Diverse diet compositions among harpaline ground beetle species revealed by mixing model analyses of stable isotope ratios

1. Species diversities of some insect lineages have been attributed to differentiation of feeding habits among species. Our objective was to determine variation in diet composition among harpaline ground beetle species occurring in a riverside grassland. 2. We examined the diet compositions of 14 species from six genera in the spring and 10 species from two genera in the autumn. We performed measurements of nitrogen and carbon stable isotope ratios in consumers and in their potential food items, and estimated relative contributions of different food items with two mixing models, IsoSource and MixSIR. 3. IsoSource and MixSIR software gave similar results, but IsoSource tended to calculate higher contributions of principal food items and smaller percentile ranges than MixSIR. Among harparine beetle species, there were diverse food utilisation patterns among four food categories (detritivorous invertebrates, herbivorous invertebrates, C3 plants, and C4 plants). Detritivores comprised the main diets of abundant harpaline species in the spring, whereas abundant harpaline species in the autumn were primarily herbivores feeding on C4 plants, or omnivores feeding on herbivorous invertebrates and C3 plants. Seasonal changes in food use were related to seasonal changes in the abundance of each food resource. 4. Mixing model analysis of stable isotope ratios is a convenient and effective method for roughly estimating diets of many species with diverse food habits (such as ground beetles). This method can contribute to determining the trophic relationships of related insects in one ecosystem.     

Structure and Role of the Five Glycopeptides of Human IgM Immunoglobulins

Carbohydrate is attached at five sites in the constant sequence region of the µ heavy chain of human IgM. The oligosaccharides are of two kinds, simple and complex and affect the conformation and properties of macroglobulins.     

Cell Fusion and Its Application to Genetic Analysis of Development in Dictyostelium discoideum

Dictyostelium cells were fused by a modification of the polyethylene glycol method of Kuhn and Parish. In the modified method Tricine buffer and Concanavalin A were used in place of Ca⁺⁺. The efficiency of genetic complementation through cell fusion was about 10 times higer by the modified method than by the original method with glycine buffer and Ca⁺⁺. Complementation between developmental mutants without any selectable growth character was clearly detected by the modified system, at efficiencies of about 1 in 10–20 surviving cells.     

A simple method to score single nucleotide polymorphisms based on allele‐specific PCR and primer‐induced fragment‐length variation

We describe a simple protocol to genotype single nucleotide polymorphisms (SNPs), which combines allele‐specific polymerase chain reaction (PCR) with fragment‐length analysis. Three primers are used in the PCR: two allele‐specific forward primers with a length‐difference and one reverse primer. The forward primers induce a length‐difference between the SNP‐variants, which can be assessed with standard fragment‐length analyses. We designed primers for 21 SNPs, and codominance was achieved for 76% of these SNPs. An inexpensive and flexible laser‐detection scoring protocol can be achieved with multiplex scoring and by incorporating the M13(‐21) genotyping method.     

The role of a glyoxylate-glycolate system in chloroplasts of higher plants

Photoreduction of glyoxylate and oxidation of glycolate wereinvestigated using unwashed chloroplasts from spinach leaves.A glyoxylateglycolate system operated in light and under aerobicconditions. Accompanying the photoreduction of glyoxylate andthe oxidation of glycolate, was the disappearance of inorganicphosphate. Photoreduction of oxalate was also observed in illuminatedchloroplasts. The reaction rate was, however, much lower thanthat for the photoreduction of glyoxylate. (Received August 4, 1969; )     

Arabidopsis thaliana ASN2 encoding asparagine synthetase is involved in the control of nitrogen assimilation and export during vegetative growth

We investigated the function of ASN2, one of the three genes encoding asparagine synthetase (EC 6.3.5.4), which is the most highly expressed in vegetative leaves of Arabidopsis thaliana. Expression of ASN2 and parallel higher asparagine content in darkness suggest that leaf metabolism involves ASN2 for asparagine synthesis. In asn2‐1 knockout and asn2‐2 knockdown lines, ASN2 disruption caused a defective growth phenotype and ammonium accumulation. The asn2 mutant leaves displayed a depleted asparagine and an accumulation of alanine, GABA, pyruvate and fumarate, indicating an alanine formation from pyruvate through the GABA shunt to consume excess ammonium in the absence of asparagine synthesis. By contrast, asparagine did not contribute to photorespiratory nitrogen recycle as photosynthetic net CO₂ assimilation was not significantly different between lines under both 21 and 2% O₂. ASN2 was found in phloem companion cells by in situ hybridization and immunolocalization. Moreover, lack of asparagine in asn2 phloem sap and lowered ¹⁵N flux to sinks, accompanied by the delayed yellowing (senescence) of asn2 leaves, in the absence of asparagine support a specific role of asparagine in phloem loading and nitrogen reallocation. We conclude that ASN2 is essential for nitrogen assimilation, distribution and remobilization (via the phloem) within the plant.     

Ultrastructural Studies on Development of the Tail Gland of a Cuttlefish, Sepiella japonica

Hatching glands in embryos of teleosts and amphibians have been reported to be indispensable for hatching of the embryos. The cephalopod has capsuled eggs, so we expected to find some exocrine organ in the embryos that functioned as a hatching gland. The tail gland (Hoyle's organ) has been suspected to be a hatching gland in the cephalopod, and therefore we examined it during the course of development of cuttlefish embryos. Cells in the tail gland appeared similar to the hatching gland cells (HGCs) of teleosts and amphibians, and contained a number of secretion granules that also resembled the hatching enzyme granules (HEGs) in HGCs of teleosts and amphibians in size, electron density and distribution in the cells. However, a few of these granules were discharged one after another from an early stages, whereas most of them were retained up to the stage just before hatching, and then discharged all at once. The former process of trickling discharge was similar to that in amphibians and the latter process of abrupt discharge resembled that in teleosts.     

Further Evidence for the Presence of a Circadian Clock in the Prothoracic Glands of the Saturniid Moth Samia cynthia ricini: Decapitated Larvae Can Respond to Light-Dark Changes

A small peak of haemolymph ecdysteroid titre precedes the gut purge that characterizes larval-prepupal transition of the saturniid moth Samia cynthia ricini. This peak shifts its phase in parallel with the phase shifts of gut purge according to the changes in light-dark conditions preceding gut purge. Decapitated larvae responded to these light-dark changes as intact larvae did, as assessed by the phase shifts of the haemolymph ecdysteroid peak. This indicates that the brain-centred PTTH clock is not prerequisite for realization of the circadian-clock-controlled timing in the initiation of prepupal development, and supports indirectly our previous notion that the prothoracic glands of Samia possess a circadian clock dictating gut purge timing.