How Do Scale Insects Settle into the Nests of Plant-Ants on Macaranga Myrmecophytes? Dispersal by Wind and Selection by Plant-Ants

This report elucidates the process of settlement by Coccus scale insects into Crematogaster plant-ant nests formed inside the hollow stems of a myrmecophytic species, Macaranga bancana, in a tropical rain forest. We collected wafting scale insect nymphs from the canopy using sticky traps and characterized the DNA sequence of the trapped nymphs. In addition, we experimentally introduced first-instar nymphs of both symbiotic and nonsymbiotic scale insects to M. bancana seedlings with newly formed plant-ant colonies. Nymphs of symbiotic species were generally carried by ants into their nests within a few minutes of introduction. Most nymphs of nonsymbiotic species were thrown to the ground by ants. Our results suggest that in Crematogaster–Macaranga myrmecophytism, symbiotic coccids disperse by wind onto host plant seedlings at the nymphal stage, and plant-ants actively carry the nymphs landing on seedlings into their nests in discrimination from nonsymbiotic scale insects

How Do Scale Insects Settle into the Nests of Plant-Ants on Macaranga Myrmecophytes? Dispersal by Wind and Selection by Plant-Ants

This report elucidates the process of settlement by Coccus scale insects into Crematogaster plant-ant nests formed inside the hollow stems of a myrmecophytic species, Macaranga bancana, in a tropical rain forest. We collected wafting scale insect nymphs from the canopy using sticky traps and characterized the DNA sequence of the trapped nymphs. In addition, we experimentally introduced first-instar nymphs of both symbiotic and nonsymbiotic scale insects to M. bancana seedlings with newly formed plant-ant colonies. Nymphs of symbiotic species were generally carried by ants into their nests within a few minutes of introduction. Most nymphs of nonsymbiotic species were thrown to the ground by ants. Our results suggest that in Crematogaster-Macaranga myrmecophytism, symbiotic coccids disperse by wind onto host plant seedlings at the nymphal stage, and plant-ants actively carry the nymphs landing on seedlings into their nests in discrimination from nonsymbiotic scale insects.ArticleSOCIOBIOLOGY. 59(2):435-446 (2012)journal articl

オオバギ属アリ植物の共生アリ巣に生息するカイガラムシについての生態学的研究

京都大学0048新制・課程博士博士(人間・環境学)甲第19070号人博第723号新制||人||173(附属図書館)26||人博||723(吉田南総合図書館)32021京都大学大学院人間・環境学研究科相関環境学専攻(主査)教授 市岡 孝朗, 教授 加藤 眞, 教授 瀬戸口 浩彰学位規則第4条第1項該当Doctor of Human and Environmental StudiesKyoto UniversityDGA

Syntheses, Structures, and Properties of Mono- and Dinuclear Acetylacetonato Ruthenium(III) Complexes with Chlorido or Thiocyanato Ligands

The mononuclear and dinuclear ruthenium(III) complexes trans-Ph4P[RuIII(acac)2Cl2] (1), Ph4P[{RuIII(acac)Cl}2(μ-Cl)3] (2) and trans-Ph4P[RuIII(acac)2(NCS)2]·0.5C6H14 (3·0.5C6H14) were synthesized. Single crystals of 1, 2·H2O and 3·CH3CN suitable for X-ray crystal structure analyses were obtained through recrystallization from DMF for 1 and 2·H2O and from acetonitrile for 3·CH3CN. An octahedral Ru with bis-chelate-acac ligands and axial chlorido or κ-N-thiocyanido ligands (for 1 and 3·CH3CN) and triply µ-chlorido-bridged dinuclear Ru2 for 2·H2O were confirmed through the structure analyses. The Ru–Ru distance of 2.6661(2) of 2·H2O is indicative of the existence of the direct metal–metal interaction. The room temperature magnetic moments (μeff) are 2.00 and 1.93 μB for 1 and 3·0.5C6H14, respectively, and 0.66 μB for 2. The temperature-dependent (2–300 K) magnetic susceptibility showed that the strong antiferromagnetic interaction (J ≤ −800 cm−1) is operative between the ruthenium(III) ions within the dinuclear core. In the 1H NMR spectra measured in CDCl3 at 298 K, the dinuclear complex 2 showed signals for the acac ligand protons at 2.50 and 2.39 ppm (for CH3) and 5.93 ppm (for CH), respectively, while 1 and 3·0.5C6H14 showed signals with large paramagnetic shifts; −17.59 ppm (for CH3) and −57.01 ppm (for CH) for 1 and −16.89 and −17.36 ppm (for CH3) and −53.67 and −55.53 ppm (for CH) for 3·0.5C6H14. Cyclic voltammograms in CH2Cl2 with an electrolyte of nBu4N(ClO4) showed the RuIII → RuIV redox wave at 0.23 V (vs. Fc/Fc+) for 1 and the RuIII → RuII waves at −1.39 V for 1 and −1.25 V for 3·0.5C6H14 and the RuIII–RuIII → RuIII–RuIV and RuIII–RuIII → RuIII–RuIV waves at 0.91 V and −0.79 V for 2

Copper(II) Carboxylates with 2,3,4-Trimethoxybenzoate and 2,4,6-Trimethoxybenzoate: Dinuclear Cu(II) Cluster and µ-Aqua-Bridged Cu(II) Chain Molecule

Copper(II) complexes with 2,3,4-trimethoxybenzoic acid (H234-tmbz) and 2,4,6-trimethoxybenzoic acid (H246-tmbz), [Cu2(234-tmbz)4(H2O)2] (6) and [Cu(246-tmbz)2(µ-H2O)2(H2O)2]n (7), were synthesized and characterized by elemental analysis, infrared and UV-vis spectra and temperature dependence of magnetic susceptibilities (1.9–300 K). The X-ray crystal structures revealed that the former 6 is a dinuclear cluster having syn-syn-bridged Cu2(µ-234-tmbz)4 core with Cu···Cu separation of 2.6009(7) Å, while the latter 7 is a µ-aqua-bridged chain molecule consisting of Cu(246-tmb)2(µ-H2O)2(H2O)2 units with Cu···Cu separation of 4.1420(5) Å. Temperature dependence of magnetic susceptibilities showed that an antiferromagnetic interaction with 2J = −272 cm−1 for 6 and a weak antiferromagnetic interaction with J = −0.21 cm−1 for 7, between the two copper(II) ions. The adsorption isotherm of 6 showed Types I behavior having a 125.4 m2g−1 of specific surface area