TL;DR: The stratigraphic record of Diplodipelta, together with the occurrence of genuine Dipelta fruits in the late Eocene of England, indicates that the divergence of these genera occurred during or prior to theLate Eocene.
Abstract: Recent phylogenetic analyses of the Caprifoliaceae and related families have paved the way for critical study and interpretation of the fossil record. A new extinct genus, Diplodipelta, is established on the basis of winged fruits from the Eocene, Oligocene, and Miocene of western North America, with two species: Diplodipelta reniptera (Becker) comb. nov. and D. miocenica (Berry) comb. nov. Although formerly attributed to Ptelea and Dodonaea, detailed comparative studies demonstrate that the fossils actually represent the Caprifoliaceae, tribe Linnaeeae, on the basis of elongate, indehiscent, longitudinally ribbed fruits with a sterile apical neck and persistent, epigynous calyces, and "supernumerary bracts." The samaroid dispersal units resemble those of extant Dipelta because the bracts are enlarged into wings that function in wind dispersal. However, Diplodipelta differs from Dipelta by the presence of a pair of fruits, rather than just one fruit, per dispersal unit, by the adnation of lateral wings to...
TL;DR: It is proposed that the flower of Victoria has evolved by (1) the adnation and connation of the proximal portions of the appendicular organs which now envelop the syncarpous gynoecium and (2) the concomitant condensation from a primitive ranalian floral apex.
TL;DR: The evolutionary history of the PI gene subfamily indicates that the two genes in Petunia result from an ancient duplication event, coinciding with the origin of core asterids, which suggest that the asterids have preferentially recruited PI duplicate genes to diverse and potentially novel roles in asterid flower development.
Abstract: Basal asterid families, and to a lesser extent the asterids as a whole, are characterized by a high variation in petal and stamen morphology. Moreover, the stamen number, the adnation of stamens to petals, and the degree of sympetaly vary considerably among basal asterid taxa. The B group genes, members of the APETALA3 (AP3) and PISTILLATA (PI) gene lineages, have been shown to specify petal and stamen identities in several core eudicot species. Duplicate genes in these lineages have been shown in some cases to have diversified in their function; for instance in Petunia, a PI paralog is required for the fusion of stamens to the corolla tube, illustrating that such genes belonging to this lineage are not just involved in specifying the identity of the stamens and petals but can also specify novel floral morphologies. This motivated us to study the duplication history of class B genes throughout asterid lineages, which comprise approximately one-third of all flowering plants. The evolutionary history of the PI gene subfamily indicates that the two genes in Petunia result from an ancient duplication event, coinciding with the origin of core asterids. A second duplication event occurred before the speciation of basal asterid Ericales families. These and other duplications in the PI lineage are not correlated with duplications in the AP3 lineage. To understand the molecular evolution of the Ericales PI genes after duplication, we have described their expression patterns using reverse transcription polymerase chain reaction and in situ hybridization, reconstructed how selection shaped their protein sequences and tested their protein interaction specificity with other class B proteins. We find that after duplication, PI paralogs have acquired multiple different expression patterns and negative selective pressure on their codons is relaxed, whereas substitutions in sites putatively involved in protein-protein interactions show positive selection, allowing for a change in the interaction behavior of the PI paralogs after duplication. Together, these observations suggest that the asterids have preferentially recruited PI duplicate genes to diverse and potentially novel roles in asterid flower development.
TL;DR: The superior ovary and the columella formed in the fruit are probably primitive characteristics, but in all other respects the flower of P. aculeata appears to be advanced.
Abstract: which become reflexed in the fruit, and its rim bears a series of small, triangular bracts, which are sharply delimited from the perianth segments. Vascular anatomy indicates that there is a short floral tube formed by the adnation and connation of the bases of the stamens and perianth segments. The inner side of this floral tube forms an extensive cylindrical nectary; the outer si'de is adnate to the receptacle. There are usually five carpels, each bearing a single ovule. Carpel tips are free, but their bases are congenitally connate. During ontogeny, the adaxial faces of the carpels grow together, forming a solid style. The base of the ovary is partially divided into locules by small partitions, which represent the fused margins of connate carpels. The tip of the floral receptacle (residual meristem) becomes a convex body which enlarges in the fruit, filling that portion of the ovary cavity not occupied by seeds. The superior ovary and the columella formed in the fruit are probably primitive characteristics, but in all other respects the flower of P. aculeata appears to be advanced. It is a product of evolutionary reduction.
TL;DR: Floral anatomy and embryology suggest a close relationship among the genera and structure and morphology of inflorescence and also flower suggest the manifestation of certain evolutionary trends, probably guided by reduction, cohesion and adnation.
Abstract: The present paper deals with certain aspects of morphology and anatomy of the Saururaceae. Floral anatomy and embryology suggest a close relationship among the genera. In floral anatomy the genus Saururus is the least specialized and Anemopsis the most highly specialized. Structure and morphology of inflorescence and also flower suggest the manifestation of certain evolutionary trends, probably guided by reduction, cohesion and adnation. Origin of inferior ovary in the Saururaceae is discussed. Carpels and nature of placentation show certain primitive features. Origin and evolution from apocarpous condition to syncarpous condition of carpels are briefly discussed. Further details will be presented in a separate paper. M. V. S. RAJU, Department of Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.