Ultrastructure of the nephrostome in Enchytraeus albidus (Annelida, Clitellata)

 The nephrostome of Enchytraeus albidus exhibits a longitudinal slit-like opening on the dorsal side of a bulbous organ which is mainly composed of three cells, one flame cell situated centrally and endowed with a ciliary flame, and two cells lying superficially, called the mantle cell and the accessory mantle cell. The mantle cell occupies the ventral side of the organ extending on both sides up to the opening to constitute its immediate border on the frontal and lateral sides. Here it forms a kind of crest which is heavily subdivided into many protrusions and infoldings endowed with long cilia which exclusively spread into the coelomic cavity. The accessory mantle cell borders the narrow posterior slit of the opening, forming the roof of the initial canal which is devoid of cilia. From its anterior region a projection arises extending above the opening. The flame cell forms a groove from which the ciliary flame arises which extends into the canal. At its posterior region it replaces the accessory mantle cell displacing it onto the dorsal surface of the organ. It is argued that the mantle cell and the accessory mantle cell have presumbly originated from coelothelial cells. Thus the metanephridium may be a composite organ developing from a nephridioblastic and a coeloblastic source. A discussion of results in other annelid species indicates that metanephridia in the Annelida may have evolved more than once. Accepted: 13 October 1997     

小地老虎成虫循环系统形态的初步研究

本文对小地老虎Agrotis ypsilon 成虫循环系统的形态作了初步研究,表明背血管由6个心室的心脏和倒V形的胸部大血管及头部分支的大血管组成.中胸辅搏动器很发达,与大血管的腔直接相连,具有一个小盾片腔前半部的肌肉搏动膜.后胸辅搏动器很小,与背血管无直接通道,具有一个没有肌肉的搏动膜.腹膈显著,具有翼肌.还描述了心脏和辅搏动器的搏动情形.     

黄鳝的泌尿系统及其功能

黄鳝腹腔左侧有盲端的中空管状结构,不是退化性腺,而是十分特化的长管囊膀胱。膀胱内壁具大量发达的绒毛,绒毛表面是移行上皮。在绒毛内部或基部有丰富的血管,因此该管囊膀胱不仅可贮存尿液,而且可能对水分等有重吸收作用。在中肾管与膀胱相接处,膀胱腔背侧出现一条明显的纵行皱襞,即在其横切面上观为巨绒毛。巨绒毛形成的原因,主要是中肾管移入膀胱壁所致。中肾管在巨绒毛内移行一程后才开口于膀胱。因此,黄鳝的生殖腺不是一对,而是一个,位于腹腔右侧。黄鳝肾脏细长,呈“丫”,在腹腔背侧,紧贴脊椎。前端为头肾,无肾单位,仅是造血器官。中肾有类似于哺乳类的肾小体,但数量较少,主要分布在肾脏周缘。肾小管包括颈段、初级近曲小管、次级近曲小管、初级远曲小管和次级远曲小管。两中肾管位于两肾叶腹内侧,其上皮间或是假复层柱状上皮,间或是移行上皮。前者含有许多杯状细胞,并可见到顶浆分泌的现象。中肾的肾小管间组织是大量的红细胞样组织,头肾似具有贮存或释放刚成熟的红细胞的组织结构,因此黄鳝肾脏可能是体内主要的造血器官。     

The scolopidial accessory organ in the Jerusalem cricket (Orthoptera: Stenopelmatidae)

Multiple mechanosensory organs form the subgenual organ complex in orthopteroid insects, located in the proximal tibia. In several Ensifera (Orthoptera), a small chordotonal organ, the so-called accessory organ, is the most posterior part of this sensory complex. In order to document the presence of this accessory organ among the Ensifera, the chordotonal sensilla and their innervation in the posterior tibia of two species of Jerusalem crickets (Stenopelmatidae: Stenopelmatus) is described. The sensory structures were stained by axonal tracing. Scolopidial sensilla occur in the posterior subgenual organ and the accessory organ in all leg pairs. The accessory organ contains 10–17 scolopidial sensilla. Both groups of sensilla are commonly spatially separated. However, in few cases neuronal fibres occurred between both organs. The two sensillum groups are considered as separate organs by the general spatial separation and innervation by different nerve branches. A functional role for mechanoreception is considered: since the accessory organ is located closely under the cuticle, sensilla may be suited to detect vibrations transferred over the leg's surface. This study extends the known taxa with an accessory organ, which occurs in several taxa of Ensifera. Comparative neuroanatomy thus suggests that the accessory organ may be conserved at least in Tettigoniidea.     

Emerging views on the distinct but related roles of the main and accessory olfactory systems in responsiveness to chemosensory signals in mice

In rodents, the nasal cavity contains two separate chemosensory epithelia, the main olfactory epithelium, located in the posterior dorsal aspect of the nasal cavity, and the vomeronasal/accessory olfactory epithelium, located in a capsule in the anterior aspect of the ventral floor of the nasal cavity. Both the main and accessory olfactory systems play a role in detection of biologically relevant odors. The accessory olfactory system has been implicated in response to pheromones, while the main olfactory system is thought to be a general molecular analyzer capable of detecting subtle differences in molecular structure of volatile odorants. However, the role of the two systems in detection of biologically relevant chemical signals appears to be partially overlapping. Thus, while it is clear that the accessory olfactory system is responsive to putative pheromones, the main olfactory system can also respond to some pheromones. Conversely, while the main olfactory system can mediate recognition of differences in genetic makeup by smell, the vomeronasal organ (VNO) also appears to participate in recognition of chemosensory differences between genetically distinct individuals. The most salient feature of our review of the literature is that there are no general rules that allow classification of the accessory olfactory system as a pheromone detector and the main olfactory system as a detector of general odorants. Instead, each behavior must be considered within a specific behavioral context to determine the role of these two chemosensory systems. In each case, one system or the other (or both) participates in a specific behavioral or hormonal response.     

Spermatogenesis inPlatynereis massiliensis (Polychaeta: Nereidae)

Stage 1 of spermatogenesis in the protandrous polychaetePlatynereis massiliensis is represented by clusters of about 60 spermatogonia which appear in the coelomic cavity. There are no testes inP. massiliensis. The origin of the spermatogonial clusters is not known. Subclusters of approximately 20 primary spermatocytes each represent stage 2. The appearance of synaptonemal figures in the spermatocyte nuclei marks the beginning of stage 3. Cells tend to lose their tight packing during stage 3 but interdigitate with cellular processes. Then very small subclusters of 4 to 8 spermatocytes appear. Meiosis is completed during stage 4, giving rise to secondary spermatocytes and then to spermatid tetrads. Spermatogonia and primary spermatocytes are interconnected by structurally specialized fusomes while secondary spermatocytes and spermatids, which are also in cytoplasmic continuity, show rather simple cell bridges. Synthesis of acrosomal material starts during stage 2. During spermiogenesis the proacrosomal vesicles of Golgi origin travel from the posterior part of the cell to its anterior part to form the acrosome proper. Acrosome formation, nuclear condensation, shaping of the long and slender sperm nucleus, and development of the sperm tail are the main events during spermiogenesis. Sperm morphology is briefly discussed wity respect to its phylogenetic bearings.     

The septal organ of the rat during postnatal development

The septal organ of Masera (SO) is a small, isolated patch of olfactory epithelium, located in the ventral part of the nasal septum. We investigated in this systematic study the postnatal development of the SO in histological sections of rats at various ages from the day of birth (P1) to P666. The SO-area increases to a maximum at P66-P105, just as the animals reach sexual maturity, and decreases thereafter, significantly however only in males, indicating a limited neurogenetic capacity for regeneration. In contrast, the main olfactory epithelium area continues to expand beyond P300. The modified respiratory epithelium ('zwischen epithelium') separating the SO and the main olfactory epithelium contains a few olfactory neurons up to age P66. Its length increases postnatally so that the SO becomes more ventral to the OE. Although the position of the SO relative to other anatomical landmarks changes with development it is consistently located just posterior to the opening of the nasopalatine duct (NPAL). Thus, a possible function of the SO is in sensing chemicals in fluids entering the mouth by licking and then delivered to the nasal cavity via the NPAL; therefore the SO may be involved in social/sexual behavior as is the vomeronasal organ (VNO). We suggest that the SO is a separate accessory olfactory organ with properties somewhat different from both OE and VNO and may exist only in species where the NPAL does not open into the VNO.     

Early segregation of the adrenal cortex and gonad in chicken embryos

The adrenal gland is an endocrine organ that plays essential roles in stress responses. This organ consists of two types of tissues, adrenomedulla and adrenocortex, deriving from different embryonic origins. Whereas it is well accepted that the adrenomedulla derives from neural crest cells, the origin of the adrenocortex remains elusive. In addition, the adrenocortex and gonads, two major steroid hormone‐producing tissues, have been thought to share the same origin, although the experimental evidence is lacking. In this study, to identify the origin of adrenocortex and to compare it to that of gonads, we scrutinized the medial portion of the coelomic epithelium (CE) after the lateral plate mesoderm has split into two CE components with a concomitant opening of the coelomic cavity in between them. We found that early medial CE consists of a two‐cell layer‐thick band of epithelial‐like cells, the outer and inner CEs. The outer CE faces the coelomic cavity, whereas the inner CE is juxtaposed to nascent blood vessels. Combining direct cell labeling with early molecular markers, we found that outer CE was the origin of the gonad but not the adrenocortex. The adrenocortex, instead, appears to derive from inner CE. Thus, the adrenocortical and gonadal progenitors are already segregated from each other when the coelomic cavity has opened. This study provides a new basis for understanding how the adrenal gland forms and how steroid hormone‐producing tissues arise during development.     

The accessory organ,a scolopidial sensory organ,in the cave cricket Troglophilus neglectus (Orthoptera: Ensifera: Rhaphidophoridae)

Mechanoreceptor organs occur in great diversity in insect legs. This study investigates sensory organs in the leg of atympanate cave crickets (Troglophilus neglectus KRAUSS, 1879) by neuronal tracing. Previously, the subgenual and the intermediate organs were recognised in the subgenual organ complex, lacking the tympanal membranes present for example in the tibial hearing organs of Gryllidae and Tettigoniidae. We document the presence of the accessory organ in T. neglectus. This scolopidial organ is located in the posterior tibia close to the subgenual organ and can be identified by position, innervation and orientation of the dendrites of sensory neurons. The main motor nerve in the leg innervates a part of the subgenual organ and the accessory organ. The dendrites of sensory neurons in the accessory organ are characteristically bent in proximo‐dorsal direction, while the subgenual organ dendrites run distally along the longitudinal axis of the leg. The accessory organ contains 6–10 scolopidial sensilla, and no differences in neuroanatomy occur between the three thoracic leg pairs. Hence, the subgenual organ complex in cave crickets is more complex than previously known. The wider taxonomic distribution of the accessory scolopidial organ among orthopteroid insects is inconsistent, indicating its repeated losses or convergent evolution.     

The Development of the Brachiopod Crania (Neocrania) anomala (O. F. Müller)and its Phylogenetic Significance

The freely spawned eggs of Crania go through radial cleavage, embolic gastrulation, and the posteroventral part of the archenteron forms mesoderm through modified enterocoely. The blastopore closes in the posterior end of the larva. The ciliated, lecithotrophic larva has four pairs of coelomic pouches and three pairs of dorsal setal bundles. At metamorphosis, the larva curls ventrally by contraction of a pair of midventral muscles, which are extensions of the first pair of coelomic sacs; the larva attaches by the epithelium just behind the closed blastopore. The brachial valve is secreted by the middle part of the dorsal epithelium and the pedicle valve is secreted by the attachment epithelium. The second pair of coelomic sacs develop small attachment areas at the edge of the dorsal valve and become the lophophore coelom (mesocoel); the third pair of coelomic sacs become the body coelom (metacoel) with the adductor muscles. The posterior position of the closing blastopore is characteristic of deuterostomes. The ventral curving of the settling larva and the formation of both valves from dorsal epithelial areas indicate that the brachiopods have a very short ventral side as opposed to the phoronids. It is concluded that both groups have originated from a creeping ancestor with a straight gut.     

Ultrastructure and formation of the body cavity lining in Phoronis muelleri (Phoronida, Lophophorata)

Among other characteristics a trimeric coelomic compartmentation consisting of an anterior protocoel, followed by a mesocoel and a posterior metacoel is traditionally believed to substantiate the sister-group relationship between Lophophorata and Deuterostomia, together forming the Radialia. As molecular data cannot support this hypothesis a reanalysis of the coelomic cavities in Phoronida is undertaken, because corresponding coelomic compartmentation is widely accepted to support the Radialia hypothesis. A coelomic cavity can be recognized on the ultrastructural level because its lining is a true epithelium with polarized cells interconnected by apical adherens junctions. This study reveals that neither in larval nor adult Phoronis muelleri (Phoronida) an anterior cavity with such a lining is present. What on the light microscopic level leads to the impression of a cavity inside the larval episphere, actually is an enlarged subepidermal extracellular matrix with an amorphous, presumably gel-like filling, into which several muscle cells are embedded. Larvae, thus, possess only one coelomic cavity, the large trunk coelom of the larva which is adopted in the adult organization. The second coelomic cavity of adult P. muelleri, the lophophore coelom, develops as a double-layer of epithelialized mesodermal cells at the base of the adult tentacle buds and becomes fluid filled during metamorphosis. Like the larval episphere, larval tentacles and most parts of the blastocoel are filled by an amorphous matrix. Reanalysis of the literature and comparison with Brachiopoda and Bryozoa allows the hypothesis that a protocoel is lacking in all Lophophorata, and that merely two unpaired coelomic cavities, one tentacle and one trunk coelom, can be assumed for the ground pattern of this taxon. These results do not provide further evidence for the Radialia hypothesis, but also do not contradict it. Accepted: 28 August 2000     

Anatomic,Histologic and Certain Enzymatic Studies on the Male Genital Organs of Hemiechinus auritus collaris Gray,the Indian Long Eared Hedgehog

Anatomically the male reproductive organs of Hemiechinus auritus collaris are of considerable interest and present a unique pattern of arrangement of different glands. The testes are inguinal and a true scrotum is absent. A pair of accessory glands, the seminal vesicles, are situated dorsal to the bladder. A pair of obviously lobulated glands, ventral to the bladder, represent the internal prostate and a pair of compact glands situated outside the pelvis in para-anal position the external prostate. The Cowper's gland and the gland of ampulla are absent. The present studies also concern enzymes of the phosphatase group, including both specific and non-specific phosphatases, in the testes and the sex accessory glands during both active and inactive periods in this insectivore.     

Temperature regulation of the testes of the bottlenose dolphin (Tursiops truncatus): evidence from colonic temperatures

Dolphins possess a countercurrent heat exchanger that functions to cool their intra-abdominal testes. spermatic arteries in the posterior abdomen are juxtaposed to veins returning cooled blood from the surfaces of the dorsal fin and flukes. A rectal probe housing a linear array of five copper-constantan thermocouples was designed to measure colonic temperatures simultaneously at positions anterior to, within, and posterior to the region of the colon flanked by the countercurrent heat exchanger. Colonic temperatures adjacent to the countercurrent heat exchanger were maximally 1.3°C cooler than temperatures measured outside this region. Temporary heating and cooling of the dorsal fin and flukes affected temperatures at the countercurrent heat exchanger, but had little or no effect on temperatures posterior to its position. These measurements support the hypothesis that cooled blood is introduced into the deep abdominal cavity and functions specifically to regulate the temperature of arterial blood flow to the dolphin testes.     

The Morphology of the Phoronid Phoronopsis harmeri

We studied the morphology and gross anatomy of the phoronid Phoronopsis harmeriusing light microscopy and scanning electron microscopy. The body of Ph. harmeriis subdivided into several regions: a lophophore, a head, anterior, and posterior parts of the body, and an ampulla. The lophophore is spiral and comprises 0.5 turns. In males, there are lophophoral organs in the tentacular crown; under the lophophore, there is an epithelial fold or collar. The internal organization shows partitioning into three coeloms: the coelom of the epistome, the tentacular coelom, and the trunk coelom. The trunk coelom is divided into a series of chambers by a complex system of mesenteries. The intestine is U-shaped, and the epistome is located above the mouth opening. The circulatory system is closed and consists of the following vessels: the efferent and afferent circular, left and right lateral (efferent), and medial (afferent) vessels. In Ph. harmeri, there is a dorsolateral (afferent) vessel running through the ampulla and the lower part of the posterior trunk region. The excretory system is composed of paired metanephridia that resemble asymmetrical U-shaped tubes. Sexual dimorphism is characteristic of the structure of the distal part of the nephridium, which opens into the body cavity. The nervous system consists of a dorsal nervous field, a circular nerve plexus, and a giant left nerve fiber. Ph. harmeriis a dioecious species; the gametes develop in a vasoperitoneal tissue that envelops the intestine in the posterior part of the trunk region.     

Accessory arteries supplying the human transverse colon

An accessory colic artery which arose from the superior mesenteric artery more proximally than the first jejunal artery and met the marginal artery at the splenic flexure was observed in 32 of 65 subjects (49.2%). Considering its constant morphological features, this accessory colic artery was given the new nomenclature 'superior left colic artery (arteria colica sinistra superior; CSS)'. The unusual middle colic artery arising from the celiac trunk was supposed to be caused by the anastomosis between the dorsal pancreatic artery from the CSS and that from the celiac trunk. An additional epiploic branch derived from the pancreatic branch (posterior epiploic branch) also sent an accessory colic artery in 2 subjects. But judging from its origin and area of distribution which overlaps with that of the middle colic artery, this accessory colic artery is not equivalent to CSS.     

Fine structure of the epistome in Phoronis ovalis: significance for the coelomic organization in Phoronida

Abstract. The hypothesis of a common ancestry of the lophophorate taxa Brachiopoda, Bryozoa, Phoronida, and the Deuterostomia can be traced back to the late 19th century when Masterman recognized a tripartite organization of the body consisting of pro-, meso-, and metasome, along with coelomic body cavities in each compartment, as characteristic for Echinodermata, Pterobranchia, Phoronida, and Brachiopoda. This idea became quite popular under the name "archicoelomate" concept. The organization of the phoronids, and especially of their transparent actinotroch larva, has for a long time been used as a touchstone for the validity of this concept. As a coelomic lining can reliably be recognized only on the ultrastructural level, this technique has been applied for adults of Phoronis ovalis , which is assumed to be a sister species to all other phoronids. Phoronis ovalis contains only two coelomic compartments, a posterior coelom inside the trunk (metasoma), occupying the space between the trunk epidermis and the digestive epithelium, and an anterior lophophoral coelom inside and basal to the tentacular crown (mesosoma). There is no coelomic cavity inside the epistome (prosoma). This part of the body is filled with myoepithelial cells, which are continuous with the epithelial lining of the lophophore cavity. These cells form a lumenless bilayer and possess long, tiny myofilamentous processes, which are completely embedded in an extracellular matrix. A comparison with data on P. muelleri shows that there is no need to assume three different coelomic cavities in Phoronida, in contrast to the predictions of the archicoelomate concept. At least for this taxon, a correspondence to the situation in deuterostomes can hardly be found.     

Olfactory metamorphosis in the coastal tailed frog Ascaphus truei (Amphibia,Anura, Leiopelmatidae)

The structure of the olfactory organ in larvae and adults of the basal anuran Ascaphus truei was examined using light micrography, electron micrography, and resin casts of the nasal cavity. The larval olfactory organ consists of nonsensory anterior and posterior nasal tubes connected to a large, main olfactory cavity containing olfactory epithelium; the vomeronasal organ is a ventrolateral diverticulum of this cavity. A small patch of olfactory epithelium (the “epithelial band”) also is present in the preoral buccal cavity, anterolateral to the choana. The main olfactory epithelium and epithelial band have both microvillar and ciliated receptor cells, and both microvillar and ciliated supporting cells. The epithelial band also contains secretory ciliated supporting cells. The vomeronasal epithelium contains only microvillar receptor cells. After metamorphosis, the adult olfactory organ is divided into the three typical anuran olfactory chambers: the principal, middle, and inferior cavities. The anterior part of the principal cavity contains a “larval type” epithelium that has both microvillar and ciliated receptor cells and both microvillar and ciliated supporting cells, whereas the posterior part is lined with an “adult‐type” epithelium that has only ciliated receptor cells and microvillar supporting cells. The middle cavity is nonsensory. The vomeronasal epithelium of the inferior cavity resembles that of larvae but is distinguished by a novel type of microvillar cell. The presence of two distinct types of olfactory epithelium in the principal cavity of adult A. truei is unique among previously described anuran olfactory organs. A comparative review suggests that the anterior olfactory epithelium is homologous with the “recessus olfactorius” of other anurans and with the accessory nasal cavity of pipids and functions to detect water‐borne odorants. J. Morphol. 2011. © 2011 Wiley Periodicals, Inc.     

The morphology and anatomy of the vestimentiferan worm Oasisia alvinae Jones, 1985 (Annelida: Siboglinidae). III. Coelomic cavity, trophosome and blood, excretory and reproductive systems

This study deals with the organization of the coelom in the all the parts of the body of the vestimentiferan Oasisia alvinae. The localization of the dissepiment between the vestimental and trunk regions in males and females differs. The histological structure and anatomy of the trophosome and the vascular, excretory, and reproductive systems is described. Three cell types are distinguishable in each trophosome lobe. Up to four bacteriocytes could be found in a row from the central blood vessel to the surface of the organ. The main blood vessels in almost all parts of the body have a well-developed muscle sheath and an endothelium that is expressed in varying degrees. In the trunk region, an intravasal body, which is represented by two modifications, is observed in the dorsal blood vessel. The excretory tree is located under the brain. The reproductive system is symmetrical in males and dissymmetrical in females. The gonoducts of females are extensive; in males, they are short and open in the front part of the reproductive coelom. The genital coeloms of both sexes perform the functions of gamete production and storage.     

Reproductive anatomy of the Australian grayling, Prototroctes maraena Gunther

Gross anatomy of Australian grayling testes showed progressive enlargement from March to the peak of the spawning season in late April–early May. The single, left testis changed from a flat, translucent wisp of tissue consisting of an anterior and posterior lobe connected by a thin filament to a three-dimensional mass of milky-white tissue which filled the coelomic cavity. Spawning lasted 2 weeks and testicular regression was apparent by 8 May when the bilobed condition of the testis was noted. The testis cleared rapidly and resembled pre-spawning conditions by mid-June. Histological examination revealed that Australian grayling testes follow the pattern of teleost spermatogenesis whereby clusters of spermatogonia arise from resting germ cells and all of the cells within a given cluster mature at approximately the same time.
The single left ovary of Australian grayling females showed a similar pattern of development, filling the body cavity with an average of 47 000 eggs of 0.9 mm diameter by late April–early May. Females exhibited swollen genital vents near spawning and males developed breeding tubercles which are illustrated by scanning electron micrograph.     

Sex Differentiation in Meloidogyne incognita and Anatomical Evidence of Sex Reversal

Sex differentiation was studied by examining the cellular structure of gonad primordia extracted from second-stage juveniles developing under different environmental conditions. In female jnveniles, divisions of the two somatic cells of the primordium occurred in mid-sccond stage and resulted in 12 cells. Two of them were differentiated as cap cells, two occupied the anterior central and eight the posterior central part of the V-shaped primordium. The two germinal cells divided at the 6-8 somatic-cell stage of the primordium; i.e., earlier than in any other plant-parasitic nematode. In male juveniles of similar developmental stage, divisions of somatic cells resulted in 10 cells: one cap cell at the posterior tip and nine cells at the anterior part of the rod-shaped primordium. Germinal cells divided at the 6-8 sontatic-cell stage. On the basis of gonad anatomy it was concluded that some female juveniles undergo sex reversal and proceed with further development as males. The degree of expression of intersexual features depends on the period at which sex reversal occurs. Sex reversal at an early period gives rise to males with one testis, almost indistinguishable front true males. Sex reversal at mid-second stage involves degeneration of the nucleus of one of the cap cells resulting in males with an atrophied testis and a well-developed testis. More delayed sex reversal results in males with two testes of approximately equal size. To explain these patterns of development, it is assumed that sex differentiation is hormonally controlled and that the environment influences hormonal balance by affecting gene expression.