Amphidiploids between Cyclamen persicum Mill. and C. purpurascens Mill. induced by treating ovules with colchicine in vitro and sesquidiploids between the amphidiploid and the parental species induced by conventional crosses

Summary We cultured colchicine-treated hybrid ovules in vitro to produce fertile amphidiploids of C. persicum (2n=2x=48. referred to as AA) × C. purpurascens (2n=2x=34, referred to as BB). Seedlings and mature plants were obtained from the ovules without colchicine and those exposed to 50 mg/l colchicine for 5, 10 and 15 days, whereas they were not obtained from the ovules exposed to 50 mg/l colchicine for 20 days and 500 mg/l for 5, 10, 15 and 20 days. Although 8 mature hybrids derived from the ovules without colchicine produced a few fertile pollen grains, they failed to produce viable seeds by self-fertilization. The hybrids had 41 somatic chromosomes. Four and 3 mature plants were derived from ovules exposed to 50 mg/l colchicine for 10 and 15 days, respectively. One each among 4 and 3 mature plants showed a high frequency of pollen grain fertility, produced several seeds by self-fertilization, and had 82 somatic chromosomes which is twice the number of hybrid chromosomes (2n=41, AB). These findings indicated that these plants are amphidiploids (2n=82, AABB) between C. persicum and C. purpurascens. Three and 2 viable seeds were derived by the conventional crosses of diploid C. persicum × the amphidiploid and the amphidiploid × C. purpurascens, respectively. Flowering plants that developed from the seeds of diploid C. persicum × the amphidiploid were barely fertile and had 65 somatic chromosomes (2n=65, AAB), whereas those that developed from the seeds of the amphidiploid × C. purpurascens were barely fertile and had 58 somatic chromosomes (2n=58, ABB). The somatic chromosomes indicated that these plants are probably sesquidiploids between the amphidiploid and either C. persicum or C. purpurascens. The interspecific cross-breeding of cyclamen using the amphidiploids and the sesquidiploids is discussed.     

Effects of protein and peptide addition on lipid oxidation in powder model system

The effect of protein and peptide addition on the oxidation of eicosapentaenoic acid ethyl ester (EPE) encapsulated by maltodextrin (MD) was investigated. The encapsulated lipid (powder lipid) was prepared in two steps, i.e., mixing of EPE with MD solutions (+/- protein and peptides) to produce emulsions and freeze-drying of the resultant emulsions. EPE oxidation in MD powder progressed more rapidly in the humid state [relative humidity (RH) = 70%] than in the dry state (RH = 10%). The addition of soy protein, soy peptide, and gelatin peptides improved the oxidation stability of EPE encapsulated by MD, and the inhibition of lipid oxidation by the protein and the peptides was more dramatic in the humid state. Especially, the oxidation of EPE was almost perfectly suppressed when the lipid was encapsulated with MD + soy peptide during storage in the humid state for 7 days. Several physical properties such as the lipid particle size of the emulsions, the fraction of nonencapsulated lipids, scanning electron microscopy images of powder lipids, and the mobility of the MD matrix were investigated to find the modification of encapsulation behavior by the addition of the protein and peptides, but no significant change was observed. On the other hand, the protein and peptides exhibited a strong radical scavenging activity in the powder systems as well as in the solution systems. These results suggest that a chemical mechanism such as radical scavenging ability plays an important role in the suppression of EPE oxidation in MD powder by soy proteins, soy peptides, and gelatin peptides.     

Naidid worms (Oligochaeta, Naididae) in paddy soils as affected by the application of legume mulch and/or tillage practice

Reproduction, intrinsic rate of natural increase and population density of naidid worms were investigated in submerged paddy fields and the laboratory. No tillage plus legume-mulching increased the population density of naidid worms. Soil treatments with neither tillage nor legume mulch, and tillage practice alone, did not increase the number of worms. Dero dorsalis Ferronnière was dominant in soil of the no-tillage treatment. In laboratory experiments, legume-mulching with the proper amount of dissolved O₂ accelerated asexual reproduction of D. dorsalis through zooid budding. For the legume and aeration treatment, (N_i+1-N_i) N_i^-1 values (where N_i and N_i+1 are the populations at times t=i and t=i+1) were plotted against N_i+1. Utilizing this linear relation, this data fitted the logistic curve (r²=0.885, P<0.05). Based on the linear relation, the intrinsic rate of natural increase (r), carrying capacity (K), and doubling time (T) were calculated as 0.2125 day^-1, 12,666 m^-2, and 3.26 days, respectively. The amounts of legumes applied were highly correlated with the population of D. dorsalis, indicating that the weight of legume is a limiting factor with respect to carrying capacity. A literature review indicated a significant correlation (P<0.01) between intrinsic rate of natural increase and maximum body length of naidids with temperature conversion of the growth rate. Sexually mature worms were rarely found in submerged paddy fields. Sexual reproduction seems to be adopted in response to soil desiccation after paddy field drainage.     

Elevational Patterns of Acid Deposition into a Forest and Nitrogen Saturation on Mt. Oyama, Japan

Virgin fir trees have been dying on Mt. Oyama, which is located in the southwestern part of Kanto Plain, although the frequency of death seems to be reducing recently. We report elevational patterns of acid deposition in precipitation and throughfall under fir and cedar canopies and nitrogen saturation in the forest ecosystem on Mt. Oyama. The deposition fluxes of major inorganic ions in precipitation were nearly constant regardless of elevation except for hydrogen and ammonium ions, whereas the deposition fluxes of all major inorganic ions in throughfall among cedar increased. The 5-year average of annual nitrate deposition in precipitation from 1994 to 1998 showed 19.3 – 23.5 kg ha^?1 yr^?1 (annual inorganic total N deposition: 9.6 – 10.7 kgN ha^?1 yr^?1) at four sites ranging in elevation from 500 to 1252 m, whereas the deposition in both cedar and fir throughfall was over 6 times greater than that in precipitation. The average soil surface nitrate concentration in 1998 was 140 µg g^?1 (the range: 21.1 – 429 µg g^?1, n=80) and the 7-year average of nitrate concentration in stream water from 1992 to 1998 was 4.81 mg L^?1 (the range: 2.38 – 20.6 mg L^?1, n=317). Our results indicate that nitrogen saturation is occurring in the forest ecosystem because of high N deposition, probably via acid fog, on Mt. Oyama.     

Magmatic dike resonances inferred from very-long-period seismic signals

Very-long-period (VLP) signals showing simple decaying harmonic oscillations with periods near 10 seconds and lasting for about 300 seconds were observed in association with an earthquake swarm that occurred beneath Hachijo Island, Japan. Results from the source-mechanism analysis and waveform simulation based on a fluid-filled crack model consistently point to the resonance of a dike filled with a basaltic magma as the source of the VLP signals. Thus, VLP signals can be used to probe the state of the fluid and dynamic processes within a volcanic system.     

Differential detection of shrimp and crab for food labeling using polymerase chain reaction

Shrimp and crab are well-known as allergenic ingredients. According to Japanese food allergy labeling regulations, shrimp species (including prawns, crayfishes, and lobsters) and crab species must be differentially declared when ≥10 ppm (total protein) of an allergenic ingredient is present. However, the commercial ELISA tests for the detection of crustacean proteins cannot differentiate between shrimp and crab. Therefore, two methods were developed to discriminate shrimp and crab: a shrimp-PCR method with postamplification digestion and a crab-PCR method that specifically amplifies a fragment of the 16S rRNA gene. The sensitivity and specificity of both PCR methods were verified by experiments using DNA extracted from 15 shrimp species, 13 crab species, krill, mysid, mantis shrimp, other food samples (cephalopod, shellfish, and fish), incurred foods, and commercial food products. Both PCR methods could detect 5 pg of DNA extracted from target species and 50 ng of genomic DNA extracted from incurred foods containing 10 ppm (μg/g) total protein of shrimp or crab. The two PCR methods were considered to be specific enough to separately detect species belonging to shrimp and crab. Although false-positive and false-negative results were obtained from some nontarget crustacean species, the proposed PCR methods, when used in conjunction with ELISA tests, would be a useful tool for confirmation of the validity of food allergy labeling and management of processed food safety for allergic patients.     

Quantitative nested real-time PCR detection of <Emphasis Type="Italic">Verticillium longisporum</Emphasis> and <Emphasis Type="Italic">V. dahliae</Emphasis> in the soil of cabbage fields

Verticillium longisporum and V. dahliae, causal agents of Verticillium wilt, are spreading through the cabbage fields of Gunma Prefecture. Using the V. longisporum-specific intron within the 18S rDNA and differences between ITS 5.8S rDNA sequences in Japanese isolates of V. longisporum and V. dahliae, we developed three quantitative nested real-time (QNRT) PCR assays. The QNRT-PCR quantification of V. longisporum or V. dahliae in cabbage field soil was consistent with the severity of Verticillium wilt disease in those fields. In field trials of resistant cultivar YR Ranpo grown for three seasons in soil infested with the pathogen, disease severity and pathogen density in the soil were significantly reduced in a field moderately contaminated by V. dahliae, but only slightly reduced in a highly contaminated field. These results suggest that continuous cultivation of a resistant cultivar is an effective way to reduce the pathogen population. QNRT-PCR assays provide a powerful analytical tool to evaluate the soil population dynamics of V. longisporum and V. dahliae for disease management.