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G T Baker

Publications and source records attributed to G T Baker.

At least 19 recordsLinked to original sources
PubMed2001

Distribution patterns and morphology of sensilla on the apical segment of the antennae and palpi of Hydradephaga (Coleoptera: adephaga).

The sensilla on the terminal antennomere of selected Hydradephagans (Coleoptera) are modified in several distinct ways as compared to the sensilla on the terminal antennomere of Geadephagans (Coleoptera). There are no long sensilla of any type on antennae of Hydradephagans, the sensilla are either short, peg-like sensilla that may be recessed in the antennal surface or they are multiporous plate-like sensilla. Multiporous plate-like sensilla have not been found on the antennae of Geadephagans. A pit sensillum occurs on the antennae of one family, Gyrinidae, in the Hydradephaga whereas it is found on the antennae of several species from the families of Geadephaga. The sensilla on the terminal antennomere of Hydradephaga are often grouped into sensory fields that could be located on a particular area of the antennomere. Sensory fields are also located on the apices of the maxillary and labial palps and the most unique sensory fields occur in the Noteridae. The maxillary palpal apex of Hydrocanthus oblongus (Noteridae) is bifurcate and a sensory field with several types of sensilla is at the apex of each branch. The terminal labial palpomere is greatly enlarged and has a long, slender sensory field at the apex and a secondary sensory field on a thumb-like projection. The sensilla on the palpal apices are more diverse and complex in form as compared to the sensilla on the palps of Geadephaga. The most complex sensillum has a cuticular collar and a dome that is divided into six or seven triangular sections. The dome may be opened or closed and a peg-like sensillum with a very wide apical pore is situated beneath the dome.

Animals↗
PubMed1993

Genetic and environmental factors regulating the expression of an extended longevity phenotype in a long lived strain of Drosophila.

We have demonstrated that the expression of the ELP in our strains is the outcome of a genetically determined, environmentally modulated, event dependent, developmental process. Given the appropriate genetic and environmental conditions, we observe an early acting temporal progression of alterations in specific gene activity patterns which appear to give rise to functional phenotypic changes. The observed patterns are consistent with the interpretations drawn from our chromosome substitution and biomarker experiments. The interaction of specific environmental and genetic factors is sufficient to explain the observed plasticity of longevity in our L strain. Independently derived long lived strains may have altered different combinations of physiological mechanisms so as to give rise to a statistically equivalent ELP. Theoretically based conclusions obtained from only one set of sister strains may be difficult to extrapolate to other strains. Future work will involve the experimental verification of the genetic-environmental circuitry discussed here, using novel molecular genetic techniques to define, characterize, and isolate the genes involved in the expression of the ELP.

Animals↗
PubMed1993

Chromosomal localization and regulation of the longevity determinant genes in a selected strain of Drosophila melanogaster.

A controlled chromosome substitution experiment was performed on a strain (NDC-L) selected for long life to determine if the genes responsible for the extended-longevity phenotype could be localized to any particular chromosome(s). All 27 different possible combinations of the three major chromosomes of Drosophila melanogaster were constructed and longevities were determined on 3875 individual animals of both sexes and analysed. The results are statistically significant and demonstrate that mean longevity is specified primarily by recessive genes on the third chromosome (c3). The extended longevity phenotype (ELP) is only expressed in those lines which are homozygous for the NDC-L type c3. Loci on the first (c1) and second (c2) chromosomes interact, both positively (c1) and negatively (c2), respectively, such that c1 represses c2 which in turn represses c3. The ELP is fully expressed in the mutual presence and mutual absence of c1 and c2. The significance of these results is discussed in the context of broader categories of molecular genetic mechanisms suggested previously to be involved in the modulation of longevity in Drosophila.

Animals↗
PubMed1993

Larval regulation of adult longevity in a genetically-selected long-lived strain of Drosophila.

Our previous work has shown that the major genes involved in the expression of the extended-longevity phenotype are located on the third chromosome. Furthermore, their expression is negatively and positively influenced by chromosomes 2 and 1, respectively. In this report we show that the expression of the extended-longevity phenotype is dependent on the larval environment. A controlled chromosome substitution experiment was carried out using a strain selected for long life (L) and its parent (R) strain. Twenty different combinations of the three major chromosomes were conducted and their longevities were determined under both high (HD) and low (LD) larval density conditions. The extended-longevity phenotype was only expressed under HD conditions. The chromosome interactions were not apparent under LD conditions. Density-shift experiments delineate a critical period for expression of the extended-longevity phenotype, extending from 60 h after egg laying (AEL) to 96 h AEL, during which the developing animal must be exposed to HD conditions if the extended-longevity phenotype is to be expressed. The change from HD to LD conditions is accompanied by statistically significant increases in body weight. The possible role of a dietary restriction phenomenon is examined and the implications of these findings discussed. It is now apparent, however, that the extended-longevity phenotype in Drosophila is a developmental genetic process.

Animals↗
PubMed1992

A historical perspective of research on the biology of aging from Nathan W. Shock.

This article describes some of the thoughts and the conceptual framework from which Nathan W. Shock prepared his last major presentation. This paper, written some 8 months following Dr. Shock's death on November 12, 1989, is based upon his extensive notes and discussions with one of the authors (George T. Baker). This presentation in no way is meant to encapsulate the long and distinguished career of Nathan Shock, but rather to provide a glimpse of his perspectives on the development of the field of aging. Furthermore, we believe that the scientific principles concerning aging research laid out by Dr. Shock in this publication are still valid today and may provide valuable insights for researchers in the field.

Aging↗
PubMed1991

Elevated paraquat resistance can be used as a bioassay for longevity in a genetically based long-lived strain of Drosophila.

A long-lived (L) strain of Drosophila melanogaster, derived from a normal-lived (R) strain by artificial selection, has a significantly different adult longevity. Previous work has shown that 1) the two strains age in the same manner, 2) the major genes responsible for much of the L strain's extended longevity are located on the 3rd chromosome, and 3) the extended longevity phenotype is significantly modulated by the larval environment. In this report, we investigate the resistance of the L and R strains to the lethal effects of dietary paraquat. We show that, within the limitations of our described chromosomal and environmental manipulations, the extended longevity phenotype always accompanies the phenotype of elevated paraquat resistance. In addition, reversed selection applied to the L strain results in the simultaneous decrease of both life span and paraquat resistance. Thus, the presence or absence of the latter phenotype may be used as a bioassay for the presence or absence of the extended longevity phenotype, without any necessary implication of causality. Use of this bioassay should greatly speed up the genetic analysis of this system by allowing us to identify long-lived animals at a young age. Finally, we show that the age-related loss of elevated paraquat resistance in both strains precedes all the other age-related functional decrements which we have previously noted in this system.

Animals↗
PubMed1988

Biomarkers of aging.

This article presents a conceptual discussion of some aspects involved in biomarkers of aging. A biomarker of aging is a biological parameter of an organism that either alone or in some multivariate composite will, in the absence of disease, better predict functional capability at some late age than will chronological age. The reasons for undertaking biomarker research, criteria for putative biomarkers, measurement and assessment of putative biomarkers, and the new initiative by the National Institute on Aging in biomarker research are discussed.

Aging↗
PubMed1987

Morphological aspects of the third instar larva of Haematobia irritans.

The main morphological features of the cephalic region of the larva of Haematobia irritans (L.) are the oral grooves, tripartite labium and the antennomaxillary protuberances that have the dorsal, terminal and ventral sensory organs. The total number of sensilla that are found on the terminal organ differs from other cyclorrhaphous-fly larvae. The fan-shaped anterior spiracles usually consist of seven bulbous digits that are unequal in length. The creeping welts consist of notched, convex plates that split into two separate plates as they approach the midline of the venter. This characteristic has not been described previously for this species or other, higher, dipterous larvae. There are two posterior spiracles with an ecdysial scar, four fan-shaped and branching spiracular hairs and irregularly-shaped spiracular openings. The longitudinal anal opening is situated in the cuticular band that is known as the anal organ.

Animals↗
PubMed1984

Developmental time and adult longevity in two strains of Drosophila melanogaster in a constant low-stress environment.

This study examines the life spans of wild type flies (Sevelen strain, n = 2991) and post-replication DNA repair-deficient flies (mei-41D5, n = 1607) as members of age-synchronized birth cohorts and as members of full sibships. Flies were individually housed from the time they were laid as eggs until they died as imagoes; environmental conditions were constant throughout the life span of these virgins. In this minimal stress experiment, developmental time and imaginal longevity were negligibly correlated (r = -0.09 to -0.25), even though developmental time was canalized at different levels in both strains. Previous research involving environmental perturbations during the life span of Drosophila (e.g. temperature, diet, population density) has demonstrated significant strong correlations, mostly positive, between developmental time and adult longevity. We have demonstrated that the duration of development and aging are not coupled in the absence of such stresses. We therefore suggest that related changes in the duration of the pre-imaginal and the adult stages of the lifecycle of Drosophila may have evolved through adaptation to environmental stresses.

Animals↗
PubMed1984

On statistical tests of significance in studies of survivorship in laboratory animals.

In many studies of longevity in experimental animals, sample sizes are small enough to warrant the use of statistical tests of significance in making judgments of scientific interest. Illustrated in this paper is a nonparametric test procedure for deciding on the statistical significance of observed differences in two empirical survival functions. This procedure takes an experimenter one step beyond comparing means and medians. For experimenters who wish to pursue the subject further, a brief entry into the extensive literature on survival analysis is also provided.

Animals↗
PubMed1979

Alteration in thermal stability of ribosomes from Drosophila melanogaster with age.

Thermal analysis of high salt (0.5 M) washed ribosomal monomers from young and old male Drosophila melanogaster revealed an 8 degrees C downshift in the mean temperature of denaturation (Tm). Moreover, there was observed a marked loss in the ability of ribosomes extracted from older flies to reassociate upon cooling. These observations suggest that age-dependent alterations in the structural integrity of the rRNA-r protein complex could, at least in part, be responsible for the diminished capacity for protein synthesis in this species with advancing age.

Aging↗
PubMed1978

Age-dependent alpha-glycerophosphate dehydrogenase activity changes in mutant and wild type Drosophila melanogaster.

The age-related changes in the activity of the extramitochondrial alpha-glycerophosphate dehydrogenase (alpha-GPDH) were compared in two mutants of Drosophila melanogaster, a vestigial-winged and an alpha-glycerophosphate dehydrogenase deficient mutant with that of the wild type. The age-dependent patterns of activity change in both mutants were shown to be identical to that of the wild type. This is in spite of the lack of flight ability in both mutants, the reduced enzyme activity levels in the alpha-glycerophosphate mutant, and in the case of the vestigial flies, of reduced life-span. The results suggest that those mechanisms responsible for the observed aged-related activity changes in alpha-GPDH are intrinsically regulated, independent of functional flight, genetic alteration of specific activity, and life-span.

Age Factors↗
PubMed1976

Changes in 80S ribosomes from Drosophila melanogaster with age.

A 23% reduction in the amount of 80S ribosomes extracted from young and old male Drosophila melanogaster on a per g wet weight basis was demonstrated. Furthermore, a significant alteration in the structural integrity of the ribosomal RNA-protein complex from older flies as demonstrated by the dissociation of protein from the 80S particle in the presence of varying concentrations of KC1 was observed.

Aging↗