The function of the glabellar 'tubercle' in Nileus and other trilobites

The glabellar 'tubercle' of Nileus armadillo (Dalman) is an inverted funnel-shaped thinning in the cuticle, covered by the outer cuticular layer. Its structure is consistent with a function as a light-sensitive organ, whose angular range of light receptivity complements that of the lateral eyes. Median cephalic tubercles of most other trilobites are unlike that of Nileus and are difforent. in structure and position; henco they are unlikely to have been homologous.     

Ventral axial organs regulate expression of myotomal Fgf-8 that influences rib development

Fgf-8 encodes a secreted signaling molecule mediating key roles in embryonic patterning. This study analyzes the expression pattern, regulation, and function of this growth factor in the paraxial mesoderm of the avian embryo. In the mature somite, expression of Fgf-8 is restricted to a subpopulation of myotome cells, comprising most, but not all, epaxial and hypaxial muscle precursors. Following ablation of the notochord and floor plate, Fgf-8 expression is not activated in the somites, in either the epaxial or the hypaxial domain, while ablation of the dorsal neural tube does not affect Fgf-8 expression in paraxial mesoderm. Contrary to the view that hypaxial muscle precursors are independent of regulatory influences from axial structures, these findings provide the first evidence for a regulatory influence of ventral, but not dorsal axial structures on the hypaxial muscle domain. Sonic hedgehog can substitute for the ventral neural tube and notochord in the initiation of Fgf-8 expression in the myotome. It is also shown that Fgf-8 protein leads to an increase in sclerotomal cell proliferation and enhances rib cartilage development in mature somites, whereas inhibition of Fgf signaling by SU 5402 causes deletions in developing ribs. These observations demonstrate: (1) a regulatory influence of the ventral axial organs on the hypaxial muscle compartment; (2) regulation of epaxial and hypaxial expression of Fgf-8 by Sonic hedgehog; and (3) independent regulation of Fgf-8 and MyoD in the hypaxial myotome by ventral axial organs. It is postulated that the notochord and ventral neural tube influence hypaxial expression of Fgf-8 in the myotome and that, in turn, Fgf-8 has a functional role in rib formation.     

Some neuroanatomical aspects of primate locomotor evolution

Primate locomotor patterns are the result of osteological and myological interactions, the effectiveness of which is governed by various afferent, internuncial and efferent central nervous system pathways. The distribution of primary afferents following lumbosacral ganglionectomies and the distribution of corticospinal fibers following lesion of contralateral motor cortex to medial and lateral ventral horn motor nuclei have been discussed for the tree shrew and bushbaby. Based on limited data it has been suggested that the tree shrew is the best living example of the quadrupedal Paleocene forms from which primates presumably evolved, and the bushbaby is one of the best examples of the vertical clingers and leapers which appeared in the Eocene. Both forms have dense primary afferent distribution to cells of the lateral portion of the ventral horn, which are related to appendicular musculature, and sparse projection to the medial part of the ventral horn which innervates axial musculature. Corticospinal fibers in the tree shrew do not synapse in any portion of the ventral horn at any spinal cord level. The bushbaby has direct cortical motor control over cells located in the medial portion of the ventral horn and, consequently, over axial musculature. Extrapolations from studies on the tree shrew and other generalized forms suggested that Paleocene quadrupeds lacked cortical control over axial and appendicular musculature and depended primarily on subcorticospinal pathways and spinal reflexes for the execution of their locomotor pattern. Eocene vertical clingers and leapers retained the reflex pathways of their Paleocene ancestors but acquired direct cortical motor control over axial musculature, thus indicating a first level of neuroanatomical adaptation related to evolving locomotor styles. It was suggested that there are correlations between locomotor style and neuromorphological specializations, and that comparative observations on key extant phylogenetic forms may provide a clearer and more complete picture of initial locomotor adaptations in the primate series.     

The chordoid larva of Symbion pandora (Cycliophora) is a modified trochophore

Developmental and free-living stages of the chordoid larva of the cycliophoran species, Symbion pandora Funch and Kristensen 1995, were studied using light and electron microscopy. In the free-living stage of the larva, about 200 μm long, four ciliated areas are found: two anterior bands, a ventral ciliated field, and a posterior unit on the ventral side of the foot. The nervous system consists of a dorsal brain and a pair of ventral longitudinal nerves. A gut is absent. A pair of protonephridia, each with a single multiciliated terminal cell and at least one duct cell, is present. Nephridiopores are not localized. A pair of corsal ciliated organs is posterior to the brain. The homology between these and the apical organ of a trochophore larva is discussed. A distinctive longitudinal rod, the chordoid organ, consists of vacuolized cells with circular myofilaments. The organ is comparable to a similar structure in gastrotrichs. In the discussion of the phylogenetic position of Cycliophora among protostomians, important morphological observations that are described in the present study indicate that, despite some dissimilarities, the chordoid larva is a modified trochophore. © 1996 Wiley-Liss, Inc.     

Dorsoventral Differences of Morphogenetic Potencies of the Loach Blastoderm in Experiments with Alteration of Mass of Explanted Fragments

We studied the influence of doubling the mass of explanted fragments of the dorsal and ventral loach blastoderm at the early gastrula stage on their capacity for differentiation of axial structures. The dorsoventral differences are as follows: the differentiation of somites correlates, according to the results of factor analysis, with the shape complication only in double dorsal explants, while the notochord is more differentiated in the ventral fragments, if it is present, than in the dorsal ones. Doubling of the mass of dorsal fragments of the blastoderm enhances their morphogenetic potencies and shifts differentiation towards the formation of trunk axial structures. The increased mass of ventral fragments does not affect their differentiation and morphogenesis, but disturbs the correlation of these processes.     

Axial complex of Crinoidea: Comparison with other Ambulacraria

The anatomy of Crinoidea differs from that of the other modern echinoderms. In order to see, whether such differences extend to the axial complex as well, we studied the axial complex of Himerometra robustipinna (Himerometridae, Comatulida) and compared it with modern Eleutherozoa. The axial coelom is represented by narrow spaces lined with squamous coelothelium, and surrounds the extracellular haemocoelic lacunae of the axial organ. The latter is located, for the most part, along the central oral-aboral axis of the body. The axial organ can be divided into the lacunar and tubular region. The tubular coelomic canals penetrating the thickness of the axial organ have cuboidal epithelial lining, and end blindly both on the oral and aboral sides. The axial coelom, perihaemal coelom, and genital coelom are clearly visible, but they connect with the general perivisceral coelom and with each other via numerous openings. The haemocoelic spaces of the oral haemal ring pass between the clefts of the perihaemal coelom, and connect with the axial organ. In addition, the axial organ connects with intestinal haemal vessels and with the genital haemal lacuna. Numerous thin stone canaliculi pierce the spongy tissue of the oral haemal ring. They do not connect with the environment. On the oral side, each stone canaliculus opens into the water ring. The numerous slender tegmenal pores penetrate the oral epidermis of the calyx and open to the environment. Tegmenal canaliculi lead into bubbles of the perivisceral coelom. Some structures of the crinoid axial complex (stone canaliculi, communication between different coeloms) are numerous whereas in other echinoderms these structures are fewer or only one. The arrangement of the circumoral complex of Crinoidea is most similar to Holothuroidea. The anatomical structure and histology of the axial complex of Crinoidea resembles the “heart-kidney” of Hemichordata in some aspects.     

Podocytes in the axial organ of echinoderms

The axial organ of two sea urchin genera, Echinometra and Eucidaris , has been analysed with the electron microscope. It is mainly built up by an extracoelomic tissue rich in various leucocytic cells and blood vessels lacking an endothelium. The axial sinus (axocoel) is located on the interior of the axial organ, and evaginations extend into this loosely constructed tissue. The epithelium of the axial sinus and its extensions are characterized by epitheliomuscular cells and abundant podocytes, which overlie the blood vessels. Since podocytes are the well known structural basis for ultrafiltration, it is postulated that this is a function of the axial organ at least in echinoids and asteroids.     

Anatomy and ultrastructure of ventral pharyngeal organs and their phylogenetic importance in Polychaeta (Annelida)

Summary Transmission electron microscopic studies were carried out on the ventral pharyngeal organs in Ctenodrilus serratus and Scoloplos armiger. The pharyngeal organs are composed of a muscle bulbus and a tongue-like organ. In both species the muscle bulbus consists of transverse muscle fibres and interstitial cells with voluminous cell bodies and dorsoventral tonofilaments; the investing muscle runs into the tongue-like organ; the nuclei of the investing muscle fibres are located in caudal bulges; salivary glands are not present, but numerous gland cells occur in the bulbus epithelium. The tongue-like organ, however, is formed by lateral folds (C. serratus) or a bridge-like structure (S. armiger). The specific structure of the bulbus muscle is probably a homologous characteristic also occurring in several other polychaete families. The phylogenetic importance of this ventral pharynx is discussed and a hypothesis is suggested to explain the differentiation of certain other ventral pharyngeal organs from this probably primitive type.     

Dorsoventral differences of morphogenetic potencies of the loach blastoderm in experiments with alteration of the mass of explanted fragments

We studied the influence of doubling the mass of explanted fragments of the dorsal and ventral loach blastoderm at the early gastrula stage on their capacity for differentiation of axial structures. The dorsoventral differences are as follows: the differentiation of somites correlates, according to the results of factor analysis, with the shape complication only in double dorsal explants, while the notochord is more differentiated in the ventral fragments, if it is present, than in the dorsal ones. Doubling of the mass of dorsal fragments of the blastoderm enhances their morphogenetic potencies and shifts differentiation towards the formation of trunk axial structures. The increased mass of ventral fragments does not affect their differentiation and morphogenesis, but disturbs the correlation of these processes.     

梭德氏蛙蝌蚪的腹吸盘--同功器官一例

本文讨论梭德氏蛙蝌蚪的腹吸盘,经它与湍蛙属蝌蚪的腹吸盘是同功器官,因而前者不可能与后者是同民各关系。按照“丰家争鸣”方针,我们主张对科学的问题采取科学的方式加以讨论,欢迎不同意见在国内外任何刊物上撰文发表,只有通过学术讨论才有得达到共识,取得尽可能符合客观实际的结论。     

Did the notochord evolve from an ancient axial muscle? The axochord hypothesis

The origin of the notochord is one of the key remaining mysteries of our evolutionary ancestry. Here, we present a multi‐level comparison of the chordate notochord to the axochord, a paired axial muscle spanning the ventral midline of annelid worms and other invertebrates. At the cellular level, comparative molecular profiling in the marine annelids P. dumerilii and C. teleta reveals expression of similar, specific gene sets in presumptive axochordal and notochordal cells. These cells also occupy corresponding positions in a conserved anatomical topology and undergo similar morphogenetic movements. At the organ level, a detailed comparison of bilaterian musculatures reveals that most phyla form axochord‐like muscles, suggesting that such a muscle was already present in urbilaterian ancestors. Integrating comparative evidence at the cell and organ level, we propose that the notochord evolved by modification of a ventromedian muscle followed by the assembly of an axial complex supporting swimming in vertebrate ancestors.     

Anatomy and Ultrastructure of Ventral Pharyngeal Organs and their Phylogenetic Importance in Polychaeta (Annelida). IV. The Pharynx and Jaws of the Dorvilleidae

An anatomical and ultrastructural investigation of the ventral pharyngeal organ, jaws and replacement of jaws was carried out in Ophryotrocha gracilis and Protodorvillea kefersteini (Dorvilleidae). The pharynx exhibits the following features: jaw apparatus present, consisting of paired mandibles and rows of maxillary plates, the latter are fused to form a single piece; cuticular jaws electron-dense, in P. kefersteini with collagen fibres; muscle bulbus solid, composed of muscle cells only; parallel running myofilaments, centrally located mitochondria and nuclei, bulbus epithelium containing the mandibles and gland cells, maxillary plates lying on folds corresponding to a tongue-like organ, connected with mandibles by longitudinal investing muscles; numerous gland cells not united to distinct salivary glands. Development of jaw replacements occurs in epithelial cavities beside the functional maxillae. Shape of maxillary plates is preformed by microvilli carrying cell processes. Maxilloblasts change their shape during the development. Synapomorphic structures occurring in ventral pharyngeal organs of other species outside the Eunicea are not present and even the closely related Dinophilidae exhibit a completely different pharyngeal organ. Therefore, convergent evolution of these organs is the most probable explanation. These findings do not agree with the hypothesis of the homology of the ventral pharyngeal organs in the Polychaeta.     

The first report of luminescent liver tissue in fishes: Evolution and structure of bioluminescent organs in the deep‐sea naked barracudinas (Aulopiformes: Lestidiidae)

Bioluminescent organs that provide ventral camouflage are common among fishes in the meso‐bathypelagic zones of the deep sea. However, the anatomical structures that have been modified to produce light vary substantially among different groups of fishes. Although the anatomical structure and evolutionary derivation of some of these organs have been well studied, the light organs of the naked barracudinas have received little scientific attention. This study describes the anatomy and evolution of bioluminescent organs in the Lestidiidae (naked barracudinas) in the context of a new phylogeny of barracudinas and closely related alepisauroid fishes. Gross and histological examination of bioluminescent organs or homologous structures from preserved museum specimens indicate that the ventral light organ is derived from hepatopancreatic tissue and that the antorbital spot in Lestrolepis is, in fact, a second dermal light organ. In the context of the phylogeny generated from DNA‐sequence data from eight gene fragments (7 nuclear and 1 mitochondrial), a complex liver with a narrow ventral strand running along the ventral midline evolves first in the Lestidiidae. The ventral hepatopancreatic tissue later evolves into a ventral bioluminescent organ in the ancestor of Lestidium and Lestrolepis with the lineage leading to the genus Lestrolepis evolving a dermal antorbital bioluminescent organ, likely for light‐intensity matching. This is the first described hepatopancreatic bioluminescent organ in fishes. J. Morphol. 276:310–318, 2015. © 2014 Wiley Periodicals, Inc.     

Review of Chinese Oligaphorurini (Collembola, Onychiuridae) with descriptions of two new Palaearctic species

A checklist of Chinese Oligaphorurini is given. Two new Chinese species, Micraphorura changbaiensissp. n. and Oligaphorura pseudomontanasp. n., are described from Changbai Mountain Range. Micraphorura changbaiensis sp. n. has the same dorsal pseudocelli formula and number of papillae in Ant. III sensory organ as Micraphorura uralica, but they can be easily distinguished by number of chaetae in Ant. III sensory organ, ventral pseudocelli formula, ventral parapseudocelli formula, number of pseudocelli on subcoxa 1 of legs I-III, dorsal axial chaeta on Abd. V and number of chaetae on tibiotarsi. Oligaphorura pseudomontana sp. n. is very similar to the species Oligaphorura montana having an increased number of pseudocelli on body dorsally, well marked base of antenna with 1 pseudocellus and 3 pseudocelli outside, subcoxa 1 of legs I-III with 1 pseudocellus each, dorsally S-chaetae formula as 11/011/22211 from head to Abd. V, S-microchaeta present on Th. II-III, claw without inner teeth and with 1+1 lateral teeth, and unguiculus with basal lamella; but they can be separated easily by the number of pseudocelli on Abd. V and VI terga, parapseudocelli on the body, number of chaetae on Th. I tergum, and number of chaetae on tibiotarsi. A key to Chinese species of Oligaphorurini is provided in the present paper.     

Role of the hindbrain in dorsoventral but not anteroposterior axial specification of the inner ear

An early and crucial event in vertebrate inner ear development is the acquisition of axial identities that in turn dictate the positions of all subsequent inner ear components. Here, we focus on the role of the hindbrain in establishment of inner ear axes and show that axial specification occurs well after otic placode formation in chicken. Anteroposterior (AP) rotation of the hindbrain prior to specification of this axis does not affect the normal AP orientation and morphogenesis of the inner ear. By contrast, reversing the dorsoventral (DV) axis of the hindbrain results in changing the DV axial identity of the inner ear. Expression patterns of several ventrally expressed otic genes such as NeuroD, Lunatic fringe (Lfng) and Six1 are shifted dorsally, whereas the expression pattern of a normally dorsal-specific gene, Gbx2, is abolished. Removing the source of Sonic Hedgehog (SHH) by ablating the floor plate and/or notochord, or inhibiting SHH function using an antibody that blocks SHH bioactivity results in loss of ventral inner ear structures. Our results indicate that SHH, together with other signals from the hindbrain, are important for patterning the ventral axis of the inner ear. Taken together, our studies suggest that tissue(s) other than the hindbrain confer AP axial information whereas signals from the hindbrain are necessary and sufficient for the DV axial patterning of the inner ear.     

In vitro effect of rabbit anti sea star lymphocyte serum on axial organ cells

The axial organ (AO-cells) of the sea star Asterias rubens is a primitive immune organ. The total population was fractionated or not into two populations: adherent (B-like) and non adherent (T-like) to nylon wool. Rabbit anti sea star lymphocyte serum induces the proliferation of axial organ cells. The T-like antiserum stimulates the T-like cells exclusively; the whole axial organ cell antiserum only stimulates the whole axial organ cell population.     

An ultrastructural investigation of the hypocerebral organ of the adult Euperipatoides kanangrensis (Onychophora, Peripatopsidae)

The hypocerebral organs of Euperipatoides kanangrensis are a pair of spherical vesicles located ventral to the cerebral ganglia. They develop in the embryo from the most anterior pair of ventral organs, in the antennal segment. The wall of each hypocerebral organ is a dense epithelium of elongate cells with peripheral nuclei. The cytoplasm of the cells includes numerous mitochondria, Golgi bodies and microtubules. The small lumen, located eccentrically within the organ, contains concentrically layered electron-dense material resembling cuticle.Each hypocerebral organ is enclosed by a layer of extracellular matrix continuous with that surrounding the adjacent cerebral ganglion. There are no nerve connections between ganglion and organ, but cellular connections traverse the intervening matrix and could serve as a communication pathway. The ultrastructure of the hypocerebral organs indicates that they are glands.     

The infundibular organ of the lancelet (Branchiostoma lanceolatum,Acrania): an immunocytochemical study

Reissner's fibers are secretions produced by different ependymal areas of the chordate brain, viz., in adult vertebrates, by the dorsal subcommissural organ, and in all stages of cephalochordates (Branchiostoma lancelets), by the ventral infundibular organ. Fibers produced by these different organs are seemingly identical and the two fiber sources also share some immunocytochemical and lectin-binding properties. The secretions in these two glands are, however, not identical; the infundibular organ cells are strongly reactive with antibodies against vertebrate Reissner's fibers, but they do not react with antibodies raised against the source of the vertebrate fibers, viz., the subcommissural organ. The results support the possibility that, in adult vertebrates, the Reissner's fibers are composed of material not only from the subcommissural organ, but also from another, not yet identified, source that is identical or equivalent to the infundibular organ of the lancelet. There are indications that the infundibular organ is immunocytochemically closely akin to some secretory cells in the vertebrate embryonic brain and also to those that produce the juvenile vertebrate Reissner's fibers, viz., secretory cells in the flexural organ.