Anke Schmitz

Organization of the superficial neuromast system in goldfish, Carassius auratus

Distribution, morphology, and orientation of superficial neuromasts and polarization of the hair cells within superficial neuromasts of the goldfish (Carassius auratus) were examined using fluorescence labeling and scanning electron microscopy. On each body side, goldfish have 1,800–2,000 superficial neuromasts distributed across the head, trunk and tail fin. Each superficial neuromast had about 14–32 hair cells that were arranged in the sensory epithelium with the axis of best sensitivity aligned perpendicular to the long axis of the neuromast. Hair cell polarization was rostro‐caudal in most superficial neuromasts on trunk scales (with the exception of those on the lateral line scales), or on the tail fin. On lateral line scales, the most frequent hair cell polarization was dorso‐ventral in 45% and rostro‐caudal in 20% of the superficial neuromasts. On individual trunk scales, superficial neuromasts were organized in rows which in most scales showed similar orientations with angle deviations smaller than 45°. In about 16% of all trunk scales, groups of superficial neuromasts in the dorsal and ventral half of the scale were oriented orthogonal to each other. On the head, most superficial neuromasts were arranged in rows or groups of similar orientation with angle deviations smaller than 45°. Neighboring groups of superficial neuromasts could differ with respect to their orientation. The most frequent hair cell polarization was dorso‐ventral in front of the eyes and on the ventral mandible and rostro‐caudal below the eye and on the operculum. J. Morphol., 2008.

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 μm to 35 μm. 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.

A new type of infrared organ in the Australian "fire-beetle" Merimna atrata (Coleoptera: Buprestidae)

Abstract The Australian buprestid beetle Merimna atrata (Coleoptera: Buprestidae) approaches forest fires because its larvae develop in freshly burnt wood. So far nothing is known about possible sensory systems enabling the beetles to detect fires and to cope with the thermal environment close to the flames. We found that M. atrata has two pairs of infrared (IR) organs on the ventrolateral sides of the abdomen. Each IR organ consists of a specialized IR-absorbing area which is innervated by one thermosensitive multipolar neuron. The primary dendritic branches ramify into more than 800 closely packed terminal endings which contain a large number of mitochondria. We called the special morphology of the dendritic region a terminal dendritic mass. The type of IR receptor found in M. atrata is unique in insects and can best be compared with the IR organs of boid snakes.

Hypoxic tolerance in air-breathing invertebrates.

Terrestrial invertebrates experience hypoxia in many habitats and under a variety of physiological conditions. Some groups (at least insects) are much more capable of recovery from anoxia than most vertebrates, but there is still a tremendous unexplained variation in hypoxia/anoxia tolerance among terrestrial invertebrates. Crustaceans and arachnids may be less often confronted with hypoxic environments than insects and myriapods and also seem to be less hypoxia/anoxia tolerant. Tracheated groups, especially those that are able to ventilate their tracheal system like many insects, cope with lower critical PO2 than nontracheated groups. Modulation of oxygen carrier proteins is normally not important in hypoxia resistance. Recent application of genetic and cellular tools are revealing that many of the same pathways documented for mammals (e.g. HIF, nitric oxide) function to regulate morphological and biochemical responses to hypoxia/anoxia in insects.

Morphology of a thermosensitive multipolar neuron in the infrared organ of Merimna atrata (Coleoptera, Buprestidae).

Two pairs of infrared (IR) organs are situated ventrolaterally on the second and third abdominal sternites of the Australian fire beetle Merimna atrata (Buprestidae). In ventral view, each IR organ has a round IR absorbing area under which a sensory complex is attached to the epidermis. The main component of the complex is a single large multipolar neuron and its mass of highly branched dendrites. All parts of this neuron are enveloped in glial cells. The proximal primary dendrites, which arise from the soma, finally branch into several hundred tightly packed terminal dendrites, which contain many mitochondria. We term this unusual morphology of the dendritic region a terminal dendritic mass (TDM). Additionally, two chordotonal organs were found in each sensory complex. Their somata are integrated in the complex and the dendrites extend to the periphery of the absorbing area. The bauplan of the dendritic region is reminiscent of the thermosensitive trigeminal nerve fibers innervating the absorbing structures in the IR receptors in boid and crotalid snakes. Because this multipolar neuron also functions as a thermoreceptor, another example of a functional analogy between insect and vertebrate sensory systems could be demonstrated.

Sensitivity threshold and response characteristics of infrared detection in the beetle Melanophila acuminata (Coleoptera: Buprestidae)

The minimum detection threshold of the infrared sensitive beetle, Melanophila acuminata, was measured with a helium-neon laser that emitted light at a wavelength of 3.39 microm. Extracellular recordings were taken both at the pit organ responsible for detection and at the interganglionic connectives in the thorax of the beetle. At the pit organ, generator and action potentials from single neurons were measured with a sharpened tungsten electrode. At the connectives that linked the fused second meso-/metathoracic and prothoracic ganglia, compound action potentials were measured with a tungsten hook electrode that encircled the connective. The latter recordings confirmed conveyance of infrared information through specific pathways to rostrally-situated sites in the nervous system of the beetle. The 50% probability irradiance threshold at which action potentials were elicited from the receptor and connectives occurred at 17.3 and 14.6 mW/cm(2), respectively. In addition to sensitivity threshold, several other characteristics of the response were quantified including dependence of generator potential latency, generator potential duration, spike frequency, and spike latency on irradiance, dependence of response strength (spike count) on exposure time, and flicker fusion frequency. The ability to detect infrared radiation is rare in nature, and these results provide valuable information necessary to understand this unique sensitivity.

Spiders on a treadmill: influence of running activity on metabolic rates in Pardosa lugubris (Araneae, Lycosidae) and Marpissa muscosa (Araneae, Salticidae).

SUMMARY The CO2 release of the well-tracheated jumping spider, Marpissa muscosa, and the poorly tracheated, Pardosa lugubris, was tested while animals were running on a treadmill at three different speeds and under a selective elimination of lungs or tracheae. Thus, the influence of a well-developed tracheal system on the metabolism during physical exercise was examined. The CO2 release in intact animals increased with the running speed in both species. The costs of transport (COT) running at the maximal sustainable speed were nearly twice as big in M. muscosa as in P. lugubris. Elimination of one lung by sealing resulted in reduced COT and running times, and increasing anaerobic proportions in metabolism. Effects were greater in P. lugubris than in M. muscosa, indicating that tracheae compensate partly for the lacking lung capacity. Sealing of the tracheae in M. muscosa reduced the COT and the running times only at the highest speed. Results indicate that tracheae in M. muscosa support the aerobic metabolism only at the most intense physical exercise. At low and medium activity, tracheae may play their main role in the local supply of organs that are not involved in running activity.

Lung morphology in rodents (Mammalia, Rodentia) and its implications for systematics

A new nomenclature of the lung lobes and of the bronchial tree is presented, with which the lungs in 40 species of 11 rodent families are described. Whole, fixed lungs and silicone casts of the bronchial tree are tested for 23 characters, based on the distribution of lung lobes, the number and geometry of first order bronchi, the pulmonary blood supply, and lung symmetry. Ten lung morphotypes are recognized, seven of them representing one or more families: Castor type (Castoridae), Cryptomys type (Bathyergidae), Ctenodactylus type (Ctenodactylidae), Eliomys type (Gliridae), Myocastor type (Myocastoridae), Octodon type (Octodontidae and Echimyidae) and Rattus type (Sciuridae, Muridae pt. and Dipodidae). The Hydromys type is found only in Hydromys chrysogaster (Muridae), while Galea type A and B both appear in Galea musteloides (Caviidae). The data are phylogenetically analyzed by the program PAUP 4.0 using as outgroup Lagomorpha or Insectivora. On the species level, there are no well‐resolved cladograms. On the family level, the cladograms do not contradict traditional rodent systematics with one exception: the Caviidae do not fall within Caviomorpha or even within the Hystricomorpha, but form a sister group to Dipodidae (Myomorpha). This appears to be a result of convergence. The lungs of Gliridae are more similar to those of Muridae than to those of Sciuridae. Included in the ingroup, Oryctolagus (Lagomorpha) forms a clade with Caviidae + Dipodidae. Thus, the “Glires hypothesis” is neither supported nor refuted. J. Morphol. 246:228–248, 2000.

Stereological estimation of surface area and barrier thickness of fish gills in vertical sections.

Previous morphometric methods for estimation of the volume of components, surface area and thickness of the diffusion barrier in fish gills have taken advantage of the highly ordered structure of these organs for sampling and surface area estimations, whereas the thickness of the diffusion barrier has been measured orthogonally on perpendicularly sectioned material at subjectively selected sites. Although intuitively logical, these procedures do not have a demonstrated mathematical basis, do not involve random sampling and measurement techniques, and are not applicable to the gills of all fish. The present stereological methods apply the principles of surface area estimation in vertical uniform random sections to the gills of the Brazilian teleost Arapaima gigas. The tissue was taken from the entire gill apparatus of the right‐hand or left‐hand side (selected at random) of the fish by systematic random sampling and embedded in glycol methacrylate for light microscopy. Arches from the other side were embedded in Epoxy resin. Reference volume was estimated by the Cavalieri method in the same vertical sections that were used for surface density and volume density measurements. The harmonic mean barrier thickness of the water‐blood diffusion barrier was calculated from measurements taken along randomly selected orientation lines that were sine‐weighted relative to the vertical axis. The values thus obtained for the anatomical diffusion factor (surface area divided by barrier thickness) compare favourably with those obtained for other sluggish fish using existing methods.

Distribution and functional morphology of photomechanic infrared sensilla in flat bugs of the genus Aradus (Heteroptera, Aradidae)

Globally the flat bug genus Aradus comprises about 200 species. About half a dozen Aradus species can be primarily found on burnt areas and, therefore, have been called pyrophilous. Bugs and their offspring feed on fungi growing on burnt wood. Recently, prothoracic infrared (IR) receptors have been described in the pyrophilous Australian species Aradus albicornis. In our study we investigated 10 Aradus species, once again including A. albicornis, and found prothoracic as well as hitherto unknown mesothoracic IR sensilla in A. albicornis, Aradus lugubris and Aradus fuscicornis. In Aradus flavicornis only prothoracic IR receptors were found. Currently the latter two species are not known as pyrophilous. However, there is considerable evidence that these flat bugs also approach forest fires. In all four species where IR receptors were identified, the dome-shaped IR sensilla look very similar. An IR sensillum consists of an internal exocuticular sphere reinforced by consecutive layers of chitin fibres. In the center of the sphere, a microfluidic core is located which consists of a cup-shaped plug of cuticle and an underlying fluid filled annular channel surrounding the tip of the dendrite of a mechanosensitive neuron. Like the IR receptors of buprestid beetles of the genus Melanophila, the IR sensilla found in Aradus species can be classified as photomechanic IR receptors.