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Life cycle optimization of automobile replacement: model and application.

Although recent progress in automotive technology has reduced exhaust emissions per mile for new cars, the continuing use of inefficient, higher-polluting old cars as well as increasing vehicle miles driven are undermining the benefits of this progress. As a way to address the "inefficient old vehicle" contribution to this problem, a novel life cycle optimization (LCO) model is introduced and applied to the automobile replacement policy question. The LCO model determines optimal vehicle lifetimes, accounting for technology improvements of new models while considering deteriorating efficiencies of existing models. Life cycle inventories for different vehicle models that represent materials production, manufacturing, use, maintenance, and end-of-life environmental burdens are required as inputs to the LCO model. As a demonstration, the LCO model was applied to mid-sized passenger car models between 1985 and 2020. An optimization was conducted to minimize cumulative carbon monoxide (CO), non-methane hydrocarbon (NMHC), oxides of nitrogen (NOx), carbon dioxide (CO2), and energy use over the time horizon (1985-2020). For CO, NMHC, and NOx pollutants with 12000 mi of annual mileage, automobile lifetimes ranging from 3 to 6 yr are optimal for the 1980s and early 1990s model years while the optimal lifetimes are expected to be 7-14 yr for model year 2000s and beyond. On the other hand, a lifetime of 18 yr minimizes cumulative energy and CO2 based on driving 12000 miles annually. Optimal lifetimes are inversely correlated to annual vehicle mileage, especially for CO, NMHC, and NOx emissions. On the basis of the optimization results, policies improving durability of emission controls, retiring high-emitting vehicles, and improving fuel economies are discussed.

Air Pollution↗

Life cycle and reproductive patterns of Triatoma rubrofasciata (De Geer, 1773) (Hemiptera: Reduviidae), under laboratory conditions.

The life cycle and reproductive patterns of Triatoma rubrofasciata were studied along with laboratory conditions for the establishment of a prolific colony. The insects were divided into four groups: two of them were maintained at room temperature (20.5 degrees C to 33 degrees C and 85% +/- 5% of relative humidity), the other two in a climatic chamber (CC) (temperature: 29 degrees C, humidity: 80% +/- 5%). The groups were fed weekly or fortnightly on Swiss mice. The females from the group kept in the CC and fed weekly had longer life span, as well as a higher number of eggs, fertile eggs and hatchings; the group kept in the CC and fed fortnightly had a shorter life span for the 1st, 2nd and 3rd instars and a lower mortality rate for all instars. It was concluded that a constant high temperature (CC at 29 degrees C) is the most suitable condition for the maintenance of a colony of T. rubrofasciata regardless of the interval between repasts.

Animals↗

Role of envelope protein gE endocytosis in the pseudorabies virus life cycle.

Several groups have reported that certain herpesvirus envelope proteins do not remain on the surface of cells that express them but rather are internalized by endocytosis in a recycling process. The biological function of membrane protein endocytosis in the virus life cycle remains a matter of speculation and debate. In this report, we demonstrate that some, but not all, membrane proteins encoded by the alphaherpesvirus pseudorabies virus (PRV) are internalized after reaching the plasma membrane. Glycoproteins gE and gB are internalized from the plasma membrane of cells, while gI and gC are not internalized efficiently. We show for gE that the cytoplasmic domain of the protein is required for endocytosis. While the gI protein is incapable of endocytosis on its own, it can be internalized when complexed with gE. We demonstrate that endocytosis of the gE-gI complex and gB occurs early after infection of tissue culture cells but that this process stops completely after 6 h of infection, a time that correlates with significant shutoff of host protein synthesis. We also show that gE protein internalized at 4 h postinfection is not present in virions formed at a later time. We discuss the differences in PRV gE and gI endocytosis compared to that of the varicella-zoster virus homologs and the possible roles of glycoprotein endocytosis in the virus life cycle.

Animals↗

DNA measurements reveal differences in the life cycles of Babesia bigemina and B. canis, two typical members of the genus Babesia.

The relative DNA levels of different developmental stages of Babesia bigemina and B. canis were measured by cytophotometry using the fluorochrome Hoechst 33258 as a staining dye. The DNA measurements provided direct proof of sexual reproduction, i.e., fusion of gametes resulting in the formation of zygotes followed by a meiotic division. Both Babesia species are considered to be typical members of the genus Babesia; however, the DNA measurements revealed important differences in the life cycle of these parasites, indicating that Babesia species are not characterized by a life cycle, which is specific for this genus.

Animals↗

Activity of a trypanosome metacyclic variant surface glycoprotein gene promoter is dependent upon life cycle stage and chromosomal context.

African trypanosomes evade the mammalian host immune response by antigenic variation, the continual switching of their variant surface glycoprotein (VSG) coat. VSG is first expressed at the metacyclic stage in the tsetse fly as a preadaptation to life in the mammalian bloodstream. In the metacyclic stage, a specific subset (<28; 1 to 2%) of VSG genes, located at the telomeres of the largest trypanosome chromosomes, are activated by a system very different from that used for bloodstream VSG genes. Previously we showed that a metacyclic VSG (M-VSG) gene promoter was subject to life cycle stage-specific control of transcription initiation, a situation unique in Kinetoplastida, where all other genes are regulated, at least partly, posttranscriptionally (S. V. Graham and J. D. Barry, Mol. Cell. Biol. 15:5945-5956, 1985). However, while nuclear run-on analysis had shown that the ILTat 1.22 M-VSG gene promoter was transcriptionally silent in bloodstream trypanosomes, it was highly active when tested in bloodstream-form transient transfection. Reasoning that chromosomal context may contribute to repression of M-VSG gene expression, here we have integrated the 1.22 promoter, linked to a chloramphenicol acetyltransferase (CAT) reporter gene, back into its endogenous telomere or into a chromosomal internal position, the nontranscribed spacer region of ribosomal DNA, in both bloodstream and procyclic trypanosomes. Northern blot analysis and CAT activity assays show that in the bloodstream, the promoter is transcriptionally inactive at the telomere but highly active at the chromosome-internal position. In contrast, it is inactive in both locations in procyclic trypanosomes. Both promoter sequence and chromosomal location are implicated in life cycle stage-specific transcriptional regulation of M-VSG gene expression.

Animals↗

Effect of temperature and relative humidity on the life cycle of Ornithodoros (Pavlovskyella) erraticus (Ixodoidea: Argasidae).

The effect of different temperatures (18, 22, 28, and 32.5 C, at constant 75% RH) and relative humidities (0, 15, 42, 60, 75, 84, and 92%, at constant 28 C) on the duration of the life cycle of Ornithodoros (Pavlovskyella) erraticus is studied in the laboratory. The egg incubation period is longer at 22 C than at the other temperatures tested; the percentage of hatched eggs was markedly increased at 28 C in comparison with other temperatures (T's) and relative humidities (RH's) tested. At constant 28 C, most larvae (86.2%) are ready to feed within 7.2 days posthatching; they feed for 5-52 min and molt to N1 in 7.8 days postfeeding. Five nymphal instars are recorded. Unfed N1-N5 survived for a longer period at 18 C than at other temperatures, whereas the effect of RH's was insignificant. After feeding, nymphal premolting periods differ from one instar to another and from one T or RH to another. At 28 C, the males emerge from N3, N4, and N5 in 9-15 days postfeeding, while females emerge only from N4 and N5 in 10-16 days. The overall sex ratio (3 male:5 female) is not affected by different T's and RH's. The female and male life spans were longer (means 720 and 500 days, respectively) at 22 C than at other T's and RH's. This study shows that the duration of the life cycle of O. erraticus decreases with rising T and increases with an increase in RH. However, the 28 C and 75% RH seem to be the optimum conditions for this species.

Animals↗

The life cycle of the policy for preventing road accidents: an empirical example of the policy for reducing drunk driving crashes in Taipei.

The purpose of this paper is to examine the temporal variation of the effect of preventive policy on reducing traffic accidents. The life cycle theory was introduced to describe the safety effect of the intervening policy over time. Poisson regression models with dummy-based and time-based specifications were used to evaluate the effect of an intervening policy over an observation period following its implementation. The policy of "Criminal sanction for drunk driving (CSFDD)" in Taipei city was evaluated as an empirical example to determine whether the temporal variation of safety effect happened to the CSFDD policy. The study results showed that alcohol consumption, arresting the drunk driving offenders, and the implementation of the CSFDD were the significant factors affecting the rate of occurrence of fatal accidents involving drunk driving. The effect of the CSFDD policy appeared to be a rapid initial response followed by a lower rate of decay. The existence of the life cycle implies that employing different observation periods following the implementation of a specific policy to evaluate its performance may obtain different effects. The results of this study are crucial for policy evaluation. The effects of safety policy should be carefully interpreted in order to avoid misleading the relevant authorities in coming to the wrong conclusions and as such make the wrong decisions.

Accidents, Traffic↗

Proteomic analysis of the potato tuber life cycle.

The tuber of potato (Solanum tuberosum) is commonly used as a model for underground storage organs. In this study, changes in the proteome were followed from tuberization, through tuber development and storage into the sprouting phase. Data interrogation using principal component analysis was able to clearly discriminate between the various stages of the tuber life cycle. Moreover, five well-defined protein expression patterns were found by hierarchical clustering. Altogether 150 proteins showing highly significant differences in abundance between specific stages in the life cycle were highlighted; 59 of these were identified. In addition, 50 proteins with smaller changes in abundance were identified, including several novel proteins. Most noticeably, the development process was characterized by the accumulation of the major storage protein patatin isoforms and enzymes involved in disease and defense reactions. Furthermore, enzymes involved in carbohydrate and energy metabolism and protein processing were associated with development but decreased during tuber maturation. These results represent the first comprehensive picture of many proteins involved in the tuber development and physiology.

Electrophoresis, Gel, Two-Dimensional↗

The C terminus of human immunodeficiency virus type 1 matrix protein is involved in early steps of the virus life cycle.

Deletion mutations at the C terminus of the matrix (MA) protein of human immunodeficiency virus type 1 (HIV-1) were generated by site-directed mutagenesis. The resultant mutant viruses had a severe defect in virus infectivity. This defect did not involve late steps of the virus life cycle, as the synthesis and processing of the Gag polyprotein and the assembly and release of mutant virions were not greatly affected. The incorporation of viral proteins and the viral RNA genome was similar for mutant and wild-type virions. In contrast, the early steps of the virus life cycle were severely affected, as the synthesis of viral DNA postinfection was dramatically reduced in mutant-virus-infected cells. One stretch of amino acids that was deleted in one of the mutants has significant homology with a region in VP1 of the picornavirus family. This region of VP1 is presumably involved in poliovirus penetration into cells. These results suggest that in addition to its functional role in virus assembly, the MA protein of HIV-1, and possibly of other retroviruses, plays an important role in virus entry.

Amino Acid Sequence↗

Growth of Azotobacter vinelandii in dialysed soil medium: studies upon the life cycle.

Azotobacter vinelandii ATCC 12837 cultured in dialysed soil medium with addition of 0.5% glucose showed four distinct morphological cell types: large cells, precyst forms, mature cysts and filterable corpuscles (0.3 micron in diameter). These results indicate that Azotobacter is a bacterium with a complex life cycle under certain culture conditions. Intracellular levels of RNA and poly-beta-hydroxybutyric acid were significantly affected when cells grown in dialysed soil were compared with those obtained after growth on defined medium (N-free). Further studies showed that the chemical composition of filterable corpuscles obtained from dialysed soil medium were different from the composition of normal Azotobacter cells produced in both culture media (dialysed soil and defined media). We suggest that filterable corpuscles represent a stage in the life cycle of Azotobacter in their natural environment.

Azotobacter↗

A proposed life cycle model of Spiroplasma mirum based on scanning electron microscopical observations of growth in liquid culture.

Cells of Spiroplasma mirum strain SMCA were grown in PPG broth and examined by scanning electron microscopy. Comparison of the results at different time intervals allowed for a model of the life cycle of S. mirum to be proposed. Under favorable growth conditions, helical filament formation was initially observed, followed by the formation of small spherical structures originating from each filament. In old culture, large spherical bodies appeared from entangled helical filaments. From the larger spherical bodies, granular bodies representing the smallest reproductive units were produced to continue the life cycle.

Culture Media↗

Life cycle, migration and antigen presenting functions of spleen and lymph node dendritic cells: limitations of the Langerhans cells paradigm.

The phenotypic and functional studies carried out in recent years on dendritic cells (DC) purified from spleen and lymph nodes has revealed the existence of heterogeneous populations with distinct life cycles, migratory properties and antigen presenting functions. A major subdivision can be made between "tissue derived" DC that migrate to the lymph nodes from peripheral tissues, both in the steady state and in the course of infections, and "blood-derived" DC, which reside in the spleen and lymph nodes throughout their life cycle. These two groups of DC can be subdivided into smaller subsets. The tissue-derived and the blood-derived DC also show fundamental differences in maturational status and antigen presenting capabilities. In this review, we summarize the roles played by the different DC types in the steady state and during pathogen infections, relating those roles to maintenance of peripheral tolerance and the induction of immunity. We point out the caveats of assuming that the DC that collect antigens are the ones involved in their presentation, emphasizing the phenomenon of antigen transfer as an important component of the immune response.

Animals↗

Environmental and endogenous control of sexuality in a rotifer life cycle: developmental and population biology.

Induction of mictic females, and hence initiation of sexuality, in the life cycle of some Brachionus requires an environmental stimulus associated with crowding. The inducing stimulus appears to be a taxonomically specific chemical released into the environment by the rotifers. Oocytes are induced to develop into mictic females before they are oviposited by their amictic mothers and begin cleavage divisions. Thus, the inducer affects the oocyte in the maternal body cavity either directly or indirectly by altering the physiology of its mother. The level of sexual reproduction expressed in populations of a Florida strain of B. calyciflorus is controlled by two types of endogenous factors and by the degree of crowding. First, some fraction of genetically identical oocytes in a clonal population fails to respond to even extreme crowding conditions, thus ensuring some potential for continued population growth by female parthenogenesis. Second, the propensity of amictic females to produce mictic daughters is extremely low when they hatch from fertilized resting eggs and then gradually increases to an asymptote after about 12 parthenogenetic generations. This multigenerational parental effect likely is due to a cytoplasmic factor in fertilized eggs that inhibits expression of the mictic-female phenotype and that is gradually diluted in successive parthenogenetic generations. The effect may increase a clone's genetic contribution to the resting-egg bank by increasing its population size through parthenogenetic generations before mictic females are induced.

Animals↗

Aquatic ecotoxicological indicators in life-cycle assessment.

This paper compares available options for the aquatic ecotoxicological effect factor component in life-cycle assessment (LCA). The effect factor is expressed here as the change in risk per unit change in cumulative exposure, delta effect/delta exposure. The comparison is restricted to approaches linked, implicitly as well as explicitly, to species-sensitivity distributions (SSDs). This draws on recent insights for chemical mixtures and identifies the implications of different model choices. In spite of the many options, assumptions, and areas for further research, it is concluded that a single effect factor basis represents the best available practice for use in LCA at this time, deltaPAF(ms)/deltaC = 0.5/HC50, where deltaPAF(ms) is the change in the (potentially affected) fraction (PAF) of species that experiences an increase in exposure above a specified effect level, accounting for the presence of complex background mixtures (ms), deltaC is the change in cumulative exposure concentration of the chemical of interest, and HC50 is the median, chronic hazardous concentration for regional, multiple-species systems. The resultant aquatic effect factors are risk-based and can be estimated readily for many chemicals using available methods, without the need to describe the entire SSDs and without the need for additional data. For example, the octanol-water partitioning coefficient provides a sufficient estimation basis for about 50% of existing chemicals that have a narcosis mode of action. This also is relevant in LCA for chemicals that are at low concentrations in the environment, concentrations below the biological thresholds at which more specific modes of action would be of relevance.

Animals↗

Speculation on possible life cycles for the clonal lineages in the genus toxoplasma.

Recent evidence suggests that the strains currently classified in the genus Toxoplasma, ie. within the species Toxoplasma gondii, may actually comprise at least two clonal lineages correlated with their virulence in mice. Here, Alan Johnson reviews these data in the context of evolution and speciation within the genus, and raises hypotheses on how the virulent lineage may undergo an asexual life cycle in nature, similar to that found for the very closely related coccidian, Neospora camnum. The putative vertical transmission life cycle of this mouse virulent lineage of T. gondii could involve passage to the foetus late in pregnancy, or transmission in milk to the neonate after birth.

Journal Article↗

The activity periods and life-cycle of the tick Ixodes uriae (Acari: Ixodidae) in relation to host breeding strategies.

We investigated the timing of seasonal activity of the seabird tick Ixodes uriae by examining engorgement rates of off-host ticks and the prevalence of infested common guillemots (Uria aalge) and kittiwakes (Rissa tridactyla) on the Isle of May, Scotland. More than 99% of I. uriae fed during the period late April to early August which coincided with the seabird breeding season. No ticks fed in the autumn and winter, and none over-wintered in the engorged state. Peak tick feeding activity was during the hosts' incubation period in May and early June, when over 70% of birds were parasitized. Few ticks were active when guillemot chicks were being brooded, or during the early part of kittiwake chick-rearing. Adult female tick feeding peaked in the first week of June, while nymphal and larval activity peaked in the third week of May. Adult female ticks fed later than nymphs on guillemots and larvae on both guillemots and kittiwakes; however, there was considerable temporal overlap in the feeding periods of the 3 stages of both hosts. All larvae and nymphs fed in May and early June, but up to 18% of adult females remained unengorged at this time, and probably deferred feeding by 1 year. A small proportion of individuals which fed as larvae in May appeared to feed again as nymphs in July of the same season, thereby shortening their life-cycle by 1 year. The duration of the life-cycle of I. uriae on the Isle of May is typically 3 years but varies from 2 to 4 years. Ticks feeding on guillemots did so significantly earlier than those feeding on kittiwakes, possibly because guillemots start breeding earlier in the year. Breeding of both guillemots and kittiwakes was later in 1994 than in 1993. This delayed the activity of all tick stages on kittiwakes and adult female ticks on guillemots, but did not affect the timing of activity of nymphs or larvae feeding on guillemots.

Animals↗

[Life cycle of Proteocephalus neglectus (Cestoda) from rainbow trout Salmo gairdneri].

Proteocephalus neglectus is described for the first time in the G.D.R. from Salmo gairdneri. The incidence of invasion was 65% and the main intensity was 2.8 with a maximum of 6 worms per fish. P. neglectus has a 2-host life-cycle. Copepods of the Cyclops strenuus-group and Cyclops furcifer were used as experimental intermediate hosts. The ontogenetic stages oncosphaera (free-living first larva), cercoscolex (second larva in the copepod haemocoel) and preadult (in the gut lumen of the definitive host) were described and compared with other proteocephalid life-cycles. When copepods invaded by oncosphaeres and captured at 14-15 degrees C were eaten by the trouts after 21 days the invasion of the definitive host took place. Parallel tests with Perca fluviatilis were not successful. A transfer of the preadult worms from trout to trout was possible. Some problems of species determination and of terminology were discussed.

Animals↗

Transcriptional regulation of metacyclic variant surface glycoprotein gene expression during the life cycle of Trypanosoma brucei.

In antigenic variation in African trypanosomes, switching of the variant surface glycoprotein (VSG) allows evasion of the mammalian host immune response. Trypanosomes first express the VSG in the tsetse fly vector, at the metacyclic stage, in preparation for transfer into the mammal. In this life cycle stage, a small, specific subset (1 to 2%) of VSGs are activated, and we have shown previously that the system of activation and expression of metacyclic VSG (M-VSG) genes is very different from that used for bloodstream VSG genes (S.V. Graham, K.R. Matthews, P.G. Shiels, and J.D. Barry, Parasitology 101:361-367, 1990). Now we show that unlike other trypanosome genes including bloodstream VSG genes, M-VSG genes are expressed from promoters subject to exclusively transcriptional regulation in a life cycle stage-dependent manner. We have located an M-VSG gene promoter, and we demonstrate that it is specifically up-regulated at the metacyclic stage. This is the first demonstration of gene expression being regulated entirely at the level of transcription among the Kinetoplastida; all other protein-coding genes examined in these organisms are, at least partly, under posttranscriptional control. The distinctive mode of expression of M-VSG genes may be due to a stochastic mechanism for metacyclic VSG activation.

Animals↗