A cortical band of gelatinous fibers causes the coiling of redvine tendrils: a model based upon cytochemical and immunocytochemical studies.

A cortical band of fiber cells originate de novo in tendrils of redvine [Brunnichia ovata (Walt.) Shiners] when these convert from straight, supple young filaments to stiffened coiled structures in response to touch stimulation. We have analyzed the cell walls of these fibers by in situ localization techniques to determine their composition and possible role(s) in the coiling process. The fiber cell wall consists of a primary cell wall and two lignified secondary wall layers (S(1) and S(2)) and a less lignified gelatinous (G) layer proximal to the plasmalemma. Compositionally, the fibers are sharply distinct from surrounding parenchyma as determined by antibody and affinity probes. The fiber cell walls are highly enriched in cellulose, callose and xylan but contain no homogalacturonan, either esterified or de-esterified. Rhamnogalacturonan-I (RG-I) epitopes are not detected in the S layers, although they are in both the gelatinous layer and primary wall, indicating a further restriction of RG-I in the fiber cells. Lignin is concentrated in the secondary wall layers of the fiber and the compound middle lamellae/primary cell wall but is absent from the gelatinous layer. Our observations indicate that these fibers play a central role in tendril function, not only in stabilizing its final shape after coiling but also generating the tensile strength responsible for the coiling. This theory is further substantiated by the absence of gelatinous layers in the fibers of the rare tendrils that fail to coil. These data indicate that gelatinous-type fibers are responsible for the coiling of redvine tendrils and a number of other tendrils and vines.

The pattern of carbon allocation supporting growth of preformed shoot primordia in Acomastylis rossii (Rosaceae).

Extreme preformation, the initiation of leaves or inflorescences more than 1 yr before maturation and function, is common in arctic and alpine habitats. This extended pattern of development provides a potential means to alleviate an apparent asynchrony between carbon supplied by photosynthesis in the summer and carbon demanded by growth in the spring. Allocation of resources to preforming organs has not been studied in herbs with multi-year patterns of preformation. Acomastylis rossii (Rosaceae) in the southern Rockies initiates leaves and inflorescences 2 yr prior to their maturation and function. Allocation to preforming organs in A. rossii was studied by means of a labeled carbon pulse chase experiment. During the summer, carbon is allocated directly to preforming organs and rhizomes from the mature leaves. Additional allocation of carbohydrate into preforming organs occurs in autumn after photosynthesis by mature leaves has ceased. Organ primordia initiated in the second year do not receive a substantial quantity of the labeled carbon from reserves stored in the rhizome the previous year. We conclude that concurrent photosynthesis is the primary source of carbon for preformation development.