scholarly journals Assessing the lockdown effect from excess mortalities

Author(s):  
Alexej Weber

AbstractBackground and AimsThe reported case numbers of COVID-19 are often used to estimate the reproduction number or the growth rate. We use the excess mortality instead, showing the difference between most restrictive non-pharmaceutical interventions (mrNPIs) and less restrictive NPIs (lrNPIs) with respect to the growth rate and death counts.MethodsWe estimate the COVID-19 growth rate for Sweden, South Korea, Italy and Germany from the excess mortality. We use the average growth rate obtained for Sweden and South Korea, two countries with lrNPIs, to estimate additional death numbers in Germany and Italy (two countries with mrNPIs) in a hypothetic lrNPIs scenario.ResultsThe growth rate estimated from excess mortality decreased faster for Germany and Italy than for Sweden and South Korea, suggesting that the mrNPIs have a non-negligible effect. This is not visible when the growth rate is calculated using the reported case numbers of COVID-19. This results in approximately 4 500 and 12 000 more death numbers for Germany and Italy, respectively.ConclusionThe reproduction numbers or growth rates obtained from reported COVID-19 cases are most likely biased. Expanding testing capacity led to an overestimation of the growth rate across all countries analyzed, masking the true decrease already visible in the excess mortality. Using our method, a more realistic estimate of the growth rate is obtained. Conclusions made for the reproduction number derived from the reported case numbers like the insignificance of most restrictive non-pharmaceutical interventions (lockdowns) might be wrong and have to be reevaluated using the growth rates obtained with our method.

2010 ◽  
Vol 138 (11) ◽  
pp. 1559-1568 ◽  
Author(s):  
J. M. GRAN ◽  
B. IVERSEN ◽  
O. HUNGNES ◽  
O. O. AALEN

SUMMARYInfluenza can be a serious, sometimes deadly, disease, especially for people in high-risk groups such as the elderly and patients with underlying, severe disease. In this paper we estimated the influenza-related excess mortality in Norway for 1975–2004, comparing it with dominant virus types and estimates of the reproduction number. Analysis was done using Poisson regression, explaining the weekly all-cause mortality by rates of reported influenza-like illness, together with markers for seasonal and year-to-year variation. The estimated excess mortality was the difference between the observed and predicted mortality, removing the influenza contribution from the prediction. We estimated the overall influenza-related excess mortality as 910 deaths per season, or 2·08% of the overall deaths. Age-grouped analyses indicated that the major part of the excess mortality occurred in the ⩾65 years age group, but that there was also a significant contribution to mortality in the 0–4 years age group. Estimates of the reproduction number R, ranged from about 1 to 1·69.


1967 ◽  
Vol 47 (3) ◽  
pp. 211-216
Author(s):  
A. D. L. Gorrill

Three groups of 10 Ayrshire bull calves born in May and June, 1963 were placed on pasture at 2 weeks of age, after weaning at 55 kg body weight, or at 15 weeks of age. Half the calves in each group also received whole oats while on pasture to a maximum of 1.4 kg/day. Prior to going on pasture, calves were fed a starter ration and timothy hay. The calves were removed from pasture at 21 weeks of age and fed hay and grain until 52 weeks of age. There were no differences between groups in rate of gain from 1 week of age to weaning, the average growth rate for all calves being 427 g/day. Calves put on pasture after weaning gained 223 g/day from weaning to 15 weeks of age, and calves put on pasture at 15 weeks of age gained only 177 g/day from 15 to 21 weeks of age. Weight gains during these same two periods for calves put on pasture at 2 weeks of age were 432 and 500 g/day, respectively. Feeding oats to calves on pasture did not increase growth rates to weaning or to 15 weeks of age. Average body weights at 52 weeks of age were 251, 228, and 242 kg, respectively for calves started on pasture at 2 weeks of age, after weaning, and at 15 weeks of age.


2021 ◽  
Author(s):  
Kenneth Bodin ◽  
Joacim Rocklov

A new virus variant of SARS-COV-2 has had a profound impact on society while governments have taken action to limit its impacts by enforcing lockdowns and limiting spread from the UK to other countries. Variants with mutations in the virus genome are likely to occur, but do not always associate to significant changes in the biology of the virus, or the disease. For the variant VOC 202012/01 (also referred to as B.1.1.7), however, preliminary reports indicate it may be more transmissible. Here we use a simulation model calibrated to the inherent random fluctuating transmission pattern of COVID-19 to investigate what the probability may be for detecting more transmissible virus variants post facto. We find that post facto identification of successful virus variants of SARS-COV-2 are likely to exhibit growth rates that are substantially larger than the average growth rate. This finding has implications for interpreting growth rate and transmissibility of new virus variants.


Author(s):  
P.D. Muir ◽  
N.B. Smith ◽  
J.C. Lane

Abstract This study set out to demonstrate what could be achieved in terms of lamb growth rates under controlled experimental conditions. Ewes with high breeding values for progeny growth rate were selected from within a flock of 900 ewes and mated using AI to a ram with a high breeding value for progeny growth rate. Of the 70 ewes mated, 44 reared 75 lambs (170%) to 12 weeks of age. Lamb birth weights averaged 4.8 kg. Ewes and lambs were fed on pasture covers between 1800 and 2600 kg DM/ha throughout lactation. At 12 weeks of age, the average weight of all lambs in the mob averaged 39 kg. Average growth rate of all lambs from birth to 12 weeks was 409 g/d, with single, twin and triplet lambs averaging 437, 407 and 380 g/d respectively. The best individual lamb grew at 549 g/d and weighed 51.6 kg at 12 weeks. This demonstration sets a new benchmark for both mob and individual lamb growth rates and indicates what can be achieved with a combination of genetics for growth, ewes with good milking ability and good pasture feeding conditions. Keywords: breeding value, lamb growth rate, milking ability, pasture quality


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 451d-451
Author(s):  
Nolan Farace ◽  
C.E. Johnson

Pecan seedlings were randomly selected and divided into two lots according to size. Seven rates and three sources of nitrogen based fertilizers were applied four times starting on 6 May, 20 June, 4 July, and 15 Aug. Leachates were taken 3 weeks after each application. The pH range after the first application ranged from 6.0 to 7.0. After the fourth the pH had dropped to a range of 5.0 to 6.0. The TDS ranged from 0 to 6.0 mS after the first application to a 2.1 to 0.5 mS after the last application. Growth rates varied slightly among treatments. The average growth rate among seedlings was only slightly affected by nitrogen fertilize rates. Within 12 weeks the average growth was 1.3 mm. There were only slight differences in growth between the low and high rates of NH4·NO3 fertilizer. The growth rate decreased somewhat in response to increased rates of application of Ca·NO3.


2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Chien Wei Wu ◽  
Wei Zhan Hung

The purpose of this study is to propose a new economic index, namely, real national income average growth rate (RNIAGR), which measures the performance of economic growth with consideration for income distribution. This study also develops another new economic index, called five-scale real national income average growth rate (FSRNIAGR), which simplifies the calculation of RNIAGR. The merits of these new indexes are discussed to justify their efficacy. This paper also justifies the use of proposed index by showing that this index can actually measure the ordering of social welfare. To highlight the difference between this new index and the traditional ones, this paper compares the index with real economic growth rate using the data of Taiwan. In addition, this paper shows that when the real growth stagnates or even declines, this new index indicates that income distribution deteriorates.


2020 ◽  
Author(s):  
Alexander Adamou ◽  
Yonatan Berman ◽  
Ole Peters

Economic growth is measured as the rate of relative change in gross domestic product (GDP) per capita. Yet, when incomes follow random multiplicative growth, the ensemble-average (GDP per capita) growth rate is higher than the time-average growth rate achieved by each individual in the long run. This mathematical fact is the starting point of ergodicity economics. Using the atypically high ensemble-average growth rate as the principal growth measure creates an incomplete picture. Policymaking would be better informed by reporting both ensemble-average and time-average growth rates. We analyse rigorously these growth rates and describe their evolution in the United States and France over the last fifty years. The difference between the two growth rates gives rise to a natural measure of income inequality, equal to the mean logarithmic deviation. Despite being estimated as the average of individual income growth rates, the time-average growth rate is independent of income mobility. (Stone Center on Socio-Economic Inequality Working Paper)


Author(s):  
Elena Vasechkina ◽  
Elena Vasechkina ◽  
Irina Kazankova ◽  
Irina Kazankova

This study presents the results of field and laboratory-based experiments performed to determine the mussel density effect on an individual mollusk’s growth and clearance rates. We measured the weight and length growth rates of single and aggregated mussels exposed into the sea for three monthly periods in summer and autumn 2015. The sample group contained 140 mollusks from natural populations within the length range of 15-20 mm. The average growth rate of aggregated mussels was almost the same as the growth rate of single ones. Clearance rate of single and aggregated mussels was measured in the laboratory using indirect method. There were selected 5 groups of mussels within the length ranges: 12-16 mm, 17-18 mm, 18-25 mm, 22-23 mm, and 35-38 mm. The clearance rate was measured for each mussel from the group and then for the whole group aggregated in a clump. Water temperature and seston concentration were the same for single and clumped mollusks. The volume of water in chambers was proportional to the weight of mussels put in water. The ratio of aggregated and single mussels’ clearance rates varied from 0.48 to 0.85 at the same density of aggregation and without regard to the animal size. Significant individual variability was recorded in all field and laboratory-based experiments.


Author(s):  
Elena Vasechkina ◽  
Elena Vasechkina ◽  
Irina Kazankova ◽  
Irina Kazankova

This study presents the results of field and laboratory-based experiments performed to determine the mussel density effect on an individual mollusk’s growth and clearance rates. We measured the weight and length growth rates of single and aggregated mussels exposed into the sea for three monthly periods in summer and autumn 2015. The sample group contained 140 mollusks from natural populations within the length range of 15-20 mm. The average growth rate of aggregated mussels was almost the same as the growth rate of single ones. Clearance rate of single and aggregated mussels was measured in the laboratory using indirect method. There were selected 5 groups of mussels within the length ranges: 12-16 mm, 17-18 mm, 18-25 mm, 22-23 mm, and 35-38 mm. The clearance rate was measured for each mussel from the group and then for the whole group aggregated in a clump. Water temperature and seston concentration were the same for single and clumped mollusks. The volume of water in chambers was proportional to the weight of mussels put in water. The ratio of aggregated and single mussels’ clearance rates varied from 0.48 to 0.85 at the same density of aggregation and without regard to the animal size. Significant individual variability was recorded in all field and laboratory-based experiments.


1981 ◽  
Vol 11 (3) ◽  
pp. 689-695 ◽  
Author(s):  
Craig G. Lorimer

Mortality and growth rates of trees in various crown classes and size classes were analyzed from 40-year permanent plot records of slope and ravine forest dominated by chestnut oak (Quercusprinus L.) and northern red oak (Quercusrubra L.). Average 5-year mortality rates for suppressed trees ≥2.5 cm dbh of chestnut oak and red oak in the slope forest were 26 and 45%, respectively. None of the suppressed red oaks survived the 40-year period, compared with 14% of the chestnut oaks and 33% of the red maples (Acerrubrum L.). Mortality of oak trees in the intermediate crown class was less than half that of suppressed trees, but still much higher than that of maples and birches on the tracts. Survival was reasonably high for oaks as long as the top of the crown was receiving direct sunlight, but the expected 40-year survival rate of red oaks in such a position is only 20%, with an average growth rate of 1.0 mm in diameter per year. Curves and equations expressing average mortality and growth rates at various levels of competition are presented for each species.


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