Occupational Sex Identification and the Assessment of Male and Female Earnings Inequality

1978 ◽  
Vol 43 (6) ◽  
pp. 909 ◽  
Author(s):  
Steven D. McLaughlin
Botany ◽  
2021 ◽  
Author(s):  
Erin Jacqueline Gilchrist ◽  
Daniela Hegebarth ◽  
Shumin Wang ◽  
Teagen D. Quilichini ◽  
Jason Sawler ◽  
...  

We report the identification of two SNPs in Cannabis sativa that are associated with female and male plant sex phenotypes, and are located on the top arm of the X chromosome. High Resolution Melt analysis was used to develop and validate a novel, rapid method for sex identification in medical/recreational cannabis as well as in hemp. This method can distinguish between dioecious male (XY) and dioecious female (XX) cannabis plants with 100% accuracy, and can also be used to differentiate between male and female Humulus lupulus (hop) plants.


Author(s):  
Sylvia Dixon

Changes in the distribution of individual earnings between 1984 and 1995 are examined using data from the Household Economic Survey. Several dimensions of changes in the earnings structure are considered, including measures of aggregate earnings inequality, the gender earnings gap and shifts in relative earnings by level of educational attainment. Changes in the variance of earnings are decomposed to identify more clearly the source of the tendencies towards and against greater inequality. Evidence is found of a rise in hourly earnings inequality among males over the decade. However, the effects of this trend on the total earnings distribution were offset by a rise in the female share of employment and a narrowing of the gap between male and female average hourly earnings.


2018 ◽  
Vol 6 (2) ◽  
pp. 358
Author(s):  
Najla Irhamni Phasa ◽  
Dwi Kartika Apriyono ◽  
Masniari Novita

Mass disaster often happened in Indonesia. Sex identification is one of the important things for determining the identity of the victims. Sex can be identified based on the size of the teeth.  The study determine the differences of maxillary first molar and mandibular caninus tooth size between male and female student in Faculty of Dentistry University of Jember. The sample of this study consisted of 34 tooth models of female and 6 tooth models of male that measured in mesiodistal and bucolingual width of maxillary first molar and mandibular caninus with a digital caliper. Data were analyzed using Independent T-test. There were significant differences (p ≤ 0,05) of maxillary first molar and mandibular caninus size between male and female. Mesiodistal and bucolingual width of maxillary first molar respectively are 10.64 mm, 11.90 mm in males, and 10.16 mm, 11.16 mm in females. The mesiodistal and bucolingual width of mandibular caninus are 7.13 mm, 7.85 mm in males, and 6.66 mm, 7.08 mm in females. It can be concluded that there was a difference in size of maxillary first molar and mandibular caninus between male and female. Keywords: sex identification, masiodistal width, bucolingual width, maxillary first molar, mandibular caninus


2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Yu Zhang ◽  
Yuexing Wang ◽  
Wanying Zhou ◽  
Shimao Zheng ◽  
Wenhui Zhang

Abstract Background Kiwifruit (Actinidia chinensis var. Chinensis) is abundant with vitamin C and is a rapidly developing crop in China, New Zealand, and other countries. It has been widely used as a raw material for food and kiwifruit wine. Among these, A. chinensis var. chinensis and A. chinensis var. deliciosa are the most valuable kiwifruit in production. Kiwifruit is a typical dioecious plant and its female and male plants have different economic values. Therefore, sex identification, especially at the seedling stage, has important implications for the scientific planning of its production and economic benefits. However, the kiwifruit sex regulation mechanism is very complex and molecular studies are in the initial stages. Currently, there is not a universal and effective sex identification method for A. chinensis. Methods In this study, we used a label-free quantitative proteomics approach to investigate differentially accumulated proteins, including their presence/absence and significantly different levels of abundances during A. chinensis var. chinensis male and female flower bud development. Results A total of 6485 proteins were identified, among which, 203 were identified in male buds, which were mainly associated with phenylalanine metabolism, tyrosine metabolism, and plant hormone signal transduction. In female buds, 241 were identified, which were mainly associated with the ErbB signaling pathway, growth hormone synthesis, secretion and action, and mRNA surveillance pathway. A total of 373 proteins were significantly differentially accumulated proteins (fold change > 2; P < 0.05), of which, 168 were upregulated and 205 were downregulated. Significant differences between proteins involved 13 signaling pathways, most of which were involved in flavonoid biosynthesis, phenylpropanoid biosynthesis, and starch and sucrose metabolism. Protein interaction analysis showed that enriched protein nodes included cell division cycle 5-like protein, 40S ribosomal protein S8, ribosomal protein, and 40S ribosomal protein like, which interact with 35, 25, 22, and 22 proteins, respectively. Conclusions This study provide valuable information for cloning key genes that control sex traits and functionally analyze their roles, which lay a foundation to the development of molecular markers for male and female kiwifruit identification.


2018 ◽  
Vol 10 (3) ◽  
pp. 533-538
Author(s):  
Ibnu Baehaqi ◽  
Tyas Rini Saraswati ◽  
Enny Yusuf Wachidah Yuniwarti

Parakeets (Melopsittacus undulates) are classified parrot order Psittaciformes. Parakeets are monomorphic birds whose sex is difficult to be distinguished. Sex identification is very important for breeding efforts in order to increase the parakeet population. External morphology was determined to identify the sex of the birds. This research was conducted to determine the sex of parakeets (male and female). This study used five male and five female parakeets aged 4 months as the study objects. This study used the quantitative and qualitative method. Results of this study was verified by performing surgery to determine the sex of parakeet based on their reproductive organs. The t-test results of morphometric characteristics showed no significant different in the length of body, upper bill, lower bill, wing, tail, femur, tibial-tarsus, tarsometatarsus and digits as well as the body weight between male and female parakeets.  The color of the cere was useful to accurately determine sex in parakeets (blue in males and white in females). This research provided information to the public about the differences between male and female parakeets for the selection of good broodstock in order to increase their population in captivity.


2019 ◽  
Vol 239 (2) ◽  
pp. 277-304 ◽  
Author(s):  
Martin Biewen ◽  
Daniela Plötze

Abstract Using data from the German Structure of Earnings Survey (GSES), this paper studies the role of changes in working hours for the increase in male and female earnings inequality between 2001 and 2010. We provide both classic decompositions of the variance of log earnings into the variances of hours, wage rates and their covariance, and decompositions based on reweighting the conditional hours distribution. Depending on the inequality measure considered, our results suggest that between 10 and 30% of the increase in male earnings inequality and 37 to 47% of the increase in female earnings inequality can be explained by changes in working hours. In addition, a large part of the inequality increase can be accounted for by changes in the composition of person and firm characteristics.


2019 ◽  
Author(s):  
Maiken Hemme Bro-Jørgensen ◽  
Xénia Keighley ◽  
Hans Ahlgren ◽  
Camilla Hjorth Scharff-Olsen ◽  
Aqqalu Rosing-Asvid ◽  
...  

AbstractDetermining the male and female representation in zooarchaeological material from hunted animal species is essential, to fully investigate the effects and means of prehistoric hunting practices, and may further provide valuable biological information on past animal life-history, behaviour and demography. However, the fragmented nature of the zooarchaeological record and a lack of clear diagnostic skeletal markers, often prevents such inference. Here, we test the usability of the dog nuclear genome (CanFam3.1) for sex identification of pinnipeds. First, a contemporary sample set (n=72) of ringed seals (Pusa hispida), with known sex was used to test the genetic sex identification method. By quantifying the proportion of X chromosome reads, as the chrX/chr1 ratio, the ratios clustered in two clearly distinguishable sex groups. Of the 72 individuals, 69 were identified to the accurate sex, which proves a high reliability of the genetic method. Second, random down sampling of a subset of the ringed seal samples to different read number, suggests at least 5000 DNA sequence reads mapped to the reference genome as the lower limit for which this method is applicable. Finally, applying this standard, sex identification was successfully carried out on a broad set of ancient pinniped samples, including walruses (Odobenus rosmarus), grey seals (Halichoerus grypus) and harp seals (Pagophilus groenlandicus), which all showed clearly distinct male and female chrX/chr1 ratio groups.


Author(s):  
R. F. Bils ◽  
W. F. Diller ◽  
F. Huth

Phosgene still plays an important role as a toxic substance in the chemical industry. Thiess (1968) recently reported observations on numerous cases of phosgene poisoning. A serious difficulty in the clinical handling of phosgene poisoning cases is a relatively long latent period, up to 12 hours, with no obvious signs of severity. At about 12 hours heavy lung edema appears suddenly, however changes can be seen in routine X-rays taken after only a few hours' exposure (Diller et al., 1969). This study was undertaken to correlate these early changes seen by the roengenologist with morphological alterations in the lungs seen in the'light and electron microscopes.Forty-two adult male and female Beagle dogs were selected for these exposure experiments. Treated animals were exposed to 94.5-107-5 ppm phosgene for 10 min. in a 15 m3 chamber. Roentgenograms were made of the thorax of each animal before and after exposure, up to 24 hrs.


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