Morphology of the haemolymph vascular system in Tanaidacea and Cumacea: - implications for the relationships of "core group" Peracarida (Malacostraca; Crustacea)

Tanaidacea and Cumacea are crucial for understanding the phylogenetic relationships of "core group" peracarids. Here, the haemolymph vascular system in three tanaidacean and four cumacean species was studied on the basis of histological sections and 3D reconstruction. The circulatory organs in Tanaidacea include a tubular heart which extends through most of the thorax. It is extended into the cephalothorax by an anterior aorta. Haemolymph enters the heart through one to two pairs of incurrent ostia. Up to five pairs of cardiac arteries emanate from the heart to supply viscera in the body cavity. In the anterior cephalothorax, the aorta forms a pericerebral ring from which the arteries for the brain and the antennae branch off. In Cumacea, the heart is shorter but more voluminous. In all cumaceans studied, five pairs of cardiac arteries supply the thoracopods and the pleon. The single pair of ostia is situated in the centre of the heart. The anterior aorta runs into the anterior cephalothorax where it supplies the brain and antennae. This paper provides a general comparative discussion of all available data from the literature and the data provided herein. In certain details, the haemolymph vascular system of the Tanaidacea resembles that of Amphipoda, and some correspondences between Cumacea and Isopoda are pointed out. These findings might support a closer relationship between the latter two taxa while they show no support for an amphipod/isopod clade.     

The circulatory system in Phreatoicidea: implications for the isopod ground pattern and peracarid phylogeny

The circulatory systems of four species of Phreatoicidea and two species of Oniscidea were studied on the basis of serial semi-thin sections and a corrosion cast method. A 3D computer reconstruction was used to visualize the circulatory organs in the head of the Phreatoicidea. In the Phreatoicidea, the circulatory system consists of a longitudinal dorsal heart extending from the third thoracic to the border between the fourth and fifth pleonal segments. It is equipped with two pairs of asymmetrically arranged ostia, while five pairs of lateral cardiac arteries and an unpaired anterior aorta extend from the heart. Entering the head, the aorta is accompanied by the two first lateral arteries, which supply the muscles of the mandibles. Four pairs of arteries branch off the aorta to supply both pairs of antennae, the eyes, and sinuses in the head. In addition, several minute capillaries extend from the aorta to supply the brain. The two oniscidean species were re-investigated with regard to some characters which have been controversially discussed. In these species, the heart extends from the border between the fifth and sixth thoracic segments to the fifth pleonal segment. Five pairs of lateral cardiac arteries and the unpaired anterior aorta lead off the heart. A ventral vessel was not observed. The ground pattern of the circulatory system in isopods is reconstructed with greater reliability through optimisation of its characters based on proposed phylogenetic relationships. The results do not support a phylogenetic position of the Isopoda as basal Peracarida or even basal Eumalacostraca.     

The circulatory system in Mysidacea--implications for the phylogenetic position of Lophogastrida and Mysida (Malacostraca, Crustacea)

The morphology of the circulatory organs in Mysida and Lophogastrida (traditionally combined as Mysidacea) is revisited investigating species so far unstudied. In addition to classical morphological methods, a newly developed combination of corrosion casting with micro computer tomography (MicroCT) and computer aided 3D reconstructions is used. Lophogastrida and Mysida show a highly developed arterial system. The tubular heart extends through the greater part of the thorax and is connected with the ventral vessel via an unpaired descending artery. It is suggested that a distinct ostia pattern supports the monophyly of Mysidacea. The cardiac artery system is more complex in Lophogastrida than in Mysida, consisting of up to 10 pairs of arteries that supply the viscera. In both taxa, an anterior and posterior aorta leads off the heart. In the anterior part of the cephalothorax the anterior aorta forms dilations into which muscles are internalized; these structures are called myoarterial formations. One of these myoarterial formations can also be found in all the other peracarid taxa but not in other Malacostraca.     

Comparative morphology of the hemolymph vascular system in scorpions--a survey using corrosion casting, MicroCT, and 3D-reconstruction

Although scorpions are one of the better known groups of Arthropoda, detailed knowledge of their anatomy remains superficial. This contribution presents the first comprehensive investigation of the gross morphology of the scorpion vascular system, based on a survey of species representing all major lineages of the order, using classical and modern non-destructive techniques in combination with three-dimensional reconstruction. The investigation reveals that the hemolymph vascular system (HVS) of Scorpiones comprises a central pumping heart which extends the entire length of the mesosoma and is enclosed in a pericardium. Several arteries branch off the heart to supply different organs and body regions. Two different anterior aorta major branching patterns are identified among the species investigated. Arteries that branch off the anterior aorta system supply the appendages (chelicerae, pedipalps, and walking legs) and the central nerve mass with a complex arterial network. This study of the HVS of scorpions provides further evidence that the vascular systems of euarthropods can be highly complex. Use of the term "open circulatory system" within arthropods is re-emphasized, as it refers to the general organization of the body cavity (i.e. mixocoely) rather than to the complexity of the circulatory system.     

树鼩(Tupaia belangeri chinensis)的脑底动脉环

用25只树鼩,从升主动脉灌注带色的橡胶乳液,在解剖显微镜下进行解剖观察,用目测微尺进行测量。大多数树鼩(22只)有完整的脑底动脉环。由左、右大脑前动脉向内侧各发一前交通动脉组成大脑前总动脉。前交通动脉口径为大脑前动脉的75～85％。后交通动脉口径与大脑后动脉相近,连于颈内动脉与大脑后动脉(基底动脉的分支)之间。测量了组成脑底动脉环有关动脉的口径。由于后交通动脉足够粗大,只有中断左、右颈总动脉和左、右椎动脉,才能造成全脑缺血。     

A radiological study of the central circulation in the lungfish, Protopterus aethiopicus

The dipnoan heart is only in part structurally developed to support a separated circulation in pulmonary and systemic circuits. In the present investigation biplane angiocardiography has been used to describe the extent of such a double circulation and the factors which may modify it in the African lungfish, Protopterus aethiopicus. Contrast injections in the pulmonary vein revealed a clear tendency for aerated blood returing from the lungs to be selectively dispatched to the anterior branchial arteries giving rise to the major systemic circulation. Contrast injections in the vena cava delineated the sinus venosus as a large receiving chamber for systemic venous blood. Contraction of the sinus venosus discharged blood into the right, posterior part of the partially divided atrial space. Contrast injection in the pulmonary vein showed that vessel to pass obliquely from right to left such that blood was emptied distinctly into the left side of the atrium. During contraction the atrial space tended to retain a residual volume in its anterior undivided part which minized mixing. Ventricular filling occurred through separate right and left atrio-ventricular connections. Right-left separation in most of the ventricle was maintained by the partial ventricular septum, the trabeculated, spongelike myocardium and the mode of inflow from the atria. Mixing in the anterior undivided portion of the ventricle during the ejection phase was slight due to a streamlined ejection pattern. The outflow through the bulbus cordis occurred in discrete streams which in part were structurally separated by well developed spiral folds. In the anterior bulbus segment the spiral folds are fused and make completely separate dorsal and ventral outflow tracts. The ventral bulbus channel provides blood to the three anterior branchial arteries. The second and third branchial arteries are large and represent direct shunts to the dorsal aorta. The fourth and fifth branchial arteries are gill bearing and receive blood form the dorsal bulbus channel. The most posterior epibranchial vessels give rise to the pulmonary arteries.     

Homeotic selector genes control the patterning of seven-up expressing cells in the Drosophila dorsal vessel

The linear cardiac tube of Drosophila, the dorsal vessel, is an important model organ for the study of cardiac specification and patterning in vertebrates. In Drosophila, the Hox segmentation gene abdominal-A (abd-A) is required for the specification of a functionally distinct heart region at the posterior of the dorsal vessel, from which blood is pumped anteriorly through a tube termed the aorta. Since we have previously shown that the posterior part of the aorta is specified during embryogenesis to form the adult heart during metamorphosis, we determined if the embryonic aorta is also patterned by the function of Hox segmentation genes. Using gain- and loss-of-function experiments, we demonstrate that the three Hox genes expressed in the posterior aorta and heart are sufficient to confer heart or posterior aorta fate throughout the dorsal vessel. Additionally, we demonstrate that Ultrabithorax and abd-A, but not Antennapedia, function to control cell number in the dorsal vessel. These studies add robustness to the model that homeotic selector genes pattern the Drosophila dorsal vessel, and further extend our understanding of how the cardiac tube is patterned in animal models.     

Review of the Australian hagfishes with description of two new species of Eptatretus (Myxinidae)

This paper revises and updates taxonomic and distributional information about hagfishes (Myxinidae) from Australia. It covers five species of the genus Eptatretus: Eptatretus cirrhatus known from eastern Australia and also distributed around New Zealand, Eptatretus longipinnis endemic to South Australia, Eptatretus strahani originally described from the Philippines and reported here as a new record from Western Australia and two new species described herein as Eptatretus alastairi and Eptatretus gomoni, both from Western Australia. Eptatretus alastairi is distinguished from all congeners by the unique combination of the following characters: six pairs of gill pouches; three‐cusp multicusps on the anterior and posterior rows of cusps; anterior unicusps 9–12; posterior unicusps 8–11; total cusps 48–56; prebranchial pores 13–16; branchial pores 5–6; trunk pores 50–55; tail pores 11–13; total pores 83–88; two bilaterally symmetrical nasal‐sinus papillae in the dorsal surface of the nasal sinus. Eptatretus gomoni is distinguished from all congeners by the unique combination of the following characters: eight pairs of gill pouches; three‐cusp multicusps on the anterior and two‐cusp multicusps on the posterior row of cusps; anterior unicusps 10–11; posterior unicusps 9–10; total cusps 50; prebranchial pores 12–13; branchial pores 7–8; trunk pores 57–58; tail pores 14–15; total pores 91–93; no nasal‐sinus papillae. An identification key for the Australian species of Eptatretus is also provided.     

SALMFamide2 and serotonin immunoreactivity in the nervous system of some acoels (Xenacoelomorpha)

Acoel worms are simple, often microscopic animals with direct development, a multiciliated epidermis, a statocyst, and a digestive parenchyma instead of a gut epithelium. Morphological characters of acoels have been notoriously difficult to interpret due to their relative scarcity. The nervous system is one of the most accessible and widely used comparative features in acoels, which have a so‐called commissural brain without capsule and several major longitudinal neurite bundles. Here, we use the selective binding properties of a neuropeptide antibody raised in echinoderms (SALMFamide2, or S2), and a commercial antibody against serotonin (5‐HT) to provide additional characters of the acoel nervous system. We have prepared whole‐mount immunofluorescent stainings of three acoel species: Symsagittifera psammophila (Convolutidae), Aphanostoma pisae, and the model acoel Isodiametra pulchra (both Isodiametridae). The commissural brain of all three acoels is delimited anteriorly by the ventral anterior commissure, and posteriorly by the dorsal posterior commissure. The dorsal anterior commissure is situated between the ventral anterior commissure and the dorsal posterior commissure, while the statocyst lies between dorsal anterior and dorsal posterior commissure. S2 and serotonin do not co‐localise, and they follow similar patterns to each other within an animal. In particular, S2, but not 5‐HT, stains a prominent commissure posterior to the main (dorsal) posterior commissure. We have for the first time observed a closed posterior loop of the main neurite bundles in S. psammophila for both the amidergic and the serotonergic nervous system. In I. pulchra, the lateral neurite bundles also form a posterior loop in our serotonergic nervous system stainings.     

Surface ultrastructure of the plagiorchid trematode Glossidium pedatum Looss, 1899 from bagrid fish in Egypt

The present study concerned the morphology and surface ultrastructure of a plagiorchid, Glossidium pedatum, from bagrid fish of the river Nile in Egypt. Adult G. pedatum have an elongate body, tapered towards the anterior and posterior ends. Their oral sucker is small, sub‐terminal and rounded, measuring 0.200 mm in diameter. Sensory papillae around the oral sucker usually occur in small clusters of three to eight each. The ventral sucker is large, situated at the anterior end of the second third of the body, 0.299 mm in diameter, and is surrounded by three pairs of sensory papillae. Both suckers have rounded rims covered by tegumental spines. On the anterior part of the ventral surface of the body tegumental spines are small, pointed and closely spaced. A small triangular area of tegument anterior to the ventral sucker is devoid of spines. Tegumental spines on the mid‐region of the body slightly increase in size and number, especially towards the lateral aspects and posterior to the ventral sucker. Towards the posterior end of the body the spines progressively decrease in both size and number. The dorsal side exhibits similar surface features but the spines are less numerous and slightly smaller.     

Functional morphology of the heart and of a new cephalic pulsatile organ in the blowfly Calliphora vicina (Diptera: Calliphoridae) and their roles in hemolymph transport and tracheal ventilation

In the blowfly Calliphora vicina (Diptera: Calliphoridae), the morphology of the dorsal vessel and of a new cephalic accessory pulsatile organ (CPO) were analysed with light-microscopic, SEM and TEM techniques. The CPO and neck aorta are reconstructed 3-dimensionally by computer-aided design. The pulse activity of the CPO and of the heart was measured in intact flies over periods of several hours or days using contact-thermography with laser beam heat-marking. The intratracheal pressure was simultaneously measured at the anterior thoracic spiracle. The dorsal vessel is constructed of pairs of left–right alternating cells. Its enlarged chamber in the anterior abdomen contains two pairs of incurrent ostia, its posterior narrower heart tube possesses three pairs of incurrent ostia and paired caudal excurrent openings. The aorta opens with a funnel-like opening in the neck. Proportions, arrangement and ultrastructure of the aorta, heart cells and pericardial muscles are described. Cushionlike sarcoplasmic protrusions of heart cells (pair no. 17) probably function as internal valves. The neck aorta is constructed of a cuticular ‘roof’ deviating from the dorsal neck membrane and a ventral longitudinal muscle ‘floor’. The aorta is not kept open because of missing muscle or connective tissue strands. The underside of the CPO is fused with air sacs that function as antagonists to the muscles. The heart reverses its beat periodically in resting and active flies. During the longer forward-pulse periods, mean frequency is lower (about 3.0 Hz at Ta 20°C), during the shorter backward periods mean frequency is higher (4.6 Hz). The CPO beats only during forward-pulse periods of the heart with an independent and slower pulse rate (1.8 Hz). The CPO-pulses produce positive pressure pulses at the anterior thoracic spiracle. During backward-pulse periods of the heart and pulse pause of the CPO, a continuous negative pressure arises at the thoracic spiracle instead of pressure pulses. The intimate connection of an accessory pulsatile organ with tracheal air sacs makes it work as a bifunctional pump for hemolymph distribution and tracheal ventilation. Neurosecretory and synapsing innervation of the CPO in connection with aorta, heart and pericardial septum muscle innervation suggest that both organs are regulated and that the duration of their periods is neuronally coordinated.     

Morphological analysis of the hagfish heart. I. The ventricle,the arterial connection and the ventral aorta

We have studied the heart in three species of hagfish: Myxine glutinosa, Eptatretus stoutii, and Eptatretus cirrhatus and report about the morphology of the ventricle, the arterial connection and the ventral aorta. On the whole, the hagfish heart lacks outflow tract components, the ventricle and atrium adopt a dorso‐caudal rather than a ventro‐dorsal relationship, and the sinus venosus opens into the left side of the atrium. This may indicate a “defective” cardiac looping during embryogenesis. The ventral aorta is elongated in M. glutinosa and E. stoutii but sac‐like in E. cirrhatus. The ventricles are entirely trabeculated. The myocytes show a low myofibrillar content and junctional complexes formed by fascia adherens and desmosomes. Gap junctions could not be demonstrated. Myocardial cells in M. glutinosa contain numerous lipid droplets. These droplets are less numerous in E. stoutii and practically absent in E. cirrhatus, suggesting different metabolic requirements. Other cell types present in the ventricle are chromaffin cells and granular leukocytes that contain rod‐shaped granules. The ventricle‐aorta connection is guarded by a bicuspid valve with left and right, pocket‐like leaflets. The leaflets extend from the cranial end of the ventricle into the aorta but the junction is asymmetrical. This junction contains a ganglion‐like structure in E. cirrhatus. The ventral aorta shows endothelial, media, and adventitial layers. The media contains smooth muscle cells surrounded by dense bands formed by tightly‐packed extracellular filaments. In addition, a short number of elastic fibers are observed in M. glutinosa and E. stoutii. Cellular and extracellular elements are more loosely organized in the aorta of E. cirrhatus. The collagenous adventitia contains ganglion‐like cells in the three species. In the absence of nerves, chromaffin and ganglion‐like cells may control the activity of the myocardium and that of the aortic smooth muscle cells, respectively. J. Morphol. 277:326–340, 2016. © 2015 Wiley Periodicals, Inc.     

Evolutionary morphology of the circulatory system in Peracarida (Malacostraca; Crustacea)

We demonstrate that by formulating guidelines for evolutionary morphology the transparency, reproducibility, and intersubject testability of evolutionary hypotheses based on morphological data can be enhanced. The five main steps in our concept of evolutionary morphology are (i) taxon sampling, (ii) structural analysis, (iii) character conceptualization, (iv) phylogenetic analysis, and (v) evolutionary interpretation. We illustrate this concept on the example of the morphology of the circulatory organs in peracarid Malacostraca. The analysis is based on recently published accounts in which detailed structural analyses were carried out, and on the older literature. Detailed conceptualizations of 22 characters of the circulatory system are given for 28 terminals. In a further step these characters are included in a recently revised matrix, resulting in 110 characters. The resulting parsimony analysis yielded a single most parsimonious tree with a length of 309 steps. The most significant results are that Peracarida is monophyletic, Amphipoda is the sister taxon to the Mancoida sensu stricto, the relict cave‐dwelling taxa Thermosbaenacea, Spelaeogriphacea, and Mictocarididae form a monophylum and Tanaidacea is the sister group to a monophylum comprising Cumacea and Isopoda. The evolutionary analysis shows that the ground pattern features of the circulatory organs in Peracarida are a tubular heart extending through the whole thorax, a posterior aorta with lateral arteries, and a ventral vessel system. Important features within the Peracarida are the backward shift of the anterior border of the heart, the reduction of the ventral vessel system, and two patterns of cardiac arteries, one common to the amphipod and tanaidacean terminals, and one to the cumacean and isopod terminals. © The Willi Hennig Society 2009.     

A new subterranean amphipod (Crustacea: Gammaridea: Niphargidae) from southern Ireland, 'with comments on its taxonomic position and the validity of the genus Niphargellus ScheOenberg.

The subterranean amphipod Niphargus vuexfordensis/i> sp. nov. (Amphipoda: Gammaridea: Niphargidae) is described and figured from a well at Kerloge, County Wexford in southern Ireland. The taxonomic position of this species is analysed and its relationship to the controversial genus Niphargellus Schellenberg discussed.     

Description of a new cryptic,shallow‐water tonguefish (Pleuronectiformes: Cynoglossidae: Symphurus) from the western North Pacific Ocean

Combined results based on morphological characters and analyses of partial sequences of the 16s rRNA and coI genes confirm the validity of a new, cryptic, symphurine tonguefish from the western North Pacific Ocean. Symphurus leucochilus n. sp., a diminutive species reaching sizes to c. 67 mm standard length, is described from nine specimens that were collected from fish‐landing ports and from trawls made at c. 150 m off Taiwan and Japan. Symphurus leucochilus shares many similar features with those of Symphurus microrhynchus and that of several undescribed species that are morphologically similar to S. microrhynchus. Symphurus leucochilus has also been misidentified as Symphurus orientalis in fish collections because of shared similarities in some aspects of their morphology. The new species differs from all congeners by the following combination of meristic, morphological and pigmentation features: a predominant 1–2–2–2–2 pattern of interdigitation of proximal dorsal‐fin pterygiophores and neural spines; 12 caudal‐fin rays; 89–92 dorsal‐fin rays; 76–80 anal‐fin rays; 49–51 total vertebrae; four hypurals; 75–83 longitudinal scale rows; 32–35 transverse scales; 15–17 scale rows on the head posterior to the lower orbit; absence of a fleshy ridge on the ocular‐side lower jaw and a membranous connection between the anterior nostril and lower part of the eye; a narrow interorbital space and dorsal‐fin origin anterior to the vertical through the anterior margin of the upper eye; absence of both dermal spots at bases of anterior dorsal‐fin rays and melanophores on the isthmus; uniformly yellow to light‐brown ocular‐side colouration without bands; dorsal and anal fins with alternating series of dark rectangular blotches and unpigmented areas; a uniform white blind side and a bluish‐black peritoneum. Despite overall similarities in morphology between S. leucochilus and S. orientalis, as well as between two of the nominal species morphologically similar to S. microrhynchus, analyses of partial 16s rRNA and coI gene sequences show that S. leucochilus, S. orientalis and the two other nominal species represent three distinct lineages within the genus Symphurus.     

Scanning electron microscopy of the dorsal vessel of Panstrongylus megistus (Burmeister, 1835) (Hemiptera: Reduviidae).

In this study we analyzed the microanatomy of the dorsal vessel of the triatomine Panstrongylus megistus. The organ is a tubule anatomically divided into an anterior aorta and a posterior heart, connected to the body wall through 8 pairs of alary muscles. The heart is divided in 3 chambers by means of 2 pairs of cardiac valves. A pair of ostia can be observed in the lateral wall of each chamber. A bundle of nerve fibers was found outside the organ, running dorsally along its major axis. A group of longitudinal muscular fibers was found in the ventral portion of the vessel. The vessel was found to be lined both internally and externally by pericardial cells covered by a thin laminar membrane. Inside the vessel the pericardial cells were disposed in layers and on the outside they formed clusters or rows.