Not all herbivory is detrimental to plants. In some cases, plants can compensate for herbivory, maintain growth and fitness following damage, or even overcompensate for herbivory and perform better ...than if left undamaged. Examples of overcompensation to vertebrate herbivory are well known, but here we review the literature for examples of reproductive overcompensation (i.e., increased production of traits associated with fitness) and increased vegetative growth (i.e., vegetative overcompensation) following insect herbivory. We used a meta-analysis to explore the effects of plant growth form, evolutionary history, herbivore feeding guild, and other plant and insect traits on the expression of reproductive and vegetative overcompensation by plants. Our literature search revealed 86 studies documenting examples of overcompensation for insect herbivory by 67 plant species representing 26 families. These plants included monocots and dicots, annuals and perennials, and woody and herbaceous plants. We also found that varied insect herbivores induce overcompensation, including 75 insect species in six orders representing 27 families and myriad feeding guilds. In our meta-analysis, we calculated 53 effect sizes from 21 publications documenting reproductive overcompensation and 89 effect sizes from 40 publications documenting vegetative overcompensation. Variation in reproductive overcompensation was seen among plant growth forms, functional groups, cultivation, herbivore feeding sites, and plant and herbivore families. Variation in vegetative overcompensation was seen among plant families, herbivore families, and latitudinal gradients. We suggest overcompensation for insect herbivory may be far more prevalent than previously thought. Additional research focusing on the mechanisms, patterns, and ecological and evolutionary consequences of overcompensation for insect herbivory is likely to provide exciting new insights into this poorly understood and largely overlooked outcome of plant–insect interactions.
Full text
Available for:
BFBNIB, FZAB, GIS, IJS, INZLJ, KILJ, NLZOH, NMLJ, NUK, OILJ, PNG, SAZU, SBCE, SBMB, UL, UM, UPUK, ZRSKP
30 years of fatal dengue cases in Brazil: a review Nunes, Priscila Conrado Guerra; Daumas, Regina Paiva; Sánchez-Arcila, Juan Camilo ...
BMC public health,
03/2019, Volume:
19, Issue:
1
Journal Article
Peer reviewed
Open access
Over the last 30 years, extensive dengue epidemics have occurred in Brazil, characterized by emergences and re-emergences of different serotypes, a change in the epidemiological profile and an ...increase in the number of severe and fatal cases. Here, we present a review on the dengue fatal cases that occurred in Brazil in 30 years (1986-2015).
We performed an ecological study by using secondary data on dengue fatal cases obtained in the National System of Reported Diseases (Sistema de Informação de Agravos de Notificação -SINAN) and in the Mortality Information System (SIM), both maintained by the Brazilian Ministry of Health. Cases were analyzed by region, demographic variables, clinical classification and complications based on the data available.
In 30 years (1986-2015), the Southeast region reported 43% (n = 2225) of all dengue deaths in the country. The Midwest region was responsible for 18% of the fatal cases. After 2000, deaths occurred in almost all states, with the exception of Santa Catarina and Rio Grande do Sul, South region. From 2006 to 2010, the number of deaths increased, with higher rates of mortality, especially in Goiás and Mato Grosso. From 2011 to 2015, Goiás became the state with the highest mortality rate in the country, and Rio Grande do Sul reported its first dengue deaths. In 30 years, a total of 2682 dengue deaths occurred in males and 2455 in females, and an equal distribution between the sexes was observed. From 1986 to 2006, dengue deaths occurred predominantly in individuals over 15 years old, but this scenario changed in 2007-2008. After 2009, fatal cases on individuals above 15 years old became more frequent, with peaks in the years of 2010, 2013 and 2015.
The Brazil is experiencing a hyperendemic scenario, which has resulted in the co-circulation of the four DENV serotypes and with the increasing occurrence of severe and fatal cases. The disease surveillance and studies characterizing what has been reported overtime, are still important tools to better understand the factors involved in the disease outcome.
Full text
Available for:
DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK
Iron deficiency has particular importance in early childhood because of its impact on growth and development. Preventive food-based strategies of iron deficiency require knowledge of intakes and ...sources of iron.
This study aimed to assess daily iron intakes (DIIs) in 2013, to compare them with the dietary reference values, to assess their evolution since 1981, and to identify iron food sources among nonbreastfed French children younger than 3 years.
This was a nationwide cross-sectional survey conducted in 2013 in France to assess DIIs by means of comparing them with the dietary reference values. Parents’ reported diet diaries were collected for 3 nonconsecutive days.
Of the 1,184 children enrolled in the study, 1,035 nonbreastfed healthy children aged 0.5 to 35 months stratified into 11 age groups were included after informed consent was obtained from parents and according to a weighted quota sampling method.
DII from the different food sources and trends in their evolution from 1981 to 2013 was assessed.
Results are expressed as median with interquartile range and range and mean ± SD. Student t test was used with the 2-sided α level of significance set at 5%.
Mean ± SD DII was 6.7 ± 2.3 mg/d before 6 months, 8.2 ± 2.7 mg/d from 6 months to 1 year, and 7.0 ± 3.2 mg/d from 1 to 3 years. The prevalence of infants older than 7 months with a DII less than the dietary reference values was 52.5%, and that of young children was 30%. After slightly increasing until 2005, DIIs decreased thereafter. Formulas contributed to most of the DIIs up to 2 years of age. Cereals were the second largest contributor to DIIs, and meat accounted for a small part of iron intake.
A substantial number of children between 6 months and 3 years of age were at risk of insufficient iron intake. This risk increased from 2005 to 2013. The role of formula in ensuring iron intake is highlighted. More research on health outcomes of low iron intakes is needed.
Full text
Available for:
GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
The two most pressing challenges to agriculture worldwide are feeding a rapidly growing human population and developing more sustainable agricultural practices that do not threaten human and ...ecosystem health. We address these challenges through research in plant-herbivore interactions, specifically overcompensatory responses in potato to herbivore damage. While herbivory is usually detrimental to most crops, some potato cultivars can overcompensate and increase crop productivity up to two-fold in response to herbivore damage. However, biotic and abiotic factors are known to influence compensatory responses. Here we tested if compensatory plant responses to herbivory increase productivity of potatoes under field conditions along gradients of altitude and landscape simplification in 15 different farms. Our results suggest that compensatory plant responses could double the mean productivity of a potato farm in relation to the productivity of undamaged plants. The compensatory response is best predicted by pest pressure on a farm with potato plants having the maximum productivity when 10% of the tubers are damaged and decreasing in productivity as pest pressure increases. To a lesser extent an interaction between altitude and landscape simplification did affect the compensatory response, suggesting that abiotic factors play an important role in compensation. Our results suggest that overcompensation-based management practices could be used to maximize yields on working potato farms. Further research is required to determine action thresholds (i.e. the damage levels at which pest control needs to be enacted to maximize yields and minimize insecticide use) to develop more sustainable ways of increasing yields in the future.
Full text
Available for:
BFBNIB, FZAB, GIS, IJS, INZLJ, KILJ, NLZOH, NMLJ, NUK, OILJ, PNG, SAZU, SBCE, SBMB, UL, UM, UPUK, ZRSKP
Background. The duration of protection in children and adults resulting from hepatitis B vaccination is unknown. In 1981, we immunized a cohort of 1578 Alaska Native adults and children from 15 ...Alaska communities aged ≥6 months using 3 doses of plasma-derived hepatitis B vaccine. Methods. Persons were tested for antibody to hepatitis B surface antigen (anti-HBs) levels 30 years after receiving the primary series. Those with levels <10 mIU/mL received 1 booster dose of recombinant hepatitis B vaccine 2–4 weeks later and were then evaluated on the basis of anti-HBs measurements 30 days after the booster. Results. Among 243 persons (56%) who responded to the original primary series but received no subsequent doses during the 30-year period, 125 (51%) had an anti-HBs level ≥10 mIU/mL. Among participants with anti-HBs levels <10 mIU/mL who were available for follow-up, 75 of 85 (88%) responded to a booster dose with an anti-HBs level ≥10 mIU/mL at 30 days. Initial anti-HBs level after the primary series was correlated with higher anti-HBs levels at 30 years. Conclusions. Based on anti-HBs level ≥10 mIU/mL at 30 years and an 88% booster dose response, we estimate that ≥90% of participants had evidence of protection 30 years later. Booster doses are not needed.
Full text
Available for:
BFBNIB, NMLJ, NUK, PNG, SAZU, UL, UM, UPUK
Plants have numerous mechanisms to cope with the negative effects of herbivory, including plant resistance, structural and chemical traits that reduce damage, and plant tolerance, the ability to ...compensate for tissues lost. It has been argued that resistance and tolerance represent alternate strategies and thus there should be a trade-off between resistance and tolerance. However, resistance and tolerance are controlled via the same molecular pathway, the oxidative pentose phosphate pathway and the process of endoreduplication. Endoreduplication is the replication of the genome without mitosis, which leads to an increase in cellular chromosome number. Increasing chromosome number and therefore gene copy number provides a means of increasing gene expression that has been shown to enhance compensation following herbivory. By measuring glucosinolate levels and seed production following the removal of apical dominance in genotypes of Arabidopsis thaliana we show that there is a positive association between tolerance and induced chemical defense. Similarly, the direct association between tolerance and resistance is demonstrated by genetically manipulating the endoreduplication pathway. By overexpressing ILP1, a positive regulator of endoreduplication, and thus compensation, we experimentally increased glucosinolate production and tolerance in the Col-0 genotype. We suggest that many herbaceous plants that endoreduplicate (∼90%) would show a positive relationship between compensation and chemical defense, given that the molecular pathways are shared in common. We discuss these findings in light of contrasting results on measures of tolerance and resistance, given that the true relationship can be masked by ignoring genetic variation in endoreduplication and the timing of chemical measurement.
Full text
Available for:
BFBNIB, FZAB, GIS, IJS, INZLJ, KILJ, NLZOH, NMLJ, NUK, OILJ, PNG, SAZU, SBCE, SBMB, UL, UM, UPUK, ZRSKP
Plant tolerance of herbivory, i.e., the ability to recover after damage, is an important component of how plants cope with herbivores. Tolerance has long been hypothesized to be constrained ...evolutionarily by plant resistance to herbivores, traits that allow plants to cope with stressful growing conditions, and traits that influence the timing of damage in relation to reproduction. Variation in tolerance and resistance can be caused by differences in the identity of the plant (e.g., genotype, species, clade) and by the context of the herbivore threat (e.g., identity of the herbivore, type of damage it causes, abiotic conditions in which the plant is growing). To date, the vast majority of studies have explored trade-offs with tolerance within species. Here, we test hypotheses of constraints on tolerance using comparative approaches in a clade of mustards, emphasizing the variety of contexts in which damage is realistically tolerated. We estimated tolerance to leaf damage, tolerance to apical clipping at the bolting stage – simulating browsing –, and resistance to a specialist and generalist lepidopteran herbivore for a group of native mustards, grown in field soils unique to each population and in a common potting soil. Resistance to herbivores was soil dependent, while surprisingly, tolerance was not. Phylogenetic signal in resistance to specialist and generalist lepidopteran herbivores was present, but only when plants were grown in field soils. Tolerance had low phylogenetic signal. Tolerance to leaf damage was unrelated to tolerance to simulated browse. We found no evidence for a resistance-tolerance trade-off, and some evidence for a soil-dependent positive correlation between tolerance and resistance to both herbivores. Drought-tolerant species had poorer ability to tolerate browse damage, and earlier flowering species tended to be less tolerant to leaf damage. Our results suggest that tolerance trades off with traits that allow mostly annual, monocarpic Streptanthus (s.l.) to persist in drought-prone conditions but is largely unrelated to resistance to herbivores. Our study highlights a need for a new framework for tolerance to herbivory that explicitly acknowledges that the relationship among tolerance, resistance, and traits that ameliorate abiotic stress.
Full text
Available for:
BFBNIB, FZAB, GIS, IJS, INZLJ, KILJ, NLZOH, NMLJ, NUK, OILJ, PNG, SAZU, SBCE, SBMB, UL, UM, UPUK, ZRSKP
As a compensatory response to herbivory, plants may branch vigorously when the growth of dormant meristems is triggered by shoot damage. Undamaged plants, on the other hand, often restrain branching, ...and this limitation on growth can be considered a cost of tolerance to herbivory. Restrained branching is caused by apical dominance and may, alternatively, be associated with fitness benefits in competitive environments that favor fast vertical growth. To test these hypotheses regarding selection for restrained branching, we compared the performance of two subspecies of the biennial grassland herb Gentianella campestris; the tall, apically dominant ssp. campestris and the short, multi-stemmed ssp. islandica, which shows reduced apical dominance. For both subspecies, we manipulated the height of surrounding vegetation (competition) and damage intensity in grasslands of differing productivity (high, medium, low), and examined population growth rates using matrix population models combined with life table response experiments. In the absence of damage, ssp. campestris exhibited a higher population growth rate than ssp. islandica in the tallest vegetation, however with the growth rate still being below one. In the medium and low productivity environments where the vegetation was shorter, the population growth rate of ssp. islandica was considerably higher than that of ssp. campestris as long as no more than about 50% of the plants were damaged. When plants were damaged, the apically dominant ssp. campestris showed a positive population growth rate (λ > 1) and often overcompensatory seed production in all productivity levels, while ssp. islandica showed no compensation and therefore the population was predicted to decline (λ < 1). We conclude that restrained branching in Gentianella cannot be selected for by competition alone, but that episodes of apical damage are required to maintain the trait. Furthermore, because of the costs of restrained branching, apical dominance should be selected against in grasslands where competition and disturbance are low.
Full text
Available for:
BFBNIB, FZAB, GIS, IJS, INZLJ, KILJ, NLZOH, NMLJ, NUK, OILJ, PNG, SAZU, SBCE, SBMB, UL, UM, UPUK, ZRSKP
PDF
