Geographical variation in mandible morphologies specialised for collembolan predation depend on prey size in the ant Strumigenys lewisi

1. Ants in the genus Strumigenys are predator ants that feed on tiny soil arthropods. The mandibles are modified into high‐speed traps to capture swift collembolan prey. The peculiar mandible morphologies of these ants have evolved depending on characteristics of the prey. Specifically, the evolution of mandible size and shape may be directly driven by prey size. 2. In the present study, the intraspecific variation of the morphological traits of Strumigenys lewisi populations were observed in central Japan. The relationships between the morphological variations and the prey body size were analysed. 3. In workers and queens, three morphological traits, head width, mandible length, and mandible width were significantly different among the multiple sites. Specifically, the mandible length was shorter in southwestern Japan than in other sampling locations. The ancova model revealed that the allometry of the mandible length to the head width was different among the sites. 4. As predicted, the mandible length was positively correlated with the average body size of collembolans in the Entomobryidae family. Furthermore, multiple regression analysis showed that the variation of the mandible length was affected by environmental factors represented as location information. However, the effect of collembolan body size was more effective at predicting mandible length. The study suggests that the geographical variation of mandible morphologies in S. lewisi has been selected by predator–prey interactions with collembolans.     

Effects of Organic Solvents on the Coupling Between ATP Hydrolysis and Sliding of Microtubules in Axonemes from Chlamydomonas Flagella

ABSTRACT. The effects of organic solvents on the ATPase activity and the sliding disintegration of axonemes from Chlamydomonas were investigated. The axonemal ATPase was markedly activated by methanol accompanying with marked inhibition of the sliding disintegration of axonemes. On the contrary, glycerol inhibited the ATPase activity without serious inhibition of the sliding disintegration. As far as the axonemes are not irreversibly denatured by extremely high concentration of solvents, the effects of solvents both on the ATPase and the ability of sliding are reversible. Therefore, the inhibition of sliding accompanied by the activation of ATPase is probably due to an inability to couple the hydrolysis of ATP to sliding between dynein and microtubule in the presence of methanol. The axonemal ATPase was less sensitive to vanadate inhibition after exposure to methanol. This indicates that methanol makes the dyneinADP.Pi complex unstable and increases product release. On the other hand, glycerol and ethylene glycol seem to stabilize the force generation responsible for the sliding through stabilizing the dynein.ADP.Pi complex.     

Metabolism of Round Spermatids: A Possible Regulation of Hexose Transport

Round spermatids (steps 1–8) were isolated from rat testes and glucose transport into the cells was examined. The exposure of spermatids to glucose resulted in an extremely low level of ATP. In contrast, the level of ATP remained constant in the presence of pyruvate. Transport of a glucose analogue, 2-deoxy-D-[³H]glucose ([³H]dGlc) into spermatids was correlated with intracellular levels of ATP and was much greater in cells with higher rather than lower levels of ATP. [³H]dGlc transport into spermatids with low levels of ATP was partially reversed when the cells were incubated with pyruvate. Inhibition of [³H]dGlc transport was exerted on Vmax and not on Km. Moreover, glucose acted as a competitive inhibitor of [³H]dGlc uptake (Km increased; Vmax unaltered). These results suggest that glucose transport into spermatids is active in vitro and probably regulated by the intracellular level of ATP.     

Reactivity of a Monoclonal Antibody Raised against Human Leukemic Cells to Embryonic and Adult Tissues of the Mouse and Teratocarcinomas

C-9-1, a monoclonal IgM antibody raised against human null cell acute lymphocytic leukemia cells reacted with restricted regions of embryonic and adult tissues of the mouse. The antigen positive sites in the embryos included embryonic ectoderm, visceral endoderm, trophoblastic cells invading the maternal decidua of 5∼7-day embryos, primordial germ cells of 10∼12-day embryos, epithelium of nasal chamber, the bronchus, Mullerian duct, epididymis and bladder of 12∼17-day embryos. In the adult mice, C-9-1 antigen was detected in renal tubules, a part of stomach, bladder, endometrium and epididymal sperm. Embryonal carcinoma cells, but not endodermal cells of teratocarcinoma expressed the antigen. Thus, C-9-1 antigen showed distribution similar to SSEA-1. However, C-9-1 antigen was not detected in preimplantation embryos, nor in oviduct, both of which are positive for SSEA-1.     

Structure of Major Surface Determinants and DNA Diagnosis of Pneumocystis carinii

Pneumocystis carinii is a pathogen which, causes fatal pneumonia in patients with the acquired immune deficiency syndrome (AIDS). To facilitate the basic study of P. carinii , we have analyzed its major surface proteins by both immunochemical and biochemical methods. The major protein components of both cysts and trophozoites are a group of proteins called "P115" with apparent masses of 105–120 kd. It includes 6 isoelcclric variants. A monoclonal antibody raised against cysts recognizes all 6 variants and reacts with epitopes located in the cell wall indicating that P115 is an immunorcactive surface component. The isoelectric variants contain identical or closely related protein components and they are mannose-rich glycoproteins. The isoelectric variation may be due primarily to differences in glycosylation. The majority of sera from humans with diagnosed pneumocystosis that were tested reacted strongly with the P115 proteins. To develop probes for DNA diagnosis and to facilitate molecular studies, a genomic DNA library of P. carinii has been constructed. Some of these clones were used for DNA hybridization analysis of rat and human lungs.     

Synergistic Inhibition of Fructose 1,6-Bisphosphatase by Fructose 2,6-Bisphosphate and Adenosine Monophosphate in Round Spermatids of Rats

The effects of adenosine monophosphate (AMP) and fructose 2, 6-bisphosphate (fruc-2, 6-P₂) on the key-enzyme of gluconeogenesis, fructose 1, 6-bisphosphatase (fruc-P₂ase; D-fructose 1, 6-bisphosphate 1-phosphohydrolase, EC 3.1.3.11) in spermatid extract from rat testes were studied. The fruc-P₂ase activity in the spermatids of rats was suppressed by AMP and fruc-2, 6-P₂. The inhibition of fruc-2, 6-P₂ was much stronger at low than at high substrate concentrations, and enhanced synergistically with AMP. The substrate saturation curve was changed by fruc-2, 6-P₂ hyperbolic to sigmoidal. Furthermore, the concentration of AMP that decreased the activity to 50% was much lower in the presence than in the absence of fruc-2, 6-P₂. These results indicate the possibility that gluconeogenesis in spermatids of rats is controlled by AMP and fruc-2, 6-P₂.     

Indices of reproductive skew depend on average reproductive success

Several indices of reproductive skew, which quantify the degree of unequal partitioning of reproductive output among members in an animal society, have been proposed. Here we point out the drawbacks of these indices. The most serious problem is the dependence of the indices on mean reproductive success: skew values tend to be larger, as average numbers of offspring decrease, due to random sampling error in numbers of offspring. Thus it is difficult to compare societies with different average lifetime reproductive success using these indices, even though we have presented methods to calculate the expected reproductive skew caused by random sampling error, especially when average numbers of offspring are small, as is often the case with cooperatively breeding vertebrates. As an alternative, we propose using the spatial dispersion indices of population ecology (Morisita's index or its standardized version) for the measurement of reproductive skew. These indices are almost independent of average fecundity and have their own method of testing for random variation in offspring numbers. This revised version was published online in July 2006 with corrections to the Cover Date.     

Parasitoid spectrum (Hymenoptera: Braconidae; Aphelinidae) of the soybean aphid Aphis glycines (Homoptera: Aphididae) in Japan and Indonesia (Java and Bali)

Aphidiine and aphelinid parasitoids collected from the soybean aphid, Aphis glycines, on Glycine max in Japan and Indonesia (Java and Bali) were identified to clarify the parasitoid spectrum of the aphid there. Nine parasitoid species from Japan (Aphidiinae: Aphidius gifuensis, Aphidius sp., Binodoxys communis, Diaeretiella rapae, Lipolexis gracilis, Lysiphlebia japonica; Aphelinidae: Aphelinus asychis, A. gossypii, A. varipes) and two parasitoid species from Indonesia (B. communis, A. gossypii) were found to be associated with A. glycines.