but as the flat top curls round the cylindrical and thin proboscis, or round a bristle, the pollinia necessarily diverge. As soon as the saddle has clasped the bristle and the pollinia have diverged, a second movement commences, which action, like the last, is exclusively due to the contraction of the saddle-shaped disc of membrane, as will be more fully described in the ninth chapter. This second movement is the same as that in O. mascula and its allies, and causes the divergent pollinia, which at first projected at right angles to the needle or bristle (see fig. F), to sweep through an angle of nearly ninety degrees towards the tip of the needle (see fig. G), so as to become depressed and finally to lie in the same plane with the needle. In three specimens, this second movement was effected in from thirty to thirty-four seconds after the removal of the pollinia from the anther-cells, and therefore in about fifteen seconds after the saddle had clasped the bristle.
The use of this double movement becomes evident if a bristle with pollinia attached to it, which have diverged and become depressed, be pushed between the guiding ridges of the labellum into the nectary of the same or another flower (compare figs. A and G); for the two ends of the pollen-masses will be found now to have acquired such a position that the end of the one strikes against the stigma on the one side, and the end of the other at the same moment strikes against the stigma on the opposite side. The secretion on the stigmas is so viscid that when the pollinia are withdrawn, the elastic threads by which the packets of pollen are bound together are ruptured; and some dark-green grains may be seen, even by the naked eye, remaining on the two white stigmatic surfaces. I have shown this little experiment to several
