Histological Aspects of Root Formation in Petioles of Detached Leaves of Pereskia grandifolia (Cactaceae): Natural Conditions and Effects of GA3 and Dark

Adventitious roots arise naturally on petioles of Pereskia grandifoliaHaw. held in light. At about the 12th day after the beginningof the experiment, the root primordia arise in a callus tissuedeveloped from the basal portion of the petiole. Associatedwith the development of the callus, noticeable structural changesoccur in the originating organ. Petioles maintained in darkalso form callus; however, they die in a few days. On the otherhand, petioles treated with GA,, maintained in light, developcallus and survive; but they do not give rise to roots. Someaspects are discussed, such as: the kind of origin observedfor the roots, and the possible physiological basis for theirformation, as wdl as for the inhibition of their appearance Pereskia grandifolia, adventitious root formation, gibberelljc acid, petiole structure, rooting     

Review of the genus Hippidion Owen, 1869 (Mammalia: Perissodactyla) from the Pleistocene of South America

This review of Hippidion is based on a multivariate analysis of the foot, and some morphological characteristics of the skull and dentition. We recognize only one genus ( Hippidion ) including all the hippidiform horses, with three different species: H. principale, H. devillei and H. saldiasi. The latter species is stratigraphically and geographically restricted to the period from 13000 to 8000 years BP in the southern part of South America. Hippidion principale and H. devillei have a large geographical distribution (Argentina, Bolivia, Chile, Perú, Uruguay, Brazil) through the Upper Pliocene-Upper Pleistocene. Both species show some morphometric variations across their geographic range; these features may result from the environmental characteristics.     

Leafminers help us understand leaf hydraulic design

Leaf hydraulics of Aesculus hippocastanum L. were measured over the growing season and during extensive leaf mining by the larvae of an invasive moth (Cameraria ohridella Deschka et Dimic) that specifically destroy the palisade tissue. Leaves showed seasonal changes in hydraulic resistance (R_lamina) which were related to ontogeny. After leaf expansion was complete, the hydraulic resistance of leaves and the partitioning of resistances between vascular and extra‐vascular compartments remained unchanged despite extensive disruption of the palisade by leafminers (up to 50%). This finding suggests that water flow from the petiole to the evaporation sites might not directly involve the palisade cells. The analysis of the temperature dependence of R_lamina in terms of Q₁₀ revealed that at least one transmembrane step was involved in water transport outside the leaf vasculature. Anatomical analysis suggested that this symplastic step may be located at the bundle sheath where the apoplast is interrupted by hydrophobic thickening of cell walls. Our findings offer some support to the view of a compartmentalization of leaves into well‐organized water pools so that the transpiration stream would involve veins, bundle sheath and spongy parenchyma, while the palisade tissue would be largely by‐passed with the possible advantage of protecting cells from short‐term fluctuations in water status.     

How river structure and biological traits influence gene flow: a population genetic study of two stream invertebrates with differing dispersal abilities

1. Determined by landscape structure as well as dispersal‐related traits of species, connectivity influences various key aspects of population biology, ranging from population persistence to genetic structure and diversity. Here, we investigated differences in small‐scale connectivity in terms of gene flow between populations of two ecologically important invertebrates with contrasting dispersal‐related traits: an amphipod (Gammarus fossarum) with a purely aquatic life cycle and a mayfly (Baetis rhodani) with a terrestrial adult stage. 2. We used highly polymorphic markers to estimate genetic differentiation between populations of both species within a Swiss pre‐alpine catchment and compared these results to the broader‐scale genetic structure within the Rhine drainage. Landscape genetic approaches were used to test for correlations of genetic and geographical structures and in‐stream barrier effects. 3. We found overall very weak genetic structure in populations of B. rhodani. In contrast, G. fossarum showed strong genetic differentiation, even at spatial scales of a few kilometres, and a clear pattern of isolation by distance. Genetic diversity decreased from downstream towards upstream populations of G. fossarum, suggesting asymmetric gene flow. Correlation of genetic structure with landscape topography was more pronounced in the amphipod. Our study also indicates that G. fossarum might be capable of dispersing overland in headwater regions and of crossing small in‐stream barriers. 4. We speculate that differences in dispersal capacity but also habitat specialisation and potentially the extent of local adaptation could be responsible for the differences in genetic differentiation found between the two species. These results highlight the importance of taking into account dispersal‐related traits when planning management and conservation strategies.     

Reproductive structures and systematics of Buxaceae

Buxaceae belong to a grade of families near the base of eudicots. Flowers of these families are characterized by a variable number and arrangement of floral organs. In this study, the anthetic structure of the gynoecium and androecium of representatives of all genera of Buxaceae were comparatively studied, and observations on the flowering processes and pollination biology were made. Styloceras and Notobuxus were studied in detail for the first time. Various features of the morphological analysis support our earlier molecular phylogenetic study. Shared reproductive characters among Sarcococca , Pachysandra and Styloceras are the occurrence of two (rarely three) carpels, the lack of interstylar nectaries, a micropyle formed by both integuments, attractive stamens in male flowers, and fleshy fruits. In addition, Styloceras and Pachysandra share a secondary partition in the ovary. Notobuxus does not seem to be clearly distinct from Buxus . Both have a similar inflorescence and perianth structure; female flowers have three carpels, interstylar nectaries, micropyles formed by the inner integument, rudimentary arils, and they develop into capsular fruits; in male flowers stamens are sessile and the central pistillode is lacking in some species. Thus, it is questionable to justify a separation of Buxus and Notobuxus at genus level. The results further strongly support the placement of Buxaceae among basal eudicots.  © The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 140 , 193–228.     

Cytological evidence of natural hybridization in Brachiaria brizantha Stapf (Gramineae)

Two accessions of Brachiaria brizantha under cytological analysis showed 2 n  = 5x = 45 chromosomes. Pentaploidy probably resulted from natural hybridization between two species that were not closely related: an apomictic tetraploid male (2 n  = 4x = 36), and a sexual diploid female (2 n  = 2x = 18). The lack of affinity between genomes was clearly indicated by asynchrony during meiosis. The haploid genome ( n  = 9) showed unique behaviour, remaining univalent during prophase I and metaphase I, and undergoing sister-chromatid segregation and lagging at anaphase I. The laggard genome did not always reach the poles in time to be included in the telophase nucleus. However, when the inclusion was effective, this genome was distributed peripherally, changing the otherwise spherical nucleus shape. In the second division, the haploid genome behaved similarly, but as there was sister-chromatid segregation during the first division, the chromatids were slow to reach the poles, forming several micronuclei at telophase II. The two accessions were characterized as allo-autopentaploids, with the tetraploid genome (2 n  = 4x = 36) designated as B (from B. brizantha ) and the haploid genome as X, representing a species with a distinct genome having little affinity with the B genome. Thus, the hybrids' genome composition is represented by BBBBX. By comparing their meiotic behaviour with that observed in synthetic hybrids between B. brizantha and B. ruziziensis analysed previously, B. ruziziensis is the putative diploid sexual parent species in these pentaploid accessions.  © 2006 The Linnean Society of London , Botanical Journal of the Linnean Society , 2006, 150 , 441–446.     

On the identity of Festuca jubata Lowe (Poaceae) and the description of a new Festuca species in the Azores Islands

The majority of authors consider Festuca jubata Lowe as an endemic species common to Madeira and the Azores. Saint-Yves proposed that F. jubata was an Azorean endemic and described a geovicarious taxon in Madeira: F. filiformis C. Sm. ex Link in Buch ssp. mandonii St.-Yves. We undertook a complete bibliographical revision of the taxonomy, nomenclature, and chorology of F. jubata s.l. , and contrasted it with morphological and anatomical studies performed on samples from the Azores and Madeira. Azorean plants usually identified as F. jubata had a character combination distinct from that of those with a Madeiran provenance. Saint-Yves' proposal of two independent taxa was correct, but he erroneously considered F. jubata as an Azorean endemic because the name F. jubata was based on Madeiran plants. Consequently, F. jubata auct. pl. from the Azores belongs to a new species.  © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society , 2008, 157 , 493–499.     

A phase II randomized clinical trial for the treatment of recalcitrant chronic leg ulcers using centrifuged adipose tissue containing progenitor cells

Background aims

Preclinical and observational reports indicate that adipose tissue (AT) is a safe and promising tool to treat non-healing venous leg ulcers (VLUs).