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1.
四种草螽雄性鸣声的研究   总被引:1,自引:0,他引:1  
对分布于我国的长瓣草螽Conocephalus(Anisoptera)gladiatus,中华草螽C.(Amurocephalus)chinensis,悦鸣草螽 C.(Anisoptera)melaenus和斑翅草螽C.(Anisoptera)maculatus雄性鸣声进行了分析.研究结果表明,这4种草螽雄性鸣声的时域波形较简单,鸣声均由1种类型的脉冲组序列构成.长瓣草螽雄性鸣声每个脉冲组持续时间约0.13 s,脉冲组间隔约0.12 s,每个脉冲组通常由8脉冲构成,鸣声的频率范围5~20 kHz.中华草螽雄性的鸣声脉冲组由2个脉冲构成,每次鸣叫持续时间约为3.3 s,两次连续鸣叫间隔约10.5 s,鸣声频率范围为20 Hz~20 kHz.斑翅草螽雄性鸣声的脉冲组由10~13个脉冲构成,脉冲组持续时间2.1~2.5 s,两次连续鸣叫间隔时间约为3 s;鸣声频率从5.5 kHz到高于20 kHz.悦鸣草螽雄性鸣声由单一规则的重复脉冲组序列构成,每个鸣声脉冲组持续时间约0.035 s,脉冲组间隔约0.023 s,每个脉冲组由3个脉冲构成,脉冲组重复率20/s,鸣声频率6.0~20.0 kHz.  相似文献   

2.
两种米纹蝗雄性鸣声的比较研究(直翅目,蝗总科)   总被引:3,自引:2,他引:1  
应用计算机技术分析了红足米纹蝗Notostaurus rubripes Mistshenko和小米纹蝗Notostaurus albicornis albicor-nis(Ev.)雄性的鸣声特征。这两种米纹蝗雄性呜叫声的脉冲组持续时间、脉冲组组份、脉冲组间隔、频率的主能峰以及呜叫行为均具有显著差异,可作为2种米纹蝗的分类依据。红足米纹蝗雄性鸣声的脉冲组间隔约为0.647s,每一脉冲组持续时间约为0.0673s,每个脉冲组有8个脉冲串,每个脉冲串仅有1个单脉冲,鸣声的主能峰频率约3.86~5.64kHz。小米纹蝗雄性鸣声的脉冲组间隔约0.529s,每一脉冲组持续时间为0.1185s,每个脉冲组有8个脉冲串,每一脉冲串有1~6个单脉冲构成,主能峰频率约8.10~9.24kHz。  相似文献   

3.
四种蝗虫雄性鸣声的比较研究(直翅目,蝗总科)   总被引:5,自引:3,他引:2  
应用计算机技术分析了肿脉蝗Stauroderus scalaris scalaris(Fischer-Waldheim)、宽须蚁蝗Myrmeleotettixpalalis(Zubowsky)、邱氏异爪蝗Euchorthippus cheui Hsia、西伯利亚蝗Aeropus sibiricus(Linnaeus)雄性的鸣声特征.这4种蝗虫雄性鸣声特征差异显著.肿脉蝗雄性鸣声具有脉冲序列的分化,每个脉冲序列分为两种不同的脉冲组,第1种脉冲组持续时间约0.081 s,有7个脉冲串组成,每个脉冲串有7个单脉冲构成;第2种脉冲组持续时间不等,有13~18个脉冲串组成,脉冲串持续时间为0.021 s,间隔为0.010 s.鸣声的主能峰频率约8.62 kHz.宽须蚁蝗雄性鸣声的脉冲组持续时间为0.23 s,脉冲组间隔为0.35 s,每个脉冲组由28~31个单脉冲组成,主能峰频率为6.89 kHz、12.75 kHz.邱氏异爪蝗雄性鸣声的脉冲组持续时间为0.22 s,脉冲组间隔为0.76 s,每个脉冲组由6~7个脉冲串组成,每个脉冲串内含有1~5个单脉冲,主能峰频率为9.65 kHz.西伯利亚蝗的脉冲组持续时间约为0.092 s,脉冲组间隔为0.08 s,每个脉冲组分化为5~6个脉冲串;主能峰频率为7.58 kHz.  相似文献   

4.
研究了北方常见的优雅蝈螽Gampsocleis gratiosa和暗褐蝈螽Campsocleis sedakovii雄性鸣声特征和发声器结构.优雅蝈螽鸣声规则,脉冲组序列由2种类型的脉冲组组成,第1种类型的脉冲组持续时间约0.09 s,脉冲持续和间隔时问约0.01 5;第2类型的脉冲组持续时间约0,04 s,脉冲持续和间隔时间均约0.003 s;鸣声的主能峰频率约7 kHz.暗褐蝈螽雄性鸣声包含短促的开翅鸣声和由2种类型的脉冲组组成的脉冲组序列构成的闭翅鸣声,第1种脉冲组持续时间约0.012 s,间隔时间约0.002 s;第2种脉冲组持续时间约0.013 s,间隔时间极短;鸣声主能峰频率约9.1kHz.2种蝈螽镜膜的形状、发声锉的形状和长度、发声齿的形状具显著差异.  相似文献   

5.
鼻优草螽和苍白优草螽鸣声和发声器的研究   总被引:14,自引:1,他引:13  
鼻优草螽[Euconocephalus nasutus(Thunberg)]和苍白优草螽[Euconocephalus pallidus (Redtenbacher)]外形相似,但其鸣声特征和发声器的结构明显不同。鼻优草螽鸣声的每个脉冲组由4个脉冲串构成。脉冲组持续时间4.5ms脉冲组间隔为1.8ms,主能峰频率为11.37kHz。苍白优草螽鸣声的每个脉冲组仅由1个脉冲串构成,脉冲组持续时间1.6ms,脉冲组间隔为4.3ms,主能峰频率为11.03kHz,鼻优草螽发声锉较弯曲,中部稍粗壮,两端稍细,苍白优草螽发声锉较直,呈棒状。  相似文献   

6.
乌苏里蝈螽和优雅蝈螽雄性鸣声结构的比较研究   总被引:1,自引:0,他引:1  
应用计算机技术分析了内蒙古草原乌苏里蝈螽Gampsocleis ussuriensis和优雅蝈螽Gampsocleis gratiosa2种螽斯雄性的鸣声结构。乌苏里蝈螽鸣声较复杂,一次鸣叫持续时间6~27s(平均12.5s),每个脉冲组由两类脉冲组组分构成,第1类脉冲组组分为振幅较大的脉冲组,脉冲组持续时间0.0065s,由6~8个脉冲串组成,每个脉冲串持续时间为0.00047s,间隔时间为0.00027s,每个脉冲串含5~10个单脉冲,脉冲串持续时间、间隔时间较短;第2类脉冲组组分为振幅较小的脉冲组,脉冲组持续时间0.0191s,约含有15个左右脉冲串,持续时间为0.00041s,间隔时间约为0.00127s,每个脉冲串含有3~5个单脉冲,脉冲串持续时间、间隔时间也较短,主能峰频率为7.98kHz。优雅蝈螽鸣声则较规则,一次鸣叫持续时间4~232s(平均41.7s)。每个脉冲组也由两类脉冲组组分构成,第1类脉冲组组分振幅较大且逐步增强,脉冲组持续时间0.119s,由10个振幅较大的脉冲串组成,每个脉冲串持续时间为0.00576s,间隔时间为0.005s,每个脉冲串含18~25个单脉冲;第2类脉冲组组分为振幅较小的脉冲组,脉冲组持续时间0.07s,约含有25个左右脉冲串,脉冲串振幅较小,含有6~9个单脉冲,主能峰频率为6.87kHz,次能峰频率为3.25kHz。结果表明乌苏里蝈螽与优雅蝈螽雄性鸣声既有相似的共同特征,同时存在较显著差异。  相似文献   

7.
蟋蟀科5属9个种的线粒体16S rRNA基因部分序列被测定或从Gen Bank获得,比较其同源性,计算核苷酸使用频率,并构建NJ和MP分子系统树。在获得的449bp的序列中A、T、C和G碱基含量分别为31.8%、36.9%、9.9%和21.4%,A T平均含量为68.7%。研究结果表明:所研究的5属9种蟋蟀聚成3个聚类簇,斗蟋属先与灶蟋属汇合,再与棺头蟋属构成聚类簇Ⅰ;油葫芦属黑脸油葫芦和北京油葫芦与蟋蟀属的家蟋相聚构成聚类簇Ⅱ;蟋蟀属的田蟋单独构成聚类簇Ⅲ。  相似文献   

8.
采用DNA测序技术并比较了蟋蟀科5个属:斗蟋属Velarifictorus、棺头蟋属Loxoblemmus、油葫芦属Teleogryllus、灶蟋属Gryllodes和蟋蟀属Gryllus以及蛉蟋科针蟋亚科Allonemobiussocius的mtDNA-COⅡ基因部分序列,依据分子数据建立了5个属的系统发育关系。结果显示A、T、C和G碱基含量分别为34.8%、35.3%、19.3%和10.6%,AT含量(70.1%)仅略高于半翅目锥猎蝽和缨尾目。分子系统树显示,油葫芦属黄脸油葫芦与蟋蟀属家蟋亲缘关系较近。显示油葫芦属与斗蟋属的亲缘关系较近。并且,棺头蟋属的多伊棺头蟋和窃棺头蟋先聚合,这与形态学特征的结果相符。  相似文献   

9.
本文由1741个叫声的分析,给出了蟋蟀的鸣声特征和黑蝉叫声的影响.雄蟋招引声的每个单次叫声(SC)平均含有7.6个节拍,每个含有2个脉冲列组,每组含有4个主要的调幅脉冲列.每个SC的声长、间隔和平均重复周期(?)及节拍速(?)分别为1.285-1.325s,0.755—0.746s和2.078s及每秒7.6个节拍.鸣声谱的主峰频率(MPF)和MPF下降20db的带宽分别为5223±79Hz和(4498±82)—(5656±68)Hz.正在歌唱的蟋蟀鸣声基本上不受黑蝉自鸣声的影响,但黑蝉的前置自鸣声对蟋蟀鸣声波形有一定的影响.黑蝉的惊叫声不仅对蟋蟀鸣声波形有明显影响,而且时间特性有一定影响,即(?)约缩短一半,(?)的变差明显扩大.但对频率特性都无影响.  相似文献   

10.
对两种常见树蟋长瓣树蟋Oecanthus longicauda Matsumura和黄树蟋O.rufescens Serville的召唤声特征进行了比较研究.研究结果表明,两种树蟋召唤声的时域特征和频域特征在脉冲组所含脉冲数、脉冲组持续时间、脉冲组间隔时间、脉冲组脉冲排列规律、单脉冲间隔时间、频域能峰数和能峰值等方面存在明显差异.长瓣树蟋脉冲组主要由3个脉冲组成,含3个脉冲的脉冲组持续时间约0.049±0.001 s,脉冲组间隔时间为0.027±0.003 s,单脉冲持续时间约0.011±O.001 s,单脉冲间隔时间约0.009±0.00l s,频谱图只有1个2.5KHz的主能峰.黄树蟋脉冲组由16~20个脉冲组成,脉冲组持续时间为0.303±0.021 s,脉冲组间隔时间为0.401±0.046 s,单脉冲持续时间约为0.012±0.001 s,脉冲间隔时间约为0.004±0.001 s,频谱图有两个能峰:主能峰频率为3.03 KHz,次能峰频率为16.78KHz.  相似文献   

11.
The cicada Okanagana rimosa (Say) has an acoustic communication system with three types of loud timbal sounds: (i) A calling song lasting several seconds to about 1 min which consists of a sequence of chirps at a repetition rate of 83 chirps per second. Each chirp of about 6 ms duration contains 4-5 pulses. The sound level of the calling song is 87-90 dB SPL at a distance of 15 cm. (ii) An amplitude modulated courtship song with increasing amplitude and repetition rate of chirps and pulses. (iii) A protest squawk with irregular chirp and pulse structure. The spectra of all three types are similar and show main energy peaks at 8-10 kHz. Only males sing, and calling song production is influenced by the songs of other males, resulting in an almost continuous sound in dense populations. In such populations, the calling songs overlap and the temporal structure of individual songs is obscured within the habitat. The calling song of the broadly sympatric, closely related species O. canadensis (Provander) is similar in frequency content, but distinct in the temporal pattern (24 chirps per second, 24 ms chirp duration, eight pulses per chirp) which is likely important for species separation in sympatric populations. The hearing threshold of the auditory nerve is similar for females and males of O. rimosa and most sensitive at 4-5 kHz. Experiments in the field show that female phonotaxis of O. rimosa depends on parameters of the calling song. Most females are attracted to calling song models with a 9 kHz carrier frequency (peak frequency of the calling song), but not to models with a 5 kHz carrier frequency (minimum hearing threshold). Phonotaxis depends on temporal parameters of the conspecific song, especially chirp repetition rate. Calling song production is influenced by environmental factors, and likelihood to sing increases with temperature and brightness of the sky. Correspondingly, females perform phonotaxis most often during sunny conditions with temperatures above 22 degrees C. Non-mated and mated females are attracted by the acoustic signals, and the percentage of mated females performing phonotaxis increases during the season.  相似文献   

12.
ABSTRACT. Both sexes of the speckled bush cricket, Leptophyes punctatissima (Bosc) (Tettigoniidae) produce sound by stridulation. The sound is used in courtship. The male sings for periods throughout the day and night, and there is a peak of activity in the early afternoon. The female sings only in response to a male chirp. The male increases his rate of singing if he receives replies from a female. After 3 days isolation from male song, the female replies most readily to male song mimics of short duration (10 ms) whose carrier frequency is 30 or 45 kHz. Females that have been isolated from male song for 10 days respond less readily than those isolated for 3 days. The short duration of the songs of both sexes reduces their value as locating signals. This disadvantage may be outweighed by the fact that a short signal reduces the chance of a predator detecting the singer by acoustic or visual cues.  相似文献   

13.
Summary Two ventral-cord neurons in the auditory system ofGryllus bimaculatus were studied electrophysiologically by stimulation with pulses of sound at a single frequency (sine-wave pulses), stridulatory songs, and artificial sounds constructed to imitate the conspecific songs. The sine-wave pulses were varied in frequency, sound intensity, duration, and repetition rate. The stridulatory songs were the conspecific calling, aggressive, and courtship songs and the calling songs of 8 sympatric gryllids (played back at different sound intensities). The artificial songs were varied in carrier frequency, pulse rate, chirp rate, and sound intensity.The LF1 neuron precisely duplicates the temporal structure of the conspecific calling (and aggressive) song over the whole intensity range (Figs. 7, 8, 10). It is sharply tuned to the carrier frequency of the song (5 kHz) and shows little or no response above 10 kHz and below 3 kHz (Figs. 1, 2). By variation of the calling song's temporal structure it can be demonstrated that the LF1 neuron is particularly suited to respond to the pulse duration and the pulse and chirp repetition rates of this song pattern (Figs. 6, 9).On the other hand, the HF1 neuron is a broad-band neuron with a maximal sensitivity at 16 kHz (Figs. 1, 4); it is tuned to the conspecific courtship song with respect to carrier frequency, the short pulse duration, and the very low pulse repetition rate (Figs. 6, 7, 8).The results demonstrate that the two ventral-cord neurons represent highly evolved channels of the auditory pathway in gryllids, each of which transmits important features of the corresponding conspecific songs to several areas of the brain (Fig. 11). But they are not ideal filters for these conspecific songs, since they also respond to many other sound signals (Fig. 10).Supported by the Deutsche Forschungsgemeinschaft as part of the program Sonderforschungsbereich 114 (Bionach), BochumUnder the auspices of the scientist exchange program of the Deutsche Forschungsgemeinschaft and the Academy of Sciences, USSRWe thank Prof. Dr. Schwartzkopff for his help and support; it was due to his initiative and organization that this work could be done in collaboration between the Sechenov Institute, Leningrad, and the Lehrstuhl für Allgemeine Zoologie, Ruhr University, Bochum. We are grateful to Mrs. I. Klotz and Mrs. B. Brücher for technical assistance.  相似文献   

14.
黑蚱蝉(Cryptotympana atrata Fabricius)鸣声的波谱特征   总被引:2,自引:2,他引:0  
本文研究了双气囊黑蚱蝉的Click声、自鸣声和群鸣声.其鸣声波形兼有调幅与鸣声主频变化特征.1.Click声主峰频率分布在2.64—5.73KHz之间.2.自鸣声主峰频率在3.6—6KHz之间,比Click声的分布宽度略窄.3.群鸣声的主峰频率分布在4—7KHz范围内.  相似文献   

15.
MM Rothbart  RM Hennig 《PloS one》2012,7(9):e43975
In Europe, several species of crickets are available commercially as pet food. Here we investigated the calling song and phonotactic selectivity for sound patterns on the short and long time scales for one such a cricket, Gryllus spec., available as "Gryllus assimilis", the Steppengrille, originally from Ecuador. The calling song consisted of short chirps (2-3 pulses, carrier frequency: 5.0 kHz) emitted with a pulse period of 30.2 ms and chirp rate of 0.43 per second. Females exhibited high selectivity on both time scales. The preference for pulse period peaked at 33 ms which was higher then the pulse period produced by males. Two consecutive pulses per chirp at the correct pulse period were already sufficient for positive phonotaxis. The preference for the chirp pattern was limited by selectivity for small chirp duty cycles and for chirp periods between 200 ms and 500 ms. The long chirp period of the songs of males was unattractive to females. On both time scales a mismatch between the song signal of the males and the preference of females was observed. The variability of song parameters as quantified by the coefficient of variation was below 50% for all temporal measures. Hence, there was not a strong indication for directional selection on song parameters by females which could account for the observed mismatch. The divergence of the chirp period and female preference may originate from a founder effect, when the Steppengrille was cultured. Alternatively the mismatch was a result of selection pressures exerted by commercial breeders on low singing activity, to satisfy customers with softly singing crickets. In the latter case the prominent divergence between male song and female preference was the result of domestication and may serve as an example of rapid evolution of song traits in acoustic communication systems.  相似文献   

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