Control of nematode parasites by grazing management—I. Decontamination of cattle pastures by grazing with sheep

Between December and June, six paddocks that had been contaminated naturally with infective larvae of nematode parasites of cattle, were each subjected to one of six grazing treatments. The effects of these treatments on the infectivity of the pastures were assessed by slaughter and total worm counts of calves which subsequently grazed the paddocks, and by counts of larvae on pasture samples. Grazing by sheep during autumn resulted in reduced populations of Ostertagia ostertagi and Trichostrongylus axei, both in calves and on the pasture for up to 12 months after treatment. Similar effects were noted on pasture grazed by cattle repeatedly dosed with anthelmintics, and on ungrazed pasture. There was little effect of any treatment on numbers of Cooperia oncophora. It was concluded that the level of autumn contamination was of importance in determining the numbers of O. ostertagi in the following spring and summer.     

Intensity-dependent effects of cattle and sheep grazing in sand grasslands — Does livestock type really matter?

Aims

By analysing cattle- and sheep-grazed sand grasslands, we tested the following hypotheses: (i) livestock type has a stronger effect on the vegetation characteristics than grazing intensity; (ii) sheep grazing results in lower biomass and species and functional diversity than cattle grazing, regardless of intensity; and (iii) increased grazing intensity causes a shift of the trait composition in grasslands.

Location

Sand grasslands in the Nyírség region, East Hungary.

Methods

We selected 26 sand grassland sites grazed by cattle or sheep and classified them into four intensity levels. Vegetation composition was surveyed in 2 m × 2 m plots. We harvested the above-ground biomass from 20 cm × 20 cm plots; then dried and sorted it to live biomass, litter, moss, and lichen. We compared Rao dissimilarity index, species richness, Shannon diversity, evenness, and the community-weighted means of nine vegetative and generative traits along a grazing intensity gradient. We calculated functional richness, evenness, and divergence for comparison.

Results

We found that some diversity metrics and community-weighted means of most studied traits were significantly affected by grazing intensity. Several characteristics were also affected by the interaction of grazing intensity and livestock type, but none of the studied characteristics was affected by livestock type in itself. Increasing Rao dissimilarity index peaking at the fourth grazing intensity level was detected, but for other multitrait indices, no such changes were proven, except for functional divergence, which was the lowest at the first intensity level. Graminoid, forb, and litter biomass were significantly affected by intensity, but none of the biomass fractions was affected by livestock type.

Conclusions

We suggest that for the management of sand grasslands, grazing intensity should be carefully adjusted, considering not only livestock units per hectare. For practical recommendations, well-defined, long-term experiments studying different livestock and habitat types along an intensity gradient would be essential.     

Orientation by helical motion—II. Changing the direction of the axis of motion

We analyse the helical motion of organisms, concentrating on the means by which organisms change the direction in space of the axis of the helical trajectory, which is the net direction of motion. We demonstrate that the direction of the axis is determined largely by the direction of the organism's rotational velocity. Changes in direction of the rotational velocity, with respect to the organism's body, change the direction in space of the axis of the helical trajectory. Conversely, changes in direction of the translational velocity, with respect to the body of the organism, have little effect on the direction in space of the axis of the trajectory. Because the axis of helical motion is the net direction of motion, it is likely that organisms that move in helices change direction by pointing their rotational velocity, not their translational velocity, in a new direction.     

Conservation tool or threatening process? management implications of interactions of cattle with vegetation and land at the Vale of Belvoir reserve

A recently purchased private reserve of high conservation value has been grazed in summer by cattle since the early nineteenth century. We ask whether the cattle are causing continuing damage and whether they are necessary to maintain any conservation values. We used five‐year‐old exclosures to determine the effects of cattle on wetland vegetation, mapped damage to soils and landforms and mapped cattle dung deposition in relation to the distributions of rare and threatened plant species. Cattle impacts on wetland plants were minor. Cattle damage to landforms by pugging and bank collapse was frequent near unfenced water bodies. Rare and threatened species were largely on well‐drained ground, while cattle dung was concentrated in wetlands and near water bodies. We conclude that cattle grazing is impacting some conservation values and is not necessary for conservation purposes. Destocking should be accompanied by careful monitoring of threatened plant populations. If necessary, alternative planned disturbances can provide regeneration niches for rare and threatened plants.     

First screening of bacterial communities of Microdon myrmicae and its ant host: do microbes facilitate the invasion of ant colonies by social parasites?

Many studies have highlighted how numerous bacteria provide their hosts essential nutrients or protection against pathogens, parasites and predators. Nevertheless, the role of symbiotic microorganisms in the interactions between social insects and their parasites is still poorly known. Microdon (Diptera, Syrphidae) is a peculiar fly genus whose larvae are able to successfully infiltrate ant colonies and feed upon the ant brood. Using high throughput 16S rRNA gene amplicon sequencing, we provide the first microbiome survey of Mi. myrmicae larvae and larvae and workers of its host, Myrmica scabrinodis, collected from two sites in England. We analyzed the microbiome of the external surface of the cuticle and the internal microbiome of the body separately. The results clearly show that the Mi. myrmicae microbiome significantly differs from that of its host, while no substantial dissimilarity was detected across the microbiome of ant workers and ant larvae. Microdon myrmicae microbiome varies across the two analyzed sites suggesting that bacteria communities of Mi. myrmicae are derived from the environment rather than by horizontal transmission between hosts and parasites. Families Streptococcaceae, Carnobacteriaceae and Rizhobiaceae are dominant in My. scabrinodis, and Spiroplasma is dominant in ant workers. Microbiome of Mi. myrmicae larvae is mainly characterized by the family Anaplasmataceae, with Wolbachia as predominant genus. Interestingly, we found Serratia within both Mi. myrmicae and Myrmica larvae. Bacteria of this genus are known to produce a family of pyrazines commonly involved in ant communication, which could play a role in Microdon/ant interaction.     

Additional characterization of the two oxygen-containing compounds formed by the interaction of phthalocyaninatoiron(II) and dioxygen. Reproducible synthesis of the species isomorphic with the α form of Fe(II)Pc

The two compounds obtained by the interaction in solution of Fe(lI)Pc with O₂, presently considered two crystalline modifications of the μ-oxo dimer of Fe(III)Pc, are further characterized by visible absorption, XPS and Mössbauer spectra. The results stress the difference between the solid state properties of the two Fe(III) compounds.The behaviour of Fe(II)Pc and the two oxidized compounds in some chlorinated and non-chlorinated solvents, at different temperatures in the presence and absence of O₂, is reported. It is seen that heating the two Fe(III) products in 1-chloronaphthalene, or dimethylformamide, in vacuum sealed tubes, gives as a final product βFe(II)Pc. However, the same procedure in chlorobenzene or nitrobenzene yields, in a reproducible way, the pure oxygen-containing species which is isomorphic with αFe(II)Pc. Until now this product was only obtained in a fortuitous manner.     

Tree composition and structure in disturbed stands with varying dominance by Pinus spp. in the highlands of Chiapas,México

We studied soil and forest floor conditions, regeneration patterns oftrees, and forest structure and floristic composition along a gradient ofdominance by Pinus spp. in disturbed stands in thehighlands of Chiapas, southern Mexico. Seedlings, saplings, and adults of treespecies were counted and measured in 2-3 circular plots (1000m² each) in 36 forest stands (a total of 38 treespecies). Dominance of broadleaved trees other thanQuercusspp. was negatively correlated with basal area of Pinusspp. (P < 0.001). Soils of pine-dominated stands weremore compacted, less acidic, and less fertile (lower C.E.C., nitrogen, andorganic matter content). Numerous broadleaved trees may depend on anoak-dominated canopy to regenerate, and changes associated to pinelandsexpansion may compromise their long-term persistence. However, seedlings andsaplings of Quercus spp. were abundant in stands with bothan oak- or pine-dominated canopy. The results suggest that a plan forsustainable forest utilization in the study region, and in other similarpopulated tropical highlands, could take advantage of the abundant oakregeneration and coexistence with pines in the canopy.     

Chronorhythms of the Circulating Erythrocytes and Leukocytes—Correlation with the E.S.R. Cycles

2750 healthy and fasting subjects, 20-30 years old, were studied over a half-year period in 1980. Considering the mean day value as a basic piece of information for statistics, the Erythrocyte Sedimentation Rate (E.S.R.) and the blood counts (erythrocytes, leukocytes, polymorphonuclears, lymphocytes, monocytes and eosinophils) were compared.

The timeless relation between E.S.R. and each cell type number or percentage is rectilinear. The stronger slope and relation apply to the polymorphonuclears (PMN) or to the overall leukocytes.

The chronological normalized variations of the E.S.R. and of the PMN or leukocyte number or percentage are highly correlated. E.S.R. is less correlated with monocytes, eosinophils and Lymphocytes. Contrary to what could have been expected, the erythrocyte situation is but an intermediate one.

The spectra derived from the time variations show that all the cell types, whatever they are, are to be taken into account to explain the E.S.R. value and variation with time, even if, for a given cell type, the correlation and timeless relation were but faint ones.

Each cell type has a specific spectrum. Erythrocytes are subject to low frequency variations (316-158 days). PMNs oscillate with time within the medium frequency range (90 days). Lymphocytes, monocytes and eosinophils fluctuate more quickly (53 days).     

Octopamine in leeches—II. Synthesis,release and reuptake of octopamine by the ventral nerve cord of Erpobdella octoculata

1. Octopamine was synthesized by the ventral nerve cords of E. octuculata during in vitro incubation in radiolabelled tyrosine and tyramine. Trace amounts of dopamine were also synthesized from tyrosine and tyramine.2. In vitro uptake of ³H-octopamine revealed the presence of a sodium sensitive and a sodium insensitive component which was linear up to 10.54 μM. The sodium sensitive component showed at least one component that was fully saturated at 1.54 μM octopamine, possessed a K_m of approximately 4 × 10⁻⁷ M and a V_max of 15.5 mM/10 ventral nerve cord ganglia/min.3. Release of preloaded ³H-octopamine from ventral nerve cords was by a calcium-dependent process. A high-potassium-induced calcium-dependent release was also demonstrated.4. Hydroxymandelic acid production was decreased in the presence of iproniazid phosphate suggesting the presence of a monoamine oxidase.5. The synthesis, release, reuptake and metabolism of octopamine are discussed in the light of octopamine as a central transmitter in the leech.     

Batwanema gen. n. and Chokwenema gen. n. (Oxyurida,?Hystrignathidae), new nematode genera?as parasites of Passalidae (Coleoptera) from the Democratic Republic of Congo

Two new genera and species parasitizing passalid beetles from the Democratic Republic of Congo are described. Batwanema congogen. n. et sp. n. is characterized by having females with the cervical cuticle armed with scale-like projections, arranged initially in rows of eight elements that gradually divide and form pointed spines toward the end of the spiny region, two cephalic annuli, clavate procorpus and genital tract monodelphic-prodelphic. Two Malagasian species of Artigasia Christie, 1934 were placed in this genus as B. latum (Van Waerebeke, 1973) comb. n. and B. annulatum (Van Waerebeke, 1973) comb. n.Chokwenema lepidophorumgen. n. et sp. n. is characterized by having females with the cervical cuticle armed with scale-like projections, arranged initially in rows of eight elements (similar to Batwanema) that divide gradually, forming spines; a single cephalic annule cone-like, truncated, moderately inflated; procorpus sub-cylindrical and genital tract didelphic-amphidelphic.     

Control of yeast cell type by the mating type locus: II. Genetic interactions between MATα and unlinked α-specific STE genes

The alleles of the yeast mating type locus, MATα and MATa, determine the yeast cell types, a,α, and a/α. It has been proposed that the MATα2 product negatively regulates expression of unlinked a-specific genes, and that the MATα1 product positively regulates expression of unlinked α-specific genes. The behavior of mutants defective in MATα2, which are deficient in mating and in production of α-factor, can thus be attributed to antagonism between a-specific and α-specific functions expressed simultaneously in matα2^? strains. If this view is correct, then elimination by mutation of the specific functions required to mate as α may allow matα2 mutants to mate as a. In order to test this possibility, we examined the interactions between matα2 mutations and various unlinked mutations that cause α cells but not a cells to be mating defective (α-specific STE mutations). Three α-specific mutations (ste3, ste13 and kex2) were found to be non-allelic. Furthermore, although matα2 mutants mate weakly as a, matα2, ste3 double mutants, but not matα2 ste13 or matα2 kex2 double mutants, mate efficiently as a. The ability of matα2 ste3 strains to mate as a supports the view that matα2 mutants express a-specific mating functions, and suggests that a mating functions are expressed constitutively in MATa cells. The mating behaviour of the matα2 ste3 double mutant is consistent with the proposal that STE3 is positively regulated by the MATα1 product.     

Control of the production of exo-β-N-acetylglucosaminidase by Bacillus subtilis B. Derepression during gluconeogenesis and initial stages of sporulation

1. The control of exo-beta-N-acetylglucosaminidase (EC 3.2.1.30) production by Bacillus subtilis B growing on a chemically defined medium was studied. 2. The enzyme was repressed during exponential growth by those carbon sources that enter the glycolytic pathway above the level of phosphoenolpyruvate. When exponential growth ceased as a result of low concentrations of the nitrogen, carbon or metal ion components of the medium, the enzyme was formed and its amount could be increased by the addition of cell-wall fragments as inducer. 3. The enzyme was de-repressed and could be induced during exponential growth on non-glycolytic compounds metabolized directly into pyruvate, acetyl-CoA or tricarboxylic acid cycle intermediates. 4. The major difference in the metabolism of the organism utilizing these two groups of compound was the existence of high activities of phosphoenolpyruvate carboxylase required for gluconeogenesis. 5. It is concluded that the de-repression of glucosaminidase occurs when the only principal change detected in the intermediary metabolism of the organism was the presence of high activities of phosphoenolpyruvate carboxylase. 6. When the organism was grown on media containing repressing compounds, the enzyme was only de-repressed on entry of the cells into the initial stages of sporulation, where phosphoenolpyruvate carboxylase activity, even in the presence of excess of glucose, increased in parallel with glucosaminidase, neutral proteinase and alkaline phosphatase activities. 7. These results suggest a strong link, at the level of the tricarboxylic acid cycle, between the control of phosphoenolpyruvate carboxylase and the control of the de-repression of glucosaminidase and sporulation.     

Phylogeny and ontogeny of the phosphoglycerate mutases—II. Characterization of phosphoglycerate mutase isozymes from vertebrates by their thermal lability and sensitivity to the sulfhydryl group reagents

• 1.1. To characterize the three phosphoglycerate mutase (PGM) isozymes present in vertebrates (types M, B and MB) their sensitivity to the reagents of the sulfhydryl groups and to heat treatment has been studied.
• 2.2. In mammals and reptiles type M PGM is not affected by the —SH group reagents, type MB PGM is inhibited about 50% and type B PGM is fully inhibited. Types B and MB PGM show greater heat lability than type M PGM.
• 3.3. In amphibians and fishes PGM isozymes do not differ in their sensitivity to the —SH reagents.
• 4.4. The results strongly support the homodimeric and heterodimeric structure suggested for PGM isozymes and favour their genetic origin.

     

Formate production and utilization by methanogens and by sewage sludge consortia — interference with the concept of interspecies formate transfer

Pure cultures of H₂/CO₂- and formate-utilizing methanogens or mixed consortia of sewage sludge generated some formate from H₂/CO₂ at H₂ partial pressure in the gas phase above 200 kPa. At decreasing H₂ partial pressure the formate was taken up again and converted to methane. If methanogenesis was inhibited by bromoethanesulphonic acid (BESA) or a high redox potential (–180 to –200 mV), formate-utilizing methanogens produced high amounts of formate from H₂/CO₂. No formate was excreted by the species, which could only utilize H₂/CO₂ for methanogenesis. In contrast, H₂ formation from formate was observed in cultures of Methanobacterium thermoformicicum and M. formicicum. Measurable amounts were, however, only formed if its immediate utilization for methane production was inhibited by BESA. In the light of the data on formate formation from H₂/CO₂ and its re-utilization by all formate-utilizing methanogens, the concept of interspecies formate transfer of Thiele and Zeikus should be reconsidered. In pure cultures of methanogens or complex ecosystems with excess H₂, formate formation seemed to serve more as a means of disposal of surplus reducing power than for H₂ transfer. Correspondence to: J. Winter