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Age Marker (age + marker)
Selected AbstractsSex ratio and maturity indicate the local dispersal and mortality of adult stonefliesFRESHWATER BIOLOGY, Issue 8 2006I. PETERSEN Summary 1.,Despite a recent upsurge in interest, there remains remarkably little information about the dispersal and survival of the adults of most stream-dwelling insects, although this is a basic requirement for understanding their long-term population dynamics. 2.,Using Malaise traps for a whole annual flight period, we captured adult stoneflies (Leuctra nigra) along transects perpendicular to three upland Welsh streams. We assessed spatial and temporal patterns in sex ratio to infer local dispersal and, using maturity as an age marker, estimated the mortality of adult females. 3.,Nearly all adult stoneflies (99%) were taken in the period 26 April,23 July, and the onset of the male and female flight periods was the same. Most males (90%) had been caught by late June. Females were classified as immature (without ripe eggs) or mature, and 90% of immature females had been caught by mid-late June (depending on catchment). As immature females declined in the catch, mature females increased, 10% having been caught by late-May to early June and 90% by early to mid-July. The median catches of immature and mature females were separated by 32 days in all three catchments. 4.,There was a female bias in the sex ratio overall, which increased as time passed and was attributable partially to the greater longevity of females. Late in the flight period, however, female bias was also greater near the stream channel implying a return of mature females (but not males) from the riparian vegetation, presumably to oviposit. 5.,The number of mature females was less than the number of immatures in two of the three channels. Over all three catchments, the overall mortality of females over the 32 days taken to mature was estimated at 29%, equivalent to an exponential daily rate of 1.1% day,1. The apparently negative mortality rate in one catchment (i.e. more matures than immatures being caught) could be due to an influx of adult females from elsewhere along the channel to oviposit. 6.,Natural markers of age and population structure, such as sex ratio and female maturity, thus enabled us to detect a return of females to the stream to oviposit, after prior limited dispersal into the riparian zone, and to infer longitudinal movements in search of suitable sites. We were also able to estimate mortality in the field. Such natural markers seem to have been underexploited in the study of adult aquatic insects. [source] Derivated fetal haemoglobin as a marker for red cell age in the human fetus reflecting stimulated or impaired red blood cell productionPRENATAL DIAGNOSIS, Issue 7 2001Margriet Huisman Abstract We have determined whether derivated fetal haemoglobin (dHbF, consisting of glycated and acetylated HbF) can be used as a cell age marker for fetal red blood cells (RBCs). Cord blood was obtained between 19 and 39 weeks of gestation from 28 alloimmunised anaemic fetuses (23 RhD+ and 5,Kell) and from 20 non-anaemic fetuses and newborns (controls). Density gradient centrifugation was applied to 36 samples (20 RhD+, 15 controls and 1,Kell) to obtain fractions of increasing cell age. Blood samples were used for measurements of mean cellular volume (MCV), mean cell haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), pyruvate kinase activity (PK) and derivated fetal haemoglobin (dHbF) by cation-exchange HPLC. Reticulocytes were counted only in the whole blood samples. In all density gradient separated RBC fractions, the values for MCV, MCH and PK activity decreased and those of MCHC and dHbF increased with increasing density (equivalent to increasing cell age). The mean density was lower for RBCs of the anaemic RHD group (1.072±0.007,g/ml) than for the non-anaemic controls (1.077±0.005,g/ml) (p<0.05) The RBC density of the Kell sensitised fetus did not differ from those of the controls. In the control group, the values of the cell age markers in whole blood changed significantly with the gestational age, showing an increase of mean age of the erythrocyte population. The best linear relationship was found for dHbF (y=6.28+0.17*weeks; r=0.84; p<0.001). In the anaemic RhD+ fetuses, the RBC age markers did not change with gestational age; the dHbF percentages were lower, and the MCV, MCH, PK values and the reticulocyte counts were higher than in the controls (0.05 Effects of dietary restriction on mortality and age-related phenotypes in the short-lived fish Nothobranchius furzeriAGING CELL, Issue 2 2009Eva Terzibasi Summary The short-lived annual fish Nothobranchius furzeri shows extremely short captive life span and accelerated expression of age markers, making it an interesting model system to investigate the effects of experimental manipulations on longevity and age-related pathologies. Here, we tested the effects of dietary restriction (DR) on mortality and age-related markers in N. furzeri. DR was induced by every other day feeding and the treatment was performed both in an inbred laboratory line and a longer-lived wild-derived line. In the inbred laboratory line, DR reduced age-related risk and prolonged maximum life span. In the wild-derived line, DR induced early mortality, did not reduce general age-related risk and caused a small but significant extension of maximum life span. Analysis of age-dependent mortality revealed that DR reduced demographic rate of aging, but increased baseline mortality in the wild-derived strain. In both inbred- and wild-derived lines, DR prevented the expression of the age markers lipofuscin in the liver and Fluoro-Jade B (neurodegeneration) in the brain. DR also improved performance in a learning test based on conditioning (active avoidance in a shuttle box). Finally, DR induced a paradoxical up-regulation of glial fibrillary acidic protein in the brain. [source] Derivated fetal haemoglobin as a marker for red cell age in the human fetus reflecting stimulated or impaired red blood cell productionPRENATAL DIAGNOSIS, Issue 7 2001Margriet Huisman Abstract We have determined whether derivated fetal haemoglobin (dHbF, consisting of glycated and acetylated HbF) can be used as a cell age marker for fetal red blood cells (RBCs). Cord blood was obtained between 19 and 39 weeks of gestation from 28 alloimmunised anaemic fetuses (23 RhD+ and 5,Kell) and from 20 non-anaemic fetuses and newborns (controls). Density gradient centrifugation was applied to 36 samples (20 RhD+, 15 controls and 1,Kell) to obtain fractions of increasing cell age. Blood samples were used for measurements of mean cellular volume (MCV), mean cell haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), pyruvate kinase activity (PK) and derivated fetal haemoglobin (dHbF) by cation-exchange HPLC. Reticulocytes were counted only in the whole blood samples. In all density gradient separated RBC fractions, the values for MCV, MCH and PK activity decreased and those of MCHC and dHbF increased with increasing density (equivalent to increasing cell age). The mean density was lower for RBCs of the anaemic RHD group (1.072±0.007,g/ml) than for the non-anaemic controls (1.077±0.005,g/ml) (p<0.05) The RBC density of the Kell sensitised fetus did not differ from those of the controls. In the control group, the values of the cell age markers in whole blood changed significantly with the gestational age, showing an increase of mean age of the erythrocyte population. The best linear relationship was found for dHbF (y=6.28+0.17*weeks; r=0.84; p<0.001). In the anaemic RhD+ fetuses, the RBC age markers did not change with gestational age; the dHbF percentages were lower, and the MCV, MCH, PK values and the reticulocyte counts were higher than in the controls (0.05 |