PRESENCE OR ABSENCE OF A "BRIM."
That the extension of the glabella to the front of the cephalon is a primitive feature is well shown by the development of Sao (Barrande, 1852, pl. 7), Ptychoparia (Beecher, 1895 C, pl. 8), and Paradoxides (Raymond, Bull. Mus. Comp. Zool., vol. 57, 1914), although in the last genus the protaspis has a very narrow brim, the larva during the stages of introduction of new segments a fairly wide one, and most adults a narrow one.
The brim of Sao seems to be formed partly by new growth and partly at the expense of the frontal lobe, for that lobe is proportionately shorter in the adult than in the protaspis. In Cryptolithus and probably in Harpes, Harpides, etc., the brim is quite obviously new growth and has nothing to do with the vital organs. Its presence or absence may not have any great significance, but when the glabella extends to the frontal margin, it certainly suggests a more anterior position of certain organs. In Sao, the only trilobite in which anything is known of the position of the hypostoma in the young, the posterior end is considerably further forward in a specimen a. 5 mm. long than in one 4 mm. long, thus indicating a backward movement of the mouth during growth, comparable to the backward movement of the eyes.
The very smallest specimens of Sao show a simple, unsegmented axial lobe, and the same simplicity has been noted in the young of other genera. Beecher considered this as due to imperfect preservation of the exceedingly small shells, which practically always occur as moulds or casts in soft shale. There is, however, a very general increase in the strength of glabellar segmentation in the early part of the ontogeny of all trilobites whose life history is known, and in some genera, like the Agnostidæ, there is no question of the comparatively late acquisition of glabellar furrows. Even in Paradoxides, the furrows appear late in the ontogeny.
If absence of eyes on the dorsal surface be primitive, as Beecher has shown, and if the large pygidium, narrow axial lobe, and long unsegmented glabella be primitive, then the known protaspis of the Mesonacidæ and Paradoxidæ is not primitive, that of the Olenidæ is very primitive, and that of the Agnostidæ is primitive except that in one group the axial lobe, when it appears, is rather wide, and in the other a brim is present.
Subsequent development from the simple unsegmented protaspis would appear to show, first, an adaptation to swimming by the use of the pygidium; next, the invagination of the appendifers as shown in the segmentation of the axial lobe indicates the functioning of the appendages as swimming legs; then with the introduction of thoracic segments the assumption of a bottom-crawling habit is indicated. Some trilobites were fully adapted for bottom life, and the pygidium became reduced to a mere vestige in the production of a worm-like body. Other trilobites retained their swimming habits, coupled with the crawling mode of life, and kept or even increased (Isotelus) the large pygidium.