Effects of Na2SO4, K2SO4 and KCl on Growth and Ion Uptake of Callus Cultures of Vaccinium corymbosum L. cv. Blue Crop

Non-selected and Na₂SO-, K₂SO₄- or KCl-selected callus culturesof Vaccinium corymbosum L. cv. Blue Crop were grown on mediasupplemented with 0, 25 and 50 mM Na₂SO₄ (non-selected and Na₂SO(-selectedonly), 0, 25 and 50mMK₂SO₄ (non-selected and K₂SO₄-selectedonly) or 0, 50 and 100 mM KCl (non-selected and KCl-selectedonly). On all media, growth of selected callus (on a fresh-weightor dry-weight basis) was greater than that of non-selected callus,and selected callus grew optimally on the level and type ofsalt on which it was selected. Selected callus was friable andmaintained a higher f. wt:d. wt ratio. Tissue water potentialin selected callus was more negative than in non-selected callus. Flame photometry and chloridometry showed Na⁺, K⁺ and Cl^–accumulated in callus to concentrations equal to or greaterthan the initial concentration in the medium. Turbidometry showedthat tissue SO₄^2- concentration was lower than the concentrationin the medium. In most cases selected callus accumulated moreNa⁺, K^sup, SO₄^2– or Cl^– than non-selected callus.Vacuolar ion concentration was measured by electronprobe X-raymicroanalysis, and on most media selected callus had highervacuolar ion concentrations than non-selected callus. SO₄^2–and Cl^– were accumulated in the vacuoles at concentrationshigher than the external medium, but vacuolar Na⁺ concentrationdid not reach external concentration on Na₂SO₄ and on potassiumsalts was maintained between 12 and 17 mM. Vacuolar K⁺ concentration(approx. 142–191 mM on no salt) decreased on Na₂SO₄ andincreased on K₂SO₄ and KCl. There was no precise correlation between total or specific ionaccumulation (Na⁺, K⁺, SO₄^2– and Cl^– and fresh-weightyield. Results suggest that selection results in adaptationin response to decreased water potential of the medium. Vaccinium corymbosum, blueberry, electronprobe X-ray microanalysis, callus, in vitro selection, salt tolerance, KCl, K₂SO₄, Na₂SO₄     

Transmission of Megatrypanum Trypanosomes to Cervus dama by Tabanidae1

Four fallow deer, Cervus dama, became infected with Trypanosoma (Megatrypanum) sp. by oral application of triturated guts from tabanids collected in an area with deer but without any cattle; four control calves remained negative. Upon challenge with triturated guts from tabanids from an area with pastured cattle, the four calves became infected with Trypanosoma (M.) theileri. The prepatent period in deer was five days or less. Haematopota spp. and Tabanus spp. were identified as vectors of the deer trypanosomes. It is concluded that the trypanosomes of C. dama belong to a Megatrypanum species that is not identical with T. theileri.     

Interaction of pheromones during food exploitation by the termite Schedorhinotermes lamanianus

Abstract. Chemical signals from secretions of different exocrine glands modulate a variety of behavioural patterns in termite societies. These signals have multiple functions and may be interactive. During food exploitation workers of the African termite Schedorhinotermes lamanianus (Isoptera: Rhinotermitidae) employ, on foraging trails, the secretion from the sternal gland both for orientation and recruitment to a food source. The secretion from the labial gland, released onto the food by gnawing termites, stimulates additional workers to gnaw at the same site, thereby forming aggregations of gnawing termites. An interaction between these two pheromones during food exploitation is demonstrated for the first time. The volatile signal from the sternal gland inhibits in a dose-dependent manner the non-volatile, highly persistent, signal from the labial gland. The development of gnawing aggregations is inhibited and established ones are dissolved. Behavioural evidence for the perception of both the volatile signal from the sternal gland by olfactory neurones and of the non-volatile signal from the labial gland by gustatory neurones on the antennae is given. The interaction of the two pheromones as a basis for the development of distinct commuting and gnawing zones on the food source, and as a means for a dynamic regulation of food exploitation, is discussed.     

Micro‐ and nano‐scale ultrastructure of cell walls in Cryogenian microfossils: revealing their biological affinity

Moczyd?owska, M., Schopf, J.W. & Willman, S. 2009: Micro‐ and nano‐scale ultrastructure of cell walls in Cryogenian microfossils: revealing their biological affinity. Lethaia, Vol. 43, pp. 129–136. Recently established protocols and methods in advanced microscopy and spectrometry applied to studies of ancient unicellular organic‐walled microfossils of uncertain biological affinities (acritarchs) provide new evidence of the fine ultrastructure of cell walls and their biochemistry that support the interpretation of some such microfossils as photosynthesizing microalgae. The micro‐scale and nanoscale ultrastructure of the cell walls of late Cryogenian sphaeromorphic acritarchs from the Chichkan Formation (Kazakhstan) revealed by the advanced techniques and studied originally by Kempe et al. (2005) is here further analysed and compared with that of modern microalgal analogues. On the basis of such comparison, we interpret the preserved cell wall ultrastructure to reflect original layering and lamination within sub‐layers of the fossil wall, rather than being a result of taphonomic and diagenetic alteration. The outer thick layer represents the primary wall and the inner layer the secondary wall of the cell, whereas the laminated amorphous sub‐layers, 10–20 nm in thickness and revealed by transmission electron and atomic force microscopy, are recognized as trilaminar sheath structure. Because two‐layered cell walls, trilaminar sheaths and the position of the TLS within the fossil cell wall are characteristic of the mature developmental state in cyst morphogenesis in modern microalgae, we infer that the Chichkan sphaeromorphs are probably resting cells (aplanospores) of chlorophyceaen green microalgae from the order Volvocales. □Biological affinity, cell wall, Cryogenian, microfossils, ultrastructure.     

Leaf architecture and epidermal characters in Zelkova, Ulmaceae

Zelkova , with six extant species in Eurasia - three in East Asia (Z. schneideriana, Z. serrata, Z. sinica) , one in south-western Asia (Z. carpinifolia) and two in southern Europe (Z. abelicea, Z. sicula) - was investigated with respect to leaf architecture and epidermal characters by LM and SEM. The leaf venation of Zelkova is relatively uniform, while leaf size and shape are highly variable. Characters such as teeth and epidermal cells, trichomes and stomata provide useful specific distinctions. Beginning in the Miocene, increasing aridity in Central Asia would appear to have been responsible for isolating the eastern Asiatic species from their European/western Asiatic counterparts. The European range underwent further changes in response to Quaternary climatic oscillations.     

Three-dimensional Raman imagery of precambrian microscopic organisms

Two major difficulties have long hindered studies of ancient permineralized micro‐organisms: (1) accurate documentation of their three‐dimensional morphology at micron‐scale resolution; and (2) direct characterization of their molecular‐structural composition. Here we introduce a technique new to palaeobiology, the three‐dimensional Raman imagery that meets both of these needs, which is a nonintrusive, nondestructive technique that can provide data by which to accurately and objectively characterize, in situ and at micron‐scale resolution, the morphology and molecular‐structural composition of permineralized micro‐organisms and their associated matrices. Application of this new technique can provide information about the morphology, taphonomy and fidelity of preservation of fossil micro‐organisms unavailable by any other means.