Circellium bacchus is a flightless telecoprid (ball-rolling) dung beetle, endemic to the afrotropical region, where it is found in a few restricted populations in the eastern Cape of South Africa. Its apterous condition and large size (mass ranges from 6 to 12 g) are considered to be adaptations to a semi-arid habitat. This beetle is active in the sun for long periods, walking between widely scattered dung pats, thus is under selection pressure to reduce water loss.
C. bacchus has eight spiracles on each side of the body. The metathoracic spiracle and six abdominal spiracles open into the subelytral cavity, which is closed. The mesothoracic spiracle is the largest and most exposed, occurring ventrally in the membrane connecting the prothorax and mesothorax.
When at rest a cyclic form of respiration, known as discontinuous gas exchange cycle, is used by C. bacchus, releasing a burst of carbon dioxide approximately once an hour when the spiracles open for about 33 minutes. Flow-through respirometry was used to measure water loss from the thorax (being the head, prothorax and mesothorax) and elytral case (containing the metathorax and abdomen) separately. The total water loss of C. bacchus could be divided up as 65% cuticular water loss from the thorax, 35% cuticular water loss from the elytral case, 4% respiratory water loss from the thorax and no measurable respiratory water loss from the elytral case. 1.51 µg of water is lost for every µl of CO2 emitted during respiration in the thorax. Thus, the main avenue for both respiration and respiratory water loss is via the mesothoracic spiracles, suggesting that the primary function of the subelytral cavity is not to reduce respiratory water loss.
It is shown that coherent electrodynamics of water molecules produces extended regions where the chemical activity of bio-molecules is governed in a selective way by a code based on frequency resonance. Coherence Domains of water act as devices able to collect low-grade energy in the environment and to transform it into high-grade energy able to produce electronic excitations.
Water is the most important constituent of all living organisms (70% of the total mass and 99% of all molecules). Other biomolecules, proteins, fats, sugars, vitamins, salts, which are usually considered the only molecules playing a remarkable role in molecular biology, make up only 1% of the total. So, biological activity is assumed to involve 1% of all molecules only.
What is the role of water then? Is it possible that 99% of all biomolecules are necessary only as a solvent whereas the ``really essential'' biomolecules enact all productive activity?
The driving and regulatory role of water in governing the biochemical activity has begun to be recognized in recent times (Voeikov, 2007).
In order to unravel this puzzle, we should take another enigma, which is the existence of biochemical codes (Barbieri, 2004), into account. Apart from the living matter or more generally far from catalysts, molecules are usually subjected to a polygamous regime; each biomolecule can interact with many others, thus producing a great number of reactions. In living matter, instead, biomolecules live inside each particular biochemical cycle in a monogamous condition (at least within definite time intervals), i.e. a biomolecule interacts only with well-defined partners and ignores the other biomolecules, with which interaction would be possible in empty space. Living matter therefore produces a ``context'' capable of preventing a great number of chemical interactions, which would theoretically be possible. The possibility of molecular interactions is governed by biochemical codes (the genetic code is the most widely known among them), to which particular biological processes correspond. Within the world of biomolecules, there are thus the prerequisites for communication. Indeed, biochemical cycles are open and capable of reacting against new influences. In this way all the codes build up and adopt flexible features, which are typical of a language.
The emergence of these biochemical codes from the dynamics of matter is undoubtedly the main problem of biology.
Naturally occurring veinless specimen of the swallowtail Papilio xuthus show an extremely aberrant colour pattern. In spite of the fact that we have no breeding data, these veinless specimen are provisionally called veins-reduced mutant. In these mutants seven longitudinal veins of the fore wing and five of the hind wing are absent. The absence of wing veins is associated with a loss of the broad black venous stripes that normally are present along the proximal portion of the veins. In addition, missing veins cause a loss of the dislocation of black bands in adjacent wing cells, so that what are discrete black segments in normal wings become continuous bands in the veinless wing. Computer simulations show that the morphology of the striped patterns on both the veinless and veined wing can be explained if the wing margin acts as an inductive source of pattern formation and the veins act simply as boundaries to the propagation of the signal from the wing margin. The vein-dependent patterns by contrast, require that the veins act as inductive sources, at least along their proximal portion. This dual role of wing veins is consistent with prior observations on the biology of colour pattern formation. The unique veinless colour pattern strongly supports the hypothesis that the wing margin is the dominant organiser of colour pattern in this species, and possibly in other Papilionidae.
The cocoons characteristic of the prepupal and pupal stages of many insects vary widely in size, durability, structure, shape and colour, as well as in other features such as orientation and attachment to the substrate. In some species they vary seasonally. Most cocoons provide little direct insulation, although they may reduce the rate at which temperature changes, but many provide the mechanical protection required for overwintering beneath insulating substrates such as soil and snow. The cocoons of some terrestrial species prevent inoculative freezing by isolating the integument from ice crystals on the cocoon surface or its surroundings. In some aquatic species, cocoons appear to limit damage by providing mechanical protection during the freezing of surrounding water. Some cocoons help in the acquisition of solar heat: dark structures are especially effective because dark pigments absorb heat, and surrounding layers trap this heat. Insects are immobilized when it is cold and so cannot move in response to environmental threats, and protective cocoons made for winter tend to be more robust than their summer counterparts. Such cocoons protect against abrasion of the waterproof layer of the cuticle. In some species, robust cocoons or complex structures impede natural enemies. Cocoon silk has anti-bacterial and anti-fungal actions. Other cocoons are more or less waterproof. These and other features withstand simultaneous constraints in addition to cold. Therefore, cocoons enhance survival during cold conditions in many species. However, this conclusion is based on fragmentary evidence, and there has been relatively little explicit examination of the roles of cocoons during winter. Therefore, specific work is required to assess resistance to or enhancement of inoculative freezing, resistance to penetration by natural enemies and water, the roles of particular cocoon silks and silk constituents, and the quantitative contributions of cocoons to winter survival in nature.
We present the Rothe method for the McKendrick-von Foerster equation with initial and boundary conditions. This method is well known as an abstract Euler scheme in extensive literature, e.g. K. Rektorys, The Method of Discretization in Time and Partial Differential Equations, Reidel, Dordrecht, 1982. Various Banach spaces are exploited, the most popular being the space of bounded and continuous functions. We prove the boundedness of approximate solutions and stability of the Rothe method in $L^\infty $ and $L^1$ norms. Proofs of these results are based on comparison inequalities. Our theory is illustrated by numerical experiments. Our research is motivated by certain models of mathematical biology.
In this paper, we study the s-Perron, sap-Perron and ap-McShane integrals. In particular, we show that the s-Perron integral is equivalent to the McShane integral and that the sap-Perron integral is equivalent to the ap-McShane integral.
Monoclonal antibody-based treatment of cancer has been established as one of the most successful therapeutic strategies for both hematologic malignancies and solid tumors. In addition to targeting cancer antigens antibodies can also modulate immunological pathways that are critical to immune surveillance. Antibody therapy directed against several negative immunologic regulators (checkpoints) is demonstrating significant success in the past few years. Immune checkpoint inhibitors, ipilimumab,
pembrolizumab and nivolumab, have shown significant clinical benefit in several malignancies and are already approved for advanced melanoma and squamous NSCLC. Based on their mechanism of action, these agents can exert toxicities that are unlike conventional cytotoxic chemotherapy, whose nature is close to autoimmune diseases -
immune related adverse events (irAEs). In this review we focus on the spectrum of irAEs associated with immune checkpoint antibodies, discussing the pharmacological treatment strategy and possible clinical impact.
A unifying picture to the hermeneutical approach to schizophrenia is given by combining the philosophical and the experimental/computational approaches. Computational models of associative learning and recall in the cortico-hippocampal system helps to understand the circuits of normal and pathological behavior.