Diurnal Cycling in Root Resistance to Water Movement

The occurrence of diurnal changes in root resistance of cotton was studied by measuring the flow of water through 35-to70-day-old root systems under a pressure of 3.10 bars or a vacuum of 0.88 bar. The volume of exudate obtained under constant pressure or constant vacuum was 2 to 3 times greater near midday than near midnight indicating that the root resistance apparently was 2 to 3 times greater at night than during the day. The salt concentration of the exudate also cycled; the concentration was lowest at midday and highest at night, hence there was little diurnal variation in the total amount of salt moved per hour. The cycle for volume of exduate, salt concentration, and apparent root resistance had a period of 22 to 26 hours at 24°C. The cycle gradually died away 2 to 3 days after removal of the shoots. The diurnal variations appeared to be controlled by signals from the shoots because the phase of the cycles could be reset by changing the light-dark cycle under which the plants were grown. Cycling was eliminated by exposure to 8 or more days of continuous light before removing the shoots, and cycling could not be entrained by a 6 hour light-6hour dark cycle. Bubbling nitrogen gas through the nutrient medium stopped cycling. A possible role of ion or growth regulator action is discussed.     

The Results of Parenteral Injections of Sporulated or Unsporulated Oocysts of Eimeria bovis in Calves

SYNOPSIS. Five experiments using newborn Holstein-Friesian and weaner Hereford calves were conducted to observe the effects caused by parenteral injections of oocysts of Eimeria bovis . Sporulated oocysts were given intraperitoneally (IP), subcutaneously (SC), intramuscularly (IM) and intravenously (IV). Unsporulated oocysts or merozoites were given IP or IM.
Coccidiosis developed in calves in three experiments after they were inoculated IP with sporulated oocysts. Immunity to reinfection resulted from these infections. No infections occurred at any time after SC, IM or IV inoculation with sporulated oocysts or after IP or IM inoculation with unsporulated oocysts or merozoites.
Coccidiosis failed to occur in two experiments when special precautions were used to prevent puncture of the intestines during IP inoculations. There was no detectable immunological response to any of the inoculations unless intestinal infections occurred.
In one experiment sporulated oocysts were exposed to 60,000 r irradiation by x-ray in an attempt to attenuate the oocysts. Calves became infected when given orally administered oocysts irradiated at this level.     

Observations on the development and maintenance of the deep sea barnacle,Octolasmis aymonini geryonophila (Pilsbry)

Thirty-two pedunculate barnacles, O. a. geryonophila, were maintained in culture for a period of 2 yr in the laboratory. These barnacles were obtained from the pleopods and mouth parts of the giant marine isopod, Bathynomus giganteus, which had been collected, at a depth of 200 fathoms, in the Gulf of Mexico.

The carina, scutum, mandible and maxilla of adult barnacles were typical of deep water species. However, the tergum and labrum were intermediate between those of shallow and deep water species.

Adults 3.1–4.1 mm in length were cultured in sea water (15–19°C), and fed on benthic copepods such as Tisbe furcata and Laophonte sp. Three broods of nauplii from 8 barnacles were obtained in 2 yr. Larvae were reared on plankton collected from Coney Island waters in which nauplii reached Stage IV in 10–14 days at 16°C. Isochrysis galbana and Thalassiosira pseudonana individually or in combination maintained nauplii to Stage IV, but with very high mortality. The lack of spines on the carapace edge of the nauplii distinguishes this deep water species from the shallow water form, O. mulleri.     

New highlights about the enigmatic marine snake Palaeophis maghrebianus (Palaeophiidae; Palaeophiinae) from the Ypresian (Lower Eocene) phosphates of Morocco

Abstract: Palaeophis maghrebianus belongs to the Palaeophiinae (Palaeophiidae). This snake subfamily is relatively poorly known, and it is mainly represented by disarticulated vertebrae and ribs and by a few vertebral segments. Its intracolumnar variability remains also poorly understood. The discovery of new isolated vertebrae and vertebral segments of Palaeophis maghrebianus in the Ypresian (Lower Eocene) Phosphates of Morocco enables us to provide a more detailed diagnosis of this species and to describe its intracolumnar variability. Moreover, the new material reveals that this species could reach gigantic size being, with Palaeophis colossaeus, one of the two longer palaeophiids. The microanatomical and histological analysis of some vertebrae illustrating diverse positions along the vertebral column reveals the presence of osteosclerosis, especially in the anterior and mid‐precloacal regions. The occurrence of this osseous specialization implies a role in buoyancy and body trim control in this taxon, which is considered a shallow marine dweller based on its anatomical features and geological data. Palaeophis maghrebianus also displays a dense vascular network suggesting a growth speed, and thus a metabolic rate, much higher than in the biggest extant snakes.     

Cryopreservation and thawing of hematopoietic stem cell CD34-induced apoptosis through caspase pathway activation: Key role of granulocytes

IntroductionCell damage inescapably occurs during both the freezing and the thawing graft processes for autologous hematopoietic stem cell (HSC) transplantation. To estimate HSC injury, a quality control is performed including: (i) CD34⁺ quantification; (ii) percentage of CD34⁺ viability and (iii) evaluation of HSC functional ability to form colony forming unit–granulocyte macrophage (CFU-GM). Apoptosis involves complex pathways such as caspase enzymes. Here, we assess the extent of apoptosis that is caspase-dependent before and after cryoconservation of CD34⁺, using a Fluorescent Labeled Inhibitor of CAspases (FLICA).MethodsCaspase pathway activation status was evaluated in 46 patients (multiple myeloma [n = 24], lymphoma [n = 22]), by flow cytometry, using a 7-aminoactinomycin-D (7AAD)/FLICA staining test, in CD34⁺, CD3⁺, CD14⁺ and CD56⁺ cells. Viable 7AAD^?/FLICA⁺ cells were then correlated with various parameters.ResultsWe showed a significant caspase pathway activation, with 23% CD34⁺/7AAD^?/FLICA⁺ cells after thawing, compared with the 2% described in fresh CD34⁺ cells (P < 0.0001). Moreover, caspase pathway was significantly activated in thawing CD3⁺, CD56⁺ and CD14⁺ cells. We also report a significant correlation between the rate of CD34⁺/7AAD^?/FLICA⁺ cells and post-thawing granulocytes count (P = 0.042) and their potential to be differentiated into CFU-GM (P = 0.004).DiscussionOur results show substantial cell death, induced by the increase of caspase pathway activation, secondary to the thawing process, and across all study cell types. This observation may affect the immune response quality during recipient aplasia, without detecting a clinical impact. Moreover, caspase pathway activation through CD3⁺ and CD56⁺ subpopulations could modify the therapeutic result of donor lymphocytes infusion (DLI).