Dry under water: Comparative morphology and functional aspects of air‐retaining insect surfaces

Superhydrophobic surfaces prevent certain body parts of semiaquatic and aquatic insects from getting wet while submerged in water. The air layer on these surfaces can serve the insects as a physical gill. Using scanning electron microscopy, we investigated the morphology of air‐retaining surfaces in five insect species with different levels of adaptation to aquatic habitats. We found surfaces with either large and sparse hairs (setae), small and dense hairs (microtrichia), or hierarchically structured surfaces with both types of hairs. The structural parameters and air‐film persistence of these surfaces were compared. Air‐film persistence varied between 2 days in the beetle Galerucella nymphaea possessing only sparse setae and more than 120 days in the bugs Notonecta glauca and Ilyocoris cimicoides possessing dense microtrichia (up to 6.6 × 10⁶ microtrichia per millimeter square). From our results, we conclude that the density of the surface structures is the most important factor that affects the persistence of air films. Combinations of setae and microtrichia are not decisive for the overall persistence of the air film but might provide a thick air store for a short time and a thin but mechanically more stable air film for a long time. Thus, we assume that a dense cover of microtrichia acts as a “backup system” preventing wetting of the body surface in case the air–water interface is pressed toward the surface. Our findings might be beneficial for the development of biomimetic surfaces for long‐term air retention and drag reduction under water. In addition, the biological functions of the different air retention capabilities are discussed. J. Morphol., 2011. © 2011 Wiley‐Liss, Inc.     

Water Striders： The Biomechanics of Water Locomotion and Functional Morphology of the Hydrophobic Surface （Insecta： Hemiptera-Heteroptera）

Water striders are insects living on the water surface, over which they can move very quickly and rarely get wetted. We measured the force of free walking in water striders, using a hair attached to their backs and a 3D strain gauge. The error was calculated by comparing force and data derived from geometry and was estimated as 13%. Females on average were stronger （1.32 mN） than males （0.87 mN）, however, the ratio of force to weight was not significantly different. Compared with other lighter species, Aquarius paludum seems stronger, but the ratio of force to weight is actually lower. A. paludum applies about 0.3 mN.cm^-1 to 0.4 mN.cm 1 with its mid-legs, thus avoiding penetrating the surface tension layer while propelling itself rapidly over the water surface. We also investigated the external morphology with SEM. The body is covered by effectively two layers of macro-and micro-hairs, which renders them hydrophobic. The setae are long （40 μm-60μm） and stiff, being responsible for waterproofing, and the microtrichia are much smaller （〈10μm）, slender, and flexible, holding a bubble over the body when submerged.     

Water Striders:The Biomechanics of Water Locomotion and Functional Morphology of the Hydrophobic Surface(Insecta:Hemiptera-Heteroptera)

Water striders are insects living on the water surface, over which they can move very quickly and rarely get wetted. We measured the force of free walking in water striders, using a hair attached to their backs and a 3D strain gauge. The error was calculated by comparing force and data derived from geometry and was estimated as 13%. Females on average were stronger (1.32 mN) than males (0.87 mN), however, the ratio of force to weight was not significantly different. Compared with other lighter species, Aquarius paludum seems stronger, but the ratio of force to weight is actually lower. A. paludum applies about 0.3 mN·cm-1 to 0.4 mN·cm-1 with its mid-legs, thus avoiding penetrating the surface tension layer while propelling itself rapidly over the water surface.We also investigated the external morphology with SEM. The body is covered by effectively two layers of macro-and micro-hairs, which renders them hydrophobic. The setae are long (40 um-60 um) and stiff, being responsible for waterproofing, and the microtrichia are much smaller (<10 um), slender, and flexible, holding a bubble over the body when submerged.     

Respiration and growth of Hyas araneus L. Larvae (Decapoda:Majidae) from hatching to metamorphosis

Rates of respiration and growth were measured for larvae of the spider crab Hyas araneus L., reared in the laboratory from hatching to metamorphosis. The moulting cycle was simultaneously monitored. In both zoeal instars individual respiration rate (R) increased as a linear function of time (t) of development, whereas growth, measured as dry weight (W), carbon (C), nitrogen (N), hydrogen (H), and energy content (E, calculated from C) followed a power function of t. Weight-specific respiration rate (QO₂) was in all instars maximum in early postmoult, and minimum in intermoult and early premoult. Zoea II and megalopa instars showed another conspicuous QO₂ increase during late premoult. Respiration (both R and QO₂)and growth of the megalopa could be described by non-linear (quadratic) functions of t. R and QO₂ during this larval stage were not correlated with W, but were controlled by events of the moulting cycle: R followed a similar pattern to QO₂ (minimum values in intermoult), whereas biomass of the megalopa changed conversely, with a maximum in intermoult and early premoult. The respiratory coefficient (i.e. the ratio of metabolic energy loss: energy gain by body growth) was far lower (<0.8) in the zoeal instars than in the megalopa (>5), suggesting a strongly reduced capability of energy conversion in the final larval stage of H. araneus.     

Larval stop,delayed development and survival in overcrowded cultures of Drosophila melanogaster: Effect of urea and uric acid

Uric acid and urea added to non-crowded cultures of D. Melanogaster are able to reproduce the larval stop (cessation in development) detected in highly competitive situations. The quantitative analysis of media as well as of larvae and pupae reveals the presence of both compounds as natural waste products of nitrogen metabolism in Drosophila. The nature of their effect is discussed in terms of larval intoxication as a mechanism which may account for the effects usually observed in crowded cultures: development delay, lower survival and also larval stop (which can only be detected by interrupting the competitive process by an overfeeding technique).     

A scanning electron microscope study of tarsal adhesive setae in the Coleoptera

Scanning electron micrographs of the tarsal adhesive setae of 84 species of beetle are described. These show a vast range of setal structure and distribution.     

欧洲伪叶甲Lagria hirta L.种群季节变化和幼虫生长发育(鞘翅目:伪叶甲科)(英)

欧洲伪叶甲Lagria hirta L.野外种群季节变化特点鲜明:成虫仅发生于6月底至8月初,幼虫除6月份外全年可见。基于野外观察和测量幼虫头宽,发现这种甲虫的生殖季节很短,在6至8月份;卵孵化后幼虫生长发育,在越冬前可达第3、4或5龄(个别达6龄);幼虫越冬后,经过总共8—10龄,于6月份化蛹。冬季幼虫发育减慢但不完全停滞(非参数型中数检验,P<0.01)。这项研究改变了以前的观点,即认为该甲虫的幼虫发育只有4或5龄,同时也对这种甲虫的生命周期研究有促进作用。     

Pre-imaginal flight motor pattern in Locusta

In a wind stream, larval stages of Locusta usually show a tonic muscle activity but they can also exhibit a rhythmic motor output. With ageing such a pattern can be released sooner, the trains become longer. The basic rhythm of 10 Hz does not change. The initial co-contraction of specific muscles is substituted later in development by an antagonistic recruitment. This activity resembles the flight motor pattern of young locusts which lack phasic sensory feedback from the wing region. Azadirachtin, an insect growth regulator, has been used to produce a permanent 5th larval instar. However, the extension of the last larval stage does not lead to a further development of the motor pattern to a level comparable to mature animals.     

POPULATION SEASONALITY AND LARVAL DEVELOPMENT OF LAGRIA HIRTA L. (COLEOPTERA: LAGRIIDAE)*

Abstract The seasonality of the field population of Lagria hirta L. is remarkable: adults occur only from the end of June to the beginning of August, whereas larvae exist in the whole year except June. Based on the data of field observations and larval head-width measuring, the author demonstrated that L. hirta would reproduce in a very short interval in June to August; eggs hatch and develop (molt) into the 3rd, 4th or 5th (sometimes 6th) instar before winter; after larval overwintering, the beetles complete the larval development after total 8–10 times of molts and pupate in June. The larval development rate is decreased but not completely stopped during winter (the nonparametric median test, P<0. 01). This result changes the hitherto opinion of 4 or 5-instar larval development of L. hirta and will stimulate the studies on its life history.     

Effect of ultraviolet radiation on growth and percent settlement of larval Lytechinus variegatus (Echinodermata: Echinoidea)

Lytechinus variegatus larvae were used to examine the effects of ecologically relevant short-term exposures of ultraviolet radiation (UVR) on larval morphology and settlement. A laboratory experiment tested the blastula, gastrula, and early pluteus stages of larval development for susceptibility to damage from exposure to UVR produced by an artificial light source. Larval post-oral arm length and percent settlement were measured to assess UVR effects. Larvae exposed at the blastula and gastrula stages had a reduction in larval post-oral arm length compared with non-exposure controls, while larvae exposed at the early pluteus stage were similar to controls. Larvae exposed in the gastrula stage had a significant reduction in percent settlement compared with controls. Negative consequences from ecologically relevant levels of UVR were differentially dependent on the larval stage at time of exposure suggesting time point in larval development at exposure will be important in interpreting effects on higher levels of biological organization.     

Influence of artificial honeydew on larval development and survival inChrysoperla carnea [Neur., Chrysopidae]

The effects of providing (a) an artificial honeydew consisting of yeast autolysate, sugar and water in the ratio 4∶7∶10 live prey (eggs ofEphestia kuehniella), and (b) water and life prey, on larval development and survival in the green lacewingChrysoperla carnea were examined. Compared with larvae provided with eggs and water, those given eggs and artificial honeydew were more likely to complete their development and did so significantly more rapidly.     

Effects of photoperiod and temperature on head-capsule size in Planotortrix octo (Lepidoptera: Tortricidae)

Abstract

The head-capsule widths of Planotortrix octo were measured atphotophases of 0, 2, 6, 12, 14, 16, 18, and 24 h under a LD 24 h cycle. The headcapsule widths of the 2nd, 4th, and 5th instar showed a photoperiodic response, being smaller under photophru;es of 12-16 h.

The critical 5th instar head-capsule size above which pupation occurred, appeared smaller at these photophases. However, the critical size could not be determined accurately—or this difference verified statistically—as there wru; some overlap in capsule size between 5 and 6 instar groups.     

Ultrastructure of larval epidermis of the nemertean <Emphasis Type="Italic">Quasitetrastemma stimpsoni</Emphasis> (Chernyshev, 1992) (Hoplonemertea)

The ultrastructure of the epidermis of free-swimming larvae of the nemertean Quasitetrastemma stimpsoni was examined. At about 24 hours after hatching, the provisional epithelium of larva is 28–35 μm thick and consists of two layers of cells—peripheral and basal. The peripheral layer consists of multiciliated cells and two kinds of gland cells. The “basal cup” zone is formed from the vacuoles of basal cells. At about 50 hours after hatching, the definitive epithelium is 14–17 μm thick and exhibits a typical hoplonemertean structure. However, it has numerous yolk vesicles, few processes of granular basal cells, and a weakly developed dermis. Thus, the replacement of the provisional epithelium by the definitive one occurs in Q. stimpsoni at an earlier stage, compared to the hidden larva of Tetrastemma candidum.