云南元谋小河地区古猿地点的小型猿类化石

本文记述的云南元谋小河地区古猿地点发现的一种小型猿类。它的牙齿形态比晚中新世的禄丰粗壮池猿进步。而牙齿的某些形态介于粗壮池猿和现生长臂猿之间,它的发现为探讨现生长臂猿的起源与进货提供了新的化石依据。依哺乳动物群的初步研究,其时代稍晚于禄丰古猿地点的时代。鉴于它的形态特征和地史分布,作者将它订为一新属新种：进步滇猿Ｄｉａｎｏ ｐｉｔｈｅｃｕｓ ｐｒｏｇｒｅｓｓｕｓ ｇｅｎ．ｅｔ ｓｐ．ｎｏｖ。     

Sarsicopia polaris gen. et sp.n., the first platycopioida (Copepoda: Crustacea) from the Arctic Ocean,and its phylogenetic significance

A new genus of Platycopioida is described from a boxcore sample taken at a depth of 534 m in the ArcticBarents Sea. This is the deepest record ofPlatycopioida so far. Sarsicopia gen. n. is thesistergroup of a taxon comprising Platycopia and Nanocopia; the sistergroup ofthese is Antrisocopia. Sarsicopia gen. n.is the only platycopioid to retain 2 inner setae onthe second endopod segment P2–P4, and 8 setae in thethird endopod segment of P2. The male antennnule isremarkable in having a geniculation located betweenancestral segments XX and XXI. It is suggested thatthis flexure zone was already present in thegroundpattern of Copepoda. Platycopia and Nanocopia have secondarily lost thisgeniculation.     

贡山竹属——我国云南竹亚科一新属

灌木状竹,有时附生于树干基部。地下茎短颈粗型。秆单丛;节问圆筒形;每节分枝单一,与主秆近等粗。秆释宿存性,革质;滓耳大,镰刀状;滓舌较低;算片外展。叶耳镰刀状;     

穿鞘花（鸭跖草科）的核形态

本文对鸭跖草科的穿鞘花Ａｍｉｓｃｈｏｔｏｌｙｐｅｈｉｓｐｉｄａ（ＬｅｓｓｅｔＡ．Ｒｉｃｈ．）Ｈｏｎｇ进行了核形态研究。其静止核和有丝分裂前期染色体分别属于复杂中央染色微粒型和中间型;染色体数目为２ｎ＝３６,核型公式为２ｎ＝４ｍ＋２８ｓｍ＋４ｓｔ。本种的核型为首次报道。     

荸荠营养器官的发育与解剖学研究

荸荠同化茎起源于肉质主茎倒２或倒３叶的叶腋内。同化茎基部着生二鞘状叶,鞘状叶对早期同化茎穿出土面具保护作用。匍匐茎大多起源于同化茎基部鞘状叶的叶腋内。当植株开始抽生花茎时,地下匍匐茎顶端开始膨大。球茎的膨大是匍匐茎顶端５－６节的基本组织经细胞有丝分裂,增加细胞数目,然后由细胞体积的扩大来实现的。球茎具足够的营养物质供来年顶芽萌发的需要,故属水生植物冬芽的性质。     

美口菌属二新种

本文报道了美口菌属 Calostoma Desv.的两个新种:云南美口菌 Calostoma yunnanensisL.J.Li et Liu sp.nov.和彭氏美口菌 Calostoma pengii Liu et Y.H.Liu sp.nov.     

Assessment of a model for intron RNA secondary structure relevant to RNA self-splicing--a review

A widespread class of introns is characterized by a particular RNA secondary structure, based upon four conserved nucleotide sequences. Among such "class I" introns are found the majority of introns in fungal mitochondrial genes and the self-splicing intron of the large ribosomal RNA of several species of Tetrahymena. A model of the RNA secondary structure, which must underlie the self-splicing activity, is here evaluated in the light of data on 16 further introns. The main body or "core structure" of the intron always consists of the base-paired regions P3 to P9 with the associated single-stranded loops, with P2 present also in most cases. Two minority sub-classes of core structure occur, one of which is typical of introns in fungal ribosomal RNA. Introns in which the core structure is close to the 5' splice site all have an internal guide sequence (IGS) which can pair with exon sequences adjacent to the 5' and 3' splice sites to align them precisely, as proposed by Davies et al. [Nature 300 (1982) 719-724]. In these cases, the internal guide model allows us to predict correctly the exact location of splice sites. All other introns probably use other mechanisms of alignment. This analysis provides strong support for the RNA splicing model which we have developed.     

Distributional patterns and an additional species of thePassiflora vitifolia complex: Amazonian species diversity due to edaphically differentiated communities

Field studies in Amazonian Peru show that thePassiflora vitifolia complex, a microcosm of many larger taxa, is concentrated in Amazonia with 4 ecologically separated species. One species is restricted to seasonally inundated forests, a second to non-inundated white sand soils, a third to non-inundated lateritic soils, and the fourth mostly to non-inundated alluvial soils. A new combination is formally proposed to recognize the white sand taxon, previously regarded as a variety, as a distinct species:P. involucrata. The importance of -diversity in maintaining high Amazonian species diversity is emphasized.     

Two Possibly Distinct Prostaglandin E1 Receptors in N1E-115 Clone: One Mediating Inositol Trisphosphate Formation, Cyclic GMP Formation, and Intracellular Calcium Mobilization and the Other Mediating Cyclic AMP Formation

Prostaglandin E1 (PGE1)-mediated transmembrane signal control systems were investigated in intact murine neuroblastoma cells (clone N1E-115). PGE1 increased intracellular levels of total inositol phosphates (IP), cyclic GMP, cyclic AMP, and calcium ([Ca2+]i). PGE1 transiently increased inositol 1,4,5-trisphosphate formation, peaking at 20 s. There was more than a 10-fold difference between the ED50 for PGE1 at cyclic AMP formation (70 nM) and its ED50 values at IP accumulation (1 microM), cyclic GMP formation (2 microM), and [Ca2+]i increase (5 microM). PGE1-mediated IP accumulation, cyclic GMP formation, and [Ca2+]i increase depended on both the concentration of PGE1 and extracellular calcium ions. PGE1 had more potent intrinsic activity in cyclic AMP formation, IP accumulation, and cyclic GMP formation than did PGE2, PGF2 alpha, or PGD2. A protein kinase C activator, 4 beta-phorbol 12 beta-myristate 13 alpha-acetate, had opposite effects on PGE1-mediated IP release and cyclic GMP formation (inhibitory) and cyclic AMP formation (stimulatory). These data suggest that there may be subtypes of the PGE1 receptor in this clone: a high-affinity receptor mediating cyclic AMP formation, and a low-affinity receptor mediating IP accumulation, cyclic GMP formation, and intracellular calcium mobilization.