Multiple-brooding in birds of prey: South African Black Sparrowhawks Accipiter melanoleucus extend the boundaries

Multiple-brooding (raising more than one brood of young in quick succession) occurs infrequently in raptors and is generally restricted to either smaller species with shorter nesting periods, co-operative breeders or species capable of capitalizing on conditions of prolonged food abundance whenever they occur. This paper presents the first recorded cases of multiple-brooding in the Black Sparrowhawk Accipiter melanoleucus from two distinct locales in South Africa. In the Western Cape (Cape Peninsula), four attempts to multiple-brood were recorded in four different years, involving three distinct pairs of birds, and in KwaZulu–Natal (Eshowe), three distinct pairs of Sparrowhawks successfully multiple-brooded on several occasions over a 5-year study period. These results establish the Black Sparrowhawk as one of only two relatively large, monogamous raptor species, and the only specialist bird-eating raptor, in which multiple-brooding has been recorded with any frequency . The species' capacity to thrive in human-modified environments (i.e. alien plantations) and particularly to exploit associated foraging opportunities (e.g. high densities of doves and pigeons in suburban areas) may, at least partly, account for the instances of multiple-brooding reported here. We suggest that biologists be more vigilant for cases of multiple-brooding in raptors, as it is possible that this trait is more common than originally thought and has previously been overlooked.     

William Trager: An Appreciation

SYNOPSIS. Additional information on host interactions with trypanosomatid membranes was obtained from studies of a monomorphic strain of Trypanosoma brucei harvested at peak parasitemia from intact and lethally irradiated rats. Pellets of trypanosomes were fixed briefly in glutaraldehyde and processed for thin section electron microscopy or freeze-cleave replicas. Observations of sectioned material facilitated orientation and comparison of details seen in replicas. Fracture faces of cell body and flagellar membranes as well as 3-dimensional views of the nuclear membrane were studied. Cell body membranes of 80% of the organisms from intact rats contained random arrays of intramembranous particles (IMP). Aggregated clusters of particles appeared on the fracture faces of 20% of the trypanosomes. Some of these membranes had nonrandomly distributed particles aligned in distinct rows on the outer fracture face of both cell body and flagellum. Many inner face fractures of the cell body membranes had a particle arrangement similar to the longitudinal alignment of cytoskeletal microtubules. No aggregated particle distribution was seen in membranes of trypanosomes harvested from lethally irradiated rats. Replicas of trypanosome pellets also had plasmanemes as a series of attached, empty, coated membrane vesicles. These structures were found in close association with, as well as widely separated from the parasites. The shedding of these vesicles and the variation of particles in cell body membranes are discussed in light of antibody-induced architectural and antigenic changes in surface properties of trypanosomatids. The convex face of the inner membrane of the nucleus also is covered with randomly arrayed particles. More IMP were observed on the inner than on the outer nuclear membranes. Images of nuclear pores were also seen. The importance of these structures in drug and developmental studies of trypanosomes is discussed. On fracture faces of the flagellar membrane there were miniature maculae adherentes, unique to the inner fracture face and occurring only at regions of membrane apposition between cell body and flagellum. Each cluster of particles exposed by the freeze-cleave method corresponds to an electron-dense plaque seen in thin section images. However, because of a unique fracture pattern, these plaques were not revealed on the apposing body membranes, as illustrated in thin sectioned organisms.     

Pentamidine Transport and Sensitivity in brucei-Group Trypanosomes*

SYNOPSIS. Sensitivity to pentamidine of bloodstream forms and culture forms of Trypanosoma brucei brucei, strains of this subspecies, and strains of T. brucei rhodesiense characteristically differs in vitro. Analyses of transport parameters for pentamidine uptake in these organisms show differences that correspond with drug sensitivity. Long slender bloodstream forms of T. b. brucei have a high affinity for the drug and high rates of uptake as indicated by K_m and V_max values for [³H]pentamidine transport. Although pentamidine and stilbamidine resistance is associated with dyskinetoplasty. this condition does not itself confer resistance to pentamidine nor does it affect pentamidine transport. However, drug-resistant strains show lower rates for pentamidine transport as does T. b. rhodesiense, which is characteristically less sensitive to the drug. Of all the forms and strains studied, procyclic trypomastigotes were least sensitive to pentamidine and had a remarkable ability to exclude the drug.     

Subcellular localization of DNA-binding protein BA by immunofluorescence and immunoelectron microscopy

Nonhistone protein BA has been shown to decrease in amount in the chromatin of growth- stimulated normal rat liver (Yeoman et al. 1975. Cancer Res. 35:1249-1255) and in mitogen-stimulated normal human lymphocytes (Yeoman et al. 1976. Exp. Cell Res. 100:47- 55.). Subsequently, protein BA was purified and was shown to prefer to bind to double- stranded A-T-rich DNAs (Catino et al. 1978. Biochemistry. 17:983-987.). Immunization of rabbits with highly purified protein BA has resulted in the production of a specific antibody. A specific immunoreactivity for chromosomal protein BA has been demonstrated by immunoelectrophoresis and double antibody immunoprecipitation analysis with rabbit anti-BA immunoglobulin and IgG fractions. Light microscope examination of normal rat liver crysections by the indirect immunofluorescence procedure has demonstrated a cytoplasmic as well as a nuclear localization for protein BA with a pronounced perinucleolar fluorescence. Immunoelectron microscopy employing the peroxidase antiperoxidase method of antigen localization has confirmed the immunofluorescence data and has show a heterochromatin localization for protein BA. The relationship of the localization of protein BA to gene control in quiescent cells or to configurations of heterochromatin as well as the marked reduction in the amounts of protein BA which occur in stimulated growth states remains to be defined.     

Trypanosoma lewisi Infections in Normal Rats and in Rats Treated with Dexamethasone

SYNOPSIS. Administration of dexamethasone to rats infected with Trypanosoma lewisi resulted in the development of exceedingly large populations of trypanosomes which were fatal to their hosts. The elevated levels of parasitemia in treated rats early in infections were thought not to be a result of an increased reproductive rate. However, trypanosomes in treated rats 2 days postinfection did have a higher coefficient of variation in total length and a greater percentage of dividing forms than those observed from infected rats which were not given the drug. The course of infection may be markedly altered not only in intensity but also in length by this corticosteroid. It is suggested that dexamethasone administered at the levels recorded to rats infected with T. lewisi inhibits the production of ablastin and trypanocidal antibodies.     

Effect of malformin on the major constituents of Phaseolus vulgaris

Malformin inhibits wet and dry weight, nitrogen accumulation,and cell wall, RNA, DNA and protein synthesis in Phaseolus vulgaris.The relative proportion of dry matter and nitrogen in malformedtissues is increased in the ethanol soluble fraction and decreasedin the residue remaining after hydrolysis with 0.5 N HCl. Inhibitionof cell wall and protein synthesis was generally greater thaninhibition of nitrogen accumulation and RNA and DNA synthesis.The effects of malformin on the composition of P. vulgaris aresimilar to alterations in composition reported for ethylene,and opposite to those reported for gibberellic acid. ¹This research was supported by grant GB-7158 from the NationalScience Foundation and grant E-146-F from the American CancerSociety. ²Journal Paper No. 3509 of the Purdue Agricultural ExperimentStation. (Received October 23, 1968; )     

Comparison of different insecticides and fabrics for anti-mosquito bednets and curtains

Abstract. Various formulations of six insecticides (a carbamate and five pyrethroids), were impregnated into bednets and curtains made from cotton, polyester, polyethylene or polypropylene fabric. For bioassays of insecticidal efficacy, female Anopheles gambiae mosquitoes were made to walk on the fabrics for 3 min and mortality was scored after 24 h. The main concentrations tested were: bendiocarb 400 mg/m², cyfluthrin 30–50 mg/m², deltamethrin 15–25 mg/m², etofenprox 200 mg/m², lambda-cyhalothrin 5–15 mg/m² and permethrin 200–500 mg/m². Field trials in Tanzania used experimental huts (fitted with verandah traps) entered by wild free-flying Anopheles gambiae, An. funestus and Culex quinquefasciatus mosquitoes. Results of testing the impregnated fabrics in experimental huts showed better personal protection provided by bednets than by curtains. Permethrin cis:trans isomer ratios 25:75 and 40:60 were equally effective, and the permethrin rate of 200 mg/m² performed as well as 500 mg/m². Bioassay data emphasized the prolonged insecticidal efficacy of lambda-cyhalothrin deposits, except on polyethylene netting. Most of the impregnated nets (including the ‘Olyset’ net with permethrin incorporated during manufacture of the polyethylene fibre) and an untreated intact net performed well in preventing both Anopheles and Culex mosquitoes from feeding on people using them overnight in the experimental huts. Anopheles showed high mortality rates in response to pyrethroid-treated nets, but only bendiocarb treated curtains killed many Culex. Holed nets treated with either cyfluthrin (5 EW formulation applied at the rate of 50 mg a.i./m²) or lambda-cyhalothrin (2.5 CS formulation at 10 mg a.i./m²) performed well after 15 months of domestic use. Treatment with deltamethrin SC or lambda-cyhalothrin CS at the very low rate of 3 mg/m² gave good results, including after washing and re-treatment.