Morphogenesis of the reproductive shoots of Welwitschia mirabilis and Ephedra distachya (Gnetales), and its evolutionary implications

For decades, Gnetales appeared to be closely related to angiosperms, the two groups together forming the anthophyte clade. At present, molecular studies negate such a relationship and give strong support for a systematic position of Gnetales within or near conifers. However, previous interpretations of the male sporangiophores of Gnetales as pinnate with terminal synangia conflict with a close relationship between Gnetales and conifers. Therefore, we investigated the morphogenesis of the male reproductive structures of Welwitschia mirabilis and Ephedra distachya by SEM and light microscopy. The occurrence of reduced apices to both halves of the antherophores of W. mirabilis gives strong support for the assumption that the male ‘flowers’ of W. mirabilis represent reduced compound cones. We assume that each half of the antherophore represents a lateral male cone that has lost its subtending bract. Although both halves of the antherophores of Ephedra distachya lack apical meristems, the histological pattern of the developing antherophores supports interpreting them as reduced lateral male cones as well. Therefore, the male sporangiophores of Gnetales represent simple organs with terminal synangia. Although extant conifers do not exhibit terminal synangia, similar sporangiophores are reported for some Cordaitales, the hypothetical sister group of conifers. Moreover, several Paleozoic conifers exhibit male cones with terminal sporangia or synangia. Therefore, we propose that conifers, Cordaitales and Gnetales originated from a common ancestor that displayed simple sporangiophores with a terminal cluster of sporangia.     

Evolution of Reproductive Organs in Land Plants

LEAFY gene is the positive regulator of the MADS-box genes in flower primordia. The number of MADS-box genes presumably increased by gene duplications before the divergence of ferns and seed plants. Most MADS-box genes in ferns are expressed similarly in both vegetative and reproductive organs, while in gymnosperms, some MADS-box genes are specifically expressed in reproductive organs. This suggests that (1) the increase in the number of MADS-box genes and (2) the subsequent recruitment of some MADS-box genes as homeotic selector genes were important for the evolution of complex reproductive organs. The phylogenetic tree including both angiosperm and gymnosperm MADS-box genes indicates the loss of the A-function genes in the gymnosperm lineage, which is presumably related to the absence of perianths in extant gymnosperms. Comparison of expression patterns of orthologous MADS-box genes in angiosperms, Gnetales, and conifers supports the sister relationship of Gnetales and conifers over that of Gnetales and angiosperms predicted by phylogenetic trees based on amino acid and nucleotide sequences. Received 30 July 1999/ Accepted in revised form 9 September 1999     

The Chloroplast trnT–trnF Region in the Seed Plant Lineage Gnetales

The trnT–trnF region is located in the large single-copy region of the chloroplast genome. It consists of the trnL intron, a group I intron, and the trnT–trnL and trnL–trnF intergenic spacers. We analyzed the evolution of the region in the three genera of the gymnosperm lineage Gnetales (Gnetum, Welwitschia, and Ephedra), with especially dense sampling in Gnetum for which we sequenced 41 accessions, representing most of the 25–35 species. The trnL intron has a conserved secondary structure and contains elements that are homologous across land plants, while the spacers are so variable in length and composition that homology cannot be found even among the three genera. Palindromic sequences that form hairpin structures were detected in the trnL–trnF spacer, but neither spacer contained promoter elements for the tRNA genes. The absence of promoters, presence of hairpin structures in the trnL–trnF spacer, and high sequence variation in both spacers together suggest that trnT and trnF are independently transcribed. Our model for the expression and processing of the genes tRNA^Thr(UGU), tRNA^Leu(UAA), and tRNA^Phe (GAA) therefore attributes the seemingly neutral evolution of the two spacers to their escape from functional constraints. [Reviewing Editor: Debashish Bhattacharya]     

The Structure Anomalous Secondary Growth of Stem in Gnetum montanum

In the stem of Gnetnm montanum Mgr. the general arrangement of various tissues and its pattern of secondary growth are very similar to those of angiosperms. The most conspicuous similarity lies in that the xylem contains vessels and the phloem, sieve elements and “companion ceils”. In climbing species of G. montanum, secondary growth initiates in s normal manner which is followed by the development of new combium at various loci among the parenehyms cells towards the periphery of each bundle. It does not initiate from the phloem parenchyma which is in agreement with the findings of Pearson (1929) and Maheshwari etc. (1961). Gradually these loci become incorporated into a continuous cylinder, producing a normally oriented ring of xylem and phloem separated by broad medullary rays. The growth of the first ring ceases at the commencement of the further formation of the outer, successive rings.     

The evolution of double fertilization and endosperm: an ”historical” perspective

 One hundred years ago, the developmental origin of endosperm from double fertilization was discovered independently by Navashin and Guignard. For much of the twentieth century, specific events related to the evolutionary origin of the endosperm of flowering plants remained a mystery. However, during the past 20 years, advances in phylogenetic reconstruction of seed plants, genetic theory associated with kin selection, and comparative study of the reproductive biology of the closest living relatives of angiosperms (Gnetales) have advanced our understanding of the evolutionary events associated with the origin of double fertilization and endosperm. Recent developmental analyses of Ephedra and Gnetum (members of Gnetales) indicate that these nonflowering seed plants undergo a regular process of double fertilization that yields two diploid zygotes. Use of explicit genetic and developmental criteria for analysis of evolutionary homology demonstrates congruence with the hypothesis that double fertilization processes in Gnetales and angiosperms were inherited from a common ancestor of the two lineages. In its rudimentary form, the second fertilization event in the ancestors of flowering plants yielded a supernumerary diploid embryo that was genetically identical to the normal embryo, a process most similar to what occurs in extant Ephedra. Subsequent to the divergence of the angiosperm stem lineage, the supernumerary embryo derived from double fertilization was developmentally modified into an embryo-nourishing structure, endosperm, that now characterizes angiosperms. Received: 25 September 1997 / Accepted: 3 November 1997     

The mycorrhizal status of Welwitschia mirabilis

This is the first report of the mycorrhizal status of Welwitschia mirabilis, a gymnosperm endemic to the Namib Desert. Like all other gymnosperms except the Pinaceae and Gnetaceae, W. mirabilis is associated with vesicular-arbuscular mycorrhizal (VAM) fungi. Mycorrhizal colonization of roots and the diversity and abundance of VAM species were determined at seven sites. Six sites received annual rainfall of 0–100 mm, varying widely from year to year. The seventh site experienced more predictable annual rainfall of 150–200 mm. Perennial vegetation was sparse at the six low-rainfall sites. Dry annual grasses from previous rain events were present at only three of these six sites and mean mycorrhizal colonization levels of W. mirabilis at these three sites were as high as 18%. W. mirabilis was not mycorrhizal at sites where grasses were absent. The seventh site, receiving higher rainfall, supported small trees and annual grasses in addition to W. mirabilis. Mycorrhizal colonization levels of W. mirabilis at this site were significantly higher than at the other six sites, closely paralleling those of the surrounding annual grasses. The mycorrhizal flora of W. mirabilis consisted of four Glomus species. These taxa were not unique to W. mirabilis, having been found with Stipagrostis and Cladoraphis grasses throughout the Namib and Kalahari deserts.     

Wood and bark anatomy of lianoid Indomalesian and Asiatic species of Gnetum

Quantitative and qualitative data on wood and bark are offered for 11 species of lianoid Indomalesian and Asiatic species of Gnetum section Cylindrostachys. Material of roots was studied for two species, material of an underground stem for one species, and stem material was studied for all species; wood from inside and outside of a large stem of G. montanum was analysed (quantitative data do not change with age in this species). Roots have shorter, narrower vessel elements, more numerous per mm², compared with those of stems; these trends run counter to those in dicotyledons. Roots and underground stems have more abundant parenchyma and less abundant sclerenchyma than do stems. Parenchyma of both roots and stems is rich in starch. All of the species studied here have both fibre-tracheids and tracheids, but tracheids are not distributed vasicentrically as they are in dicotyledons. Tori are reported for tracheary elements of three species studied here. Vasicentric axial parenchyma (which usually is thick-walled) is present in all species; thick or thin-walled diffuse or diffuse-in-aggregates apotracheal parenchyma is present in almost all of the species studied. Rays are mostly dimorphic in size, but show various conditions with respect to wall thickness, sclerenchyma presence, and crystal presence. As in other lianoid species of Gnetum, the species of the present study show origin of lateral meristem activity in parenchyma of the innermost cortex. Cortex and bark of the species studied here are relatively uniform in distribution of gelatinous fibres, nests of sclereids, the cylinder of brachysclereids that extends around the stem, and sclerenchymatous phelloderm. Laticifers were observed in bark of only two species studied. Although a few species characters are evident, the species that comprise Section cylindrostachys differ from each other mostly in degree rather than in presence or absence character state distributions. Secretory cavities are newly reported for the genus.     

麻黄属种子表面纹饰的多样性及其系统学意义

麻黄属(Ephedra)的分子系统学研究结果明显不同于基于雌球果成熟苞片质地的传统分类,指出麻黄属的形态特征和分子特征存在冲突。对麻黄属53种植物的种子表面微形态特征进行了研究,结果表明麻黄属的种子表面纹饰包括3种主要类型,即横向片层型(T型)、乳突型(P型)和扁平型(S型)。麻黄属的种子表面纹饰特征既与宏观形态特征不相关,也与分子系统学的研究结果不相关,表明该属微形态特征、宏观形态特征和分子特征之间的更多冲突。在欧洲和东亚发现的与买麻藤类有关的几个大化石带有T型种子表面纹饰,暗示具有T型纹饰的麻黄类植物在早白垩纪就十分多样。     

Sequence Peculiarity of Gnetalean Legumin-Like Seed Storage Proteins

The development of seeds as a specialized organ for the nutrition, protection, and dispersal of the next generation was an important step in the evolution of land plants. Seed maturation is accompanied by massive synthesis of storage compounds such as proteins, starch, and lipids. To study the processes of seed storage protein evolution we have partially sequenced storage proteins from maturing seeds of representatives from the gymnosperm genera Gnetum, Ephedra, and Welwitschia—morphologically diverse and unusual taxa that are grouped in most formal systems into the common order Gnetales. Based on partial N-terminal amino acid sequences, oligonucleotide primers were derived and used for PCR amplification and cloning of the corresponding cDNAs. We also describe the structure of the nuclear gene for legumin of Welwitschia mirabilis. This first gnetalean nuclear gene structure contains introns in only two of the four conserved positions previously characterized in other spermatophyte legumin genes. The distinct phylogenetic status of the gnetalean taxa is also reflected in a sequence peculiarity of their legumin genes. A comparative analysis of exon/intron sequences leads to the hypothesis that legumin genes from Gnetales belong to a monophyletic evolutionary branch clearly distinct from that of legumin genes of extant Ginkgoales and Coniferales as well as from all angiosperms. Received: 5 June 1997 / Accepted: 31 March 1998