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Different wing colors in a harlequin ladybeetle specimen

The ladybeetle Harmonia axyridis is naturally distributed over eastern Asia, but was imported to the United States already at the beginning of the 20th century as pest control. At first, there was no population development in the open fields. These were at first reported from Louisiana in 1988. In 2001 the first free living specimens were for Europe discovered in Belgium. Since then the beetle distributed over several European countries, such as France, entire Germany or Switzerland.

 

Variations of Harmonia axyridis

 

The beetle is well known for its great form variations. Worldwide more than 200 different color pattern forms of thorax and elytrae are described. They are distinctly shaped and maintain in this shape and arrangement of pattern. But four forms dominate within natural populations. Speaking about the elytrae (not the thorax patterns), the reddish form with dark spots, as visible in my film, is one of them.

These distinct different forms must be named a polymorphism and are based on genetic information as well as on environmental conditions, such as temperature, humidity and light intensitivity. According to that even the term polyphenism might be adequate.

 

 

 

 

Transcription factor pannier responsible for color pattern polymorphism

 

According to the work of M. Gautier et al. (the genomic basis of color pattern polymorphism  in the harlequin ladybird, Current biology, 28, 20), the transcription factor pannier is responsible for the genetically based control of this polymorphism. They discovered that different pannier alleles determine the color pattern in the different known forms. The authors furthermore report that pannier was never found before to play a keyfactor role in the pigmentation of insects.

 

Ladybeetle species on a meadow in Berlin

 

The specimen in my footage was discovered on an urban meadow in the park area „Nordhafen“ in Berlin. It’s a meadow in autumn predominantly consisting of lucerne and clover, sorrel and yellow field cress. Different ladybeetle species could be in greater numbers found there between September and October 2019. The sevenspot-ladybird, the adonis ladybird (Hippodamia variegata) and most abundant the harlquin ladybird in all its developmental stages.

 

Asymmetrical wing colors and possible explications

 

 

Harlequin beetle specimen from Berlin with asymmetrically colored wings, copyrights Stefan F. Wirth, please like my video also on Youtube

 

The most conspicuous character of „my“ harlequin ladybird specimen was its distinct asymmetrically colored wings (elytrae). One side reddish with black spots, the other side brownish with black spots. During my research about such asymmetries in ladybirds, I didn’t find recent studies, which distinctly focussed on that topic. H. E. Roy et al. reported in their book „ladybirds“ (original version 1989, revised version 2013) about the existance of such differently colored wings in the same specimen. They emphasized that the phenominon was not studied in detail, but assumed different factors being eventually responsible for such a development of a beetle individual: 1) disruption of pigment production, 2) mitotic mutation in early development, 3) environmental conditions, eventually influencing the colors of an originally normal developed young adult (exposed for longer time to different light intensities etc.). The latter might in the case of „my“ specimen being an indeed possible factor, as it is clearly visible that also the brownish wing has at its edges some of the reddish pigments.

 

 

Filming/ photography conditions

 

The beetles was filmed and photographed under artificial conditions in a soil and grass-set in my video lab. There, mites of the Gamasina (Parasitiformes, evtl. mostly Laelapidae) were common. They interestingly showed a phoretic behavior by quickly climbing onto the wings of that ladybeetle. They obviously recognized it as a suitable carrier to new habitats. I assume ladybeetles in the field not being of much attraction for phoretic dispersal, based on their life-cycles and preferred habitats.

 

Berlin, September/ October 2019, Copyrights Stefan F. Wirth

Diving, feather cleaning and water bathing of the Inca tern Larosterna inca


Inca terns live along the South American Pacific coast and breed along rocky coastlines of Peru and North Chile. They can be easily identified by their grey plumages, their distinctly red beaks and feeds as well by their conspicious white feather curls on the bases of their beaks.

 

Geographic distribution and life-strategy aspects of Larosterna inca

 

Larosterna inca breeds inside rocky walls of coastlines either inside rocky cavities or in old nesting holes of other seabird species. Its hunting ground is the  Humboldt Current, which is famous for its cold temperature, but also its enormous fish wealth. To increase its chances for fishing success, the Inca tern might follow sea lions, cormorants and whales  and is then hunting fishes, which were flushed up by these bigger sea animals. They also follow fisher boats to catch some rests of their fishery.

 

Phylogenetic (systematic) relationships

 

According to phylogenetic reconstructions L. inca, which represents the only recent species of its genus, branches off in the Animalia tree within the monophyletic clade of terns. Based on DNA sequences E. S. Bridge, A. W. Jones and A. J. Baker reconstructed in their 2005 paper (Molecular phylogenetics and evolution) a sister-clade relationship between Larosterna and species of the taxa Sterna, Thalasseus and Chlidonias (mitochondrial DNA was used to reconstruct the tern phylogeny).

Terns themselves seem representing an own clade (Sternidae), being for example based on characters of behavioral pattern, and are considered as a sister taxon of gulls (Laridae).

 

Filming conditions and filming locality

 

My footage was recorded in the Zoo Berlin, where terns together with other sea birds inhabit a for tourists accessible free-flight enclosure. There I captured scenes about the diving and „fishing“ behavior (specimens fished repeatedly wooden sticks) as well as their plumage cleaning activities on shore and their conspicuous plumage cleaning behaviors via extended bathing trips inside areas of low water. Size of my entire video is 4K. But parts of the scenes were originally recorded in Full HD to enable a better slow motion effect based on 100 frames per second. Such footage was subsequently digitally magnified into the 4K size to fit in the entire video project.

All behavioral activities are at first presented in a slow motion (ca. three to four times slowlier than  original speed), then in the much faster original speed.

 

Plumage cleaning

 

Plumage cleaning is part of the hygienic behaviors of birds. Feathers can only stay in full function, thermoregulation and flying, when dirt and parasites are removed regularly. Typical plumage parasites are represented by feather mites (no phylogenetic clade), which consist of taxa of the Astigmata (Acariformes) and of taxa of the Dermanyssoidea (Parasitiformes). Feather lice represent  a subclade of the (Phthiraptera = lice), named Mallophaga. The monophyletic situation of Mallophaga is seemingly doubtful.

 

Plumage cleaning and hunting behavior of Larosterna inca, video (4K9, copyrights Stefan F. Wirth. Please like my video on youtube too.

 

Putative reasons for plumage cleaning behaviors

 

I couldn’t research sufficient information about specific plumage parasites of Larosterna inca. There is indication that terns generally are relatively free of predators and parasites. Seemingly, plumage parasites of this particular species are still a more or less open research field. But the existence of a regular and visibly careful plumage cleaning might indicate a sensitiveness for corresponding parasites. L. inca can be according to literature (e.g. W. Pieters et al., Avian Diseases, 2014) fatally infested with the trematode Ichthyocotylurus erraticus.

 

Copyrights Stefan F. Wirth, Zoo Berlin July/ September 2019

Mite Histiostoma sp., putatively new species, from mud around ponds (Berlin) and its morphology

Gravel pit area „Im Jagen 86“ in Berlin as biotope

 

„Im Jagen 86“ is a former gravel pit area in the Berlin urban forest Grunewald. It today represents a dynamic biotope, consisting of different types of habitats: mud around ponds, sand dunes, dry grassland and forest. Since the early 2000th, its habitat composition partly changed remarkably. Out of several (smaller) ponds, only one bigger pond remained. All ponds originally were surrounded by sapropel, a habitat for different interesting organisms, such as beetles of Heterocerus, Elaphrus and Bembidion. The mite Histiostoma maritimum was commonly found phoreticaly on Heterocerus and Elaphrus. I additionally in those early 2000th described the new mite Histiostoma palustre from Hydrophilidae of Cercyon and Coelostoma, living inside the saporopel as well. Today only a few small areas with open sapropel exist. I so far did not look for Histiostoma maritimum again and don’t know, how common it still is. At least Heterocerus beetles are harder to find than in earlier years. I so far did not found Histiostoma palustre again.

 

Rearing conditions of a putatively new mite species

 

I collected new mud samples in March 2019 at different areas, but found developing histiostomatid mites in a sample from the edge between mud (sapropel) and mosses. It is a species I never found before there and which might represent a new species. Only females could be morphologically studied. Nymyphal stages (not deutonymphs) are only available as video footage. No males were found. I had added bigger potato pieces to stimulate microorganism growth as mite food into the soil sample (room temperature). After about one month, a few mites (females and proto/tritonymphs) developed on only one of these potato pieces and quickly died out shortly after my filming activities and after I could prepare a few females. I actually try to get them reared again. Due to the low temperatures in March, it is considered that these mites hibernate independently from insects in the substrate. No bigger insects could be found in the substrate, which might be the corresponding carriers. But different dipterans (e.g. Ceratopogonidae) developed, they had no mite deutonymphs after hatching in my sample.

 

 

 

 

Morphological reconstruction of females and important characters as well as behavioral observations

 

The females of Histiostoma sp. differ from other females, which I know, by the mosaic of the following characters: body conspicuously elongated with a distinctly big distance between hind ringorgans and anus, digitus fixus almost simple shaped, fringes or ridges on palparmembrane, 6 dorsal humps, unusually big copulation opening. Leg setation not yet studied. One pair of ventral setae hardly visible (not in the drawing). Nymphs were observed during burrowing activities (footage), females are may be also able to. Deutonymphs or males would be useful to decide, whether the species is new. Some species are only described by deutonymphs.

 

Berlin, March/ June 2019 All copyrights Stefan F. Wirth

Oribatida mites: Fast runners and slow crawlers

Microhabitats often consist of a complexity of organism species. Under suitable conditions, samples can be kept „alive“ for months and even for years by regularly adding moisture and organic tissue, in case of my sample of this footage: patato pieces.

 

 

Mites of the Oribatida and their different ways of locomotion. Copyrights: Stefan F. Wirth, Berlin April 2019. Please give the video a like on youtube too.

 

Soil samples from island Norderney

 

This soil sample was collected in summer 2018 on the North Sea island Usedom during my participation at the „Geo Tag der Natur“. It contained several specimens of the predatory chilopode Lithobius sp. and pieces of rotting wood, moss and forestground, everything collected under rotting treetrunks and tree branches. The samples additionally contained the carabid beetle Pterosticus cf. niger and ants of genus Lasius. Samples were collected in a small forest area with wetland aspects. The soil quality was rather moist.

 

Astigmatid mites

 

I later added potato pieces and regularly some water droplets to the sample with still living big arthropods/ insects. After some weeks, specimens of the astigmatid mite Acodyledon cf. schmitzi developed on dryer areas of the potato pieces. These mites were presumably phoretic associates of the carabid beetles. They died out after several months, after the sample had dried out a little bit and may be due to changes of the room temperature during winter time.

 

Oribatida

 

Now, almost a year later, the micro habitat is inhabited by mites of the Oribatida in greater numbers of specimens of at least three species: Nothrus sp. (genus not yet clarified), Nothrus palustris (already found for the first time shortly after the sample collection) and a species of Phthiracarida.

 

Locomotion and biodiversity

 

Purpose of the short film is to show different organisms, cultured after about a year in this sample: mites, nematodes, collembolans and microorganisms, fungae and bacteria. Of the bigger arthropods/insects, only one Lithobius species survived until now.  Also the diversity of ways of locomotion in different oribatid species is emphasized: There are slow crawlers (Nothrus) and fast runners (Phthiracarida).

 

Berlin, April 2019, Copyrights Stefan F. Wirth

Late winter insect life: winter aconite blossoms and dipteran visitors

When do the first insect activities in the new year occur? Can insects be active in winter, even in the presence of snow? The answer is generally yes, different insect species even use to appear on warmer winter days on top of snow layers. Examples are the limoniid crane fly Chionea belgica, a wingless dipteran, which can be observed on milder winter days on snow surfaces along forest edges in Central Europe. Also the fly Trichocera hiemalis belongs to the winter crane flies (Trichoceridae) and can be characterized by a very well developed cold resistance. It appears on sunny winter days between branches of leafless trees in swarms around invading sunlight beams.

 

The winter aconite as an early blooming flower and its biology

 

But what about insects, visiting blooming flowers? This requires the existance of early blossoms, which can grow and bloom under winter conditions. A well known example is the winter aconite Eranthis hyemalis, which outlasts the summer period only by its underground tubers. Their conspicuous yellow blossoms belong to the first blooming flowers in the year. In Central Europe, they begin to grow under suitable conditions in mid February. They require milder temperatures, but even persist in case an unusual cold snap would happen. The blossoms open only at sunshine and thus close shortly after sunset. Opening and closing is a growth process, which depends on temperature conditions. Such a phenomenon is called thermonasty.

 

The winter aconite as a neophyte in Germany

 

In Central Europe, such as in Germany, E. hyemalis is a neophyte. It is originally native to Southern European areas, Turkey, South-East-France, Italy, Bulgaria and Hungary.

The species was introduced to Central Europe (and North America) as ornamental plant for gardens. It is proven that it was in Germany already cultivated since the 16th century. The German botanist, nature researcher and medical doctor Joachim Camerarius reared the winter agonite, which he brought from Italy, since 1588 in his backyards.

 

Common pollinating insects

 

Pollinating insects of E. hyemalis are flies, bumblebees and bees. To reach the nectar inside the blossoms requires a proboscis length of about two mm, which is mostly given in bumblebees and bees.

 

Flowerbed in Berlin urban park Schillerpark

 

I documented via my videography (4K) and photography a smaller area of winter aconites in front of a wall at urban park „Schillerpark“ (honoring the German poet Friedrich Schiller) in Berlin. The bright bricks of that wall reflected efficiently the solar warmth and thus created suitable conditions for a late winter flowerbed full of life.

 

Video with winter aconite blossoms and pollunating flies, copyrights Stefan F. Wirth.

 

Most abundant insects in that winter aconite bed

 

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Western honey bee, copyrights Stefan F. Wirth

 

The western honey bee Apis mellifera was often seen on blossoms, but unfortunately was not captured via video footage. Our honey bee hibernates in a so called winter clusters with lower temperatures and low activities in workers. Beginning in late winter/ early spring, workers increase the nest temperature due to body movements up to 35°C. This is exactly the body temperature, workers need to fly out and collect first nectar and pollen, for example from the winter agonite.

 

Drone fly on blossom of the winter aconite, copyrights Stefan F. Wirth

 

The drone fly Eristalis tenax belongs to the hoverflies (Syrphidae). Their larvae develop in watery environments, where they use their conspicuous snorkel tube to breath air at the water surface. Adults are typical blossom visitors, preferring Asteraceae and Apiaceae. Interesting highlight of their biology is the migratory behavior. These migratory insects form swarms, which cross the Alpes towards Southern European areas by using suitable wind conditions, where they finally hibernate and reproduce. The next generation returns the same way back. Not all individuals participate these migratory flights and would try to hibernate in Central Europe. Hibernating individuals are always females, which were fertilized prior to their winter diapause or their migration and which lay their eggs in the subsequent spring or in southern regions during winter. In Germany they only survive in greater numbers in milder winters, which they persist in temperature-stable hideways, such as gaps inside walls or wooden habitats. These specimen can be usually observed early in the year, beginning with March, when visiting blooming flowers. Their numerous very early appearance in mid February 2019 might be due to a very warm summer 2018 and a subsequent very mild winter in north-eastern Germany (Berlin). I have no comparative findings regarding the usual blooming time of the winter aconite and the abundance of drone flies there for Berlin or even this specific urban park. I also don’t know about indications that due to a global warming, as in some migratory birds, less specimens of the fly would migrate and more stay to hibernate here around.

The research station „Randecker Maar“ in the Swabian Jura records changes in migratory flights of birds and insects. They discovered a distinct decline of numbers of migrating drone flies and interpret it as a result of the increasing application of poisonous substances in the agricultural sector. Whether they additionally consider this being due to more individuals hibernating, where they are, based on generally warmer temperatures (global warming) is unknown to me.

 

Blow fly on blossom of the winter aconite, copyrights Stefan F. Wirth

 

The blow fly Calliphora vicina is a common blossom visitor in early spring and autumn. This fly, typically appearing in human settlements in Europe and the New World, is well adapted for an activity at lower temperatures (more than 13°C). While larvae develop in decomposing organic tissue (such as cadavers of animals), adults feed on nectar and pollen. They additionally incorprate saps from organic material with a strong odor.

C. vicina produces about five generation per year and throughout the year. The flies can even be active in winter, when temperatures reach a suitable level.

 

Other fly species were existant, but I did not determine them.

 

Time of footage and photo recording

 

Video footage and photos were recorded between 16 and 18 February 2019 in the urban park Schillerpark in Berlin.

 

Copyrights: Stefan F. Wirth, Berlin 2019.

Mite Histiostoma sachsi (Astigmata): Juvenile dispersal instar deutonymph and its orientation behavior

Some animals live in environments, where there is (almost) no light available. It makes no sense to see in the dark, but it is important for a specimen to know, where it actually is, where it is going to, whether there is enough food and what the conspecifics are doing. Predators need to be recognized in time, and a sexual partner must be found. There is also need for an efficient communication between specimens of a species. How can all this be performed by mites of the Astigmata, which usually live inside decomposing soil habitats in a more or less permanent darkness?

 

Olfactory sense organs in mites of the Histiostomatidae

 

Histiostoma sachsi (Histiostomatidae, Astigmata) is such a mite, living inside cow dung or compost. It might have a rudimentary ability for a light perception, but has not visible or functional eyes. It cannot produce any sounds. It can only feel and smell. Seemingly very limited abilities, but the contrary is fact: Due to evolution this mite is perfectly adapted to its life-style. It can feel objects by touching on them using its body setation (= body hairs). And it smells by means of very specialized body hairs, which are called solenidia and appear in different types, shapes and functions. These mites don’t smell on the level of us humans, which would be very insufficient. If at all, it should be compared with a dog. I am always fascinated when seeing blind dogs and how perfectly they can interact with their environment, despite their handicap. That’s may be how the efficiency of olfactory perception abilities of such a mite must be imagined. They do not only perceive scent particles from other animals, plants and soil components. Even olfactory signals from their conspecifics will be correctly and differentiatedly interpreted. And that not only marginally.  Olfactory signals represent indeed the major mode of their intraspecific communication.

 

Chemical communication of mites of the Histiostomatidae

 

Communication always requires contributions from both sides, a signal and an answer. These mites smell the signal of a conspecific using their solenidia, and they answer by the secretion of biochemical components. For these purposes, they possess a huge and complex gland system located on the upperside of their backs. Volatile excretions aggregate inside a big and rounded reservoir and finally leak to the outside via a pore, called oilgland opening. These gland systems are located symmetrically on both sides, each with one reservoir and one pore.

The meaning of the sent volatile message simply depends on the composition of the correspondingbiochemical components. Even diffferent stereochemical configurations of the same molecule can have different meanings. Citral for instance is a major component and has in different stereoisomers different functions. Such cummunicative volatile signals are usually named pheromones. And mites of the Histiostomatidae can indeed produce different kinds of pheromnes via the same gland system. Aggregation pheromones inform specimens about a suitable place to stay together with their conspecifics, for example due to a sufficient amount of food resources. Alarm pheromones solicit mites nearby to flee from an unpleasant situation. Sexual pheromones attract adult partners to each other in order to perform the mating procedure. But the gland secretions can even more. As allomones, they communicate with specimens of other species. They function as defenses against predators or other dangerous cohabitants.

 

Deutonymphs need to find a carrier for dispersal

 

Another form of communicative interspecific interactions is performed by a specific juvenile instar, the deutonymph. It looks morphologically quite different from all other instars (heteromorphic situation), does not need or possess a functional mouth, has a thicker cuticle as protection against drying out and a complex sucker organ on its underside in order to attach itself to an insect or another bigger arthropod. Deutonymphs of the astigmatid mites search for bigger carrier-arthropods to get carried from one habitat to another (dispersal strategy  is calledphoresy). While doing so, they again use their specifically modified leg setation (hairs) on the first pairs of legs to perceive scents for the detection of a suitable and passing by carrier. Basically it is still unknown, whether the term „communication“ is indeed appropriate in this context as we don’t know yet about a mutual interaction between deutonymphs and their carriers, before the phoretic ride begins.

 

 

Olfactory orientation of the deutonymph of Histiostoma sachsi, copyrights Stefan F. Wirth, February 2019.

 

Specific way of walking in deutonymphs

 

In detail, different kinds of behaviors can be observed in deutonymphs, when searching a carrier. The detailed behavioral patterns in this context can slightly differ between even closer related species. Deutonymphs of Histiostoma sachsi as all deutonymphs show a characteristic mode of walking, in which especially the first pair of legs plays an important role. During each step, performed by four pairs of legs, the first legs are lifted up much higher than all other hind legs. While doing so, they slightly tremble up and down. A behavior that mostly supports a better basic orientation inside a „jungle-„micro-landscape, being filled up with soil particles and decomposing plant tissues. But what H. sachsi deutonymphs additionally need in order to find their carriers is repeatedly to rest between the walking activities. Thus the first legs, which normally are still walking legs, are made free and that way available for the perception of carrier-scent-components only. These  namely are the legs that bear the highest densiy of solenidia.

 

Two different behavioral modes for an efficient orientation towards a carrier

 

Two different modes of resting with olfactory searching activities could be observed: In periodic intervals the deutonymph attached to the ground by using its sucking structures. They were then more or less laying on their entire undersides with only their forebodies slightly lifted up. By alternating moving the first legs up and down, olfactory information could be perceived from all directions without having the own body as a barrier to backwards. To improve its orientation situation, the deutonymph additionally turned on its own axis around, being stabilized by its sucking structures, which are flexible enough to follow these movements. When the deutonymph intended to continue its walk, it first needed to detach from the ground, which happened via muscle contractions that caused an abrupt detachment of the corresponding suckers. But main aim of the deutonymph is to find an elevated place, where the probability of a passing by carrier is especially high and from where a bigger insect (or other arthropod) can easier be ascended. There the second behavioral mode was performed. The deutonymph only fixed the edge of its hind body to the ground, again using the suckers on its underside, which are located close to this edge. This time the entire mite body stood in an upright position. The first legs again „waved“ alternating up and down and could under these especially elevated conditions even perceive scents from bigger distances. By occasionally slightly and alternating turning their upright bodies to both sides, olfactory information could be easier detected from all directions.

 

Carrier of H. sachsi still unknown

 

The frequency of such movements in mites increases typically as closer a suitable carrier approaches. But this was not yet observed or documented for Histiostoma sachsi. Its carrier inside the compost substrate is still unknown, which is why I so far could’t perform corresponding experiments. The species‘ describer, Scheucher (1957), found her mite specimens in cow dung and also didn’t identify the corresponding carriers there.

The observations presented in my video are part of my research project about morphologies and behaviors of deutonymphs in the Histiostomatidae.

 

Berlin, February 2019. All copyrights Stefan F. Wirth.

 

Arapaima gigas, einer der größten Süßwasserfische – doch was sind Fische eigentlich?

Sie sind beeindruckende Fische, nicht nur aufgrund ihrer Größe. Und doch kennen die meisten Menschen sie nur aus den Aquarienhäusern zoologischer Gärten. Arapaima gigas wird mindestens zwei Meter lang und erreicht in Ausnahmefällen sogar Längen von über drei Metern. Beheimatet ist die Art im Bereich des Amazonas-Beckens und ist in Peru, Brasilien und Guyana verbreitet.

 

Arapaima gigas, einer der größten bekannten Süßwasserfische aus dem Amazonas-Gebiet

 

Arapaima ist ein Räuber. Erwachsene Fische ernähren sich von anderen Fischen sowie Tieren in vergleichbarer Größe, wie zum Beispiel auch kleineren Säugern. Besonders auffällig sind die kräftig gestalteten großen Schuppen, die den Körper der Tiere umschließen. Sie dienen unter anderem als mechanischer Schutz gegen Angriffe durch Feinde. So können sie beispielsweise den Attacken der im selben Lebensraum beheimateten Piranhas, die zwar wesentlich kleiner sind, aber bekanntlich empfindliche Beißwerkzeuge besitzen, wirkungsvoll widerstehen. Das schützt Arapaima freilich nicht vor seinem größten Feind, dem Menschen. Er ist ein beliebter Speisefisch, der durch massenhafte Bejagung in seinem Bestand immer wieder gefährdet wird.

Arapaima gigas wird häufig als größter Süßwasserfisch der Welt bezeichnet. Dies basiert jedoch auf Übertreibungen. In Wahrheit befindet er sich in der Größenordnung des Europäischen Welses, dem größten europäischen Süßwasserfisch.

 

„Fische“ ist keine spezielle systematische Gruppierung

 

Ich verwendete bislang stets unkommentiert den Begriff „Fisch“. Was sind Fische eigentlich?Welche sogenannte Fische kennt man noch? Wie verhält es sich beispielsweise mit dem Bullenhai, der über drei Meter lang werden kann und neben marinen Habitaten auch im Süßwasser auftreten kann. Kann er als Gigant des Süßwassers mit dem Arapaima, dem Gigant aus dem Amazonas verglichen werden? Nach evolutionsbiologisch-systematischen (=phylogenetisch) Gesichtspunkten kann er das nicht. Der Begriff „Fisch“ bezeichnet nämlich keine spezielle, systematisch in sich geschlossene Gruppe. Stattdessen haben wir es mit einem deskriptiven Begriff zu tun, der alle Tiere umfasst, die in ihrer Gestalt ganz grundsätzlich eine gewisse Ähnlichkeit mit dem Goldfisch aufweisen.

Wenn wir außer Acht lassen, dass auch „Tintenfische“ und „Walfische“ nach demselben Muster benannt wurden, die bekanntlich zu den Mollusken und Säugetieren gehören, weist die Fischgestalt zumindest in den meisten Fällen auf eine irgendwie gestaltete Verwandtschaft hin. Jedoch sind Haie und Arapaima dennoch nicht sonderlich nahe miteinander verwandt.

 

Arapaima gigas im Aquarium des Zoos Berlin, ein gigantischer Süßwasserfisch, der regelmäßig atmosphärische Luft an der Wasseroberfläche aufnehmen muss. Copyrights Stefan F. Wirth

 

Bei den „Fischen“ handelt es sich nämlich um eine sogenannte paraphyletische Gruppe. Das heißt, sie umschließt zwar eine ihnen allen gemeinsame Stammart, jedoch keineswegs alle dazu gehörigen Tochtergruppen. Dazu würden nämlich auch alle Landwirbeltiere gehören. Eine vergleichbare paraphyletische Gruppe stellen beispielsweise die „Reptilien“ dar, zu denen Eidechsen/Schlangen, Schildkröten, Krokodile und alle Dinosaurier gehören. Da die Vögel aus den Dinosauriern hervorgingen, jedoch nicht zu den „Reptilien“ gezählt werden, haben wir es unter dieser Bezeichnung wieder mit einer Stammart und nur einem Teil aller Tochtergruppen zu tun, die allerdings im Stammbaum der Tiere nebeneinander stehen und daher näher miteinander verwandt sind, so wie auch bei den „Fischen“.

Im Falle der „Fische“ (paraphyletische Gruppen werden häufig in Anführungszeichen gesetzt) verhält es sich so, dass die verschiedenen als Fische bezeichneten Gruppen neben nur ihnen eigenen Merkmalen auch unterschiedliche Merkmale aufweisen, die auf eine Ahnenlinie hin zu den Wirbeltieren zurückgeführt werden müssen. Was unterscheidet also Knorpelfische (zum Beispiel Haie) und Strahlenflosser (Actinopterygii = echte Fische) voneinander? Eine Frage, die so in der modernen Systematik, die stets nach Gemeinsamkeiten sucht, eigentlich nicht gestellt wird. Richtiger ist es, zu fragen: Welche Merkmale teilen die Knorpelfische mit den Landwirbeltieren (z. B. knöcherner Schädel, Kiefer) und welche die Strahlenflosser (z.B. Lunge). Wenn man dennoch über Unterschiede sprechen möchte, ist festzustellen, dass Knorpelfische noch keine Lunge, die mit jener der Landwirbeltiere homolog ist, besitzen, Strahlenflosser aber schon. Die Lunge ist also auf der Ahnenlinie der Knorpelfische hin zu den Strahlenflossern evolviert. Anders als die „Fische“ sind die Strahlenflosser, die ich hier auch als echte Fische bezeichne, sehr wohl eine geschlossene systematische Einheit (=Monophylum), die auf Merkmale einer gemeinsamen Stammart zurückgeführt werden kann, die nur dieser Gruppe eigen sind. Ein Beispiel ist die namengebende Gestalt der Flossen, die durch Flossenstrahlen durchsetzt sind.

 

Zuerst gab es Lungen, aus denen Schwimmblasen evolvierten

 

Die Strahlenflosser (Actinopterygii), zu denen neben unzähligen Arten auch Arapaima gehört, besitzen also in der Tat ursprünglich paarige Lungen als Respirationsorgane. Diese sind demzufolge nicht erst vor dem Abzweig der Lungenfische entstanden, die als nächste Verwandte der Landwirbeltiere gelten. Die dortige Neuerung betrifft, anders als der Name Lungenfisch vermuten lässt, die Evolution eines Lungenkreislaufs, den es bei urtümlichen „Fischen“ mit Lunge noch nicht gegeben hat.

Aber besitzen echte Fische (Actinopteryii) nicht Schwimmblasen und atmen ausschließlich durch Kiemen? Mitnichten. Ursprüngliche Vertreter der echten Fische werden beispielsweise durch die Flösselhechte (Polypteriformes) representiert, die paarige sackförmige Lungen besitzen und neben der Kiemenatmung daher auch atmosphärische Luft veratmen können. Diese beeindruckenden Tiere können sich mithilfe ihrer Flossen nicht nur an Land fortbewegen, sondern lassen sich (es gibt Experimente an Senegal-Flösselhechten) auch unter vorwiegend terrestrischen Bedingungen in Terrarien halten.

Erst innerhalb der echten Fische ist die Schwimmblase entstanden, die sich durch Evolution aus den Lungen heraus bildete. Die fachgerechte Beschreibung lautet daher: Lunge und Schwimmblase sind einander homologe Organe. Innerhalb der Actinopterygii gibt es einen evolutiven Trend, demzufolge die Schwimmblase bei urtümlicheren Vertretern (noch) der Atmung dient, bei evolutiv weiter abgeleiteten Vertretern hingegen nur noch die Funktion der Austarierung im Wasser übernimmt.

Allerdings ist es innerhalb der echten Fische oftmals schwierig zu entschlüsseln und noch immer Gegenstand phylogenetischer Studien, ob die Lungenfunktion einer Schwimmblase einen Hinweis auf Urtümlichkeit darstellt, oder ob sekundär aus einer Schwimmblase mit Tarierfunktion erneut ein Atmungsorgan entstanden ist. In der Evolutionsbiologie werden im Übrigen unabhängige Entwicklungsschritte stets als Konvergenzen bezeichnet.

 

Arapaima gigas veratmet mithilfe seiner Schwimmblase atmosphärische Luft

 

Auch Arapaima gigas ist ein Luftatmer, der auf den Einsatz seines zusätzlichen Atmungsorgans in Form einer Schwimmblase sogar angewiesen ist. Er ist ein obligater Schwimmblasenatmer, der atmosphärische Luft an der Wasseroberfläche mithilfe seiner Mundöffnung aufnehmen muss. Dies wird als Anpassung an den häufig sauerstoffarmen Lebensraum der Tiere interpretiert, die sich häufig in Überflutungszonen des Amazonasbeckens aufhalten, wo wenig im Wasser gelöster Sauerstoff zur Verfügung steht. Der Literatur zufolge muss Arapaima gigas alle fünf bis fünfzehn Minuten die Wasseroberfläche aufsuchen, um dort mit seinem oberständigen Maul Luft einzuschnappen.

 

Berlin, Februar 2019, copyrights Stefan F. Wirth

Phoretic Mites waiting on Ant Pupae

Greater numbers of pupae from a nest of the myrmecine ant Myrmica rudinodis are attached by phoretic mites, which wait for these pupae to hatch. They would then attach the newly developed ants to be carried around and dispersed this way. They this way had already occupied their later ants before, namely during their pupal stage, one could call this phenomen „pupa-guarding“. In my samples, I discovered two species of mites performing this pupa guarding behavior. Most abundant were deutonymphs of the mite Forcellinia wasmanni (Astigmata). But also individuals of a mite species of the Gamasina were repeatedly discovered sitting on pupae, where they were hiding between head, ventrum and limbs of the pupa. They even seemed to defend their pupae, when they felt disturbed, e.g. by my filming activities.

 

Ant pupa guarding by mitees, looking for a carrier for dispersal

 

These pupa guarding-findings concerning this ant and with these corresponding mite species might be new to science (so far I didn’t found literature indications) and thus need to be studied closer in the future in order to understand the whole context of behaviors. In the footage, two types of pupae are visible, pupae of the winged alates and those of workers. Mites generally prefered both, but especially the deutonymphs of Forcellinia wasmanni seemed to appear more often on the pupae of later workers. Most pupae had at least one deutonymph attached, rarely, there were found up to four individuals. This is different to what could be found on older workers. They on their ventral side can have 4-6 deutonymphs. Many workers seem to be covered with the deutonymphs, but I didn’t check more workers until now, so I can’t say, how many were without mites. It is unknown, how deutonymphs come to the pupae, whether they simply leave older workers for the pupa-guarding or whether they were waiting in the soil for the pupae to arrive (due to the brood caring activitoes of the ants).

Mite-Life inside an ant nest. Copyrights Stefan F. Wirth 2015/18

 

Astigmatid mite with a strict relationship to ants

 

The mite Forcellinia wasmanni is known to be strictly associated with ants (e.g. Türk & Türk 1957). It is clear that attaching young female alates would secure the dispersial of the mite into a new ant nest. It is not clear, which function the transport via ant workers can have. But Türk & Türk (1957) mention that the free living instars of Forcellinia wasmanni would feed on dead ants. Such a kind of microhabitat for the development is not unique in astigmatid mites. Some species within the Astigmata are known to have such preferences for decaying cadavers, but are then feeding on microorganisms, which grow on these (insect) cadavers. Ant workers might be ideal to carry mite deutonymphs to new cadavers, where they would leave and develop. Ants generally have a very well developed hygienic behavior. This guarantees the mites to get access to cadavers regularly. I do not know any other video footage, showing living deutonymphs attached to their carriers on such a magnification level as visible in this film. The original footage of these deutonymphs is much longer.

 

Morphology and behavior of the dislersal-instar, the so called „deutonymph“

 

The function of the proterosoma (dorsal shield of the forebody) is acting as a flexible structure, protecting the mouthpart-area (non-functional in deutonymphs) and the fore-legs, but being very motile and being easily pushed backwards (under the following hyterosoma-shield), when the mite lifts up from the surface of the ant pupa. I cannot state much more concerning the second mite, found on pupae, which is a species of the Gamasina. I discovered this phenomenon only on three of my pupae. Ant nests represent complex communities of organisms, to which fungae, other insects, mites and nematodes can belong. The samples visible in this film were collected in July 2015 on the German island Usedom inside a forest area between the villages Zinnowitz and Karlshagen. The ant nest was quite small. An ant hill was not visible.

 

Complexity of life in ant nests

 

The complexity of life within ant nests is a result of evolution. I am an enemy of creationistic movements, including all modern faces of creationism. Creationism stimulates carelessness und illiteracy in the believing people.

 

 

Berlin August 2015/ December 2018, copyrights Stefan F. Wirth

Male and female of Histiostoma sachsi and unsuccessful mating with a „stranger“

Mites of the Acariformes vary in very different forms and life-strategies. One taxon of very tiny and soft-skinned mites is named Astigmata. Within them the familiy Histiostomatidae is especially rich of species, most of them surely not yet described or discovered.

 

Modyfied mouthparts and a specific mode of dispersal

 

These mites feed on microorganisms using a complex mouthpart-apparatus with multifunctional abilities. They can be found in habitats, which dry out quickly. When it’s getting too dry, a specific instar of the mites takes a ride on insects or other bigger arthropods for dispersal to a new and fresh habitat ( strategy called Phoresy).

Histiostoma sachsi is one of numerous (often closely related) long haired (in females) species. It was originally in 1957 described from cattle-dung. I found it in compost.

 

Long upper-setation in females and tactile camouflage (mimesis)

 

Adult females are characterized by a long setation on their uppersides. They use them to hold parts of the old nymphal cuticle and soil particles on their backs. This seems to be due to a strategy named mimesis or camouflage. It’s a tactile camouflage as an optical sense in this kind of microhabitats plays almost no role.

 

Normal and unusual copulation position, trial of an interspecific copulation

 

Males mate their females via a dorsal copulation opening and thus need to ride on them. In H. sachsi, that copulation opening is located very close to the hind-edge of the body. That way it is even despite of the camouflage cover accessible. It seems even slightly being elevated out of the body surface in order to surmount adjacent soil particles. This is an adaptation of this particular species. It might share such morphological characters only with very closely related (not yet described) species In other members of genus Histiostoma, the copulation opening is usually more centered related to the hind body.

The copulation position requires that males insert their aedeagus („penis“) into the copulation opening. They additionally use their legs to grasp into the females body. That kind of leg arrangement and thus the whole copulation position can differ from species to species.

This is why copulations between members of different species already fail, because the right copulation setting does not fit, nor does the shape of the aedeagous. Nevertheless the phenomenon of unsuccessful trials for interspecific copulations can sometimes be observed in laboratory cultures. Such a trial is also visible in this video, where a male of Histiostoma feroniarum (also appears in my compost samples regularly) tries to mate a female of H. sachsi. It cannot even almost get in a proper copulation position and seems to hold on to the dorsal camouflage cover of the female. it could only remain in a transverse position related to the female body and thus not get access to the copulation opening, normal would be a longitudinal position with the sameame orientation of female and male.

Adult mites of the family Histiostomatidae (Astigmata) and a „false“ copulation. Copyrights Stefan F. Wirth, Berlin December 2018. Please like my video also at Youtube, in case you like it.

 

Chemical communication and chemo-sensitive leg setation

 

Mites of the Astigmata communicate and find their general orientation due to chemo-sensitive setae, mostly on legs I and II, which are named solenidia. They are even on the magnification level of my footage well visible on the male’s legs. Although a direct body contact is not necessary for a innerspecific communication by chemically interpreting scents produced from mite glands, the observed male in my video repeatedly was seeking for intense body-contacts and obviously „observed“ his conspecific while doing so with its first two legs. This might have intensified the perception of pheromones.

It showed this behavior also, when passing by the „false copulation-pair“ described above. It additionally seemed to invest power in its leg movements as if it would try to remove the „competitor“ on the female, in this case even belonging to another species.

 

Competitive fights between males

 

That mites of the Histiostomatidae can use their strongly sclerotized first legs to fight under each other for an access to a female is known to me from my older observations about the species Histiostoma palustre and Histiostoma feroniarum.

 

Origin of the compost samples

 

The compost samples were collected in SW-Germany (Saarland in October 2018). The footage was recorded in December 2018 in Berlin.

 

Berlin December 2018, copyrights Stefan F. Wirth

Habitat compost: Mite Histiostoma sachsi carries old cuticle and dirt as camouflage

My parents have a compost area in their backyards. I use it as reference habitat for two mite species of the family Histiostomatidae (Astigmata): Since I began my research in 2000, the compost regularly contained Histiostoma feroniarum with its typical male dimorphism. Since summer 2017 another species appears additionally regularly: Histiostoma sachsi. Both species do not appear under the same conditions. While H. feroniarum prefers fresher decaying material, H. sachsi on visibly older decomposed tissue. There mite be even more mites of the Histiostomatidae exist in this complex compost habitat, but under my laboratory conditions, only the two named species were so far successfully reared out of samles always again. Regarding the determination of H. sachsi on a species level, I was more careful in my comments to a former video (June 17), in which I named it Histiostoma cf. sachsi due to doubts about a correct identification. Meanwhile, also due to the morphology of the deutonymph, I determine „my“ compost mite as Histiostoma sachsi Scheucher, 1957. But it is still to emphasize that Scheucher described H. sachsi from cattle dung, not from compost. But generally, both habitats can sometimes share the same inhabitants.

 

Adult females carry their old cuticles and „dirt“ on their backs as tactile comouflage

 

Biologically conspicuous is darkish material, which especially adult females carry on their backs. Unlike males, females posses elongated setae on their backsides. These setae support the holding of material such as old cuticle and soil particles. In slide preparations, this cover usually appears amorphic and contains substrate from the mite’s environment. My video footage indicates that the basis of this cover is a retained old cuticle from the former nymphal instar . That this cannot easily be proven with the light microscope is due to the very soft and fine character of the cuticles in these mites. Remnants might become decomposed by microorganisms after a while.

Compost: the habitat of the mite Histiostoma sachsi Scheucher, 1957 (Acariformes, Astigmata, Histiostomatidae). Copyrights Stefan F. Wirth, please like my video also on youtube, in case you like it.

 

The phoretic dispersal instar, named deutonymph, in mites of the Astigmata controls its body position due to sticky leg endings and suckers on their undersides

 

Deutonymphs of H. sachsi represent one of my resent models to study mite-dispersal behavior. My research focus since a while concerns ultrastructure and function morphology of the deutonympal suckerplates and other structures to attach to insects for dispersal (this dispersal strategy is called phoresie). The anterior front-suckers on the suckerplate of the mite’s underside is extendable and very flexible, not only to find a suitable position on the insect carrier. When falling, the deutonymphs use it to lift their bodies up into a proper position again. Additionally they will try to get hold using „sticky“ lobe-shaped setae on the endings of legs I and II. Both is visible in my footage. The forelegs seem generally to make the first contact, when trying to get on a suitable carrier.

 

Deutonymphs of Histiostoma sachsi take a ride on other mites (Oribatida)

 

The suitable carrier of H. sachsi is unknown to me. Some astigmatid species have even a range of carrier-„hosts“. In my samples, deutonymphs at least attach to other mites, especially to mites of the Oribatida. This is in a very short scene visible in my video too.

 

Copyrights Stefan F. Wirth, Berlin December 2018