A new species of saw‐scaled viper of the Echis coloratus complex (Ophidia: Viperidae) from Oman,Eastern Arabia

A study of 353 museum specimens of the Echis coloratus complex from its entire range of distribution revealed an undescribed species in the United Arab Emirates and northern Oman. The results of UPGMA clustering and principal coordinate analysis of 138 male and 142 female specimens yielded for both sexes two major clusters, one with specimens from the UAE and northern Oman and one from southern and western Arabia, the Levant and Egypt. The new species has a longer tail with higher subcaudal counts; the lower prenasal scale is often missing and the upper prenasal is frequently fused with the nasal; the subnasal is often missing or fused with the nasal. The gular scales between the chin‐shield and the preventrals are round or only slightly elongate, not elongate as in Echis coloratus, and their number is higher. Other differences in characters of the gular area indicate a different scale structure of the ventral surface of the head. The new species is allopatric or parapatric with E. coloratus, but sympatric with Echis carinatus sochureki.     

Feeding in extinct jawless heterostracan fishes and testing scenarios of early vertebrate evolution.

How long-extinct jawless fishes fed is poorly understood, yet interpretations of feeding are an important component of many hypotheses concerning the origin and early evolution of vertebrates. Heterostracans were the most diverse clade of armoured jawless vertebrates (stem gnathostomes), and the structure of the mouth and its use in feeding are the subjects of long-standing and heated controversy. I present here evidence that heterostracan feeding structures exhibit recurrent patterns of in vivo wear, are covered internally by microscopic oral denticles, and that the mouth may have been less flexible than has been thought. These data, particularly the absence of wear at the tips of oral plates, and the evidence that the mouth was lined with delicate outwardly directed denticles, effectively falsify all but one hypothesis of feeding in heterostracans: heterostracans were microphagous suspension feeders. This has a direct bearing on hypotheses that address ecological aspects of early vertebrate diversity and evolution, contradicting the widespread view that the pattern of early vertebrate evolution reflects a long-term trend towards increasingly active and predatory habits.     

Histology and affinity of the earliest armoured vertebrate

Arandaspids are the earliest skeletonizing vertebrates known from articulated remains. Despite a wealth of data, their affinity remains questionable because they exhibit a random mixture of primitive and derived characteristics. We constrain the affinity of arandaspids by providing the first detailed characterization of their dermoskeleton which is revealed to be three-layered, composed of a basal laminated, cancellous middle and tubercular superficial layers. All three layers are composed of acellular bone but the superficial layer also includes dentine and enameloid, comprising the tubercles. As such, the composition of the arandaspid dermoskeleton is common to heterostracans and astraspids, supporting existing hypotheses of early vertebrate phylogeny. This emphasizes the peculiarity of existing interpretations of aranadaspid anatomy and there is need for a complete reappraisal of the existing anatomical data.     

First Ordovician vertebrate from south America

The first Ordovician vertebrate from South Americais described from the Anzaldo Formation (Caradoc, Upper Ordovician) of Central Bolivia. It is referred to a new taxon, Sacabambaspis janvieri nov. gen. nov. sp., within the jawless vertebrate group Heterostraci, and displays some resemblance to both Astraspis and Arandaspis. It differs from all other known heterostracans by having very broad sensory-line grooves on the exoskeleton. Consideration of the palaeobiogeography of Ordovician vertebrates suggests that the early forms have been restricted to warm regions.     

Microrestes de Vertébrés du Siluro-Dévonien d'Algérie,de Turquie et de Thaïlande

Acanthodian («Shark-like spiny fishes) scaleshave been collected in three Uppermost Silurian-Lowermost Devonian localities from Algeria, southeastern Turkey and Thailand, in association with agnathan remains (heterostracans in Algeria, thelodonts in Thailand). These vertebrate microremains are the oldest ones for those three countries. They were associated with marine invertebrate faunas and are supposed to have lived in littoral environments. Their world-wide biogeographical distribution by the Silurian-Devonian boundary leads to analyse the palaeogeographical relations of north-Atlantis and Siberia on one hand, with southern Europe, southeastern Asia and Gondwanaland on the other hand.     

Histologic studies of ostracoderms, placoderms and fossil elasmobranchs. 6. Hard tissues of Ordovician vertebrates

Size and distribution of dermal elements in Ordovician eriptychiids and astraspids are considered relative to phases of skeletal assimilation and regression. The phyletic significance of acellularity in aspidin is discussed, as also is the alleged relationship claimed to exist in initial developmental stages between that hard tissue and dentine proper. To judge from hard tissue histology the astraspids may not, like the eriptychiids, have belonged to the heterostracans but to another group, of early agnathans, still incompletely known.     

The wors of I.I. Schmalhousen on comparative morphology of vertebrates: Significance for paleontological reconstructions (Data on the seismo-sensory system of agnathans)

The morphology and function of the seismo-sensory system of agnathans (Agnatha: Heterostraci) are analyzed. This system has been reconstructed in Cyathaspidiformes and Amphiaspidiformes. The seismo-sensory system of agnathans was compared with the lateral line system of fishes: the difference between these systems in the density of seismo-sensory lines and the contribution level of these systems to orientation in the water was detected. The possibility of reconstruction of the length and direction of heterostracans cranial nerves has been shown using the position of seismo-sensory lines and departments of the brain.     

Evolution of taxonomic diversity in amphiaspids (Agnatha,Heterostraci: Amphiaspidiformes) and the causes of extinction in ecologically favorable conditions

Changes in the taxonomic composition of Early Devonian amphiaspids represented in Siberia by two assemblages (from the northwestern Siberian Platform and Taimyr) are analyzed. The study is performed at the generic level and represented by diagrams. Changes in the amphiaspid composition are compared with changes in the development of the Taimyr and platform paleobasins. It is shown that shifts in ecological conditions at the stages of extinction of amphiaspids occurred within the limits of changes of abiotic factors (depth, salinity, etc.) that are usual for heterostracans. The disappearance (extinction) of amphiaspids is attributable to the level of their morphological organization, which caused inefficient adaptations to the developing paleoecosystems. The disappearance (extinction) of groups resulting from inadequate vital adaptations to the changing structure of paleoecosystems is considered to be a general law of evolution.     

THE HETEROSTRACAN FISHES

1. The heterostracan fishes were jawless, microphagous, devoid of paired fins and encased in a bony armour. The classification is based on the arrangement of the plates of the carapace — the primitive forms possessed a tessellated armour made up of numerous small polygonal plates. Several genera had a tessellated carapace ventrally but large discrete plates dorsally. All further groups are characterized by distinct patterns of plates which remain constant within each order. The proportions in some species suggest sexual dimorphism. 2. A study of the superficial ornamentation reveals patterns of growth. From the primitive tessellated condition different evolutionary lines can be followed leading to the fusion of these small elements into large discrete plates. Among the latest group of heterostracans there was a secondary redevelopment of tesserae. 3. Impressions on the inner surface of the plates of the carapace enable certain aspects of the internal anatomy to be reconstructed. The nasal sacs were double, the acousticolateralis system was primitive. The brain was little more than the nerve cord swollen in three places, there was no cranial flexure. Impressions of two pre-otic somites were present, indicating that they had not migrated to form the extrinsic eye muscles. The branchial arches appear to have been of gnathostome type and in some genera spiracles were formed as an adaptation to a benthonic mode of life. 4. Microscopic sections of the armour demonstrate the existence of four tissues: aspidin, dentine, enameloid and calcified cartilage. Aspidin was originally acellular but later became cellular; the organic matrix was first organized like dentine, but subsequently like bone. Furthermore aspidin was capable of remodelling. Dentine appears to have acted as a skin-like tissue and was capable of regeneration. The significance of enameloid and calcified cartilage in the dermal armour is not well understood. 5. Until the end of the Silurian the heterostracans inhabited marine waters but from the beginning of the Devonian they colonized the fresh-water lakes and rivers of the Old Red Continent. One major group flourished in a large embayment on the edge of the Tungussian land mass. When the stratigraphical range and geographical distribution of the heterostracans is listed, evolutionary centres can be recognized and also migration routes: during the Upper Silurian the cyathaspids in the Canadian Arctic, the Lower Devonian pteraspids in Eastern Europe, the later Lower Devonian amphiaspids in north-west Siberia (Tungussian Realm), and the Middle and Upper Devonian psammosteids in the Baltic province. Periods of migration from the Baltic to Scotland, the Timan, Ellesmereland, the Urals and Donbas have been documented. For the illustrations the author is indebted to Miss Jennifer Middleton and Mr John Smith.     

Epithelia are interchangeable between facial primordia of chick embryos and morphogenesis is controlled by the mesenchyme

The embryonic chick face is composed of a series of facial primordia, epithelium-covered buds of mesenchyme, which surround the presumptive mouth. The protruding adult upper beak containing the prenasal cartilage is formed from the frontonasal mass, the paired maxillary primordia form the sides of the face, while the lower beak is derived from the paired mandibular primordia which contain the two Meckel's cartilages. When grafted to a host wing bud, the frontonasal mass and the mandibular primordia both form elongated outgrowths, whereas the maxillary primordium forms a ball of tissue. Facial epithelium is required for growth and morphogenesis of all primordia. Recombinations between epithelium and mesenchyme from different primordia show that the epithelia are interchangeable and appear to be equivalent. Even the epithelium from the maxillary primordium that does not grow out in a polarized fashion can support outgrowth of the frontonasal mass and mandibular mesenchyme. The form of the recombined graft is determined by the mesenchymal component.     

Intraspecific variation in the external morphology of the sand skate

In male sand skate Psammobatis extenta , from the commercial fishery of Puerto Quequén, Argentina, six of 13 proportional dimensions analysed were constant (isometric) with total length, while seven proportions remained constant in females. The nature of the allometric and isometric relationships of disc length, disc width, interspiracular distance and interorbital distance did not vary between the sexes, and no sexual dimorphism occurred between these morphometric dimensions. A stepwise discriminant function analysis separated the sexes and was able to correctly classify 90·8% of the original grouped cases. The variables that best discriminated between sexes were prenasal length, distance from the cloaca to caudal fin tip, and distance from the snout to cloaca. The study also revealed that several of the meristic characters studied showed much intraspecific variation and, therefore, should be used with caution in taxonomic studies.     

Reconstruction of the Terminal of an Abandoned Fractured Unipolar Coronary Sinus Lead: a Feasible Solution to Restore Effective Cardiac Resynchronization Therapy

Complications related to coronary sinus lead are not infrequent in recipients of cardiac resynchronization devices. We describe the case of a patient with a biventricular implantable cardioverter defibrillator with persistent phrenic nerve stimulation, previous coronary sinus lead fracture, and severe left subclavian vein stenosis. The reimplantation of a new coronary sinus lead on the left side, ipsilateral to the original implant, was unsuccessful. In order to avoid more complex and risky procedures, we performed the repair of the fractured abandoned lead with the reconstruction of the unipolar lead terminal. Effective biventricular pacing was obtained with satisfactory electrical parameters and it was maintained at twelve months follow-up.     

Origins of bone repair in the armour of fossil fish: response to a deep wound by cells depositing dentine instead of dermal bone

The outer armour of fossil jawless fishes (Heterostraci) is, predominantly, a bone with a superficial ornament of dentine tubercles surrounded by pores leading to flask-shaped crypts (ampullae). However, despite the extensive bone present in these early dermal skeletons, damage was repaired almost exclusively with dentine. Consolidation of bone, by dentine invading and filling the vascular spaces, was previously recognized in Psammolepis and other heterostracans but was associated with ageing and dermal shield wear (reparative). Here, we describe wound repair by deposition of dentine directly onto a bony scaffold of fragmented bone. An extensive wound response occurred from massive deposition of dentine (reactionary), traced from tubercle pulp cavities and surrounding ampullae. These structures may provide the cells to make reparative and reactionary dentine, as in mammalian teeth today in response to stimuli (functional wear or damage). We suggest in Psammolepis, repair involved mobilization of these cells in response to a local stimulatory mechanism, for example, predator damage. By comparison, almost no new bone is detected in repair of the Psammolepis shield. Dentine infilling bone vascular tissue spaces of both abraded dentine and wounded bone suggests that recruitment of this process has been evolutionarily conserved over 380 Myr and precedes osteogenic skeletal repair.     

Anuran postnasal wall homology: An experimental extirpation study

The nasal placode was extirpated unilaterally in Gosner stage 18–20 embryos of Rana sylvatica, R. palustris and R. pipiens, in order to test alternative proposed schemes of homology for the ethmoidal attachment of the palatoquadrate in anurans and urodeles. Absence of the nasal sac has no pronounced effect on the formation of larval chondrocranial structures. In contrast, in metamorphosed animals the lamina orbitonasalis and inferior prenasal process are the only nasal capsule structures present on the operated side. The medial nasal branch of the deep ophthalmic nerve passes forward over the dorsal surface of the lamina orbitonasalis, rather than through an orbitonasal foramen. Comparison with previous experimental work on urodeles supports the traditional homology of the anuran lamina orbitonasalis with the antorbital process of urodeles and other vertebrates. J. Morphol. 238:343–353, 1998. © 1998 Wiley-Liss, Inc.     

Homology and evolution of the orbitotemporal venous sinuses of humans.

The orbitotemporal venous sinuses accompany the intracranial branches of the stapedial artery. These sinuses are large in primitive primates and drain the extensive territories supplied by the stapedial artery as well as the brain. The orbit is drained by a wide cranio-orbital sinus which empties into the postglenoid emissary vein. Also emptying into the postglenoid vein is the petrosquamous sinus. The latter diverts cerebral blood from the transverse sinus and also drains the temporalis muscle. Emptying into both the cranio-orbital and petrosquamous sinuses are meningeal tributaries, which drain the cranial side wall and the dura mater. The relatively small sinus communicans runs in the angle between the petrosal bone and the cranial side wall. It commences at the postglenoid vein and connects the distal end of the petrosquamous sinus to the pterygoid venous plexus. In humans, the orbitotemporal sinus system is greatly modified. Its remnants persist for the most part as "middle meningeal veins." The system no longer drains the orbit, the temporal fossa, or the brain. The petrosquamous sinus becomes attenuated or obliterated along part or all of its length. The postglenoid vein vanishes. The cranio-orbital sinus is reduced in diameter and its connection to the orbit is feeble or absent. During development, the posterior end of the cranio-orbital sinus migrates inferiorly along the sinus communicans. In most individuals, this migration ceases at the foramen spinosum, site of the emissary vein of the sinus communicans. Meningeal tributaries are relatively large in humans, and drain principally into the cranio-orbital sinus or sphenoparietal sinus. The sphenoparietal sinus is an evolutionary novelty restricted to hominoids and is frequently developed in only Homo and Pongo.     

The AV junction region of the heart: a comprehensive study correlating gross anatomy and direct three-dimensional analysis. Part II. Morphology and cytoarchitecture

This "Part II morphology and cytoarchitecture" study is based on paraffin-embedded specimens in which the extracellular and intracellular matrix are preserved; single parallel, perpendicular, and transverse serial sections of the entire atrioventricular (AV) junction region (AVJR) and their correlation with photographs of the tissue blocks. As in Part I, the same major new findings are: 1) a coronary sinus fossa is formed by the superoposterior right medial atria wall (MAW), the left atrium, and the coronary sinus roof; 2) the posterior MAW forms two myocardial bridges and is isolated from the sinus venarum by the floor of the inferior vena cava; 3) the tendon of Todaro terminates in the superior lip of the coronary sinus ostium; 4) only ordinary myocardium contacts the annulus fibrosus, and there is little to no collagen separating its myofibers and tissues; 5) the ventricular septum shoulder is humped shaped, completely overlaid by annular myocardium, and joined by struts of papillary muscle; 6) the membranous septum joining the ventricular septum shoulder to the crista supraventricularis forms part of the aortic valve sinus walls; and 7) myocardium of the atrionodal bundles is aggregated into numerous small fascicles encased by collagen and is outside of the MAW as are the other specialized tissues. The proximal AV bundle and medial atrionodal bundle are aligned to the medial leg of Koch's triangle and the tendon of Todaro. These data show, therefore, that the AVJR contains two overlapping atrial circuits. In the MAW, acivation of the posterior region is delayed because of the two myocardial bridges. Puncture of the AVJR can produce communication with an extracardiac space, posteriorly and medially, and with the aorta, anteriorly.     

An allometric study of the frontal sinus in Gorilla, Pan and Pongo

There is considerable speculation about the role and significance of the paranasal sinuses in the Hominoidea, and this study aims to present new data about an old problem from cephalograms of dried crania. Measurements of frontal sinus volumes were determined for Gorilla gorilla gorilla; G. gorilla beringei and Pan troglodytes. By adopting an allometric approach it was determined that the frontal sinus volume of Gorilla is relatively smaller than that of Pan, and that the frontal sinus of G. g. gorilla is relatively smaller than that of G. g. beringei. Frontal sinus volume scales in a positive allometric fashion relative to skull length. Since the slope is steeper for Pan, frontal sinus volume is increasing at a faster rate than in Gorilla. Sexual dimorphism in frontal sinus volume is present. Thirty crania of Pongo were investigated for evidence of pneumatization of the frontal bone. In no case was secondary invasion of the frontal bone by the maxillary antrum observed. In Gorilla, the nasal cavity volume scales isometrically with skull length. The scaling relationships discussed do not support any 'functional' role of the frontal sinus associated with nasal function but suggest a 'structural' role associated with craniofacial architecture.     

Development of the ethmoidal structures of the endocranium in Discoglossus pictus (Anura: Discoglossidae)

We use histological techniques and computer‐aided three‐dimensional reconstructions made from serial histological sections to describe the ontogeny of the ethmoidal endocranium of discoglossid frog Discoglossus pictus. We identify a pattern of development for the suprarostral cartilage that differs from previous findings and probably represents the ancestral anuran pattern. The nasal cartilages, including the inferior prenasal cartilage, are de novo adult structures. The only larva‐derived structures of the adult nasal capsules are the posterior aspects of the solum nasi and septum nasi. We also identify patterns of development for the ethmoid plate and postnasal wall that occur during early in ontogenesis. These patterns are associated with development events during metamorphic climax. The pattern of timing of chondrification of the anterior nasal cartilages more closely coincides with that of the neobatrachian species than that recorded for the pelobatid frog Spea. In addition, this study supports a sister taxon relationship between Discoglossus and Alytes. J. Morphol. 271:1078‐1093, 2010. © 2010 Wiley‐Liss, Inc.     

Studies of the neurohaemal organ (sinus gland) of the portunid crab Portunus sanguinolentus (Herbst) (Brachyura). 1. Morphology and histology in relation to moulting

The morphological and histological characters of the neurohaemal organ (sinus gland) of Portunus sanguinolentus are described in detail. The sinus gland lies on the dorsal surface of the optic ganglia, opposite the medulla interna. Histological techniques showed the presence of three tinctorially different secretory granules in the sinus gland. The predominant type of secretory material is basophilic and occurs as large granules, while two types of acidophilic material occur near the basement membrane. Cyclic changes in the relative amounts of acidophilic and basophilic material in correlation to moulting are also discussed. Allochthonous cells present in the sinus gland are identified.     

Ultrastructural morphometric study of efferent nerve terminals on murine bone marrow stromal cells, and the recognition of a novel anatomical unit: the "neuro-reticular complex"

In order to extend our understanding of the role of nerve fibers in the structure and function of bone marrow stroma, we have examined nerve terminals, arterioles, and capillaries in femoral bone marrow tissues of 50 C57BL strain mice, using electron microscopy and morphometric methods. Within the adventitia of arterioles, a particular type of cell, termed periarterial adventitial (PAA) cell, is characterized by a thin veil-like cytoplasm which concentrically surrounds both nerves and arterioles. Nerve fibers containing both unmyelinated and myelinated axons are distributed mainly between the layers of PAA cells, but are found rarely on the sinus walls or within the hematopoietic parenchyma. Quantitatively, the efferent nerve terminals with many synaptic vesicles are distributed mainly beside arterial smooth muscle cells (Type I: 58.8%) or between the layers of PAA cells (Type III: 33.2%), and rarely in hematopoietic parenchyma (Type II: 5.3%) or on sinus walls (Type IV: 2.7%). In the case of Type II-IV nerve terminals, efferent (autonomic) nerves and bone marrow stromal cells which are connected by gap junctions (sinus adventitial reticular cells, intersinusoidal reticular cells, and PAA cells) appear to constitute a potential functional unit for signal conduction. We would like to propose a new term for this anatomical unit in marrow, the "neuro-reticular complex."