Biological Nitrogen Fixation in Pachyrhizus ahipa (Wedd.) Parodi

The patterns of plant growth and N₂ fixation capability in Pachyrhizusahipa (Wedd) Parodi inoculated with Bradyrhizobium ‘PachyrhizusSpec 1’ strains (Lipha Tech) were investigated in a zero-Nculture system under greenhouse conditions The P ahipa plantis day-neutral with respect to reproductive development Competitionoccurred between the two storage organs (legume and tuber) andprevented high tuber yield in P ahipa The symbiotic effectivenessof the association was high, as the profuse nodulation providedthe inoculated plants with adequate amounts of N Nodules werepresent throughout the cycle of P ahipa The change in rate ofN₂ fixation (RNF) and relative growth rate (RGR) was almostparallel during ontogenesis The developmental pattern of N₂fixation activity revealed that 65% of total N₂ fixation occurredafter N began to accumulate in the reproductive (pod wall plusseed) tissue During pod filling allocation of N compounds tothe seeds exceeded N₂ fixation, the pod walls being the primarysource of redistributed N, followed by the leaves. Pachyrhizus ahipa (Wedd) Parodi, ahipa, tuber crop, dinitrogen fixation, dry matter, N partitioning, reproductive growth     

Life-cycle regulation and life history plasticity in the speckled wood butterfly: are reaction norms predictable?

We investigated whether interpopulational variation in life-cycle regulation and life-history plasticity, in response to photoperiod, is predictable from considerations of what would be the adaptive life cycle and life history in a given environment. The investigation was performed on five populations of the speckled wood butterfly, Pararge aegeria (L.) (Lepidoptera: Nymphalidae), from central and south Sweden, England, Spain and Madeira. Insects from all five populations were reared at all daylengths from 10 h to 20 h at 17^oC. Larval and pupal development times were noted. Predictions were met regarding the type of life-cycle regulation and the shape of reaction norms. Evidence for diapause (larval summer and winter diapause, pupal winter diapause) was found in the three northern populations (P. a. tircis) but not in the two southern populations (P. a. aegeria). Photoperiodic thresholds for diapause induction followed the predicted latitudinal patterns, and this was also the case regarding quantitative regulation of development time (by photoperiod) among directly developing individuals. Under direct development, development time was progressively shorter in shorter daylengms in the two Swedish populations, where this signals progressively later dates. This was not found in the English, Spanish and Madeiran populations where such a response is likely to be maladaptive, because one or more generations of larvae are present before summer solstice. There were also unexpected results, for which we propose preliminary adaptive explanations.     

Computer-assisted visualization of the rat epididymis: a methodological study based on paraffin sections autometallographically stained for zinc ions

A concept for the computer-assisted visualization of tubular organs is presented. Unmarked histological zinc-stained serial sections from the epididymis of the Wistar rat were aligned to demonstrate the concept. Virtual images were made through the aligned sections and served as controls for the alignment process. Animation of the serial sections and the virtual images revealed new information about the structure of the organ under investigation. The analysis was used to upgrade the anatomical knowledge of rat epididymis by describing how the epididymal duct runs through the structure. The proximal parts of the epididymis contain large communicating septa of connective tissue dividing the caput and the upper part of the corpus epididymidis into segments. The tortuousness was high in the caput with many turns within a small area of the epididymis, whereas longer loops were found in the lower part of the corpus and cauda epididymidis. The tube of the vas deferens was found to become an integrated part of the ductal system in the cauda epididymidis, although it was histologically easy to distinguish from the epididymal duct. The total number of cross-sections of the ductus epididymidis in the 2254, 15-mu m-thick, tissue sections analysed was 104 700, giving a minimum length of the ductal system of 1.5 m. © 1998 Chapman & Hall