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Spurious Relationship of AR(P) Stable Sequences in Presence of Trends Breaks 趋势断裂存在下AR(P)稳定序列的伪关系
Pub Date : 2013-06-26 DOI: 10.3968/J.ANS.1715787020120602.2560
Cong Yu, Xuefeng Wang, J. Ma
This paper analyzes spurious regression phenomenon involving AR(p) stable processes with trend breaks. It shows that when those time series are used in ordinary least squares regression, the convenient t-ratios procedures wrongly indicate that the spurious relationship is present as the pair of independent stable series contains trend changes. The spurious relationship becomes stronger as the sample size approaches to infinite. As a result, spurious effects might occur more often than we previously believed as they can arise even between AR(p) stable series in present of trend breaks.
本文分析了具有趋势中断的AR(p)稳定过程的伪回归现象。结果表明,当这些时间序列用于普通最小二乘回归时,方便的t比率程序错误地表明,由于独立稳定序列对包含趋势变化,因此存在虚假关系。当样本量接近无穷大时,虚假关系变得更强。因此,虚假效应可能比我们以前认为的更频繁地发生,因为它们甚至可以出现在当前趋势中断的AR(p)稳定序列之间。
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引用次数: 0
Fossilised Neanderthal Matrilineal Societies, Neo-Neanderthal Hybrids, Endosymbiotic Actinidic Archaea and Civilisational Diseases 尼安德特人母系社会化石,新尼安德特混血儿,内共生的放射线古细菌和文明疾病
Pub Date : 2013-06-26 DOI: 10.3968/J.ANS.1715787020120602.2432
K. A. Ravikumar, P. A. Kurup
Neanderthal genes have been related to human disease. The human genome has been found to have up to 10 percent Neanderthal genes. The pyruvate dehydrogenase gene as well as those coding for MHC alleles are of Neanderthal origin. Neanderthal genes have been related to autism and autoimmune disease. There is high incidence of autism and Neanderthal anthropometry in the matrilineal and Dravidian language speaking nair community of Kerala. The autistic brain is comparable to the large-sized Neanderthal brain. Metabolic patterns were compared among the following groups: matrilineal nairs, non nairs, autism, schizophrenia and systemic diseases to find out a pattern of Neanderthal metabolism. The aim of the study aimed to detect fossilized Neanderthal matrilineal societies and new Neanderthal hybrids in relation to civilisational diseases. Four groups, 25 numbers in each group were chosen for the study—the autistic population diagnosed according to DSM criteria, the normal nair population, the normal non-nair population and civilisational disease group including metabolic syndrome x, alzheimer’s disease, cancer, schizophrenia and multiple sclerosis. Archaeal cholesterol catabolism as well as PDH activity, glycolytic pathway, the GABA shunt, porphyrins, homocysteine and ammonia metabolism were studied to find out a pattern of Neanderthal metabolism. Autistic metabolonomic patterns include low pyruvate dehydrogenase activity, mitochondrial dysfunction, GABA shunt, Warburg glycolytic phenotype, hyperammonemia, hyperhomocysteinemia, porphyria, low cholesterol/bile acid levels and a similar pattern is seen in the normal nair population of Kerala. Neanderthal metabolonomic patterns include a low efficiency PDH activity. Autistic and matrilineal societies like nair can be considered as remnants of the Neanderthals. The autistic and nair population have increased cytochrome F420 activity suggestive of endosymbiotic archaeal growth resulting in PDH and mitochondrial suppression. The increased archaeal digoxin synthesis later on shuts down the metabolic machinery the neuronal and other tissue cells and the human cells and tissues including the brain are taken over by an atavistic actinidic colony network. This leads onto a Neanderthal hybrid zombie syndrome. The increased archaeal growth in ice age conditions contributed to the neanderthal evolution and similar endosymbiotic archaeal growth related to global warming leads to neanderthalisation of homo sapiens. The autistic and neanderthalic metabolonomic patterns are also seen in civilisational diseases like syndrome X, schizophrenia, cancer, multiple sclerosis and alzheimer’s disease. The results suggest neanderthalisation of the humans due to global warming and archaeal growth. The Neanderthalisation of the human species is the basis of the global autistic, schizophrenic and civilisational disease epidemic—epidemic Neanderthal hybrid zombie syndrome. The matrilineal societies are fossilized Neanderthal remnants
尼安德特人的基因与人类疾病有关。研究发现,人类基因组中有多达10%的尼安德特人基因。丙酮酸脱氢酶基因以及那些编码MHC等位基因的基因是尼安德特人的起源。尼安德特人的基因与自闭症和自身免疫性疾病有关。在喀拉拉邦的母系和说德拉威语的奈尔社区,自闭症和尼安德特人人体测量学的发病率很高。自闭症患者的大脑与尼安德特人的大大脑相当。研究人员比较了以下人群的代谢模式:母系神经症患者、非神经症患者、自闭症患者、精神分裂症患者和全身性疾病患者,以找出尼安德特人的代谢模式。这项研究的目的是检测尼安德特人母系社会化石和与文明疾病有关的新尼安德特混血儿。选取四组,每组25人,分别为DSM诊断的自闭症人群、正常皮肤人群、正常非皮肤人群和包括代谢综合征x、阿尔茨海默病、癌症、精神分裂症和多发性硬化症在内的文明疾病组。研究了古细菌胆固醇分解代谢以及PDH活性、糖酵解途径、GABA分流、卟啉、同型半胱氨酸和氨代谢,以找出尼安德特人的代谢模式。自闭症的代谢模式包括低丙酮酸脱氢酶活性、线粒体功能障碍、GABA分流、Warburg糖酵解表型、高氨血症、高同型半胱氨酸血症、卟啉症、低胆固醇/胆酸水平,在喀拉拉邦的正常人群中也有类似的模式。尼安德特人的代谢模式包括低效率的PDH活性。像奈尔这样的自闭和母系社会可以被认为是尼安德特人的残余。自闭症和非自闭症人群细胞色素F420活性增加,提示内生古细菌生长导致PDH和线粒体抑制。古细菌地高辛合成的增加随后关闭了代谢机制,神经元和其他组织细胞以及人类细胞和组织,包括大脑,被一个返祖的放光细胞集落网络接管。这就引出了尼安德特人混血僵尸综合症。冰河时期古细菌的增长促进了尼安德特人的进化,而与全球变暖相关的类似内生古细菌的增长导致了智人的尼安德特化。自闭症和尼安德特人的代谢模式也出现在X综合征、精神分裂症、癌症、多发性硬化症和阿尔茨海默病等文明疾病中。结果表明,由于全球变暖和古细菌的生长,人类的尼安德特人化。人类物种的尼安德特化是全球自闭症,精神分裂症和文明疾病流行的基础-流行病尼安德特人混合僵尸综合症。母系社会是尼安德特人遗存的化石,而尼安德特人的混血儿导致了文明疾病。
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引用次数: 0
Thermodynamics Since Einstein 爱因斯坦以来的热力学
Pub Date : 2013-06-26 DOI: 10.3968/J.ANS.1715787020120602.2121
Chih-Yueh Wang
Relativistic thermodynamics is a relatively unknown theory. Thermodynamic laws apply only to quasi-static processes that quickly change between states that are in a long-term equilibrium. However, special relativity postulates that the propagation speed of physical signals is constrained, thus limiting the speed of change in thermal states. Einstein was especially interested in the concept of temperature and the transformation formula of thermodynamic quantities in a moving frame of reference, having inspired numerous investigations for two centuries. This article reviews the historical development of relativistic thermodynamics since Einstein, beginning from the initial idea of Planck-Einstein in which a moving body warms up, to the notion of Blanusa-Ott in which a moving body cools down, and to that of Landsberg in which the temperature remains unchanged—depending on how the observer’s thermometer is defined. Current research focuses on identifying the correct form of relativistic Maxwell distribution to validate the related theory. Recent computational results using molecular dynamic simulations and their relevance to astrophysics are outlined as well.
相对论热力学是一个相对不为人知的理论。热力学定律只适用于在长期平衡状态之间快速变化的准静态过程。然而,狭义相对论假定物理信号的传播速度是受限的,因此限制了热态变化的速度。爱因斯坦对温度的概念和运动参照系中热力学量的变换公式特别感兴趣,两个世纪以来激发了无数的研究。本文回顾了自爱因斯坦以来相对论热力学的历史发展,从普朗克-爱因斯坦提出的运动物体变暖的最初想法,到布兰萨-奥特提出的运动物体变冷的概念,再到兰茨伯格提出的温度保持不变的概念,这取决于观察者的温度计是如何定义的。目前的研究重点是确定相对论麦克斯韦分布的正确形式,以验证相关理论。本文还概述了分子动力学模拟的最新计算结果及其与天体物理学的相关性。
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引用次数: 7
Nonlinear Genetics Inbreeding and Genetic Load 非线性遗传、近交与遗传负荷
Pub Date : 2013-03-26 DOI: 10.3968/4164
Volobuev Andrey Nikolaevich, Romanchuk Peter Ivanovich, Malishev Vladimir Kirikovich
Comparison of concepts of occurrence and accumulation of the genetic load in result of inbreeding for a family tree and a population is given. It is shown that for the population the analysis of the genetic load concerns to area of nonlinear genetics. The nonlinear differential equation of the second order being the special case of the Hardy-Weinberg law at presence inbreeding for the population is found. The numerical decision of this equation allowed to find the law of increase of recessive allele frequency in the population is given. Some aspects of the traditional theory of the genetic load are considered.
比较了家族树和群体近亲繁殖引起的遗传负荷的发生和积累的概念。结果表明,对群体的遗传负荷分析涉及非线性遗传领域。研究了群体近交时Hardy-Weinberg定律的二阶非线性微分方程。给出了该方程的数值求解方法,从而找到了群体中隐性等位基因频率增加的规律。考虑了遗传负荷传统理论的一些方面。
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引用次数: 2
Linear Body Measurements and Carcass Characteristics of Rabbits Fed Orange (Citrus sinensis) Waste Meal as Alternative Fibre Source in Diet 以柑桔废粕为饲粮替代纤维源家兔的线性体测量和胴体特性
Pub Date : 2013-03-26 DOI: 10.3968/J.ANS.1715787020130601.2407
A. J. Henry, G. William, O. Effiong
A study was conducted to assess the effect of orange waste meal as an alternative fibre source on linear body measurements of rabbits. Twenty-four (24) weaned rabbits of cross breed and mixed sexes were used for the study. Experimental animals which weighed between 676.67g to 686.67g were allotted to four dietary treatments in a completely randomized design. Results of the study showed that head length (HL), body length (BL), heart girth (HG), length of hind limb (LHL) and length of fore limb (LFL) differed (p 0.05) statistically between the treatment groups. At the end of the experimental period of ten weeks, rabbits fed diet T 4 (endocarp + mesocarp) recorded higher (p 0.05) influenced by dietary treatments. Therefore, rabbits can effectively utilize orange waste meal as an alternative fibre source without adverse effects on linear body measurements and carcass characteristics.
本研究评价了橙废粉作为替代纤维源对家兔线性体测量的影响。试验选用24只杂交和杂交断奶兔。体重在676.67 ~ 686.67g之间的实验动物采用完全随机设计,分为4组饮食处理。研究结果显示,治疗组间头长(HL)、体长(BL)、心围(HG)、后肢长(LHL)、前肢长(LFL)差异有统计学意义(p 0.05)。在试验期10周结束时,饲粮t4(内果皮+中果皮)对试验兔的影响显著(p 0.05)。因此,家兔可以有效地利用橙色废粉作为替代纤维来源,而不会对线性体测量和胴体特性产生不利影响。
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引用次数: 1
Effect of External Electric Field Upon Selected Model Dipeptides 外电场对选定模型二肽的影响
Pub Date : 2013-03-26 DOI: 10.3968/4294
J. Mazurkiewicz, P. Tomasik
Effect of external electric field (EEF) of 0.001, 0.005 and 0.01 a.u. upon molecular energy, charge distribution and dipole moments of non-dissociated and inner salt forms of selected dipeptides formed from alanine (Ala), glutamic acid (GluA), and ornithine (Orn) that is, Ala-Ala, Ala-GluA, GluA-Ala, Ala-Orn, Orn-Ala involving α-amino group of Orn and Orn-Ala involving δ-amino group of Orn. For that purpose HyperChem 8.0 software was used together with the AM1 method for optimization of the conformation of the molecules in a computer vacuum.
0.001、0.005和0.01 a.u.的外加电场(EEF)对丙氨酸(Ala)、谷氨酸(GluA)和鸟氨酸(Orn)形成的二肽的非解离和内盐态的分子能量、电荷分布和偶极矩的影响,即Ala-Ala、Ala-GluA、GluA-Ala、Ala-Orn、涉及Orn α-氨基的Orn-Ala和涉及Orn δ-氨基的Orn-Ala为此,使用HyperChem 8.0软件和AM1方法在计算机真空中优化分子的构象。
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引用次数: 1
Effects of Silica Ceramic Particle Sizes on the Properties of Recycled Polyethylene Composites 二氧化硅陶瓷粒径对再生聚乙烯复合材料性能的影响
Pub Date : 2013-03-26 DOI: 10.3968/J.ANS.1715787020130601.1630
J. Agunsoye, S. I. Talabi, V. Aigbodion, A. Olumuyiwa
Particulate filled polymeric composites are becoming attractive because of their wide applications and lower production cost. To evaluate the possibility of using waste silica based ceramic materials as reinforcing filler in recycled polyethylene (PE) composite, the effect of  ceramic (PC) particle sizes on the mechanical, wear and thermal behaviours of polyethylene (PE) composites were investigated at  (2wt% filler) and grain sizes (40µm-150µm). The wear behaviour was characterized using analysis of variance (ANOVA) and linear regression to determine the main and interactive effects of the process parameters such as speed, load and time on the wear behaviour of the fabricated PE-PC composites. Test results show that the decreasing the ceramic particles 150µm-40µm improved the mechanical, wear and thermal properties of the recycled polyethylene (PE) composites. Factorial design of the experiment can be successfully employed to describe the wear behavior  of the samples and developed linear equation for predicting wear rate with in selected experimental conditions.
颗粒填充聚合物复合材料因其广泛的应用和较低的生产成本而越来越受到人们的关注。为了评估在回收聚乙烯(PE)复合材料中使用废二氧化硅基陶瓷材料作为增强填料的可能性,研究了在(2wt%填料)和晶粒尺寸(40µm-150µm)下,陶瓷(PC)粒径对聚乙烯(PE)复合材料力学、磨损和热性能的影响。利用方差分析(ANOVA)和线性回归分析表征了PE-PC复合材料的磨损行为,确定了速度、载荷和时间等工艺参数对复合材料磨损行为的主要影响和交互影响。试验结果表明,减少150µm ~ 40µm的陶瓷颗粒,提高了再生聚乙烯(PE)复合材料的力学、磨损和热性能。实验的析因设计可以成功地描述样品的磨损行为,并建立了在选定的实验条件下预测磨损率的线性方程。
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引用次数: 8
Climate Change Mediated Actinidic Archaeal Endosymbiosis Generates Neanderthal Hybrids and Mind-Body Phenotypic Change 气候变化介导的锕系古菌内共生产生尼安德特人杂交体和身心表型变化
Pub Date : 2013-03-26 DOI: 10.3968/3925
R. Kurup, P. A. Kurup
Actinidic archaea has been related to global warming and human diseases especially autoimmune disease, neuro-degeneration, neuropsychiatric disorder, neoplasm and metabolic syndrome x. The growth of endosymbiotic actinidic archaea in relation to climate change and global warming leads to nean-derthalisation of the human mind-body system. Neanderthal anthropometry and metabolonomics has been described in autoimmune disease, neuro-degeneration, neuropsychiatric disorder, neoplasm and metabolic syndrome x especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces Nean-derthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to autoimmune disease, neuro-degeneration, neuropsychiatric disorder, neoplasm and metabolic syndrome x in this communication. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. Actinidic archaeal related cerebellar dominance leads to changes in brain function. The data is described in this paper.
放线菌与全球变暖和人类疾病有关,特别是自身免疫性疾病、神经变性、神经精神障碍、肿瘤和代谢综合征。与气候变化和全球变暖有关的内共生放线菌的生长导致人类身心系统的新灭绝。尼安德特人的人体测量学和代谢学已经在自身免疫性疾病、神经变性、神经精神疾病、肿瘤和代谢综合征中得到了描述,特别是Warburg表型和高地高辛血症。由古菌胆固醇分解代谢产生的地高辛产生尼安-去盐化。在这种交流中,前额皮质萎缩和小脑增生与自身免疫性疾病、神经变性、神经精神障碍、肿瘤和代谢综合征x有关。这导致自主神经异常伴交感神经亢进和副交感神经病变。放线菌相关的小脑优势导致脑功能的改变。本文对数据进行了描述。
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引用次数: 0
Archaeal Symbiosis and Digoxin Status Modulates Evolution of Homo Sapiens and Homo Neanderthalis - Digoxin Is a Neanderthal Hormone 古菌共生和地高辛状态调节智人和尼安德特人的进化——地高辛是尼安德特人的一种激素
Pub Date : 2013-03-26 DOI: 10.3968/4382
R. Kurup, P. A. Kurup
Introduction: The climate change and global warming/ice age results in endosymbiotic actinidic archaeal growth in the human system and cholesterol catabolism resulting in endogenous digoxin synthesis. The increased endosymbiotic archaeal growth detected in autism and matrilineal communities with increased incidence of autism and neanderthalic origin leads to the conclusion that digoxin acts as neanderthalic hormone. The increased endosymbiotic archaeal growth and resultant endogenous digoxin synthesis in relation to climate change and global warming results in neanderthalisation of homo sapiens and human disease resulting in homo sapien extinction. Digoxin can inhibit reverse transcriptase activity and RNA editing resulting in suppression of endogenous retroviral growth. This produces inhibition of HERV expression and jumping gene phenomena producing in adynamicity of the human genome. HERV related jumping genes are crucial in synaptic diversity, HLA expression and immunomodulation as well as metabolic diversity. Digoxin produces alteration in sodium-hydrogen exchange producing an acidic pH and acts like a growth factor producing stem cell transformation of adult cells. Stem cells have a distinct metabolism with increased glycolysis and suppression of PDH and mitochondrial function. This can result in cancer and metabolic syndrome. The digoxin interference with RNA editing can lead to mutated RNA viruses and wide spread RNA viral epidemics. The digoxin interference with HERV expression and RNA editing and resultant inhibition of genomic, metabolic, neural and immune diversity produces autoimmune disease, cancer, metabolic syndrome, degenerations, schizophrenia and autism which are increasing at epidemic rates in human population. Materials and Methods: Endogenous digoxin levels and serum cytochrome F420 levels as a marker of archaeal growth were estimated in matrilineal communities, SLE, multiple sclerosis, parkinson’s disease, alzheimer’s disease, CNS glioma, multiple myeloma, metabolic syndrome x with CAD and CVA, schizophrenia and autism. 15 numbers were included in each group and each patient had an age and sex matched control. Endogenous digoxin was estimated by Elisa and cytochrome F420 estimated by spectrophotometry. The statistical analysis was done by ANOVA. Results: Endogenous digoxin levels and cytochrome F420 levels were elevated in matrilineal neanderthalic communities, SLE, multiple sclerosis, parkinson’s disease, alzheimer’s disease, CNS glioma, multiple myeloma, metabolic syndrome x with CAD and CVA, schizophrenia and autism. Endogenous digoxin and cytochrome F420 levels were low in non-matrilineal homo sapien population. Conclusion: Homo sapiens tend to have low levels of endosymbiotic actinidic archaea and low digoxin synthesis. Homo sapiens have low incidence of autoimmune disease, cancer, schizophrenia, autism and metabolic syndrome. The neanderthalisation of homo sapiens consequent to endosymbiotic actinidic archaeal growth a
导语:气候变化和全球变暖/冰河时代导致人体系统内共生的锕系古菌生长和胆固醇分解代谢导致内源性地高辛合成。在自闭症和母系社区中检测到的内共生古细菌生长增加,自闭症和尼安德特人的发病率增加,这导致地高辛作为尼安德特人激素的结论。与气候变化和全球变暖有关的内共生古细菌生长增加以及由此产生的内源性地高辛合成导致智人尼安德特化,人类疾病导致智人灭绝。地高辛可以抑制逆转录酶活性和RNA编辑,从而抑制内源性逆转录病毒的生长。这产生了抑制HERV表达和跳跃基因现象产生在人类基因组的动态。HERV相关跳跃基因在突触多样性、HLA表达、免疫调节和代谢多样性中起着至关重要的作用。地高辛使钠-氢交换发生改变,产生酸性pH值,并像生长因子一样使成体细胞发生干细胞转化。干细胞有一个独特的代谢,增加糖酵解和抑制PDH和线粒体功能。这会导致癌症和代谢综合征。地高辛干扰RNA编辑可导致RNA病毒突变和广泛传播的RNA病毒流行。地高辛干扰HERV表达和RNA编辑,从而抑制基因组、代谢、神经和免疫多样性,从而产生自身免疫性疾病、癌症、代谢综合征、变性、精神分裂症和自闭症,这些疾病在人群中以流行病的速度增加。材料和方法:在母系社区、SLE、多发性硬化症、帕金森病、阿尔茨海默病、中枢神经胶质瘤、多发性骨髓瘤、伴有CAD和CVA的代谢综合征x、精神分裂症和自闭症中,评估内源性地高辛水平和血清细胞色素F420水平作为古菌生长的标志物。每组15个数字,每个患者有一个年龄和性别匹配的对照。Elisa法测定内源性地高辛,分光光度法测定细胞色素F420。统计分析采用方差分析。结果:内源性地高辛水平和细胞色素F420水平在母系尼安德特人社区、SLE、多发性硬化症、帕金森病、阿尔茨海默病、中枢神经胶质瘤、多发性骨髓瘤、伴有CAD和CVA的代谢综合征x、精神分裂症和自闭症中升高。内源性地高辛和细胞色素F420水平在非母系智人群体中较低。结论:智人具有较低水平的内共生放线菌和较低的地高辛合成。智人的自身免疫性疾病、癌症、精神分裂症、自闭症和代谢综合征的发病率较低。内共生的放线菌古菌生长和地高辛合成导致智人的尼安德特化,导致人类病理和灭绝。尼安德特人有更高的锕系古菌共生率和地高辛合成率,自身免疫性疾病、癌症、精神分裂症、自闭症和代谢综合征的发病率更高。放线菌分泌地高辛作为尼安德特人激素的功能。
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引用次数: 0
The Homo Neanderthalis and the Dravidians: A Common Origin and Relation to Harappan Civilisation and Vedas 尼安德特人和德拉威人:哈拉帕文明和吠陀的共同起源和关系
Pub Date : 2013-03-26 DOI: 10.3968/4384
R. Kurup, P. A. Kurup
INTRODUCTION: The postulated Lemurian part of the Indian sub-continent in South India is inhabited by the dominant Nair community. The dominant Nair community also has a high incidence of autism. Neanderthal anthropometric features have been described in autism. Neanderthal metabolonomics have also been described in autism. It is possible that homo neanderthalis would have originated in the super continent which occupied the southern ocean. The island of Sumatra is home to another human species homo floresiensis which lived along with homo neanderthalis. This suggests an oceanic origin of homo neanderthalis in the supercontinent in the southern ocean. Recurrent Tsunamis would have forced the migration of homo neanderthalis to the Eurasian land mass especially to Harappa, Sumeria, Etruscia, Egypt and Basque country. There is a high incidence of Neanderthal genes in the Basque population. The language spoken in Harappa, Sumeria, Etruscia, Egypt and Basque country had a Dravidian sub-stratum. The population in these areas are matrilineal and female dominant. MATERIALS AND METHODS: Neanderthal anthropometric features were evaluated in the Nair community and in autism. The parameters checked include dolichocephalic skull, prominent supraorbital ridge and mid face large flat nose and ring finger index finger ratios. RESULTS: The Nair community had a high prevalence of Neanderthal anthropometric features. Neanderthal anthropometric features were also dominant in autism. CONCLUSION: This suggests an out of oceania hypothesis for the origin of homo neanderthalis.
简介:印度次大陆假定的利莫里亚部分位于印度南部,居住着占主导地位的奈尔社区。占主导地位的Nair社区也有很高的自闭症发病率。尼安德特人的人体测量特征已经被描述为自闭症。尼安德特人的代谢学也被描述为自闭症。尼安德特人有可能起源于占据南大洋的超级大陆。苏门答腊岛是另一个人类物种弗洛勒斯人的家园,他们与尼安德特人一起生活。这表明尼安德特人起源于南大洋的超大陆。反复发生的海啸会迫使尼安德特人迁移到欧亚大陆,特别是哈拉帕、苏美尔、伊特鲁西亚、埃及和巴斯克地区。在巴斯克人群中,尼安德特人基因的发生率很高。哈拉帕、苏美尔、伊特鲁西亚、埃及和巴斯克地区使用的语言有德拉威语的底层。这些地区的人口以母系和女性为主。材料和方法:在Nair社区和自闭症中评估尼安德特人的人体测量特征。检查的参数包括头侧颅骨、突出的眶上脊和中脸、大扁鼻和无名指食指比。结果:Nair社区具有较高的尼安德特人人体测量特征。尼安德特人的人体特征在自闭症中也占主导地位。结论:这表明尼安德特人的起源可能来自大洋洲。
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引用次数: 1
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