Trans‐Atlantic,trans‐Pacific and trans‐Indian Ocean dispersal in the small Gondwanan Laurales family Hernandiaceae

Aim To investigate the historical biogeography of the pantropical flowering plant family Hernandiaceae (Laurales), which today comprises 62 species in five genera. Location Hernandiaceae occur in Africa (9 species), Madagascar (4), the Neotropics (25), Australia (3), southern China, Indochina, Malesia, and on numerous Pacific Islands (32). These numbers include two widespread species, Hernandia nymphaeifolia, which ranges from East Africa to the Ogasawara Islands and New Caledonia, and Gyrocarpus americanus, thought to have a pantropical range. Methods We sampled 37 species from all genera, the widespread ones with multiple accessions, for a chloroplast DNA matrix of 2210 aligned nucleotides, and used maximum likelihood to infer species relationships. Divergence time estimation relied on an uncorrelated‐rates relaxed molecular clock calibrated with outgroup fossils of Lauraceae and Monimiaceae. Results The deepest split in the family is between a predominantly African–Madagascan–Malesian lineage comprising Hazomalania, Hernandia and Illigera, and an African–Neotropical lineage comprising Gyrocarpus and Sparattanthelium; this split may be 122 (110–134) Myr old. The stem lineages of the five genera date back at least to the Palaeocene, but six splits associated with transoceanic range disjunctions date only to the Oligocene and Miocene, implying long‐distance dispersal. It is inferred that Hernandia beninensis reached the West African islands of São Tomé and Bioko from the West Indies or the Guianas; Hernandia dispersed across the Pacific; and Illigera madagascariensis reached Madagascar from across the Indian Ocean. Main conclusions The disjunct ranges and divergence times of sister clades in the Hernandiaceae are partly congruent with the break‐up of West Gondwana, but mostly with later transoceanic dispersal. An exceptional ability to establish following prolonged oceanic dispersal may be largely responsible for the evolutionary persistence of this small clade.     

Embryology of Siparunaceae (Laurales): characteristics and character evolution

Embryological characters of Siparunaceae, which are poorly understood, were studied on the basis of two constituent genera, an African Glossocalyx and a South American Siparuna, to better understand their evolution within Laurales. These two genera have many embryological characteristics in common with the other lauralean families. Noticeably, they share the multi-celled ovule archesporium (uncertain in Glossocalyx) as a synapomorphy with all the other lauralean families except Lauraceae, the anthers dehisced by valves as a synspomorphy with all the other lauralean families except Calycanthaceae and Monimiaceae, and the bisporangiate anther as a synapomorphy with Gomortegaceae and Atherospermataceae. Siparunaceae are, however, distinct from all other laularean families in having unitegmic ovules that were derived from bitegmic ovules, probably due to an elimination of the outer integument. Likewise, the lack of the testa (i.e., developed outer integument), the "endotegmic" seed coat, and the perichalazal seed at maturity are also characteristics of Siparunaceae. Within the family, Siparuna differs from Glossocalyx in having plural tetrads of megaspores and plural, starchy-rich, one-nucleate, tubular embryo sacs (autapomorphies). On the other hand, Glossocalyx is characterized by having bilaterally flattened seeds (autapomorphy). Although functional aspects of those autapomorphies are uncertain, both Glossocalyx and Siparuna show evolution in different embryological characters.     

Embryology of Hortonioideae and Monimioideae (Monimiaceae,Laurales): characteristics of the ‘lower’ monimioids

We investigated the embryology of the ‘lower’ monimioids, i.e. Monimioideae (Monimia, Palmeria and Peumus) and Hortonioideae (Hortonia), which are poorly described embryologically. Our results show that, contrary to what has been reported in the literature, ‘lower’ monimioids show very little variation in their embryological characters. Comparisons with Mollinedioideae (a large derived subfamily in Monimiaceae) and other families in Laurales show that the ‘lower’ monimioids are relatively consistent in sharing predominantly isobilateral tetrads of microspores and megaspores, a non‐specialized chalaza, and a mesotestal–endotestal seed coat (with tracheoidal cells of the meso‐ and endotesta). It is likely that, while the shared successive cytokinesis during meiosis of microspore mother cells supports the Monimiaceae–Hernandiaceae–Lauraceae clade obtained by molecular evidence, no synapomorphies exist to support a sister‐group relationship of Monimiaceae with Hernandiaceae or Lauraceae. Instead, the lack of hypostase in ovules and/or young seeds, the lack of endosperm in mature seeds and the amoeboid tapetum in the anther are likely synapomorphies of Hernandiaceae and Lauraceae. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158 , 228–241.     

Embryology of Gomortegaceae (Laurales): characteristics and character evolution

The embryological characteristics of Gomortegaceae, which are poorly understood, were investigated on the basis of Gomortega nitida, the only species of the family, to understand better the evolution of this group within Laurales. Comparisons with other Laurales and Magnoliales (a sister group of Laurales) show that Gomortega has many embryological features in common with the other lauralean families. Notably, Gomortega shares a testa without or with at best only a poorly developed mesotesta as a synapomorphy with all other Laurales. The genus further shares anthers dehisced by valves as a synapomorphy with the other Laurales (except for Calycanthaceae and Monimiaceae), and a non-multiplicative testa and bisporangiate anther as synapomorphies with Atherospermataceae and Siparunaceae (although the non-multiplicative testa occurs as a homoplasy in Monimiaceae, and the bisporangiate anther in Monimiaceae pro parte, Lauraceae pro parte and Hernandiaceae, respectively). Gomortega shows simultaneous cytokinesis to form pollen grains, a one-celled ovule archesporium and non-specialized chalaza, all or part of which may be synapomorphies shared with Atherospermataceae. Gomortega appears to have no embryological autapomorphies, but further comparison with Atherospermataceae is required.Kweon Heo and Yukitoshi Kimoto contributed equally to this work.     

Comparative seed morphology of <Emphasis Type="Italic">Leandra</Emphasis> (Miconieae,Melastomataceae)

The seed morphology of 79 species of neotropical Miconieae (Melastomataceae) is presented. These species have been chosen, in majority, from the polyphyletic genus Leandra. A few other species from the polyphyletic genera Miconia, Ossaea, and Clidemia were also sampled, because of potential similarities. Sixteen morphological seed types are defined after analysis through light microscopy and scanning electron microscopy. The seed morphology appears to possess a great deal of variability on the level of the overall shape as well as the structure and the surface of the testa. The different types defined here do not match with genera or sections, but rather are composed of species coming from different genera. In comparison with a preliminary molecular phylogeny study done on Leandra, some types of seeds are related to well supported clades. In some cases seed morphology corresponds with natural groups of species, thus being of high phylogenetic importance.     

Chromosome evolution in the Laurales based on analyses of original and published data

We present a summary of currently available chromosome information for all seven families in the order Laurales on the basis of original and previously published data and discuss the evolution of chromosomes in this order. Based on a total of 53 genera for which chromosome data were available, basic chromosome numbers appear consistent within families: x = 11 (Calycanthaceae); x = 22 (Atherospermataceae and Siparunaceae); x = 19 (Monimiaceae); and x = 12 and 15 (Lauraceae). The Hernandiaceae have diverse numbers: x = 15 (Gyrocarpoideae) and x = 18 and 20 (Hernandioideae). Karyotype analyses showed that Hennecartia, Kibaropsis, and Matthaea (all Monimiaceae) contained two or three sets of four distinct chromosomes in 38 somatic chromosomes, suggesting that 2n = 38 was derived by aneuploid reduction from 2n = 40, a tetraploid of x = 10. In light of the overall framework of phylogenetic relationships in the Laurales, we show that x = 11 is an archaic base number in the order and is retained in the Calycanthaceae, which are sister to the remainder of the order. Polyploidization appears to have occurred from x = 11 to x = 22 in a common clade of the Siparunaceae, Atherospermataceae, and Gomortegaceae (although 2n = 42 in the Gomortegaceae), and aneuploid reduction from x = 11 to x = 10 occurred in a common clade of the Hernandiaceae, Lauraceae, and Monimiaceae. To understand chromosome evolution in the Lauraceae, however, more studies are needed of genera and species of Cryptocaryeae.     

大果马蹄荷(Exbucklandia tonkinensis)群落的纬度地带性

大果马蹄荷主产南亚热带至中亚热带南缘,南至海南岛,北至罗霄山脉中段的井冈山、桃源洞地区,是常绿阔叶林的特征种。以纬度地带性(海南霸王岭、广东黑石顶、广东南岭、江西金盆山、江西井冈山、湖南桃源洞)为依托,选定6个具代表性的大果马蹄荷群落开展群落生态学研究,结果表明:(1)各样地物种多样性较高,尤以金盆山蕨类植物9科10属11种、种子植物42科78属128种和桃源洞蕨类植物9科11属12种、种子植物41科79属134种最为丰富。群落组成的优势科主要为金缕梅科、壳斗科、樟科、山茶科、杜鹃花科、山矾科等。(2)从区系特征和环境梯度看,大果马蹄荷群落以南亚热带为分布中心,向南或向北其物种多样性Simpson指数、Shannon-Wiener指数及相应的均匀度指数均呈下降趋势,其中霸王岭、黑石顶、南岭、金盆山、井冈山、桃源洞的Shannon-Wiener指数分别为3.453、4.021、4.130、3.790、3.415、3.712。(3)群落相似性聚类分析显示群落随纬度和随海拔高度形成两个梯度系列,一是以黑石顶、金盆山、井冈山、桃源洞的纬度地带性为一支,相似性系数0.51;二是以南岭和霸王岭聚成海拔梯度较高的另一支,但其相似性系数0.50,为0.33—0.48。(4)大果马蹄荷群落种类组成在区系性质上很相似,具有明显的南亚热带特征;同时,受海拔、地形、气温、降雨条件等因素的影响,种子植物属的热带成分随纬度增加而呈波动性下降趋势。(5)大果马蹄荷种群在各群落中的重要值水平和径级结构表现出一致性,在纬度地带性差异上无明显的相关性。霸王岭大果马蹄荷的径级结构为增长型,但重要值排名为32,说明向南分布该种群优势度明显下降;在南岭、黑石顶、金盆山、桃源洞该种群优势度较大,且为稳定型种群;在井冈山该群落受到人为干忧,大果马蹄荷的重要值排名第1,但为衰退型种群。     

Gynoecium diversity and systematics of the Laurales

Carpel and ovule structure was comparatively studied in representatives of all eight families of the Laurales: Amborellaceae, Calycanthaceae, Chloranthaceae, Gomortegaceae, Hernandiaceae, Lauraceae, Monimiaceae, and Trimeniaceae. In all representatives the carpels are closed at anthesis. As in Magnoliales/winteroids, closure takes place in three different modes: (1) by postgenital fusion of the stylar (and ovarial) ventral slit (Calycanthaceae, Gomortegaceae, Lauraceae, Hernandiaceae); (2) by occlusion of the inner space by secretion (Amborellaceae, Chloranthaceae, Trimeniaceae, Mollinedioideae of Monimiaceae), all having extremely ascidiate carpels; (3) by a combination of (1) and (2), whereby the ventral slit in the style is postgenitally fused but a central canal remains open, which is filled by secretion (Monimiaceae except Mollinedioideae). The carpels have a single ovule in ventral median placentation; only Calycanthaceae have two lateral ovules, although the upper ovule degenerates. In contrast to Magnoliales/winteroids, several representatives have orthotropous or almost orthotropous ovules (Amborellaceae, Chloranthaceae, Gomortegaceae). Mature ovules vary in length between 425 μm (some Monimiaceae) and 1500 urn (some Calycanthaceae, Trimeniaceae). Although all ovules are crassinucellar, nucellus breadth varies between 60 μm (Chimonanthus, Calycanthaceae) and 500 μm (Hemandia, Hernandiaceae). In almost all representatives the single ovule (two in Calycanthaceae) tightly fills out the ovarial cavity. The micropyle is mostly formed by the inner integument. In a few cases there is no micropyle and the nucellar apex makes direct contact with the inner ovary surface or the funicle (Lauraceae p.p., Calycanthaceae p.p., Hernandiaceae p.p., Monimiaceae p.p.). The ovule is pachychalazal (or perichalazal) in Lauraceae, some Hernandiaceae, and Gomortegaceae. Both integuments are variously lobed or unlobed. The outer integument is semiannular or annular, and this may vary within a family (Calycanthaceae, Hernandiaceae, Monimiaceae); it is also exceedingly diverse in thickness (2–23 cell layers). Gynoecial traits support the association of Chloranthaceae, Trimeniaceae, and Amborellaceae, and also separately Gomortegaceae, Hernandiaceae, and Lauraceae. In addition, affinities of the first group with Schisandraceae, Illiciaceae and Austrobaileyaceae may also be supported.     

Embryology and relationships of Lauraceae (Laurales)

Embryology of Lauraceae, hitherto poorly known, was investigated on the basis of 35 species from 23 genera to contribute to a better understanding of familial and generic relationships. Data from the genera investigated and from the literature show that the genera of Lauraceae are very similar embryologically, but that differences do exist in a few characters among the genera. Based on comparisons with other families of Laurales, Lauraceae consistendy had a pachychalazal ovule or seed with a ramified raphal vascular bundle at chalaza (an apomorphy) in common with Hernandiaceae. However, since several core lauralean families such as Amborellaceae, Monimiaceae, and Gomortegaceae are little known embryologically, these must be studied for critical comparison. Wimin Lauraceae, Cassytha is clearly distinct from the rest of the family in having an ab initio cellular type endosperm (a plesiomorphy, also reported in Umbellularia ) instead of a nuclear type endosperm (an apomorphy) as in the rest of the family, in lacking the nucellar cap and in having the micropyle formed by bom the inner and outer integument, facts supporting the traditional taxonomic placement of Cassytha in its own subfamily and the remainder of the family in the other subfamily. Widiin the rest of the family, the amoeboid tapetum (an apomorphy) distinguishes 15 genera ( Actinodaphne, Cinnamomum, Laurus , etc.) from the six genera with the glandular tapetum. In addition, a mature embryo sac protruding from the nucellus (an apomorphy) distinguishes five genera ( Beibchmiedia, Caryodaphnopsis, Cryptocarya, Endiandra, Potamria) and one species of Ocotea (O. rubra ) from the rest of the family. These results can properly be incorporated in a future suprageneric classification. The distinctness of Ocotea rubra wimin the genus is also discussed.     

Plastid phylogenomics improve phylogenetic resolution in the Lauraceae

Abstract The family Lauraceae is a major component of tropical and subtropical forests worldwide, and includes some commercially important timber trees and medicinal plants. However, phylogenetic relationships within Lauraceae have long been problematic due to low sequence divergence in commonly used markers, even between morphologically distinct taxa within the family. Here we present phylogenetic analyses of 43 newly generated Lauraceae plastomes together with 77 plastomes obtained from GenBank, representing 24 genera of Lauraceae and 17 related families of angiosperms, plus nine barcodes from 19 additional species in 18 genera of Lauraceae, in order to reconstruct highly supported relationships for the Lauraceae. Our phylogeny supports the relationships: sisterhood of the Lauraceae and a clade containing Hernandiaceae and Monimiaceae, with Atherospermataceae and Gomortegaceae being the next sister groups, followed by Calycanthaceae. Our results highlight a monophyletic Lauraceae, with nine well‐supported clades as follows: Hypodaphnis clade, Beilschmiedia–Cryptocarya clade, Cassytha clade, Neocinnamomum clade, Caryodaphnopsis clade, Chlorocardium–Mezilaurus clade, Machilus–Persea clade, Cinnamomum–Ocotea clade, and Laurus–Neolitsea clade. The topology recovered here is consistent with the patterns of plastome structural evolution and morphological synapomorphies reported previously. More specifically, flower sex, living type, inflorescence type, ovary position, anther locus number, leaf arrangement, leaf venation, lateral vein number, tree height, and inflorescence location all represent morphological synapomorphies of different lineages. Our findings have taxonomic implications and two new tribes, Caryodaphnopsideae and Neocinnamomeae, are described, and the composition of four other tribes is updated. The phylogeny recovered here provides a robust phylogenetic framework through which to address the evolutionary history of the Magnoliids, the third‐largest group of Mesangiospermae.     

Host-specificity of a root borer,Bembecia chrysidiformis [Lep.: Sesiidae], a potential control agent forRumex spp. [Polygonaceae] in Australia

Bembecia chrysidiformis (Esper) [Lep.: Sesiidae] was examined for its natural history and specificity toRumex spp. (Polygonaceae) which are weeds in Australia. Adults of this southern European insect appear in late spring to summer. Eggs are laid on the dried, seed bearing stems of perennialRumex plants. The larvae tunnel inside the root during summer through to the next spring. In nature, the larvae are round inRumex species of the subgeneraRumex andAcetosa. In host-specificity tests with 1st instar larvae, the roots of a number of genera within thePolygonaceae were attacked. Larvae died on a range of plants from other families except inPersea americana Miller(Lauraceae), Helianthemum nummularium (L.) Miller (Cistaceae) andQuercus ilex L. (Fagaceae) where larvae fed on the stems. The insect was judged safe for release in Australia by assessing aspects of its biology, its known host plants, and the lack of reported attack on other plants.      

Requirement for particular seed-borne fungi for seed germination and seedling growth of <Emphasis Type="Italic">Xyris complanata</Emphasis>, a pioneer monocot in topsoil-lost tropical peatland in Central Kalimantan,Indonesia

Hawaii yellow-eyed grass (Xyris complanata: Xyridaceae) inhabits infertile, acidic peat soil in the rainy tropical zone in Southeast Asia. This monocot plant produces a large number of dormant seeds in order to make a large deposit to seed bank in the soil. Under laboratory conditions, surface-sterilized X. complanata seeds are rarely able to germinate on sterilized peat moss bed; they require inoculation with either seed epiphytic or soil fungi to facilitate active seed germination. In the present study, three different genera of seed epiphytic fungi were isolated, and two common fungal genera, Fusarium sp. (strain R-1) and Penicillium sp. (strain Y-1), were found to promote seed germination of X. complanata. In sterile peat moss beds, the germination-stimulating fungi also showed growth-promoting effects on X. complanata seedlings. These results suggest that the seed germination-promoting fungi likely function as genuine partners for X. complanata in tropical open peat lands.     

Comparative seed morphology and character evolution in the genus Lysimachia (Myrsinaceae) and related taxa

Summary We investigated seed morphology in 34 species of the genus Lysimachia and in 14 species and two subspecies of six additional genera (Anagallis, Ardisiandra, Asterolinon, Glaux, Pelletiera, Trientalis), which have been shown to be closely related to, or are placed within Lysimachia in previous molecular studies. We studied seed shape, seed coat structure, and seed coat surface patterns. Three major types of seed shape were identified: (1) sectoroid, (2) polyhedral, and (3) coarsely rugose with concave hilar area. In addition, seeds may be keeled or winged. The outer layer of the seed coat is either sponge-like and adhering only loosely to the inner seed coat or it is thin and tightly adhering to the underlying tissue. Seed surface patterns can be divided into six main types: (1) reticulate, (2) tuberculate, (3) vesiculose, (4) colliculate, (5) undulate, or (6) poroid-alveolate. Seed surface patterns are mostly congruent with molecular phylogenetic relationships. A reticulate surface pattern is diagnostic of, e.g. Lysimachia subgenera Palladia and Hawaiian Lysimachiopsis. Mapping seed characters onto a recent phylogenetic tree, reveals that they provide potentially synapomorphic character states for various subclades of Lysimachia. Salient examples include a rugose seed shape, which turns out to be synapomorphic for the clade comprising the genus Pelletiera plus Asterolinon linum-stellatum and a sponge-like outer seed coat layer, which characterizes a clade with Lysimachia vulgaris, L. thyrsiflora, and L. terrestris, with an analogue that apparently evolved in parallel in Trientalis europaea. We also discuss possible habitat factors that may have favored the independent evolution of particular seed types such as winged seeds in various lineages.     

COMPARATIVE MORPHOLOGY AND PHYLOGENY OF THE RANALES

Comparative morphological studies of woody Ranales have established the primitive status of the group and hence their key place in angiosperm phylogeny. Significant advances in our knowledge of some ranalian families have been made in recent years. An attempt is made in the present review to bring together a range of morphological data (vegetative and floral anatomy, palynology and embryology) on the Ranales (sensu lato), with particular reference to research work published after the publication of Eames's (1961) book, and to discuss the relationships of the families. Recent ontogenetic studies have shown that the carpel of Drimys is ascidial and not conduplicate as earlier suggested. The inclusion of Degeneria in the Winteraceae is not supported by morphological data. Melville's gonophyll theory has been shown to be inapplicable to the magnoliaceous flower. The pollen of Schisandra is interpreted as derived and specialized rather than primitive as previously supposed. The removal of Schisandra from Magnoliaceae is upheld by morphological evidence. Recent morphological studies do not support a close relationship between Schisandraceae and Illiciaceae suggested by earlier authors. The Canellaceae shows similarities to Winteraceae, Magnoliaceae, Illiciaceae, Eupteleaceae and Myristicaceae. Transitional types of division of pollen mother cells found in Winteraceae, Schisandraceae and Annonaceae and their probable phylogenetic significance have been discussed. The Annonaceae, Winteraceae, Degeneriaceae, Magnoliaceae, Schisandraceae and Cercidiphyllaceae share several embryological features in addition to similarities in floral structure. Ruminate endosperm is regarded either as an archaic feature retained in some taxa or as a later and parallel development in others. Thus its value in assessing relationships seems to be doubtful. Myristicaceae has been shown to be closely related neither to the the Annonaceae nor to the Lauraceae. The suggested relationship of Eupomatiaceae to Annonaceae is not supported by palynology. Floral cortical vascular systems in Magnoliaceae, Annonaceae, Calycanthaceae and Myristicaceae have been compared and it is concluded that they may be vestigial structures. A great deal of similarity has been found between Lauraceae and Calycanthaceae in wood, node, flower structure and embryology. Further floral anatomical evidence has been adduced to support the removal of Scyphostegia from Monimiaceae. The Hernandiaceae show similarities to some members of Monimiaceae while the Gyrocarpaceae resemble the Lauraceae, Gomortegaceae and certain other genera of Monimiaceae. Available evidence from wood and floral anatomy and embryology indicates close relationships among Lauraceae, Monimiaceae and Hernandiaceae. Vegetative and floral anatomical and embryological data seem to indicate a place for the Chloranthaceae in the ranalian complex. Recent anatomical studies in the Nymphaeaceae show that the floral structure is of a primitive type with similarities to the woody Ranales. Available morphological evidence is considered inadequate to express an opinion on the splitting of the family. Ceratophyllaceae is regarded as a highly reduced ranalian family derived most probably from a nymphaeaceous stock. The gynoecium in Berberidaceae is interpreted as monocarpellate. No evidence has been found to support the tricarpellate view. Berberidaceae, Lardizabalaceae and Menispermaceae share several embryological features, while at the same time showing evidence of specialization, each in its own way. Thus they might have arisen from a common stock and early diverged along different lines. The occurrence of several types of embryo sac in Ranunculaceae may well be an indication of specialization, but their probable taxonomic value, if any, is not yet clear. The occurrence of numerous primitive features in Paeonia has been suggested as an argument for its retention in the Ranales. No evidence has been found to preclude the inclusion of Dilleniaceae in the Ranales. On the other hand, as opposed to similarities in wood and pollen characters between Dilleniaceae and Theaceae, floral anatomical and embryological features offer a sharp contrast between the two. The Ranales are believed to be polyphyletic. It has been tentatively suggested that two major phyletic lines may be recognized in each of the woody and herbaceous series: the magnolialian and lauralian lines in the former and the nymphaealian and berberidalian lines in the latter.     

Fossil flowers and pollen ofLauraceae from the Upper Cretaceous of New Jersey

A fossil trimerous flower from the Turonian (ca. 90 MYBP, Upper Cretaceous) of New Jersey is described as a new genus in the familyLauraceae. The fossil flower is charcoalified and preserved in exceptional detail. This fossil specimen is particularly remarkable in that several pollen grains have been preserved; pollen grains ofLauraceae generally have very thin exine and are rarely preserved in the fossil record. Although the specimen is incomplete and lacks anthers, there are sufficient structural details preserved to permit an assignment to theLauraceae, as well as comparisons with the tribePerseeae. This new genus provides an important addition to our knowledge of systematic and structural diversity in CretaceousLauraceae.     

Upper Cretaceous aquatic plants from Northern Mexico

Two aquatic plant genera assignable to Decodon (Lythraceae) and Ceratophyllum (Ceratophyllaceae) are described based on reproductive structures collected from the Cerro del Pueblo Formation (late Campanian [73.5 ma]), Coahuila, Northeast Mexico. Decodon is represented by three small seeds with a pyramidal shape, rounded borders, and a concave ventral surface with a rectangular valve towards the center of the seed ventral surface. The Ceratophyllum spiny fruit has an ellipsoidal central body and two proximal long spines flanking a short pedicel opposite the stylar projection. These new reports confirm the presence of both genera in the Upper Cretaceous sediments of Northeastern Mexico, and add to our recognition of diversity within the widely distributed freshwater communities along the margin of the epicontinental sea.     

The natural delimitation ofCentaurea (Asteraceae: Cardueae): ITS sequence analysis of theCentaurea jacea group

Taxonomic complexity has hindered partitioning the genusCentaurea into natural subdivisions, even though it has long been recognized as an unwieldy, artificial assemblage. Most of the remaining difficulties center in theCentaurea jacea group, whose taxa share a common advanced type of pollen. Because it comprises half the species of the genusCentaurea, as well as five other disputed genera previously segregated fromCentaurea (Chartolepis, Cheirolepis, Cnicus, Grossheimia andTomanthea), theCentaurea jacea group is a significant taxonomic challenge. Newer molecular approaches are useful for resolving complex relationships because they provide more precise inferences of evolutionary relationships than traditional morphological characters. Sequences of the Internal Transcribed Spacers (ITS) of nuclear ribosomal DNA were analyzed for a comprehensive sample of this group. Results indicated that theCentaurea jacea group is monophyletic and includes the segregated genera, but not two other genera (Oligochaeta andZoegea), whose inclusion in theCentaurea jacea group was doubtful. In addition to pollen morphology, the ITS phylogeny is also supported by karyological evidence and by good correlation with biogeographic distribution of the species. The monophyly of theCentaurea jacea group suggests that a natural delimitation ofCentaurea that minimizes nomenclatural changes is possible, but only if a new type of the genus is designated.     

Synchronized dichogamy and dioecy in neotropicalLauraceae

In hermaphrodite neotropicalLauraceae a highly evolved dichogamous system is present which represents a kind of temporal dioecy. This system involves the existence of two flower morphs which are characterized by reciprocal phases of receptivity of the stigmas and pollen release. In some genera (Persea, Cinnamomum), nectar is produced as a reward for the flower visitors, while in other genera (Aniba, Clinostemon, Licaria), nectar is absent and pollen seems to be the only reward. This implies that in this case the flowers in the female stage must be deceptive flowers. In dioecious species of the generaOcotea andNectandra, both the male and female flowers attract the visitors with nectar. The pollen-ovule ratio of theLauraceae is comparatively low. — The type of reproductive system that characterizes theLauraceae, comprising functional dioecy, small, inconspicuously coloured flowers, pollination by small bees, and large, one-seeded fruits dispersed by birds, is quite prominent among trees of various families in the tropical lowland forest. The relationship between the different modes of flowering within theLauraceae and the causes for the correlation of their reproductive traits are discussed.     

Phylogenetic relationships of graminicolous downy mildews based on cox2 sequence data

Graminicolous downy mildews (GDM) are an understudied, yet economically important, group of plant pathogens, which are one of the major constraints to poaceous crops in the tropics and subtropics. Here we present a first molecular phylogeny based on cox2 sequences comprising all genera of the GDM currently accepted, with both lasting (Graminivora, Poakatesthia, and Viennotia) and evanescent (Peronosclerospora, Sclerophthora, and Sclerospora) sporangiophores. In addition, all other downy mildew genera currently accepted, as well as a representative sample of other oomycete taxa, have been included. It was shown that all genera of the GDM have had a long, independent evolutionary history, and that the delineation between Peronosclerospora and Sclerospora is correct. Sclerophthora was found to be a particularly divergent taxon nested within a paraphyletic Phytophthora, but without support. The results confirm that the placement of Peronosclerospora and Sclerospora in the Saprolegniomycetidae is incorrect. Sclerophthora is not closely related to Pachymetra of the family Verrucalvaceae, and also does not belong to the Saprolegniomycetidae, but shows close affinities to the Peronosporaceae. In addition, all GDM are interspersed throughout the Peronosporaceae s lat., suggesting that a separate family for the Sclerosporaceae might not be justified.