笼养朱鹮繁殖期的鸣声特征

于2005年4月采集到笼养朱鹮(Nipponia nippon)4种行为状态的鸣叫声,对其繁殖期求偶鸣叫、交尾鸣叫、假交尾鸣叫和惊叫的鸣声特征进行了分析,探讨了不同行为状态的鸣声差异。求偶鸣叫振幅小,主要频率范围在156±13.2 Hz-1 568±120.3 Hz之间(n=30),声谱谐波丰富,频带呈直线型和拱型。交尾鸣叫由7-21声连续、急促的鸣叫和一声长鸣组成,声音宏亮有力,频域特征表现为主频呈现双峰,主要频率范围在346±16.7 Hz-2 396±138.2 Hz之间(n=14),音节高度重复并多有谐波。假交尾叫声有三种声模式,模式1包含2-10声短促鸣叫声和一声长鸣;模式2仅发出多声短促鸣叫声;模式3仅一声长鸣,频域特征在三种声模式下表现不同,模式1主频呈现双峰,模式2和模式3仅有一个峰值,主要频率范围在328±18.2 Hz-2 067±189.1 Hz之间(n=38),声谱多谐波,频带形状呈下滑状或直线状。遇险惊叫声信号振幅最大,每一声信号中包含多个脉冲组,惊叫声主频较高,主要频率范围在375-2 300 Hz之间,声谱多谐波,低频频带呈直线型,高频频带呈半拱形,声音末尾有明显的降调。     

噪音环境下花臭蛙求偶鸣声特征分析

2012年7月份,在黄山浮溪地区利用超声录音设备录制并分析了繁殖季节雄性花臭蛙(Odorrana schmackeri)个体的求偶鸣声。观察发现花臭蛙繁殖活动主要集中在7月中旬,繁殖高峰期活动无昼夜规律,全天均可见求偶鸣叫及抱对产卵等行为,并且多在浅水滩处活动。花臭蛙鸣声根据音节数和声谱特征可分为4种类型:即单音节音、婴儿音、双音节音和多音节断奏音,其中,单音节音、双音节音和婴儿音较为常见。利用Selena软件给出4种声音的语图以及各自对应的能谱图,利用Sound Analysis pro v1.2对单音节音、双音节音和婴儿音的鸣声特征参数进行定量分析,分析的声音参数包括鸣叫持续时间、音节数、音节持续时间、音节间隔、主频、脉冲率等。结果表明,花臭蛙鸣声的主频范围为1.8~4.5 k Hz(n=65)。鸣声不包括超声组分,主频峰值(3.1±0.7)k Hz,与前人电生理实验所得花臭蛙听觉敏感峰值一致,说明花臭蛙主要在这一频段进行通讯。对3种常见鸣叫音声音参数的单因素方差分析结果表明,双音节音与单音节音和婴儿音在声音持续时间上存在显著性差异(P0.01),双音节音和单音节音在第二谐波声强上也具有显著性差异(P=0.01)。花臭蛙的双音节音在3种常见鸣叫音中具有最长的持续时间,为(99.5±8.4)ms,故推测,双音节音为花臭蛙繁殖期主要求偶鸣声,并通过其鸣声时长的变化来体现自身品质的好坏。     

大壁虎两种群的求偶鸣叫变异

大壁虎Gekko gecko俗称蛤蚧,可分为黑蛤蚧和红蛤蚧.黑蛤蚧主要分布在中国的广东、广西和越南的东北部,而红蛤蚧则主要分布在东南亚地区,包括越南南部、老挝、泰国等.本文对这两种蛤蚧种群的求偶鸣叫进行了定性和定量研究.经比较分析结果表明这两个种群蛤蚧的求偶鸣叫声学特征存在明显差异.大壁虎的求偶鸣叫由一系列的音节组成,可分为3段:第一段由0～5个脉冲串组成,每个脉冲串含多个脉冲(7～10);第二段由4～10个双音节组成;第三段由1～3个单音节组成,只有红蛤蚧的求偶鸣叫具有第三段.此外,黑蛤蚧和红蛤蚧的求偶鸣叫差异也表现在第二段,即双音节的结构上.黑蛤蚧的双音节呈现出复杂的频率调节模式,且第一音节和第二音节之间有明显的沉默间隔.红蛤蚧的求偶鸣叫很少或基本没有频率调节,第一音节和第二音节之间没有沉默间隔.结合这两种蛤蚧在形态、染色体和基因结构方面的显著差异,推测传统认为的大壁虎可能由两个不同的物种以及一个亚种组成.     

同一噪音环境下武夷湍蛙与凹耳蛙的求偶鸣声特征比较及其适应策略

为了解同域分布的两种无尾两栖类动物武夷湍蛙(Amolops wuyiensis)和凹耳蛙(Odorrana tormotus)在高噪音环境下的求偶鸣声特征及其适应策略,该研究利用超声录音设备录制并分析了繁殖季节武夷湍蛙和凹耳蛙雄性个体在同一噪音环境下的求偶鸣声。结果显示,繁殖期武夷湍蛙在不同时段均能发出3~6个音节数不等的单一鸣声,每个音节由2~10个声脉冲组成,鸣声平均持续时间为2198.20ms,主频为2231.90Hz,信噪声强差为33.00dB,且鸣声不含超声组分,不具备超声通讯的基础。凹耳蛙在每天的18:00—21:00有集中鸣叫行为,鸣声平均持续时间为331.80ms,主频为6665.50Hz,信噪声强差为37.00dB,且鸣声谐波包含超声组分,与前人描述一致。经进一步分析发现,武夷湍蛙和凹耳蛙的鸣声主频和声强均高于背景噪音,噪音不会对其鸣声产生掩蔽作用。通过比较分析得知,武夷湍蛙鸣声主频率<凹耳蛙,推测其声信号传播距离相对后者更远,该蛙在噪音环境下有可能通过调整自身的发声策略(即采用多音节鸣叫声、增加鸣叫时长和鸣叫频次等)来完成种内通讯,并通过改变鸣声时长来体现雄性自身的品质,以便提高对雌性的吸引力。而相同噪音环境下的凹耳蛙则可能采用较为节约能量的方式提高声信号频率的通讯策略,完成种内竞争和交流。     

褐飞虱求偶鸣声中有效声段及其特征

对褐飞虱Nilaparvata lugens (Stal) 雌、雄虫播放求偶鸣声信号的不同声段及其组合,结果表明在它们求偶识别过程中,由多个规则连续的声脉冲所组成的声段是有效的。播放不同声脉冲重复频率和主振频率组合的模拟信号,表明褐飞虱雌、雄虫求偶信号的声脉冲重复频率是它们识别异性的敏感声学特征参数,其敏感范围较窄,分别为70～90 Hz和22 Hz左右;而对主振频率的敏感范围较宽,分别为200 ～1 700 Hz和100～300 Hz。     

丹顶鹤性活动的声行为研究

丹顶鹤繁殖期的性活动可分为雄鹤求偶、雌鹤对雄性求偶的应答、两性交配和交配完结4个阶段,其相应的鸣声模式分别为雄性的求偶鸣声、雌性对雄性求偶的应答声和两性的对鸣声、两性对唱的交配声和两性的高声合唱。4个阶段鸣声都是以基本音的主频率(PF)为主音的单音调声,前3个阶段都带数个近似fn=nf0(f0=FP)关系的低幅值谐频成分。第4个阶段带数个近似fn=nf0(f0=FP)关系的高幅值谐频成分;品质因数(Q3dB)多半为4～6,声脉冲重复频率(RFP)一般为150～180Hz,而第2阶段声的RFP一般为180～260Hz。雄性鸣声的每个单次叫声中含有的音节数较少,一般不超过4个;而雌性鸣声比较复杂。每个单次叫声中含有的音节数较多,一般都在7～8个以上;但雌雄鸣声的每个音节都是由3个声脉冲组成。雄鹤鸣唱声频率变化范围较小,而雌鹤鸣唱声频率变化形式是由低到高达到高峰后又开始下降。4个阶段的鸣声都具有较好共鸣。只有第2阶段发声运动较快。而且发现雄鹤鸣唱单次鸣叫声的音节数“增多”。各阶段鸣声特性均存在差异,不同配偶间均存在显著差异,研究结果表明丹顶鹤雌雄都具有不同的鸣声,且其性活动过程中不同的鸣声行为具有较高的个体识别信号潜能。另外,求偶鸣叫声和求偶应答与对鸣声在性活动鸣声中起着决定性的作用。     

回放雄虫第二种鸣声对稻褐飞虱生殖过程的抑制作用

结果表明：1. 回放稻褐飞虱雄虫第二种鸣声 (SMVS) 1～12 h可以显著降低雌雄虫的成功交配率,而回放SMVS 24 h则对此无明显影响;2. 回放SMVS对交配率的影响主要在于对试虫相遇前的求偶过程,表现为雌虫鸣叫率显著下降,对雄虫求偶声 (FMVS) 的反应延迟;雄虫对雌虫求偶声 (FVS) 的反应程度有所降低;雌雄虫的相遇前期显著延长;3. 回放SMVS不影响交配试虫的授精率和产卵量,但影响授精的质量, 表现在精包明显变小,卵的发育率下降。     

多频大幅脉冲传感系统监测3种食源性致病菌的生长趋势

【目的】探究智能电子舌伏安法结合特定的统计分析系统是否适用于示踪食品致病性细菌生长情况的快速监测。【方法】利用智能电子舌――多频大幅脉冲传感系统的伏安法,监测液体培养基中3种食源性致病菌的16个时段生长情况所致液体基质变化过程的综合信息;结合主成分分析法对获得的复杂综合信息数据进行统计学分析,按获得的主成分得分图分析检测样品。【结果】监测能力强的电极、频率段分别是：金黄色葡萄球菌的为钨电极的100 Hz、铂电极的1 Hz、银电极的10 Hz和钛电极的10 Hz频率段;大肠杆菌O157:H7的为金电极的100 Hz、铂电极的1 Hz、钛电极的1 Hz和钨电极的100 Hz频率段;枯草芽孢杆菌的为钯电极的1、10和100 Hz 3个频率段。【结论】本试验首次用多频大幅脉冲传感系统伏安法结合主成分分析法,能够有效的监测样品细菌的生长情况,有望成为一种具有多种优点的新型检测细菌生长情况的快速监测系统。     

瓦屋山国家森林公园锄足蟾科6种的繁殖鸣声特性

在地处四川省洪雅县的瓦屋山国家森林公园录取了锄足蟾科 6种的繁殖期求偶鸣叫声。它们分隶 4属 ,即角蟾属 (Megophrys)、齿蟾属 (Oreolalax)、齿突蟾属 (Scutiger)和掌突蟾属 (Leptolalax)。在IBMPC上用“SIGNAL”软件 (EngineeringDesign ,USA)对获取的鸣声资料进行分析 ,分析的频率范围设置为 0～ 10kHz。声学分析结果表明 :峨山掌突蟾 (L oshanensi) ,小角蟾 (M minorr) ,角蟾 1种 (M sp) ,金顶齿突蟾[S (S )chintingensis],峨眉齿蟾 (O omeimontis)和无蹼齿蟾 (O schmidti)的主能峰频率平均值分别是45 2 1 9、 34 5 6 4、 2 2 93 8、 10 76 5、 10 71 0和 1849 4Hz ,每声持续时间的平均值分别是 46 2、 90 8、 99 6、72 2、 78 8和 110 3ms ,声距的平均值分别是 140 4、 2 5 3 0、 6 81 4、 15 17 7、 46 1 3和 6 19 5ms。单因子方差分析结果表明主能峰频率、每声持续时间和各声距在 6个种间差异极显著 (P <0 0 1)。LSD法多重比较的结果指出金顶齿突蟾和峨眉齿蟾间的主能峰频率无显著差异 (P =0 917>0 0 5 ) ;在每声持续时间上 ,只有峨山掌突蟾与小角蟾、角蟾 1种、峨眉齿蟾、无蹼齿蟾间差异极显著 (P <0 0 1) ;在声距上 ,峨山掌突蟾与小角蟾间无显著差异 ,角蟾 1种与无蹼齿蟾之间、峨     

四川梅花鹿发情期的几种发声行为

2006 年9 ～11 月在四川省若尔盖县铁布自然保护区,对四川梅花鹿发情期的声行为进行了初步观测,结果表明:在发情期,四川梅花鹿的发声行为可分为雌、雄鹿的报警叫声,雄鹿的吼叫声和求偶叫声。雌鹿的报警叫声持续时间257 ～ 539 ms,频率范围1409. 5 ～ 4474. 6 Hz,主频率3534. 8 ±89.12 Hz;雄鹿的报警叫声持续时间136 ～187 ms,频率范围271.8 ～3910.5 Hz,主频率3244.3 ±79.32 Hz;两者在持续时间、最低频率、最高频率上差异极显著(P < 0.01),在间隔时间上差异不显著(P = 0.624)。吼叫是雄鹿的主要发情行为之一。雄鹿每次吼叫1 声,持续时间1580 ～4972 ms,频率范围234.6 ～6171.4 Hz,主频率2264.6 ± 166.44 Hz。雄鹿吼叫声的主频率存在显著的个体差异(P <0.01)。在整个吼叫过程中,一只雄鹿的吼叫常会引起周围其它雄鹿的吼叫反应。雄鹿每日吼叫的次数与其在繁殖群中的等级序列有关,不同序列等级雄鹿的吼叫频次存在显著差异(P<0.01)。雄鹿的吼叫声在白天和夜晚均能听到,但主要发生在06:00 ～ 08:00、17:00 ～ 19:00 和01:00 ～ 03:00 三个时间段。四川梅花鹿雄鹿的求偶叫声有4 种,其生物学意义与发情炫耀、追逐、激惹和爬跨等行为有关。     

Perception of harmonics in the combination long call of cottontop tamarins, Saguinus oedipus

A number of nonhuman primates produce vocalizations with time-varying harmonic structure. Relatively little is known about whether such spectral information plays a role in call type classification. We address this problem by utilizing acoustic analyses and playback experiments on cottontop tamarins‘ combi nation long call, a species-typical vocalization with a characteristic harmonic structure. Specifically, we used habituation-discrimination experiments to test whether particular frequency components, as well as the relationship between components, have an effect on the perception and classification of long calls. In Condition 1, we show that tamarins classify natural and synthetic exemplars of the long call as perceptually similar, thereby allowing us to use synthetics to manipulate components of this signal precisely. In subsequent conditions, we tested the perceptual salience and discriminability of long calls in which we deleted (1) the second harmonic, (2) the fundamental frequency, or (3) all frequencies above the fundamental; we also examined the effects of frequency mistuning by shifting the second harmonic by 1000 Hz. Following habituation to unmanipulated long calls, tamarins did not respond (transferred habituation) to long calls with either a missing fundamental frequency or the second harmonic, but responded (discriminated) to long calls with the upper harmonics eliminated or with the second harmonic mistuned. These studies reveal the importance of harmonic structure in tamarin perception, and highlight the advantages of using synthetic signals for understanding how particular acoustic features drive perceptual classification in nonhuman primates. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

The separate and combined effects of harmonic structure, phase, and FM on female preferences in the barking treefrog (Hyla gratiosa)

In natural advertisement calls of the barking treefrog, Hyla gratiosa, a small amount of incoherent frequency modulation (FM) is present. Incoherency in the FM of a call creates inharmonicity and phase changes between its frequency components. In this study, the combined and separate effects of the harmonic structure, phase spectrum, and FM of an advertisement call on female choice were tested. The harmonic structure of a call can have a direct effect on female preference; females showed a significant preference for static-inharmonic calls over static-harmonic calls. Neither differences in phase or FM alone conferred a preference in two choice tests. However, when FM is present in both calls it does influence female preference for harmonic structure -namely harmonic calls become preferable to inharmonic calls. This reversal of female preference for inharmonicity in a call by the presence of FM suggests that call parameters may interact, and thereby effect mate choice.Abbreviations AP amphibian papilla - BP basilar papilla - FM frequency modulation - PM phase modulation - HS harmonic structure - GB Gaussian Band     

猕猴(Macaca mulatta)叫声特点的研究

本文对海南岛南湾半岛野生猕猴的正常和受惊叫声进行了分析和研究：成年母猴与幼体正常和受惊时的叫声是一种谐波结构,其叫声的变化表现为谐波频数上不同的幅值组台。成年母猴正常和受惊叫声的高幅谐波SHHA_1,2 分别为300Hz、550Hz和300Hz、1.2KHz;幼年猴正常和受惊叫声的高幅谐波SHHA_1,2,3． 分别为300Hz、1KHz、2KHz和350Hz、IKHz、3KHz。SHHA₁是波形结构中周期波上叠加的低幅波动LAP在功率谱上的反映,而SHHA_2,3,是与波行中高幅阵脉冲列HAPT相对应的,波形结构中周期波的平均周期T始终保持一致为20ms。     

Acoustic communication in the Bocon toadfish (<Emphasis Type="Italic">Amphichthys cryptocentrus</Emphasis>)

The soundscapes of many coastal habitats include vocalizations produced by species of the family Batrachoididae (toadfish and midshipman). We describe the calling and grunting behavior of male Amphichthys cryptocentrus, a tropical toadfish, and predict how these vocalizations are influenced by conspecifics. We recorded individual males, which produced broadband grunts and multi-note, harmonic “boatwhistle” calls. Grunts were either in combination with calls or stand-alone. We used a null model to test if these latter grunts were produced at random or in response to calls from conspecifics. The model supports the hypothesis that grunts were in response to calls from neighboring males, suggesting acoustic competition. Using the most conservative estimate of hearing abilities we predict that males responded to the second harmonic of neighbor’s calls (230 Hz) at amplitudes of approximately 100–125 dB re 1μPa²/Hz. We also observed that call and grunt rates increased when males were exposed to higher rates of acoustic activity from neighboring fish. Fish used grunts to respond to background calls that occurred at different amplitudes, suggesting they responded to the calls of multiple neighboring fish and not just the highest amplitude neighbor. This communication with multiple fish within hearing range suggests a communication network in which the spatial distribution of individual toadfish relative to one another will impact their vocal behavior. Thus, the density and distribution, and not just abundance, of these toadfish at a given site will influence the characteristics of the chorus and the role of this species in the local soundscape.     

Acoustically induced call modification in the white-lipped frog,Leptodactylus albilabris

The vocalization behaviour of Leptodactylus albilabris was investigated using field playback experiments. To assess the response of males to pre-recorded natural ‘chirp’ (advertisement call) and natural ‘chuckle” (aggressive call) stimuli of gradually increasing broadcast intensity, three parameters (intensity, dominant frequency and repetition rate) of the chirp call were analysed. Of the males tested, 69% showed a significant increase in chirp intensity with increased levels of both stimulus types. In response to playback of the chirp stimulus, males actively modified the dominant frequency of their chirp calls over a mean range of 91·42 Hz, and in one case as much as 400 Hz. Moreover, 12 of 17 males shifted the frequency of their call towards the dominant frequency of the chirp stimulus (2175 Hz) by either increasing or decreasing the dominant frequency of their chirp calls. In response to the natural chuckle stimulus, 83% of the males showed either a decrease or no significant change in the dominant frequency of their chirps. All eight males for which both the chirp frequency and intensity were analysed and that showed an increase in chirp intensity also showed a concomitant increase in chirp dominant frequency. These results are the first to document quantitatively the plasticity of advertisement call intensity and dominant frequency in an anuran. The possible effects of advertisement call modification on male mating success in L. albilabris is discussed.     

Loud calls ofGalago crassicaudatus andG. garnettii and their relation to habitat structure

Long distance vocalizations have been shown to be good indicators of genetic species in primates. Here the loud calls of two recently identified greater galago taxa —Galago crassicaudatus andG. garnettii — are compared and analyzed statistically. Observed differences in call structures are investigated further as potential indicators of differences in the structures of habitats frequented by the two species. Although the calls share a repetitive structure, and show similar dominant frequency bands (1,000 – 1,500 Hz), they differ significantly in the number of units per call, unit duration, inter-unit interval, highest frequency, lowest frequency, dominant frequency band, first harmonic, and call duration. The duration of theG. crassicaudatus call is more than twice that ofG. garnettii. Strong intraspecific consistency is seen in the most energetic frequency bands (dominant frequency band and first harmonic), and durations of the individual units and inter-unit intervals. Information important to species recognition is thus most likely to be contained in these features. Individual recognition may be encoded in the relative emphasis of higher level harmonics. The frequency structures of the calls will reflect requirements for acoustical transmission in a forest environment, as well as structural constraints imposed by body size. Higher frequencies detected in theG. garnettii call (up to 8,500 Hz) may have a functional significance related to distance estimation, or may simply be a reflection of smaller body size. The greater modulation of theG. garnettii call suggests that its habitat constitutes a denser or more turbulent medium for sound transmission than does the habitat ofG. crassicaudatus.     

Advertisement calls of Guenther’s frog Hylarana guentheri (Anura: Ranidae) during the breeding season

Acoustic signalling is the most important form of communication in anuran amphibians. Here we recorded and analysed the calls of 18 male Guenther’s frogs (Hylarana guentheri) from the wild during the breeding season. The advertisement calls of H. guentheri were composed of from a single note to five notes, with three-note calls the most recorded. All individuals produced calls around 600 Hz but calls ranged from 470 to 2600 Hz. Comparing the differences between individuals calls, we found within-male coefficients of variation (CV_w) of call intensity, the fundamental frequency, the first formant, the second formant, the third formant and the fourth formant were static (less than 5% variation), whereas those of note duration, call duration, call interval, numbers of pulses and dominant frequency were dynamic (larger than 15% variation). Comparisons of the call characteristics of H. guentheri in this study with other studies from China, Singapore and Vietnam found call characteristics varied greatly between the five different locations.     

Advertisement calls of two anuran amphibians,Rana tigrina andTomopterna breviceps

Rana tigrina andTomopterna breviceps occur as sympatric species at Dharwad, India. Sexually mature males produce advertisement calls. The advertisement call of both the species consist of a number of calls produced in series forming a call group. Each call group ofRana tigrina comprises 10–40 calls, whereas that ofTomopterna breviceps consists 13–141 calls. Each call consists of a pulse group with variable number of pulses which lack pulse interval. Calls of both the species exhibit similarities in (i) call consisting of series of calls with a pulse group in each call, (ii) absence of pulse interval within the pulse group, (iii) the amplitude of the first pulse being always small, and (iv) the frequency spectrum beginning from 200 Hz. Based on the similarities in the spectral features of the calls, it is suggested that the two species may be closely related to each other.     

Correlation between auditory evoked responses in the thalamus and species-specific call characteristics

This evoked potential study of the bullfrog's auditory thalamic area (an auditory responsive region in the posterior dorsal thalamus) shows that complex processing, distinct from that reported in lower auditory regions, occurs in this center. An acoustic stimulus consisting of two tones, one which stimulates either the low-frequency or the mid-frequency sensitive population of auditory nerve fibers from the amphibian papilla and the other the high-frequency sensitive population of fibers from the basilar papilla, evoked a maximal response. The amplitude of the response to the simultaneous stimulation of the two auditory organs was, in some locations, much larger than the linear sum of the responses to the individual tones presented separately. Bimodal spectral stimuli that had relatively long rise-times (greater than or equal to 100 ms) evoked much larger responses than similar sounds with short rise-times. The optimal rise-times were close to those occurring in the bullfrog's mating call. The response was dependent on the waveform periodicity and harmonic content, with a fundamental frequency of 200 Hz producing a larger response than those with fundamentals of 50, 100 or 300 Hz. Six of the natural calls in the bullfrog's vocal repertoire were tested and the mating call and warning call were found to evoke the best responses. Each of these calls stimulate the two auditory organs simultaneously. The evoked response had a long refractory period which could not be altered by lesioning the efferent telencephalic pathways. The type of spectral and temporal information extracted by the auditory thalamic area suggests that this center is involved in processing complex sounds and likely plays an important role in the bullfrog's detection of some of its vocal signals.     

Changes in the Frequency Structure of a Mating Call Decrease Its Attractiveness to Females in the Cricket Frog Acris crepitans blanchardi

In many species, females often prefer male signals that are more complex than in nature or beyond the range of calls naturally produced by conspecific males in spectral, temporal and amplitude features. In this study we examined both the ability of females to recognize signals outside the normal range of spectral frequency variation seen in male advertisement calls, and the influence of increasing call complexity by adding spectral components to enhance the attractiveness of a male advertisement call in the cricket frog Acris crepitans blanchardi, while keeping its amplitude constant. We used two different natural male call groups and created the following synthetic call groups: with a dominant frequency at 3500 Hz, i.e. at the normal dominant frequency with a frequency band within the sensitivity range of the inner ear basilar papilla; with a dominant frequency at 700 Hz, i.e. outside the normal range of variation and with a frequency band outside the sensitivity range of the basilar papilla but within the range of the amphibian papilla; with two dominant frequencies, one at 700 Hz and another at 3500 Hz, stimulating the basilar and amphibian papilla simultaneously. In double choice experiments we tested all combinations of the three call groups, and we tested the 3500 Hz call groups against the same natural call groups. Additionally, we tested the 700 Hz call groups against white noise to see whether these signals are meaningful in mate choice. Females preferred 3500 Hz call groups over all other call groups. The synthetic call group was as attractive to females as the same natural call group. The 700 Hz call group was not meaningful in mate choice. The combined (700 Hz + 3500 Hz) call group was significantly less attractive to females than the 3500 Hz call group. Thus, making a call more spectrally complex without increasing its overall amplitude decreases its attractiveness to cricket frog females.