Evolution of the relative width of the head and alveolar surfaces in map turtles (Testudines: Emydidae: Graptemys)

Replicate adaptive radiations are dichotomous morphological patterns related to resource use and repeated in a series of isolated habitats. Biologists have long noted a dichotomy in relative head width and alveolar width among species of map turtles ( Graptemys ), particularly with regard to adult females, which are much larger dian adult males in all 12 species. I measured plastron length (PL), head width (HW), and alveolar width (AW) of nearly 2300 specimens representing the 12 recognized species, and used allometric regressions to investigate this genus as an example of both sexual dimorphism in trophic morphology and replicate adaptive radiation. Sexual dimorphism was noted in HW after correction for PL, with females having wider heads than males of similar body sizes, but AW as corrected for HW was not dimorphic, thus absolute differences in AW are the simple result of differences in HW. Sexual differences in HW probably relate to the dimorphic niches of Graptemys , as females of three species have been reported to occupy deeper water further from shore than conspecific males. Based on predicted HW at maximum PL in adult females, species were categorized as mega-, meso-, or microcephalic. Differences in relative head width are related to differences in degree of molluscivory, with little molluscivory in microcephalic females, moderate to high molluscivory in mesocephalic females, and high molluscivory in megacephalic females. Distributions of Graptemys species in sympatry and allopatry reveal patterns consistent with structuring of distributions via competitive interactions. Superimposing data on relative HW on a phylogeny of the genus suggests there may have been one or two episodes of character displacement, widi subsequent character assortment, in Graptemys evolution. This conclusion is similar to the current model for the evolution of body size during the radation of Anolis lizards in the northern Lesser Antilles.     

Coccidian parasites (Apicomplexa: Eimeriidae) of Graptemys caglei and Graptemys versa (Testudines: Emydidae) from Texas

Nineteen map turtles, Graptemys caglei and Graptemys versa were collected from the Guadalupe and Colorado River watersheds of south-central Texas and examined for coccidial parasites. Thirteen of the 19 turtles (68%), including 11 of 16 (69%) G. caglei and 2 of 3 (67%) G. versa, were infected with at least 1 coccidian. Five Eimeria spp. (E. chrysemydis, E. graptemydos, E. lutotestudinis, E. pseudogeographica, and E. trachemydis) were harbored by G. caglei, and 2 eimerians (E. graptemydos and E. mitraria) infected G. versa. This represents new host records for these previously described coccidians and is the first time parasites have been documented in turtles of both species.     

Molecular mechanisms of photoreception. VI. Cyclic nucleotide- and light-dependent phosphorylation of rod outer segment proteins in the frog retina

Phosphorylation of proteins in purified rod outer segment from frog retina was investigated. Phosphorylation of 18, 17, 12 and 11.5 kDa proteins was stimulated by cAMP (Ka approximately equal to 10(-7) M) and cGMP (Ka approximately equal to 10(-4) M). 32P-incorporation into 18 and 17 kDa proteins was much lower than into 12 and 11.5 kDa, which are in the group of main phosphoproteins of the rod outer segment: 12 and 11.5 kDA phosphoproteins appear to be present in cytoplasm or are slightly bound to disk's membranes. However, they are not discovered in the cytoplasmic membranes. The dephosphorylation of low-molecular weight proteins, discovered earlier by Polans et al., occurs slowly: the light doesn't change the level of phosphorylation of proteins in living retina within the time of photoresponse. It is suggested that the process of light-dependent phosphorylation-dephosphorylation of 12 and 11.5 kDa proteins controls the light sensitivity of the photoreceptor.     

A comparison of the second harmonic generation from light-adapted, dark-adapted, blue, and acid purple membrane.

The second order nonlinear polarizability and dipole moment changes upon light excitation of light-adapted bacteriorhodopsin (BR), dark-adapted BR, blue membrane, and acid purple membrane have been measured by second harmonic generation. Our results indicate that the dipole moment changes of the retinal chromophore, delta mu, are very sensitive to both the chromophore structure and protein/chromophore interactions. Delta mu of light-adapted BR is larger than that of dark-adapted BR. The acid-induced formation of the blue membrane results in an increase in the delta mu value, and formation of acid purple membrane, resulting from further reduction of pH to 0, returns the delta mu to that of light-adapted BR. The implications of these findings are discussed.     

The transducer model for contrast detection and discrimination: formal relations, implications, and an empirical test

The transducer function mu for contrast perception describes the nonlinear mapping of stimulus contrast onto an internal response. Under a signal detection theory approach, the transducer model of contrast perception states that the internal response elicited by a stimulus of contrast c is a random variable with mean mu(c). Using this approach, we derive the formal relations between the transducer function, the threshold-versus-contrast (TvC) function, and the psychometric functions for contrast detection and discrimination in 2AFC tasks. We show that the mathematical form of the TvC function is determined only by mu, and that the psychometric functions for detection and discrimination have a common mathematical form with common parameters emanating from, and only from, the transducer function mu and the form of the distribution of the internal responses. We discuss the theoretical and practical implications of these relations, which have bearings on the tenability of certain mathematical forms for the psychometric function and on the suitability of empirical approaches to model validation. We also present the results of a comprehensive test of these relations using two alternative forms of the transducer model: a three-parameter version that renders logistic psychometric functions and a five-parameter version using Foley's variant of the Naka-Rushton equation as transducer function. Our results support the validity of the formal relations implied by the general transducer model, and the two versions that were contrasted account for our data equally well.     

Towards a cognitive niche: divergent foraging strategies resulting from limited cognitive ability of foraging herbivores in a spatially complex environment.

A model was developed to explain one mechanism whereby differential optimal foraging strategies can occur between species as a result of selection for competition avoidance. This is the primary requirement for niche differentiation to evolve without a difference in the underlying foraging ability or morphology. The model used an individual-based patch choice mechanism, whereby herbivores move from patch to patch seeking food with the highest nutrient intake characteristics. The choice of patch was governed by a parameter, mu, which determined to what extent information in the landscape at different distances from the herbivore was used by it to make foraging decisions. A genetic algorithm was used to optimise the value, mu, in a complex landscape. The value of mu quickly converged to a single value with stabilising selection occurring when there was only a single species foraging. When there was a competing species with a fixed value of mu, the value of mu evolved to be above or below the mean for the single species mean depending on whether the value of mu for the competitor was below, or above the single-species mean, respectively. This was indicative of niche segregation. However mu tended to vary unstably over time when allowed to vary simultaneously in both species, although there was evidence for interaction between the two values. These results indicate that there can be a competitive advantage in choosing a cognitive strategy that is complementary to that used by other species.     

Cover Image,Volume 234, Number 10, October 2019

Cytoskeleton which includes microtubule and actin filaments plays important roles during mammalian oocyte maturation. In the present study, we showed that protein kinase C mu (PKC mu) was one potential key molecule which affected cytoskeleton dynamics in mouse oocytes. Our results showed that PKC mu expressed and localized at the poles of the spindle during oocyte maturation, and PKC mu expression reduced in the oocytes from 6-month-old mice or 24 hr in vitro culture. We knocked down the expression of PKC mu in oocytes using morpholino injection to explore the relationship between PKC mu and subcellular structure defects. The loss of PKC mu reduced oocyte maturation competence, showing with decreased polar body extrusion rate and increased rate of symmetric division. Further analysis indicated that PKC mu decrease caused the spindle organization defects, and this could be confirmed by the decreased tubulin acetylation level. Moreover, we found that PKC mu affected the phosphorylation level of cofilin for actin assembly, which further affected cytoplasmic actin distribution and spindle positioning. In summary, our data indicated that PKC mu is one key factor for oocyte maturation through its roles on the spindle organization and actin filament distribution.     

A new mite superfamily Cloacaroidea and its position within the Prostigmata (Acariformes)

The external morphology of 2 closely related mite families, Cloacaridae and Epimyodicidae (Acari: Prostigmata), comprising highly specialized endoparasites of vertebrates, is analyzed. These mites exhibit strong regression of many structures ancestrally present in other Prostigmata as a consequence of their endoparasitic mode of life. The relationships of these 2 families with other taxa in the infraorder Eleutherengona are still not clear. Our reinterpretation of the chelicerae as unfused precludes inclusion of this lineage in the Cheyletoidea as proposed previously. A new superfamily, Cloacaroidea superfam, nov., incertae sedis, within the infraorder Eleutherengona is established for these 2 families, and their host-parasite relationships are briefly discussed. A new cloacarid species, Caminacarus dawsoni n. sp., from Graptemys pseudogeographica (Testudines: Emydidae) from the United States is also described.     

Muscle temperature transients before, during, and after exercise measured using an intramuscular multisensor probe.

Seven subjects (1 woman) performed an incremental isotonic test on a Kin-Com isokinetic apparatus to determine their maximal oxygen consumption during bilateral knee extensions (Vo(2 sp)). A multisensor thermal probe was inserted into the left vastus medialis (middiaphysis) under ultrasound guidance. The deepest sensor (tip) was located approximately 10 mm from the femur and deep femoral artery (T(mu 10)), with additional sensors located 15 (T(mu 25)) and 30 mm (T(mu 40)) from the tip. Esophageal temperature (T(es)) was measured as an index of core temperature. Subjects rested in an upright seated position for 60 min in an ambient condition of 22 degrees C. They then performed 15 min of isolated bilateral knee extensions (60% of Vo(2 sp)) on a Kin-Com, followed by 60 min of recovery. Resting T(es) was 36.80 degrees C, whereas T(mu 10), T(mu 25), and T(mu 40) were 36.14, 35.86, and 35.01 degrees C, respectively. Exercise resulted in a T(es) increase of 0.55 degrees C above preexercise resting, whereas muscle temperature of the exercising leg increased by 2.00, 2.37, and 3.20 degrees C for T(mu 10), T(mu 25), and T(mu 40), respectively. Postexercise T(es) showed a rapid decrease followed by a prolonged sustained elevation approximately 0.3 degrees C above resting. Muscle temperature decreased gradually over the course of recovery, with values remaining significantly elevated by 0.92, 1.05, and 1.77 degrees C for T(mu 10), T(mu 25), and T(mu 40), respectively, at end of recovery (P < 0.05). These results suggest that the transfer of residual heat from previously active musculature may contribute to the sustained elevation in postexercise T(es).     

On three methods for estimating mutation rates indirectly.

Methods for estimating a mutation rate mu has been proposed by Kimura and Ohta; Nei; and Rothman and Adams. It is shown here that all three methods are best applied to rare alleles and that they are all based upon the assumption that all alleles ultimately become extinct. If there is a neutral allele in a growing population, there is conditioning on ultimate extinction, which implies that the underlying stochastic process can be approximated by a branching process for which the mean number of offspring is less than 1. The low numerical values of t0, the mean time to extinction of a line descended from a single mutant, found in two simulation studies, can be attributed to two features. First, the data on which these studies were based came from a fairly rapidly growing population. In such a population, we would expect that extinction, if it does occur, takes place quickly. A second factor is that the effective population size is somewhat lower than the actual number of adults. Population subdivision and migration does not seem to play a significant role. Conservative high and low estimates of mutation rates are computed, and an estimate is obtained for the standard deviation of the estimate of mu. These allow a rough estimate of a 95% confidence interval, which contains estimates of mu found by Neel and Rothman.     

Cytonuclear equilibrium following interspecific introgression in a turtle lacking sex chromosomes

When reproductive barriers break down, interspecific hybridization can lead to gene flow between evolutionarily distinct species. Studying the fate of these introgressing elements can offer valuable insights into the factors contributing to reproductive isolation. We have identified a population of false map turtles (Graptemys pseudogeographica) that hybridized historically with the common map turtle (Graptemys geographica), but were subsequently isolated from interbreeding for several generations by unique geological events. Although many studies conclude that genic interactions involving sex chromosomes impact the introgression of mitochondrial or nuclear genomes, Graptemys turtles have environmental sex determination, and thus introgression can be explored while controlling for the effects of sex‐specific heterogameity. We identified and sequenced a species‐specific mitochondrial control region marker, as well as two nuclear markers (ODC and HNFAL), in turtles from across the ranges of these species. We found both nuclear and mitochondrial introgression in our study population, and present evidence consistent with the proposed time range of reproductive contact and isolation. We also report an absence of cytonuclear or linkage disequilibrium among markers, indicating that some important pre‐ and postzygotic barriers to gene flow that characterize other systems are absent in Graptemys. Finally, we show that Graptemys turtles have a complex molecular evolutionary history, and that leaks in reproductive barriers probably occur frequently. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 106 , 405–417.     

Genetic diversity in natural populations of mammalian reoviruses: tryptic peptide analysis of outer capsid polypeptides of murine, bovine, and human type 1 and 3 reovirus strains.

We have studied the structural relationships between the outer capsid polypeptides of eight murine, bovine, and human isolates of type 1 and 3 mammalian reoviruses. Our results show that the outer capsid polypeptides of reoviruses isolated from different mammalian species, in different years and different geographical areas, have both conserved and unique methionine-containing tryptic peptides. We found that tryptic peptides from mu 1C polypeptides of two human, one murine, and two bovine type 3 isolates and one human and two bovine type 1 reoviruses are highly conserved. Our data show that only one tryptic peptide pattern of the mu 1C polypeptide (encoded by the M2 gene) was present in reoviruses isolated from the three different mammalian species. The mu 1C polypeptide of the type 3 Dearing strain contained one tryptic peptide not found in any other reovirus isolate examined. In marked contrast to the mu 1C polypeptides, the sigma 3 polypeptides (encoded by the S4 gene) of three type 1 and three type 3 isolates were divided into two patterns based on significant differences in their tryptic peptides. In addition, at least seven tryptic peptides were conserved among the sigma 3 polypeptides of all virus strains examined. The sigma 3 polypeptide of the type 3 Dearing strain was distinguishable from the sigma 3 polypeptides of all other strains examined. The one mu 1C and two sigma 3 tryptic peptide patterns were found to occur interchangeably in isolates of type 1 or type 3. About 1/3 of the tyrosine-containing tryptic peptides of sigma 1 polypeptides of four type 3 isolates examined were conserved. Comparison of peptide differences in sigma 1 polypeptides of these isolates showed that each had one or more unique tryptic peptides, suggesting that the S1 genes coding for these polypeptides had undergone genetic drift or, alternatively, that there are at least two tryptic peptide patterns present among the sigma 1 polypeptides of these isolates. Our results suggest that genetic drift and reassortment are the most likely explanation for the extensive genetic diversity found in natural populations of mammalian reoviruses.     

Morphology and behaviour of sex chromosomes during meiosis in Ascaris suum.

The morphology and behaviour of sex chromosomes was studied in A. suum during meiosis. It was found that the five sex chromosomes have their proper characteristic. The largest is submetacentric, of 2 microns mean length. The second largest is acrocentric, mean length of 1.4 mu. The third largest is metacentric, 1.2 mu mean length. The fourth and the fifth are metacentric, of mean length of 1 mu. In primary and secondary spermatocyte cells the sex chromosomes are close to each other, most often in the peripheral part of the cell. During anaphase I the pentad sex chromosomes lie freely between the two sister cells. It is assumed that in anaphase II the five sex chromosomes divide equally and are regularly distributed in the daughter cells. It was found that the chromosomes set of female Ascaris in metaphase I contains 24 bivalent chromosomes n = 24 and of male Ascaris 19 bivalents and 5 univalents. It is assumed that the univalent chromosomes, found in spermatocyte cells, determine sex.     

Quantitative analysis of idiotypic mimicry and allelic exclusion in mice with a mu Ig transgene

Analysis of C57BL/6 mice (IgM allotype, Igh-6b or mu b) that carry an Ig H chain transgene of a different allotype (mu a) shows that IgM molecules of mixed allotype (mu a mu b) are present among serum antibodies. The finding was extended to hybridomas prepared from nonimmune transgenic mice, many of which also failed to exhibit allelic exclusion. The proportions of mu a and mu b secreted by individual hybridomas varied markedly, and the product of an individual hybridoma was found to be heterogeneous with respect to the allotype content of individual molecules. The ratio of mu a:mu b chains secreted by individual hybridomas was found to correlate with the number of transgene copies remaining in each hybridoma, and several hybridomas that secrete only mu b-positive molecules had apparently lost all but one copy of the transgene. An idiotype characteristic of the transgene was found to be present only in association with the transgenic (mu a) allotype, and indirect evidence strongly suggests that the idiotype was present only on mu a polypeptide chains. Thus, there is no evidence in this system for the induction of idiotypically cross-reactive endogenous molecules.     

Molecular cloning and tissue-specific expression of the mutator2 gene (mu2) in Drosophila melanogaster.

We present here the molecular cloning and characterization of the mutator2 (mu2) gene of Drosophila melanogaster together with further genetic analyses of its mutant phenotype. mu2 functions in oogenesis during meiotic recombination, during repair of radiation damage in mature oocytes, and in proliferating somatic cells, where mu2 mutations cause an increase in somatic recombination. Our data show that mu2 represents a novel component in the processing of double strand breaks (DSBs) in female meiosis. mu2 does not code for a DNA repair enzyme because mu2 mutants are not hypersensitive to DSB-inducing agents. We have mapped and cloned the mu2 gene and rescued the mu2 phenotype by germ-line transformation with genomic DNA fragments containing the mu2 gene. Sequencing its cDNA demonstrates that mu2 encodes a novel 139-kD protein, which is highly basic in the carboxy half and carries three nuclear localization signals and a helix-loop-helix domain. Consistent with the sex-specific mutant phenotype, the gene is expressed in ovaries but not in testes. During oogenesis its RNA is rapidly transported from the nurse cells into the oocyte where it accumulates specifically at the anterior margin. Expression is also prominent in diploid proliferating cells of larval somatic tissues. Our genetic and molecular data are consistent with the model that mu2 encodes a structural component of the oocyte nucleus. The MU2 protein may be involved in controlling chromatin structure and thus may influence the processing of DNA DSBs.