Respiratory system of arachnids I: morphology of the respiratory system of Salticus scenicus and Euophrys lanigera (Arachnida, Araneae, Salticidae)

The book-lungs and the tracheal systems of two species of jumping spider, Salticus scenicus and Euophrys lanigera, were investigated using gross anatomical, light and electron microscopic methods. Both species possess well-developed book-lungs of similar size and tracheal systems with a basically similar branching pattern. The tracheal spiracle opens into a single atrium, where it gives rise to four thick 'tube tracheae', from which small secondary tube tracheae originate in groups. The secondary tracheae (diameter 1-5 mum) run parallel, without further branching, into the prosoma. In the opisthosoma, they lie ventrolaterally, where they contact muscles and internal organs. In the prosoma, the secondary tracheae may penetrate the gut epithelium and central nervous tissue. The structure of the tracheal walls is very similar to that of insects, consisting of a striated inner cuticular layer with taenidial structures and a surrounding outer hypodermal layer. The wall thickness appears similar in all secondary tracheae, indicating that lateral gas diffusion may be possible through the walls of all small tube tracheae.     

Respiratory system of arachnids II: morphology of the tracheal system of Leiobunum rotundum and Nemastoma lugubre (Arachnida, Opiliones)

The tracheal system of two species of harvestmen with different life styles was investigated: the long-legged, Leiobunum rotundum (Phalangioidea, Phalangiidae) and the short-legged Nemastoma lugubre (Troguloidea, Nemastomatidae). The morphology of the tracheae is very similar in both species: The branching pattern is basically asymmetric and dichotomous, and the tracheae taper between branching points. The tracheal diameters range from 160 to 0.3 mum in L. rotundum (mean body mass 25.3 mg), and from 70 to 0.5 mum in N. lugubre (mean body mass 3.8 mg). Ultrastructurally, the tracheal walls are similar to those of insects, consisting of an outer hypodermal layer and an inner cuticular layer with taenidial structures. Tracheae of all diameters have close contact with organs and muscles, indicating that diffusive gas exchange may take place through the walls of all tracheae. The finest tracheae end freely in the hemolymph or at the surface of organs and muscles. Exceptions are tracheal penetration of the central nerve mass in the prosoma in both species, and of the muscles in L. rotundum. The latter may correlate with the active perambulatory life style of L. rotundum.     

Morphometric analysis of the tracheal walls of the harvestmen Nemastoma lugubre (Arachnida, Opiliones, Nemastomatidae)

The tracheal system of harvestmen consists of two stem tracheae, which give rise to higher order tracheae that supply the extremities and internal organs. In this study, we used stereological morphometric methods to investigate diffusing capacities of the walls ('lateral diffusing capacity') of the tracheae of adult males and females of Nemastoma lugubre. Diffusing barriers of the tracheal walls tend to be thinnest (0.17-0.19 microm) for the smallest tracheae (inner diameter 0.5-2 microm). In other tracheal classes the diffusing barriers increase with increasing diameters. Calculation of the mass-specific diffusing capacity for oxygen (D(O2)) of the walls of all higher order tracheae revealed 10.57 microl min(-1)g(-1)kPa(-1) for the females (mean body mass 3.8 mg) and 25.23 microl min(-1)g(-1)kPa(-1) for the males (mean body mass 1.4 mg). In both animal groups, the main D(O2) (58-67%) lies in the tracheae with an inner diameter of 0.5-2 microm, but also tracheae up to an inner diameter of 20 microm allow gas exchange via the tracheal walls. Stem tracheae are of no importance for lateral diffusion. Our results are consistent with the hypothesis that the functional morphology of the tracheal system of harvestmen represents an 'intermediate state' between the tracheal system of insects in which gas exchange is focused on the distal portions and that of spiders, in which the walls of all tracheae serve in gas exchange.     

Stereological determination of tracheal volume and diffusing capacity of the tracheal walls in the stick insect Carausius morosus (Phasmatodea, Lonchodidae)

First instars of Carausius morosus provide a good model for morphometric evaluation of the diffusing capacity between the tracheal system and hemolymph: air sacs are lacking, tracheoles do not penetrate the organs and muscles, and entire animals can be evaluated electron microscopically without subsampling. The tracheal volume makes up 1.3% of the volume of the whole insect excluding appendages. We calculated the lateral diffusing capacity for oxygen and carbon dioxide for five classes of tracheae according to their diameters, from 0.2 microm to 35 microm. The harmonic mean thickness of the tracheal epithelium is lowest in smallest tracheae and increases with increasing tracheal diameter. Although the smallest tracheae make up 70% (O2) and 60% (CO2) of the total diffusing capacity, the proximal four classes may also be significant in diffusion of oxygen and particularly of carbon dioxide. The suppression of the development of respiratory pigments in the evolution of terrestrial insects may have increased the relative importance of small tracheal elements for local oxygen consumption.     

Tracheal ultrastructure of protura (Insecta : Apterygota)

The tracheal systems of Sinentomon and Eosentomon (Apterygota : Protura) were examined in thin sections and compared with the tracheae of collembolan, Allacma. The tracheal system of Protura consists of spiracles and tracheae. The spiracle is a simple, concave cuticular cavity known as an atrium. A globular chamber is present between the atrium and trachea. The atrium of Eosentomon is decorated with ridges and has 2 small openings to tracheal recesses beside the central tracheal opening. The tracheae of Protura are characterized by a high frequency of taenidia and the absence of intima folds and intertaenidial spaces. The taenidia of Sinentomon have a rectangular section and those of Eosentomon are gable-shaped. The results also suggest that the tracheal recess of Eosentomon is a kind of stigmatic gland. The tracheal structure of Protura was compared with that of collembolans, insects, and other arthropods, and discussed in terms of phylogeny.     

Spider tracheal systems

1. The tracheal structures of spiders belonging to 15 families were investigated. Techniques developed primarily for use with insects were used to visualize spider tracheae. The tracheae were investigated in whole spiders and with serial sections. A macerating agent is described which dissolves the soft-tissues of the spiders without harming the tracheae, or decolourizing the injected dye. 2. A variety of tracheal systems are illustrated using diagrammatic line-drawings and photographs. 3. The variation in the tracheal structures of the spiders investigated in this study is discussed, as well as the use of tracheal structures in spider classification. Spider tracheae are compared with those of insects. 4. A list is given of the major investigations into spider tracheal systems this century.     

The tracheal system of the developing primary olfactory pathway of Manduca sexta: tracheae do not play a guidance or targeting role for ingrowing receptor axons

Axons navigate to their targets by detecting signals within the environment through which they are growing. The surfaces of tracheae, which are prominent features of the insect body plan, could be detected as favorable pathways for sensory axons growing toward the brain. The pattern of the tracheal investment of the adult antennal lobe of the moth Manduca sexta suggested two specific possibilities for interaction between tracheae and axons during development: that tracheae might be involved in guiding olfactory receptor axons to their target region of the brain, the antennal lobe; and that tracheae could provide an address system within the lobe that defines the sites of glomeruli, which are olfactory-axon target areas within the lobe. To determine whether tracheae contribute to development of the primary olfactory pathway, the distribution of tracheae in the adult and developing antennal lobes was examined with both confocal and electron microscopes. During the major stages in which axons are growing into the antennal lobe and in which glomeruli are forming, the tracheal investment of the nerve and lobe was found to be minimal. Tracheae thus cannot serve as axon guides or as local address sites for newly forming glomeruli during the initial targeting of receptors onto the antennal lobe.     

Caterpillars have evolved lungs for hemocyte gas exchange

Since insect blood usually lacks oxygen-carrying pigments it has always been assumed that respiratory needs are met by diffusion in the gas-filled lumen of their tracheal systems. Outside air enters the tracheal system through segmentally arranged spiracles, diffuses along tubes of cuticle secreted by tracheal epithelia and then to tissues through tracheoles, thin walled cuticle tubes that penetrate between cells. The only recognized exceptions have been blood cells (hemocytes), which are not tracheated because they float in the hemolymph. In caterpillars, anoxia has an effect on the structure of the hemocytes and causes them to be released from tissues and to accumulate on thin walled tracheal tufts near the 8th (last) pair of abdominal spiracles. Residence in the tufts restores normal structure. Hemocytes also adhere to thin-walled tracheae in the tokus compartment at the tip of the abdomen. The specialized tracheal system of the 8th segment and tokus may therefore be a lung for hemocytes, a novel concept in insect physiology. Thus, although as a rule insect tracheae go to tissues, this work shows that hemocytes go to tracheae.     

Association of tracheal placodes with leg primordia in Drosophila and implications for the origin of insect tracheal systems

Adaptation to diverse habitats has prompted the development of distinct organs in different animals to better exploit their living conditions. This is the case for the respiratory organs of arthropods, ranging from tracheae in terrestrial insects to gills in aquatic crustaceans. Although Drosophila tracheal development has been studied extensively, the origin of the tracheal system has been a long-standing mystery. Here, we show that tracheal placodes and leg primordia arise from a common pool of cells in Drosophila, with differences in their fate controlled by the activation state of the wingless signalling pathway. We have also been able to elucidate early events that trigger leg specification and to show that cryptic appendage primordia are associated with the tracheal placodes even in abdominal segments. The association between tracheal and appendage primordia in Drosophila is reminiscent of the association between gills and appendages in crustaceans. This similarity is strengthened by the finding that homologues of tracheal inducer genes are specifically expressed in the gills of crustaceans. We conclude that crustacean gills and insect tracheae share a number of features that raise the possibility of an evolutionary relationship between these structures. We propose an evolutionary scenario that accommodates the available data.     

Involvement of mind the gap in the organization of the tracheal apical extracellular matrix in Drosophila and Nilaparvata lugens

The tracheal apical extracellular matrix (aECM) is vital for expansion of the tracheal lumen and supports the normal structure of the lumen to guarantee air entry and circulation in insects. Although it has been found that some cuticular proteins are involved in the organization of the aECM, unidentified factors still exist. Here, we found that mind the gap (Mtg), a predicted chitin‐binding protein, is required for the normal formation of the apical chitin matrix of airway tubes in the model holometabolous insect Drosophila melanogaster. Similar to chitin, the Mtg protein was linearly arranged in the tracheal dorsal trunk of the tracheae in Drosophila. Decreased mtg expression in the tracheae seriously affected the viability of larvae and caused tracheal chitin spiral defects in some larvae. Analysis of mtg mutant showed that mtg was required for normal development of tracheae in embryos. Irregular taenidial folds of some mtg mutant embryos were found on either lateral view of tracheal dorsal trunk or internal view of transmission electron microscopy analysis. These abnormal tracheae were not fully filled with gas and accompanied by a reduction in tracheal width, which are characteristic phenotypes of tracheal aECM defects. Furthermore, in the hemimetabolous brown planthopper (BPH) Nilaparvata lugens, downregulation of NlCPAP1‐N (a homolog of mtg) also led to the formation of abnormal tracheal chitin spirals and death. These results suggest that mtg and its homolog are involved in the proper organization of the tracheal aECMs in flies and BPH, and that this function may be conserved in insects.     

The tracheal supply and muscle metabolism during muscle growth in the puparium of Calliphora vomitoria

Thirty hours after puparium formation in Calliphora, the larval tracheal system is replaced by an air-filled pupal system. This is characterized initially by many tufts of tracheae and coiled tracheoles lying in the blood. Between the third and fourth day, the sixth dorsal longitudinal flight muscles are practically without attached tracheae and their longitudinal growth can partially occur when oxygen uptake is inhibited with potassium cyanide. Sodium iodoacetate prevents muscle growth. After the fifth day of development the pupal tracheoles spread out over the surface of the developing adult muscles. Between the seventh and ninth day, longitudinal growth and increases in the diameter of the myofibrils are halted by cyanide and iodoacetate. Some longitudinal growth and an increase in the total protein content of the muscles can occur in 1% oxygen. Air filling of the adult tracheae takes place 2–3 hr before the emergence of the adult and is accompanied by an increase in oxygen consumption of the thorax. The metabolism and growth of the muscles is discussed with respect to their changing oxygen supply.     

Ontogeny of tracheal dimensions and gas exchange capacities in the grasshopper, Schistocerca americana

How does body size affect the structure and gas exchange capacities of insect tracheae? Do insects become more oxygen-limited as they grow? We addressed these questions by measuring the dimensions of two transverse tracheae within the abdomen of American locusts of different ages, and evaluating the potential for diffusion or convection to provide adequate gas exchange. The grasshopper abdomen has longitudinal tracheae that run along the midgut, heart, nerve cord, and lateral body wall. Transverse tracheae run from each spiracle to the longitudinal tracheae. Dorsal air sacs attach near each spiracle. In both transverse tracheae studied, diffusive capacities increased more slowly than metabolic rates with age, and calculated oxygen gradients necessary to supply oxygen by diffusion increased exponentially with age. However, surgical studies demonstrated that transport of gas through these transverse tracheae occurred by convection, at least in adults. Convective capacities paralleled metabolic rates with age, and the calculated pressure gradients required to sustain oxygen consumption rates by convection were independent of age. Thus, in growing grasshoppers, tracheal capacities matched tissue oxygen needs. Our morphological and physiological data together suggest that use of convection allows older grasshoppers to overcome potential limitations on size imposed by diffusion through tracheal systems.     

Ontogeny of tracheal dimensions and gas exchange capacities in the grasshopper, Schistocerca americana

How does body size affect the structure and gas exchange capacities of insect tracheae? Do insects become more oxygen-limited as they grow? We addressed these questions by measuring the dimensions of two transverse tracheae within the abdomen of American locusts of different ages, and evaluating the potential for diffusion or convection to provide adequate gas exchange. The grasshopper abdomen has longitudinal tracheae that run along the midgut, heart, nerve cord, and lateral body wall. Transverse tracheae run from each spiracle to the longitudinal tracheae. Dorsal air sacs attach near each spiracle. In both transverse tracheae studied, diffusive capacities increased more slowly than metabolic rates with age, and calculated oxygen gradients necessary to supply oxygen by diffusion increased exponentially with age. However, surgical studies demonstrated that transport of gas through these transverse tracheae occurred by convection, at least in adults. Convective capacities paralleled metabolic rates with age, and the calculated pressure gradients required to sustain oxygen consumption rates by convection were independent of age. Thus, in growing grasshoppers, tracheal capacities matched tissue oxygen needs. Our morphological and physiological data together suggest that use of convection allows older grasshoppers to overcome potential limitations on size imposed by diffusion through tracheal systems.     

Tracheal development in the Drosophila brain is constrained by glial cells

The Drosophila brain is tracheated by the cerebral trachea, a branch of the first segmental trachea of the embryo. During larval stages the cerebral trachea splits into several main (primary) branches that grow around the neuropile, forming a perineuropilar tracheal plexus (PNP) at the neuropile surface. Five primary tracheal branches whose spatial relationship to brain compartments is relatively invariant can be distinguished, although the exact trajectories and branching pattern of the brain tracheae are surprisingly variable. Immunohistochemical and electron microscopic studies demonstrate that all brain tracheae grow in direct contact with the glial cell processes that surround the neuropile. To investigate the effect of glia on tracheal development, embryos and larvae lacking glial cells as a result of a genetic mutation or a directed ablation were analyzed. In these animals, the tracheal branching pattern was highly abnormal. In particular, the number of secondary branches entering the central neuropile was increased. Wild-type larvae possess only two central tracheae, typically associated with the mushroom body and the antennocerebral tract. In larvae lacking glial cells, six to ten tracheal branches penetrate the neuropile in a variable pattern. This finding indicates that glia-derived signals constrained tracheal growth in the Drosophila brain and restrict the number of branches entering the neuropile.     

The direct transport of oxygen in insects by large tracheae

Vast numbers of large and small tracheae in the abdomen of adult Calliphora are so modified that they can transfer oxygen directly by diffusion to the developing ovaries. Tracheoles are scarce but. instead, a system of distended tubules, evaginated into the cytoplasmic surface of the trachea, cover the entire tracheal surface with permeable tubes diffusing oxygen to the developing tissues. A similar development occurs also in the male fly.     

Adherence of Bordetella bronchiseptica 276 to porcine trachea maintained in organ culture

Two organ culture models have been adapted for porcine tracheae in order to study colonization by Bordetella bronchiseptica. Rings or segments excised from tracheae of newborn piglets were incubated overnight at 37 degrees C in a nutrient medium under 5% CO2-95% air conditions. Tracheal segments were infected with B bronchiseptica 276, and after different incubation times, bacterial counts were done. B. bronchiseptica adhered well to tracheae maintained in culture, and no statistically significant differences between the two models were observed. Noninfected tracheal mucosae maintained a normal appearance for several days, whereas infected mucosae showed typical damage caused by B. bronchiseptica, namely, loss of ciliary activity and cilia and sloughing of ciliated cells. Our data indicated that porcine tracheal organ culture could be advantageously used to study in vitro colonization by B. bronchiseptica.     

The physiological basis of anterior inhibition of puparium formation in ligated fly larvae

Fly larvae ligated after the critical period of ecdysone release frequently fail to pupariate in the anterior part. Evidence is presented against anterior inhibition being caused by a hormonal imbalance, such as a decreased titre of ecdysone, an increased titre of juvenile hormone, and/or a lack of the neurohormonal factors that accelerate the process of pupariation. It is unlikely that the anterior inhibition results from a sustained stimulus from the sense organs, or from the presence of an inhibitory substance. The oxygen consumption in the inhibited anterior parts is 25 per cent of that in the anterior parts that pupariate. This suggests that the inhibition of pupariation is a result of oxygen deficiency. When anteriorly inhibited larvae are subjected to pure oxygen the inhibited anterior ends that would never tan in air commence to tan. The dissection of anteriorly inhibited larvae showed that the tracheal trunks were severed at the point of ligation and that the tracheae were filled with haemolymph. In the pupariated posterior parts the tracheae showed melanotic plugs at the severed ends of the tracheae preventing the flooding. Reducing the injury, by careful ligation, or by immobilizing the anterior ends by cold or tetrodotoxin reduces the incidence of anterior inhibition. Thus, anterior inhibition results from a lack of oxygen caused by the injury to the tracheal system during ligation.     

Phenotypic variation in susceptibility of honey bees,Apis mellifera,to infestation by tracheal mites,Acarapis woodi

A laboratory bioassay was used to study phenotypic differences in susceptibility of honey bees,Apis mellifera L., to tracheal mites,Acarapis woodi Rennie. Significantly different infestation frequencies were found in bees from 23 colonies containing queens that were instrumentally inseminated with single drones. Queens and drones originated from a closed population composed of commercial stock from various areas of the United States.Mites were randomly distributed with respect to right and left prothoracic tracheae. Tracheae containing mites were no more or less attractive to migrating mites than non-infested tracheae. The same quantity of progeny per female was produced in tracheae containing 1–3 mites. Female mites apparently do not migrate a second time after egg laying begins.The degree of phenotypic variation suggests that selection of honey bees for tracheal mite resistance is feasible.     

Adherence of Bordetella bronchiseptica 276 to porcine trachea maintained in organ culture.

Two organ culture models have been adapted for porcine tracheae in order to study colonization by Bordetella bronchiseptica. Rings or segments excised from tracheae of newborn piglets were incubated overnight at 37 degrees C in a nutrient medium under 5% CO2-95% air conditions. Tracheal segments were infected with B bronchiseptica 276, and after different incubation times, bacterial counts were done. B. bronchiseptica adhered well to tracheae maintained in culture, and no statistically significant differences between the two models were observed. Noninfected tracheal mucosae maintained a normal appearance for several days, whereas infected mucosae showed typical damage caused by B. bronchiseptica, namely, loss of ciliary activity and cilia and sloughing of ciliated cells. Our data indicated that porcine tracheal organ culture could be advantageously used to study in vitro colonization by B. bronchiseptica.     

Tracheation of abdominal ganglia and cerci in the house cricket Acheta domesticus (Orthoptera,Gryllidae)

Patterns of tracheation in the abdominal central nervous system and the cerci of Acheta domesticus are described from whole mounts, and light and electron microscopy. The tracheal supply of the ganglia is derived from ventral longitudinal tracheal trunks which have segmental connections to the spiracels. Each abdominal ganglion is served by a single pair of tracheal trunks, except the terminal ganglion, which has two pairs. Within the ganglia, tracheoles occur principally in association with glia-rich areas of the neuropile. We suggest that the respiratory exchange may be concentrated in the cell bodies of neurons and glia. Each cercus has a tracheal supply in paralle with a large air sac which, it is suggested, serves to lighten the cercus, functions as a resonator for sound reception, or facilitates tidal flow of hemolymph and postecdysial expansion of the cercus. No tracheae run continuously between ganglia or between the terminal ganglion and the cerci, and they do not appear to have a potential role as a contact guidance pathway for cercal nerve growth.