Morphology and taxonomy of Rhabdias spp. (Nematoda: Rhabdiasidae) from reptiles and amphibians of southern Ontario

1978 ◽  
Vol 56 (10) ◽  
pp. 2127-2141 ◽  
Author(s):  
M. R. Baker

Rhabdias americanus n.sp., Rhabdias ranae Walton, 1929, Rhabdias fuscovenosa (Railliet, 1899), and Rhabdias eustreptos (MacCallum, 1921) from amphibians and reptiles of southern Ontario are described. Rhabdias americanus n.sp. and R. ranae have two large lateral pseudolabia beside the oral opening whereas R. fuscovenosa and R. eustreptos each have six lips arranged in lateral groups of three. Rhabdias americanus n.sp. is distinguished from R. ranae by the shape of the pseudolabia and by the presence of a cuticular ring on the posterior border of the buccal cavity which is absent in the buccal cavity of R. ranae. Rhabdias fuscovenosa is distinguished from R. eustreptos by its significantly smaller size and by the shape of the posterior quarter of the body which is straight in R. fuscovenosa and corkscrew shaped in R. eustreptos. Rhabdias fuscovenosa is the only species examined in which eggs in the uteri of gravid hermaphrodites were always at an early cleavage stage of development. In other species examined most eggs in the uteri contained first-stage larvae.

2000 ◽  
Vol 8 (3) ◽  
pp. 241-287 ◽  
Author(s):  
GM Jones

The transfer of a blastocyst established the first human clinical pregnancy following in vitro fertilization (IVF). Nine years later Cohen et al. reported pregnancies resulting from the transfer of cryopreserved human blastocysts. However, it was another six years before the first report of births resulting from the transfer of human blastocysts produced in vitro appeared in the medical literature. In the intervening period clinics have opted to transfer embryos at the early cleavage stage to the uterus, despite the fact that in vivo the embryo does not enter the uterus until two to three days later at the morula to blastocyst stage of development. The viability and potential for implantation of blastocysts is high, as indicated by the finding that more than 60% of in-vivo-derived blastocysts, recovered by uterine lavage following artificial insemination of fertile donors, implant and develop into viable fetuses when transferred to recipients. This is in stark contrast to the 10–20% of in-vitro-produced embryos transferred at the early cleavage stage of development that result in a live-birth. This reduction in viability following transfer of in-vitro-derived early cleavage stage embryos may have several possible explanations: (1) a failure of implantation due to poor synchronization between the embryo and the uterine endometrium; (2) a hostile environment in the uterus for early cleavage stage embryos; (3) sub-optimal in vitro culture conditions which result in a reduction in embryo viability; (4) the assumption that all oocytes retrieved in an IVF cycle have an equal ability to develop into viable embryos; and (5) the failure to identify the most viable embryo in a cohort. Certainly, improving culture conditions and laboratory techniques for developing high quality blastocysts routinely in vitro will not only address many of the above questions but will also improve the quality and viability of earlier stages of embryo development.


1999 ◽  
Vol 202 (12) ◽  
pp. 1649-1654 ◽  
Author(s):  
R.I. Rowe ◽  
C.D. Eckhert

Boron is the only element known to be essential for plants, but only circumstantial evidence for essentiality exists in animals. We report here that boron is essential for the embryonic development of zebrafish (Danio rerio). Zebrafish were maintained in water with a boron concentration of 0.1 micromol l-1 or supplemented to a concentration of 45 micromol l-1 using ultrapure boric acid. Both groups were fed boron-depleted brine shrimp. This procedure depleted the boron content of the blastulas from low-boron parents to only 5 % of the boron content of the blastulas from boron-supplemented parents. Sperm from low-boron males successfully fertilized eggs from low-boron females, but 92 % of the embryos died within 10 days. The early cleavage stage of development was the most sensitive to boron deficiency. Of the fertilized embryos, 46% did not live to complete the blastula stage. Repletion of low-boron embryos during the first hour after fertilization rescued them from death. These observations provide strong evidence that boron is essential for zebrafish development.


Author(s):  
Dwi Darwati

Reproductive  health education should be given since early childhood by using language that is adapted to the stage of development. If you procrastinate and wait until the teenager it is already too late because in the days of the digital era, as now, all the information can be easily accessed by anyone including children early age. If the early childhood misinformed about their reproductive organs it would disrupt the physical and psychological development due to the wrong behavior in caring for and maintaining reproductive organs. Qur’an as the holy book of Muslims describes the steps of reproduction and  imparting education wisely as well as how to apply such education. This kind of education must be in accordance with the conditions of children and there should not be a lie about it We can also use media and methods such as pictures, songs, tap or other visual  media which can give clearer information, so that children can clearly see parts of the body, their characteristics, and how to treat and care them. The impropriate approach in conveying this kind of knowledge will be very dangerous for children. The provision of early age reproductive organs education can prevent the occurrence of deviant behavior as well as protect children from dangerous influence in early childhood development.


1996 ◽  
Vol 45 (1) ◽  
pp. 180 ◽  
Author(s):  
H. Nagashima ◽  
M. Kuwayama ◽  
C.G. Grupen ◽  
R.J. Ashman ◽  
M.B. Nottle

1995 ◽  
Vol 43 (1) ◽  
pp. 285 ◽  
Author(s):  
H. Nagashima ◽  
N. Kashiwazaki ◽  
R.J. Ashman ◽  
M.B. Nottle

1985 ◽  
Vol 63 (11) ◽  
pp. 2684-2688 ◽  
Author(s):  
R. C. Ko ◽  
L. Margolis ◽  
M. Machida

Pseudascarophis kyphosi n.gen., n.sp. (Nematoda: Cystidicolidae) is described for specimens collected from the stomach of Kyphosus cinerascens (Forskål) from the southeast coast of Japan. The new genus is distinguished from all other genera of Cystidicolidae by its oral structure (presence of four submedian, longitudinally directed, digitiform processes in the buccal cavity projecting slightly beyond the oral opening; smooth margined mouth; absence of submedian labia and sublabia; and unique shape of the medial region of the pseudolabia) and numbers of caudal papillae in the male (3 pairs preanal, 7 pairs postanal).


2021 ◽  
pp. 8-14
Author(s):  
Светлана Тарасовна Быкова ◽  
Тамара Григорьевна Калинина ◽  
Ирина Макаровна Московская

Полноценное, сбалансированное питание - основной фактор в формировании здоровья детей, когда в организме наиболее интенсивно протекают процессы роста и развития, формируются и созревают многие органы и системы, совершенствуются их функции. В статье приведены основные направления исследований зарубежных и отечественных ученых по лечению генетических заболеваний, таких как фенилкетонурия. Одним из приоритетных направлений в области здорового питания населения России в соответствии со Стратегией научно-технологического развития РФ до 2030 г. является развитие производства пищевых продуктов, обогащенных незаменимыми ингредиентами, специализированных продуктов детского питания, продуктов функционального назначения, диетических пищевых продуктов и биологически активных добавок. По данным ВОЗ от структуры питания на 70 % зависят здоровье и физическое развитие детей и подростков. Фенилкетонурия (ФКУ) - наследственное заболевание, вызывающее нарушение метаболизма аминокислоты фенилаланина у ребенка, одно из первых, рекомендованных ВОЗ для ранней диагностики у новорожденных. Отсутствие лечения вызывают серьезное поражение центральной нервной системы, отставание в умственном и физическом развитии. Особенностью современного этапа развития диетотерапии для детей, страдающих различными заболеваниями, в том числе наследственными, является разработка качественных функциональных продуктов питания, способствующих сохранению и улучшению здоровья ребенка за счет регулирующего и нормализующего воздействия на организм с учетом его физиологического состояния и возраста. Данные продукты можно широко использовать в практике лечебного питания не только в составе гипофенилаланиновой диеты, но и при любых заболеваниях, требующих ее соблюдения. В настоящее время единственным методом лечения ФКУ является диетотерапия, организованная с первых дней жизни с использованием специализированных смесей без фенилаланина. Из питания исключаются высокобелковые продукты растительного и животного происхождения. Целью лечебного воздействия диеты на ребенка является поддержка концентрации фенилаланина (ФА) в крови в пределах 2-12 мг на 100 мл в зависимости от возраста ребенка. Full-fledged balanced nutrition is the main factor in the formation of children's health, when the processes of growth and development are most intense in the body, many organs and systems are formed and mature, and their functions are improved. The article presents the main research areas of foreign and domestic scientists on the treatment of genetic diseases, such as phenylketonuria. One of the priority areas in the field of healthy nutrition of the Russian population in accordance with the Strategy for Scientific and Technological Development of the Russian Federation until 2030 is the development of the production of food products enriched with essential ingredients, specialized children's food products, functional products, dietary food products and biologically active additives. According to WHO, the health and physical development of children and adolescents depends on the nutritional structure by 70%. Phenylketonuria (PKN) - an inherited disease that causes impaired metabolism of the amino acid phenylalanine in a child - is one of the first recommended by WHO for early diagnosis in newborns. Lack of treatment causes serious damage to the central nervous system, a lag in mental and physical development. A feature of the modern stage of development of dietary therapy for children suffering from various diseases, including hereditary ones, is the development of quality functional food products that contribute to the preservation and improvement of the health of the child, due to the regulatory and normalizing effect on the body, taking into account its physiological state and age. These products can be widely used in the practice of therapeutic nutrition not only in the sastava of the hypophenylalanine diet, but also for any diseases requiring its observance. Currently, the only method of treating PKN is diet therapy, organized from the first days of life using specialized mixtures without phenylalanine. High-protein products of vegetable and animal origin are excluded from nutrition. The goal of the therapeutic effect of the diet on the child is to maintain the concentration of phenylalanine (FA) in the blood in the range of 2-12 mg per 100 ml, depending on the age of the child.


Nematology ◽  
2021 ◽  
pp. 1-22
Author(s):  
Azadeh Gharahkhani ◽  
Ebrahim Pourjam ◽  
Daniel Leduc ◽  
Majid Pedram

Summary The Desmodoridae is a diverse and widespread family of free-living nematodes. Here, we provide the first record of the group in the Persian Gulf and describe three new species: Metachromadoroides sinuspersici sp. n., Zalonema iranicum sp. n. and Z. supplementorum sp. n. Metachromadoroides sinuspersici sp. n. is characterised by finely annulated cuticle, short and stout cephalic sensilla, amphidial fovea on cuticular thickening, pharyngeal bulb well developed and partitioned into three sections, absence of precloacal supplements, and presence of 6-8 pairs of rounded postcloacal papillae. Zalonema iranicum sp. n. is characterised by papilliform subcephalic sensilla (best observed with SEM), convex cephalic capsule, large multispiral amphidial fovea with 4-5 turns in both males and females, buccal cavity with one ventrosublateral and two dorsal teeth and posterior body of males with lateral alae extending from the last third of the body to the cloacal aperture and ventral alae extending 1395-2250 μm anterior to the cloacal aperture, and no precloacal supplements. Zalonema supplementorum sp. n. is characterised by four subcephalic sensilla 1-2 μm long, multispiral amphidial fovea with three turns in both males and females, buccal cavity with one dorsal and two ventrosublateral teeth, males with lateral alae present on each side of body from posterior half of body to cloacal aperture, ventral alae extending 942-1257 μm anterior to cloacal aperture, strongly cuticularised spicules 41-43 μm long, and 12-16 precloacal supplements. Near full length SSU and partial D2-D3 LSU sequences are provided for M. sinuspersici sp. n. and Z. iranicum sp. n., and the COI sequence is provided for Z. iranicum. The SSU phylogeny suggests a close relationship between M. sinuspersici sp. n. and Metachromadora and Metachromadoroides species and the monophyly of Zalonema (after currently available data). The LSU phylogeny suggests an affinity between Metachromadoroides and Zalonema with Spirinia and Acanthopharynx, respectively.


1971 ◽  
Vol 26 (8) ◽  
pp. 816-821 ◽  
Author(s):  
Larry E. Bockstahler

Incorporation of uridine in cleavage stage eggs of the sea urchin Paracentrotus lividus was investigated. It was shown by ion exchange and thin layer chromatography that most of the uridine taken up during the 16-cell stage was converted into UTP with some incorporation into UDP and UMP. Conversion of uridine to these phosphorylated nucleosides occurred throughout early cleavage stages. A very small amount of uridine taken up by cleavage stage eggs is incorporated into RNA heterogeneous in size. This RNA was examined by polyacrylamide gel electrophoresis.


2019 ◽  
Vol 4 (2) ◽  
pp. 114-129
Author(s):  
Hamam Burhanuddin

The study in this paper are explain about the studies of medical (medicine) blood type have the same relationship to human character because the blood producing antibodies and antigens. It could determine a person helpless hold strong or weak body, has an allergy to something or not, in the blood also contains various nutrients (like protein) and also the oxygen being supplied to the brain and nerves and body affect performance someone will then be emanated from the attitude of the person and social interaction. As has been explained, but keep in mind, there is blood in the genes, the nature of which is carried in the body/genotif rightly so it is, but we can not ignore the fenotif/nature arising or visible, this trait appear due to interaction between genes and the environment, so even if the person is smart in the intelligentsia and emotional, but grew up in a bad environment is going to be a bad trait. The theory of personality based on blood type can be used as a reference in parenting children through an understanding of the fundamental principles of the application of personality accompanied by parenting. Furthermore, the taking of steps in the care tailored to the stage of development of the child, in the Qur'an explicitly did not mentioned paragraph that discusses about blood type, but in the Qur'an there are blood (ad-Dam), Islamic studies in the study of Children is seen as a mandate from God, forming 3-dimensional relationships, with parents as the central figure. First, her parents relationship with God that is backed by the presence of children. Second, the relationship of the child (which still need a lot of guidance) with God through his parents. Third, the relationship of the child with both parents under the tutelage and guidance of God.


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