Root apical meristem (RAM) organization in lycophytes could be a key to understanding the early evolution of roots, but this topic has been insufficiently explored. We examined the RAM organization of lycophytes in terms of cell division activities and anatomies, and compared RAMs among vascular plants. RAMs of 13 species of lycophytes were semi-thin-sectioned and observed under a light microscope. Furthermore, the frequency of cell division in the RAM of species was analyzed using thymidine analogs. RAMs of lycophytes exhibited four organization types: type I (Lycopodium and Diphasiastrum), II (Huperzia and Lycopodiella), III (Isoetes) and RAM with apical cell (Selaginella). The type I RAM found in Lycopodium had a region with a very low cell division frequency, reminiscent of the quiescent center (QC) in angiosperm roots. This is the first clear indication that a QC-like region is present in nonseed plants. At least four types of RAM are present in extant lycophytes, suggesting that RAM organization is more diverse than expected. Our results support the paleobotanical hypothesis that roots evolved several times in lycophytes, as well as in euphyllophytes.

In the unusual aquatic Podostemaceae, the root is the leading organ of the plant body and is variously compressed and submerged as it adheres to rock surfaces in rapid water. In an anatomical comparison of the root apical meristems and root caps of 33 species that represent the major lineages of the family, the dorsiventrality of root meristems varied and was classified into four patterns: (1) The root cap is produced outward from a nearly radially symmetrical meristem. (2) The meristem and root cap are markedly dorsiventral; the outermost cells of the hood-shaped cap are acroscopic derivatives from bifacial initials on the ventral side, while the pattern on the dorsal side is similar to pattern 1. (3) Bifacial initials are on both the dorsal and ventral sides. (4) No root cap is present. An evolutionary polarity may be evident from pattern 1 to 2 and then to 3. Pattern 2 arose in the early evolution of the subfamily Podostemoideae and subsequently, pattern 3 arose in species with crustose roots, while the least specialized pattern 1 is retained in Tristichoideae and Weddellinoideae. Pattern 4 characterized by caplessness may have appeared recurrently in Tristichoideae and Podostemoideae. These evolutionary changes in the meristem preceded the specialization of external root morphologies.

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The developmental morphology of Terniopsis malayana, an unusual aquatic angiosperm from Thailand, was examined. A unique vegetative structure called the "ramulus" arises endogenously in the root tissue. The ramulus has an actively growing apical meristem. The ramulus branches several times to form a "ramulus complex" consisting of up to six ramuli, which are distichously arranged in almost a single plane. In a ramulus complex, the new ramulus (ramulus branch) is initiated on the adaxial side of the first (the basalmost) scale in the first ramulus, but at a site lateral to the first scale in later ramuli, suggesting that the new ramulus arises from axillary or extra-axillary buds of the immediately older ramulus. Ramulus growth is terminated in association with the loss of the apical meristem, and its axillary or extra-axillary buds begin to grow to form the next new ramulus instead. The flower occurs in place of the youngest ramulus, when reproductive. It seems likely that the Terniopsis ramulus and its scale are comparable to the shoot and leaf, and thus a ramulus complex is interpreted as a sympodially branched shoot.