scholarly journals And thereby hangs a tail: morphology, developmental patterns and biomechanics of the adhesive tails of crested geckos ( Correlophus ciliatus )

2021 ◽  
Vol 288 (1953) ◽  
pp. 20210650
Author(s):  
Aaron H. Griffing ◽  
Thomas J. Sanger ◽  
Lilian Epperlein ◽  
Aaron M. Bauer ◽  
Anthony Cobos ◽  
...  

Among the most specialized integumentary outgrowths in amniotes are the adhesive, scale-like scansors and lamellae on the digits of anoles and geckos. Less well-known are adhesive tail pads exhibited by 21 gecko genera. While described over 120 years ago, no studies have quantified their possible adhesive function or described their embryonic development. Here, we characterize adult and embryonic morphology and adhesive performance of crested gecko ( Correlophus ciliatus ) tail pads. Additionally, we use embryonic data to test whether tail pads are serial homologues to toe pads. External morphology and histology of C . ciliatus tail pads are largely similar to tail pads of closely related geckos. Functionally, C . ciliatus tail pads exhibit impressive adhesive ability, hypothetically capable of holding up to five times their own mass. Tail pads develop at approximately the same time during embryogenesis as toe pads. Further, tail pads exhibit similar developmental patterns to toe pads, which are markedly different from non-adhesive gecko toes and tails. Our data provide support for the serial homology of adhesive tail pads with toe pads.

2013 ◽  
Vol 275 (3) ◽  
pp. 295-312 ◽  
Author(s):  
Yuta Mashimo ◽  
Rolf G. Beutel ◽  
Romano Dallai ◽  
Chow-Yang Lee ◽  
Ryuichiro Machida

2018 ◽  
Vol 92 (6) ◽  
pp. 1018-1027 ◽  
Author(s):  
Lukáš Laibl ◽  
Peter Cederström ◽  
Per Ahlberg

AbstractThis study documents the early post-embryonic developmental stages (protaspides and early meraspides) of the Cambrian trilobite Ellipsostrenua granulosa (Ahlberg, 1984) from the Gärdsjön Formation of Jämtland, Sweden. The early protaspid stage is characterized by a circular outline of the exoskeleton, two pairs of fixigenal spines, a short preglabellar field, a genal swelling, and prominent bacullae. The late protaspid stage differs only in having the trunk portion discernible. Early meraspid cranidia are sub-rectangular with prominent palpebral lobes, a wide anterior margin, a proportionally long anterior branch of the facial suture, and intergenal spines. Meraspid pygidia tentatively assigned to this species possess comparatively long macrospines. Small hypostomes associated with E. granulosa bear at least four pairs of marginal spines. A comparison of the early developmental stages of E. granulosa with some other species of Ellipsocephalidae and with species of the closely related Estaingiidae reveals several similarities. The conservative morphology of the early protaspid stage with only two pairs of fixigenal spines, the timing of the development of the trunk portion, and the presence of genal swellings and prominent bacullae could be phylogenetically informative. The range of size variation of the early protaspid stages in two families may be related either to taxonomical differences between Ellipsocephalidae and Estaingiidae, or to environmental differences in various paleogeographic settings.


Development ◽  
1970 ◽  
Vol 23 (3) ◽  
pp. 705-718
Author(s):  
N. M. Tyrer

An understanding of the physiological and structural development of an embryo requires a knowledge of the precise state that development has reached. Without this knowledge it is not possible to compare findings from experiments performed on different embryos or to relate them to structural changes during development. In previous work on Acridid embryos two methods have been used in estimating the stage of development. Some authors have defined embryonic stages by their age from the time of oviposition (Slifer, 1932; Roonwal, 1936, 1937; Hong, 1968), while others have described development in a series of arbitrarily chosen stages, which are based primarily on changes in the external morphology (Steele, 1941; Jhingran, 1947; Mathée, 1951; Shulov & Pener, 1959, 1963). The eggs of Schistocerca gregaria are laid in pods of 30–90. Pods were collected and kept under constant conditions in order to investigate the development of the embryonic muscle (Tyrer, 1968, 1969).


2014 ◽  
Vol 30 (4) ◽  
pp. 1285-1296 ◽  
Author(s):  
Jorge Torre ◽  
Omar Vidal ◽  
Robert L. Brownell

2015 ◽  
Vol 44 (1) ◽  
pp. 42-68 ◽  
Author(s):  
Maximilian Fraulob ◽  
Rolf Georg Beutel ◽  
Ryuichiro Machida ◽  
Hans Pohl

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