[Retinal adaptations to habitat].

Revue canadienne de biologie Pub Date : 1981-03-01
M A Ali
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Abstract

Vertebrates have, through the process of evolution, adapted to their photic environment. This is well manifested in the retinal adaptations to various habitats. Although all vertebrates are considered, emphasis is placed on fishes because they form about 50% of the vertebrate species. In addition, they occupy a wide range of habitats, thus retinal modifications of fishes serve as models for all other vertebrates. The present article reviews morphological, physiological and biochemical retinal adaptations. The quality and quantity of light reaching the aquatic organism are functions of the incident light as well as the aquatic environment. Thus, in well lit, clear waters fishes are arhythmic and possess almost equal populations of rods and cones; whereas fishes in dimly lit environments (due to turbidity or depth) have retinas that are more specialised for high sensitivity-multi-banked retinas, long outer segments, grouped photoreceptors, hypertrophied ellipsoid mitochondria, reflecting tapetum. Similarly, the ratio and distribution of visual pigments (rhodopsin and porphyropsin) and S-potential change with respect to fresh/sea water, clear/turbid water and air/aquatic environments. Thus, in fresh waters, where the photic environment shifts to longer wavelengths, porphyropsin predominates; while in land vertebrates and almost all marine fishes the dominant pigment is rhodopsin. With respect to the latter, fishes in turbid, greenish or yellowish coastal waters have 'rhodopsins' with lambda mas above 500 nm; fishes in clear coastal habitats have 'rhodopsins' with lambda max near 500 nm; while those in the blue-lit environment of deep seas have lambda max below 500 nm. The retinal pigment composition is also associated with habitat changes during diadromous migrations in fishes or during amphibian metamorphosis. It is interesting to note that the dorsal and ventral retinas of Rana catesbeiana and Anableps microlepis which view aquatic and aerial environments, respectively, show a predominately porphyropsin-rich dorsal retina compared to a rhodopsin-rich ventral retina. Similar shifts in the S-potential are observed with change in habitats. Fresh water fishes exhibit L-responses with lambda max in longer wavelengths compared to marine fishes where the maximum of the L-response shifted towards shorter wavelengths.

[视网膜适应栖息地]。
脊椎动物通过进化的过程,已经适应了它们的光环境。这在视网膜对各种栖息地的适应中得到了很好的体现。虽然所有脊椎动物都被考虑在内,但重点放在鱼类上,因为它们占脊椎动物物种的50%左右。此外,它们占据了广泛的栖息地,因此鱼类的视网膜修饰可以作为所有其他脊椎动物的模型。本文综述了视网膜的形态、生理和生化适应。到达水生生物的光的质量和数量是入射光和水生环境的函数。因此,在光线充足、清澈的水中,鱼类是有节奏的,并且拥有几乎相等数量的杆状和锥状细胞;然而,在光线昏暗的环境中(由于浑浊度或深度),鱼类的视网膜更适合高灵敏度——多视网膜、长外节、成组的光感受器、肥大的椭球状线粒体、反射绒毡层。同样,视色素(视紫红质和卟啉质)的比例和分布以及s电位在淡水/海水、清澈/浑浊水和空气/水生环境中也会发生变化。因此,在淡水中,光环境转向更长的波长,卟啉占主导地位;而在陆地脊椎动物和几乎所有的海洋鱼类中,主要的色素是视紫红质。在后一种情况下,在浑浊、淡绿色或淡黄色沿海水域的鱼类,其“视紫红质”的λ大于500纳米;在清澈的沿海栖息地的鱼类具有“视紫红质”,λ Max接近500 nm;而深海蓝光环境中的λ Max则低于500纳米。视网膜色素的组成也与鱼类双产卵洄游或两栖动物变态过程中栖息地的变化有关。值得注意的是,分别观察水生和空中环境的斑蛙(Rana catesbeiana)和小鳞蛙(Anableps microlepis)的背侧和腹侧视网膜,与富含视紫红质的腹侧视网膜相比,主要表现为富含卟啉的背侧视网膜。s势也随着生境的变化而发生类似的变化。淡水鱼类在较长的波长上表现出l -响应,而海洋鱼类在较短的波长上表现出l -响应的最大值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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