云南省悠背蚱属二新种记述（直翅目：蚱科）

记述采自云南省横断山地区悠背蚱属2新种,即毛股悠背蚱Euparatettix barbifemura sp．nov．及景东悠背蚱Euparatettix jingdongensis sp．nov．,模式标本保存于西南林学院昆虫标本室。     

广西北部湾地区蚱科二新种记述(直翅目,蚱总科)

记述采自广西北部湾地区蚱总科昆虫2新种,即圆肩悠背蚱Euparatettix circinihumerus sp.nov.,桂南悠背蚱Euparatettix guinanensis sp.nov.。模式标本保存在陕西师范大学动物研究所昆明标本室。     

广西南部地区蚱总科一新属和七新种

记述采自广西南部地区蚱总科一新属七新种,即横刺郑蚱Zhengitettix transpicula sp.nov.,拟奇蚱属Miriatroides gen.nov.,方顶拟奇蚱Miriatroides quadrivertex sp.nov., 长背蟾蚱Hyboella longinota sp.nov.,二瓣庭蚱Hedotettix bivalvatus sp.nov.,防城柯蚱Coptotettix fangchengensis sp.nov.,桂南蚱Tetrix guinanensis sp.nov.,波股悠背蚱Euparatettix sinufemoralis sp.nov。模式标本保存于陕西师范大学动物研究所标本室。     

云南省蚱科四新种记述(直翅目:蚱总科)

记述采自云南省西双版纳及大理苍山地区蚱科4新种,即狭顶庭蚱Hedotettix strictivertex sp.nov.,版纳柯蚱Coptotettix bannaensis sp.nov.,长翅蚱Tetrix longipennis sp.nov.及勐仑悠背蚱Euparatettix menlunensis sp.nov.。模式标本保存于陕西师范大学动物研究所昆虫标本室。     

中国悠背蚱属的分类研究及二新种记述(直翅目,蚱科)

记述中国悠背蚱属56种,内有2新种,即察隅悠背蚱Euparatettix zayuensis sp.nov.及景洪悠背蚱Euparatettix jinghongensis sp.nov.。附有中国悠背蚱属分种检索表和分布。模式标本保存于陕西师范大学动物研究所。     

广西北部地区蚱总科七新种记述(直翅目)

记述采自广西北部蚱总科昆虫7新种,即黑股羊角蚱Criotettix nigrifemurus,sp．nov．,横刺羊角蚱Criotettix transpinius,sp．nov．,拟圆头波蚱Bolivaritettix circocephalosoides．sp．nov．,宜州蚱Tetrix yizhouensis,sp．nov．,丘背蚱Tetrix cliva,sp．nov．,白条悠背蚱Euparatettix albostriatus,sp．nov．及九万山悠背蚱Euparatettix jiuwanshanensis,sp．nov．。模式标本保存于陕西师范大学动物研究所昆虫标本室。     

西藏地区蚱总科三新种及西藏拟科蚱雄性的发现（直翅目）

记述采自西藏墨脱地区的蚱总科3新种,即弧肩波蚱Bolivaritettix arcihumerus sp.nov.,短角蚱Tetrix brevicornis sp.nov.及墨脱悠背蚱Euparatettix motuoensis sp.nov.。同时报道西藏拟科蚱Cotysoidestibetanus(Zheng)雄性新发现。     

云南省西南部蚱科的新种(直翅目)

记述云南省西南部蚱科7新种,即云南夏蚱Xiaitettix yunnanensis Zheng et Mao,sp.nov.、粗角版纳蚱Bannatettix oedicerus Zheng et Xu,sp.nov.、断隆蚱Tetrix interrupta Zheng et Xu,sp.nov.、五老山台蚱Formosatettix wulaoshanensis Zheng et Xu,sp.nov.、宽顶突眼蚱Ergatettix lativertex Zheng et Xu,sp.nov.、孟连悠背蚱Euparatettix menglianensis Zheng et Xu,sp.nov.及白斑悠背蚱Euparatettix albomaculatus Zheng et Xu,sp.nov.。模式标本保存于陕西师范大学动物研究所昆虫标本室。     

滇西横断山地区台蚱属三新种(直翅目,蚱科)

记述云南省西部横断山地区台蚱属3新种,即香格里拉台蚱Formosatettix xianggelila sp.nov.,凹缘台蚱Formosatettix camurimargina sp.nov.及无量山台蚱Formosatettix wuliangshanensia sp.nov..此外还记载因异物同名而改名的拟双背蚱属Paramphinotus.模式标本保存于西南林学院昆虫标本室.     

广西大瑶山地区蚱总科六新种记述(直翅目)

记述扁角蚱科及短翼蚱科昆虫6新种及1种雄性新发现,即齿股扁角蚱Flatocerus dentifemura sp.nov.,钩顶棒蚱Rhopalotettix uncusivertex sp.nov.,金秀玛蚱Mazarredia jinxiuensis sp.nov.,断隆玛蚱Mazarredia interrupta sp.nov.,短背波蚱Bolivaritettix brachynotus sp.nov.,圆肩波蚱Bolivaritettix circinihumerus sp.nov.及湖南希蚱Xistrella hunanensis Wang雄性新发现。模式标本保存于中国科学院动物研究所。     

Importance of biological and abiotic factors for geochemical cycling in a freshwater eutrophic lake

Here we report the results of a comprehensive biogeochemical monitoring of Rostherne Mere in 1998, including changes in dissolved oxygen, organic carbon and nitrogen, nitrate/nitrite, ammonia, Al, Na, S, K, Mg, Ca, Si, Fe, Mn, orthophosphate, particulate N & P, suspended solids, temperature, pH, chlorophyll-a and zooplankton. The results demonstrated the major influence of primary producers on the overall geochemical cycling of N, P and Si, and suggested that the significance of zooplankton might have been previously underestimated. For major anions and cations, however, the influence of biota on lake water concentrations appeared to be negligible, reflecting the fact that these chemicals were present far in excess of plankton requirements. Thus changes in concentrations of Ca, K, Na, Mg and S were rather limited and must have reflected changes in hydrological and meteorological parameters. K, however, demonstrated a transitional pattern, reflecting some influence of biological uptake. During the stratification period, the slow processes of bacterial decomposition in the hypolimnion gradually released chemicals contained in the materials accumulated in the bottom layer, remarkably increasing the concentrations of dissolved compounds of those elements present in amounts comparable with the pool stored in the sedimenting detritus (e.g. orthophosphate P, ammonia N, Si and DOC). The decomposition also resulted in a drop in the redox potential, followed by partial denitrification and chemical release from the sediments. The hypolimnion of the Mere was confirmed to remain at the stage of Mn release, characterised by accumulation of DOC, orthophosphates, ammonia and initial stages of denitrification. High levels of P released from the sediments during the stratification period suggest that the lake’s recovery after sewage diversion might be further delayed.     

派伦螨属1新种和革板螨属1新种及都匀革板螨雄螨描述(蜱螨亚纲:中气门目:派盾螨科)

记述派伦螨属1新种:遵义派伦螨Parholaspulus zunyiensis sp.nov.和革板螨属1新种:江西革板螨Gamasholaspis jiangxiensissp.nov.,并描述都匀革板螨Gamasholaspis duyunensis Chen,Guo et Gu,1994雄螨.     

Seed-coat anatomy in Fumariaceae-Fumarioideae

Seed-coat anatomy is described in 122 species of Fumarioideae, which represent all the genera, subgenera, and most sections. Nine seed-coat types were recognized: (I) Dicentra subg. Hedycapnos , (II) Dicentra subg. Chrysocapnos , (III) Dicentra subg. Macranthos , (IV) Dicentra subg. Dicentra , (V) Corydalis p.p. , (VI) rest of Corydaleae, Cysticapnos, Pseudofumaria and Ceratocapnos , (VII) Discocapnos and Sarcocapnos p. p. , (VIII) Sarcocapnos p. p., Platycapnos and Trigonocapnos , and (IX) Fumariinae. Variable characters are polarized based on the comparison with Fumariaceae Hypecooideae, Papaveraceae and Pteridophyllaceae. It is assumed that endotestal seed-coat type (I) is most primitive, that exotestal seed coat types (II—VIII) are derived therefrom, and that the reduction of the mechanical layer, including the origin of thin seed-coat type (IX) occurred repeatedly in combination with indehiscent, hard-walled fruits. Dicentra subg. Hedycapnos (with type I) possesses a combination of primitive testal characters unique within the subfamily, suggesting it represents a sister group to the rest of the subfamily. Each of the other subgenera (with II, III or IV) is also characterized by a unique combination of seed-coat characters, which are found in the outgroups but not in the other genera. Seed-coat characters support the monophyly of Fumarioideae exclusive of Dicentra subg. Hedycapnos , Fumarioideae exclusive of Dicentra , of Dicentra subg. Dicentra , of Corydalis p.p. , and of Fumariinae.     

Embryology of Swertia (Gentianaceae) relative to taxonomy

The embryological features of three species of Swertia ( s.l.) – S. erythrosticta , S. franchetiana , and S. tetraptera – were characterized, and the observations were used, together with previously gathered data on other species, to evaluate a recently proposed polyphyly, based on molecular data, of Swertia s.l. Comparisons of species within the genus showed that they have diversified embryologically, and there are significant between-species differences. Notable features that vary between species include the number of cell layers that form the anther locule wall, the construction of the wall of the mature anther, tapetum origin, the cell number in mature pollen grains, the structure of the fused margins of the two carpels, the ovule numbers in placental cross-sections, the shape of the mature embryo sac, the degree of ovule curvature, antipodal variation and the presence of a hypostase, and seed appendages. They share characters that are widely distributed in the tribe Gentianeae, such as a dicotyledonous type of anther wall formation, a glandular tapetum with uninucleate cells, simultaneous cytokinesis following the meiosis of the microsporocytes, tetrahedral microspore tetrads, superior, bicarpellary and unilocular ovaries, unitegmic and tenuinucellar ovules, Polygonum -type megagametophytes, progamous fertilization, nuclear endosperm, and Solanad-type embryogeny. The presence of variation in embryological characters amongst the species of Swertia s.l. strongly supports the view that Swertia s.l. is not a monophyletic group. Frasera is better separated from Swertia s.l. as an independent genus, and is only distantly related to Swertia s.s. judging from the numerous differences in embryology. Swertia tetraptera is very closely related to Halenia , as they show identical embryology.  © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society , 2007, 155 , 383–400.     

A review of studies on Pichavaram mangrove, southeast India

We studied a tropical mangrove ecosystem, situated at Pichavaram, southeast India. We found 13 species of mangrove trees, with Avicennia marinaand Rhizophora species predominant, besides 73 spp. of other plants, 52 spp. of bacteria, 23 spp. of fungi, 82 spp. of phytoplankton, 22 spp. of seaweeds, 3 spp. of seagrass, 95 spp. of zooplankton, 40 spp. of meiobenthos, 52 spp. of macrobenthos, 177 spp. of fish and 200 spp. of birds. The bacteria performed activities like photosynthesis, methanogenesis, magnetic behaviour, human pathogens and production of antibiotics and enzymes (arysulphatase, L-glutaminase, chitinase, L-asparaginase, cellulase, protease, phosphatase). The microzooplankton included tintinnids, rotifers, nauplius stages of copepods and veliger larvae of molluscs, with a predominance of tintinnids. Tintinopsis spp. alone accounted for 90% of abundance. The macrozooplankton consisted of 95% of copepods and coelenterates. The meiofauna was rich with nematodes (50–70% of the component), followed by foramifera. The macrofauna included polychaetes, bivalves, gastropods, tanaids, isopods, amphipods, cirripedes, crabs, hermit crabs and shrimps. The mangrove harboured a large number of juvenile fishes, especially during summer and post-monsoon. The water was fertile and productive in having several fold-higher levels of nutrients, microbes, plankton and other biological resources, than the adjoining estuarine, backwater and neritic environments. The gross primary production was 8 g cm^-3 d^-1; about 21% of which was contributed by phytoplankton of 5–10 m size. Unfortunately, 90% of the mangrove cover in the study area was degraded. Possible factors that cause degradation of the ecosystem are detailed and remedial measures suggested. Techniques for regeneration of the degraded areas are proposed.     

Early Cretaceous Palynofloras from Tarim Basin,Xinjiang

One hundred and eight species of fossil spores and pollen referred to 55 genera found from the Lower Cretaceous Kapushaliang (Kizilsu) Group in the Tarim Basin of Xinjiang have been studied in this paper. The Kapushaliang Group may be divided into the Yageliemu Formation, the Shushanhe Formation and Baxigai Formation in ascending order. The Yageliemu palynoflora is characterized by the predominance of gymnospermous pollen, the relative abundance of pteridophytic spores and the absence of angiospermous pollen. Coniferae is dominant, while Lygodiaceae and Schizaeaceae are important in the flora. The most common species of palynomorphs are Todisporites minor, Cicatricosisporites dorogensis, C. australiensis, Lygodiumsporites subsimplex, Schizaeoisporites cretacius, S. zizyphinus, S. certus. Cibotiumspora paradoxa, Cyathidites australis, C. minor, Biretisporites potoniael, Cycadopites minimus, Pseudowalchia hiangulina, Parvisaccites radiatus, Podocarpidites multesimus, P. canadensis, Alisporites bilateralis, Cedripites cretaceus, C. canadenris, Abietineaepollenites microalatus, Clarsopollis classoides, C annulatus, C. xinjiangensis (sp. nov.), Ephedripites multicostatus, E. tarimensis (sp. nov.), etc . The palynoflora is comparable with those of the lower part of the Lower Xinminbu Formation in northwestern China and the lower part of the Lower Mannville Formation in western Canada, which is considered corresponding from Berriasian to Valanginian in age. The Shushanhe palynoflora is also characterized by dominance of gymnosperms and subdominance of pteridophyta. Some primitive angiospermons pollen grains are found in the upper part of the formation. In addition to the most common species of the above mentioned palynoflora, the important species in the present palynoflora comprise Cicatricosisporites potomacensis, C. orbiculatus, C. subrotundus, Concavissimisporites punctatus, C. verrucosus, C. globosus, lmpardecispora apiverrucata, Trilobosporites crassus, T. trioreticulosus, Pilosisporites verus, P. trichopapillosus, Klukisporites pseudoreticulatus, Verrucosisporites obscurilaesuratur, Converrucosisporites saskatchewanensis, Foraminisporis wonthaggiensis, Cingulatisporites valdensis, C. ruginosus, Jiaohepollis verus, Pityosporites constrictus, etc. More than 40 in dicative species of Early Cretaceous occur in the assemblage. The palynoflora compares clcsely with those of the middle part of the Lower Xinminbu Formation and the Quartz Sand Member of the Lower Mannville Formatton. It is suggested that the Shushanhe Formation should belong to Hauterivian of Barremian in age. The Baxigai palynoflora is basically similar to the Shushanhe palynoflora. But the palynoflora shows an obvious increase in abundance of lygodiaceous spores and angiospermous pollen accompanied by a great reduction of Classopollis and Ephedripltes. Most of the Early Cretaceous species occurring in the above mentioned palynofloras are present. In addition, some Cretaceous species recorded from Aptian and Albian Stages in Europe, North America and Australia, such as Trilobosporites tribotrys, T. trioreticulosus, Coptospora paradoxa, Camarozonosporites insignis, Crybelosporites punctatus, etc., appear in the assemblage. In comparison with the microfloras of the upper part of the Lower Xinminbu Formation, the Upper Mannville Formation and the lower part of the Lower Colorado Group, the Baxigai Forma- tion should be referred to Aptian to Albian in age. Judging from the palynofloras, the early Cretaceous palaeoclimate in the basin should belong to the arid or semi-arid type of the subtropic zone. However, from Barremtan through Albian the climatic conditions might appear relatively wet.     

Identification of asymmetrically winged samaras from the Western Hemisphere

A key is presented for use in identifying asymmetrically winged fruits (samaras) with either proximal or distal locules. It aids identification based on dispersed fuit morphology and can be used to identify undetermined extant herbarium specimens or fossil fruits to the correct extant family and genus. The 39 genera from 11 families (Aceraceae, Anacardiaceae, Fabaceae, Malpighiaceae, Phytolaccaceae, Polygalaceae, Polygonaceae, Rutaceae, Sapindaceae, Trigoniaceae, Ulmaceae) are distinguished on the basis of wing venation, size of fruit, presence and position of attachment surface, presence and type of subsidiary wings on the ovary wall. ornamentation, size and shape of the ovary, locule position, shape of locule cross section, style position and ornamentation, distinction between ovary wall and wing, and angle of attachment between individual samaras. The developmental origins of some of these features are discussed.     

Concentration of 17 trace elements in serum and whole blood of plains viscachas (Lagostomus maximus) by ICP-MS, their reference ranges, and their relation to cataract

The reference ranges of the trace elements Al, As, Be, B, Cd, Co, Cu, Fe, Mn, Mo, Ni, Pb, Li, Rb, Se, Sr, and Zn were determined by inductively coupled plasma-mass spectrometry (ICP-MS) in sera of a group of free-ranging plains viscachas of the pampa grasslands of Argentina. The values were compared with those of a small group of captive plains viscachas of the Zurich Zoo with diabetes and bilateral cataracts. In addition, a method for digestion of whole-blood samples is described for the trace element determination. Significant differences in the concentration of trace elements in the two groups of animals are discussed. No correlation was found between the levels of selenium and of other trace elements compared to the formation of cataracts.     

Origin,Differentiation, and Geographic Distribution of the Chenopodiaceae

Numbers of species and genera,endemic genera,extant primitive genera,relationship and distribution patterns of presently living Chenopodiaceae(two subfamilies,12 tribes,and 118 genera)are analyzed and compared for eight distributional areas,namely central Asia,Europe,the Mediterranean region,Africa,North America,South America, Australia and East Asia． The Central Asia,where the number of genera and diversity of taxa are greater than in other areas,appears to be the center of distribution of extant Chenopodiaceae．North America and Australia are two secondary centers of distribution． Eurasia has 11 tribes out of the 12,a total of 70 genera of extant chenopodiaceous plants,and it contains the most primitive genera of every tribe． Archiatriplex of Atripliceae,Hablitzia of Hablitzeae,Corispermum of Corispermeae,Camphorosma of Camphorosmaea,Kalidium of Salicornieae,Polecnemum of Polycnemeae,Alexandra of Suaedeae,and Nanophyton of Salsoleae,are all found in Eurasia,The Beteae is an Eurasian endemic tribe,demonstrating the antiquity of the Chenopodiaceae flora of Eurasia．Hence,Eurasia is likely the place of origin of chenopodiaceous plants． The presence of chenopodiaceous plants is correlated with an arid climate．During the Cretaceous Period,most places of the continent of Eurasia were occupied by the ancient precursor to the Mediterranean,the Tethys Sea．At that time the area of the Tethys Sea had a dry and warm climate．Therefore,primitive Chenopodiaceae were likely present on the beaches of this ancient land．This arid climatic condition resulted in differentiation of the tribes Chenopodieae,Atripliceae,Comphorosmeae,Salicornieae,etc．,the main primitive tribes of the subfamily Cyclolobeae. Then following continental drift and the Laurasian and Gondwanan disintegration, the Chenopodiaceae were brought to every continent to propagate and develop, and experience the vicissitudes of climates, forming the main characteristics and distribution patterns of recent continental floras. The tribes Atripliceae, Chenopodieae, Camphorosmeae, and Salicornieae of recent Chenopodiaceae in Eurasia, North America, South America, southern Africa, and Australia all became strongly differentiated. However, Australia and South America, have no genera of Spirolobeae except for a few maritime Suaeda species. The Salsoleae and Suaedeae have not arrived in Australia and South America, which indicates that the subfamily Spirolobeae developed in Eurasia after Australia separated from the ancient South America-Africa continent, and South America had left Africa. The endemic tribe of North America, the tribe Sarcobateae, has a origin different from the tribes Salsoleae and Suaedeae of the subfamily Spirolobeae. Sarcobateae flowers diverged into unisexuality and absence of bractlets. Clearly they originated in North America after North America had left the Eurasian continent. North America and southern Africa have a few species of Salsola, but none of them have become very much differentiated or developed, so they must have arrived through overland migration across ancient continental connections. India has no southern African Chenopodiaceae floristic components except for a few maritime taxa, which shows that when the Indian subcontinent left Africa in the Triassic period, the Chenopodiaceae had not yet developed in Africa. Therefore, the early Cretaceous Period about 120 million years ago, when the ancient Gondwanan and Laurasian continents disintegrated, could have been the time of origin of Chenopodiaceae plants.The Chinese flora of Chenopodiaceae is a part of Chenopodiaceae flora of central Asia. Cornulaca alaschnica was discovered from Gansu, China, showing that the Chinese Chenopodiaceae flora certainly has contact with the Mediterranean Chenopodiaceae flora. The contact of southeastern China with the Australia Chenopodiaceae flora, however, is very weak.     

Molecular phylogeny of the gobioid fishes (Teleostei: Perciformes: Gobioidei)

The phylogeny of groups within Gobioidei is examined with molecular sequence data. Gobioidei is a speciose, morphologically diverse group of teleost fishes, most of which are small, benthic, and marine. Efforts to hypothesize relationships among the gobioid groups have been hampered by the prevalence of reductive evolution among goby species; such reduction can make identification of informative morphological characters particularly difficult. Gobies have been variously grouped into two to nine families, several with included subfamilies, but most existing taxonomies are not phylogenetic and few cladistic hypotheses of relationships among goby groups have been advanced. In this study, representatives of eight of the nine gobioid familes (Eleotridae, Odontobutidae, Xenisthmidae, Gobiidae, Kraemeriidae, Schindleriidae, Microdesmidae, and Ptereleotridae), selected to sample broadly from the range of goby diversity, were examined. Complete sequence from the mitochondrial ND1, ND2, and COI genes (3573 bp) was used in a cladistic parsimony analysis to hypothesize relationships among the gobioid groups. A single most parsimonious topology was obtained, with decay indices indicating strong support for most nodes. Major phylogenetic conclusions include that Xenisthmidae is part of Eleotridae, and Eleotridae is paraphyletic with respect to a clade composed of Gobiidae, Microdesmidae, Ptereleotridae, Kraemeriidae, and Schindleriidae. Within this five-family clade, two clades are recovered. One includes Gobionellinae, which is paraphyletic with respect to Kraemeriidae, Sicydiinae, Oxudercinae, and Amblyopinae. The other contains Gobiinae, also paraphyletic, and including Microdesmidae, Ptereleotridae, and Schindleriidae. Previous morphological evidence for goby groupings is discussed; the phylogenetic hypothesis indicates that the morphological reduction observed in many goby species has been derived several times independently.