关于费尔干蚌Ferganoconcha

在追溯费尔干蚌属与科的最初定义及过去学者对此属归科的不同意见后,从我国标本所获对此属铰齿构造了解,说明此属为蚌类化石。认为额尔古纳蚌Arguniella。也是蚌类化石,作者过去将它与费尔干蚌属合并是错误的,同时肯定了原苏联马廷生（G.G.Martinson）对费尔干蚌铰板与铰齿合并的解释。费尔干蚌属的区别特征,在其扁而无壳顶脊的外壳与狭细片状齿无铰板的发育。文末简述了陈金华1999新的不同意见,并作了评论。     

Dental ontogeny of a white shark embryo

Unlike most viviparous vertebrates, lamniform sharks develop functional teeth during early gestation. This feature is considered to be related to their unique reproductive mode where the embryo grows to a large size via feeding on nutritive eggs in utero. However, the developmental process of embryonic teeth is largely uninvestigated. We conducted X‐ray microcomputed tomography to observe the dentitions of early‐, mid‐, and full‐term embryos of the white shark Carcharodon carcharias (Lamniformes, Lamnidae). These data reveal the ontogenetic change of embryonic dentition of the species for the first time. Dentition of the early‐term embryos (∼45 cm precaudal length, PCL) is distinguished from adult dentition by 1) the presence of microscopic teeth in the distalmost region of the paratoquadrate, 2) a fang‐like crown morphology, and 3) a lack of basal concavity of the tooth root. The “intermediate tooth” of early‐term embryos is almost the same size as the adjacent teeth, suggesting that lamnoid‐type heterodonty (lamnoid tooth pattern) has not yet been established. We also discovered that mid‐term embryos (∼80 cm PCL) lack functional dentition. Previous studies have shown that the maternal supply of nutritive eggs in lamnoid sharks ceases during mid‐ to late‐gestation. Thus, discontinuation of functional tooth development is likely associated with the completion of the oophagous (egg‐eating) phase. Replacement teeth in mid‐term embryos include both embryonic and adult‐type teeth, suggesting that the embryo to adult transition in dental morphology occurs during this period. J. Morphol. 278:215–227, 2017. © 2016 Wiley Periodicals,Inc.     

Leaf architecture and epidermal characters in Zelkova, Ulmaceae

Zelkova , with six extant species in Eurasia - three in East Asia (Z. schneideriana, Z. serrata, Z. sinica) , one in south-western Asia (Z. carpinifolia) and two in southern Europe (Z. abelicea, Z. sicula) - was investigated with respect to leaf architecture and epidermal characters by LM and SEM. The leaf venation of Zelkova is relatively uniform, while leaf size and shape are highly variable. Characters such as teeth and epidermal cells, trichomes and stomata provide useful specific distinctions. Beginning in the Miocene, increasing aridity in Central Asia would appear to have been responsible for isolating the eastern Asiatic species from their European/western Asiatic counterparts. The European range underwent further changes in response to Quaternary climatic oscillations.     

Tooth Replacement in Late Jurassic Dryolestidae (Eupantotheria, Mammalia)

The discovery of juvenile dentitions of late Jurassic (Kimmeridgian) Dryolestidae (Eupantotheria, Mammalia) from Guimarota, Portugal, yields for the first time information on the mode of tooth replacement in therian mammals prior to the dichotomy of placentals and marsupials. As in extant placentals, tooth replacement occurs at all antemolar positions [incisors (I1–I4), canine (C), premolars (P1–P4)]. P1 and P2 have premolariform milk predecessors, whereas the large premolariform third (P3) and fourth premolars (P4) are preceded by molariform deciduous premolars (dP3, dP4). Tooth replacement takes place in two waves, at least in the lower jaw, with I₂, I₄, P₁, and P₃ in the first series and I₁, I₃, C, P₂, and P₄ in the second. P₄ is the last premolar to erupt, and it is present when the sixth molar (M₆) starts to break through. The reduced tooth replacement pattern of marsupials (with only dP3 being replaced postnatally) evolved secondarily from the primitive or plesiomorphic mammalian condition, which was retained in Dryolestidae and Eutheria.     

The trade-off between tooth strength and tooth penetration: predicting optimal shape of canine teeth

We investigate the shape of canine teeth under the assumption that the tooth's morphology is optimized by the evolutionary trade-off to minimize breakage and maximize ease of the penetration of prey. A series of experiments using artificial teeth to puncture the hides of a deer Odocoileus virginianus and pig Sus scrofa domesticus were conducted to establish the relationships between the tooth shape and the force needed to puncture the hide. The shapes of these teeth were also used in a beam theory analysis to calculate the strength of the teeth. Because the relative costs of puncturing and breakage were not known, a complete prediction of tooth shape was not possible. Instead, we used two independent measures of tooth shape: aspect ratio (total tooth length/tooth width at base) and rate of taper along the shank of the tooth. We quantified rate of taper in several species of felids, and by assuming this was the optimal design, we determined the relative costs of breakage and puncturing that would produce such a taper. Then, we used the relative costs to predict the aspect ratio of the optimum tooth. The average predicted value is about 2.5, very close to the average value in extant species of cats.     

广西南宁渐新世基于咽齿的鲤亚科一新属

记述了产自广西南宁盆地渐新世早—中期的鲤科鲤亚科一新属种——伍氏南宁鲤(+Nanningocyprinus wui gen.et sp.nov).化石材料包括一些咽喉骨和咽齿.这些咽喉骨和咽齿的以下特征组合明显不同于其他鲤科鱼类:齿式-3·2·1,主行第一枚咽齿大小是第二枚的3～4倍,第二枚咽齿及第二行第一枚咽齿咀嚼面上各仅有一条沟纹,咽骨前角很发育.该属种的发现进一步证明鲤亚科是鲤科中较早的分支,中国南方很有可能是鲤亚科的起源和分化中心.     

Dentition of the apron ray Discopyge tschudii (Elasmobranchii: Narcinidae)

The present study provides quantitative and qualitative analyses of the dentition of Discopyge tschudii. Overall, 193 individuals (99 males and 94 females) of D. tschudii were collected on scientific trawl surveys conducted by the National Institute for Fisheries Research and Development (INIDEP) and commercial vessels in Argentina. Discopyge tschudii has rhombic‐shaped teeth, arranged in a semipavement‐like dentition; each tooth has an erect cusp slightly inclined posteriorly and holaulachorized root. Mature males have greater tooth lengths than females and immature specimens. Discopyge tschudii exhibits dignathic homodonty and gradient monognathic heterodonty where teeth of the commissural row are shorter than those of the symphyseal and internal rows.     

禄丰古猿前部牙齿的釉面横纹与牙冠形成时间

釉面横纹的数目可用于推断个体牙齿的牙冠形成时间,在生长发育研究中具有重要的意义。本研究运用数码体视显微镜和扫描电镜观察了云南石灰坝禄丰禄丰古猿(简称禄丰古猿)30枚齿冠完整的前部牙齿,包括上下颌中门齿6枚、侧门齿10枚和犬齿14枚。根据唇侧面釉面横纹计数的观察结果,分别以7天和9天芮氏线生长周期,估算各齿型的牙冠形成时间,结果显示:以生长周期7天计算,中门齿牙冠形成时间约为3.6-4.1年,侧门齿牙冠形成时间约为2.7-3.7年,犬齿牙冠形成时间约为4.2-7.0;以生长周期9天计算,中门齿牙冠形成时间约为4.4-5.2年,侧门齿牙冠形成时间约为3.4-4.7年,犬齿牙冠形成时间约为5.2-8.8年。为更深入地了解禄丰古猿牙冠形成时间在不同齿型及性别间足否存在明显差异,本文用SPSS软件对其进行显著性差异检验。采用小样本平均值的t值假设检验(置信区间为95%),结果如下:禄丰古猿前部牙齿的牙冠形成时间在各类牙齿的上下颌中不存在显著性差异;犬齿牙冠形成时间存在非常显著的性别差异,雄性牙冠形成时间明显长于雌性,侧门齿也存在显著的性别差异,而中门齿性别间则无显著性差异。此外对禄丰古猿中门齿,侧门齿和犬齿的牙冠形成时间进行单因素方差分析并两两对比,结果显示中门齿与侧门齿的牙冠形成时间不存在显著性差异,而犬齿与中门齿和侧门齿均存在显著性差异,犬齿牙冠形成时间明显长于门齿。同时也对禄丰古猿前部牙齿的牙冠形成时间与齿冠高进行相关性分析,其结果表明两者有显著的正相关性。将禄丰古猿与其他古猿和现生大猿、南方古猿以及人属成员进行对比,结果显示其前部牙齿牙冠形成时间长于原修康尔猿、南方古猿、傍人、人属成员,接近于蝴蝶禄丰古猿和大猩猩,而明显小于黑猩猩、华南化石猩猩及现生猩猩。