Ground beetle species in heathland fragments in relation to survival, dispersal, and habitat preference.

Local numbers of ground beetle species of heathland appeared to be significantly associated with size of total area, whereas such relationships were not found for the total number of ground beetle species and eurytopic ground beetle species. Presence of species with low chances of immigration was highly associated with area. This is accordance with the "area per se" hypothesis for islands as far as extinction rates are concerned. The habitat diversity hypothesis and the random sampling hypothesis are of less importance for explaining this phenomenon. The importance of dispersal for presence and survival in fragmented habitats could be demonstrated. This result supports the founding hypothesis, under which founding of new populations is considered the main effect of dispersal. The frequency of heathland species with low powers of dispersal in habitats smaller than 10 ha was 76% lower on average than in areas larger than 100 ha. For heathland species with high powers of dispersal this frequency was only 22% lower on average. The period of isolation of the habitats studied, 26-113 years, appeared to be too long to persist for many populations of heathland species with low powers of dispersal.

Evaluation of the immunogenicity of polymerized hemoglobin solutions in a rabbit model.

Chemical modification of proteins carries the risk that neo-antigens are introduced. To investigate the potential immunogenicity of human glutaraldehyde-polymerized hemoglobin (polyHbX1), we analyzed the antibody responses of rabbits after hyperimmunization with complete Freund's adjuvant. In view of the species difference, we also tested rabbit hemoglobin that was modified in the same way as human polyHbX1. Thereafter, we studied the antibody response after weekly intravenous infusion of clinically relevant doses of polyHbX1 to evaluate whether an immune response is likely to occur when modified hemoglobin is used as blood substitute. The occurrence of an antibody response was tested by using an enzyme immunoassay (ELISA). To find out whether antibodies were directed against neo-epitopes on human polyHbX1 we used a competitive ELISA. The results showed that polymerized hemoglobin may weakly activate the immune system in special conditions, but is unlikely to do so when it is used as blood substitute.

Prevention of side effects by hemoglobin solutions; the selection of optimal test models, especially concerning thrombogenicity.

Modification of hemoglobin (Hb) by crosslinking and polymerization results in an improved oxygen release capacity and a prolonged vascular retention time. Modification improves the efficacy and prevents certain side effects. It eliminates leakage of Hb through the kidneys and accumulation in the tubuli. Another important issue is the degree of purification of Hb solutions. Traces of membrane fragments may cause immunogenic and thrombogenic side effects. To determine the contamination with erythrocyte membrane fragments, we developed assays for glycophorin-alpha and phospholipids. Special models were evaluated for testing the maximum allowable level of membrane contamination. As an in vitro model for thrombogenicity we used confluent monolayers of human umbilical vein endothelial cells. These cells were incubated with Hb solutions and subsequently tested on tissue factor (TF) procoagulant activity. TF was tested by the factor VII-catalyzed activation of factor X. The lower detection limit of this assay for endotoxin was 0.5 ng/ml. Hb did not cause any tissue factor expression even after prolonged incubation. No cooperation was found within endotoxin. As an in vivo test on thrombogenicity we developed a guinea pig model in which we can follow the generation of fibrinopeptide A (FPA). This is one of the most sensitive markers for thrombin activation in vivo. When slightly contaminated Hb solutions (phospholipid content 2 nmol/ml) were infused in the presence of factor Xa at a dose (9 micrograms/kg) which in itself did not induce FPA generation, we observed an increase in FPA levels in the plasma from 1.2 +/- 0.4 ng/ml to 5.2 +/- 0.7 ng/ml. Factor Xa is used to mimic a stressed clinical condition with activated coagulation.(ABSTRACT TRUNCATED AT 250 WORDS)

Measurement of interleukin-6 production by monocytes for in vitro safety testing of hemoglobin solutions.

Induction of interleukin-6 (IL-6) production by isolated human mononuclear blood cells was taken as in vitro model for the induction of inflammatory reactions. The model was very sensitive to bacterial endotoxin (detection limit < 10pg/ml). Hemoglobin (Hb) solutions, prepared under non-sterile conditions also induced IL-6 production, which correlated with a positive reaction in the Limulus assay. Purification of the Hb solutions with a detergent prevented IL-6 production, showing that pure Hb itself does not activate the monocytes. We conclude that this assay is a useful and sensitive test of contamination with components that can induce inflammatory reactions, especially microbial products.

Preparation and characterization of crosslinked and polymerized hemoglobin solutions.

In 1982 we synthesized 2-Nor-2-formylpyridoxal 5'-phosphate (NFPLP) and subsequently showed that coupling of the beta chains of hemoglobin (Hb) by this organic phosphate compound according to Benesch et al. (1) lowers the oxygen affinity and prolongs the retention time in the circulation of rats and rabbits with a factor 3 by prevention of excretion via the kidneys. Optimal conditions for the purification of HbNFPLP either by ion-exchange chromatography or by heat treatment were established with recoveries of 70% and 85%, respectively. By extrapolation from the data in rats and rabbits a half life of about 8 hours can be expected in the circulation of humans. However, under some conditions a further prolongation is required. The aim of further modification of HbNFPLP was to achieve a retention time of about 24 hours. Polymerization with glutaraldehyde to polyHbNFPLP resulted in a mixture of polymers of different size. We determined the optimal degree of polymerization with respect to the effects on vascular retention time, oncotic activity, viscosity and oxygen affinity. Depending on the degree of polymerization we found in rats a 5- to 7- fold increase in vascular half-life compared to native Hb. The change in oxygen affinity was found to be independent of the polymer size (P50 = 18-22 mmHg). A limiting factor for polymerization is the increase in viscosity, which was dramatic when large polymers (greater than 300 kD) were present in the preparation.(ABSTRACT TRUNCATED AT 250 WORDS)

Intravascular reduction of methemoglobin in plasma of the rat in vivo.

The formation and reduction of extracellular methemoglobin (metHb) in plasma was studied in vivo in conscious rats after isovolemic exchange transfusions with polymerized hemoglobin solutions. After exchange transfusions of 40 and 70% of the blood volume with hemoglobin solutions, containing less than 6% methemoglobin, the methemoglobin level remained below 15%, whereas exchange transfusions of greater than 90% resulted in an increase in the metHb level to about 30% after 24 hours. The reduction of metHb was studied after exchange transfusions with fully oxidized hemoglobin. A gradual decrease in the metHb level to 20% was observed after exchanges of 5 or 40%. A higher exchange transfusion (70%) resulted also in a decrease in the metHb level but only to approximately 40% in 24 hours. In another series of experiments the reduction of metHb was studied in vitro with isolated human erythrocytes. Incubation of the erythrocytes in the presence of oxidized polymerized hemoglobin (3 g%) resulted in a decrease in the percentage of metHb from 91% to 64%. In the presence of 0.2 mM ascorbic acid the metHb level declined to 22%, suggesting a synergistic effect. These results indicate (1) that there is a potent reducing mechanism present in blood that can reduce extracellular oxidized polymerized hemoglobin and (2) that isolated erythrocytes have a large capacity to reduce extracellular metHb, and may also play an important role in the reduction of extracellular metHb in vivo.

Effect of polymerization on clearance and degradation of free hemoglobin.

In the present study we investigated the mechanism of prolongation of the plasma retention of free hemoglobin by polymerization. Polymerization of intramolecularly crosslinked hemoglobin with glutaraldehyde yields a mixture of large polymers, small polymers and monomers. In exchange transfusion experiments in rats we analyzed plasma samples by gel filtration to determine the clearance of polymers of different size. A positive correlation was found between polymer size and vascular retention. Furthermore, the clearance of large polymers appeared to be highly dose-dependent: after 20% and 70% exchange transfusions, we observed for large polymers a plasma half-life of 12 and 26 hours, respectively, whereas the half-life for 64 kD monomers was 4 hours in both cases. The degradation of hemoglobin was followed by measuring the bilirubin excretion. The infused heme was recovered as bilirubin within 72 hours. The delay between the disappearance of free hemoglobin from the plasma and the recovery as bilirubin was about six hours and was not affected by polymerization or dose. We conclude that polymerization prevents the operation of certain clearance mechanisms, while still allowing a route of clearance that is easily saturated. The intracellular degradation of heme into bilirubin is not affected by the modifications of hemoglobin and is not easily saturated.

The life histories and population dynamics of two carabid species on a Dutch heathland : 1. Fecundity and the mortality of immature stages.

We deal with the causes of the synchronously fluctuating numbers of subpopulations of the carabid species Calathus melanocephalus as compared with the asynchronously fluctuating numbers of subpopulations of the carabid Pterostichus versicolor. Both species continuously occupy a large heath area, Dwingelder Veld (1600 ha), in The Netherlands, and are studied there in the same localities with the same methods. Of the adults of C. melanocephalus, 90% do not cover more than 2 ha during the entire reproductive season, while 90% of adults of P. versicolor cover no more than 12 ha. In C. melanocephalus egg production in the field is usually similar to that under optimal feeding conditions in the laboratory, but in P. versicolor egg production seems to be much lower in the field. In the field 70-80% of the eggs most probably are killed by eelworms, followed by more than 90% mortality among the remaining larvae. Comparing mortality of developmental stages in laboratory experiments with that in field experiments in enclosures, it appears that mortality of larvae is not density-dependent, even when density in the experiments is much higher than it ever is in the field. Larval mortality mainly results from the poor ability of the larvae to find prey, even when in field experiments prey density is increased far above natural densities. We discuss why these poor prey-finding abilities are not improved by natural selection. In the spring breeder P. versicolor differences between localities both in abiotic factors, soil moisture and surface temperature, and biotic factors, reactions of prey species to abiotic factors, in spring and summer when the larvae are maturing contribute to the asynchronous fluctuations of numbers between subpopulations. In the autumn breeder C. melanocephalus possible differences in biotic factors between sites are outnumbered by the effects of winters with a higher or lower than normal amount of precipitation respectively. During a wet winter mortality among the larvae is much higher than during a dry winter. As these winter conditions are similar over large areas (many km2) the fluctuations of numbers between subpopulations are synchronous.

Immunochemical detection of DNA damage induction and repair at different cellular stages of spermatogenesis of the hamster after in vitro or in vivo exposure to ionizing radiation.

An immunochemical method has been used to detect quantitatively DNA damage caused by ionizing radiation in germ cells. With this method, DNA strand breaks as well as lesions converted into breaks in alkaline medium are measured as a function of controlled partial unwinding of the DNA, a time-dependent process starting at each breakage site, followed by the determination of the relative amount of single-stranded regions by use of a single-strand specific monoclonal antibody. With this method the induction and repair of DNA damage in different cellular stages of spermatogenesis (spermatocytes, round and elongated spermatids) of the hamster were investigated. Germ cells were irradiated in vitro with 60Co-gamma-rays, at doses between 0 and 5 Gy. A linear dose-response relationship was observed. Spermatocytes and round spermatids had normal, fast repair of the lesions when compared with the repair of these sites in cultured V79 or CHO cells and human lymphocytes. The elongated spermatids, however, showed hardly any repair. Similar results were obtained after the in vivo gamma-irradiation of hamsters with doses of 0. 4, and 8 Gy and subsequent isolation of germ cells. The damage was still detectable in the elongated spermatids at 24 h after exposure. The results of the experiments show substantial differences in repair capacity between different stages of germ cell development. Because DNA is the major target for mutation induction, this assay may be useful for assessment of the genetic risk of exposure of male germ cells to ionizing radiation, in relation to the stage of development.

Seeing the trees for the wood: random walks or bounded fluctuations of population size?

It is often claimed that the fluctuation of numbers in field populations is fundamentally different from random walks of densities, in that population size is kept between certain positive limits. To test this hypothesis patterns of fluctuation in field populations were compared with random walks of density of about the same duration. It was found that the boundaries (Log-Range) between which numbers fluctuate in field populations increase with time to about the same extent as in comparable random walks of density. Moreover, deviations of the trend of numbers over years (Average lnR) from zero trend in populations of 62 (carabid) species were just those expected for simulated random walk runs, with the median value of Var(lnR), and different values for mean population size that cover the possible range of "survival times" for these species. This means that the null hypothesis that in the field numbers would fluctuate as random walks of densities could not be rejected. Although it is not very probable that field populations fluctuate exactly like random walks of densities, random walk models appear to mimic the fluctuation patterns of field populations sufficiently closely to explain what happens in nature, and to deny the need for regulation. The same conclusion was drawn in earlier studies where statistical tests were applied to fluctuation patterns of field populations (Den Boer and Reddingius 1989; Den Boer 1990a). Random walks of densities do not exclude the possibility that local populations can persist for some centuries.

Glutathione-dependent defence mechanisms in isolated round spermatids from the rat.

The different mechanisms for glutathione-dependent inactivation of a number of oxidizing compounds and other xenobiotics were studied using isolated round spermatids from rats. For the estimation of cellular GSH a flow cytometric assay was used. The cells were exposed to the oxidizing compounds cumene hydroperoxide and diamide, to study the activity of the GSH redox cycle. Incubation of the isolated cells with these compounds showed that the cells had a limited capacity to withstand the oxidative stress associated with their inactivation. The GSH level of the spermatids was maintained during 18 h of incubation in the presence of low concentrations of cumene hydroperoxide and diamide, whereas spermatids exposed to higher concentrations showed a loss of both GSH and ATP. No partial loss of GSH from individual cells was observed. Diethyl maleate and 1,2-epoxy-p-(nitrophenoxy)propane (ENPP) were used to study the effect of glutathione S-transferase-catalysed GSH conjugation on the GSH content of spermatids. Exposure of the cells to low concentrations of diethyl maleate and ENPP resulted in a decrease in GSH content. The flow cytometric analysis showed that this was a partial loss of GSH from all cells, rather than GSH depletion in a part of the cell population. This diminution of the cellular GSH pool, however, did not affect the ATP content and viability of the cells. The present results indicate that spermatids can utilize GSH-dependent defence mechanisms against a number of model compounds.

Effect of glutathione depletion on the cytotoxicity of xenobiotics and induction of single-strand DNA breaks by ionizing radiation in isolated hamster round spermatids.

The role of glutathione (GSH) in cellular protection mechanisms in round spermatids from hamsters was studied. Isolated spermatids were largely depleted of GSH by treating the cells for 2 h with the GSH conjugating agent diethyl maleate (DEM). This treatment resulted in a 90% decrease of the cellular GSH content, but did not affect the ATP content. Exposure of isolated spermatids to cumene hydroperoxide (CHP), a compound which is detoxicated by the GSH redox cycle, showed that the cytotoxicity of the peroxide was markedly potentiated by GSH depletion of the cells. The cytotoxicity was reflected by the cellular ATP content. A decrease of the ATP content of the GSH-depleted spermatids was observed at 5-6-fold lower CHP concentrations, as compared to control cells. An increased cytotoxicity in GSH-depleted cells was also observed using 1-chloro-2,4-dinitrobenzene (CDNB), which is a reactive compound that is detoxicated by glutathione conjugation. The induction of single-strand DNA breaks by gamma radiation was 3-5-fold higher in GSH-depleted spermatids as compared to control cells. This radiation-induced damage was estimated under hypoxic conditions (500 p.p.m. O2 in N2). GSH depletion did not affect the repair of single-strand DNA breaks following the irradiation. The present results indicate that cellular GSH has an important function in the defence mechanisms of round spermatids against peroxides, electrophilic xenobiotics and radiation-induced DNA damage.

Effects of glucose and adenosine on the ATP content of hamster spermatids.

Effects of glucose and adenosine on ATP metabolism were studied using isolated round spermatids from hamsters. The ATP content of the spermatids was strongly decreased after 1 h of incubation of the cells in the presence of 0.1 mM D-glucose. Glucose (1 mM) had no effect during 18 h of incubation in the presence of 12 mM sodium DL-lactate. However, 10 mM glucose caused an almost complete loss of cellular ATP in the presence of lactate. The effect of adenosine was estimated in the absence of glucose with lactate as the energy-yielding substrate. The cellular ATP content was approximately 4 and 8 nmol/10(6) cells, after 18 h of incubation in the absence and presence of 0.1 mM adenosine, respectively. This two-fold increase was prevented by inhibitors of adenosine uptake and phosphorylation and was slowly reversed after removal of the exogenous adenosine. Treatment of the cells with adenosine had no effect on the energy charge, which was higher than 0.90, and did not alter the cellular cyclic AMP content. The suggestion that the physiological ATP content of the round spermatids is probably stabilized in the region of 4 nmol/10(6) cells is discussed.

On the stabilization of animal numbers. Problems of testing : 3. What do we conclude from significant test results?

When testing census data of insect populations for regulation, and/or for overall density dependence in the course of numbers over years, certain conditions, which follow from the testing models, should be fulfilled. Even if the series of densities may be considered a piece of first-order Markov chain (a necessary condition) significant test results need not obviously point to regulation of numbers by dominant density-dependent processes. Such a case is presented by the pine looper population at "Hoge Veluwe" studied by Klomp. A drastic drop in density from 1952 to 1953, which takes 78-97% of the log-density range (LR) over all years, most probably wrongly causes significant test results. This is supported by some simulation experiments. Moreover, we cannot be sure that the population was sufficiently isolated, i.e. that dispersal of adults from surrounding populations did not importantly influence population numbers. Among 6 Panolis-populations studied by Schwerdtfeger during 17 years a single one scored significantly with all tests. This resulted, however, from such a drastic drop in density that it covered the entire log-density range (LR=9.39), which therefore is wider than in any of the other (non-significant) populations. Another Panolis-population that maintained itself during 60 years, and which also scored significantly, most probably was kept within limits by supplementation of very low densities with immigrants, on the one hand, and by restriction of high densities by defoliation caused by other species, on the other. It is discussed whether this can be considered "regulation", or results from spreading of risk. It is concluded that the range stability of particular populations must be considered generally to be the result of stabilization by both internal and external processes among which both density-dependent and density-independent processes play a significant part, and from which the contribution of the density-dependent processes need not be separated. The most interesting aspect of the stabilization of animal numbers is its relationship with the expected survival time of the population.

Glutathione metabolism in cultured Sertoli cells and spermatogenic cells from hamsters.

Isolated spermatocytes and spermatids from hamsters contained a large amount of glutathione (GSH) (approximately 40 and 30 nmol GSH/mg protein, respectively), but showed a spontaneous decrease of GSH content during prolonged incubation (t1/2 approximately 35 h). Incubation of the germ cells in the presence of the glutathione biosynthesis inhibitor buthionine sulphoximine (BSO) provided evidence that the cells can perform glutathione synthesis. This synthesis, however, was not sufficient to maintain the GSH content of the isolated cells, or to restore the cellular GSH pool after depletion caused by exposure of the cells to the glutathione S-transferase substrate, diethyl maleate (DEM). Cultured Sertoli cells, containing approximately 10 nmol GSH/mg protein, had a more active BSO-sensitive GSH synthesis system. The Sertoli cells, but also tubule fragments containing Sertoli cells and germ cells, were able to restore their GSH pool after DEM-induced depletion. DEM treatment of the tubule fragments resulted in a 90% decrease of the GSH content of the spermatocytes and spermatids present within the fragments. The GSH levels of the tubule fragments and the enclosed germ cells were restored during a subsequent incubation in the absence of DEM. As indicated above, such a recovery was not observed for isolated spermatocytes and spermatids. The results illustrate the importance of Sertoli cell-germ cell interaction, and point to a role of Sertoli cells in glutathione synthesis by the germ cells.

On the stabilization of animal numbers. Problems of testing : I. Power estimates and estimation errors.

It is tried to remove some misunderstandings about the "regulation" of animal numbers by density-dependent processes. Staying between limits is called "stabilization", and only when this results from density-dependent processes it is considered "regulation". We discuss two tests that may be used to detect the existence of regulation: the parametric tests of Bulmer and a nonparametric "permutation" test. The powers of these tests are compared. The first test of Bulmer and the permutation test do not differ very much in power, but the second test of Bulmer has hardly any power and therefore cannot be used in cases where densities were only estimated. The arguments from which Bulmer's second test is derived are critically discussed and found not to be very convincing. We propose, rather than using Bulmer's second test, to correct the test statistic of his first test for estimation error, and present a possible solution for this. In a following paper this method will be applied to some long series of population counts of univoltine insects, for, a basic assumption of all regulation-tests is, that the sequence of population counts is a realization of a piece of first-order Markov chain. This highly restricts the usefulness of regulation-tests. Some other recent attempts to construct such tests are discussed within the present context.

On the stabilization of animal numbers. Problems of testing : 2. Conforntation with data from the field.

When testing for regulation of population numbers, rather than using Bulmer's second test in cases where population numbers are estimated instead of measured, we prefer to correct Bulmer's first test for estimation error. A correction method is expounded, discussed, and applied to two series of census data: the pine looper of Klomp and the garden chafer of Milne. In neither case the tentative conclusion from using the uncorrected test was changed after correction. Therefore, in practice Bulmer's first test without correction can be used well as a first orientation. Twelve long series (more than 10 years) of census data of both univoltine and semelparous (a necessary condition) insects were tested for significant density dependence in the fluctuations of numbers with the randomization test of Pollard et al. None of the series, all we could find to meet the necessary condition as well as being longer than 10 years, showed significant density dependence at the 0.05 level, though the pine looper of Klomp did so at the 0.1 level. Next, the same series were tested for regulation in the sense of "keeping density within limits" with both the first test of Bulmer and the permutation test of Reddingius and Den Boer. Onky Klomp's pine looper population at "Hoge Veluwe" scored significantly. In a following paper this population will be considered more closely, in order to enable understanding of this test result.

Mechanism of action of (-)gossypol on ATP production in isolated hamster spermatids.

The ATP content of round spermatids isolated from hamsters was decreased 90% after 18 h of incubation in the presence of 4 microM-(-)gossypol and 0.10% bovine serum albumin (BSA). The (+)-enantiomer had no effect under these incubation conditions. The Michaelis-Menten constant Km and the maximal initial velocity Vmax of cellular LDH-C4 were not significantly altered after 18 h of incubation of the spermatids with (-)gossypol. Furthermore, there was no effect of (-)gossypol on the production of 14CO2 from L-[U-14C]lactate. It is concluded that (-)gossypol does not inhibit ATP production in spermatids by an effect on the sperm-specific LDH-C4 enzyme or on the mitochondrial oxidation of pyruvate. Rather, (-)gossypol may have an effect on the coupling between electron transport and ATP synthesis in the mitochondria. This action of (-)gossypol may not involve the H+-conducting activity of gossypol, but could be produced through binding of (-)gossypol to specific mitochondrial proteins.