Premature Drying, Fluridone-Treatment, and Embryo Isolation During Development of Maize Kernels (Zea mays L.) Induce Germination, but the Protein Synthetic Responses are Different. Potential Regulation of Germination and Protein Synthesis by Abscisic Acid

Freshly harvested, developing kernels of maize (Zea mays L.)do not germinate up to 77 d after pollination, but can be inducedto do so by fluridone, premature desiccation, and isolationof the developing embryo. The pattern of protein synthesis indeveloping maize embryos is distinct from that during germinationand subsequent seedling growth. Premature desiccation at 35DAP elicits a pattern of protein synthesis upon rehydrationwhich is similar to that in germinated embryos from mature drykernels. Fluridone-induced viviparous germination is accompaniedby changes in the synthesis of some proteins to a post-germinativepattern, but some developmental proteins continue to be synthesized.Embryos isolated from developing kernels at 35 DAP germinatewhen incubated on water; they also produce some developmentalproteins during germination. Kernels from developing cobs at35 DAP which are detached from the mother plant and maintainedin an atmosphere of high relative humidity (moist controls)do not germinate, but neither do they continue a clearly definedpattern of either developmental or germinative protein synthesis.Drying is thus critical to effect a clear transition of proteinsynthesis from a developmental to a germinative mode in maizeembryos. Abscisic acid within the developing embryos is reduced by fluridone,but to a lesser extent by premature drying or maturation drying.Changes in sensitivity to abscisic acid by the developing embryomay be as, or more, important in permitting germination, andthe attendant synthesis of proteins, than changes in abscisicacid content. Key words: Maize (Zea mays L.), germination, vivipary, desiccation, abscisic acid     

Proximate developmental mediators of sexual dimorphism in size: case studies from squamate reptiles

Sexual dimorphism in size (sexual size dimorphism; SSD) is nearlyubiquitous, but the relative importance of genetic versus environmentalcontrol of SSD is not known for most species. We investigatedproximate determinants of SSD in several species of squamatereptiles, including three species of Sceloporus lizards andthe diamond-backed rattlesnake (Crotalus atrox). In naturalpopulations of these species, SSD is caused by sexual differencesin age-specific growth. Males and females, however, may oftenshare similar potentials for growth: growth is strongly responsiveto the availability of food, and sexual differences in growthcan be greatly suppressed or completely absent under commonenvironmental conditions in the laboratory. Sexually divergentgrowth is expressed in natural environments because of inherentecological differences between males and females and becauseof potential epigenetic effects of sex-specific growth regulators.In field-active Sceloporus, sexual differences in growth rateare associated with sexual divergence in plasma testosterone.Experiments confirm that testosterone inhibits growth in speciesin which females are larger (for example, S. undulatus and S.virgatus) and stimulates growth in those in which males arelarger (for example, S. jarrovii). Interestingly, however, sexualdivergence in plasma testosterone is not accompanied by divergencein growth in S. jarrovii or in male-larger C. atrox in the laboratory.Furthermore, experimental effects of castration and testosteronereplacement on growth are not evident in captive S. jarrovii,possibly because growth effects of testosterone are supersededby an abundant, high-quality diet. In female-larger S. undulatus,growth may be traded-off against testosterone-induced reproductivecosts of activity. In male-larger species, costs of reproductionin terms of growth are suggested by supplemental feeding ofreproductive female C. atrox in their natural environment andby experimental manipulation of reproductive cost in femaleS. jarrovii. Growth costs of reproduction, however, do not contributesubstantially to the development of SSD in male-larger S. jarrovii.We conclude that the energetic costs of testosterone-induced,male reproductive behavior may contribute substantially to thedevelopment of SSD in some female-larger species. However, despitestrong evidence that reproductive investment exacts a substantialcost in growth, we do not support the reproductive cost hypothesisas a general explanation of SSD in male-larger species.     

Gene expression patterns, and uptake and fate of fed ABA in white spruce somatic embryo tissues2

Changes in cellular protein accumulation and in in vivo andin vitro protein synthesis, in somatic embryo tissues of whitespruce during a 42 d maturation period were followed by two-dimensionalsodium dodecyl sulphate-polyacrylamide gel electrophoresis (2-DSDS-PAGE). These investigations were complemented by an analysisof uptake and fate of fed abscisic acid (ABA) in somatic embryotissues grown on maturation medium. When Stage 1 somatic embryoswere cultured on ABA-containing maturation medium, many changeswere observed in patterns of gene expression and in proteinsynthesis and accumulation which could be associated with embryodevelopment. The polypeptides observed could be categorizedas constitutive, embryo-abundant, embryo maturation-relatedand embryo stage-related, as well as those with non-specificchanges. Accumulation of label from fed ³H-(+)-ABA in embryotissues reached a plateau 3 d after Stage 1 somatic embryoswere placed on maturation medium. ABA taken into tissues wasrapidly metabolized, and 40% of radioactivity in tissues after1 d of culture resulted from ABA metabolites. This value increasedto 90% after 3 weeks culture. Conjugated ABA and oxidized ABA(phaseic acid and dihydrophaseic acid) were major forms of ABAmetabolites in spruce embryo tissues. Using a single 42 d cultureperiod following transfer to medium with ABA, the conditionsthat stimulate the sequence of developmental changes of somaticembryo maturation during the first 21 d do not reoccur duringthe second 21 d. Unless greater synchronization of Stage 1 culturescan be achieved, it is therefore unlikely that yields of maturesomatic embryos will be increased by this method. Key words: Abscisic acid, gene expression, Picea glauca (Moench) Voss, protein synthesis, somatic embryo maturation     

Ultrastructure, Development and Secretion in the Nectary of Banana Flowers

The nectaries of Musa paradisiaca L. var. sapientum Kuntze werefound to secrete in addition to the sugar solution, a polysaccharidemucilage and a very electron dense, homogenous material whichwas apparently protein. The polysaccharide had already startedto appear outside the epithelial cells of the nectary at veryearly stages of nectary development. At somewhat later developmentalstages the very dense homogenous material appeared in the formof droplets between the plasmalemma and cell wall in massesin the nectary lumen. Nectar secretion started in flowers whenthe bract in the axil of which they occurred had just recoiled.The ER elements were dilated and formed vesicles and the Golgibodies were very active, at the stage of the nectar secretionand at stages preceding it, except at the stage just beforesecretion. In all stages of nectary development the dilatedER elements and most large Golgi vesicles contained fibrillarmaterial. It is suggested that both ER and the Golgi apparatusare involved in the secretion of the sugar solution and of thepolysaccharides. There was not enough evidence as to where inthe cell the very dense homogenous material is synthesized. A few developmental stages of the nectaries of the male flowersof the Dwarf Cavendish banana, which do not secrete nectar,were also studied. It was seen that at early stages of development,the ultra-structure of the nectary of this banana variety wassimilar to that of M. paradisiaca var. sapientum. However, theepithelial nectary cells of the Dwarf Cavendish banana disintegratedbefore maturation of the nectary. Musa paradisiaca L, banana, floral nectaries, ultrastructure     

Studies on the Development of the Air Pores and Air Chambers of Marchantia paleacea: 1. Light Microscopy

The ontogeny of the air pores and air chambers of Marchantiapaleacea begins with the schizogenous development of protodermalintercellular spaces of the initial apertures, and is completedwith the formation of the air pores and giant sub-epidermalair chambers bearing numerous photosynthetic filaments. Intercellularspace formation commences from the thallus surface and proceedsinwards to the first internal layer of cells. The cells amongwhich spaces develop do not originate from one mother cell.Spaces are formed only in the regions of the intersection ofthe anticlinal walls of three, four, or sometimes more successivederivatives of S₁, S₃ and S₄ segments of the apical cell, oneor two of which have been divided periclinally and the restanticlinally. Protodermal intercellular spaces appear in mostor all the corners of these cells, the anticlinal walls of whichexhibit an opposite disposition. The S₁, S₂, S₃ and S₄ segmentsare produced by definite divisions of a five-sided apical celland by a series of divisions give rise to initial cells of theinternal layers of the thallus and initial cells of the protodermaland sub-protodermal layers. The concept of a quiescent apicalcell cannot be accepted, since dividing apical cells have beenobserved, and the pattern of wall disposition of the thallusapex cannot be explained without the active participation ofthe apical cell. The air chambers are apparently of exogenous origin. They resultfrom the broadening of the bottom of the initial apertures bythe coordination of the rate of anticlinal divisions and growthof the protodermal and sub-protodermal cells surrounding theintercellular spaces of the initial apertures. The ontogenyof the pore rings starts at an advanced stage of air chamberformation not from a mother cell but from the cells which surroundthe closed entrance of the air chamber, by a shift of the planeof division from anticlinal to periclinal. Before the periclinaldivisions a new axis of growth perpendicular to the thallussurface is established in the mother cells of the pore. By a polarized growth into the air chamber followed by periclinaldivisions, the cells of the floor form initial cells of thephotosynthetic filaments. The latter divide again to form singleor branched photosynthetic filaments. Marchantia paleacea, air pore, air chamber     

Plumage coloration, not length or symmetry of tail-streamers, is a sexually selected trait in North American barn swallows

Sexual adornments often vary markedly across a species' range,which presumably is owing to differences in local environmentalconditions and the associated selection pressures, such as naturalversus sexual selection or the relative signaling value of differentornamental traits. However, there are only a few reported examplesin which the information content of mating signals varies geographically,and even fewer in which a set of secondary sexual traits servesdifferent signaling functions in different populations. Classicstudies of sexual selection in the European barn swallow (Hirundorustica rustica) demonstrate that elongate tail-streamers provideseveral reproductive advantages to males and females and areused as reliable signals of mate quality. Here, we show thattail-streamers do not appear to confer these same benefits ina population of barn swallows from North America (Hirundo rusticaerythrogaster). Instead, ventral plumage coloration, which ismore exaggerated in North American swallows compared with theirEuropean counterparts, predicts patterns of assortative matingand annual reproductive success in H. r. erythrogaster. Theseobservations support the idea that ornamental traits can servedifferent functions among animal populations and suggest thatgeographic variation in different sexual signals may facilitatepopulation divergence, which may ultimately lead to speciation.     

Variable Development and Cellular Patterning in the Epidermis of Ruscus hypoglossum

The general problem was the meaning of the variability of cellulardevelopment of the stomata-bearing epidermis of Ruscus hypoglossumin which 'immature stomata' occur, i.e. cells that have gonethrough part but not the final stages of stomatal development.The development of the epidermis was followed in vivo, by makingrepeated replicas of the same developing tissues using dentalimpression material. The development of stomata occurred overthe entire surface of large phyllodes and was not synchronous.The early development of future and 'immature stomata' couldnot be distinguished, neither by the form of the cells nor bythe timing of the initial, unequal divisions. The process ofstomatal development did not stop at any one, characteristicsstage. Statistical analyses indicated that the pattern of functionalstomata would have been less orderly if all stomatal initialshad developed into mature structures. The results suggest thatin Ruscus epidermal patterning occurs during, rather than preceding,stomatal development: many stomata are initiated, but they followa labile developmental program and cellular interactions selectthose that reach the mature functional state.Copyright 1993,1999 Academic Press Cellular patterns, epigenetic selection, immature stomata, Ruscus hypoglossum, spacing patterns, stomata, subsidiary cells, unequal divisions     

The Mexican Axolotl, Ambystoma mexicanum: Its Biology and Developmental Genetics, and Its Autonomous Cell-lethal Genes

SYNOPSIS. The Mexican axolotl, a neotonous salamander, has foundwidespread use as an experimental animal for studies in embryologyand physiology. The convenience with which the axolotl can bemaintained as a laboratory animal and the high quality of theeggs it produces contribute to its popularity in laboratoryresearch. A large array of mutant genes has been recognizedin the axolotl. These genes affect one or another process duringdevelopment of the organism, and have provided a basis for carryingout research in developmental genetics. Approximately threedozen mutant genes in the axolotl are known. These genes havebeen grouped into 5 different categories which reflect, forthe most part, the developmental stage at which the mutant phenotypecan first be recognized. One group of mutant genes, the autonomous cell-lethals, is discussedin detail. These genes share the common feature that homozygousembryos cannot be rescued by parabiosis with normal embryos.In addition, grafts of mutant tissue (e.g., gill or limb primorida)do not survive on normal hosts. These genes probably are responsiblefor metabolic or regulatory defects which affect all cells andtissues in the organism. The mutant phenotypes and potentialusefulness of these genes are discussed in detail.     

Control and Consequences of Alternative Developmental Modes in a Poecilogonous Polychaete

SYNOPSIS. The poecilogonous polychaete Streblospio benedicti(Webster) exhibits both planktotrophic and lecithotrophic modesof larval development. The alternative trophic modes are associatedwith differences in age and size at maturation, offspring number,size and energetic investment, larval planktonic period, morphologyand survivorship. This paper reviews a decade of research intothe control and consequences of the traits associated with planktotrophyand lecithotrophy in S. benedicti. The dominant control on reproductiveand developmental characters is genetic. Significant additivegenetic variance has been detected for egg diameter, fecundity,larval planktonic period and aspects of larval morphology. However,environmental factors such as temperature, food quality andphotoperiod, and intrinsic factors such as maternal age, exertconsiderable influence on non-trophic developmental traits (e.g.,offspring number, size and energy content). Demographic consequencesof development mode are reviewed for field and laboratory demesof S. benedicti dominated by individuals exhibiting either planktotrophyor lecithotrophy. Similar population size structure, fluctuationsin abundance, P: B ratios, and estimated population growth ratesare achieved through trade-offs between survivorship and fecundity. Development mode may best be viewed as a complex set of traitsthat are intimately linked developmentally and evolutionarilyto other aspects of an organism's life history. Greater insightinto the control and consequences of development mode shouldresult from further investigation of these linkages     

Development of the Recalcitrant (Homoiohydrous) Seeds of Avicennia marina: Anatomical, Ultrastructural and Biochemical Events Associated with Development from Histodifferentiation to Maturation

Early histodifferentiation of the embryo of Avicennia marina(Forssk) Vierh was characterized by the formation of endospermhaustoria Once the growth phase was initiated, subsequent embryodevelopment was extra-ovular The mature seed, therefore, wasenclosed by a pericarp originating entirely from the ovary wallGrowth and reserve deposition was not initiated until 45–50d after fruit set (DAFS), when respiratory activity had peakedWater content remained constant from the earliest stages ofembryogenesis to seed abscission and respiratory activity, althoughdeclining somewhat after the completion of histodifferentiation,remained relatively high throughout seed development The ultrastructureof the meristematic root primordia was indicative of metabolicactivity, remaining essentially similar in all respects fromthe end of histodifferentiation until the mature seeds wereabscised During this phase cotyledon cells became highly vacuolatedand the soluble sugars, which constituted the major nutrientreserves of mature seeds, increased considerably Seeds of A,marina initiate germination, without the requirement for additionalwater, as soon as they are shed It is proposed that the accumulationof soluble sugars, rather than insoluble complex reserves, isa major factor in the developmental strategy of these highlyrecalcitrant seeds Anatomy, Avicennia marina, biochemistry, homoiohydrous, recalcitrant, seed development/maturation, ultrastructure     

Changes in Seed Constituents During Germination and Seedling Growth of Precociously Matured Soybean Seeds(Glycine max)

During 7 d of precocious maturation of soybean seed (Glycinemax), the starch content declined and soluble sugar levels increasedin patterns similar to natural seed dehydration and maturation.Total seed protein content and total seed dry weight increasedwhereas oil content remained relatively unchanged. Overall,the proportions of the constituents in precociously maturedseeds were comparable to naturally mature seeds. Precociouslymatured soybean seeds showed much the same germination and seedlinggrowth frequency patterns as naturally matured seeds. Duringgermination and seedling growth of precociously matured seeds,starch, soluble sugar, protein and oil levels followed patternssimilar to naturally mature, germinating seeds and seedlings.Therefore, precocious maturation may be used as a model systemto investigate the control of the physiological and biochemicalevents occurring during seed maturation which lead to germinationand subsequently, seedling growth. Glycine max (L.) Merr., soybean, cotyledons, maturation, germination/seedling growth     

The effect of temperature on the post-embryonic growth of Neomysis intermedia Czernlawsky (Crustacea, Mysidacea) under laboratory conditions

The effect of temperature on post-embryonic growth of Neomysisintermedia was investigated under unlimited food conditionsin the laboratory. The effect of temperature on the size ofnewly released animals was negligibly small, but body size wasinversely related to temperature in adults. This was mainlycaused by the difference in the number of molts before maturation.The specific growth rate of N. intermedia increased exponentiallywith a temperature coefficient, Q₁₀ of 4.6 from 0.018 d^–13C to 0.21 d^–1 at 20C in juveniles, and with a temperaturecoefficient of 2.7 from 0.006 d^–1 at 3C to 0.05 d^–1at 25C in adults. The rate in juveniles levelled off above20C, and dropped at 29C. Brood size and brood interval decreasedwith temperature increase, while the daily specific reproductionrate increased. The specific growth rate of gravid females,including production of egg matter, increased exponentiallywith a temperature coefficient of 3.3 from 0.015 d^–1 at10C to 0.093 d^–1 at 25C. The present laboratory experiments confirmed the temperaturecontrol on the growth of N. intermedia suggested in a hyper-eutrophiclake.     

Pollen-pistil Interaction in a Non-pseudogamous Apomict,Commiphora wightii

Structural and cytochemical details of the pistil and the interactionof pollen and pistil were studied in a non-pseudogamous apomict,Commiphorawightii.The anthers in the male and bisexual flowers producefunctional pollen grains. The stigma is of the wet and papillatetype. The style is typically solid with two strands of transmittingtissue that traverse the entire length of the style. There isa marked reduction in the area occupied by the transmittingtissue from the stigma to the base of the style. The cells ofthe transmitting tissue are isodiametric in transverse as wellas longitudinal section and do not form longitudinal files ofelongated cells as reported for other taxa. Proteins could notbe localized in the intercellular matrix. Although pollen grainsgerminate on the stigma, pollen tubes do not grow beyond theproximal one third of the style. Changed orientation of thecells of the transmitting tissue and absence of proteins inthe intercellular matrix could account for the failure of thepistil to support pollen growth.Copyright 1998 Annals of BotanyCompany Guggul, pollen-pistil interaction, non-pseudogamous apomict,Commiphora wightii, transmitting tissue     

Patterns of growth and sexual size dimorphism in two species of box turtles with environmental sex determination

An adaptive explanation for environmental sex determination is that it promotes sexual size dimorphism when larger size benefits one sex more than the other. That is, if growth rates are determined by environment during development, then it is beneficial to match developmental environment to the sex that benefits more from larger size. However, larger size may also be a consequence of larger size at hatching or growing for a longer time, i.e., delayed age at first reproduction. Therefore, the adaptive significance of sexual size dimorphism and environmental sex determination can only be interpreted within the context of both growth and maturation. In addition, in those animals that continue to grow after maturation, sexual size dimorphism at age of first reproduction could differ from sexual size dimorphism at later ages as growth competes for energy with reproduction and maintenance. I compared growth using annuli on carapace scales in two species of box turtles (Terrapene carolina and T. ornata) that have similar patterns of environmental sex determination but, reportedly, have different patterns of sexual size dimorphism. In the populations I studied, sexual size dimorphism was in the same direction in both species; adult females were, on average, larger than adult males. This was due in part to males maturing earlier and therefore at smaller sizes than females. In spite of similar patterns of environmental sex determination, patterns of growth differed between the species. In T. carolina, males grew faster than females as juveniles but females had the larger asymptotic size. In T. ornata, males and females grew at similar rates and had similar asymptotic sizes. Sexual size dimorphism was greatest at maturation because, although males matured younger and smaller, they grew more as adults. There was, therefore, no consistent pattern of faster growth for females that may be ascribed to developmental temperature. Received: 20 March 1996 / Accepted: 10 March 1998     

Environmental effects on adult growth patterns in the male sailfin molly,Poecilia latipinna (Poeciliidae)

Synopsis Widespread male body size variation in P. latipinna appears to be attributable to genetic variation in the size at maturation. The contribution of adult growth needs to be assessed because adult growth rates may vary with size at maturation and local environment. In our laboratory study we examined adult growth patterns as a function of size at maturation and juvenile experience (favorable or unfavorable conditions). In our field study we assessed adult growth as a function of initial size and environmental condition (using males in enclosures in contrasting habitats). Adult growth rates in the laboratory were an order of magnitude higher than rates observed in field enclosures. Growth rates varied with male size, increasing with increasing male size in the laboratory study but decreasing with increasing male size in the field study. The laboratory results alone would have cast considerable doubt on the ability to interpret size distributions of field-collected males, but the field results indicate that adult growth is sufficiently low that it can be ignored as a source of body size variation within and among populations.     

PYRUVATE KINASE ISOZYMES IN NEURONS, GLIA, NEUROBLASTOMA, AND GLIOBLASTOMA

Abstract– The distribution of pyruvate kinase isozymes (EC 2.7.1.40) was examined in cells and tissues from the central and peripheral nervous system of the rat. Most tissues contain significant quantities of both the K₄ (fetal type) and M₄ (skeletal muscle type) isozymes plus tetrameric hybrids comprised of various combination of the type M and type K subunits. Retina, for example, contains a five-mem-bered hybrid set weighted toward K₄, while sciatic nerve and spinal cord have patterns very similar to that of adult brain, consisting predominantly of M₄ with small amounts of K₄ and K-M hybrids. This adult pattern is achieved by a gradual shift from a hybrid set dominated by K₄ in fetal life, to the pattern at birth at which time the two most prominent bands were M₄ and K₂M₂, and finally to the adult pattern by about 28 days after birth. Neurons and glial cells were isolated from rat and mouse brains at the various developmental levels. The pyruvate kinase isozyme patterns in the two cell types were similar to each other and to the patterns seen in whole brain homogenates at all ages, indicating similar rates of isozymic maturation in the two cell types. The correlation of maturation with pyruvate kinase isozyme patterns was further tested in cultures of malignant cell lines. A K-M hybrid set, weighted toward K₄, was seen in two clonal lines of mouse neuroblastoma under normal culture conditions. However, lowering the serum concentration in the culture medium or adding bromodeoxyuridine caused a shift in the patterns toward type M as the cells differentiated, mimicking in part the in vivo maturation of normal cells. On the other hand, a rapidly growing and poorly differentiated line of rat glioblastoma had only K₄ under all conditions examined.     

Reduced reproductive effort in male field crickets infested with parasitoid fly larvae

Some populations of the field cricket Teleogryllus oceanicusare parasitized by the phonotactic fly Ormia ochracea. Flieslocate crickets by their song and deposit larvae onto them.The larvae develop inside the cricket for 1 week before killingthe host upon emergence. The reproductive compensation hypothesispredicts that parasitized crickets should increase their reproductiveeffort during the initial stages of infestation to offset theloss of fitness resulting from their shortened life span. An alternative hypothesis predicts that parasitized crickets willdecrease reproduction, either because they are unable to reproduceor because selection acting on the parasitoid favors decreasedhost reproduction. In laboratory experiments, parasitized malecrickets had reduced reproductive effort (spermatophore production,calling, mating activity, and mass allocated to reproductivetissue) compared to unparasitized males. Parasitized males fedad libitum showed no evidence of allocating a greater proportionof their resources to reproduction. Parasitized and healthymales did not differ significantly in resting or maximal metabolicrates, although this may have been due to the substantial contributionof larval respiration to the metabolic rate of the host—parasitoidcomplex. These results are consistent with previous studiesand suggest that T. oceanicus males parasitized by O. ochraceado not increase their reproductive effort. We discuss potentialreasons that crickets do not increase reproductive effort inresponse to fly larvae and address difficulties in demonstratingaltered life-history patterns in response to parasitism.