ALBERT

Notes: Summary The corneas of some nocturnal Lepidoptera carry an array of surface protuberances (nipples), about 200 mμ high, that acts as an impedance transformer equalizing by gradual transition the refractive index of air to that of the cornea. A screening of the insect class has been carried out in the present study with respect to the variation in corneal topography seen in previous obsarvations. 361 species in most insect orders were prepared for EM by thin sectioning or platinum replication. Using the amplitude of the surface protuberances as parameter, a grouping of the cornea types was made on the basis of the well-defined variation of nipple heights observed between individuals of certain species. Thus, the corneas of one extreme group were either smooth (Fig. 4A) or possessed protrusions (Fig. 4B and C) less than about 50 mμ high, arranged either irregularly or in a regular, hexagonal array (group I). At the other extreme, there was a group with “full-sized” nipples (Figs. 1 and 3) ranging in amplitude around 250 mμ (group III). An intermediate group of nipple heights (group II) comprised corneas with “low-sized” nipples (Fig. 6) between 50 and about 200 mμ high. Regularity in the arrangement of the various types of protuberances was observed both in groups I and II (compare Figs. 4C and 8). Irregularity tended to be associated with low amplitudes (e.g. Fig. 4B), being found only in group I corneas. Full-sized nipples (group III corneas) were found only among the anagenetically highest orders, Trichoptera and Lepidoptera (Tables 3 and 4), which, however, also had corneas with low protrusions (group I) and low-sized nipples (group II). In one of the two mecopteroid orders, Diptera (Table 2), protrusions and low-sized nipples were found (the latter only in Culicomorpha). The corneas of all other orders (Table 1) had only group I corneas with one noteworthy exception, Thysanura, the most primitive order investigated. All four thysanuran species examined had corneas with low-sized nipples (Fig. 8), thus belonging to group II. The morphological findings demonstrated in the present study can be taken to illustrate the following trends. 1.a)The higher relative number of group II and III corneas (low- and full-sized nipples) in the anagenetieally highest orders and the exclusive occurrence of group III corneas in the most advanced orders, Trichoptera and Lepidoptera, may indicate a progressive development of nipples during phylogenesis. Thus, the full-sized nipples may represent an apomorphous condition. Parallelisms — leading to the appearance of low- and full-sized nipples — may have occurred several times during insect phylogenetic development, thus possibly reflecting an evolutionary potential (with or without a selective pressure for this character). b)Low-sized nipples were found in the most primitive insect order, Thysanura. This circumstance may point to regression from full-sized nipples that were present in an ancestor common to all insects. In such a case, the full-sized nipples in Trichoptera and Lepidoptera are to be considered plesiomorphous. At present nothing supports conclusively a preference for one of these two alternatives. 2.Among the Lepidoptera, a greater relative number of butterflies than moths lack full-sized nipples. This may be taken to indicate a regression of nipples in the day-flying group of insects in comparison with their possible moth-like, nocturnal ancestors. That in many species there are low-sized nipples (the regression thus being incomplete) may indicate that a function of the nipples in ranges of shorter wavelengths has brought about an arrest of the regression at lower amplitudes.

Notes: Fibroblast chemotaxis has usually been determined in Boyden-type chambers with polycarbonate filters, assuming that a stable concentration gradient of the attractant develops that causes directional migration of the cells. This view has been repeatedly challenged, and development of such gradients in vivo is unlikely. The present experiments were designed to test if a stable concentration gradient was required for normal dermal fibroblasts to migrate toward platelet-derived growth factor. It was found that a brief pulse of the attractant was required and sufficient to induce chemotaxis. The pulse had to contain a specific concentration of attractant and was ineffective when not unilateral. The observed effects could not be attributed to induction of random migration or migration on a mediator-coated surface. It is not clear which machinery is regulating this cellular behaviour, but it is suggested that cells may migrate in vivo by similar mechanisms, because the establishment of stable concentration gradients of attractants in tissues is deemed unlikely.