HAPTOTROPISM 



495 



contact but perhaps by pressure against the support. Longitudinal growth in the 

 basal region comes rapidly to a standstill, although the tendril may by no means 

 have reached the length attainable if a support be not grasped. Further, 

 a spiral twisting manifests itself in the basal region, which is of great service to 

 the plant inasmuch as it is the means of drawing the branch closer to the support. 

 For purely mechanical reasons this intermediate spiral changes its direction at 

 least once, but several such reversals of the spiral may frequently be noticed 

 (Fig. 153 W). That this reversal is mechanically necessary, may be readily 

 demonstrated by attempting to produce a spiral coiling in a cord or piece of 

 rubber-tubing fixed at both ends. This spiral coiling recalls the autonomous 

 curvatures already noted as occurring in older tendrils that have found no 

 supports, since it always arises by excessive growth on the upper side. There 

 are good reasons for believing, however, that the two phenomena are not iden- 

 tical, since intermediate spiral coils occur, after the clasping of the support, 

 in tendrils which exhibit no free senile coiling (Vitis, DARWIN, 1876 a). [FITTING 

 (1903 b) has shown that the incoiling of the base of the tendril after attachment 

 to a support is a stimulus phenomenon which takes place in consequence of a 

 growth acceleration in the median region.] 



The following additional changes taking place in tendrils which have suc- 

 ceeded in finding a support, may also be noted. Not 

 infrequently secondary thickening accompanied by 

 a large development of sclerenchyma appears not only 

 in the part immediately in contact with the support 

 but also in the basal region of the tendril as well, which 

 renders the tendril more capable of fulfilling its function 

 (TREUB, 1882-3 ; EWART, 1898). Some tendrils also 

 give off a secretion which helps them to adhere (O. 

 MULLER, 1887) ; as to these and other morphogenic 



results of contact stimulus compare p. 315. Finally Fi 7 tendril whose 



we must note that functional tendrils remain alive for tip has just begun to coil round 



a much longer time than those which have been un 



successful in finding a support ; the latter soon die, tion . n the support and on the 



wither, or are thrown off. 



Haptotropism manifests itself not merely in tendrils ace 



ace 



serving as specific climbing organs and which have somedWancefromthe 

 entirely relinquished their previous functions and ^ 

 become adapted specially for that purpose, but it is the original coiim/; the point 



Tiii ji 1-11 j marked 4 is now in contact 



manifested also in other organs which have remained with the support. (After FITT- 



functional so far as their main duties are concerned, ING) - 



but which add as a subsidiary function that of acting as 



climbing organs. Thus, for instance, ordinary roots may become sensitive to 



contact in their growing regions and may respond with haptotropic curvatures 



(SACHS, 1873, 436 ; [NEWCOMBE, 1902 ; NEMEC, 1904]) ; and this capacity is so 



to many different families, e.g. Clematis, Maurandia, Lophospermum, Tro- 

 paeolum, Solanum jasminoides, &c., grasp supports by means of their petioles, 

 while the leaf blades continue to act purely as assimilatory organs. Fumaria 

 officinalis also climbs by means of unaltered laminae. Nepenthes may also be 

 referred to in this connexion, where a certain part of the leaf functions as a tendril, 

 while of the remainder, one part assimilates carbon-dioxide and one part acts as 

 an insect-trap. Lophospermum may be specially mentioned as an example of a 

 climber whose principal axis is sensitive to contact and twines round a support 

 and in addition possesses both sensitive petioles and internodes. None of the 

 examples cited have as yet been fully investigated from a physiological stand- 



