LIRIODENDRON (MAGNOLIACEAE) FROM THE MIOCENE CLARKIA FLORA OF IDAHO

Miocene Liriodendron carpels, whole fruiting structures and leaves from Clarkia and Oviatt Creek sites in northern Idaho are preserved as imprints and compressed fossils in soft lacustrine clays. The isolated carpels are indistinguishable from those described as L. hesperia Berry from the Spokane Latah flora. Fruit aggregates from the type Clarkia and Oviatt Creek localities and leaves from three Clarkia sites are considered to be within the range of variation of the single species L. hesperia. Comparisons were made regarding leaf architecture, lower leaf epidermal structures, leaf flavonoid and steroid analysis, morphological features of receptacles and carpels, and the venation pattern of carpels of the fossil material to the two extant species, L. tulipifera L. (native to southeastern United States) and L. chinense Sarg. (native to southeastern Asia). Leaf architecture features analyzed by standard statistical and canonical tests and marginal venation patterns near the base of leaves suggest that L. hesperia is more similar to L. tulipifera, whereas the size dimensions of lower epidermal cells and the common presence of two sterane compounds imply that L. hesperia is more similar to L. chinense. The fossil species, however, is a distinct taxon indicated by statistical discriminant and canonical tests, leaf base shape, often smaller epidermal cell dimensions, and the shape of round receptacle carpel scars. Both the fossil and the two living Liriodendron species are associated with comparable mixed mesophytic floras.     

COMPARATIVE MORPHOLOGY OF THE CARPEL IN THE ROSACEAE VI. POMOIDEAE: ERIOBOTRYA,HETEROMELES, PHOTINIA,POURTHIAEA, RAPHIOLEPIS,STRANVAESIA

The pomoid genera, Eriobotrya, Photinia, Pourthiaea, Raphiolepis, Stranvaesia, and Heteromeles, have compound inflorescences and biovulate carpels which become papery at maturity. The carpels of all of these except Heteromeles are fused with one another. There are open sutures in the carpels of Heteromeles, Photinia, Pourthiaea, and Raphiolepis, and in these four genera the extent of fusion of the ovular bundle with the wing bundle is related directly to the state of tegumentary fusion and to the extent of fusion of the carpel with the floral cup. In those species of Eriobotrya and Stranvaesia with closed sutures the integuments tend to be fused, as do the ovular and wing bundles, and the carpels are adnate with the floral cup for a considerable distance; in species with open sutures the integuments tend to be free, the ovular and wing bundles tend to be separate, and the extent of fusion of carpel with floral cup tends to be shorter. In genera with connate carpels the wing bundles of adjoining carpels may also be fused. The greatest extent of fusion occurs in Eriobotrya and Raphiolepis, in which there may also be attenuation and disappearance of the wing bundles above the region of ovular insertion and even reduction and disappearance of the carpellary margin.     

乌鲁木齐乌头, 新疆毛茛科一新种

该文描述了发现自中国新疆天山北部的毛茛科乌头属一新种,即乌鲁木齐乌头(Aconitm urumqiense),此新种与新疆乌头(A. sinchiangense)近缘。两者的区别在于此新种(乌鲁木齐乌头)的茎无毛,不存在基生叶,总状花序轴和花梗被黄色腺毛,萼片背面疏被柔毛、边缘被缘毛,上萼片较宽,花瓣唇在顶端啮蚀状,子房幼时疏被柔毛。     

COMPARATIVE MORPHOLOGY OF THE CARPEL IN THE ROSACEAE. III. POMOIDEAE: CRATAEGUS,HESPEROMELES, MESPILUS,OSTEOMELES

The carpels in Crataegus, Hesperomeles, Mespilus, and Osteomeles appear to constitute a morphologically related group: all have bony pits, ovules that tend to be acollateral (usually superposed), and clearly separate ovular and wing bundles, i.e., no “ventral” bundles, at the level of ovular insertion. In species whose carpels have no sutural opening, the integuments are more extensively fused with one another, the degree of intercarpellary fusion tends to be greater, and the carpels are fused with the floral cup to relatively higher levels than in those species whose carpels have a sutural opening. In the few cases in which wing and ovular bundles are adnate at the locular base (Crataegus monogyna, Mespilus, Osteomeles anthyllidifolia, O. Schwerinae), the extent of inter- and extracarpellary fusion and sutural closure is among the most advanced.     

ONTOGENY AND ANATOMY OF THE FLOWER OF LIMNOCHARIS FLAVA (BUTOMACEAE)

The flowers of Limnocharis flava (L.) Buch. are borne in an indeterminate umbel and each consists of three sepals, three yellow petals, and about 18 carpels surrounded by numerous stamens and staminodia. The androecium is centrifugally developed, and the last-formed members are staminodial; it is supplied by branching vascular systems. Carpels arise almost simultaneously, and a prominent residual floral apex remains. The carpels are partially conduplicately closed and are also primitive in possessing laminar placentation and in lacking differentiation of a style. The gynoecium is essentially apocarpous, but there are slight fusions of adjacent carpels near their ventral margins where they are attached to the receptacle. It is suggested that the Limnocharis flower is the most primitive in the family.     

INFLORESCENCE AND FLOWER DEVELOPMENT IN THE PIPERACEAE III. FLORAL ONTOGENY OF PIPER

Floral development in Piper was compared between four-staminate species (P. aduncum and P. marginatum) and six-staminate species (P. amalago). All Piper species have a syncarpous gynoecium composed of three or four carpels. The floral apex is initiated by a periclinal division in the subsurface layer in the axil of a bract 40-55 μm high; initiation of the bracts occurs separately and considerably earlier. The floral primordium widens and the first pair of stamens are initiated at either side. The median anterior stamen forms next, and the median posterior later. This sequence is common to all species studied. In the six-staminate P. amalago, the last two stamens form simultaneously in lateral-anterior positions. The stamens hence arise as pairs, and symmetry is bilateral or dorsiventral. The three or four carpels arise simultaneously; they are soon elevated on a gynoecial ring by growth of the receptacle below the level of attachment of the carpels to produce a syncarpous gynoecium. The floral apex lastly produces the solitary basal ovule and is used up in its formation.     

COMPARATIVE STUDY OF THE FLORAL VASCULATURE IN SAURURACEAE

The floral vascular systems are compared among all six taxa of Saururaceae, including the two species of Gymnotheca which have not been studied previously. All are zygomorphic (dorsiventrally symmetrical), not radial as sometimes reported, in conformity with dorsiventral symmetry during organogenesis. Apocarpy in the two species of Saururus (with four carpels and six free stamens) is accompanied by a vascular system of four sympodia, each of which supplies a dorsal carpellary bundle, two ventral carpellary bundles, and one or two stamen traces. The level at which the ventral bundles diverge is the major difference in vasculature between the two species. The other four taxa are all syncarpous, and share some degree of stamen adnation and/or connation. The vascular systems also show varying degrees of fusion. The two species of Gymnotheca (with four carpels and six stamens) are very similar to each other; in both, the ventral traces of adjacent carpels fuse to form a placental bundle, which supplies the ovules and then splits into a pair of ventral strands. The flowers of Houttuynia cordata (with only three carpels and three adnate stamens) are sessile. Each flower is vascularized by three sympodia; the median adaxial sympodium is longer than the other two sympodia before it diverges to supply the adaxial organs. Three placental bundles also are formed in Houttuynia, but the three bundles differ in their origin. The median abaxial placental bundle diverges at the same level as the three sympodial bundles of the flower, while the other two lateral placental bundles diverge at a higher level from the median adaxial sympodium. Anemopsis californica, with an inferior ovary of three carpels, sunken in the inflorescence axis, and six stamens adnate to the carpels, has a vascular system very similar to that of Houttuynia cordata. The modular theory of floral evolution is criticized, on the bases of the known behavior of apical meristems and properties of vascular systems. The hypothesis is supported that saururaceous plants may represent a line of angiosperms which diverged very early.     

INITIATION AND DEVELOPMENT OF INFLORESCENCE AND FLOWER IN ANEMOPSIS CALIFORNICA (SAURURACEAE)

All flowers of Anemopsis californica, the most specialized taxon of the family Saururaceae, are initiated as individual primordia subtended by previously initiated bracts, in contrast to the common-primordium initiation of all flowers of Saururus cernuus and of most flowers of Houttuynia cordata. Floral symmetry is bilateral and zygomorphic, and the sequence of initiation among floral parts is paired or whorled. In A. californica, the six stamens arise as three common primordia, each of which later bifurcates to form a pair. The three common primordia occupy sites corresponding to the positions of the three stamens in H. cordata flowers. In Anemopsis, the filaments of each pair are connate. Each stamen pair is vascularized by a single bifurcating vascular bundle. The three carpels per flower are usually initiated simultaneously although there may be some variation. Adnation between stamens and carpels results from zonal growth. Downward extension of the locule, and proliferation and expansion of receptacular tissue and inflorescence cortical tissue around the locule below the bases of the carpels produce the inferior ovary. The inflorescence terminates its activity as a flattened apical residuum, surrounded by bracts subtending reduced flowers most of which have stamens only.     

Two new fossil flowers of magnoliid affinity from the Late Cretaceous of New Jersey

Two taxa of cupulate magnoliid fossil flowers, Cronquistiflora and Detrusandra, are described from the Late Cretaceous (Turonian, ∼90 million years before present [MYBP]) Raritan (or lower Magothy) Formation of New Jersey. The fossil taxa are represented by flowers at various stages of development, associated fragments of cup-shaped floral receptacles with attached anthers, and isolated anthers. Both taxa have laminar stamens with adaxial thecae and valvate dehiscence. Pollen is boat-shaped and foveolate in anthers associated with Cronquistiflora and spherical with reticulate ornamentation in Detrusandra. Cup-shaped receptacles are externally bracteose in both taxa. The receptacle of Cronquistiflora is broader than the campanulate one of Detrusandra. Cronquistiflora also has more carpels (∼50 in a spiral vs. ∼5 in a whorl or tight spiral). In Detrusandra the carpels are surrounded by dorsiventrally flattened structures (pistillodes?) that are remote from the attachment of the stamens near the distal rim of the receptacular cupule. Detrusandra stigmas are rounded and bilobed, while those of Cronquistiflora, although bilateral in symmetry, are somewhat peltate. The fossil taxa share prominent characters with extant cupulate magnoliids (e.g., Eupomatia, Calycanthus), but also share characters with other magnoliids including Winteraceae. These fossils represent taxa that are character mosaics relative to currently recognized families. Inclusion of these fossils in existing data matrices and ensuing phylogenetic analyses effect changes in tree topologies consistent with their mosaicism relative to modern taxa. But such analyses do not definitively demonstrate the affinities of the fossils other than illustrating that these fossils are generalized magnoliids. Additional analysis of modern and fossil magnoliids is necessary to fully appreciate the phylogenetic significance and positions of these fossil taxa. However, the results of the phylogenetic analyses do introduce the possibility that extinct taxa of Magnoliales with cupulate floral receptacles were transitional between basal angiosperms and those with tricolpate pollen. The fossils provide insights into the timing of evolution of character complexes now associated with coleopteran pollination.     

THE COMPARATIVE MORPHOLOGY AND RELATIONSHIPS OF THE MAGNOLIACEAE. III. CARPELS

Canright , James E. (Indiana U., Bloomington.) The comparative morphology and relationships of the Magnoliaceae. III. Carpels. Amer. Jour. Bot. 47(2): 145—155. Illus. 1960.–The morphology and vascular anatomy of the carpels of 49 species in 9 of the 10 genera of the Magnoliaceae are described. Assuming that the conduplicate carpel of Australasian species of Drimys (Winteraceae) represents the primitive condition, various carpellary modifications are indicated for the Magnoliaceae. These evolutionary spcializations from the basic type include: basal adnation, lateral concrescence, reduction in number of ovules, closure of the ventral suture, and localization of stigmatic areas. Among the examined species it was determined that carpels of the genera Elmerrillia and Manglietia retain the most primitive features, whereas those of the genus Liriodendron possess the most advanced. Comparisons are made with the gynoecia of related ranalean families, viz., Himantandraceae, Degeneriaceae and Annonaceae.     

DISPERSAL ECOLOGY OF VANCOUVERIA (BERBERIDACEAE)

All Vancouveria species are habitual myrmecochores of the Viola odorata type. The anatropous, bitegmic seed develops an unusual elaiosome in the form of a large, empty, folded and lobed sac of epidermal tissue. The thin-walled assimilating capsule dehisces along an oblique weak zone that probably represents the suture between two fused and unequal carpels. In V. hexandra the capsule opens early to expose immature assimilating seeds. Decurved pedicels, down-turned fruits, and weak funiculi produce tachyspory. The related Epimedium, Jeffersonia, and Plagiorhegma have appendaged seeds and other possible myrmecochorous features resembling those of Vancouveria. Myrmecochory was probably established in the early or middle Tertiary period. The Vancouveria-Epimedium complex indicates that enormous plant migrations may be accomplished by means of ants.     

Heat and drought determine flower female allocation in a hermaphroditic Mediterranean plant family

• In animal‐pollinated hermaphroditic species, larger and xenogamous flowers increase male‐biased resource allocation, whereas smaller and selfing flowers invest disproportionally more resources to female function. In Cistaceae, an entomophilous and hermaphroditic Mediterranean family, this pattern generally follows a phylogenetic signal. However, resource allocation to carpels is independent of phylogeny, which suggests trait divergences among closely related species during the diversification into different environmental conditions.
• We tested this hypothesis across 37 species of Cistaceae along a temperature and precipitation gradient, including semiarid, dry, subhumid and humid sites. We quantified the proportions of dry mass and nutrient investment to carpels and tested the influence of the climatic gradient and site‐specific precipitation on the interspecific variation in carpel resource allocation.
• Lowest and highest percentages of resource allocation to carpels ranged from 1.5–4.2% to 24.2–36.6%, respectively. The proportion of resources comprised in carpels significantly decreased with increasing precipitation/decreasing temperature. Thus, carpels comprised proportionally more resources under drier and hotter conditions, especially in semiarid sites.
• Our results demonstrate how the extent of climatic constraints is more important than phylogenetic relationships in determining stress‐induced differences in carpel resource allocation across species of Cistaceae in a Mediterranean environment. We suggest that allocation of proportionally more resources to carpels in drier and hotter sites lies within a strategy to deal with the most stressful conditions by means of a high reproductive effort.

     

Sinocarpus decussatus gen. et sp. nov., a new angiosperm with basally syncarpous fruits from the Yixian Formation of Northeast China

An Early Cretaceous angiosperm, Sinocarpus decussatus gen. et sp. nov., is described from the Yixian Formation in Liaoning, China, based on an infructescence fragment. It is probably ebracteate, consisting of one terminal fruit and two pairs of pedicellate lateral fruits arranged decussately. Carpels are probably borne on a small convex receptacle. There are no distinct remnants of a perianth although fragments observed at the base of immature fruits may represent perianth parts. No remnants of androecial parts have been observed, and it is unknown whether the flowers were unisexual or bisexual. The basally syncarpous ovary is superior and composed of 3 or 4 carpels. Each carpel contains about 10 anatropous ovules/seeds borne along the linear placentae. Seeds are flattened and embedded in a thick amorphous material. The character combination of Sinocarpus indicates a systematic position among the basal grade of eudicots or the basal core eudicots, and particularly shows similarities to extant Ranunculaceae, Buxaceae, and Myrothamnaceae, but based on the available data the fossil cannot unambiguously be placed in any modern family.     

The Diatom Attachment Scar Ophthalmichnus lyolithon igen. et isp. n.

A number of benthic diatoms (including species of the genera Cocconeis, Achnanthes, and Amphora) etch shallow attachment scars in carbonate hard substrates. The morphology of these microbioerosion traces mirrors the elliptical to biconvex outline of the diatoms, which, in its most common appearance, is expressed as a distinct ring-shaped groove. The traces are established as new ichnogenus and -species Ophthalmichnus lyolithon. The diatoms are assumed to form the etching scars by means of their adhesive mucilage composed of acidic polysaccharides, probably in order to enhance adhesion.     

STUDIES ON THE FLORAL ANATOMY OF THE CUNONIACEAE

Twenty-two genera representing sixty-two species of Cunoniaceae and Davidsonia were examined with respect to floral anatomy. Sepals are vascularized by three traces with the lateral traces of adjacent sepals united. Pancheria is unique for the family with species in which the sepals are vascularized by a single, undivided bundle. Petals, when present, and stamens, are uniformly one-trace structures. A general tendency exists within the family for the principal floral bundles to unite in various ways, with fusions evident between calyx, corolla, and androecial vascular supplies. Carpel number ranges from two to five and the gynoecium is generally surrounded by a prominent disc. Gynoecia of Ceratopetalum and Pullea are “half-inferior.” The number of ovules per carpel locule ranges from one to numerous. Ventral carpel sutures range from open to completely sealed at the level of placentation. Carpels of the apocarpous genus Spiraeanthemum (incl. Acsmithia) are vascularized by a dorsal bundle and either three or four bundles constituting the ovular and wing vasculation in the ventral position, a condition unlike other members of the family. Ovules are supplied by the median ventral bundle. More advanced bicarpellate gynoecia within the family are predominately vascularized by a dorsal and two ventral bundles although a variable number of additional lateral wall traces may be present. A major trend exists toward fusion of the ventral bundles of adjacent carpels in the ovary of both bicarpellate and multicarpellate plants. At the base of the styles the fused ventral strands separate and extend along with the dorsal carpellary bundles into styles of adjacent carpels. In Pullea the ventral bundles terminate within the ovules. The united ventral carpellary bundles in Aphanopetalum, Gillbeea, and Aistopetalum lie in the plane of the septa separating adjacent carpels. Ovules are vascularized by traces originating from the vascular cylinder at the base of the gynoecium or by traces branching from the ventral bundles. Ovular traces in each carpel are united, or remain as discrete bundles, prior to entering the placenta. Tannin and druses are common throughout all floral parts. Although floral anatomy generally supports the position of Cunoniaceae near Saxifragaceae and Davidsoniaceae, the evolutionary relationship of the Cunoniaceae to the Dilleniaceae is uncertain.     

STRUCTURALLY PRESERVED SPHENOPHYTES FROM THE TRIASSIC OF ANTARCTICA: VEGETATIVE REMAINS OF SPACIINODUM,GEN. NOV.

Sphenophyte remains of Early-Middle Triassic age are described from silicified peat collected in the Transantarctic Mountains of Antarctica. The new sphenophyte, Spaciinodum collinsonii sp. nov., is represented by ribbed, jointed stems with characteristic pith and carinal canals. Stems are relatively small, ranging from 1.8–3.0 mm in diameter, lack secondary tissues, and are characterized by vallecular canals that are restricted to nodal regions. The internodal vascular system consists of 12–18 collateral bundles which alternate between successive internodes. A complete vascular ring is present in the nodal region and is surrounded by a continuous double endodermis. Xylem is endarch and composed of elements ranging from annular to reticulate. The Antarctic sphenophyte is compared with other Gondwana fossil articulates and extant Equisetum. Superficial stomata suggest affinities with modern Equisetum subgenus Equisetum; however, some anatomical differences preclude assignment with living species.     

EARLY ANGIOSPERM REPRODUCTION: CALODA DELEVORYANA GEN. ET SP. NOV., A NEW FRUCTIFICATION FROM THE DAKOTA FORMATION (CENOMANIAN) OF KANSAS

A new angiosperm fructification, Caloda delevoryana, is described from the Cenomanian age Dakota Formation of central Kansas. It consists of a long, narrow, main axis with numerous secondary axes arranged helically around the main axis. These secondary axes are each terminated in a small receptacle bearing numerous conduplicate carpels. No evidence of a perianth or androecium was found. This fructification bears some similarity to a number of different modern orders, such as the Hamamelidales, Alismatales, Najadales, and Piperales, and families, particularly the Platanaceae and the Aponogetonaceae, but cannot definitely be assigned to any modern taxon within the angiosperms. C. delevoryana exhibits several characters traditionally assumed to be primitive in the angiosperms, and several other features of this fossil are proposed as primitive in the evolution of angiosperms. This floral axis, with its compact mass of numerous secondary axes bearing very small fruits and seeds, may be the product of reduction through diminished growth of internodes and carpels, and elaboration through increased repetition of floral modules. This record adds to the rapidly growing body of paleobotanical data on early angiosperm reproductive structures, which should prove important in the assessment of the extent and direction of angiosperm evolution.     

COMPARATIVE MORPHOLOGY OF THE CARPEL IN THE ROSACEAE VII. POMOIDEAE: CHAENOMELES,CYDONIA, DOCYNIA

The multi-ovulate pomoids, Chaenomeles, Cydonia, and Docynia, all have closed sutures and extensive fusion between carpel and floral cup and between ovular and wing bundles. Although the ovules in Docynia are generally apotropic and few in number (4–7), the ovules in the other two genera are pleurotropic and numerous (15–48). A statistical treatment of the whole tribe of Pomoideae shows that in carpels with open sutures ovular and wing bundles definitely tend to be separate while in those with closed sutures these bundles tend to be fused. To a lesser degree carpels with open sutures also tend to have bitegmic ovules, separate carpels, and a lesser extent of fusion between carpel and floral cup, while carpels with closed sutures tend to have monotegmic ovules, united carpels, and a greater extent of fusion between carpel and floral cup.     

Floral development in Adonideae (Ranunculaceae)

Floral development and floral phyllotaxis in species of Adonis, Callianthemum, and Trollius (Ranunculaceae) were studied with scanning electron microscopy. The floral organs are initiated in spiral sequence and the flowers have spiral phyllotaxis. The sepal primordia are broad, crescent-shaped, and truncate, but those of petals, stamens, and carpels are rather hemispherical. A relatively long plastochron appears to be present between the last sepal and the first petal as compared with the short and equal plastochrones of all subsequent floral organs. Maturation of the stamens within the androecium appears to be centripetal. The carpels have a short ascidiate zone. Placentation is uniformly lateral, even in Adonis and Callianthemum, which have only one fertile ovule per carpel (versus median in other genera of Ranunculoideae with a single fertile ovule). In Adonis and Callianthemum at the tip of the carpel the ventral slit is gaping and the stigma is broadly exposed, whereas in Trollius the stigma is narrower and more pronouncedly decurrent along the ventral slit. The petals in Callianthemum and Trollius are more conspicuously delayed in development than those in Adonis as compared with sepals and stamens. A short carpel stipe is formed early in Callianthemum but later in Adonis and Trollius. In Trollius farreri (commonly having only five carpels in contrast to other species of Trollius) the carpels form a single (spiral) series. Thus floral development is similar in all three genera and, at a lower level, Adonis and Callianthemum are especially close but have different autapomorphies, which reflects the current classification of the genera.     

Comparative floral anatomy and ontogeny in Magnoliaceae

Floral anatomy and ontogeny are described in six species of Magnoliaceae, representing the two subfamilies Liriodendroideae (Liriodendron chinese and L. tulipifera) and Magnolioideae, including species with terminal flowers (Magnolia championi, M. delavayi, M. grandiflora, M. paenetalauma) and axillary flowers (Michelia crassipes). The sequence of initiation of floral organs is from proximal to distal. The three distinct outermost organs are initiated in sequence, but ultimately form a single whorl; thus their ontogeny is consistent with a tepal interpretation. Tepals are initiated in whorls, and the stamens and carpels are spirally arranged, though the androecium shows some intermediacy between a spiral and whorled arrangement. Carpels are entirely free from each other both at primordial stages and maturity. Ventral closure of the style ranges from open in Magnolia species examined to partially closed in Michelia crassipes and completely closed in Liriodendron, resulting in a reduced stigma surface. Thick-walled cells and tannins are present in all species except Michelia crassipes. Oil cells are normally present. Floral structure is relatively homogeneous in this family, although Liriodendron differs from other Magnoliaceae in that the carpels are entirely closed at maturity, resulting in a relatively small stigma, in contrast to the elongate stigma of most species of Magnolia. The flower of Magnolia does not terminate in an organ or organ whorl but achieves determinacy by gradual diminution.