chinese Babax. Furthermore, we describe a new egg colour for the Large Hawk‐Cuckoo. The parasitism rate of Chinese Babax nests over 4 years was 6.9% (11 of 159 nests), with significant temporal variation. The Large Hawk‐Cuckoo laid immaculate white eggs that appeared non‐mimetic to the blue Babax eggs, an impression that was confirmed by avian visual modelling. Nevertheless, most Cuckoo eggs were accepted by the host, suggesting that this host–parasite system may be evolutionarily recent.