Nitrogen and carbon isotope ratios in termites: an indicator of trophic habit along the gradient from wood-feeding to soil-feeding

1. Nitrogen and carbon stable-isotope ratios (δ¹⁵N and δ¹³C) of body tissues, mound/nest materials and dietary substrates were determined in termite species with differing trophic habits, sampled from the Mbalmayo Forest Reserve, southern Cameroon.
2. δ¹⁵N of termite tissues was enriched gradually along a spectrum of species representing a trophic gradient from wood- to soil-feeding. Species that could be identified from their general biology and from gut content analysis as feeding on well-rotted wood or as wood/soil interface feeders showed δ¹⁵N intermediate between sound-wood-feeders and soil-feeders. It is proposed that δ¹⁵N is therefore a possible indicator of the functional position of species in the humification process. Differences in δ¹³C were also observed between wood-feeding and soil-feeding forms.
3. High values of δ¹⁵N in soil-feeding termites suggest that nitrogen fixation is of little importance in these species.
4. A wide range of isotope effects (the difference in isotope ratios between termites and their diet) was observed for both nitrogen (Δδ¹⁵N = –1.6 to + 8.8‰) and carbon (Δδ¹³C = –2.2 to + 3.0‰), which suggests a diversity of nutrient acquisition mechanisms within termites and diverse relationships between termites and their intestinal micro-organisms.     

Fish species richness in spring‐fed ponds: effects of habitat size versus isolation in temporally variable environments

1. Species richness in a habitat patch is determined by immigration (regional) and extinction (local) processes, and understanding their relative importance is crucial for conservation of biodiversity. In this study, we applied the Island Biogeography concept to spring ponds connected to a river in southwestern Japan to examine how immigration and extinction processes interact to determine fish species richness in temporally variable environments. 2. Fish censuses were conducted 15 times in 13 study ponds at 1–4 month intervals from August 1998 through October 2000. Effects of habitat size (pond area), isolation (distance from the river) and temporal environmental variability (water level fluctuation) on (i) species richness, (ii) immigration and extinction rates and (iii) population size and persistence of each fish species were assessed. 3. The results revealed predominant effects of distance on species richness, immigration/extinction rates and population size and persistence. Species richness decreased with increasing distance but was not related to either pond area or water level fluctuation. A negative effect of distance on immigration rate was detected, while neither pond area nor water level fluctuation had significant effects on extinction rate. Further, population size and persistence of four species increased with decreasing distance, suggesting that, in ponds close to the river, immigrants from the river reduce the probability of extinction (i.e. provide a rescue effect), contributing to the maintenance of high species richness. 4. Overall results emphasise the importance of immigration processes, rather than extinction, in shaping patterns of species richness in our system. The predominant importance of immigration was probably because of (i) high temporal variability that negates habitat‐size effects and (ii) continuous immigration that easily compensates for local extinctions. Our results suggest that consideration of regional factors (e.g. connectivity, locations of source populations and barriers to colonisation) is crucial for conservation and restoration of local habitats.     

Syntheses of Alkaline Phosphatase in Embryonic Cells during Aggregate Formation

CELL interaction, an important process in morphogenesis, seems to regulate in some way the expression of genetic information, thereby giving rise to differentiation of the cell; but little is known about the mechanism of such regulation at the molecular level. Our results suggest that the synthesis of alkaline phosphatase is regulated at the translation level in embryonic cells.     

Meiosis of Primary Spermatocytes and Early Spermiogenesis in the Resultant Spermatids in Newt, Cynops pyrrhogaster in vitro

Dissociated spermatogenic cells were cultivated within the collagen matrix at low cell density. The largest cell type in the culture was identified as the primary spermatocytes by their size and the morphological characteristics revealed by ultra-thin sections. Chromosome analysis showed that about 90% of the cells examined were either in first or second meiosis. Within the collagen matrix, the fates of 282 single primary spermatocytes at meiotic stage in diakinesis or metaphase were followed. In a few days, most of them gave rise to four spermatids, passing through first and second meiotic divisions. About 80% of the spermatids formed motile flagella. They grew about 20–60 μm a day. The final state of the differentiation attained in our culture conditions was the spermatids with localized spherical nuclei and motile flagella, about 500 μm in length after 1-month's culture. Ultra-thin sections of the spermatids show that the rings, neck-pieces, and acrosomes developed in the cells.     

Development of the Embryo Sac in Amitostigma kinoshitae (Makino) Schltr. (Orchidaceae)

The embryo sac of Amitostigma kinoshitae was studied. The ovuleis anatropous, bitegmic, and tenuinucellate. The inner integumentalone forms a micropyle. The megaspore of a tetrad nearest tothe chalaza develops into an eight-nucleate embryo sac of thetypical Polygonum-type. Double fertilization takes place normally.     

AN ANALYSIS OF DIFFERENTIATIVE CAPACITY OF PIGMENTED EPITHELIAL CELLS OF ADULT NEWT IRIS IN CLONAL CELL CULTURE

Singly dissociated cells from dorsal and ventral iris epithelia ( iris iridica ) of adult newts were cultured separately at clonal density to analyse their growth and differentiative capacity. Usually some attached cells began to proliferate on 12th day of culture, and grew with loss of melanosomes to form clonal cell colonies. Up to 30 days after inoculation, most of the clonal colonies formed typical epithelial monolayer sheets which consisted mostly of nonpigmented cells. Then, in some of those colonies, cells piled up together and form typical lens structures containing lens antigens. A month and a half after culturing, 30 to 40% of single iris cells, which had been previously marked, grew to form clonal colonies consisting of more than 100 cells. About 30% of these colonies expressed lens specificity and no significant differences in efficiency of colony formation and differentiation were detected between the dorsal cells and the ventral, suggesting that potent cells capable of transdifferentiating into lens cells are evenly distributed in all parts of the newt iris epithelium.     

Ethnobotanical Studies in Gaoligong Mountains: II. The Dulong Ethnic Group

The traditional agro - ecosystem and indigenous botanical knowledge of the Dulong ethnic group in the Dulong Jiang (Dulong River) watershed of northern Gaoligong Mountains in western Yunnan, China are extensively investigated and studied through the approaches of human ecology and ethnobotany. Living in a very isolated environment, the Dulong people have established very close relationships with plants and the plant environment. The agro - ecosystem in the Dulong Jiang watershed is a typical montane swidden agro -ecosystem in which there are various traditional cultivars and local landraces of crops with potential value out-side of their area.     

Mitosis in Beating Cardiac Muscle Cells from Newt Embryos In Vitro

Cardiac muscle cells from newt embryos were cultured at relatively low cell density. Within 10 days in culture, 2 cell types (spindle and flat type) were distinguished both among beating and non-beating cells. Mitosis in single beating cells was frequently observed both in spindle and flat cells. Some cells maintained almost constant contractile activities throughout the mitotic stages, while the others transiently stopped beating during mitosis, which accords well to the case in chick embryos (1). Ultra-thin section shows the presence of myofibril's structure in a dividing cell, as shown in newborn rats (2, 3, 4), chick embryos (1, 5, 6, 7) and adult newts (8, 9). As a consequence of mitosis, 3 types (spindle, flat and mixed type) of beating colonies developed after 34 weeks in culture. Cell proliferation was accompanied with pulsation and could be directly pursued till the 4th division, suggesting that differentiated myocardiac cells with myofibrils proliferate by their mitoses in vivo , maintaining rhythmic contraction.     

Periodic Rotation of Chromosomes During the Mitotic Divisions in Secondary Spermatogonia of Newt, Cynops Pyrrhogaster

Mitosis was frequently observed in the secondary spermatogonia of newt in in vitro cultures. From prometaphase to mid-anaphase, the whole set of the chromosomes rotated alternately clockwise and counterclockwise generally in the same plane as the bottom of a plastic dish. The axis of rotation was almost always perpendicular to the bottom of a dish, passing through the central part of the cell. This rotation of chromosomes was so fast that we could discern it directly by a phase contrast microscope. It was a rhythmic and regular motion with almost the constant frequency and magnitude. The average period of each cycle during metaphase varied from cell to cell and between 70 to 20 seconds (0.9–3.0 rotations/min) and the average angle traversed during each motion also varied and between 10 to 90 degrees at 25°C. By marking the cell surface with iron particles, it was demonstrated that the inner part of the cell actively rotated and not the cell as a whole. Colcemid at the concentration of 1.0 μg/ml reversibly arrested the chromosomal rotation and karyokinesis. Cytochalasin B (4.0 μg/ml) also reversibly disturbed the rotation though the karyokinesis continued. These results suggest that the rotation of chromosomes as a set may be mediated by filamentous organelles such as microtubules in the mitotic spindle and cytoplasmic microfilaments.