fine bristle of hair, into the minute and rounded orifice of the nectary, which, small as it is, is partly choked up by the rostellum. This contrivance of the guiding ridges may be compared to the little instrument sometimes used for guiding a thread into the fine eye of a needle.
Now let us see how these parts act. Let a moth insert its proboscis (and we shall presently see how frequently the flowers are visited by Lepidoptera) between the guiding ridges of the labellum, or insert a fine bristle, and it is surely conducted to the minute orifice of the nectary, and can hardly fail to depress the lip of the rostellum; this being effected, the bristle comes into contact with the now naked and sticky under surface of the suspended saddle-formed disc. When the bristle is removed, the saddle with the attached pollinia is removed. Almost instantly, as soon as the saddle is exposed to the air, a rapid movement takes place, and the two flaps curl inwards and embrace the bristle. When the pollinia are pulled out by their caudicles, by a pair of pincers, so that the saddle has nothing to clasp, I observed that the tips curled inwards so as to touch each other in nine seconds (see Fig. D), and in nine more seconds the saddle was converted by curling still more inwards into an apparently solid ball. The probosces of the many moths which I have examined, with the pollinia of this Orchis attached to them, were so thin that the tips of the saddle just met on the under side. Hence a naturalist, wo sent me a moth with several saddles attached to its proboscis, and who did not know of this movement, very naturally came to the extraordinary conclusion that the moth had cleverly bored through the exact centres of the so-called sticky glands of some Orchid.
Of course this rapid clasping movement helps to fix the saddle with its pollinia upright on the proboscis, which is very important; but the viscid matter rapidly setting hard would probably suffice for this end, and the real object gained is the divergence of the pollinia. The pollinia, being attached to the flat top or seat of the saddle, project at first straight up and are nearly parallel to each other; 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 seventh 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 nearly 90 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 30 to 34 seconds after the removal of the pollinia from the anther-cells, and therefore in about 15 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 pollinia will be found to have acquired exactly 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. These stigmas are so viscid that they rupture the elastic threads by which the packets of pollen are bound together; and some dark-green grains will be seen, even by the naked eye, remaining on the two white stigmatic surfaces. I have shown this little experiment to several persons, and all have expressed the liveliest admiration at the perfection of the contrivance by which this Orchid is fertilised.
As in no other plant, or indeed in hardly any animal, can adaptations of one part to another, and of the whole to other organized beings widely remote in the scale of nature, be named more perfect than those presented by this Orchis, it may be worth while briefly to sum them up. As the flowers are visited both by day and night-flying Lepidoptera, I do not think that it is fanciful to believe that the bright-purple tint (whether or not specially developed for this purpose) attracts the day-fliers, and the strong foxy odour the night-fliers. The upper sepal and two upper petals form a hood protecting the anther and stigmatic surfaces from the weather. The labellum is developed into a long nectary in order to attract Lepidoptera, and we shall presently give reasons for suspecting that the nectar is purposely so lodged that it can be sucked only slowly (very differently from in most flowers of other families), in order to give time for the curious chemical quality of the viscid matter on the under side of the saddle setting hard and dry. He who will insert a fine and flexible bristle into the expanded mouth of the sloping ridges on the labellum will no doubt that they serve as guides; and that they effectually prevent the bristle or proboscis from being inserted obliquely into the nectary. This circumstance is of manifest importance, for, if the proboscis were inserted obliquely, the saddle-formed disc would become attached obliquely, and after the compounded movement of the pollinia they could not strike the two lateral stigmatic surfaces.
Then we have the rostellum partially closing the mouth of the nectary, like a trap placed in a run for game; and the trap so complex and perfect, with its symmetrical lines of rupture forming the saddle-shaped disc above, and the lip of the pouch below; and, lastly, this lip so easily depressed that the proboscis of a moth
