Responses of the cinnabar moth Hypocrita jacobaeae to various temperature/photoperiod régimes

Subjecting larvae of Hypocrita jacobaeae to temperatures of 21 and 28°C and photoperiods of $\text{0}\text{24}$, $\text{10}\text{14}$, $\text{12}\text{12}$, and $\text{18}\text{6}$ does not interfere with the phenomenon of diapause. The last larval instar is particularly affected by the higher temperature. Effects include numerous deaths, a high proportion of ill-formed pupae, and failure of adults to emerge properly from the pupal case. The significance of these findings is discussed.     

Patterns of temperature sensitivity in Contrabithorax/Ultrabithorax heterozygotes of Drosophila

Contrabithorax (Cbx) is a dominant homeotic mutant of Drosophila which transforms wings to halteres, while Ultrabithorax (Ubx) is a dominant mutant which transforms halteres to wings. Therefore $\text{Cbx}\text{Ubx}$ flies carry dominant homeotic mutants engaged in opposing transformations. This article reports that $\text{Cbx}\text{TM2 Ubx}{}^{130}$ is temperature sensitive. At 29°C, flies express strong Cbx transformation of wings, and minor Ubx transformation of halteres. Larvae shifted to 17°C prior to 72 hr express strong Ubx transformation of halteres toward wings, and slight Cbx transformation of wings. Seventeen-degree temperature-pulse experiments show that the $\text{Cbx}\text{TM2 Ubx}{}^{130}$ system is temperature sensitive continuously during embryonic and larval life. Expression of the Cbx transformation in left and right wings is highly correlated in all conditions studied, as is expression of the Ubx transformation in left and right halteres, but the Cbx transformation in wings and Ubx transformation in halteres can be negatively correlated or uncorrelated. The temperature sensitivity in $\text{Cbx}\text{TM2 Ubx}{}^{130}$ is not found in $\text{Cbx}\text{Ubx}{}^{\mathrm{61D}}$, and Ubx is only weakly expressed in $\text{Sb}\text{TM2}$Ubx¹³⁰ flies. These results show that Cbx in trans to Ubx can enhance Ubx expression, although Cbx also causes an opposing transformation to Ubx; that the $\text{Cbx}\text{Ubx}$ system acts in both the mesothorax and metathorax to modulate their phenotypes; and that both transformations are broadly temperature sensitive through embryonic and larval life. This suggests that the $\text{Cbx}\text{TM2 Ubx}{}^{130}$ system functions continuously during embryonic and larval development to maintain mesothoracic and metathoracic commitments. The results are interpreted in terms of a $\text{Cbx}\text{Ubx}$ feedback loop which maintains the mesothorax in a state of low $\text{Cbx}\text{Ubx}$ activity, and metathorax in a state of high $\text{Cbx}\text{Ubx}$ activity.     

Larval adipose tissue of homoeotic bithorax mutants of Drosophila.

In the homoeotic bithorax mutant combination bx³$\text{pbx}\text{Ubx}{}^{105}$ of Drosophila melanogaster, the metathoracic segment is transformed to a mesothoracic segment and the adult flies have an extra pair of wings in place of the paired halteres [Lewis, E. B. (1963). Amer. Zool.3, 33–56]. The morphology of the larval fat body, the number of cells in the fat body, and the distribution pattern of kynurenine autofluorescent materials (KAF+) in this tissue were compared in the homoeotic mutant and a wild-type strain. The mutant has an additional mass of adipose cells anterior to the posterior margin of the ventral commissure of the fat body. However, the total number of adipose cells in the two strains as well as the limits of the KAF+ cell population do not differ. Therefore, the bithorax transformation in the larval fat body involves rearrangement of the same cell population as that in the normal strain. This study suggests (1) that the bithorax mutant genes affect the pattern of cell segregation and/or migration of preblastoderm nuclei during embryogenesis and (2) that the larval fat body of Drosophila has a segmental origin.     

Hormonal regulation of epidermis-specific protein and messenger RNA synthesis in amphibian metamorphosis

Experiments using a monospecific antibody directed against one type of epidermis-specific keratin from adult skin of the amphibian Xenopus laevis have demonstrated that polysomes synthesizing this protein first appear within larval skin during natural metamorphosis. Further experiments demonstrated that the synthesis of keratin within larval skin could be induced precociously by the thyroid hormone, 3,3′,5-triiodo-l-thyronine, both in vivo and when the isolated larval skin is cultured in vitro. The earliest developmental age responsive to such hormone induction appeared to be Stage $\text{50}\text{52}$ of larval development. This is about 20–24 days before keratin would normally make its appearance within the skin during natural metamorphosis. Hormone treatment of tadpoles at this age will also cause a precocious increase in the amount of keratin messenger RNA present within larval skin. This has been demonstrated directly by the isolation of poly(A)-containing messenger RNA from hormone-treated larvae and its translation in a wheat germ cell-free system to give immunoprecipitable keratin. Peptide analysis of the in vitro translation product indicates that the hormone-induced mRNA probably codes for an initial protein product that is slightly larger than keratin itself.     

Letter: Studies on histidinol dehydrogenase preliminary crystallographic data

Crystals of histidinol dehydrogenase (EC 1.1.1.23) from Salmonella typhimurium have been obtained in large size suitable for single crystal X-ray studies. The following crystal data were obtained on examination of a number of X-ray precession photographs; crystal system monoclinic, $\text{a = 149.6}\text{A}\text{?}$, $\text{b = 88.9}\text{A}\text{?}$, $\text{c = 105.6}\text{A}\text{?}$, β = 124.5 °, space group C2. The density of the crystal measured by flotation in bromobenzene/xylene mixture is 1.186 g/cm³. There is one dimer molecule of molecular weight 80,000 in one crystallographically asymmetric unit.     

Proteins with haemagglutinin activity in larvae of the Colorado beetle, Leptinotarsa decemlineata

The haemagglutinating activity of larval haemolymph of Leptinotarsa decemlineata against red blood cells of various origins has been examined. This activity appeared to be unspecific, since all the different types of erythrocytes were agglutinated by a haemolymph dilution of $\text{1}\text{128}$ to $\text{1}\text{512}$. Only horse erythrocytes were agglutinated to a greater degree ($\text{1}\text{3200}$. Red blood cells became much more sensitive after treatment with trypsin, while formol fixation also resulted in a better agglutinability. Sulphated polysacchrides (heparin, mucin, dextran sulphate) were good inhibitors of the haemagglutination reaction. A weaker inhibition was obtained with hexosamines. As demonstrated by immunoelectrophoresis, two haemagglutinins occur in larval haemolymph. One is specific for larvae and pupae, and is therefore called the larval-pupal haemagglutinin. It is absent in adults. The second haemagglutinin is the well-known chromoprotein 2, which is present in all developmental stages, including the egg, where it constitutes an important element of yolk proteins. The affinity of chromoprotein 2 toward dextran sulphate was confirmed by precipitation tests in agarose.     

A simple “Width” Method for easy determination of diffusion coefficients with maximum utilization of data

This paper extends the study of Gaussian curves and describes a simple, fast, and reliable Width Method for evaluating diffusion coefficients from the spreading of $\text{dc}\text{dx}$ vs x curves with time. The procedure involves measuring the widths as a function of time at a number of different heights that are fixed fractions of the maximum heights of the curves. A major advantage of the Width Method is that it allows use of virtually all of the available data, instead of only one height, or one height and one width, from each curve. As a result, with the data from a single experiment, the method can be used to calculate a large number of independent values of the diffusion coefficient, one for each fixed fractional height used; in comparison, most other methods yield only a single value of D. It is also shown that certain other methods, including the Area/Height Method, the Width/Height Method and the Error Function Method, are mathematically special cases of this more general and, in most cases, simpler method. Finally, procedures are also described by which these principles can be used to calculate diffusion coefficients from c vs x curves. Although more involved than the analysis using $\text{dc}\text{dx}$ vs x curves, the c vs x method is still simpler than the methods used in analyzing data from fringe patterns using Rayleigh interference optics.     

Development of a model for prediction of target insect mortality following field application of a Bacillus thuringiensis formulation

A model for predicting mortality of Schizura concinna larvae on Cercis occidentalis trees following application of Bacillus thuringiensis formulations is based on an estimation of the effective dose. This is calculated from the initial application level and field persistence characteristics of the pathogen and from the feeding rate of the target insects. Using the estimated effective dose and the time the pathogen was on the host plant, the probability of larval mortality is calculated by means of a multiple logistic dose-response model. Predicted mortalities for B. thuringiensis applications at concentrations 0.00025, 0.0025, 0.025, and 0.25%, $\text{w}\text{v}$, were 7.7, 23.3, 46.2, and 87.1%, respectively. Corresponding, observed mortalities adjusted for larval loss due to forces unrelated to the B. thuringiensis application were 6, 54, 66, and 100%.     

Macrophages as effector cells of protective immunity in murine schistosomiasis: IV. Coincident induction of macrophage activation for extracellular killing of schistosomula and tumor cells

Peritoneal macrophages from Schistosoma mansoni-infected mice are activated both for nonspecific tumor cytotoxicity and for killing of skin-stage schistosomula in vitro. In the current study, mechanisms for induction of macrophage tumoricidal and schistosomulacidal activity have been compared. Examination of macrophages activated in vivo by BCG infection or C. parvum treatment, or in vitro by exposure to lymphokine prepared from antigen-stimulated BCG-immune spleen cells, showed that these effector functions were closely linked. Indeed, fractionation of lymphokine-rich supernatant fluids by Sephadex G-100 gel filtraction showed that activities responsible for induction of schistomula killing by inflammatory macrophages and for induction of tumoricidal activity cochromatographed as a single peak in the 50,000 MW region. Thus, development of macrophage-mediated cytotoxicity against these two extracellular (tumor cell or helminth) targets was coincident in several cell populations activated in vivo or in vitro. However, activation for tumoricidal and schistosomulacidal capacity appeared to be quantitatively dissociated in macrophages from mice with chronic schistosomiasis; those cells demonstrated low, yet significant, levels of larval killing ($\text{1}\text{3}$ to $\text{1}\text{5}$ those of BCG or lymphokine-activated cells) but maximal levels of tumor cell cytotoxicity. Furthermore, cytotoxicity by peritoneal cells from S. mansoni-infected mice was not increased in vitro by exposure to lymphokine. Identification of this functional alteration in S. mansoni-activated cells may help to clarify the role of macrophages in the partial immunity against challenge infection which is demonstrated by mice with chronic primary S. mansoni infection.     

Effects of depurination on the fidelity of DNA synthesis.

The effect of depurination of polynucleotide templates on the fidelity of DNA synthesis in vitro has been determined. The fidelity of DNA synthesis with Escherichia coli DNA polymerase I, avian myeloblastosis virus DNA polymerase and human placenta DNA polymerase-β is decreased as a result of depurination of the poly[d(A-T)], poly[d(G-C)]and poly[d(A)]templates. The error rate with poly[d(A-T)]increased from $\text{1}\text{17,500}$ to $\text{1}\text{2100}$ using E. coli Pol I, and from $\text{1}\text{4100}$ to $\text{1}\text{1500}$ using the myeloblastosis virus DNA polymerase. Depurination of poly[d(A)]increased the error rate from $\text{1}\text{21,000}$ to $\text{1}\text{6500}$ using E. coli Pol I, and from $\text{1}\text{19,300}$ to $\text{1}\text{6100}$ using the DNA polymerase-β from human placenta. Depurination of poly[d(G-C)]resulted in an increase in the error rate with E. coli Pol I from $\text{1}\text{9200}$ to $\text{1}\text{2200}$, and with the virus DNA polymerase from $\text{1}\text{2400}$ to $\text{1}\text{1300}$. This misincorporation is shown to be directly proportional to the extent of depurination. Deletion experiments and alkaline sucrose gradient analyses suggest that the incorporation of complementary and non-complementary nucleotides is dependent on polymerization, and occurs in the same newly synthesized product. Kinetic studies and nearest-neighbor analyses indicate that the incorporation of non-complementary nucleotides occurs randomly as single-base substitutions. The nearest-neighbor studies also suggest that any of the four deoxynucleotides can be incorporated opposite apurinic sites. The number of each nucleotide incorporated relative to the number of apurinic sites was determined to be $\text{1}\text{490}$ for dGTP, $\text{1}\text{115}$ for dCTP, $\text{1}\text{2·5}$ for dATP and $\text{1}\text{1·7}$ for dTTP with both the poly[d(A-T)] and poly[d(A)] templates. The frequencies of misincorporation relative to the number of apurinic sites with the poly[d(G-C)]template were $\text{1}\text{230}$ for dATP, $\text{1}\text{120}$ for dTTP, $\text{1}\text{2·4}$ for dGTP and $\text{1}\text{1·8}$ for dCTP. Hydrolysis at the apurinic sites by alkali treatment reversed the effects of depurination on fidelity. The error rates with the depurinated templates were reduced to within 2% of those obtained prior to depurination, providing additional evidence that the misincorporation after depurination results from apurinic sites on the template. These results suggest a possible relationship between depurination of DNA and errors in DNA replication and/or repair.     

What determines the number of ovarioles in a fly ovary?

The relation between the size of a fly and the number of ovarioles in its ovary was investigated in Phormia regina and Sarcophaga bullata. Small flies of varying size were produced by taking larvae prematurely off the food. The smallest flies thus obtained were derived from larvae only $\text{1}\text{8}$ of the weight of a normal larva. The number of ovarioles in an ovary is directly proportional to the size of the fly and, in the extreme case, is about $\text{1}\text{5}$ the normal number in Sarcophaga and about $\text{1}\text{3}$ in Phormia. Larvae prematurely taken off the food, but fed again after starving for several days, grow to normal or almost normal size and develop ovaries with about the normal number of ovarioles. Small or re-fed Sarcophaga do not show any changes in the anatomy of individual ovarioles but in Phormia disorders in ovariole development and a consequent reduction of fertility are frequent. The number of ovarioles remains identical from the early pupal stage all through the development of the pharate fly and then through ovarian development in the adult fly: it is determined by the size of the larva when it was taken off the food. This shows that it is not lack of space in a small adult fly abdomen which determines the number nor the occurrence of degenerative processes during ovarian development.     

Amino acid and protein changes in the haemolymph of developing fourth instar Chironomus tentans

The concentration of free amino acids, total soluble protein, and haemoglobin in the haemolymph of fourth instar Chironomus tentans was investigated.The concentration of the free amino acid pool increases between the early (15.7 mM/l) and mid-(33.9 mM/l) fourth larval stages followed by a decline during the late (16.9 mM/l) fourth larval period. Alanine, serine, and the amides of aspartic acid and glutamic acid are the predominant free amino acids at all stages. Physiological fluid analysis of late fourth instar haemolymph detected 32 ninhydrin positive components including 18 common amino acids plus homoarginine, ornithine, citrulline, β-alanine, α-aminoadipic acid, α-aminoisobutyric acid, and sarcosine.The concentration of total soluble protein steadily increases during fourth instar larval development to a maximum of $\text{9.3}\text{g}\text{100}\text{ml}$ followed by a decline during the pharate pupal period. A similar pattern of variation occurs in haemoglobin content which comprises from 51 to 66% of Chironomus tentans haemolymph protein.The mM percentage of individual amino acids of total haemolymph protein varies little during the fourth instar. At all stages alanine and aspartic acid are the predominant amino acids.     

An ultrastructural examination of everted rat jejunum

Male, albino, Sprague-Dawley rats were sacrificed by cervical separation. Segments of jejunum were excised, everted and examined with the electron microscope. Examination of tissue fixed immediately after eversion revealed the following changes as compared to non-everted segments fixed $\text{in}$$\text{situ}$ and $\text{in}$$\text{vitro}$: 1) an increase in the length of microvilli from (mean ± S. E.) 0.991 ± 0.011μ for normal tissue to 1.389 ± 0.023μ for everted tissue, 2) an increase in width of microvilli from (mean ± S. E.) 0.089 ± 0.001μ for normal tissue to 0.097 ± 0.001μ for everted tissue, 3) an increase in length and number of lateral membrane interdigitations, and 4) the appearance of intercellular “lakes” in the lateral spaces. The above changes are in those structures hypothesized to be involved with salt and water transport across epithelia and may reflect altered transport rates $\text{in}$$\text{vitro}$ as compared to $\text{in}$$\text{vivo}$.     

Histopathology of Aerococcus viridans var. homari infection (Gaffkemia) in the lobster, Homarus americanus, and a comparison with histological reactions to a gram-negative species, Pseudomonas perolens

Histological response of lobsters to injection of Aerococcus viridans var. homari, cause of gaffkemia, was followed over a 14-day period. Salient features in infected lobsters, Homarus americanus, were: aggregations of hemocytes occurring in hemal spaces throughout the tissues and increasing in number and size with time; the early phagocytosis of bacteria by the system of fixed phagocytes (FPs) present in hemal spaces of the hepatopancreas; and premature release of differentiating hemocytes from the hemopoietic tissue, so that by 14 days that tissue consisted mainly of large stem cells. Mass release of differentiating hemocytes presumably occurred to replace hemocytes lost from the circulation by their incorporation into aggregations or by lysis of individual cells ruptured through the pressure of phagocytized bacteria that were multiplying in them. Bacteria and their remains were present in FPs at 2 days but not visible in single or aggregated hemocytes until 6 days, when free bacteria were also present in the hemolymph. By 6 days, all bacteria, whether phagocytized or free, appeared normal and were surrounded by nonstaining halos that extended well beyond the stainable capsular material. As predicted earlier in physiological studies, gaffkemia is a nontoxic, noninvasive bacteremia. There was hemal stasis and consequent injury in the antennal gland due to free and aggregated hemocytes that occluded hemal spaces of that organ, but other tissues and organs appeared normal except for depletion of glycogen. Aggregations of hemocytes were present in lobsters 2 and 12 days after injection of a nonpathogenic, Gram-negative bacterium, Pseudomonas perolens. Unlike the case with gaffkemia, necrotic hemocytes were common in the aggregations, presumably in response to damage by endotoxin. A further difference was that aggregations were common in the heart of P. perolens-injected lobsters but rare in the heart of gaffkemic lobsters. Bacteria were not seen in hemolymph, hemocytes, or other cells of P. perolens-injected lobsters.     

RNA in the degenerating silk gland of Bombyx mori

Nucleic acids in the degenerating posterior silk gland of Bombyx mori were analysed during the period from larval maturation to early pupal stage, by methylated albumin column chromatography and sucrose density gradient centrifugation. During the first half of the period, the amount of RNA decreased rapidly, but no accumulation of degradation products was detected. The ratio $\text{26}\text{S}\text{17}\text{S}$ rRNA decreased slightly. A decrease of sRNA-like polynucleotide (∼4S RNA) was faster than that of rRNA. During the latter half of the period, rRNA continued to decrease, while ∼4S RNA increased in content. This probably resulted from the degradation of rRNA. There was a significant fall in the ratio of $\text{26}\text{S}\text{17}\text{S}$, suggesting that rRNA, at least in part, was degraded by the scheme of 26 S→17 S→∼ 4S. The possibility that a part of rRNA may be released outside the tissue without complete decomposition is discussed.     

Estimation of mutation rates in cultured mammalian cells

The factors that affect reliable estimations of mutation rates (μ) in cultured mammalian somatic cell populations by fluctuation analysis are studied experimentally and statistically. We analyze the differential effect of the final cell population size in each culture (N_t) and the number of parallel cultures (C) on the variation in the rate estimates ($\text{μ}$) inferred from the P₀ method. The analysis can be made after the derivation of the variance of $\text{μ}$, which is a measure of variation of $\text{μ}$ for a given combination of N_t and C in a number of repeat experiments. The variance of $\text{μ}$ is inversely proportional to C and to the square of N_t. N_t determines the probability of occurrence of mutation in a cell culture. By influencing the size of P₀, N_t also determines whether a rate estimate is obtainable from the experiment. Since P_o is estimated from the fraction of cultures containing no mutation in a set of C cultures, C becomes a determining factor for the accuracy of $\text{μ}$. The rate estimated from $\text{P}\text{?}{}_0$ is biased, but the bias is in general 2 orders of magnitude smaller than $\text{μ}$. By the selection of an appropriate combination of N_t and C for the experiment, this bias can be reduced even further.Based on the notion of comparing two proportions, we propose a test statistic and have applied it to experimental results for a test of equality of mutation rates in different cell lines. This development places the comparison of mutation rates on a statistical basis.     

Coevolution in resource-limited competition communities

A coevolutionary model of species packing is developed which allows evolutionary adjustment in both niche position and within-phenotype niche width of from one of three competing species. The environment is specified as a single resource dimension x and availability of resources along x is given by a Gaussian curve with parameters ($\text{x}\text{?}{}_{\mathrm{R}}\text{and}\text{σ}{}_{\mathrm{R}}$). The model predicts that for S species the ratio of optimal niche width (?) to σ_R is roughly independent of σ_R and can be approximated by $\text{1}\text{S}$ when the competitors are completely resource limited. Niche separation ($\text{d}\text{?}\text{w}\text{?}$) increases only moderately with increases in resource diversity σ_R and is greater for two than for three competing species. To the extent that the competitors do not utilize all resources, both optimal niche separation and niche width decrease. Many of the general trends in niche width and niche separation predicted by this coevolutionary model parallel those from optimal foraging theory and limiting similarity models of community structure. The coevolutionary model stands out, however, in the singularly high values predicted for niche separation, making coevolved communities highly invadeable. Hence, the theory suggests, as some empirical evidence indicates, that coevolved competition communities can only exist as such on remote islands or in other habitats which might be free from invasion by outside species. For such communities, resource diversity (σ_R) should have much less effect on species packing than either species number itself or the extent that these competitors are resource limited.     

Babesia major in Britain: blood-induced infections in splenectomized and intact calves

A strain of Babesia major, originally isolated from field collections of Haemaphysalis punctata in Kent, England was maintained in splenectomized calves by the intravenous inoculation of infected blood. Rapid passage from carrier calves, that had recovered from a tick-induced infection, resulted in a marked increase in virulence; 4 out of 6 calves of the second passage underwent fatal infections and the others suffered severe reactions.Five splenectomized and 5 intact calves of the same breed and age were infected with the same number of infected erythrocytes (RBC). The intact calves reacted mildly with maximum parasite counts ranging from < $\text{1}\text{1000}$ RBC to $\text{5}\text{1000}$ RBC; haemoglobin levels and packed cell volume values, however, fell sharply but recovered swiftly. The group of splenectomized calves exhibited one fatal case, 2 severe reactions and 2 mild infections; maximum parasitaemias varied from $\text{7}\text{1000}$ RBC to $\text{322}\text{1000}$ RBC. Packed cell volumes and haemoglobin concentrations declined to low levels and took several weeks to return to normal.It is concluded that B. major should be regarded as a potential pathogen of British cattle.     

Variation in flavonoid patterns in relation to chromosome changes in Gibasis schiedeana

The distribution of $\text{C-}\text{glycoflavones}$ has been examined in the leaves of plants from five diploid and 12 tetraploid populations of Gibasis schiedeana. Five different chromatographic patterns were found; one occurs only in a single population of diploid plants, two were found in seven populations of tetraploids and the other two in the remaining plants from both diploid and tetraploid populations. Flavonoids were also investigated in three different types of artificially produced triploids. The effects of the changes in ploidy, which are accompanied by Robertsonian fusion and variation in the number of B chromosomes as contributory factors in the observed differences in flavonoid patterns are discussed.