spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online January 3, 2006
Journal of Experimental Biology 209, 202-226 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02007
This Article
Right arrow Summary Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lillywhite, H. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lillywhite, H. B.

Water relations of tetrapod integument

Harvey B. Lillywhite*

Department of Zoology, University of Florida, Gainesville, FL 32611-8525, USA



View larger version (49K):

[in a new window]
 
Fig. 1. Generalized features of integument in four major clades of vertebrates. {alpha} and ß indicate alpha- and beta-type keratins, respectively. OG and IG indicate outer and inner epidermal generations that might be present in a squamate reptile prior to skin shedding. The mesos layer of squamates is a specialized cell type derived from {alpha} keratins and contains extracellular, laminated lipids, comprising the principal water barrier in these species.

 


View larger version (51K):

[in a new window]
 
Fig. 2. Schematic illustrations of the water permeability barrier in relation to the stratum corneum of the epidermis in four principal lineages of vertebrates. The images on the left depict the morphology of generalized integument, and drawings to the right illustrate the stylized arrangement of barrier lipids (dark bars) in relation to horny layers of stratum corneum (thin broken lines). The stratum germinativum is represented by the thick broken lines. The features shown are not to scale.

 


View larger version (175K):

[in a new window]
 
Fig. 3. Electron micrographs showing details of stratum corneum and permeability barrier of terrestrial vertebrates. (A) Section through a portion of cocoon of a burrowing hylid frog, Pternohyla fodiens. The layers of squamous epidermal cells are separated by granular extracellular materials in the subcorneal spaces. Scale bar, 500 nm. Reproduced with permission (Ruibal and Hillman, 1981Go). (B) Section through mesos layer of snake epidermis (Natrix natrix), which is the recognized permeability barrier of squamates. Laminated lipids occur between the darker bands of keratin layers. Scale bar, 100 nm. Courtesy of Lukas Landmann. (C) Section through stratum corneum of human skin. Lipids (unstained) occur between the distinct layers of keratin. Scale bar, 200 nm. Courtesy of Gopi Menon. (D) Section through epidermis of a canary, showing nucleated layers as well as stratum corneum (top). Lipids occur between the distinct layers of keratin toward top of figure. Note the multigranular bodies (source of lipids; arrows). Scale bar, 200 nm. Courtesy of Gopi Menon.

 


View larger version (46K):

[in a new window]
 
Fig. 4. Schematic illustration of the process involved in formation of intercellular stratum corneum lipids of a mammal following extrusion from lamellar bodies. The lipid content of lamellar bodies is altered in composition and rearranged into long lipid lamellae that fill the extracellular regions in the stratum corneum. Reproduced from Bouwstra et al. (2003bGo), with permission.

 


View larger version (86K):

[in a new window]
 
Fig. 5. Electron micrograph showing ultrastructure of epidermis in hatchling king snakes Lampropeltis getula, sampled on the day of hatching (A) and 2 days after the first ecdysis (B). The photos feature the mesos layer (m), which pre-shed has disorganized bilayer structures (arrows) but well-organized and continuous bilayers in the extracellular domains of post-shed skin (arrows). The number of bilayers is doubled in the post-shed skin relative to pre-shed. After Tu et al. (2002Go).

 


View larger version (13K):

[in a new window]
 
Fig. 6. Whole body resistance to water vapor diffusion (solid circles) and cutaneous evaporation rates (broken line) as a function of ambient temperature in pigeons, Columba livia. Data are re-plotted from Webster et al., 1985Go.

 





© The Company of Biologists Ltd 2006