The role of picoplankton (cyanobacteria and plastidic picoflagellates) in the diet of tintinnids

Food vacuole contents in naturally occurring populations oftintinnids in surface waters at the mouth of the Bay of Villefranchewere examined from November 1988 to December 1989. Three typesof prey were considered: cyanobactena (Synechococcus spp.),plastidic pico- and nanoflagel lates. The relative frequency(%) of these were observed in the diet of 18 tintinnid species.Results confirm that nanoflagellates constitute the dominantfraction in the diet of most of the tintinnids examined. Theyare preferentially ingested by some species, such as Amphoridesquadrilineata and Favella sp. Nevertheless, picoplankton isingested throughout the year by all the tintinnids, and canreach up to 100% of the ration mainly during winter and summer.Cyanobacteria are the prey most ingested by Rhabdonella spiralisand the only prey observed in food vacuoles of Salpingella acuminaia.As indicated by the Strauss linearity index values, picoflagellatesare actively grazed by some species (e.g. Dictyocysta elegans,Eutintinnus spp.). The implications of the ingestion of picoplanktonby tintinnids in the food webs are discussed.     

Changes in the optical properties of a particle suspension caused by protist grazing

The effect of grazing within microbial food webs on the opticalproperties of seawater was studied in the laboratory by inoculatinga culture of cyanobacteria Synechocystis with an oligotnchousciliate, Strombidium. During the 4 week experiment sequentialmeasurements of spectral absorption and scattering coefficientswere supplemented by determinations of the particle size distribution,prey and predator numbers and pigment concentration. All ofthese parameters changed dramatically during the course of theexperiment. Protist grazing caused a large decrease in the concentrationof particles that ranged from 0.75 to 2.5 µm in size;Synechocystis is within this range. On the other hand, the concentrationof particles <0.75 µm increased. These fine particlesconsist of small heterotrophic bacteria and disintegrated detritalmaterial. In addition, the concentration of particles in therange of 2.5–16 µm also increased; this size rangeincluded a growing population of pigmented flagellates and detritus.Such particle dynamics were associated with large decreasesin both the scattering and the absorption coefficient. The spectralshape of the scattering coefficient flattened, and the spectralabsorption coefficient shifted to enhanced absorption at shorterwavelengths. These changes suggest that detrital particles andpigmented microflagellates were the dominant contributors tolight scattering and absorption at the end of the experiment.     

Dynamics of transparent exopolymeric particles (TEP) production by Phaeocystis globosa under N- or P-limitation: a controlling factor of the retention/export balance

The concentration of transparent exopolymeric particles (TEP) was monitored during Phaeocystis globosa blooms that developed in mesocosms under different initial N:P ratios (from N- to P-limited conditions). TEP concentration was measured using the microscopic (TEP_micro, ppm) and the colorimetric (TEP_color, Xanthan equiv. L⁻¹) methods. TEP concentrations varied from 5 to >75 ppm and from 60 to >1500 μg Xanthan equiv. L⁻¹, and were relatively low until the mesocosms reached nutrient (either N or P) depletion and then increased abruptly. From the TEP_micro versus TEP_color concentrations comparison and from their relation to chlorophyll a concentrations, two phases for the dynamics of TEP production were identified: (1) production through active release of precursors during the growth phase of P. globosa — defined as TEP₁ — and their integration into the TEP pool through coagulation processes; (2) release of large TEP from the mucilaginous matrix of P. globosa colonies subsequent to disruption caused by nutrient depletion — defined as TEP₂ — and their direct integration into the TEP pool outside the constraint of coagulation. The formation of a multiorigin TEP pool during P. globosa blooms may have implications for the fate of the blooms, due to difference in TEP bioreactivity according to their source and to difference in timing and intensity of TEP₁ versus TEP₂ production according to N- or P-depletion. For P. globosa blooms developing under N-limiting conditions, the transition from the first source (i.e. TEP₁) to the second one (i.e. TEP₂) was a slow and continuous process. In contrast, the P. globosa bloom developing under P-limiting conditions showed the sudden formation of heavy mucous aggregates when P became depleted, that may have been caused by a massive release of TEP₂. Our study suggests that the nutrient regime may control the export vs. retention balance during P. globosa blooms, via production of a multiorigin TEP pool.     

Serum nitric oxide metabolite levels in a general healthy population: relation to sex and age

This study aims at determining serum nitrite/nitrate (NO(x)) levels in healthy subjects within the framework of a population-based study. NO(x) concentration was measured in 3505 subjects aged >/=20 years. Subjects with diabetes, renal dysfunction, those undergoing treatment for dyslipidemia and hypertension, were excluded; also excluded were smokers, pregnant women, and subjects with cardiovascular and infectious diseases or cancer; leaving 1983 (667 men, 1316 women) asymptomatic non-smoking subjects for the analysis. NO(x) concentrations were determined in serum and compared in different age groups. Mean+/-SE of NO(x) concentration was 24.8+/-0.02 and 24.4+/-0.01 micromol/l in men and women respectively. Men aged 20-29 years had significantly higher NO(x) levels compared to corresponding women (25.1+/-0.03 vs. 22.7+/-0.02). Serum NO(x) concentration peaked at 50-59 years in both genders. Comparison between lower and upper quartiles of NO(x) levels was performed in both genders. Women with high serum NO(x) were older and had significantly higher body mass index and fasting plasma glucose. The results of this study determine the normal levels of serum NO(x) concentrations in asymptomatic non-smoker subjects; also show that serum NO(x) concentrations indicate sex and age differences in these subjects.     

P53-dependent expression of the stress-induced protein (SIP)

The mouse stress-induced protein (SIP) mRNA is activated in the pancreas with acute pancreatitis and in several cell lines in response to various stress agents. The SIP gene is alternatively spliced, generating two proteins (SIP'8 and SIP27). Both proteins, located mainly in the nucleus, promote cell death when overexpressed in vitro. We show that induction by stress agents of the expression of SIP18 and SIP27 mRNAs, observed in human- and mouse-derived cell lines, is absent from cells with deleted, mutated or inactive p53, suggesting that regulation of SIP gene expression is dependent on p53. That hypothesis is consistent with the presence of a functional p53-response element within the promoter region of the mouse SIP gene and confirmed by the induction of SIP mRNA expression in mouse embryo fibroblasts upon activation of a p53-dependent pathway by transfection with rasV12 or rasV12/E1A. In conclusion, SIP being a proapoptotic gene induced through p53 activation could be a stress-induced gene with antitumour properties.     

Morphology and mechanics of myosepta in a swimming salamander (Siren lacertina)

In contrast to the complex, three-dimensional shape of myomeres in teleost fishes, the lateral hypaxial muscles of salamanders are nearly planar and their myosepta run in a roughly straight line from mid-lateral to mid-ventral. We used this relatively simple system as the basis for a mathematical model of segmented musculature. Model results highlight the importance of the mechanics of myosepta in determining the shortening characteristics of a muscle segment. We used sonomicrometry to measure the longitudinal deformation of myomeres and the dorsoventral deformation of myosepta in a swimming salamander (Siren lacertina). Sonomicrometry results show that the myosepta allow some dorsoventral lengthening, indicating an amplification of myomere shortening that is greater than that produced by muscle fiber angle alone (10% muscle fiber shortening produces 28.7% myomere shortening). Polarized light and DIC microscopy of isolated hypaxial myosepta revealed that the collagen fiber orientation in hypaxial myomeres is primarily mediolateral. The mediolateral collagen fiber orientation, combined with our finding that the hypaxial myosepta lengthen dorsoventrally during swimming, suggests that one possible function of hypaxial myosepta in S. lacertina is to increase the strain amplification of the muscle fibers by reducing the mediolateral bulging of the myomeres and redirecting the bulging toward the dorsoventral direction.     

Expression profiling in pancreas during the acute phase of pancreatitis using cDNA microarrays

Most attacks of acute pancreatitis are self-limiting, suggesting that the pancreatic cells adapt their phenotype to prevent progression of the disease. Such phenotypic change must involve a coordinated modification in the expression of numerous genes. To identify differentially expressed genes, high-density mouse cDNA microarrays were hybridized with cDNA probes from both healthy pancreas and pancreas affected by acute pancreatitis. From the 7981 mouse genes analyzed, 239 showed significant changes in their expression during the acute phase of pancreatitis. Among them, 107 genes were up-regulated whereas 132 were down-regulated. They include genes whose function was not previously related to pancreatitis, suggesting that they are involved in some way into the acute pancreatic response. Finally, 40% of differentially expressed genes corresponded to ESTs. Demonstration that a large quantity of unexpected or yet uncharacterized genes showed altered expression during acute pancreatitis underscores the interest of a genome-based investigation. Some of these genes are certainly involved in the cellular defense against pancreatitis and, as such, deserve being studied further.     

Increased central AT(1)-receptor activation, not systemic vasopressin, sustains hypertension in ANP knockout mice

We tested the hypothesis that hypertension in atrial natriuretic peptide (ANP) knockout mice is caused in part by disinhibition of angiotensin II-mediated vasopressin release. Inactin-anesthetized F(2) homozygous ANP gene-disrupted mice (-/-) and wild-type (+/+) littermates were surgically prepared for carotid arterial blood pressure measurement (ABP) and background intravenous injection of physiological saline or vasopressin V(1)-receptor antagonist (Manning compound, 10 ng/g body wt) and subsequent intracerebroventricular (left lateral ventricle) injection of saline (5 microl) or ANP (0.5 microg) or angiotensin II AT(1)-receptor antagonist losartan (10 microg). Only (-/-) showed significant decrease in ABP after intracerebroventricular ANP or losartan. Both showed significant hypotension after intravenous V(1) antagonist, but there was no difference between their responses. We conclude that 1) vasopressin contributes equally to ABP maintenance in ANP-disrupted mice and wild-type controls; 2) permanently elevated ABP in ANP knockouts is associated with increased central nervous angiotensin II AT(1)-receptor activation; 3) disinhibition of central nervous angiotensin II AT(1) receptors in ANP-deficient animals does not lead to a significant increase in the importance of vasopressin as a mechanism for blood pressure maintenance.