Gynoecium and fruit histology and development in Eugeissona (Calamoideae: Arecaceae)

The Malesian genus Eugeissona, with six species, is sister to all other Calamoideae, which are in turn sister to all other Arecaceae. The structure of its gynoecium and fruit is thus potentially of great interest in understanding gynoecium evolution in calamoid palms and in Arecaceae as a whole. The wall of the incompletely trilocular gynoecium of Eugeissona is thick and differentiated into several topographic zones, with a well‐developed vascular system even before pollination. During gynoecium and fruit development, the outer and inner epidermises are little specialized and form the exocarp and endocarp (obliterated in the mature fruit), respectively. In contrast, the mesophyll of the carpels differentiates strongly and is markedly specialized: four massive topographic zones are easily distinguished within the mesocarp. The peripheral zone of the mesocarp forms the body of the scales (a synapomorphy for Calamoideae). The second and the fourth zones are multilayered and parenchymatous with a massive derived vascular system in the former. The third zone of the mesocarp comprises a stout sclerenchymatous pyrene, made of fibre‐like sclereids, the innermost bundles of the derived vascular system and dorsal, ventral and lateral vascular bundles. The fruits of all other Calamoideae lack the sclerenchymatous pyrene and thus differ dramatically from Eugeissona fruits. The similarity of the processes of histogenesis during gynoecium and fruit development in Eugeissona with those in Nypa and borassoid palms, suggests these features could be plesiomorphic for the family. © 2012 The Linnean Society of London, Botanical Journal of the Linnean Society, 2012, 168 , 377–394.     

Discovery of the Quedius antipodum Sharp larva from New Zealand: phylogenetic test of larval morphology for Staphylinini at the intratribal level (Coleoptera: Staphylinidae)

Quedius antipodum Sharp is an endemic species from New Zealand. Here we describe its larva, the first of the species‐rich group of the south temperate ‘Quedius’ spp. This finding throws light on the controversy between the conventional systematics of Quedius Stephens and newer phylogenetic analyses, both of which are based on non‐larval characters only. We compare the larva of Q. antipodum with those of the north temperate Quedius (Quediina), where it was traditionally placed, and with the known larvae of Amblyopinina, a group where Q. antipodum was placed by recent phylogenetic studies. Sister‐group relationships of Q. antipodum within the tribe Staphylinini are explored based on larvae by means of parsimony analysis: 77 morphological characters scored for 20 species from 17 genera. Consistent with the adult morphology and DNA sequences, larvae‐based cladistic analysis confirms that Q. antipodum should not be placed in the north temperate genus Quedius. However, larval analysis alone remains dubious with respect to finding the exact sister relationships of that species.     

Alesiella gen.n. and a newly discovered relict lineage of Staphylinini (Coleoptera: Staphylinidae)

This study aimed to identify the sister group of the poorly known and morphologically isolated Burmese species Quedius lineipennis within the tribe Staphylinini (Staphylinidae: Staphylininae) using morphological characters. Phylogenetic analysis of a broad taxon sample demonstrated that this Asian species is not a member of the genus Quedius but forms the sister taxon to the Neotropical genus Quediomacrus. Both taxa were shown to be members of a hitherto unrecognized lineage with a highly disjunct distribution. The lineage is hypothesized to be Asian in origin, with dispersals to the Americas during the early Eocene climatic maximum via Beringia and to Australia via land connections in the late Miocene. The current distribution of the lineage is considered to be relictual. New phylogenetic hypotheses within ‘Quediina’ and Staphylinini as a whole are proposed and the general tree topology of Staphylinini recovered by recent morphological studies is refined. Phylogenetic relationships within the Quedius complex remain unclear. Alesiella Brunke and Solodovnikov gen.n. , is erected for Quedius lineipennis and the Quedius subgenus Quedionuchus is reinstated to genus level with new combinations as follows: Quedionuchus atl (Smetana, 1975), comb.n. ; Quedionuchus calli (Smetana, 1976), comb.n. ; Quedionuchus cipactli (Smetana, 1976), comb.n. ; Quedionuchus coatl (Smetana, 1976), comb.n. ; Quedionuchus ehacatl (Smetana, 1976), comb.n. ; Quedionuchus ollin (Smetana, 1976), comb.n. ; Quedionuchus ozomatli (Smetana, 1975), comb.n. ; Quedionuchus reitterianus (Bernhauer, 1944), comb.n. ; Quedionuchus samuraicus (Bernhauer and Schubert, 1916), comb.n. ; Quedionuchus schultzei (Smetana, 1975), comb.n. ; Quedionuchus tecpatl (Smetana, 1976), comb.n. ; Quedionuchus xochitl (Smetana, 1976). Quedius lugubris Lokay, 1913 is transferred from the subgenus Quedionuchus to the subgenus Distichalius and placed in synonymy: Quedius punctatellus (Heer, 1839) = Quedius lugubris Lokay, 1913, syn.n . This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:9C7D3C90‐FCB9‐414F‐911B‐194A1A6602DE .     

Fruit structure of Amborella trichopoda (Amborellaceae)

The indehiscent fruitlets of the apparently basalmost extant angiosperm, Amborella trichopoda, have a pericarp that is differentiated into five zones, a thin one‐cell‐layered skin (exocarp), a thick fleshy zone of 25–35 cell layers (outer mesocarp), a thick, large‐celled sclerenchymatous zone (unlignified) of 6–18 cell layers (middle mesocarp), a single cell layer with thin‐walled (silicified?) cells (inner mesocarp), and a 2–4‐cell‐layered, small‐celled sclerenchymatous zone (unlignified) derived from the inner epidermis (endocarp). The border between inner and outer mesocarp is not even but the inner mesocarp forms a network of ridges and pits; the ridges support the vascular bundles, which are situated in the outer mesocarp. In accordance with previous observations by Bailey & Swamy, no ethereal oil cells were observed in the pericarp; however, lysigenous cavities as mentioned by these authors are also lacking; they seem to be an artefact caused by re‐expanding dried fruits. The seed coat is not sclerified. The fruitlets of Amborella differ from externally similar fruits or fruitlets in other basal angiosperms, such as Austrobaileyales or Laurales, in their histology. © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society, 2005, 148 , 265–274.     

A new genus of Staphylinidae (Coleoptera) from the Lower Cretaceous: the first fossil rove beetles from the Southern Hemisphere

The fossil genus of rove beetles Apticax gen.n . with two new species, A. volans sp.n . and A. solidus sp.n., is described from the Nova Olinda Member of the Crato Formation in north‐eastern Brazil (Aptian–Albian, dated as 125–99.6 Ma old). Both species belong to the clade Staphylininae + Paederinae in the staphylinine group of subfamilies and are the first fossil true Staphylinidae to be described from the entire Southern Hemisphere. Although they resemble Paederinae, the low number of satisfactorily preserved characters do not allow definite placement of either A. volans or A. solidus in any of the subfamilies of Staphylinidae.     

Structure, expression, and developmental function of early divergent forms of metalloproteinases in Hydra

Metalloproteinases have a critical role in a broad spectrum of cellular processes ranging from the breakdown of extracellular matrix to the processing of signal transduction-related proteins. These hydrolytic functions underlie a variety of mechanisms related to developmental processes as well as disease states. Structural analysis of metalloproteinases from both invertebrate and vertebrate species indicates that these enzymes are highly conserved and arose early during metazoan evolution. In this regard, studies from various laboratories have reported that a number of classes of metalloproteinases are found in hydra, a member of Cnidaria, the second oldest of existing animal phyla. These studies demonstrate that the hydra genome contains at least three classes of metalloproteinases to include members of the 1) astacin class, 2) matrix met-alloproteinase class, and 3) neprilysin class. Functional studies indicate that these metalloproteinases play diverse and important roles in hydra morphogenesis and ce     

Seed morphology and anatomy of Austrotaxus spicata (Taxaceae) and its systematic position

The anatomy and ultrastructure of seed envelopes of a New Caledonian endemic Austrotaxus spicata were examined for the first time. The systematic position and phylogenetic relations of Austrotaxus were analysed in light of these data. The structure of aril and spermoderm were investigated to demonstrate the similarities with Phyllocladus as well as with Taxus and Pseudotaxus . On the basis of all female reproductive organ characters, Austrotaxus appeared to be fairly isolated and its placing in the independent family Austrotaxaceae was confirmed from the standpoint of comparative anatomy of the seed coat. Taking into consideration that the heterobathmy of features can be the most distinctively traced in the structure of reproductive organs, evaluating the extent of evolutionary advancement of Austrotaxus seems to be rather difficult. However, it is evident that the relationship of Austrotaxus either with Taxaceae or with Podocarpaceae s.l . is considerably remote.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 145 , 437–443.     

Revised systematics and biogeography of ‘Quediina’ of sub‐Saharan Africa: new phylogenetic insights into the rove beetle tribe Staphylinini (Coleoptera: Staphylinidae)

Abstract Quediina, a mega‐diverse conventional subtribe of the rove beetle tribe Staphylinini, is remarkably species rich in the north and south temperate regions of the world. Tropical faunas of this group, and the fauna of the entire Afrotropical biogeographical region (= Ethiopian region, = sub‐Saharan Africa), in contrast, are remarkably poor. The taxonomic study of the quediine genera of Staphylinini from the Afrotropical region reveals misidentifications for many of them. Their phylogenetic study demonstrates polyphyly of Quediina and reveals a new evolutionary pattern for the entire tribe Staphylinini. In particular, the formerly quediine genera Euristus Fauvel, 1899 , Ioma Blackwelder, 1952, Natalignathus Solodovnikov, 2005 , all endemic in the Afrotropical region, belong to the non‐related ‘Staphylinina’, ‘Philonthina propria’ and ‘Tanygnathinina sensu novo’ lineages of Staphylinini, respectively. Contrary to earlier records, the genus Quedius Stephens, 1929 does not occur in Africa south of Sahara: Quedius angularis Cameron, 1948 and Quedius cinctipennis Cameron, 1951 are moved to the genus Philonthus Stephens, 1829. The same is established for the Asian genus Algon Sharp, 1874, formerly for a long time associated with Quediina: African species Algon robustus Wendeler, 1928 is moved to the genus Moeocerus Fauvel, 1899 (here in the ‘Philonthina propria’ lineage); and the misidentification of Algon africanus Bernhauer, 1915, a species that probably belongs to a new genus, is discussed. The phylogenetic affiliation of Afroquedius Solodovnikov, 2006 , a South African endemic, is still ambiguous. Overall, the formerly seen bipolar distribution pattern for the ‘Quediina’ is demonstrated to be an artefact, not a reality to explain. Historical biogeographical explanations are proposed for some of the Afrotropical endemics, partly as an attempt to apply biogeography as an external criterion for the evaluation of the new phylogenetic pattern revealed for Staphylinini. The monotypic genera Euristus and Ioma, as well as Heterothops megalops Cameron, 1959 , the only representative of this widespread genus in the Afrotropical region, are redescribed. Limits and synapomorphies of the genus Heterothops are discussed. The following new combinations and new names are proposed: Philonthus cinctipennis ( Cameron, 1951 ) comb.n. (preoccupied by Philonthus cinctipennis Fauvel, 1875), here replaced by Philonthus pseudoquedius Solodovnikov nom.n. ; Philonthus angularis ( Cameron, 1948 ) comb.n. ; Moeocerus robustus ( Wendeler, 1928 ) comb.n. [preoccupied by Moeocerus robustus (Gestro, 1881)], here replaced by Moeocerus wendeleri Solodovnikov nom.n. A lectotype is designated for Heterothops megalops Cameron, 1959 .