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Development Period (development + period)
Selected AbstractsLife history of the bird cherry-oat aphid, Rhopalosiphum padi, on transgenic and non-transformed wheat challenged with Wheat streak mosaic virusENTOMOLOGIA EXPERIMENTALIS ET APPLICATA, Issue 1 2009Edgardo S. Jiménez-Martínez Abstract The life history of the bird cherry-oat aphid, Rhopalosiphum padi (L.) (Hemiptera: Aphididae), was studied via laboratory assays on Wheat streak mosaic virus (WSMV)-infected and non-infected transgenic and non-transformed wheat [Triticum aestivum L. (Poaceae)]. Although R. padi is not a WSMV vector, it is known to colonize WSMV-infected wheat plants. Two transgenic soft white winter wheat genotypes, 366-D03 and 366-D8, that express the WSMV coat protein gene, and the WSMV-susceptible non-transformed cultivar Daws were tested. All genotypes showed disease symptoms when infected with WSMV. Whereas plant height was significantly reduced on virus-infected compared to non-infected plants of all genotypes, virus-infected transgenic plants exhibited lower virus titer and lower disease rating scores than Daws. No significant effects of WSMV infection or genotypes were observed on the length of R. padi nymphal development period, nor on their pre-, and post-reproductive periods. Rhopalosiphum padi reproductive period was significantly longer on Daws infected with WSMV than on non-infected plants of this cultivar. In contrast, there were no significant differences in length of R. padi reproductive period between virus-infected and non-infected transgenic plants within a genotype. Rhopalosiphum padi daily fecundity was significantly lower and adult longevity significantly longer on virus-infected than on non-infected plants of all genotypes. Total aphid fecundity and intrinsic rate of increase were not significantly different among treatments. The percentage of winged aphids that developed was greater on WSMV-infected compared to non-infected plants within a genotype. Results indicate that both virus infection status of plants and wheat genotype influence the life history of R. padi. [source] Genetic evidence for `leaky' cohorts in the semivoltine stonefly Peltoperla tarteri (Plecoptera: Peltoperlidae)FRESHWATER BIOLOGY, Issue 3 2002ALICIA S. SCHULTHEIS 1.,Genetic techniques are being used increasingly to address questions about dispersal and gene flow of freshwater invertebrates. However, population genetic structure can be affected by factors other than dispersal. Many stream insects have long life cycles that result in the simultaneous existence of multiple cohorts throughout the larval development period. If larval development is fixed, successive cohorts may be reproductively isolated and, as a result, genetically distinct. In such cases, significant levels of genetic differentiation between cohorts could confound estimates of dispersal based on population genetic structure. 2.,Peltoperla tarteri is a stonefly that can be abundant in Appalachian headwater streams. Although P. tarteri is univoltine at the type locality (Big Paint Hollow, WV, U.S.A.), the study populations in southwestern Virginia, U.S.A., were semivoltine. This semivoltine life cycle results in the simultaneous existence of multiple cohorts with the potential for significant genetic differentiation among them. 3.,Levels of genetic differentiation among P. tarteri cohorts were analysed with mitochondrial DNA (mtDNA) sequence data from the non-coding origin of replication or `control' region from 93 individuals from two successive cohorts (collected in 1998 and 1999). 4.,Analysis of molecular variance (AMOVA) indicated no genetic differentiation among cohorts (FST=0.0), and gene flow among cohorts was very high (Nm=,). 5.,High levels of gene flow among cohorts suggest that larval development of P. tarteri is not fixed. Gene flow among cohorts most likely occurs as a result of a cohort split in which some individuals complete development in one or three years instead of two. [source] Control of fledging age in Leach's Storm-Petrel, Oceanodroma leucorhoa: chick development and prefledging mass lossFUNCTIONAL ECOLOGY, Issue 1 2005R. A. MAUCK Summary 1Leach's Storm-Petrel (Oceanodroma leucorhoa) chicks accumulate fat through most of the nestling period, near the end of which they typically weigh 50,100% more than their parents. Much of this excess mass is lost abruptly prior to leaving the nest and fledging itself marks the termination of parental care. 2In this study, we evaluated the hypothesis that the onset of the prefledging mass loss period coincides with the end of the development period and the completion of structural growth. 3We characterized the pattern of prefledging mass loss and the timing of fledging with respect to a point (T), based on wing growth, at which structural development stops. Variation in T suggested that development rate is partially influenced by parental food provisioning, particularly early in the nestling period (age 16,20 days) just prior to the onset of rapid primary feather growth. 4The timing of mass loss and fledging in relation to T suggested that prefledging mass loss begins upon completion of wing growth and that fledging occurs after chicks have reached a mass compatible with sustained flight. Thus, the time to fledging is positively correlated with nestling mass at the end of the development period. 5The prefledging period of mass loss is a unique phase of anorexia placed between parental feeding and self-feeding in the life of the young petrel. [source] Fly or die: the role of fat stores in the growth and development of Grey-headed Albatross Diomedea chrysostoma chicksIBIS, Issue 2 2000KEITH REID Chicks of albatrosses, like other Procellariiformes, become independent at a mass similar to their parents but during growth attain a peak mass some 30% or more greater, before losing mass prior to fledging. The current views are that this high peak mass represents chicks storing fat reserves as an energy sink, or as an insurance against periodic food scarcity, or as a Consequence of natural stochastic variation in provisioning rate. We analysed growth and body composition of Grey-headed Albatross Diomedea chrysostoma chicks at Bird Island, South Georgia in 1984 and 1986, two years of very different food availability. In 1984 when overall breeding success was only 28% (the lowest in 20 years and less than halt that in 1986), chicks were significantly smaller in terms of peak mass (by 37%), primary length (by 25%), liver, lung, heart and kidney size (by 18,34%) and fat (by 75,80%) but not significantly different in terms of skeletal (tarsus, culmen, ulna, sternum) or muscle (pectoral, leg) size. Despite these differences, there were some important similarities in the patterns of growth in both years. Up to the attainment of peak mass, most of the growth of organs and of skeletal structures was completed and little fat was deposited. In the remaining part of the chick-rearing period, feather growth and acquisition of fat stores were undertaken. Thus Grey-headed Albatross chicks begin to acquire substantial fat stores only during the later part of the development period; this is contrary to the predictions of any of the existing hypotheses concerning provisioning patterns and the role of fat stores in Procellariiformes. We propose that the deposition of fat in the later stages of chick growth is an adaptation to: (a) ensure against energy demands and/or nutritional stress affecting the quality of flight feathers (many of which are not renewed for up to three years after fledging); and (b) provide an energy reserve for chicks to use in the critical period immediately after independence. [source] Size compensation in moth larvae: attention to larval instarsPHYSIOLOGICAL ENTOMOLOGY, Issue 3 2010TOOMAS ESPERK Environmental perturbations such as starvation and poor diet often prevent animals from attaining their optimal sizes. When the perturbation has a transient character, compensatory responses are expected in terms of faster growth or a prolonged developmental period. In the case of insect larvae, details of such responses are insufficiently known at the proximate level. Attention to responses at the level of particular larval instars should promote an understanding of insect developmental plasticity also in a more general context. To provide an instar-specific analysis of compensatory growth, larvae of the moth Orgyia antiqua (L.) are reared on inferior diet during one larval instar. Responses in growth parameters are recorded in the course of the manipulated instars, as well as at the level of the entire larval period. The negative relationship between development time and size in response to the inferior food quality, typical of the entire larval periods, is also observed within the manipulated instars taken separately. The manipulated larvae remain smaller than the larvae of the control group (significant in males only), even by the end of the subsequent instar during which all individuals are provided with superior host. In males, close to full size compensation by the time of pupation is achieved only by means of adding an extra larval instar. The inability of larvae to fully compensate during one and even two instars is considered as an indication of the presence of constraints on the within-instar growth pattern. An alternative, adaptational explanation for the incomplete compensation could be based on the cost of prolonged development period. Given the ecological context of the species' life history, such an explanation appears less likely. [source] | |||||||||||||||||||