A new genus of Canuellidae (Copepoda, Harpacticoida) associated with Atlantic bathyal sea-urchins

Both sexes of Echinosunaristes bathyalis gen. ct sp. n. are described from the rectum of a deepwater spatangoid sea-urchin Palaeopneustes sp. taken off San Salvador Island, Bahamas. The new genus displays strong sexual dimorphism in body form, size, antennules and caudal rami. E. bathyalis can also be readily distinguished from the other members of the family by the specialized geniculation mechanism of the male antennule, the atypical reductions in the mouthparts and the unusual facies of the swimming legs. On the basis of the structure of the genital field in both sexes, Echinosunaristes is placed in the Sunaristes lineage which groups species that arc primarily associated with crustacean hosts. A ncw genus Intersunaristes is established to accommodate Sunaristes curticaudata Thompson & A. Scott, 1903 and S. dardani Humes & Ho, 1969. Canuella paenelanitica Fiers, 1992 is formally transferred to the genus Elanella Por, 1984. Records of Canuellidae associated with other invertebrates arc compiled and a key to the 17 genera of the family is presented.     

Studies on the Cylindropsyllidae (Copepoda, Harpacticoida). 1. The status of Leptastacus laticaudatus Nicholls

Leptastacus laticaudatus Nicholls, 1935, commonly found interstitially in fine sands of European boreal waters, is redescribed and figured. As a result, the subspecies names L. laticaudatus laticaudatus and L. laticaudatus intermedius Kunz, 1938 are nullified. Some variable characters, i.e. caudal rami and structure of the fifth leg, are discussed and the distribution of the species is summarized. The most closely allied species L. macronyx (T. Scott, 1892) and L. spatuliseta Mielke, 1982 constitute, together with L. laticaudatus , the 'macronyx -group'. L. laticaudatus intermedius sensu Apostolov, 1973 is considered species inquirenda . An amended diagnosis of the genus Leptastacus T. Scott, 1906 is presented.     

A new species of the marattialean fern Scolecopteris (Zenker) Millay from the uppermost Permian of Guizhou Province, south-western China

Several isolated marattialean synangia and sporangia are reported from coal balls collected from Coal Seam No.1 (C605) in the uppermost Permian Wangjiazhai Formation in Guizhou Province, south-western China. The synangia are radially symmetrical with diameters between 0.8 and 1.2 mm and are 1.7 mm long, consisting of 3–4 elongate sporangia that are fused basally, free distally and possess a pointed apex. The outer-facing sporangial wall is 4–5 cells thick and conspicuously differentiated. Spores are trilete, have a granular ornamentation and are nearly round equatorially with a diameter of 55–60 µm. Comparisons with other anatomically preserved Palaeozoic marattialean synangia from the Euramerican and Cathaysian floras permit their assignment to the genus of Scolecopteris (Zenker) Millay. In this species the thick, outer-facing sporangial walls and large trilete spores are features consistent with those of the Oliveri Group within Scolecopteris , a group that has previously been considered primitive within this genus. Distinctions from all other previously recognized species within the Oliveri Group lead to the creation of a new species, S. guizhouensis sp. nov. This species is the youngest of the reported species of Scolecopteris recognized from the Euramerican and Cathaysian floras, and provides important evidence on the organization of marattialean ferns from the Upper Permian strata of south China.  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 151 , 279–288.     

Towards a revision of Ameira Boeck, 1865 (Harpacticoida, Ameiridae): reinstatement of Psammameira Noodt, 1952

Both sexes of Ameira hyalina (Noodt, 1952) and A. parasimulans Lang, 1965 are redescribed. The genus Psammameira Noodt, 1952 previously regarded as a junior subjective synonym of Ameira. is reinstated to accommodate these two species and a revised diagnosis for the genus is presented. Examination of the type material of Psammameira reducta Wells, 1967 and P. gradis (Nicholls, 1939) revealed that they should be removed from the genus. The possible relationships of two species of doubtful affinity, A. esigun T. Scott, 1894 and A. simulans T. Scott, 1912 are reconsidered. The phylogenetic position of Psammameira within the Ameiridae is briefly discussed.     

Comparative floral structure and systematics in Crossosomatales (Crossosomataceae, Stachyuraceae, Staphyleaceae, Aphloiaceae, Geissolomataceae, Ixerbaceae, Strasburgeriaceae)

Floral structure of all putative families of Crossosomatales as suggested by molecular studies was comparatively studied. The seven comprise Crossosomataceae, Stachyuraceae, Staphyleaceae, Aphloiaceae, Geissolomataceae, Ixerbaceae, and Strasburgeriaceae. The entire clade (1) is highly supported by floral structure, also the clades (in sequence of diminishing structural support): Ixerbaceae/Strasburgeriaceae (2), Geissolomataceae/Ixerbaceae/Strasburgeriaceae (3), Aphloiaceae/Geissolomataceae/Ixerbaceae/Strasburgeriaceae (4), and Crossosomataceae/Stachyuraceae/Staphyleaceae (5). Among the prominent floral features of Crossosomatales (1) are solitary flowers, presence of a floral cup, imbricate sepals with outermost smaller than inner, pollen grains with horizontally extended endoapertures, shortly stalked gynoecium, postgenitally united carpel tips forming a compitum, stigmatic papillae two‐ or more‐cellular, ovary locules tapering upwards, long integuments forming zigzag micropyles, cell clusters with bundles of long yellow crystals, mucilage cells, seeds with smooth, sclerified testa and without a differentiated tegmen. Clade (2) is characterized by large flowers, petals forming a tight, pointed cone in bud, stamens with long, stout filaments and sagittate anthers, streamlined, conical gynoecium, antitropous ovules, rudimentary aril, lignified, unicellular, T‐shaped hairs and idioblasts with striate mucilaginous cell walls. Clade (3) is characterized by alternisepalous carpels, punctiform stigma formed by postgenitally united and twisted carpel tips, synascidiate ovary, only one or two pendant ovules per carpel, nectary recesses between androecium and gynoecium. Clade (4) is characterized by pronounced ‘pollen buds’. Clade (5) is characterized by polygamous or functionally unisexual flowers, x‐shaped anthers, free and follicular carpels (not in Stachyuraceae). Crossosomataceae and Aphloiaceae, although not retrieved as a clade in molecular studies, share several special floral features: polystemonous androecium; basifixed anthers without a connective protrusion; stigma with two more or less decurrent crests; camplyotropous ovules and reniform seeds; simple, disc‐shaped nectaries and absence of hairs. © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society, 2005, 147 , 1–46.     

Comparative floral structure and systematics in Celastrales (Celastraceae, Parnassiaceae, Lepidobotryaceae)

Floral morphology, anatomy and histology in the newly circumscribed order Celastrales, comprising Celastraceae, Parnassiaceae and Lepidobotryaceae are studied comparatively. Several genera of Celastraceae and Lepidobotrys (Lepidobotryaceae) were studied for the first time in this respect. Celastraceae are well supported as a group by floral structure (including genera that were in separate families in earlier classifications); they have dorsally bulged‐up locules (and thus apical septa) and contain oxalate druses in their floral tissues. The group of Celastraceae and Parnassiaceae is also well supported. They share completely syncarpous gynoecia with commissural stigmatic lobes (and strong concomitant development of the commissural vascular bundles but weak median carpel bundles), only weakly crassinucellar or incompletely tenuinucellar ovules with an endothelium, partly fringed sepals and petals, protandry in bisexual flowers combined with herkogamy by the movement of stamens and anther abscission, and stamens fused with the ovary. In contrast, Lepidobotryaceae are more distant from the other two families, sharing only a handful of features with Celastraceae (not Parnassiaceae), such as pseudohermaphroditic flowers, united stamen bases forming a collar around the gynoecium and seeds with a conspicuous aril. However, all three families together are also somewhat supported as a group and share petals that are not retarded in late floral bud development, 3‐carpellate gynoecia, ventral slits of carpels closed by long interlocking epidermal cells and pollen tube transmitting tissue encompassing several cell layers, both integuments usually more than two cell layers thick, and only weak or lacking floral indumentum. In some molecular analyses Celastrales form an unsupported clade with Malpighiales and Oxalidales. This association is supported by floral structure, especially between Celastrales and Malpighiales. Among Celastrales, Lepidobotryaceae especially share special features with Malpighiales, including a diplostemonous androecium with ten fertile stamens, epitropous ovules with an obturator and strong vascularization around the chalaza. © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society, 2005, 149 , 129–194.     

Khaosokia caricoides, a new genus and species of Cyperaceae from Thailand

Khaosokia caricoides , D.A. Simpson, Chayam. & J. Parn., a newly discovered genus and species of Cyperaceae is described and illustrated. The genus is characterized by a narrowly paniculate dioecious inflorescence with 2–4 nodes, each of the nodes having a leaf-like inflorescence bract that exceeds the inflorescence. Spikelets in both sexes are linear-cylindric and each flower has seven perianth bristles. The nutlet was immature in the specimens examined. The photosynthetic pathway is C₃. Khaosokia is endemic to limestone cliffs in peninsular Thailand; its conservation status is assessed as Vulnerable (VU B1a + 2a). It has affinities to tribes Cariceae, Dulichieae and some members of Scirpeae, but the exact nature of these relationships has yet to be determined. A revised key to the genera of Cyperaceae in Thailand is presented.  © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society , 2005, 149 , 357–364.     

A summary of fossil records for Arecaceae

Of all monocotyledons the Arecaceae displays by far the richest fossil record, and there is an extensive literature. The earliest unequivocal fossil palm material probably dates from the early to mid Late Cretaceous (Turonian > Coniacian > Santonian). The records are geographically widespread and comprise a wide range of organs: leaves, cuticles, stems, rhizomes, roots, fruits, seeds, endocarps, rachillae, peduncles, inflorescences, individual flowers and pollen. For some of these organs records are rare while for others, such as leaves, stems and pollen, records are abundant. However, fossil material often lacks sufficient diagnostic detail to allow reasonable association with living palm taxa beyond, or even to, subfamilial level. Nevertheless, many fossil genera and numerous species have been described. A brief survey of palm fossil records is presented, and their taxonomy and morphological limitations are considered. © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 151 , 39–67.