Cutting xylem under tension or supersaturated with gas can generate PLC and the appearance of rapid recovery from embolism

We investigated the common assumption that severing stems and petioles under water preserves the hydraulic continuity in the xylem conduits opened by the cut when the xylem is under tension. In red maple and white ash, higher percent loss of conductivity (PLC) in the afternoon occurred when the measurement segment was excised under water at native xylem tensions, but not when xylem tensions were relaxed prior to sample excision. Bench drying vulnerability curves in which measurement samples were excised at native versus relaxed tensions showed a dramatic effect of cutting under tension in red maple, a moderate effect in sugar maple, and no effect in paper birch. We also found that air injection of cut branches (red and sugar maple) at pressures of 0.1 and 1.0 MPa resulted in PLC greater than predicted from vulnerability curves for samples cut 2 min after depressurization, with PLC returning to expected levels for samples cut after 75 min. These results suggest that sampling methods can generate PLC patterns indicative of repair under tension by inducing a degree of embolism that is itself a function of xylem tensions or supersaturation of dissolved gases (air injection) at the moment of sample excision. Implications for assessing vulnerability to cavitation and levels of embolism under field conditions are discussed.     

Effects of sand sedimentation on the macroinvertebrate fauna of lowland streams: are the effects consistent?

1. In lowland streams sand sedimentation can produce sand slugs: very slow moving, discrete volumes of sand that are created episodically. Hypothetically, such sedimentation causes losses of habitat and fauna but little is known about the effects of sand slugs. In south‐eastern Australia sand slugs are widespread, especially in streams with granitic catchments. 2. This study in north‐central Victoria was centred on three streams that rise in the Strathbogie Ranges and flow out onto lowland plains, where they contain sand slugs. Below the sand slugs, the streams are slow‐flowing ‘chains of ponds’ with a clay streambed. To correct for potential upstream‐downstream confounding of comparisons, two unsanded, nearby streams were included as potential controls. Habitat measurements and faunal samples were taken in Spring 1998, from three sites in the sand slug and three sites in the clay‐bed, downstream sections of each impacted stream, as well as from three sites in commensurate upstream and downstream sections of the control streams. 3. The sand‐slugged sections had significantly higher velocities, shallower depths and less coarse woody debris than the unsanded downstream sections. Macroinvertebrate taxon richness and abundance showed some significant differences between the sand and clay sections compared with commensurate up‐ and downstream locations in the control streams. Effects were not uniform, however. In Castle Creek there were no significant differences between the sand and clay sections, in Pranjip‐Ninemile Creek taxon richness and abundances were higher in sand than in the clay sections, whereas in Creightons Creek the ‘expected’ results of lower taxon richness and abundance in the sand were found. 4. Of the 40 most common taxa, only eight provided a clear signal related to sand and, of these, one (Slavina sp.) occurred only in the sand slugs, whereas the other seven had significantly higher numbers in the clay sections. Of these taxa, three were ostracods, three were chironomids and one was a tubificid oligochaete, all taxa that live in detritus‐rich environments. Overall faunal composition did not show a clear distinction though, between sandy and clay sites. The sand slug community of Creightons Creek was very different from the other communities in all of the streams. There were clear differences in community composition between the sand‐affected and the control streams, even for downstream, clay sections, suggesting they cannot act as controls for the impacted sections of the sand‐slugged streams. 5. Differences between streams within categories (particularly between sand‐slugged streams) and between sites in the same section of stream accounted for most of the variability in species richness and the abundances of each of the 40 most common taxa. That finding was repeated when data were examined at the family level, for both numbers of families per sample and collated lists of families occurring across sites. These results strongly suggest that the effects of sedimentation by sand slugs do not overwhelm background variation in macroinvertebrate density and diversity. Overall the results suggest that many taxa may respond individually, and that there is much variation between sand‐affected streams even over relatively small (approximately <10 km) spatial scales.     

AGE DEPENDENCE OF THE NUMBER OF THE STEM CELLS IN HAEMOPOIETIC TISSUES OF RATS

The number and concentration of haemopoietic stem cells in the femoral bone marrow and spleen of Wistar rats of different ages were investigated. Stem cells were assayed by the spleen colony technique in irradiated rat recipients. The ability of the recipient spleen to harvest transplanted tissue as a macroscopic colony was found to be dependent on the recipient's age. Changes with senescence were observed also in the concentration and the size of the stem cell compartment both in the marrow and spleen. No differences were demonstrated in the seeding of transplanted colony-forming units into the spleen of recipients of 1 and 4 months of age. A rats-mice strain difference in the effect of senescence on the haemopoietic stem cells is discussed.     

Low population genetic structuring of two cryptic bat species suggests their migratory behaviour in continental Europe

Although two cryptic pipistrelle bat species, Pipistrellus pipistrellus and Pipistrellus pygmaeus , belong among the most common bat species in Europe, it is still unclear whether they can migrate over long distances between summer and winter roosts. Long-distance migratory species may be expected to show low levels of genetic structuring in large areas due to regular mixing of the gene pool by mating that occurs during migration and/or hibernation. Conversely, the dispersal of gametes in sedentary species is spatially restricted, populations are more genetically structured, and isolation by relatively short distance is visible. By analysing diversity of highly variable microsatellites within and among summer colonies of both studied species in central Europe, we found that differentiation between populations is very weak. Both classical F _ST and Bayesian clustering approach failed to detect genetic structure among colonies and there was no significant isolation-by-distance pattern. The analyses of relatedness, however, revealed that individuals within colonies are more related than random suggesting philopatry of at least one sex. The results were very similar for the two species. The high level of gene flow among central European populations, even on large geographic distances, is discussed in relation with migrations, dispersal, and mating behaviour.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 96 , 103–114.     

Cluster biodiversity as a multidimensional structure evolution strategy: checkerspot butterflies of the group Euphydryas aurinia (Rottemburg, 1775) (Lepidoptera: Nymphalidae)

In the present paper, we explore the evolution of cluster structure in closely related species in the Euphydryas aurinia complex based on morphological (wing pattern, genital armatures) and molecular (cytochrome c oxidase subunit I) characters. Male genitalia differ in the length and shape of the uncus, harpe and juxta branches, by the shape of some parts of the phallus, and by the amount of spikes on the ventral section of the valva. The main trends in the vertical distribution of the E. aurinia group are dwarfism with increasing altitude, coupled with enlargement of paler and darker‐coloured elements of the wing pattern, increasing the overall contrast. Unlike the Euphydryas maturna, the E. aurinia complex forms many local populations specialized under different ecological conditions, probably affected by different evolutionary scenarios. The phylogenetic analysis of the group reveals two ecologically distinct subgroups: one associated with the boreal forest‐mesophyllic meadow biome and one associated with the xeromesophyllic steppe biome. Within each group, two major ecological strategies have evolved in parallel: montane and lowland. Based on the results of the analyses, we revise the nomenclature as follows: E. aurinia pyrenesdebilis (Verity, 1928), stat. rev. (= debilis Oberthür, 1909, syn.n. , nomen nudum), E. aurinia bulgarica (Fruhstorfer, 1916), stat. rev. , E. aurinia provincialis (Boisduval, 1828), stat. rev. and E. beckeri (Lederer, 1853), stat. rev. The following name‐bearing types are designated: neotype of Papilio aurinia Rottemburg, 1775, neotype of Papilio merope de Prunner, 1798, lectotype of Melitaea beckeri Lederer, 1853, and lectotype of Melitaea aurinia banghaasi Seitz, 1908. All name‐bearing types are figured. A new subspecies, Euphydryas laeta ostracon Korb, Bolshakov, Fric, ssp.n. , is described (type locality by holotype data: Kazakhstan, Vostochno‐Kazakhstanskaya Oblast, Shemonaikha).