Spatial variability and major controlling factors of CO2 sink strength in Asian terrestrial ecosystems: evidence from eddy covariance data

Asian terrestrial ecosystems cover an extensive area characterized by a large variety in climates and ecosystem properties. The observations of ecosystem CO₂ flux in this area are increasing both in duration and spatial density, but no synthesis has yet been conducted. We surveyed CO₂ flux observation data obtained by eddy covariance methods at 49 sites in terrestrial Asia. The measurements at most sites (44 of 49) began after 2000. The net ecosystem uptake of CO₂ (NEE) varied greatly among sites and years and averaged −132.6±73.7, −250.1±206.1, and −180.1±361.7 g C m⁻² yr⁻¹, in boreal, temperate, and tropical Asia, respectively, and the coefficient of variation among sites increased from boreal to tropical Asia. The site-averaged annual NEE was correlated linearly with the mean annual temperature (T_air) and also correlated logarithmically with the precipitation. Multiple regression analysis and stepwise analysis indicated that photosynthetic active radiation (PAR) and T_air were the most significant predictors of the annual NEE. The study results suggest that Asian terrestrial ecosystems are currently significant net CO₂ sinks and that the sink strength is largely controlled by temperature, moisture, and light conditions.     

MAINTENANCE OF PHENOTYPIC PROPERTIES BY CHONDROCYTES CULTURED IN SUSPENSION*

Sternal chondrocytes obtained from 13-day-old chick embryos could be cultured in suspension without any mechanical agitation for 8 weeks. The cells in suspension retained all characteristics of chondrocytes when examined from morphological, histochemical and biochemical points of view. The floating cells were round in shape, rich in Golgi apparatus-associated vesicles. Each cell was covered with a thin coat of matrix showing metachromasia when stained with toluidine blue. Autoradiographic studies suggested an active synthesis of proteochondroitin sulfates by the individual floating cells. The biochemical analyses revealed that the floating cells continued to synthesize type H proteochondroitin sulfate and type II collagen, both of which are known to be characteristic products of differentiated chondrocytes.     

Role of photoperiod and temperature in seasonal morph determination of the butterfly Eurema hecabe

ABSTRACT. Environmental cues affecting seasonal morph determination of the pierid butterfly Eurema hecabe L. were examined in laboratory experiments and in the field. A sexual difference exists in the photoperiodic response for seasonal morph determination: in short days at 25C the proportion of the autumn morph is higher in females than in males, and as the rearing temperature is decreased the proportion of autumn morphs increases in both sexes. A 5C drop in temperature during the final larval stadium induces 100% autumn morph production in short-day animals. This increase in autumn morph production induced by temperature decrease explains the seasonal morph change of this butterfly occurring in early autumn in the field. The role of this sex-linked photoperiodic response is discussed as a seasonal strategy of reproduction.     

Wolbachia‐induced feminisation newly found in Eurema hecabe,a sibling species of Eurema mandarina (Lepidoptera: Pieridae)

1. Complete feminisation of genetic males into functional females, a unique case among insects, is known in Eurema mandarina (former Eurema hecabe Y type) that are infected with two strains of Wolbachia, wCI^Em and wFem^Em. 2. Here, we newly found that a proportion of wild‐caught E. hecabe (former E. hecabe B type) produced only female offspring. Cytogenetic observations indicated that individuals of E. hecabe displaying the all‐female trait were genetically male (i.e. feminisation). 3. Multilocus sequence typing analyses demonstrated that the feminised individuals of E. hecabe were infected with two Wolbachia strains, wCI^Eh and wFem^Eh, that were indistinguishable from wCI^Em and wFem^Em, respectively. 4. Even identical strains of Wolbachia can be regulated differently depending on the host genetic background. Therefore, we compared the infection densities and vertical transmission efficiencies of Wolbachia between feminised E. mandarina and E. hecabe, but detected no significant differences in these traits. 5. The possible routes by which the two Wolbachia strains have transferred between E. mandarina and E. hecabe are discussed.     

Removal and subsequent ingestion of rivals' semen during copulation in a tree cricket

ABSTRACT. A novel combination of adaptations resulting from sperm competition is demonstrated for the tree cricket Truljalia hibinonis (Matsumura) (Podoscirtinae: Gryllidae: Orthoptera). 87.5% of the semen of previous males is displaced onto the penis of the copulating male and is removed at the end of copulation. Semen thus removed is ingested during post-copulatory oro-genital grooming. No overt morphological adaptations for sperm removal were observed and, on the basis of anatomical evidence, it is suggested that rivals' semen is flushed out of the female?s sperm storage organ by the semen of the last male.     

Ca2+ and UVB Radiation Have No Effect on E-Cadherin-Mediated Melanocyte-Keratinocyte Adhesion

Direct cell-cell contact between melanocytes and keratinocytes has been shown to play an important role in the regulation of human melanocyte function and skin pigmentation. An important role for the calcium-dependent epithelium-specific cell adhesion molecule, E-cadherin, in melanocyte-keratinocyte adhesion was suggested previously. To further clarify regulation of E-cadherin-mediated melanocyte-keratinocyte interactions, we investigated the effects of physiological (Ca²⁺) and environmental (ultraviolet B [UVB] radiation) stimuli on the expression and functional activity of E-cadherin in melanocyte-keratinocyte adhesion. Expression of E-cadherin mRNA was detected by Northern blot analysis in cultured normal human melanocytes at levels similar to those in keratinocytes. Flow cytometry analysis with anti-human and anti-mouse-E-cadherin antibodies (anti-uvomorulin and ECCD-2) showed that cultured normal human keratinocytes, melanocytes, and two metastatic melanoma cell lines express E-cadherin strongly on the cell surfaces. Melanocyte adhesion, particularly to differentiating keratinocytes (cultured in 1.2 mM calcium) but not to proliferating keratinocytes or to fibroblasts, was decreased by 41.7 ± 4.5% in the absence of 1 mM Ca²⁺ during the binding assay. Addition of anti-mouse-E-cadherin antibody (ECCD-1) to the binding assay inhibited the adhesion of melanocytes to differentiating keratinocytes by 88.2 ± 1.1%, while addition of anti-P-cadherin antibody (PCD-1) had no effect. The levels of E-cadherin expression in melanocytes were not changed by the presence of calcium (1 mM) in the medium or by UVB irradiation (20 mJ/cm²) for one day before flow cytometry analysis. Moreover, these treatments had no effect on melanocyte-keratinocyte adhesion. These results demonstrate that E-cadherin is strongly involved in melanocyte adhesion to keratinocytes and suggest the implication of E-cadherin in the overall regulation of the skin pigmentary system.