两种米纹蝗雄性鸣声的比较研究(直翅目,蝗总科)

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。     

乌苏里蝈螽和优雅蝈螽雄性鸣声结构的比较研究

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。     

四种草螽雄性鸣声的研究

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.     

历山自然保护区四种蟋蟀鸣声结构的比较研究(直翅目:蟋蟀总科)

应用计算机技术,分析了山西历山自然保护区的白须双针蟋,短翅灶蟋,银川油葫芦,迷卡斗蟋4种蟋蟀雄性的鸣声结构,白须双针蟋雄性鸣声的每个脉冲组持续时间和每个脉冲组的脉冲数不同,主能峰频率为6．5kHz,短翅灶蟋雄性鸣声的时域波形较规则,每个脉冲组由3个脉冲构成,每个脉冲组的持续时间,脉冲组间隔基本相同,主能峰频率6．6kHz,银川油葫芦雄性的鸣声由两类脉冲组构成,主能峰频率为3．94kHz,迷卡斗蟋雄性鸣声的时域波形较规则,每个脉冲组由6－7个脉冲构成,主能峰频率为3．86kHz。     

北方两种常见蝈螽鸣声与发声器的比较研究

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.     

新疆四种螽斯雄性鸣声结构的比较研究

比较分析了新疆短翅姬螽Metrioptera brachyptera(Linnaeus)、疣谷盾螽Decticus verrucivorus(Linnaeus)、灰螽斯Platycleis grisea (Fabricius)和长瓣螽斯Tettigonia caudata(Charpentier)雄性鸣声结构.研究结果表明,短翅姬螽和疣谷盾螽雄性鸣声具单一脉冲序列,灰螽斯和长瓣螽斯雄性鸣声具有多个脉冲序列组成.短翅姬螽脉冲组持续时间为0.290 s ～0.525 s,间隔时间较长,每个脉冲组有6～7个脉冲构成.疣谷盾螽脉冲组持续时间为0.080 s±0.003 s,有6个脉冲构成.灰螽斯的脉冲序列数较多,脉冲序列持续时间为0.20 s～0.27 s,间隔时间较短,为0.20 s～0.40s,有3～4个脉冲组组成,脉冲组持续时间为0.066 s±0.003 s,脉冲组重复率为13.2次/s.长瓣螽斯脉冲序列持续时间为2.590 s ～6.670 s,脉冲组持续时间为0.009 s-0.018 s.     

鼻优草螽和苍白优草螽鸣声和发声器的研究

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。     

四种网翅蝗鸣声结构分析(直翅目,蝗总科)

分析了网翅蝗科4种蝗虫雄性的鸣声。研究结果表明,宽翅曲背蝗Pararcyptera microptera meridionalis(Ikonn.)具有2类脉冲组,脉冲组持续时间分别为0.016~0.028s,0.20±0.01s;隆额网翅蝗Arcyptera coreanaShiraki有3类脉冲组,脉冲组的持续时间分别为0.11±0.02s,0.034±0.005,0.885±0.020s。曲线越度蝗Podismopsis sinucarinataZhengetLian每1脉冲序列含4~7脉冲组,脉冲组持续时间为0.023~0.030s;二声越度蝗Podismopsis bisonita Zheng etal.每1脉冲序列含2~4个脉冲组,脉冲组持续时间为0.119~0.140s。     

中国两种常见树蟋雄性鸣声的比较研究(直翅目,树蟋科)

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.     

三种蛙鸣声特征比较研究

本文用计算机鸣声分析技术对杭州地区的黑斑蛙、泽蛙和饰纹姬蛙的鸣声进行了分析。黑斑蛙鸣声一般由４个较长的脉冲组成,每个脉冲持续时间３０－５０ｍｓ,脉冲率（ＰＲ）８－１１个／ｓ。每声持续时间３７０－５１０ｍｓ,各脉冲的能量主要集中在３个能峰上,主能峰位于２．０－２．４ｋＨｚ之间。泽蛙鸣声由６－７个前后紧接的纺锤形的脉冲串组成,ＰＲ为７１．７次／ｓ,每声持续时间８４．２５±７．１２ｍｓ,主峰频率为１．３９５±０．０２３ｋＨｚ。但嵊泗岛上的泽蛙在鸣声的结构、频谱与时域特征上有些差异。在泽蛙的变音鸣声中,纯音占大部分,纯音的频率约为１．２８ｋＨｚ。饰纹姬蛙的鸣声由１１－１３个间隔较开的减幅振荡脉冲组成,每个脉冲持续时间１６．０６±２．０８ｍｓ,ＰＲ为３６．２３次／ｓ,每声持续时间３０８．６４±２２．９３ｍｓ,主峰频率为１．３６±０．０２ｋＨｚ。但与安徽宣城地区饰纹姬蛙的分析结果差异较大。３种蛙鸣声的波形结构和频谱特性各不相同,可能与它们的声囊构造有关。不同的地区蛙鸣声物理结构上的差异,可能是环境差异所致。     

Acoustic communication in Okanagana rimosa (Say) (Homoptera: Cicadidae)

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.     

The ultrasonic mating signal of the male lesser wax moth

Abstract. Male lesser wax moths, Achroia grisella (Fabricius) (Lepidoptera: Pyralidae: Galleriinae), produce both a pheromone and an ultrasonic acoustic signal that function in mate attraction. We describe the structure of the acoustic signal, in particular the interpulse intervals and the spectral properties of the pulses. The song consists of a train of ultrasonic pulses. The interpulse interval is usually bimodally distributed, but can sometimes be unimodal. This reflects variation in the duration of the up and down wing strokes. The pulses are also usually paired which can produce multimodality of the interpulse intervals. These paired pulses probably reflect wingbeat asynchrony because they are not found in males in which the signalling capability of one wing's sound producing structure is abolished.
The song's frequency spectrum has peaks at around 80 and 100 kHz. The first peak varies significantly with male size, with larger males producing a lower frequency peak. The second peak is associated with male age, with 1-day-old males producing songs with a lower frequency second peak. Thus the ultrasonic song of lesser wax moths is more complex in structure than previously reported and could provide potentially important cues to females. However, the ability of females to discriminate such detail is not known.     

Brain projections and information processing of biologically significant sounds by two large ventral-cord neurons ofGryllus bimaculatus DeGeer (Orthoptera,Gryllidae)

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.     

鸣鸣蝉(Oncotympana maculaticollis Motschulsk)自鸣声信息及其频谱的双倍频特征

本文报道庐山鸣鸣蝉自鸣声信息的长码与短码结构及其部分频谱的双倍频特征。庐山鸣鸣蝉多次重复的“MUYING……MUYING MU A”叫声,仅由三种信息MU(简称M),YING(I)及“A”重复编排而成。M与A的特征类似:持续时间大于170ms,波形具有约为6ms的周期,频谱主峰频率(MPF)约为4kHz,谱能量主要分布在2—7kHz频带内。这是鸣鸣蝉自鸣声长码的近似不变特征。长码I与M,A的不同点是持续期多在300ms以上,MPF为变频特征,在2.7—7.2kHz之间变化,谱能量较均匀地分布在0—14kHz频带内。约为6ms的准周期内含有几个频率不同的脉冲串(PT),这些不同频率的PT称为短码。这表明鸣鸣蝉自鸣声中长码是由变频短码组成的。M与A部分频谱具有双倍频特征,即构成频谱的子谱峰频率为两个倍频序列,其中一序列的共振峰为主峰,另一序列的共振峰为次峰。     

黑蚱蝉(Cryptotympana atrata Fabricius)鸣声的波谱特征

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.