BLUMEA 23 345—348 (1977) The pattern of in the and its vasculat bundles Nymphaea lotus stamens of bearing on W.A. van Heel Rijksherbarium, Leiden, 1969 I published, In with P. G. together Netherlands Heinsbroek, a of Victoria amazonica. The flowers used in that stamens paper study could be excluded that the not house conditions, I plants, which Garden at then observed structures subsequently took the opportunity were cultivated in the Bogor*). The results bundles consisting under the open air exactly the were of abaxial bundles, adaxial bundles. All bundles fertile region of the and stamen. run vein’ (Moseley, Apart from the 1958). Its This vein played thinks the the a fellner auxiliary peripheral (1956), diplophyllous is opposed advocated vein bundle who to to system is course a central of set peripheral sheath of the stamen, branch well as upwards as into the the lower end of the pollen in the middle between the the normal median vein, and its xylem Ranales is a explicable the on blade, in Meeuse this is our as My sincere opportunity schappelijk to situation thanks work a are due to there for Onderzoek van de as a paper in analogy that the teratology, laminar stamens with the 1972) (1976) hand, a stamens are medianly. By in Ranales had been as the median Meeuse (1972) that the of 1969, namely axial system. an structure, On the other terms. ventral blade fused stamen took vascula- flattened axis component Coniferous female proof of his thesis that the structure of the cone stamen scale. in the However, careful comparison with show that the vascular patterns are described above. the Director period in of the Kebun 1969. This Tropen (WOTRO), Tropen (Treub Maatschappij), stamen welcomed by authors like Lein- was of American stamens. vein. Schneider requested by the theory. the results of Cécile Lemoine-Sebastian (a.o. a in functional ground the flat insignificant an bract component (the abaxial bundles) and a bract amalgamated with different from on of laminar the auxiliary vein could be considered now central and adaxial bundles), to as apparently homogeneous suggestion brought forward According it that is consist of a dorsal and explain. However, consisted of primitiveness median auxiliary vein vascular bundle of the fused ventral the the by considering thought, mainly structures, this view the existence of difficult de its role in diverse morphological opinions the discovery of the opposed *) up ones anastomose at pursues be mentioned vascular bundle had been named the ‘auxiliary position 1961), who (Eames, disposed of ture to way green- developed conditions of the Botanic tropical same. and the central anastomoses the effect of is inverted. authors (the anatomy of the from plants which flowers of well study terminating half parallel The adaxial bundles of the resulting one thecae. In literature the last up the partly were to vascular bundles, normal in laminar structures, there proved pole on came cultivated in the green-house of the Leiden Botanic Garden. Because the possibility were sacs L. stamen morphology the GreshofF's the visit Raya, Bogor, Indonesia, was subsidized Maatschappij Rumphius Fonds, voor by the who Stichting Wetenschappelijk gave voor ine the Weten- Onderzoek and the Van Leersumfonds. in BLUMEA 346 Nymphaea lotus — Fig. 1. Outer stamen, cleared. Abaxial ground; dotted lines: vascular bundles Ibidem, adaxial view. 7 7 x. — Fig. x. — inner 5. Detail of background. 30 Fig. VOL. 23, No. 2, 3. in the background; Inner stamen, abaxial two view. 7 lower end of pollen cleared. Anther turned stamen at Interrupted view. crosses: 1977 sacs. x. abaxial — lines: pollen sacs bundles. system Fig. Interrupted 7 in the backx. — lines: vascular bundles x. Nymphaea gigantea — Fig. 6. Stamen, 90 degrees. Fig. 2. 4. Inner stamen, adaxial view. Pollen sacs removed. 7 x. in the W. A. study of 1969 showed that, Our all the floral appendages in only It is petals. is blocked. In at the vein in Victoria anastomosing, normal set, pollen peripheral a innermost separated by are of be to nothing peripheral a than more and occurs outermost a an Schneider (1976) straight a the members, member of special bundle system. wider stretch of a instead of system all the intermediate androecial comparing of bundles set stamens that the formation of the adaxial bundles sacs stamens, in which the thecae appears part a 347 slightly anastomosing adaxial bundle a vein. After auxiliary next to Nymphaea intermediate between the location of the outer sterile tissue, there is Heel : van auxiliary adaxial, distally with these agrees observations. The Bogor material permitted the study of the bundles. The central bundles are and outward sequence. The lignification lower end of the pollen and of the auxiliary In the its same stamens restricted the the similar results (figs, stamen a the adaxial bundles form straight with the thecae. There are In the that is they following forms a all. All gular I were separate transverse are according section. broadened base with the thecae two gives lateral branches off to Conard (1905), which anastomose if only sterile tissue with median bundle tangential Nymphaea excepted; forming a extension occurs. conclusion I think be considered must as sterile tissue, which is stamens ed by *) stamens homology. have laminar outermost a an (the abaxial vein' 'auxiliary quadrangular certain radial extension a bear and constant There is that, or on structures Eames, from natural localities the an quadran- system), the Secondly, In it the to occur only sterile terete tissue with consistent correlation between the ground stamens of the in all vasculature, for these groups. The cases the starting Townsville these stamens are by that stamens sacs, a the certain occurrence in an the these of taxa increase condition may of have theory adopt- and the terete and from the Missouri Botanic primitive, (Queensland, Australia), may studied. stamens flat microsporangiophores. Therefore, that some appears the location of the pollen if basal two show it a anther peripheral bundles anther occurs. and may have may in the In which stamens at anther stamens that which have become large and stating near a relation may thickness of the specialization with the form of Moseley Material Garden. a a lateral bundles vascular bundles and the width been that the suggested not proof as stamen. of the lateral members of the main central system of vascular bundles in flat of Victoria and in As 'auxiliary be adduced Nymphaea gigantea*), does of the radial branches ramifications. The conclusion is that also in none cannot instead of system median stretch of tissue, well vascularised (fig. 6). anastomosing of the median that the of unknown structures Only the filaments a study is absent. In or small short lateral vascular bundles. However, separated by median bundle occur, system. It amend this. Firstly, the Australian subgenus 1), reason have terete filaments with a single vascular bundle, and stamens in to fig. slightly anastomosing adaxial a flattened three-dimensional will try the network in the whole of also present in are of 1969, Heinsbroek and the present author study in crosses for the amalgamation theory of the nor at time. same lotus is cultivated. A Therefore it follows with stronger neither for the diplophyllous the at variations. The abaxial system is some vein' is part of the adaxial peripheral anastomosing investigated place Nymphaea upward often connections between the central and adaxial there is stamens 'auxiliary vein'. an of the adaxial system large anastomosing a the site of the thecae, at except Also in the inner system. i—5) simple basal short bundles (indicated by two outer stamens region between vein take general there is In ones. anastomoses of the Bogor Botanic Garden pond gave to sacs of the of lignification of the vascular sequence ahead of the peripheral BLUMEA 348 of the other Dicotyledons stamens as Victoria, the anatomy does in the VOL. derived, No. 23, 2, 1977 be discarded. Also, must Nymphaea lotus in fit in with the amalgamation theory of Meeuse, and not diplophyllous theory of Leinfellner. It has been (Carlquist 1969, Gottsberger plants is well known a for reported during the night stamens The at conclusion My 1974). The lotus Nymphaea used 1899). Recently for the present study in these was again Meeuse by Cramer, that grounds the increase in size & flowered also with slender — of the is in accordance with the view of Prance plants, the cantharophily in Victoria amazonica is secondary, spondence between it these plants flowered in day-time. ; anatomical on therefore the pollination by beetles for Victoria (Knoch, plants and pollination by crude beetles Bogor. The pollination method of Nymphaea gigantea in these specialisation is related with and Stebbins 1974, feature, especially is undescribed — that the increase in size, bundles, nocturnally flowering species of Nymphaea, two (1975). Teunissen authors suggested by several increase in the number of vascular increase in size and not & stamens Arias is a (1975) that primitive, given that the corre- is real. cantharophily REFERENCES S. CARLQUIST, 1969. Toward acceptable evolutionary interpretations of floral anatomy. Phytomorphology 19: 332—362. CONARD, H. CRAMER, J. M., S. 1905. 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