Two-stage life cycle of a Cordylophora population in the Netherlands

A population of Cordylophora caspia was studied during a number of years in interconnected waters of different salinity and pollution. The distribution pattern of the colonies is only partly accounted for by these properties of the water. Part of it is also due to the availability of suitable substratum.Evidence is given that colonies of Cordylophora grow and survive on stones along the banks, but flourish during the summer on free-floating water-lily stalks.Zoological Laboratory, University of AmsterdamZoological Laboratory, University of Amsterdam     

POPULATION ECOLOGY OF SEALS: RETROSPECTIVE and PROSPECTIVE VIEWS

This review focuses on population ecology, with critical accounts of past work and future possibilities in age determination, body growth and condition, estimating abundances, mortality rates and lifespans, reproduction, comparative life histories, population dynamics, population modelling and seals in ecosystems. We suggest ways to reduce errors in age determination and to improve methods of obtaining and presenting growth data. Generalized von Bertalanffy growth equations are promoted as a basis for analysing species differences and intra-population variation in body lengths. Indices other than blubber thickness may be better for following body condition. Catch-effort and survival-index methods of estimating abundances have limited applicability, total counts are only locally useful, and sample counts may only be accurate for scattered, ice-breeding species. Some new techniques for population indices are promising. Pre-adult mortality remains difficult to assess. Although not always recognized, adult mortality rates do increase with age, as well described by Gompertz functions. Existing estimates of lifespans are unreliable, and a new approach is outlined. There are methodological problems in estimating ages of maturity. Corpora albicantia should not be used for back-extrapolation, and more study is needed of use of teeth annuli as indicators of maturity. Age-specific proportions of females parous based on reproductive tracts may disagree with proportions recruited in breeding groups, suggesting that the former may often be in error. Allometric relationships among body sizes and life-history variables need more reliable data, especially since the residuals of such relationships are of greatest interest. Brain size may be a better scalar. Direct evidence of density dependence in population growth of seals is sparse. Early survival has been more widely shown to be density-dependent, but only among polygynous species where crowding on land may be a byproduct of sexual selection; there is as yet no good evidence of trophic restraints. Evidence of density dependence of ages of maturity is generally unconvincing. Predation, especially by sharks, may be critical in some species. Characteristics of equilibrium populations might profitably be sought in mass remains in middens and historic kill sites. More attention should be paid to the search for density-independent influences. Supposed impacts of fisheries and pollutions are not wholly convincing. Natural epidemics may keep some populations below resource or space saturation, and some high-latitude species may show large year-to-year variations in recruitment and abundances. Evidence for such density-independent effects should be sought in residuals of growth curves and in teeth layers. Although surplus yield and production/biomass models have been tried, realistic pinniped models must be completely age-structured and time-dependent. Simple models have questionably assumed stationarity to derive life-history parameters. The best available estimates of density dependence of such parameters give no resolution when extrapolated toward equilibrium, and only limited efforts have been made to introduce stochasticity. Better data, not improved model structures, are needed for better understanding. Recent work has contradicted the assumed voraciousness of seals, but their system impacts and dependencies are not well understood. Extended Lotka-Volterra equations used to model Antarctic food webs, including seals, are merely heuristic. Fixed seal biomasses enter as top-down, driving functions in a Bering Sea model, which accordingly cannot be used to analyse or manage their populations. Some Soviet models are tantalizing but ill-specified. The introduction of harbor seals in well-chosen lakes might give mote insights into system roles than would more elaborate modelling. We wonder if pinniped ecology is well served by too many enthusiasts operating under too many restraints.     

The distribution,life cycle and production of Leptophlebia vespertina (L.) (Ephemeroptera) in a lowland lake

Oak Mere, the water body studied, is a moderately productive base-poor lowland lake. It has zones of submerged marginal vegetation growing on sand at the south-west end and on peat at the north-east end. The distributions of L. vespertina and other macroinvertebrates are described in relation to these two distinct areas. Laboratory experiments on behaviour and survival are described in an attempt to explain the patterns of distribution. The seasonal distribution, variations in population density, spatial distribution variance in relation to mean density, life cycle, length-weight relationship, growth and biomass of L. vespertina are then described during two years at the sandy south-west end. The data are used to estimate annual production. Distribution, life cycle, growth and production are compared with populations in water bodies of lower conductivity in the British Isles and Scandinavia.     

Multigenerational experimental simulation of climate change on an economically important insect pest

Long‐term multigenerational experimental simulations of climate change on insect pests of economically and socially important crops are crucial to anticipate challenges for feeding humanity in the not‐so‐far future. Mexican bean weevil Zabrotes subfasciatus, is a worldwide pest that attacks the common bean Phaseolus vulgaris seeds, in crops and storage. We designed a long term (i.e., over 10 generations), experimental simulation of climate change by increasing temperature and CO₂ air concentration in controlled conditions according to model predictions for 2100. Higher temperature and CO₂ concentrations favored pest''s egg‐to‐adult development survival, even at high female fecundity. It also induced a reduction of fat storage and increase of protein content but did not alter body size. After 10 generations of simulation, genetic adaptation was detected for total lipid content only, however, other traits showed signs of such process. Future experimental designs and methods similar to ours, are key for studying long‐term effects of climate change through multigenerational experimental designs.     

Incidence of Fungal Necrotrophic and Biotrophic Pathogens in Pioneer and Shade‐tolerant Tropical Rain Forest Trees

This study assessed the hypothesis that plant life history traits determine the incidence of fungal biotrophic and necrotrophic pathogens in pioneer vs. shade‐tolerant tropical plant species. Considering that pioneer species mainly invest in induced defenses, we expected a negative relationship between the incidence of biotrophic and necrotrophic pathogens; in contrast, as shade‐tolerant species invest heavily in constitutive defenses, we expected to find no correlation between the incidence of biotrophic and necrotrophic pathogens. These ideas were evaluated by assessing standing levels of fungal damage in a set of pioneer and shade‐tolerant species from the Lacandona tropical rain forest (Mexico). The results showed that among pioneer plant species, leaves with biotrophic lesions were between 34 and 44 percent more abundant than those with necrotic lesions. In contrast, among shade‐tolerant species, the proportions of leaves with necrotic lesions were 17–23 percent higher than those of leaves with injuries caused by biotrophic pathogens. Our study suggests that tropical tree species might present different defense strategies depending on the life‐style of the pathogens that attack them, and the life history strategy of the attacked host plant species. Thus, the host constitutive and induced defenses, as well as the mechanisms used by different types of pathogens to circumvent those defenses maybe responsible for the patterns of attack observed in perennial tropical plants. Abstract in Spanish is available at http://www.blackwell‐synergy.com/loi/btp .     

The geological setting of the earliest life forms

Summary Life on Earth may have begun about 4×10⁹ years (4 Ga) ago. Plate tectonics probably operated in the early Archaean, with rapid spreading at mid-ocean ridges, a komatiitic (magnesium-rich) oceanic crust, active volcanic arcs and the development of extensional basins on continental crust. Shallow water environments would have been more restricted and probably shorter-lived than in later geological times; however, extensive shallow seas existed in the later phases of the development of extensional basins. Bacterial communities-presumably photosynthetic-have probably existed in such shallow-water settings and probably at shallow depths in the oceans for at least 3.5 Ga. Because the mid-ocean ridges were probably subaqueous, hydrothermal systems would have been very vigorous and would have offered suitable habitats for early chemo-autotrophic bacterial communities. Early life forms probably also occupied vesicles in lavas, pumice and volcanic breccias, and pores in soft sediments, living in the constant flux of fluid flushing through permeable strata. Other, similar habitats would have existed in volcanic island arcs and in extensional basins.     

Effects of fluctuating thermal regimes on cold survival and life history traits of the spotted wing Drosophila(Drosophila suzukii)

Drosophila suzukii is an invasive pest causing severe damages to a large panel of cultivated crops.To facili tate its biocontrol with stratcgies such as sterile or incompatible insect techniques,D.suzukid must be mass-produced and then stored and transported under low temperature.Prolonged cold exposure induces chill injuries that can be mitigated if the cold period is interrupted with short warming intervals,referred to as fluctuating thermal regimes(FTR).In this study,we tested how to optimally use FTR to extend the shelf life of D.suzukii under cold storage.Several FTR parameters were asessed:temperature(15,20,25℃),duration(0.5,1,2,3 h),and frequency(every 12,24,36,48 h)of warming intervals,in two wild-type lines and in two developmental stages(pupac and adults).Generally,FTR improved cold storage tolerance with respect to constant low temperatures(CLT).Cold mortality was lower when recovery temperature was 20℃ or higher,when duration was 2 h per day or longer,and when warming interruptions occurred frequently(every 12 or 24 h).Applying an optimized FTR protocol to adults greatly reduced cold mortality over long-term storage(up to 130 d).Consequences of FTR on fitness-related traits were also investigated.For adults,poststorage survival was unaffected by FTR,as was the case for female fecundity and male mating capacity.On the other hand,when cold storage occurred at pupal stage,postorage survival and male mating capacity were altered under CLT,but not under FTR.After storage of pupae,female fecundity was lower under FTR compared to CLT,suggesting an energy trade-off between repair of chill damages and C22 production.This study provides detailed information on the application and optimization of an FTR-based protocol for cold storage of D.suzuki that could be useful for the biocontrol of this pest.     

康复运动对冠脉支架植入术后患者相关因素的影响

目的：研究心脏康复运动对冠脉支架植入术后患者血脂、血糖、体重指数及生活质量的影响。方法：对实施冠脉支架植入术的 146例患者进行比较分析，根据随机原则分为试验组76 例及对照组70 例。对照组患者给予常规的健康教育及冠心病二级预防指 导，给予定期随访。试验组患者在此基础上给予规律的康复运动指导。经过6 个月随访，比较两组患者血脂、HbA1C、体重指数及 生活质量情况。结果：试验组患者通过为期6 个月的规律的心脏康复运动指导，其血脂、HbA1C等冠心病危险因素控制情况优于 对照组，差异有统计学意义(P<0.05)。同时，6个月后，试验组康复运动六月后sF 量表各项评分与对照组同期比较，差异均有统计 学意义(P<0.05)。结论：规范的心脏康复运动指导能够有效改善冠脉支架植入术后患者血脂、血糖情况，提高患者生活质量。     

Physiological mechanism governing slow and fast development in predatory ladybirds

Aphidophagous and coccidophagous ladybirds, similar to their prey, show marked differences in their pace of life (Dixon, 2000), in particular in their rate of development, with all stages of aphidophagous species developing much faster than those of coccidophagous species. Two hypotheses are proposed to account for the large difference in the pace of life of these two groups. These are that differences in the rate of development are a result of differences in lower temperature thresholds for development or the quality of their respective prey as food (Dixon et al., 2011). Analysis of published results on the rates of development of the eggs of ladybirds indicates that the inverse relationships between the number of day‐degrees required for development (K) and the lower temperature threshold for development (td_min) of these two groups are significantly different. In particular, the respective td_min overlap and K of the aphidophagous and coccidophagous species with a similar td_min are, on average, 38 and 117 day‐degrees (D^o). The relationship between the rate of development (R) and temperature (T) for aphids reared on poor‐ or high‐quality foods indicates that, although the value of td_min of a species depends on food quality, K does not, showing that it is unlikely that K is governed by food quality. Thus, there is little support for differences in either the td_min or food quality governing the difference in the pace of life of these two groups of ladybirds. The results indicate that the physiological mechanism that may govern the difference in the pace of life between these two groups is the number of day‐degrees (K) needed to complete their development. The possible evolutionary reason for this is discussed.