Growth responses of individual roots of Opuntia ficus-indica to salinity

Responses of individual roots of the widely cultivated cactus Opuntia ficus-indica to salinity stress were evaluated using a split-root system. Three roots from a plant with at least 20 roots were isolated from the remainder of the root system and exposed to 0, 30 or 100 mol m^-3 NaCl for up to 28 d. Cortical cells became shorter and lateral root development was substantially reduced as salinity increased. Compared with the control, the increase in dry weight for the isolated roots was reduced 40% by 30 mol m^-3 NaCl and 93% by 100mol m^-3 NaCl. The sodium content of roots increased only two-fold with increasing salinity. Respiration rates of roots exposed to 30 or 100 mol m^-3 NaCl were higher than those of the control. Carbon accumulation in roots measured 2 d after exposing shoots to ¹⁴CO₂ was not initially affected by 30 mol m^-3 NaCl but was substantially reduced at 100 mol m^-3 NaCl. Thus, roots exposed to short periods of moderate salinity stress maintained sufficient carbon sink strength for continued growth of the roots. Moreover, increased salinity led to decreased efficiency of carbon usage for the expansion of root surface area.     

Effects of Ultraviolet Irradiation on the Cell Cycle

Cultured mouse Cloudman melanoma cells, EMT6 breast carcinoma cells, and 3T3 fibroblasts all accumulated in the G2/M phase of the cell cycle when exposed to UVB radiation. The effects of UVB were maximal at 20–30 mJ/cm² for all three cell lines, and could be observed by flow cytometry as early as 12 hr post irradiation. It has been known since the mid-1970s that MSH receptor binding activity is highest on Cloudman melanoma cells when they are in the G2/M phase of their cycle. Here we show that either UVB irradiation or synchronization of Cloudman cells with colchicine results in a stimulation of MSH binding within 24 hr following treatment, a time when both treatments have resulted in accumulation of cells in the G2/M phase of the cycle. Furthermore, the two treatments performed together on the melanoma cells stimulated MSH receptor activity to the same extent as either treatment performed separately, suggesting that each may be influencing MSH receptor activity solely through a G2/M accumulation of cells. Together, these results raise the possibility that an increase in the number of cells in the G2 phase of the cell cycle is a generalized cellular response to injury, such as UV irradiation. However, in the case of pigment cells this response includes a mechanism for increasing melanin formation, i.e., increased MSH receptor activity. Should this be the case, similar G2/M “injury responses” of other cell types might be expected, consistent with their differentiated phenotypes.     

On Paraptychostomum almae N. G., N. Sp., a Commensal Ciliate from the Digestive Tract of Oligochaetes of the Cameroons, in a New Subclass Hysterocinetia

ABSTRACT. Morphological and ultrastructural studies on a new ciliate, Paraptychostomum almae , from the digestive tract of an oligochaete ( Alma emini ) from the Cameroons are carried out. The flattened cell has a large size; its left lateral face bears an anterior thigmotactic zone that includes seven-nine short kinetal segments. The somatic cortex is composed of flattened alveoli, a thin epiplasm and a microfibrillar ecto-endoplasmic boundary. Kineties are made of monokinetids, each particularly characterized by a long anteriorly directed kinetodesmal fiber, and a hyperdivergent postciliary ribbon. The postero-ventral buccal apparatus consists of a short peristome and a deep longitudinal infundibulum. The paroral organelle is a long stichodyad. The three adoral organelles are of different types: ADI and AD3 are of the membranoid type, respectively with two and one rows of ciliated kinetosomes; AD2 is of the peniculus type with six-seven rows of ciliated kinetosomes. A microfibrillar network with nodes arises from all the buccal kinetosomes and extends under the naked wall. Mitochondria are small and numerous and dispersed throughout the whole cell. The existence of an AD2 with more than two rows of kinetosomes warrants the creation of the new genus Paraptychostomum and a new family, Ptychostomatidae. The presence of a distinct ecto-endoplasmic boundary and of somatic kinetids exclusive without transversal dense tractus, hyperdivergent postciliary ribbons, and dispersed numerous mitochondria, added to particularities of the stomatogenesis, allow us to clearly separate hysterocinetians from the scuticociliates and to set up for them the new subclass Hysterocinetia, within the class Oligohymenophorea, with a single new order Hysterocinetida.     

Cretaceous Promecognathinae (Goleoptera: Garabidae): a new genus, phylogenetic reconstruction and zoogeography

A fossil carabid (Coleoptera) belonging to the subfamily Promecognathinae is described from Cretaceous crater lake deposits at Orapa, Botswana. The specimen, which is the first ever fossil promecognathine, is placed in a new genus Palaeoxinidium. The fossil supports a Cretaceous age determination for the sediments, and it indicates that the Orapa crater was, at least in part, heavily vegetated at the time of deposition. Cladistic analysis of the fossil and extant Promecognathinae indicates that the fossil represents the sister group of the extant taxa and that the latter, in turn, comprise a pair of sister groups. It is, therefore, proposed that the Promecognathinae should be divided into two tribes: the Palaeoaxinidiini, represented by the fossil, and the Promecognathini, represented by the extant groups. The Promecognathini should be subdivided further into the subtribes Promecognathina and Axinidiina, represented by the American and African species, respectively. Three alternative zoogeographic hypotheses that explain the distributions of the fossil and extant promecognathines are discussed and tests for the hypotheses are proposed.     

Effect of Chilling Temperatures on the Protoplasmic Streaming of Plants from Different Climates

A microscope mount was designed so that specimen temperaturescould be monitored and controlled without impairing phase contrastoptics and used to measure rates of protoplasmic streaming between0 and 25 ?C in trichome cells of Lycopersicon esculentum, Lycopersiconhirsutum, Citrullus vulgaris, Tradescantia albiflora, Digitalispurpurea, and Veronica persica. Between 10 and 20 ?C the rates of streaming varied from 2–6µm s^–1 depending on the temperature, and differencesbetween the species were small. The temperature coefficientof streaming rates was found to increase as the temperaturewas lowered so that the plot of log rate against temperaturehad a steeper slope at the lower temperatures. The largest temperature cofficients were for the warmth-requiringL. esculentum (tomato) and C. vulgaris (water melon), and thesmallest for the temperate-zone plants V. persica (speedwell)and D. purpurea (foxglove). The changes in rate always occurredover a range of temperature; no ‘critical temperature’wasobserved below which streaming abruptly stopped and above whichit was active, although the amount of streaming as well as therate decreased as the lowest temperatures were approached. The temperatures experienced by the specimens during the experimentdid not affect the recovery of normal streaming rates betweenabout 10 and 20 ?C. In a population of a wild tomato, Lycopersicon hirsutum Humb.and Bonpl., collected from different altitudes in Peru and Ecuador,i.e. from locations of different environmental temperature,the rate of protoplasmic streaming at 5 ?C was greatest in thevarieties collected from the highest altitudes. The resultssuggest that streaming rates correlate with genetic adaptationto low temperature in the species examined.     

Plasmodium falciparum: Differential Sensitivity In Vitro to E-64 (Cysteine Protease Inhibitor) and Pepstatin A (Aspartyl Protease Inhibitor)

ABSTRACT We investigated the effect of a cysteine proteinase inhibitor (E-64) and an aspartyl proteinase inhibitor (Pepstatin A) on asexual erythrocytic stages of Plasmodium falciparum in culture. These two protease inhibitors showed different patterns of activity. E-64 acted preferentially against trophozoite and schizont stages. After 48 h incubation at high concentrations of E-64 (28, 140, 280 μM), growth was totally abolished and the parasites presented characteristic enlarged food vacuoles. Morphological alterations were also seen after shorter incubation periods (6 h at 28 μM) or 12 h at the inhibitory concentration 50% (12 μM), but an additional culture period (24 h) in inhibitor-free medium allowed normal parasite development, demonstrating a parasitostatic effect. E-64 acts on parasite multiplication; the normal merozoite maturation was altered and the normal reinvasion process partially impaired. Pepstatin A used at the inhibitory concentration 50% (4 μM) killed the parasites before trophozoite development and had a major effect on schizonts maturation. No altered parasite development occurred during an additional culture period without Pepstatin A, demonstrating a parasiticidal effect. E-64 and Pepstatin A used in combination inhibit the parasite growth with a strong synergistic effect.