Dynamic comparison of the development of combinatory manipulations between chimpanzee and human infants

2001 ◽  
Vol 24 (1) ◽  
pp. 65-66
Author(s):  
Hideko Takeshita

I present my observations of combinatory manipulations by three infant chimpanzees in a series of test tasks. Common characteristics of motor patterns were observed across the tasks between both infant chimpanzees and 1-year-old infants. Based on the results, I point out that comparative approach can illuminate Thelen et al.'s arguments.

2009 ◽  
Vol 12 (4) ◽  
pp. 621-631 ◽  
Author(s):  
Gabriella Lakatos ◽  
Krisztina Soproni ◽  
Antal Dóka ◽  
Ádám Miklósi

1996 ◽  
Vol 83 (2) ◽  
pp. 611-614 ◽  
Author(s):  
Shoji Itakura

In human infants, index finger extension is shown frequently even from 3 months old, and it is considered that such pointing develops into deictic and communicative pointing; however, there are many reports that chimpanzees do not point with the index finger. In the present study the manual actions of two infant chimpanzees were observed when the experimenter was trying to make eye contact with them. The result shows that pointing was shown very rarely by these infant chimpanzees even morphologically.


Author(s):  
Guillaume Dezecache ◽  
Klaus Zuberbühler ◽  
Marina Davila-Ross ◽  
Christoph D Dahl

Abstract How did human language evolve from earlier forms of communication? One way to address this question is to compare prelinguistic human vocal behavior with nonhuman primate calls. An important finding has been that, prior to speech and from early on, human infant vocal behavior exhibits functional flexibility, or the capacity to produce sounds that are not tied to one specific function. This is reflected in human infants’ use of single categories of protophones (precursors of speech sounds) in various affective circumstances, such that a given call type can occur in and express positive, neutral, or negative affective states, depending on the occasion. Nonhuman primate vocal behavior, in contrast, is seen as comparably inflexible, with different call types tied to specific functions and sometimes to specific affective states (e.g. screams mostly occur in negative circumstances). As a first step toward addressing this claim, we examined the vocal behavior of six wild infant chimpanzees during their first year of life. We found that the most common vocal signal, grunts, occurred in a range of contexts that were deemed positive, neutral, and negative. Using automated feature extraction and supervised learning algorithms, we also found acoustic variants of grunts produced in the affective contexts, suggesting gradation within this vocal category. In contrast, the second most common call type of infant chimpanzees, the whimpers, was produced in only one affective context, in line with standard models of nonhuman primate vocal behavior. Insofar as our affective categorization reflects infants’ true affective state, our results suggest that the most common chimpanzee vocalization, the grunt is not affectively bound. Affective decoupling is a prerequisite for chimpanzee grunts (and other vocal categories) to be deemed ‘functionally flexible’. If later confirmed to be a functionally flexible vocal type, this would indicate that the evolution of this foundational vocal capability occurred before the split between the Homo and Pan lineages.


2019 ◽  
Author(s):  
Guillaume Dezecache ◽  
Klaus Zuberbühler ◽  
Marina Davila-Ross ◽  
Christoph D. Dahl

ABSTRACTHow did human language evolve from earlier forms of communication? One way to address this question is to compare prelinguistic human vocal behavior with nonhuman primate calls. Here, an important finding has been that, prior to speech, human infant vocal behavior exhibits functional flexibility, the capacity of producing protophones that are not tied to one specific function. Nonhuman primate vocal behavior, by contrast, is comparably inflexible, with different call types tied to specific functions. Our research challenges the generality of this claim, with new findings of flexible vocal behavior in infant chimpanzees. We used artificial intelligence consisting of automated feature extraction and supervised learning algorithms to analyze grunt and whimper vocalizations from free-ranging infants during their first year of life. We found that grunt production was highly flexible occurring in positive, neutral and negative circumstances, as already shown in human infants. We also found acoustic variants of grunts produced in different affective contexts, suggesting gradation within this vocal category. By contrast, the second most common call type of infant chimpanzees, the whimpers, was produced in only one affective context in line with standard models of nonhuman primate vocal behavior. We concluded that the most common chimpanzee vocalization, the grunt, qualifies as functionally flexible, suggesting that evolution of vocal functional flexibility occurred before the split between the Homo and Pan lineages.


Author(s):  
Miki Takahasi ◽  
Kazuo Okanoya ◽  
Reiko Mazuka

Abstract Human infants acquire motor patterns for speech during the first several years of their lives. Sequential vocalizations such as human speech are complex behaviors, and the ability to learn new vocalizations is limited to only a few animal species. Vocalizations are generated through the coordination of three types of organs: namely, vocal, respiratory, and articulatory organs. Moreover, sophisticated temporal respiratory control might be necessary for sequential vocalization involving human speech. However, it remains unknown how coordination develops in human infants and if this developmental process is shared with other vocal learners. To answer these questions, we analyzed temporal parameters of sequential vocalizations during the first year in human infants and compared these developmental changes to song development in the Bengalese finch, another vocal learner. In human infants, early cry was also analyzed as an innate sequential vocalization. The following three temporal parameters of sequential vocalizations were measured: note duration (ND), inter-onset interval, and inter-note interval (INI). The results showed that both human infants and Bengalese finches had longer INIs than ND in the early phase. Gradually, the INI and ND converged to a similar range throughout development. While ND increased until 6 months of age in infants, the INI decreased up to 60 days posthatching in finches. Regarding infant cry, ND and INI were within similar ranges, but the INI was more stable in length than ND. In sequential vocalizations, temporal parameters developed early with subsequent articulatory stabilization in both vocal learners. However, this developmental change was accomplished in a species-specific manner. These findings could provide important insights into our understanding of the evolution of vocal learning.


Author(s):  
Dean A. Handley ◽  
Lanping A. Sung ◽  
Shu Chien

RBC agglutination by lectins represents an interactive balance between the attractive (bridging) force due to lectin binding on cell surfaces and disaggregating forces, such as membrane stiffness and electrostatic charge repulsion (1). During agglutination, critical geometric parameters of cell contour and intercellular distance reflect the magnitude of these interactive forces and the size of the bridging macromolecule (2). Valid ultrastructural measurements of these geometric parameters from agglutinated RBC's require preservation with minimal cell distortion. As chemical fixation may adversely influence RBC geometric properties (3), we used chemical fixation and cryofixation (rapid freezing followed by freeze-substitution) as a comparative approach to examine these parameters from RBC agglutinated with Ulex I lectin.


2020 ◽  
Vol 477 (7) ◽  
pp. 1261-1286 ◽  
Author(s):  
Marie Anne Richard ◽  
Hannah Pallubinsky ◽  
Denis P. Blondin

Brown adipose tissue (BAT) has long been described according to its histological features as a multilocular, lipid-containing tissue, light brown in color, that is also responsive to the cold and found especially in hibernating mammals and human infants. Its presence in both hibernators and human infants, combined with its function as a heat-generating organ, raised many questions about its role in humans. Early characterizations of the tissue in humans focused on its progressive atrophy with age and its apparent importance for cold-exposed workers. However, the use of positron emission tomography (PET) with the glucose tracer [18F]fluorodeoxyglucose ([18F]FDG) made it possible to begin characterizing the possible function of BAT in adult humans, and whether it could play a role in the prevention or treatment of obesity and type 2 diabetes (T2D). This review focuses on the in vivo functional characterization of human BAT, the methodological approaches applied to examine these features and addresses critical gaps that remain in moving the field forward. Specifically, we describe the anatomical and biomolecular features of human BAT, the modalities and applications of non-invasive tools such as PET and magnetic resonance imaging coupled with spectroscopy (MRI/MRS) to study BAT morphology and function in vivo, and finally describe the functional characteristics of human BAT that have only been possible through the development and application of such tools.


2009 ◽  
Vol 18 (1) ◽  
pp. 3-12
Author(s):  
Andrea Vovka ◽  
Paul W. Davenport ◽  
Karen Wheeler-Hegland ◽  
Kendall F. Morris ◽  
Christine M. Sapienza ◽  
...  

Abstract When the nasal and oral passages converge and a bolus enters the pharynx, it is critical that breathing and swallow motor patterns become integrated to allow safe passage of the bolus through the pharynx. Breathing patterns must be reconfigured to inhibit inspiration, and upper airway muscle activity must be recruited and reconfigured to close the glottis and laryngeal vestibule, invert the epiglottis, and ultimately protect the lower airways. Failure to close and protect the glottal opening to the lower airways, or loss of the integration and coordination of swallow and breathing, increases the risk of penetration or aspiration. A neural swallow central pattern generator (CPG) controls the pharyngeal swallow phase and is located in the medulla. We propose that this swallow CPG is functionally organized in a holarchical behavioral control assembly (BCA) and is recruited with pharyngeal swallow. The swallow BCA holon reconfigures the respiratory CPG to produce the stereotypical swallow breathing pattern, consisting of swallow apnea during swallowing followed by prolongation of expiration following swallow. The timing of swallow apnea and the duration of expiration is a function of the presence of the bolus in the pharynx, size of the bolus, bolus consistency, breath cycle, ventilatory state and disease.


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