Animal or Plant: Which Is the Better Fog Water Collector?

Occasional fog is a critical water source utilised by plants and animals in the Namib Desert. Fog basking beetles (Onymacris unguicularis, Tenebrionidae) and Namib dune bushman grass (Stipagrostris sabulicola, Poaceae) collect water directly from the fog. While the beetles position themselves optimally for fog water collection on dune ridges, the grass occurs predominantly at the dune base where less fog water is available. Differences in the fog-water collecting abilities in animals and plants have never been addressed. Here we place beetles and grass side-by-side in a fog chamber and measure the amount of water they collect over time. Based on the accumulated amount of water over a two hour period, grass is the better fog collector. However, in contrast to the episodic cascading water run-off from the grass, the beetles obtain water in a steady flow from their elytra. This steady trickle from the beetles' elytra to their mouth could ensure that even short periods of fog basking--while exposed to predators--will yield water. Up to now there is no indication of specialised surface properties on the grass leafs, but the steady run-off from the beetles could point to specific property adaptations of their elytra surface.     

Polarized iridescence of the multilayered elytra of the Japanese jewel beetle, Chrysochroa fulgidissima

The elytra of the Japanese jewel beetle Chrysochroa fulgidissima are metallic green with purple stripes. Scanning electron microscopy and atomic force microscopy demonstrated that the elytral surface is approximately flat. The accordingly specular green and purple areas have, with normal illumination, 100-150 nm broad reflectance bands, peaking at about 530 and 700 nm. The bands shift progressively towards shorter wavelengths with increasing oblique illumination, and the reflection then becomes highly polarized. Transmission electron microscopy revealed that the epicuticle of the green and purple areas consists of stacks of 16 and 12 layers, respectively. Assuming gradient refractive index values of the layers between 1.6 and 1.7 and applying the classical multilayer theory allowed modelling of the measured polarization- and angle-dependent reflectance spectra. The extreme polarized iridescence exhibited by the elytra of the jewel beetle may have a function in intraspecific recognition.     

Frictional surfaces of the elytra-to-body arresting mechanism in tenebrionid beetles (Coleoptera : Tenebrionidae) : design of co-opted fields of microtrichia and cuticle ultrastructure

In beetles, the system responsible for an attachment of forewings (elytra) to the thorax consists of interlocking fields of microtrichia (MT) located between thorax and body and between left and right elytra. The present study provides comparative data about microtrichia design on the thorax and elytra in three species of tenebrionid beetles (Tribolium castaneum, Tenebrio molitor, Zophobas rugipes) (Coleoptera : Tenebrionidae), which are different in their size. The length, width, density and directionality of microtrichia in 13 MT fields (4 on the thorax, 1 on the abdomen, 7 on the elytra, and 1 on the costal vein of the hindwing) were quantified. (1) Parameters studied are dependent on the dimension of an insect. The length of the microtrichia of most fields compared increases with an increase in body size. The MT width in the majority of fields increases with an increase in the elytra length. The MT density decreases with an increase in the elytra length. (2) Both width and length of microtrichia increase with an increase in the distance between single MT. The density of outgrowths increases with an increase in their length and width. (3) The fields oriented along the same spatial axis constitute functional groups responsible for a particular direction. Co-opted fields can be oriented in the same or opposite directions. (4) The design of MT correlates in co-opted surfaces. There are 3 field groups, which were stated as functionally corresponding to one another : the medial, anterio-lateral, and posterio-lateral. The lengths and widths of microtrichia from fields of these functional groups were quite similar in corresponding fields. Length-to-width ratios of MT in elytral fields were usually weakly correlated with those of thoracic fields. The distances between microtrichia on the elytra surface directly depended on those of the thorax. Distance-to-width ratio of MT of one surface slightly increased with an increase in this parameter on the co-opted surface. The MT densities on co-opted fields were usually quite different. (5) The ultrastructure of the cuticle suggests differences in the material properties of the cuticle between MT fields. The thoracic fields usually consist of elastic cuticle, whereas elytral fields are much harder. Usually, a MT field of elastic cuticle corresponds to the field composed of hard cuticles. The study also provides information about the ultrastructure of epidermal cells and about the design of pore channels, which are presumably responsible for production and transport of an adhesive secretion into the area of contact between lateral fields. Sensory organs monitoring contact between co-opted binding sites were also studied. The results of this study may aid in understanding the morphological basis of cuticular microsculptures acting as frictional devices.     

Brilliant camouflage: photonic crystals in the diamond weevil, Entimus imperialis

The neotropical diamond weevil, Entimus imperialis, is marked by rows of brilliant spots on the overall black elytra. The spots are concave pits with intricate patterns of structural-coloured scales, consisting of large domains of three-dimensional photonic crystals that have a diamond-type structure. Reflectance spectra measured from individual scale domains perfectly match model spectra, calculated with anatomical data and finite-difference time-domain methods. The reflections of single domains are extremely directional (observed with a point source less than 5°), but the special arrangement of the scales in the concave pits significantly broadens the angular distribution of the reflections. The resulting virtually angle-independent green coloration of the weevil closely approximates the colour of a foliaceous background. While the close-distance colourful shininess of E. imperialis may facilitate intersexual recognition, the diffuse green reflectance of the elytra when seen at long-distance provides cryptic camouflage.     

Physiological colour change in the elytra of the hercules beetle, Dynastes hercules

The male of the hercules beetle, Dynastes hercules, is able to change the colour of its elytra from yellowish to black and back again to yellowish within a few minutes. The epicuticle of the elytra is transparent and about 3 μm thick. Below it is a yellow spongy layer that is usually about 5 μm thick. The cuticle below the yellow sponge is black. When the layer of yellow sponge is air filled it becomes optically heterogeneous, and the light reflected from the elytra is yellow. When the yellow sponge is liquid filled it becomes optically homogeneous, and the black cuticle below is seen.If a beetle that has yellowish elytra is placed in a saturated atmosphere, the elytra become black. When the relative humidity is appreciably reduced, yellow patches begin to appear on the elytra, usually within 30 sec to 2 min. However, if the beetle is kept at a constant relative humidity that previously caused yellowing, it will become black given enough time. Most colour changes observed were clearly in response to changes in the ambient humidity and were not affected when the beetles were kept in the light or in total darkness nor by blackening their eyes or prodding them or exposing them to sounds of different intensities or frequencies.If an elytron is removed from a live beetle, it changes colour in response to changes in relative humidity exactly like the elytron left attached. When a restricted area of the elytra is subjected to a humidity that normally causes blackening and an adjacent area to a humidity that normally causes yellowing, both change colour in the expected way. This local control of colour change seems to preclude hormonal control. It is suggested that the epidermal cells or both the epidermal and blood cells in the elytra are responsible for the hydration and dehydration of the layer of yellow sponge.     

Compound Microstructures and Wax Layer of Beetle Elytral Surfaces and Their Influence on Wetting Properties

A beetles’ first line of defense against environmental hazards is their mesothoracic elytra – rigid, protective forewings. In order to study the interaction of these wings with water, the surface microstructures of various beetles’ elytra were observed by Environment Scanning Electron Microscopy (ESEM) and Atomic Force Microscopy (AFM). Chemistry components were ascertained using X-ray photoelectron spectroscopy (XPS). All the beetles of various habitats (including desert, plant, dung, land and water) exhibited compound microstructures on their elytra. The wetting properties of these elytra were identified using an optical contact angle meter. In general the native elytra exhibited hydrophilic or weak hydrophobic properties with contact angles (CAs) ranging from 47.5° to 109.1°. After treatment with chloroform, the CAs all increased on the rougher elytral surfaces. The presence of wax is not the only determinant of hydrophobic properties, but rather a combination with microscopic structures found on the surfaces. Irregularities and the presence or absence of tiny cracks, hairs (or setae), pores and protrusions are important factors which influence the wetting properties. Rougher elytral surfaces tended to present a stronger hydrophobicity. Effects on hydrophobicity, such as surface microstructures, chemistry, environment and aging (referring to the time after emergence), are also included and discussed. Our results also provide insights into the motion of water droplets when in contact with beetle elytra.     

Field trapping of the flathead oak borer Coroebus undatus (Coleoptera: Buprestidae) with different traps and volatile lures

The flathead oak borer Coroebus undatus F. (Coleoptera: Buprestidae) is one of the primary pests of cork oak Quercus suber L. in the Mediterranean region causing great economic losses to the cork industry. Very little is known about its biology and behavior and, so far, no control measures have been established. We present the results of a pilot study aimed to develop an efficient trapping method for monitoring this harmful pest. In a 3‐year field study, purple‐colored prism traps baited with a mixture of green leaf volatiles (GLVs) from the host have been shown the most effective combination to catch C. undatus adults (solely females) compared to other trap and lure types tested. Wavelength and reflectance measurements revealed that purple traps exhibit reflectance peak values similar to those found in the abdominal and elytral cuticle of both sexes, suggesting the involvement of visual cues for mate location in this species. The data presented are the first to demonstrate captures of adults of the genus Coroebus by an attractant‐based trapping method.     

Species Identification of Food Contaminating Beetles by Recognizing Patterns in Microscopic Images of Elytra Fragments

A crucial step of food contamination inspection is identifying the species of beetle fragments found in the sample, since the presence of some storage beetles is a good indicator of insanitation or potential food safety hazards. The current pratice, visual examination by human analysts, is time consuming and requires several years of experience. Here we developed a species identification algorithm which utilizes images of microscopic elytra fragments. The elytra, or hardened forewings, occupy a large portion of the body, and contain distinctive patterns. In addition, elytra fragments are more commonly recovered from processed food products than other body parts due to their hardness. As a preliminary effort, we chose 15 storage product beetle species frequently detected in food inspection. The elytra were then separated from the specimens and imaged under a microscope. Both global and local characteristics were quantified and used as feature inputs to artificial neural networks for species classification. With leave-one-out cross validation, we achieved overall accuracy of 80% through the proposed global and local features, which indicates that our proposed features could differentiate these species. Through examining the overall and per species accuracies, we further demonstrated that the local features are better suited than the global features for species identification. Future work will include robust testing with more beetle species and algorithm refinement for a higher accuracy.     

Disentangling thermal from alternative drivers of reflectance in jewel beetles: A macroecological study

Aim

To predict future colour–climate relationships, it is important to distinguish thermal drivers of reflectance from other evolutionary drivers. We aimed to achieve this by comparing relationships between climate and coloration in ultraviolet–visible (UV–Vis) and near-infrared (NIR) light, separately.

Location

Samples were distributed primarily across Australia and North America, with some from Africa and Asia.

Major taxa studied

Coleoptera: Buprestidae.

Methods

We used jewel beetles as models to identify climatic drivers of reflectance, because jewel beetles have highly diverse coloration and a wide distribution and are often active in hot conditions. Specifically, we tested the association between climate, body size and reflectance using a phylogenetic comparative analysis for three wavebands (UV–Vis, NIR and total).

Results

Reflectance of jewel beetles was more strongly predicted by body size than by climate. NIR reflectance and total reflectance were not associated with climate, but larger beetles had higher NIR reflectance. For UV–Vis reflectance, small beetles were darker in warmer and more humid environments, whereas there was no association with climate for large beetles.

Main conclusions

Our study suggests that variation in reflectance of jewel beetles is not driven by thermal requirements and highlights the importance of considering NIR reflectance when evaluating explanations of the effects of colour on thermoregulation.     

A scaleless scale worm: Molecular evidence for the phylogenetic placement of Pisione remota (Pisionidae, Annelida)

Pisionidae is a group of interstitial worms whose phylogentic affinities have been enigmatic. They have been allied to different Phyllodocida taxa. Although originally associated with Glyceridae and Phyllodocidae, they are more recently considered to be related to scale worms. Scale worms are a well-defined taxon, Aphroditiformia, within Annelida due to the unique possession of dorsal scales called elytra. Pisionidae lack elytra but they have been grouped with scale worms because they possess two pairs of jaws with venom glands, also found in Glyceridae. Determining the phylogenetic position of Pisionidae is important for understanding if features such as elytra and venomous jaws are evolutionarily labile in annelid history. Therefore, we explored 18S rDNA and Cytochrome c Oxidase subunit I data from several Aphroditiformia, Pisionidae, and other Phyllodocida to determine the phylogenetic placement of Pisionidae. Maximum likelihood and Bayesian inference of separate and combined data sets were conducted. All analyses support a derived position of Pisionidae within Aphroditiformia, close to Pholoidae and Sigalionidae. The loss of elytra in Pisionidae is probably due to adaptation for interstitial life. Furthermore, the results reject a monophyletic Aphroditoidea comprising Acoetidae, Aphroditidae, Eulepethidae and Polynoidae. Thus, the possession of only simple chaetae is either symplesiomorphic or convergent.     

Lehr's fields of campaniform sensilla in beetles (Coleoptera): Functional morphology. III. Modification of elytral mobility or shape in flying beetles

Some flying beetles have peculiar functional properties of their elytra, if compared with the vast majority of beetles. A “typical” beetle covers its pterothorax and the abdomen from above with closed elytra and links closed elytra together along the sutural edges. In the open state during flight, the sutural edges diverge much more than by 90°. Several beetles of unrelated taxa spread wings through lateral incisions on the elytra and turn the elytron during opening about 10–12° (Cetoniini, Scarabaeus, Gymnopleurus) or elevate their elytra without partition (Sisyphus, Tragocerus). The number of campaniform sensilla in their elytral sensory field is diminished in comparison with beetles of closely related taxa lacking that incision. Elytra are very short in rove beetles and in long-horn beetles Necydalini. The abundance of sensilla in brachyelytrous long-horn beetles Necydalini does not decrease in comparison with macroelytrous Cerambycinae. Strong reduction of the sensory field was found in brachyelytrous Staphylinidae. Lastly, there are beetles lacking the linkage of the elytra down the sutural edge (stenoelytry). Effects of stenoelytry were also not uniform: Oedemera and flying Meloidae have the normal amount of sensilla with respect to their body size, whereas the sensory field in the stenoelytrous Eulosia bombyliformis is 5–6 times less than in chafers of the same size but with normally linking broad elytra.     

Mechanical and Frictional Properties of the Elytra of Five Species of Beetles

The mechanical and frictional properties of different parts of the elytra of five species of beetle were measured using a nano-indenter and a micro-tribometer. The surface microstructures of the elytra were observed by optical microscopy and scanning white light interferometry. The surface microstructures of the elytra of all five species are characterized as non-smooth concavo-convex although specific morphological differences demonstrate the diversity of beetle elytra. Young's modulus and the hardness of the elytral materials vary with the species of beetle and the sampling locations, ranging from 1.80 GPa to 12.44 GPa, and from 0.24 GPa to 0.75 GPa, respectively. In general, both the Young's modulus and the hardness are lower in samples taken from the center of the elytra than those taken from other regions, which reflects the functional heterogeneity of biological material in the process of biological evolution. The elytra have very low friction coefficient, ranging from 0.037 to 0.079, which is related to their composition and morphology. Our measurements indicate that the surface texture and its microstructural size of beetle elytra contribute to anti-friction effects.     

Indirect closing of elytra by the prothorax in beetles (Coleoptera): general observations and exceptions

Voluntary movements of the prothorax and the elytra in tethered flying beetles and manually induced movements of these parts in fresh dead beetles were recorded in 30 species representing 14 families. Participation of prothoracic elevation in the closing of the elytra was demonstrated in three ways. (i) The elevation was always simultaneous with elytral closing, in contrast to depression and elytral opening; a rare exception occurred in Lucanus cervus, whose elytra sometimes started to close before the cessation of wing strokes and the elevation of the prothorax. (ii) The manipulated elevation always induced closing of the spread elytra; the mechanical interaction between the hind edge of the pronotum and the roots of the elytra is a universal mechanism of closing the elytra in beetles. (iii) The prevention of pronoto-elytral contact in live beetles by the excision of the hind edge of the pronotum in front of the root prevented elytral closing after normal flight. Exceptions to this rule included some beetles that were able to close their elytra after such an excision: tiger beetles and diving beetles (seldomly) and rose chafers (always). This ability in Adephaga may be explained by attachments of the muscle actuating the 4th axillary plate, which differ from the attachments in Polyphaga. Cetoniinae open their elytra only by a small amount. It is proposed that their small direct adductors in combination with the elasticity of the sclerites are enough to achieve elytral closing without additional help from the prothorax.     

Beetle elytra: evolution,modifications and biological functions

Conversion of forewings into hardened covers, elytra, was a ground-breaking morphological adaptation that has contributed to the extraordinary evolutionary success of beetles. Nevertheless, the knowledge of the functional aspects of these structures is still fragmentary and scattered across a large number of studies. Here, we have synthesized the presently available information on the evolution, development, modifications and biological functions of this crucial evolutionary novelty. The formation of elytra took place in the earliest evolution of Coleoptera, very likely already in the Carboniferous, and was achieved through the gradual process of progressive forewing sclerotization and the formation of inward directed epipleura and a secluded sub-elytral space. In many lineages of modern beetles, the elytra have been distinctly modified. This includes multiple surface modifications, a rigid connection or fusion of the elytra, or partial or complete reduction. Beetle elytra can be involved in a very broad spectrum of functions: mechanical protection of hind wings and body, anti-predator strategies, thermoregulation and water saving, water harvesting, flight, hind wing folding, diving and swimming, self-cleaning and burrow cleaning, phoresy of symbiotic organisms, mating and courtship, and acoustic communication. We postulate that the potential of the elytra to take over multiple tasks has enormously contributed to the unparalleled diversification of beetles.     

Passive aerodynamic stabilization by beetle elytra (wing covers)

Summary. Most beetles extend their elytra laterally during flight, where they can act as fixed airfoils; typically, such elytra are held at a pronounced dihedral angle. We fixed extended elytra of June beetles (Scarabaeidae: Melolonthinae) and tiger beetles (Cicindelidae) over a range of dihedral angles (-10° to 45°) and towed them in a water tunnel. We also towed them with flexed elytra (i.e. in the resting position). (Reynolds number was used to maintain dynamic similarity with air.) We measured the maximum rolling angle and the lateral oscillation rate as two indices of stability. There was no relationship between oscillation rate and dihedral angle, or between maximum roll angle and dihedral angle. At all dihedral angles tested, however, beetles were much more stable than when they were towed with the elytra flexed. We also included a third beetle type, flower beetle (Scarabaeidae: Cetoniine), which normally flies with flexed elytra. We measured stability indices for these beetles with elytra only in the flexed position. When all beetles were tested with flexed elytra, flower beetles showed no difference in maximum roll angle, but more stability in oscillation rate than the other two beetle types.     

Mechanical properties of elytra from Tribolium castaneum wild-type and body color mutant strains

Cuticle tanning in insects involves simultaneous cuticular pigmentation and hardening or sclerotization. The dynamic mechanical properties of the highly modified and cuticle-rich forewings (elytra) from Tribolium castaneum (red flour beetle) wild-type and body color mutant strains were investigated to relate body coloration and elytral mechanical properties. There was no statistically significant variation in the storage modulus E′ among the elytra from jet, cola, sooty and black mutants or between the mutants and the wild-type GA-1 strain: E′ averaged 5.1 ± 0.6 GPa regardless of body color. E′ is a power law function of oscillation frequency for all types. The power law exponent, n, averaged 0.032 ± 0.001 for elytra from all genotypes except black; this small value indicated that the elytra are cross-linked. Black elytra, however, displayed a significantly larger n of 0.047 ± 0.004 and an increased loss tangent (tan δ), suggesting that metabolic differences in the black mutant strain result in elytra that are less cross-linked and more pigmented than the other types. These results are consistent with the hypothesis that black elytra have a β-alanine-deficient and dopamine-abundant metabolism, leading to greater melanin (black pigment) production, probably at the expense of cross-linking of cuticular proteins mediated by N-β-alanyldopamine quinone.     

Cuticular hydrocarbons on elytra of the Diaprepes root weevil Diaprepes abbreviatus (L.) (Coleoptera: Curculionidae)

Abstract 1 External gland openings and associated structures on the elytra of teneral and mature Diaprepes root weevils, Diaprepes abbreviatus (L.), were elucidated by scanning electron microscopy (SEM). 2 There were clear differences between teneral, callow adults and fully mature adults. In the field, teneral adults remain in the pupal chamber in the soil until sclerotization of the cuticle is complete or nearly so. 3 Phenotypic variation of the elytra in this species consists of varying patterns and coloration of scaled intervals between a variable number of raised ridges devoid of scales. In addition to being thinner and lighter in colour than fully mature adults, the elytra of teneral adults were devoid of waxy hydrocarbon secretions. 4 External gland openings at the base of each scale were observed on teneral elytra and mature elytra washed with methylene chloride. 5 SEM evidence to document the production of waxy filaments by these glands and partial characterization of these by gas chromatography and mass spectrometry are presented.     

Macro-/Micro-Structures of Elytra, Mechanical Properties of the Biomaterial and the Coupling Strength Between Elytra in Beetles

Macro-/Micro-structures and mechanical properties of the elytra of beetles were studied. The Scan Electron Microscope (SEM) and optical microscopy were employed to observe the macro-/micro-structure of the surface texture and cross-section structure of elytra. Nano-indentation was carried out to measure the elastic modulus and the hardness of elytra. Tensile strengths of elytra in lateral and longitudinal directions were measured by a muhifunctional testing machine. The coupling force between elytra was also measured and the clocking mechanism was studied. SEM images show the similar geometric structure in transverse and longitudinal sections and multilayer-dense epicuticle and exocuticle, followed by bridge piers with a helix structured fibers, which connect the exocuticle to the endodermis, and form an ellipse empty to reduce the structure weight. The elastic modulus and the hardness are topologically distributed and the mechanical parameters of fresh elytra are much higher than those of dried elytra. The tensile strength of the fresh biological material is twice that of dried samples, but there is no clear difference between the data in lateral and longitudinal directions. Coupling forces measured are 6.5 to 160 times of beetles' bodyweight, which makes the scutellum very important in controlling the open and close of the elytra. The results provide a biological template to inspire lightweight structure design for aerospace engineering.     

How Could Beetle＇s Elytra Support Their Own Weight during Forward Flight？

The aerodynamic role of the elytra during a beetle＇s flapping motion is not well-elucidated, although it is well-recognized that the evolution of elytra has been a key in the success of coleopteran insects due to their protective function. An experimental study on wing kinematics reveals that for almost concurrent flapping with the hind wings, the flapping angle of the elytra is 5 times smaller than that of the hind wings. Then, we explore the aerodynamic forces on elytra in free forward flight with and without an effect of elytron-hind wing interaction by three-dimensional numerical simulation. The numerical results show that vertical force generated by the elytra without interaction is not sufficient to support even its own weight. However, the elytron-hind wing interaction improves the vertical force on the elytra up to 80%; thus, the total vertical force could fully support its own weight. The interaction slightly increases the vertical force on the hind wind by 6% as well.