Fossil flowers of ericalean affinity from the Late Cretaceous of Southern Sweden

Charcoalified fossil flowers of a new genus and species (Paradinandra suecica) with affinities to Ericales s.l. (sensu lato) are described from the Late Cretaceous (Santonian-Campanian) from Southern Sweden. The flowers are pentamerous, hypogynous, and actinomorphic. Aestivation of sepals and petals is imbricate-quincuncial. The androecium consists of an outer whorl with single episepalous stamens and an inner whorl with paired epipetalous stamens. Pollen is small and probably tricolpate. Three carpels form a syncarpous ovary with numerous campylotropous ovules on parietal placentae. The styles are free for most of their length. The structure of mature fruits and seeds is unknown. Clear distinction of sepals and petals, possible dehiscence of anthers by restricted slits, presence of a nectary, and the general floral construction (salverform corolla) with a canalized access to the floral center clearly indicate insect pollination of the fossil flowers. Comparisons with extant taxa demonstrate that Paradinandra suecica shares many similarities with Ericales s.l. and in particular with members of Ternstroemiaceae, Theaceae, and Actinidiaceae. However, it is neither identical to any one genus of these families nor to any of the previously described ericalean taxa from the Cretaceous and thus provides further evidence of the diversity of Cretaceous ericalean plants.     

Floral Development and Anatomy ofMoringa oleifera(Moringaceae): What is the Evidence for a Capparalean or Sapindalean Affinity?

Floral development and anatomy ofMoringahave been investigatedin the context of the disputed view of a capparalean affinity.Flowers arise in terminal or axillary panicles. Sepals arisesequentially and petals simultaneously. Antepetalous stamensarise simultaneously and precede the antesepalous staminodes,which emerge sequentially. Within their respective whorls, thepetals and stamens become twisted along different orientations.The gynoecium develops as a ring primordium on which three carpellarylobes become demarcated simultaneously. A saccate ovary bearsnumerous ovules on a parietal placentation and is topped bya hollow style. The interpretation of laminal placentation isdenied. Monothecal anthers are formed by the failure of onehalf to initiate. The flowers present a peculiar form of zygomorphyrunning transversally from the petal between sepals 3 and 5to sepal 4. The shape and position of petals and stamens isrelated to a pollen presentation mechanism with bowl-shapedanthers on different levels. The floral anatomy also reflectsthe zygomorphy of the flower. AlthoughMoringashares importantmorphological features with certain members of the Sapindalesand Capparales, differences in ontogeny make a close relationshipwith either Capparales or certain Sapindales appear uncertain.Copyright1998 Annals of Botany Company Moringa,Moringaceae, Capparales, Sapindales, floral ontogeny, floral anatomy.     

STUDIES IN THE FLORAL ANATOMY OF POLYGALA (POLYGALACEAE)

Flowers of Polygala are irregular, each having three small and two long winglike sepals, three petals, eight stamens, and a bilocular ovary. These flowers have been considered pentamerous, and placentation has been subject to various interpretations. Development and anatomy of flowers of Polygala alba, P. lanceolata, and P. lutea were studied to see if evidence of pentamery and change in placentation could be found. These studies reveal no evidence of vestigial petals or stamens nor of vascular traces to organs that are missing in the three species studied. Neither are there abortive sporangia in the bisporangiate anthers. Observations on development of carpel primordia and on the vascular plan of mature carpels indicate that placentation is fundamentally parietal rather than axile. Speculation is offered as to the derivation of this type of placentation.     

A SCANNING ELECTRON MICROSCOPIC STUDY ON THE INITIATION AND DEVELOPMENT OF FLORAL ORGANS OF BRASSICA NAPUS (CV. WESTAR)

The initiation and development of the floral organs of Brassica napus L. (cv. Westar) were examined using the scanning electron microscope. After transition of the vegetative apex into an inflorescence apex, flower primordia were initiated in a helical phyllotactic pattern. The sequence of initiation of the floral organs in a flower bud was that of sepals, stamens, petals and gynoecium. Of the four sepal primordia, the abaxial was initiated first, followed by the two lateral and finally the adaxial primordium. The four long stamens were initiated simultaneously in positions alternating with the sepals. The two short stamens were initiated basipetal to and outside the long stamens, and opposite the lateral sepals. The petals arose on either side of the two short stamens and the gynoecium was produced from the remainder of the apex. During development, the sepal primordia curved sharply at the tips and tightly enclosed the other organs. Stamen primordia developed tetralobed anthers at an early stage while filament elongation occurred just prior to anthesis. A unique pattern of bulbous cells was present on the abaxial surface of the anther. Growth of petal primordia lagged relative to the other floral organs but expansion was rapid prior to anthesis. The gynoecium primordium was characterized by an invagination early in development. At maturity, there was differentiation of a papillate stigma, an elongated style and a long ovary marked externally by sutures and divided internally by a septum. Distinct patterns of cuticular thickenings were observed on the abaxial and adaxial surfaces of the petals and stamens and on the surface of the style. The patterns were less obvious on the sepals and ovary. Stomata were present on both surfaces of the mature sepals, on the style and restricted areas on the abaxial surface of the anthers and nectaries but were absent from the petals, the adaxial surface of the stamens and the ovary. No hairs were present on any of the floral organs.     

Floral ontogeny of Sinojackia xylocarpa (Styracaceae), with special reference to the development of the androecium

Using scanning electron microscopy, we studied the floral ontogeny of Sinojackia xylocarpa. There are 6–7 (–8) sepals. Sepal initiation is staggered; adaxial sepals arise later than abaxial and lateral ones. There are (5–) 6–7 (–8) petals, initiated simultaneously. Petals alternate with the sepals, and occasionally there are two petals instead of one between two sepals. The (10–) 12–14 (–16) stamens are initiated centripetally in two sets (whorls). These floral organ numbers deviate from those of the otherwise mostly pentamerous family Styracaceae. The ovary consists of three (rarely four) locules. In each of the locules, two rows of ovules are differentiated basipetally. Placentation is axile with (5–) 6 (–7) ovules in each locule. Ovules are unitegmic and are ascending with the micropyle directed downwards. Intra‐ovarian trichomes are present as in other representatives of Styracaceae and seem to be an apomorphic character of the family as they are absent in the closely related Symplocaceae and Diapensiaceae. Various levels of organ union occur in anthetic S. xylocarpa. The calyx is synsepalous and the ovary syncarpous. Possibly, the basal connation of petals and stamens is postgenital (and not congenital), but this needs further study. The outward curvature of the young anthers of the inner stamen whorl superficially simulates an obdiplostemonous androecium. However, the sequence of stamen initiation shows a diplostemonous pattern.     

Development of the gametophytes, flower, and floral vasculature in Dichorisandra thyrsiflora (Commelinaceae)

The flowers of Dichorisandra thyrsiflora (Commelinaceae) are monosymmetric and composed of three sepals, three petals, six stamens, and three connate carpels. The anthers are poricidal and possess a wall of five cell layers (tapetum included). This type of anther wall, not previously observed in the Commelinaceae, is developmentally derived from the monocotyledonous type via an additional periclinal division and the persistence of the middle layers through anther dehiscence. Secondary endothecial thickenings develop in the cells of the two middle layers only. The tapetum is periplasmodial and contains raphides. Microsporogenesis is successive and yields both decussate and isobilateral tetrads. Pollen is shed as single binucleate grains. The gynoecium is differentiated into a globose ovary, hollow elongate style, and trilobed papillate stigma. Each locule contains six to eight hemianatropous to slightly campylotropous crassinucellar ovules with axile (submarginal) placentation. The ovules are bitegmic with a slightly zig-zag micropyle. Megagametophyte development is of the Polygonum type. The mature megagametophyte consists of an egg apparatus and fusion nucleus; the antipodals having degenerated. The floral vasculature is organized into an outer and inner system of bundles in the pedicel. The outer system becomes ventral carpellary bundles. All other floral vascular traces originate from the inner system.     

Sul Dioicismo Di Idesia Polycarpa Maxim

Summary

On the dioecism in idesia polycarpa maxim.

Idesia polycarpa Maxim. is a dioecious species, native of Japan and China. Two specimens have been studied for this research, a ♀ and a ♂ one, growing in the Botanical garden of Siena.

The female plant does not present anomalies in the sex behaviour; the male plant, on the contrary, bears occasionaly some flowers with ovaries, which exceptionally develop into fruits.

In the Botanical Garden of Pisa a case of complete sex inversion has been observed (male into female).

In both the ♀ and the ♂ the first development stage is identical and hermaphrodyte. The flower is tendentially proterandrous, unisexuality being attained only successively.

In the male flowers the pystil degenerates while the pollen mother cells undergo meiosis. The ovary ceases developing farther, at the ovule forming stage from the placentae. The only cellular line which degenerates is the epithelium, which lines the ovary inner surface and extends as far the upper surface of the stygma. The microspores tetrads form contemporarily. The tapetum is of the secretory type.

The stamens degenerates in female flowers at the moment corresponding to the passage from the vegetative to the reproductive stage; i. e. the stamens of the female flowers are not capable to carry out the meiosis. The first cellular layer to be reached by a degeneration process is the tapetum; the second is the archesporial tissue. During the degeneration of these two tissues ovules are developing. The female gamethophyte is of the monomegasporial, normal, eightnucleate type. The fruits born by the female plant are roundish, with 8–30 fertile seeds and 50–65 sterile ones. Thè fruits which are exceptionally born by the male plant are bigger, pear-shaped, and countain 20–40 fertile seeds and 65–85 sterile ones.

The epithelium lining the ovaries undergoes total degeneration in normal male flowers; a partial one in the occasional male flowers which have more or less developed pistils. When only the stygma epithelium degenerates, the ovary produces a higher number of ovules even through the whole style region, so that a style does not form and the ovary does not shut, giving a pear-haped fruit.

A higher number of seeds are therefore produced by such an ovary, not only because the placentae go on producing ovules for a longer period, but because also their stylar region is active in this process. It is evident then, that the stigma plays a very important role in the normal closing of the ovary.

In the cases of partial degeneration, ovules remain vital only where the corresponding epithelium is unaltered. This shows that the epithelium has a great importance in the ovule producing phase of the placentae.

Everything seems to point out that the anthers degeneration is autonomous, owing to its own incapacity to undergo meiosis. On the contrary the suppression of the ovary in the male flower is not autonomous and does not occur in a particular moment of the ovary development, but it coincides with microsporogenesis. The suppressor of the ♀ sex therefore acts through the opposite sex. In a male plant where the anthers happen to degenerate, pystils develop in various degree, even completely.

The flowers of the female plant reache the microsporogenesis stadium about 15 days later than those of the male. The author suggests that this delay may be responsible for the realization of the female sex, checking the normal development of the anthers, probably under the influence of environmental factors. On this base he has tried to explain anomalies in male flowers.     

Gender variation in Actinidia deliciosa,the kiwifruit

Summary Flower and fruit characters were measured in ten female, five male and five fruiting male selections of A. deliciosa var deliciosa (A. Chev) Liang and Ferguson. Flowers from female vines had functional pistils, which contained many ovules. Stamens appeared to be fully developed but produced only empty pollen grains. Flowers from male vines had functional stamens that produced high percentages of pollen grains with stainable cytoplasmic contents. Pistils did not contain ovules and were generally small with vestigial styles. Fruiting male vines had both staminate and bisexual flowers. Staminate flowers were similar to those found on strictly male vines. Bisexual flowers produced ovules and stainable pollen. Pistils were smaller than in pistillate flowers. Although the three flower sexes differed in style length, ovary dimensions and ovules per carpel, staminate and bisexual flowers were similar in number of flowers per inflorescence, stamen filament length, pollen stainability, inflorescence rachis length and carpel number, and differed from pistillate flowers in these characters. The three flower sexes had similar sepal and petal numbers. The fruit of fruiting males were considerably smaller than those of females. Low ovule number appears to be the major factor limiting fruit size in the fruiting males studied. Prospects for developing hermaphroditic kiwifruit cultivars through breeding are discussed.     

Floral ontogeny in legume genera Petalostylis, Labichea, and Dialium (Caesalpinioideae: Cassieae), a series in floral reduction

Floral ontogeny of taxa of two subtribes (Labicheinae, Dialiinae) of caesalpinioid tribe Cassieae, characterized by reduced number of floral organs, was compared. All three taxa studied are distichous; Petalostylis labicheoides flowers are solitary in leaf axils, Labichea lanceolata has few-flowered racemes, and Dialium guineense has numerous-flowered cymes. The first sepal primordium in each is initiated abaxially and nonmedianly. Order of organogenesis in Petalostylis is: five sepals bidirectionally, five petals and carpel simultaneously, then five stamens bidirectionally, starting abaxially. The order in Labichea is: five sepals helically (one lagging in time), five petals unidirectionally starting abaxially, the carpel and petals concurrently, then two stamens successively, starting laterally. Order in Dialium is: five sepals bidirectionally, the single petal adaxially, and lastly the carpel and two stamens concurrently. Specializations include (1) reduction of the five sepals to four by fusion in Petalostylis and Labichea; (2) reduction of petal number to one in Dialium; (3) reduction of stamen number to two in Labichea and Dialium, and reduction of functional stamens to three in Petalostylis; and (4) an elaborate, late-developing style in Petalostylis. Floral asymmetry, another specialization, characterizes Labichea, expressed by dissimilar stamens, while the other genera have zygomorphic flowers. Floral ontogenies are compared with other taxa of Cassieae.     

The breeding system of Fumana ericifolia: first evidence of autogamy in woody Cistaceae

Fumana ericifolia belongs to the family Cistaceae, in which all perennial species previously studied have been reported to be self-incompatible and xenogamous. Here we show that F. ericifolia is self-compatible and autogamous. Its flowers last only four to eight hours and produce a small amount of pollen and ovules. Self-pollination depends on changes in the relative position of the stigma and the anthers, triggered by the abscission of the petals; this in turn causes closing of the sepals, which push the anthers onto the stigma. Pollen remains highly viable and germinable, and the stigma keeps its receptivity several hours after the loss of the petals. Hand pollination treatments revealed that fruits are produced both in selfed and crossed flowers. The germination of pollen grains on the stigma, the rate of pollen tube growth along the style, and the penetration into the ovules were similar in self-and cross-pollinations; also, there were no significant differences in fruit set, seed set and weight of seeds. Thus, we report the first evidence of autogamy in a woody Cistaceae and suggest that selfing may ensure reproductive success when pollinators are limited.     

Fossil Clusiaceae from the late Cretaceous (Turonian) of New Jersey and implications regarding the history of bee pollination

The Turonian flora from Sayreville New Jersey includes one of the world's most diverse assemblages of Cretaceous angiosperm flowers. This flora is made even more interesting by its association with a large insect fauna that is preserved by charcoalification as well as in amber. Floral diversity includes numerous representatives of Magnoliidae, Hamamelididae, Rosidae, Dilleniidae, and Asteridae (Ericales sensu lato). Included are hypogynous, five-merous flowers with uniseriate hairs on the pedicels and stamens in bundles most frequently borne opposite the petals. There is considerable variation in filament length, and some filaments are branched. On some anthers, strands of residue, suggesting the former presence of a liquid of unknown nature, partially occlude the apparent zone of dehiscence. In other cases, open anthers are fully occluded by an amorphous substance. pollen is rarely found associated with anthers, but is common on stigmatic surfaces. pollen is prolate and tricolporate with reticulate micromorphology. The superior syncarpous ovary is five-carpellate with axile/intruded parietal placentation and numerous anatropous ovules/carpel. Ovary partitions have closely spaced, parallel ascending channels (secretory canals?), and there are apparent secretory canals/cavities in receptacles, sepals, and petals. Individual stigmas are cuneiform with a central groove and eccentrically peltate. Styles are short and fused. In aggregate, the stigmas form a secondarily peltate stigma. Seeds have a reticulate sculpture pattern, a pronounced raphe, and funicular arils with sculpture similar to the seeds. phylogenetic analyses of several data matrices of extant taxa place this fossil in a monophyletic group with the modern genera Garcinia and Clusia within the Clusiaceae. As such, these fossils represent the earliest fossil evidence of the family Clusiaceae. Some modern Clusiaceae are notable, in particular, for their close relationship with meliponine and other highly derived bee pollinators; the fossil flowers share several characters that suggest a similar mode of pollination. This possibility is consistent with other floral and insect data from the same locality.     

Interrelationship between the Different Flower Parts during Emasculation-Induced Senescence in Cymbidium Flowers

In Cymbidium flowers emasculation by removal of the anther capand the pollinia, led to rapid colouration of the lip and advancedwilting of the petals and sepals. The ethylene production ofwhole flowers showed an emasculation-induced early peak in ethyleneevolution followed some days later by a second increase concomitantwith the wilting of the flower. In non-emasculated flowers theethylene production increased later and simultaneously withcolouration of the lip and wilting of the petals and sepals.At all stages of senescence, the contribution of the lip, petals,and sepals to the total amount of ethylene produced was negligible. Parallel to the increase in ethylene production of whole flowers,an increase in 1-aminocyclopropane-l-carboxylic acid (ACC) andmalonyl-ACC (MACC) in the central column and, to a lesser extent,in the ovary was observed. Also an increase in internal ethyleneconcentration was demonstrated and this, in contrast, was apparentin all the different flower parts. The activity of the ethylene-formingenzyme in lips, petals, and sepals showed an increase afteremasculation and such an effect could also be induced by treatmentof isolated lips with low concentrations of ethylene. The data indicate that senescence in Cymbidium flowers is regulatedby the central column and perhaps the ovary and that both ACCand ethylene may play a signalling role in inter-organ communication. Key words: 1-aminocyclopropane-l-carboxylic acid, ethylene, Cymbidium, senescence     

Fossil flowers and fruits of the Actinidiaceae from the Campanian (Late Cretaceous) of Georgia

A new genus and species of Actinidiaceae (Parasaurauia allonensis gen. et sp. nov.) are established for fossil flowers and fruits from the early Campanian (Late Cretaceous) Buffalo Creek Member of the Gaillard Formation in central Georgia, USA. The fossil flowers, which are exquisitely preserved as charcoal, have five imbricate, quincuncially arranged sepals and petals. The androecium consists of ten stamens with anthers that are deeply sagittate proximally. The gynoecium is tricarpellate, syncarpous, and has three free styles that emerge from an apical depression in the ovary. The fruit is trilocular and contains numerous ovules on intruded axile placentae. The structure of mature fruits is unknown. Comparisons with extant taxa clearly demonstrate that the affinities of Parasaurauia allonensis are with the Ericales, and particularly with the Actinidiaceae, which have been placed among the Ericales in recent cladistic analyses. Because Parasaurauia allonensis is not identical to any one genus of Actinidiaceae, or other member of the Ericales, phylogenetic relationships of the fossil were evaluated through a cladistic analysis using morphological and anatomical characters. Results of this analysis place Parasaurauia allonensis within the Actinidiaceae as sister to the extant genera Saurauia and Actinidia. Parasaurauia allonensis differs from extant Saurauia only in having ten rather than numerous stamens.     

COMPARATIVE REPRODUCTIVE BIOLOGY OF HERMAPHRODITIC AND MALE-STERILE IRIS DOUGLASIANA HERB. (IRIDACEAE)

A comparative study of the reproductive biology of male-sterile and hermaphroditic plants in a gynodioecious population of Iris douglasiana Herb. (Iridaceae) was conducted at the University of California's Marine Laboratory at Bodega Bay, California, between 1976–1979. Each year of the study, there were 11.1% male-sterile plants in the population, some of which began blooming at the same time as the earliest blooming hermaphrodites. Male-sterile flowers made up between 7–21% of the flowers produced during the male-sterile flowering period. Male-sterile flowers had smaller sepals and petals than hermaphrodites, there were fewer of them per square meter, and they had fewer pollinated stigmas than did hermaphroditic flowers. In a test to determine pollinator preference, intact hermaphroditic flowers tended to have more pollinated stigmas than did hermaphrodites with their stamens removed or those flowers with shortened sepals made to resemble the smaller male-sterile flowers. Floral phenology and nectar-flow patterns were similar in both types of flowers as were the kinds of amino acids and sugar rewards in the nectar. Male-sterile flowers, however, produced much less nectar per flower. There were no significant differences in the number of ovules per flower or the number of seeds produced per capsule between the two flower types, but the loss of seeds through larval predation was much greater in capsules from hermaphroditic flowers. Early flowering and setting of seed by plants with male-sterile flowers could give them a reproductive advantage over plants with hermaphroditic flowers which experience higher levels of larval predation later in the growing season.     

A comparison of early floral ontogeny in wild-type and floral homeotic mutant phenotypes of <Emphasis Type="Italic">Primula</Emphasis>

Primula flowers are heteromorphic with individual plants producing either pin-form or thrum-form flowers. We have used scanning electron microscopy to observe early development of wild-type flowers of primrose (Primula vulgaris), cowslip (P. veris), and the polyanthus hybrid (P. x tommasinii x P. vulgaris). Floral ontogeny in Primula is different from that observed in the well-studied models Antirrhinum majus and Arabidopsis thaliana and our studies reveal morphological landmark events that define the sequence of early floral development in Primula into specific stages. Pin-form and thrum-form flowers are indistinguishable during early development with differentiation of the two floral morphs occurring beyond the differentiation of floral organs. Early ontogeny of flowers with homeotic mutant phenotypes was also studied to determine the timing of developmental reprogramming in these mutants. Phenotypes studied included Hose in Hose and Jack in the Green that develop petaloid sepals and leafy sepals, respectively, and Jackanapes plants that carry both these dominant mutations. Recessive double and semi- double flowers that produce additional whorls of petals and/or stamens in place of carpels were also studied. We describe a previously undocumented recessive Primula mutant phenotype, sepaloid, that produces sepals in place of petals and stamens, and a new non-homeotic, dominant mutant phenotype Split Perianth, in which sepals and petals fail to fuse to form the typical calyx and corolla structures. The molecular basis of these mutant phenotypes in relation to the ABC model is discussed.     

FLORAL ANATOMY OF KRAMERIA LANCEOLATA

The anatomy of each of the series of floral organs of Krameria lanceolata was examined. The sepals are characterized by three main veins each, an undifferentiated mesophyll, and stomata on the upper epidermis. The fleshy petals are distinguished by their numerous veins as well as by palisade-like epidermal cells on the outer surface. The three partially united petals have each a single vein and long, narrow epidermal cells similar to those on other floral organs. The stamens are united at their bases and bear tetra-sporangiate, conical anthers. The gynoecium includes a sterile and a fertile carpel. In the receptacle the veins to the sepals and petals are separated by a wide gap; those to the petals and stamens, by a narrow gap. Anatomical characteristics of the flower dissociate Krameriaceae from the legumes with which they have frequently been thought to be allied.     

STUDIES IN THE FLORAL ANATOMY OF CLAYTONIA (PORTULACACEAE)

Claytonia virginica has a regular flower with two sepals, five petals with an equal number of stamens in positions opposite the petals and a many-seeded tricarpellate gynoecium with basal placentation. The flower has been interpreted as uniseriate, the putative sepals as bracts and the corolla as modified calyx lobes. Anatomical and developmental studies were undertaken to find evidence for the existence of vestigial or rudimentary parts whose existence would illuminate the true nature of the flower. Vascular and epidermal anatomy of sepals are both similar to that of leaves. Corolla and androecium develop basipetally and petals and stamens share common vascular traces in the lower part of the receptacle. Thus, in terms of both anatomy and development, evidence supports the conclusion that the perianth is essentially biseriate. Vestigial or rudimentary parts are not present which would alter the manifest design of the mature flower.     

FLORAL DEVELOPMENT OF A FLOWER-STRUCTURE MUTANT IN SOYBEANS,GLYCINE MAX (L.) MERR. (LEGUMINOSAE)

A flower-structure mutant with cleistogamous flowers (but often with an exposed style and stigma) and very low seed set was found in soybeans (Glycine max (L.) Merr.). The mutant, assigned Genetic Type Collection Number T269, is controlled genetically by duplicate recessive genes, fs₁ and fs₂. A study of flower development in T269 plants was undertaken to determine the cause of the low seed set. Both normal and mutant flower buds were observed with a light microscope by using paraffin serial sections and with a scanning electron microscope. Measurements of various floral structures were taken to verify differences observed between mutant and normal flowers. Young mutant flower buds had longer carpels and larger receptacles than did normal flower buds. These two factors caused the sepals to be positioned abnormally, which, in turn, prevented normal development of the petals. The abnormal petal development prevented staminal tube elongation, and a spatial separation between the anthers and stigma existed at anthesis, preventing self-pollination. Observations of the gynoecium of mutant flowers revealed that megasporogenesis and megagametogenesis were normal but that other features of ovule ontogeny were abnormal. In all ovules examined, the outer integuments failed to form micropyles. In addition, many ovules were positioned abnormally. The degree of aberration varied even within a carpel, but we estimated that at least 75% of the ovules were too aberrant to be functional. Therefore, the low seed set on T269 plants was due both to a lack of self-pollination and to partial female sterility. It is the only naturally occurring structural sterile reported in soybeans to date.     

Comparative floral structure and systematics in Oxalidales (Oxalidaceae, Connaraceae, Brunelliaceae, Cephalotaceae, Cunoniaceae, Elaeocarpaceae, Tremandraceae)

Floral morphology, anatomy and histology were studied in representatives of all families of current Oxalidales, which were recently constituted as a result of molecular systematic studies by other authors, and are composed of families of different positions in traditional classifications (Oxalidaceae, Connaraceae, Brunelliaceae, Cephalotaceae, Cunoniaceae, Elaeocarpaceae, Tremandraceae). Two of the three pairs of sister (or nested) families that come out in molecular analyses are highly supported by floral structure: Oxalidaceae/Connaraceae and Elaeocarpaceae/Tremandraceae, whereas Cephalotaceae/Cunoniaceae are not especially similar at the level of Oxalidales. Oxalidaceae and Connaraceae share petals that are postgenitally united into a basal tube (although they are imbricate in both) but free at the insertion zone, stamens that are congenitally united at the base, uniseriate glandular hairs on the stamen filaments, and ovules that are hemianatropous to almost orthotropous. The sharing of a special type of sieve-tube plastids and of trimorphic heterostyly, studied by other authors, should also be mentioned. With Brunelliaceae, the two families share an androgynophore and nectaries at the base of the stamens in alternisepalous sectors. Elaeocarpaceae and Tremandraceae share buzz-pollinated flowers and a syndrome of features functionally connected with it. In addition, petals are larger than sepals in advanced bud, they are valvate, involute and enwrap part of the adjacent stamens, they have three vascular traces. Lignified hairs are common on the anthers and are found in the ovary locules and on the ovules (not lignified) of representatives of both families. Ovules have a chalazal appendage, and the inner integument is much thicker than the outer.  © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 140 , 321–381.     

Comparative floral structure and systematics in Chrysobalanaceae s.l. (Chrysobalanaceae, Dichapetalaceae, Euphroniaceae, Trigoniaceae; Malpighiales)

Chrysobalanaceae s.l. , one of the few suprafamilial subclades of Malpighiales that is supported by molecular phylogenetic analyses, and containing Chrysobalanaceae, Dichapetalaceae, Euphroniaceae, and Trigoniaceae, was comparatively studied with regard to floral structure. The subclade is well supported by floral structure. Potential synapomorphies for Chrysobalanaceae s.l. are the following shared features: floral cup; flowers obliquely monosymmetric; sepals congenitally united at base; sepals of unequal size (outer two shorter); fertile stamens concentrated on the anterior side of the flower and sometimes united into a strap; staminodes absent in the posteriormost antepetalous position; anthers extremely introrse, with thecae almost in one plane; endothecium continuous over the dorsal side of the connective; dorsal anther pit; gynoecium completely syncarpous up to the stigma; carpel flanks slightly bulged out transversely and thus carpels demarcated from each other by a longitudinal furrow; flowers with dense unicellular, non-lignified hairs, especially on the gynoecium; light-coloured, dense indumentum on young shoots and inflorescences. Potential synapomorphies for Chrysobalanaceae + Euphroniaceae include: spur in floral cup; clawed petals; lignified hairs on petals; nectary without lobes or scales and mostly annular. Potential synapomorphies for Dichapetalaceae + Trigoniaceae include: special mucilage cells in sepals in mesophyll (in addition to epidermis); anthers almost basifixed; gynoecium synascidiate up to lower style; nectary with lobes or scales and semi-annular.  © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society , 2008, 157 , 249–309.