TL;DR: Definition of some vascular plant families is unsatisfactory and, consequently, it is impossible to classify them adequately and the lack of an analytical key to the families based on easily observed, widespread characters sometimes results in surprising misinterpretations.
Abstract: Definition of some vascular plant families is unsatisfactory and, consequently, it is impossible to classify them adequately. The lack of an analytical key to the families based on easily observed, widespread characters sometimes results in surprising misinterpretations. A striking example in this regard is the Casuarinaceae. Engler (1897) considered them to be true Angiospermae (Dicotyledoneae, Order 1. Verticillatae). Melchior (Engler's Syllabus der Pflanzenfamilien, vol. 2. 1964) and Wettstein (1935) concur with Engler, but Hutchinson (1973) placed the Casuarinales (Order 18) between the Juglandales and Urticales. According to Takhtajan (1969, 1973) the Casuarinaceae probably arose from the Hamamelidales. Gaussen (1940) derived the Casuarinaceae from the Articulatae. Hegnauer (1964) recalls that authors have noted similarities between Casuarina, Equisetum, Ephedra, and the Coniferae, but states the chemistry of the family is not well enough known to determine its position in the system. The Nymphaeaceae is another difficult family to place in the system. In Engler's Syllabus, Order 16 Ranunculales includes the suborders Ranunculineae and Nymphaeineae. The latter contains families Nymphaeaceae, and Ceratophyllaceae. The first of these is divided into the subfamilies Cabomboideae, Nymphaeoideae and Nelumbonoideae. Wettstein places the Nymphaeaceae in Order 18, Polycarpicae, following Family 20, Berberidaceae. The Nymphaeaceae contains the same subfamilies as in Engler's Syllabus. The following family is Ceratophyllaceae, which is considered closely related to the Nymphaeaceae. Hegnauer (1969) states that the evidence is not sufficient to form an opinion with respect to the relationships of all the genera included in the Nymphaeaceae. Hutchinson puts the family in the Ranales and it includes Nelumbo, Euryale, Nuphar and Barclaya. He treats Cabombaceae and Ceratophyllaceae as separate families. According to Kubitzki (1972), the Nymphaeaceae, s. str., do not belong in the Polycarpicae. A third example is the Cyclanthaceae. Wettstein placed them in the Order Synanthae, with the Palmae and Araceae but the plants of the three families are very different. The Palmae are mostly derived, the Cyclanthaceae include at least two different plant types, and the Araceae, mostly herbaceous, exhibit distinctive features. In Engler's Syllabus, the Order Synanthae (Cyclanthales) comprises the family Cyclanthaceae with subfamilies Carludovicoideae and Cyclanthoideae. These are herbs of palm-like habit and deeply bilobed leaves. They are very old, reduced and derived relicts. Hegnauer considers the Palmae, Cyclanthaceae and Pandanaceae more closely related to one another than to the herbaceous Araceae, Typhaceae and Sparganiaceae. According to Takhtajan, the Arales, Arecales and Cyclanthales were derived from the immediate ancestors of the Liliales.
TL;DR: The genus Nuphar (Nymphaeaceae) is described to include 11 species native to fresh waters of the Northern Hemisphere and Evolutionary reconstructions position the genus at the base of the family, most closely allied to Barclaya.
Abstract: The genus Nuphar (Nymphaeaceae) is described to include 11 species native to fresh waters of the Northern Hemisphere. This assessment utilized morphometric analyses, cladistic analyses, evaluation of randomly amplified polymorphic DNA, and seed and pollen fertility estimations. Evolutionary reconstructions position the genus at the base of the family, most closely allied to Barclaya. Comprehensive cladistic analyses of morphological and molecular data have permitted a general phylogenetic interpretation of the genus. Two major evolutionary lineages are evident and recognized taxonomically at the section level. One (sect. Nuphar) includes N. lutea, N. × spenneriana, N. japonica, and N. × saijoensis, with an ultimate branch involving N. pumila and N. microphylla. The other lineage (sect. Astylus) includes N. polysepala, N. × rubrodisca, N. variegata, N. sagittifolia, and N. advena. All studies illustrate high morphological variability and close relationships of species within each section. The biol...
TL;DR: Placentation in Barclaya longifolia Wall is laminar and Weberbauer's contention that Barclaya should be retained at the generic level in the Nymphaeaceae is supported.
Abstract: Placentation in Barclaya longifolia Wall. (Nymphaeaceae) is laminar. Each ovule is bitegmic and crassinucellate. A small embryo sac of the Polygonum type is formed from which a tubular, haustorial-like projection is produced into the surrounding perisperm. Mature seeds are spinate and exarillate. The mature embryo is minute and bears two large, separate cotyledons. Weberbauer's contention that Barclaya should be retained at the generic level in the Nymphaeaceae is supported.
TL;DR: Floral structure reveals vasculature and developmental support for the hypothesis that the hypogynous appendages are sepals, that pollen is zonasulculate, and that floral ontogeny is similar to that previously described for epigynous members of the Nymphaeaceae s.
Abstract: Barclaya, endemic to Southeast Asia, includes four species: B. longifolia Wallich. B. motleyi Hooker f., B. kunstleri (King) Ridley, and B. rotundifolia Hotta. The genus has been traditionally assigned monotypic status in the family Barclayaceae or tribe Barclayeae primarily based on the occurrence of a hypogynous calyx, originally interpreted as an involucre in an otherwise epigynous flower, orthotropous ovules, lack of an aril, and inaperturate pollen. Cladistic and molecular studies support the association of Barclaya with Euryale, Victoria, Nymphaea, Ondinea, and Nuphar in the family Nymphaeaceae. Floral structure reveals (1) vasculature and developmental support for the hypothesis that the hypogynous appendages are sepals, (2) that pollen is zonasulculate, (3) that floral ontogeny is similar to that previously described for epigynous members of the Nymphaeaceae s. str., and (4) anatomical and morphological similarities with other Nymphaeaceae s. str. The cleistogamous and chasmogamous flowers are self-pollinating, the latter perhaps facilitated by flies in emergent flowers.