Comparative analysis of the circulatory system in Amphipoda (Malacostraca, Crustacea)

We present data on the haemolymph vascular system (HVS) in four representatives of the major amphipod lineages Gammaridea, Hyperiidea and Caprellidea based on corrosion casting and three‐dimensional reconstructions of histological semi‐thin sections. In all these species the HVS comprises a dorsal pulsatile heart, which is continued in the body axis by the anterior and posterior aortae. The heart is equipped with three pairs of incurrent ostia. The number of cardiac arteries that lead off the heart varies among species: in the studied Gammaridea four pairs occur, in Hyperia galba only the three posterior pairs of cardiac arteries occur, while in Caprella mutica cardiac arteries are absent. In all the studied species the posterior aorta leads as a simple tube into the pleon attached to the dorsal diaphragm. The anterior aorta runs from its origin in the anterior part of the second thoracic segment into the cephalothorax. Both pairs of antennae have an arterial supply off the anterior aorta. An overview of previously studied species including our present findings shows the amphipod HVS to be relatively uniform and the gammarid form is discussed as being closest to the ground pattern of Amphipoda.     

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.     

The circulatory system and its spatial relations to other major organ systems in Spelaeogriphacea and Mictacea (Malacostraca, Crustacea) – a three-dimensional analysis

Spelaeogriphacea and Mictacea are enigmatic taxa within malacostracan crustaceans that play a pivotal role in peracarid phylogeny. Anatomical data on both taxa that are suitable for use in cladistic analyses are still scarce. Here, we provide for the first time detailed three-dimensional information on the major organ systems of Spelaeogriphacea and Mictacea (the circulatory system, the digestive system, and the central nervous system) using semithin sections in combination with computer aided three-dimensional reconstruction techniques. The digestive system in both Spelaeogriphus lepidops and Mictocaris halope is made up of a short oesophagus leading to a voluminous stomach chamber. Posteriorly, a pylorus is attached to the stomach chamber. An antechamber of the midgut glands is situated at the transition into the midgut, from which up to four tubular midgut glands emanate. The midgut is a straight tube running through the body terminating in a short hindgut. The central nervous system in the cephalothorax is made up of a brain and a suboesophageal ganglion. Both species show some reduction of the protocerebrum caused by the lack of eyes. The circulatory system is made up of a tubular heart that is situated in the thorax. It is equipped with two pairs of incurrent ostia in S. lepidops and one pair in M. halope . The only artery leading off the heart is the anterior aorta, which runs into the cephalothorax. A dilation is formed between the brain and the anterior stomach wall, into which oesophageal dilator muscles are internalized. The function of this so-called 'myoarterial formation a' as an accessory pulsatile structure in the anterior cephalothorax of these animals is discussed.  © 2007 The Linnean Society of London, Zoological Journal of the Linnean Society , 2007, 149 , 629–642.     

Same same but different: a stunning analogy between tracheal and vascular supply in the CNS of different arachnids

Described herein is an as yet unprecedented structural and functional analogy of both the tracheal supply of the prosomal ganglion in opilionids and the arterial supply of the prosomal ganglion in pulmonate arachnids. Within Arachnida, two different modes of respiration can be observed: the so-called book lungs, and the tube-like tracheae. These different respiratory modes always correlate with a specific setup concerning the complexity of the circulatory system. This fact has a particular influence on the supply of certain organ systems, such as the central nervous system. It has recently been shown that pulmonate arachnids possess a highly complex pattern of intraganglionic arteries. Here, we show that Opiliones (harvestmen) possess a complex tracheal system (which supplies the different organ systems with oxygen) and only a relatively simple vascular system, comprising a short heart and an anterior aorta that runs directly to the prosomal ganglion. Using a variety of modern and classical morphological methods, we studied the vascular, tracheal and nervous systems of different representatives from all higher taxa of Opiliones. We show that the prosomal ganglion is extensively supplied with intraganglionic tracheae. What is especially surprising is the high degree of correspondence between the pattern of these ganglionic tracheae in harvestmen and the pattern of arteries in the prosomal ganglion of pulmonate arachnids. We aim to provide mechanistic causal explanations of these analogous patterns by applying the concepts of role analogy and constructional analogy. We also aim to establish the circulatory system as a model organ system and hope that this may, in turn, provide a starting point for future research programmes.     

金钱豹和猪獾冠状动脉的解剖

为了阐明金钱豹(Panthera pardus)和猪獾(Arctonyx collaris)心冠状动脉的分支分布特征及血供情况,为心脏生物学及动物学研究提供结构基础资料,利用血管铸型和组织透明方法观察研究了金钱豹与猪獾心左、右冠状动脉的分支分布.结果表明,金钱豹和猪獾的心均由左右冠状动脉营养.金钱豹左冠状动脉分为室间隔支、前降支和旋支.前降支又分出左室上支、左室中支和左室下支.右冠状动脉沿途分出右室前支、右室后下支和右室后上支.猪獾左冠状动脉分为前降支和旋支.前降支又分出室间隔支和左室前支,旋支又分出左缘支和左室后支.其右冠状动脉沿途分出右室前支、右缘支和右室后支.金钱豹和猪獾心的室间隔均由发自左冠状动脉的独立的室间隔支营养,二者左右冠状动脉在膈壁的分布属于均衡型.     

Gill microcirculation of the air-breathing climbing perch, Anabas testudineus (Bloch):relationships with the accessory respiratory organs and systemic circulation

The general macrocirculation and branchial microcirculation of the air-breathing climbing perch, Anabas testudineus, was examined by light and scanning electron microscopy of vascular corrosion replicas. The ventral aorta arises from the heart as a short vessel that immediately bifurcates into a dorsal and a ventral branch. The ventral branch distributes blood to gill arches 1 and 2, the dorsal branch to arches 3 and 4. The vascular organization of arches 1 and 2 is similar to that described for aquatic breathing teleosts. The respiratory lamellae are well developed but lack a continuous inner marginal channel. The filaments contain an extensive nutritive and interlamellar network; the latter traverses the filament between, but in register with, the inner lamellar margins. Numerous small, tortuous vessels arise from the efferent filamental and branchial arteries and anastomose with each other to form the nutrient supply for the filament, adductor muscles, and arch supportive tissues. The efferent branchial arteries of arches 1 and 2 supply the accessory air-breathing organs. Arches 3 and 4 are modified to serve primarily as large-bore shunts between the dorsal branch of the ventral aorta and the dorsal aorta. In many filaments from arches 3 and 4, the respiratory lamellae are condensed and have only 1-3 large channels. In some instances in arch 4, shunt vessels arise from the afferent branchial artery and connect directly with the efferent filamental artery. The filamental nutrient and interlamellar systems are poorly developed or absent. The respiratory and systemic pathways in Anabas are arranged in parallel. Blood flows from the ventral branch of the ventral aorta, through gill arches 1 and 2, into the accessory respiratory organs, and then returns to the heart. Blood, after entering the dorsal branch of the ventral aorta, passes through gill arches 3 and 4 and proceeds to the systemic circulation. This arrangement optimizes oxygen delivery to the tissues and minimizes intravascular pressure in the branchial and air-breathing organs. The efficiency of this system is limited by the mixing of respiratory and systemic venous blood at the heart.     

The evolution of thunniform locomotion and heat conservation in scombrid fishes: New insights based on the morphology of Allothunnus fallai

Two significant functional differences–a more anterior and internally positioned red myo‐tomal muscle mass and modification of the red‐muscle vascular supply to form counter‐current heat exchangers–distinguish the tunas (tribe Thunnini) from other species in the teleost family Scombridae. Neither of these characteristics is found in the bonitos (tribe Sardini), the sister group to the Thunnini. The most recent scombrid classification places the slender tuna, Allothunnus fallai, in the tribe Sardini, but some earlier studies suggested that this species should be a member of the Thunnini. Allothunnus fallai does not possess the lateral subcutaneous arteries and veins or the lateral heat‐exchanging retia typical of tunas. However, we have found that this species has a highly modified central circulation (dorsal aorta, post cardinal vein, and associated branch vessels) similar to the central heat‐exchanging retia of certain tunas, an enlarged haemal arch to accommodate this structure, and the anterior, internal placement of red muscle characteristic of tunas. With these new characters, phylogenetic reconstructions based on parsimony place A. fallai as the sister taxon to the tunas, establish that it is the most basal tuna species, and support the hypothesis that the derivation of tunas from a bonito‐like ancestor occurred through selection for an integrated set of characteristics affecting locomotion and endothermy. The major features of this hypothesis are as follows. (1) Selection for continuous, steady, and efficient swimming resulted in changes in body shape (the result of enlargement of the anterior myotomes, the anterior and internal shift of red muscle, and a narrowing of the caudal peduncle) which increased streamlining and led to the adoption of the thunniform swimming mode unique to the tunas. (2) Alterations in blood supply necessitated by the anterior shift in red muscle led to the interdigitation of numerous arterial and venous branches which set the stage for heat conservation. (3) The evolution of endothermy, together with thunniform swimming, contributed significantly to the ecological radiation and diversification of tunas during the Early Tertiary Period. Our studies of A fall thus suggest that the shift in red muscle position and changes in central circulation preerded the evolution of red‐muscle endothermy. Co‐evolutionary changes in red muscle quantity and distribution and in vascular specializations for heat conservation have led to different macroevolutionary trajectories among the now five genera and 14 tuna species of tunas and appear to reflect the influence of changing paleocological and paleoccanographic conditions, including cooling, that occurred in the Tertiary     

Invited review: aging and the cardiovascular system.

Aging is associated with complex and diversified changes of cardiovascular structure and function. The heart becomes slightly hypertrophic and hyporesponsive to sympathetic (but not parasympathetic) stimuli, so that the exercise-induced increases in heart rate and myocardial contractility are blunted in older hearts. The aorta and major elastic arteries become elongated and stiffer, with increased pulse wave velocity, evidence of endothelial dysfunction, and biochemical patterns resembling early atherosclerosis. The arterial baroreflex is sizably altered in aging, but different components are differentially affected: there is a definite impairment of arterial baroreceptor control of the heart but much better preserved baroreceptor control of peripheral vascular resistance. Alterations at the afferent, central neural, efferent, and effector organ portions of the reflex arch have been claimed to account for age-related baroreflex changes, but no conclusive evidence is available on this mechanistic aspect. Reflexes arising from cardiopulmonary vagal afferents are also blunted in aged individuals. The cardiovascular and reflex changes brought about by aging may have significant implications for circulatory homeostasis in health and disease.     

Form and Function in Reptilian Circulations

Consistent with the great variation in their circulatory morphology,there are distinct variations in the cardiovascular physiologyof extant reptiles. The chelonian and squamate reptiles havea complexly structured heart that includes three partially separatedventricular cava. In most species (under most conditions), theventricle acts as a single pressure pump perfusing both thepulmonary and systemic circuits. However, the varanid lizardsprovide a striking exception. Subtle evolutionary changes incardiac morphology allow the ventricle of the varanid lizardto divide functionally during systole into a low pressure, pulmonarypump and a high pressure, systemic pump. The crocodilians representyet another anatomical and physiological pattern. The ventricleis completely divided into left and right chambers as in homeotherms,but the systemic and pulmonary circuits may still communicatethrough the left aorta that arises from the right ventricle. A fundamental feature of all reptilian circulations is the abilityto regulate the distribution of cardiac output between systemicand pulmonary circuits via central vascular blood shunts.Regardlessof species, mechanisms for regulating intracardiac shuntinginvolve changes in the balance between peripheral resistanceof the pulmonary and systemic circulations, and adjustmentsin cardiac performance per se. Several hypotheses are presentedthat suggest selective advantages for central vascular shuntingin intermittent breathing reptiles with variable body temperatureand metabolic rate.     

A congenital malformation of the systemic heart complex inSepia officinalis L. (Cephalopoda)

In semi-adultSepia officinalis L. (Cephalopoda) from the Bay of Arcachon (France) a congenital malformation of the systemic heart is described by macro-and microscopical methods. It concerns an atypical doubling of the site of insertion at the cephalic aorta at the apical ventricle. Its comparison with the paired anlagen of the systemic heart complex in normal embryogenesis and the central circulatory system ofNautilus gives rise to interpret it as a form of atavism. The possible causal role of mutagenic antifoulings is discussed.     

Noninvasive three-dimensional viewing of the motion and anatomical structure of the heart, lungs, and circulatory system by high speed computerized X-ray tomography.

A new generation X-ray computerized tomography system now under construction, the Dynamic Spatial Reconstructor (DSR), will record 1680 multiple view X-ray video images of the chest or other segments of the body per second. This allows com0utation of stop-action and 60-per-second instant replay motion pictures of the dynamic three-dimensional changes in shape and dimensions of the full anatomic extents of the internal and external surfaces of the heart chambers or the vascular anatomy and circulatory dynamics in any region of the body. Current commercially available scanners require one or more seconds per cross-sectional scan and lack the synchronous volumetric scanning capabilities of the DSR. These capabilities allow nondestructive mathematical selection and removal of any subvolume of interest from a reconstructed volume. The associated abilities to "zoom in" and "section" this subvolume so as to examine its structure and physiologic function in detail allow direct visualization of the internal anatomy and function of organ systems within the body. These capabilities of "noninvasive numerical biopsy" and "vivisection" have heretofore been the preserve of pathologists at autopsy or surgeons at the operating table. Possible future availability of these techniques to the practicing internist carries promise of revolutionary improvements in clinical diagnosis and treatment of the myriad of disease processes, including cancer, which may affect the heart, lungs, vascular anatomy or circulatory dynamics in any region of the body.