Latimeria chalumnae and its pedigree

Synopsis Latimeria is the product of a long coelacanth lineage, usually viewed as having changed very little. In this paper a classification of better known coelacanth genera is proposed based on a cladistic computer analysis of 56 morphological characters. Biometrical data are then matched with the classification to explore the possibility of identifying subtle change. It is concluded that throughout coelacanth history there have been changes in the structure of the vertebral column involving an overall increase in the number of vertebral elements, and a consequent crowding of these elements within the abdominal region. These changes may be associated with increasing lobation of the second dorsal and anal fins. In the skull, parameters involving the intracranial joint have also changed in such a way that the anterior part of the skull has lengthened in relation to the posterior part and this may be associated with an increase in length of the basicranial muscle.Abbreviations in text figures Ang angular - a.o.r anterior opening of th rostral organ - Art articular - ba.cr.m basicranial muscle - Basi basisphenoid - Boc basioccipital - bpt.pr basipterygoid process - c.p.l cheek pit line - De dentary - Esc extrascapular - eth.sp etmosphenoid - f.e frontoethmoid - Fr frontal - Fr.d descending process of frontal - intr. j intracranial joint - io.s interorbital septum - sc jugal sensory canal - L.e lateral ethmoid - m.Cor modified coronoid - Mm memtomeckelian - m.ot.sc medial branch of otic canal - Op operculum - o.p.l oral pit line - ot,occ otico-occipital - Pa parietal - Pa.d descending process of parietal - Par parasphenoid - pa.s parietal shield - p.Cor principal coronoid - Po postorbital - Pop preoperculum - p.o.r posterior openings of the rostral organ - Pmx premaxilla, Pre-preorbital - Pro prootic - Pro.p posterior process of prootic - Rart retroarticular - Sc.o sclerotic ossicle - So supraorbital - Soc supraoccipital - Sop suboperculum - Sp spiracular - spl splenial - Sq squamosal - Stt supratemporal - Stt.com supratemporal commissure - Stt.d descending process of supratemporal - Par.a.w ascending wing of parasphenoid - Te tectal - X level of vagus exit     

<Emphasis Type="Italic">Hongeo</Emphasis>, a new skate genus (Chondrichthyes: Rajidae), with redescription of the type species

Hongeo gen. nov. is proposed following examinations of several individuals, including adult males, of the type species Raja koreana, previously described from a single adult female specimen from the southern coast of the Korean Peninsula. A number of external (including claspers, squamation, and ampullary and lateral line canal systems) and skeletal characters are newly described. The phylogenetic position of R. koreana among 26 nominal rajid supraspecific taxa plus 2 unnamed supraspecific taxa of Rajidae and 3 outgroups was estimated. According to a strict consensus tree of 20 equally parsimonious trees of 139 steps (CI = 0.626; RI = 0.850; RC = 0.532; HI = 0.374), Hongeo gen. nov. is defined by the two derived character states: rostral cartilage continuous with neurocranium and stout proximally, but very slender and uncalcified distally; and anterior fontanelle broad, extending forward onto the basal part of rostral cartilage slightly beyond the leading edge of nasal capsules. The new genus also differs from all other supraspecific taxa of Rajidae in the following combination of characters: dorsal surface of tail with a row of distinct thorns along midline in both sexes; most thorns directed anteriorly; a pair of longitudinally elongated black blotches having undulated contours on middle of dorsal surface of disc; three groups of outer buccal ampullae and tubules; three groups of nasal ampullae and tubules; hyoidean ampullae and tubules on ventral surface posteriorly extending past cloaca; rostral shaft narrow with filamentous cartilage at base; scapulocoracoid comparatively short and high with dorsoventrally elliptical anterior fenestra and expanded postventral fenestra; external margin of mesopterygium of pectoral fin slightly undulated, not sinuous, and not fused with pectoral radials; and clasper component eperon and pent present.     

A new camuropiscid arthrodire (Pisces: Placodermi) from Gogo, Western Australia

A new camuropiscid arthrodire, Latocamurus coulthardi gen. et sp. nov., is described from the Upper Devonian Gogo Formation, Western Australia. Latocamurus , known from two complete specimens, is recognized as a camuropiscid by its narrow, spindle-shaped armour, deep postnasal plates participating in the orbits, preorbital plates which meet mesially, cheek unit firmly sutured to skull roof, posterior check plates tightly interconnected and much reduced, and the robust durophagous dentition. It is characterized by its downturned snout, broad, flat rostral plate, and narrow, deep parasphenoid. It is placed phyletically as the plesiomorphic sister taxon to all other camuropiscids which are more derived in having, inter alia , an anterior lateral plate which anteriorly contacts the anterior ventrolateral plate and pointed rostral plates. The family Camuropiscidae Dennis & Miles 1979b is redefined to incorporate features of the new genus. Camuropiscids and Incisoscutum are closely related by features of the postnasal plate and cheek.     

Development and morphology of rostral cartilages in batoid fishes (Ghondrichthyes: Batoidea), with comments on homology within vertebrates

The rostral cartilages of batoid fishes were examined to elucidate their development, morphology and homology. Comparison of a variety of rostral cartilages among elasmobranchs with other groups of vertebrates shows that rostral cartilages originate embryologically from the trabecula and/or lamina orbitonasalis. Because different morphogenetic patterns of the derivatives of the two embryonic cartilages give rise to a wide variety of forms of rostral cartilages even within elasmobranchs, and because morphogenesis involves complex interactions among participating structures in the ethmo-orbital area, we put forward conceptual and empirical discussions to elucidate the homology of the rostral cartilages in batoid fishes. With six assumptions given in this study and based on recent discussions of biological and historical homology, our discussions centre on: (1) recognition of complex interactions of participating biological entities in development and evolution; (2) elucidation of a set of interacting biological and evolutionary factors to define a given morphological structure; (3) assessment of causal explanations for similarities or differences between homologous structures by determining genetic, epigenetic and evolutionary factors. Examples of conceptual approaches are given to make the approaches testable. Although a paucity of knowledge of rostral cartilage formation is the major obstacle to thorough analysis of the conceptual framework, several tentative conclusions are made on the homology of rostral cartilages that will hopefully attract more research on development and evolution in vertebrate morphology. These are: (1) the rostral cartilage in each group of vertebrates examined can be defined by both developmentally associated and adult structural attributes, yet such data do not allow us to assess homology of a variety of forms of rostral cartilages at higher taxonomic categories; (2) the entire rostral cartilage in elasmobranchs is formed by the contribution of the embryonic trabecula and lamina orbitonasalis. The status of the development and homology of the rostral cartilage in holocephalans remains uncertain; (3) there is no simple picture of evolution of rostral cartilages among three putative monophyletic assemblages of elasmobranchs, galeomorphs, squaloids (possibly plus Squatina, Chlamydoselachus and hexanchoids as the orbitostylic group) and batoid fishes. It is highly likely that rostral cartilages in each subgroup or subgroups of these assemblages may be of phylogenetic significance but that it may not serve as a basis to unite these assemblages into much higher assemblages; (4) the tripodal rostral cartilage is unique in form in the group including some carcharhinoid and lamnoid sharks. The status of the analogous tripodal cartilage in some squaloids remains uncertain. The unfused tripodal cartilage of the electric ray Narke is interpreted as developmentally equivalent to, but not homologous with, the unfused or fused ones in the sharks; (5) the rostral cartilage in the electric ray Torpedo is uniquely formed because of its embryonic origin solely from the ventro-medial part of the lamina orbitonasalis, but it is regarded as homologous with the rostral cartilages which are formed by the trabecula and other components of the lamina orbitonasalis in other batoid fishes; (6) the cornu trabecula contributes to the formation of the ventral stem of the rostral cartilage at least in elasmobranchs, especially to a particular set of rostral cartilages, i.e. the tripodal rostral cartilage in the shark Scyliorhinus and dorso-ventrally flattened rostral shaft in the narcinidid electric rays; (7) there is a unique form of a rostral shaft with rostral appendix in skates and probably guitarfishes; (8) there is no rostral cartilage in adult benthic stingrays, pelagic stingrays Dasyatis violacea and Myliobatidae, although it is present in embryonic stages; (9) there is a unique form of the rostral cartilage as a rostral projection from the dorso-lateral part of the lamina orbitonasalis in pelagic stingrays Rhinopteridae and Mobulidae, which together with part of the pectoral fins, forms a pair of cephalic fins; (10) different developmental mechanisms may be responsible for the absence or loss of rostral cartilages in different groups, i.e. absence of the cartilage derived from the medial area of the trabecula in Torpedo vs absence of the rostral cartilage in benthic stingrays; (11) the rostral cartilages in some placental mammals (cetaceans and sirenians) arise only from the medial area of the trabecula because monotreme and placental mammals do not form the trabecula cranii; (12) some actinopterygians and sacropterygians possess a rostral cartilage which originates only from the medial area of the trabecula. One scombroid group, including Sardini and Thunnini, Scomberomorus, Acanthocybium, Istiophoridae and Xiphias, possesses a unique larval beak composed of the rostral cartilage, ethmoid cartilage and premaxillar bone. The development and homology of other rostral cartilages remain to be further elucidated; (13) urodeles possess a medial rostral process whose anlage is probably developmentally equivalent to that in batoid fishes but the occurrence in urodeles is either atavistic or unique (autapomorphic); (14) the upper jaw of tadpoles is unique in possessing the suprarostral cartilage; the anlage of the cartilage is probably developmentally equivalent to the outgrowth of the cornu trabecula in batoid fishes.     

滇东南早泥盆世无颌类

文中记述了华南鱼类两个新属,即 Gantarostrataspis gengi gen. et sp. nov. 和 Gumuaspis rostrata gen. et sp. nov.,同时对含鱼层的时代进行了讨论.     

记江西一新的中华弓鳍鱼化石

本文记述了在江西弋阳石溪组发现的一中华弓鳍鱼。其形态特征虽与华北的师氏中华弓鳍鱼很相似,但又有很明显的差别,因此建立一新种——Sinamia poyangica, sp. nov.。在此基础上,对中华弓鳍鱼的形态变异和石溪组的时代作了讨论,并对师氏中华弓鳍鱼的复原图提出了修正的建议。     

中国鲨类脑颅的研究

本文解剖观察了我国有代表性的鲨类脑颅共32种,分隶于8目14科24属。研究结果认为鲨类的脑颅共可分为9个式型和12个亚型。现存虎鲨目、须鲨目的鲸鲨科和扁鲨目吻软骨缺如,六鳃鲨目、须鲨目、角鲨目和锯鲨目均具一吻软骨,它们是一些古老和一些特化的类群。现存大多数种类均具3根吻软骨。在各不同分类阶元常有其不同的形态特征,可作为分类依据之一,亦可显示其亲缘关系。     

大泷六线鱼仔稚鱼头部骨骼发育观察

采用软骨-硬骨双染色方法, 对大泷六线鱼仔稚鱼头部骨骼的发育过程进行详细观察与分析。结果显示: 大泷六线鱼初孵仔鱼头部已存在迈克尔氏软骨、腭方骨、舌棒骨和第一基舌软骨等骨骼元件; 当仔鱼4 DPH时, 第二基鳃软骨出现在第一基鳃软骨后端, 缘带向后延伸, 且软骨桥出现, 将头盖骨分为前卤和后卤; 9 DPH时, 3对鳃下骨, 第五对角腮骨可见; 13 DPH时, 迈克尔氏软骨背中部突, 4对鳃上骨、鼻骨、中筛板和侧筛板相继出现; 16—21 DPH时, 基舌骨出现在第一基鳃软骨前方; 23 DPH时, 齿骨开始骨化; 26 DPH时, 前颌骨和上颌骨开始骨化; 至35 DPH时, 前颌骨和上颌骨完成骨化; 50 DPH时, 副蝶骨、前鳃盖骨、缘带、后翼骨、鼻骨和续骨完成骨化; 60 DPH时, 大泷六线鱼头部骨骼, 除舌棒骨外, 基本骨化完成。研究摸清了大泷六线鱼仔稚鱼头部骨骼不同骨元件的发育时序, 阐释了头部骨骼的发育规律及其特殊性, 为大泷六线鱼早期骨骼功能发育研究及头部骨骼畸形鉴定提供了科学依据。     

The relationship between ontogeny, morphology, and diet in the Chinese hook snout carp (Opsariichthys bidens)

The relationship of changes of body and mouth shape with diet during ontogeny in the Chinese hook snout carp Opsariichthys bidens was examined. Shape changes were analyzed using geometric morphometrics. Body shape changed from a shallow body to a deep body as size increased. Similarly, the head of O. bidens changed from an upward-pointing direction to a downward-pointing directing as size increased. The position of the eye also changed during ontogeny, with large individuals having an eye situated higher on the head than small individuals. The conspicuous symphyseal knob on the lower jaw of O. bidens results in a typical zigzag pattern of the jaw. The zigzag pattern became more pronounced as fish grew larger. No difference in body shape or jaw shape was found between males and females. The shape changes were associated with changes in diet, suggesting that diet choice over the course of ontogeny has a strong impact on body shape. Benthic macroinvertebrates and zooplankton dominated the diet of small individuals, medium-size individuals specialized in benthic macroinvertebrates, and fish dominated the diet of large individuals.     

Morphology–diet relationships in four killifishes (Teleostei, Cyprinodontidae, Orestias) from Lake Titicaca

This study explores the relationship between morphology and diet in four Andean killifishes ( Orestias ) from Lake Titicaca that are known to differ in habitat use. Species that fed preferentially on amphipods ( Orestias albus ) or molluscs ( Orestias luteus ) separated in multivariate space from other species that feed on cladocera and algae ( Orestias agassii and Orestias jussiei ). Generally, specimens feeding on cladocera were characterized by a short, blunt nose with a small mouth; whereas, specimens feeding on amphipods exhibited a long snout with a large mouth. Specimens including molluscs in their diet tended to have a larger posterior part of the head and the larger opercles than others; while the occurrence of substratum in gut content was generally related to a short but deep head. The present analysis suggests that the littoral O. jussiei has an intermediate phenotype and diet between the pelagic ( O. agassii ) and benthic ( O. albus and O. luteus ) species. Results suggest that resource partitioning was occurring and that several morphological traits relate to characteristics of the diet, and it is inferred that the benthic, the pelagic and the littoral zones in the lake host different prey communities constituting distinct adaptive landscapes.     

The impacts of comparative anatomy of electric rays (Batoidea: Torpediniformes) on their systematic hypotheses

The Comparative anatomy of the 11 recognized genera within Torpediniformes is described, systematically categorized, and illustrated in a comprehensive photo‐atlas. Data are compiled into a character matrix and cladistically analyzed using parsimony to test hypotheses about the previously recognized subfamilies, while reconstructing the possible evolutionary history of Torpediniformes. Results are consistent with the previous rank‐based classifications, regardless of the parsimony criteria used to generate the phylogenetic hypothesis, with one notable exception: a monophyletic Narcininae was never recovered. Torpedinoidea (=Hypnos + Torpedo) is supported by the presence of long, slender, flexible jaw cartilages, absence of a large rostral fontanelle, presence of suprascapular antimeres that are each shorter than the scapular process of the scapulocoracoid, antorbital cartilages that articulate on the anterior aspect of the nasal capsules and absence of a frontoparietal fontanelle. Subfamilial names Hypninae and Torpedininae are redundant with the genus names Hypnos and Torpedo and are not adopted here. Narcinoidea (=nontorpedinoid torpediniforms) is supported by unambiguous character transformations to the presence of a divided lower lip, labial cartilages, laterolingually compressed palatoquadrates, bifurcated antorbital cartilages, a rostral fontanelle, ventrally projecting nasal capsules, a dorsal rim of the synarcual mouth posterior to occipital condyle, posteriorly positioned lateral stays, and obtuse anterior margins of lateral stays. Narkidae is supported by unambiguous character transformations to the presence of an uncovered eye that protrudes above dorsal surface, a shared rim between the spiracle and the eye, an anterior nasal turret that projects ventrally, a nasal curtain that covers the upper lip and dentition when the mouth is closed, tab‐like prepelvic processes, a mesopterygium that is shorter than propterygium but longer than metapterygium, a slender median rostral cartilage, and a basibranchial cartilage with an anterior margin that is depressed medially and a posterior margin that tapers. J. Morphol. 275:597–612, 2014. © 2013 Wiley Periodicals, Inc.     

Divisispiculimermis mirus n. gen., n. sp. (Mermithidae: Nematoda) Parasitizing Midges in Córdoba,Argentina

Divisispiculimermis mirus n. gen., n. sp., a mermithid parasitizing larvae of Chironomus sp. in the Cajón o Grande Stream, Córdoba, Argentina, is described. The new genus differs from all other mermithid genera in having paired spicules which are separated and divided into proximal and distal sectors. The other diagnostic characters of the genus are medium size, nematodes with the cuticle appearing smooth (lacking cross fibers under the light microscope); head separated from the rest of the body by a slight constriction at the level of the amphids, six cephalic papillae, mouth papillae absent, mouth opening posterior to level of cephalic papillae; six hypodermal chords at midbody; weakly S-shaped vagina; postparasitic juvenile with a tail appendage.     

Scanning Electron Microscope Studies of Steinernema anomali Kozodoi, 1984

This paper presents SEM micrographs of portions of the male, female, and infective-stage juvenile of Steinernema anomali. Included are micrographs of the cephalic and caudal region, spicules, and gubernaculum of the male, the cephalic and vulval region of the female, and the cephalic region of the infective-stage juvenile. Males have six labial and four prominent cephalic papillae and small amphids. There are 11-14 pairs and one single genital papillae; of these, 6-9 pairs are preanal and subventral, one pair preanal, lateral, one pair adanal, and three pairs postanal. Spicules have a short head, a long blade, and a reduced shaft. The distal end is enlarged and bears a dorsal aperture. Gubernaculum much shorter than spicules; cuneus of gubernaculum short and bifurcate anteriorly. Females have six labial and four cephalic papillae and small amphids. Vulva with a thickened posterior lip. Infective juveniles have a smooth head, prominent amphids, and four cephalic papillae. Labial papillae, if present, are not evident.     

Twisted story of eye migration in flatfish

Early molecular markers for flatfish metamorphosis and eye migration must be linked to the ethmoid region, the earliest part of the flatfish cranium to change, as well as chondral and dermal ossification processes. Serial sections, morphological landmarks, and stereology were used to determine where and when the remodeling of tissues and asymmetry occurs in the head region of metamorphosing Atlantic halibut, Hippoglossus hippoglossus. Not all parts of the head remodel or migrate, and those that do may be asynchronous. Normal metamorphosis limits the torsion of the Atlantic halibut head to the anterior part of the neurocranium and excludes the tip of the snout and the general jaw area. The first cranial structure displaying eye migration-related asymmetric development is the paraethmoid part of the ethmoid cartilage. In early eye migration the medial frontal process moves apace with the eyes, whereas near completion the migrating eye moves significantly closer to the frontal process. Structures of the jaw remain mostly symmetrical, with the exception of the adductor mandibulae muscle and the bone maxillare, which are larger on the abocular than on the ocular side, the muscle occupying the space vacated by the migration of the eye. Thus, normal eye migration involves a series of temperospatially linked events. In juveniles lacking eye migration (arrested metamorphosis), the dermal bone, the prefrontal, does not develop. The two abnormal paraethmoids develop symmetrically as two plate-like structures curving anteriorly, whereas normal elongate fused paraethmoids curve at their posterior. The abocular side retrorbital vesicles are largest in volume only after the completion of normal eye migration. Factors involved in completion of normal metamorphosis and eye migration in flatfish affect chondral and dermal ossification signals in the ethmoid group, as well as remodeling of the mineralized frontal, a series of linked events not involving the entire neurocranium.     

<Emphasis Type="Italic">Dipturus wuhanlingi</Emphasis>, a new species of skates (Elasmobranchii: Rajidae) from China

Dipturus wuhanlingi, a new rajid species, is described from an immature male and female collected from the southern East China Sea and off Haimen, Shantou, in the South China Sea, respectively. The specimens conform to the genus Dipturus in having the combination of the following characters: a long rostral cartilage (length more than 60% of dorsal head length), greatly depressed and laterally expanded mesocondyle, and a total length greater than 55 cm when adult. Dipturus wuhanlingi is distinct from all other Dipturus species in the following combination of characters: a pair of scapular thorns, three or four nuchal thorns, an irregular row of lumbar thorns along the dorsal midline of the disc, a single row of tail thorns in both sexes, pores of ampullae of Lorenzini extending to just anterior to the pelvic girdle, anterior fenestra of scapulocoracoid strongly horizontally elliptical, mesocondyle located at about the middle between the procondyle and metacondyle, and three pairs of obturator foramina on the pelvic girdle.     

Raja koreana, a new species of skate (Elasmobranchii, Rajoidei) from Korea

A new rajid species,Raja koreana, is described from a single adult female specimen, 735 mm in total length, collected off the southwestern coast of the Korean Peninsula. AlthoughR. koreana is included in the group of species characterized by the scapulocoracoid lacking an anterior bridge and having the postventral fenestra expanded, it is unique among the latter in possessing: pectoral girdle propterygium not extending to snout tip; rostral shaft of neurocranium narrow and thick, unsegmented base with filamentous cartilage; snout fleshy; pores of ampullae of Lorenzini densely distributed over much of ventral surface to behind cloaca; most thorns on tail directed anteriorly; tail short; a pair of longitudinally elongated black blotches on middle of dorsal surface of disc when fresh; a pair of black blotches (grayish at center) posteriorly on pectoral fins; ventral surface of dise uniformly blackish-brown, except for areas around pores.     

Porocottus leptosomus sp. nov., from the west coast of Korea, Yellow Sea (Scorpaeniformes: Cottidae)

 A new cottid species, Porocottus leptosomus, is described on the basis of 12 specimens collected from Taean, west coast of Korea, Yellow Sea. The species is distinguished from other species of Porocottus by the following combination of characters: a strongly compressed body, two pairs of branched cirri on the dorsal surface of the head, bases of head cirri smooth, a single cirrus on the dorsal tip of each spine of the first dorsal fin, a single opening of the sixth canaliculus of the infraorbital sensory canal, a long posterior medial canaliculus of the occipital canal with the terminal pore and a few supplementary pores, and melanophores on the isthmus hidden beneath the branchiostegal membrane. Received: January 11, 2001 / Revised: February 7, 2002 / Accepted: March 4, 2002     

Why is grouper larval rearing difficult?: an approach from the development of the feeding apparatus in early stage larvae of the grouper,Epinephelus coioides

The osteological development of elements forming the oral cavity was examined in early stage larvae of the grouper,Epinephelus coioides, from hatching to 242.5 hours after hatching. By the time of initial mouth opening, at 54 hours after hatching, the fundamental elements, composed of the trabecula, some components of the lower branchial and hyoid arches, the quadrate and symplectic-hyomandibular cartilages, maxilla and Meckel's cartilage, had appeared. No further elements were observed until 165 hours after initial mouth opening, except some components in the lower branchial arch and head region. The appearance of new elements and initial ossification of existing cartilage occurred thereafter, but all elements related to feeding either had not appeared or had not started ossifying until 188.5 hours after initial mouth opening. Based on the morphology and developmental modes of these elements, the feeding mode of grouper larvae was considered to be “sucking/grasping.” However, the appearance and ossification of elements occurred slowly, with no transitional phase from sucking to grasping modes of feeding being observed during the study; such delayed development of the feeding-related bony elements was considered to be a cause of the difficulty in rearing early stage grouper larvae.     

Ethmoidal endocranium in primitive triassic amphibians

Three-dimensionally preserved and chemically prepared skulls and natural casts of representatives of the families Benthosuchidae, Melosauridae, and Capitosauridae yield data on the structure of the ethmoidal endocranium, i. e. of those nasal cranial structures that consisted originally of cartilage. This study demonstrates that the ethmoidal endocranium was principally a dorsoventrally compressed plate, pierced by a broad and oblique canal which communicated anteriorly with the outer dorsal surface by the fenestra endonarina and posteriorly with the mouth cavity by the fenestra endochoanalis(seu foris). The canal was very short, and housed the olfactory organ. The ethmoidal endocranium was connected with the palatoquadrate by the commissura quadratocranialis anterior; there was no lateral ethmoidal commissure, however, in older individuals the anterior section of the palatoquadrate might also contact the postchoanal part of the nasal endocranial skeleton.