Bøger af Ravikumar Kurup

Climate change, global warming and archaeal endosymbiosis leads to neanderthalisation of the human brain. The archaeal magnetite and porphyrions are capable of quantal perception and leads to a cerebellar cognitive affective disorder consequent to cerebral cortical atrophy and cerebellar dominance. This leads to impulsive behaviour, violent behaviour, terrorist acts which leads to surrealistic state and transcendence. The Yellow-vest movement dominating France and spreading to other parts of Europe and the world signifies this brain change consequent to archaeal endosymbiosis and brain neanderthalisation. The quantal perception of the neanderthalised brain leads to a sense of spirituality and collective consciousness among individual groups. The Yellow-vest movement is a merger of the far-right and far-left of the European political spectrum. The movement represents a type of global anarchy and is leaderless and is a form of democratic protest based on grass-root network and bottom up organisation of the socio-political movement. This can be characterised as the return of the Nazis in the modern world.

Panpsychism and connection to the protoconsciousness field forms the basis of tantric states. The tantric states associated with sexuality help to connect with the protoconsciousness field. Sexuality was used as a instrument for cortical suppression and cerebellar dominance creating a surrealistic transcendental state. The sexual transcendence can be heterosexual or alternate. The growth of endosymbiotic actinidic archaea in relation to climate change and global warming leads to neanderthalisation of the human mind-body system. The primitive parts of the brain dominate with cerebellum and brain stem undergoing hypertrophy. The atrophy of the cortex results in behavioural changes. The cortex has different hemispheric dominance in males and females. When the cortex atrophies the hemispheric differentiation and the effect on behaviour is obliterated. The cortical effect on male and female behaviour is lost. Behaviour becomes uniform and single and is dominated by the primitive brain stem and cerebellar cortex. It results in impulsive behaviour dominated by the will to power and individuality. This forms the basis of the androgynous state and alternate forms of sexuality.

Climate change, global warming and archaeal endosymbiosis leads to neanderthalisation of the human brain. The archaeal magnetite and porphyrions are capable of quantal perception and leads to a cerebellar cognitive affective disorder consequent to cerebral cortical atrophy and cerebellar dominance. This leads to impulsive behaviour, violent behaviour, terrorist acts which leads to surrealistic state and transcendence. The quantal perception of the neanderthalised brain leads to a sense of spirituality and collective consciousness among individual groups. The sense of quantal perception gives a spirituality or collective consciousness to the group. This leads to environmental consciousness and rise of pagan religions. The groups include workers, small business owners, religious leaders, groups with sexual orientation, anarchist, leftist and hard-core rightist groups brought together by a sense of togetherness as a small community. These small groups are pitched against the nation-states and global organizations leading to an anarchic revolt.

The theory of hereditability of acquired characteristics puts natural cooperation as opposed to natural selection as the basis of evolution. The endosymbiotic archaea secrete RNA viroids. The archaeal RNA viroids are converted to DNA viroids by endogenous HERV reverse transcriptase and integrated into the genome by HERV integrase. Archaeal endosymbiosis can occur consequent to global warming which leads to increased colonic archaeal growth and endosymbiosis. Archaeal endosymbiosis can occur following dietary fibre deficiency, stress and exposure to EMF. The archaea will secrete RNA viroids which can get converted to DNA viroids and get integrated into the genome functioning as jumping genes modulating gene expression. The RNA viroids and their DNA templates getting integrated into the genome consequent to environmental stress leads to genomic flexibility and dynamicity which can be inherited. The archaeal endosymbiosis and symbiotic genomics lead to human evolution and development of the human brain with its unique characteristics. Symbiotic genomics can regulate brain function, immunity, metabolism and cell cycle changes. It is the symbiotic archaea that make us humans.

The female dominant model of human evolution raises the question of who evolved first- the male or the female. The original fossils of human species are predominantly female and the male fossils evolved after billions of years. The original human species would have been a cluster of female bipedals in swampy waters feeding on tubers of water lilies and lotus as well as fish, mussels and shell fish. The women can reproduce by parthenogenesis like lower animals. Therefore it is natural for the female of the species to evolve first. The sexual relationship in such female only societies in primodial times was lesbian. The evolution of males occurred at a later date. The macho model of human evolution with male hunter and male toolmaker and a female accomplice evolving together is highly unlikely. The next stage of human evolution has been postulated to be interspecies hybrids.

Climate change and global warming leads to endosymbiotic archaeal growth and alteration in brain structure and function. The archaeal endosymbiosis produces cholesterol catabolism and depletion of sex hormones resulting in asexual phenotypes and phenotypes with alternate sexuality. There is also a decrease in fertility producing a shrinkage in population. This is compensated by an increase in longevity produced by implantation of biochips to improve ageing organ function resulting in functional cyborgs. The cerebellar dominant autistic adult phenotype is capable of quantal perception and intergalactic communication. The civilization of adult onset autistic cyborgs produces a world without empathy, affection, compassion, tolerance or logic. This results in a surreal syntheistic evil world of autistic asexual unemotional cyborgs, hermits and the tribe of modern male eunuchs.

The Neanderthal phenotype gives clues as to the origin of the humans. The Naga tribes of South India were hypothesized to originate in the ancient Lemurian landmass which got broken up by tsunamis and earthquakes. The remnants of the Neanderthal phenotype are seen in the Australian aboriginals, the New Zealandian Maoris, the Dravidian Tamils and Nairs. These societies are predominantly matriarchal and serpent worshipping. The homo neanderthalic possibly arose in the Lemurian oceanic landmass supporting the theory of the aquatic ape origin of humans. The homo neanderthalis would have originated from the bonobo monkeys in the Lemurian backwaters communicating with the sea. The bonobo monkeys owing to shortage of food would have started foraging the backwaters and sea for fish and tubers of water lilies. The bonobo monkeys would have waded into water and stood in water generating the phenomena of bipedalism. The bonobo Lemurian monkeys would have evolved into homo neanderthalis by archaeal endosymbiosis in the actinidic shores of backwaters, lakes and oceans of peninsular India. This points to a out of South India origin of homo neanderthalis and human species.

The Neanderthal diet is a 3500 calorie diet rich in proteins and fat with low levels of carbohydrate intake. It is a paleoketogenic diet. Thus protein toxicity leads to the generation of a new metabolic, genomic and neuronal phenotype susceptible to civilizational disease. The lipids especially short chain fatty acids like butyrate generated by archaeal cholesterol catabolism is neuroprotective, organ protective, immunosuppressive, promotes insulin sensitivity, suppress cell growth and modulate neurotransmission. The medium chain triglycerides derived from coconut oil also is neuroprotective and organ protective. The Neanderthals survived in peninsular India due to the consumption of high short chain fatty acid and medium chain triglyceride diet as well as high fibre diet. The Neanderthals evolved from aquatic apes in peninsular India surviving on a diet of medium chain triglycerides from coconut, polyunsaturated fatty acids from backwater fish and short chain fatty acids from dietary fibre obtained from the lush tropical vegetation. This leads to the concept of protein toxicity syndrome and dietary fibre/lipid tissue protection syndrome.

Reason judgment and logic is a function of the cerebral cortex especially the prefrontal lobe. Prefrontal lobe function needs dynamic synaptic connectivity which is produced by jumping genes mediated by human endogenous retroviral sequences. The cerebellum is the site of impulsive behavior and the unconscious behavior. The cerebellar and subcortical brain connections are predominantly archaeal colony networks. The global warming and exposure to low level of EMF leads to actinidic archaeal growth in the brain and increased archaeal magnetite mediated perception of low level of EMF. This leads to prefrontal cortex atrophy and cerebellar dominance. The conscious becomes minimal and unconscious brain takes over. This leads to dominance of pagan religions in the globalised world of internet.

The homo neanderthalis, Indo-Europeans, the Dravidian elite and the Aryans may have a common origin in the Lemurian land mass. The homo neanderthalis arising out of the Lemurian land mass consisting of peninsular India, Antarctica and Australia would have been the forerunner of the Indo-European population. The Indo-European languages like Sanskrit and Akkadian have a Dravidian substrate. The Dravidian elite would have been synonymous with Indo-Europeans, Aryans and homo neanderthalis. This suggests that the Vedas and Vedic civilization may have an Antarctic or Lemurian origin and an Indo-European Aryo-Dravidian Neanderthalic species.

Actinidic archaea has been related to human diseases especially cancer, neurodegeneration, metabolic syndrome, autoimmune disease and neuropsychiatric disorders. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in human diseases especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to diseases. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of human diseases. Archaeal Digoxin functions as the Master Modulator of Symbiosis.

Actinidic archaea has been related to human diseases especially multinodular goitre, chronic calcific pancreatitis, endomyocardial fibrosis and mucoid angiopathy. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in these disorders especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to these disorders. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of multinodular goitre, chronic calcific pancreatitis, endomyocardial fibrosis and mucoid angiopathy.

Actinidic archaea has been related to chronic ophthalmologic disease (type 2 diabetes mellitus with retinopathy, cataract, congestive glaucoma, optic neuritis and optic atrophy). The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in chronic ophthalmologic disease especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to chronic ophthalmologic disease. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in chronic ophthalmologic disease. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic ophthalmologic disease.

Actinidic archaea has been related to aging. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in aging especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to aging. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in aging. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of aging and related diseases.

Actinidic archaea has been related to neurogenetic and neurodevelopmental disorders (Huntington¿s disease, trisomy 21 and cerebral palsy), chronic congenital and acquired speech disorders (dyslexia, delayed onset speech milestone, delayed recovery from aphasia). The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system and neanderthal metabolonomics has been described in neurogenetic and neurodevelopmental disorders- the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to neurogenetic and neurodevelopmental disorders. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated the treatment of neurogenetic and neurodevelopmental disorders

Actinidic archaea has been related to human diseases especially chronic bone and joint disease (osteoporosis, osteoarthritis and spondylosis). The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in chronic bone and joint disease especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to chronic bone and joint disease. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in chronic bone and joint disease. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic bone and joint disease.

Actinidic archaea has been related to human diseases especially chronic pulmonary disease (bronchial asthma, chronic bronchitis emphysema, interstitial lung disease and sarcoidosis). The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in chronic pulmonary disease especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to chronic pulmonary disease. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in chronic pulmonary disease. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic pulmonary disease.

Actinidic archaea has been related to human diseases especially chronic renal failure. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in chronic renal failure especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to chronic renal failure. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in Chronic Renal failure. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic renal failure.

Actinidic archaea has been related to human infections- superbugs, emerging virus infection, retroviral disease and prion disease. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in human infections- superbugs, emerging virus infection, retroviral disease and prion disease especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to metabolic syndrome. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these human infections. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated treatment of human infections- superbugs, emerging virus infection, retroviral disease and prion disease.

Actinidic archaea has been related to human diseases especially chronic gastrointestinal disease (cirrhosis, inflammatory bowel disease, ischemic bowel disease and peptic ulcer disease). The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in chronic gastrointestinal and liver diseases especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to chronic gastrointestinal and liver diseases. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic gastrointestinal and liver diseases.

Actinidic archaea has been related to human diseases especially neuropsychiatric diseases like schizophrenia, autism and epilepsy. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in neuropsychiatric diseases especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to neuropsychiatric diseases. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic neuropsychiatric disorders.

Actinidic archaea has been related to human diseases especially autoimmune diseases like systemic lupus erythematosis, multiple sclerosis and rheumatoid arthritis. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in autoimmune diseases like systemic lupus erythematosis, multiple sclerosis and rheumatoid arthritis especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to autoimmune diseases. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic autoimmune disease.

Actinidic archaea has been related to human diseases especially cancer. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in cancer especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to cancer. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of cancer.

Actinidic archaea has been related to human diseases especially neurodegenerations ¿ Alzheimer¿s Disease, Parkinson¿s Disease and motor neuron disease. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in neurodegenerations especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to neurodegenerations. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in these disorders. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of chronic neurodegenerations.

Actinidic archaea has been related to human diseases especially metabolic syndrome (Type 2 Diabetes, Coronary Artery Disease, Cerebral Vascular Disease, Hypertension and Dyslipidemia. The growth of endosymbiotic actinidic archaea leads to neanderthalisation of the human mind-body system. Neanderthal metabolonomics has been described in metabolic syndrome especially the Warburg phenotype and hyperdigoxinemia. Digoxin produced by archaeal cholesterol catabolism produces neanderthalisation. Prefrontal cortical atrophy and cerebellar hyperplasia has been related to metabolic syndrome. This leads on to dysautonomia with sympathetic hyperactivity and parasympathetic neuropathy in metabolic syndrome. A method to modulate archaeal symbiosis and interconverting homo sapien to homo neanderthalis and vice versa is described. This is done by a high fibre versus a low fibre diet, administration of antioxidant antibiotic and colonic microflora from human and cow dung. This can be called as a therapeutic archaeal symbiotic modulated human evolution for the treatment of metabolic syndrome.

The theory of hereditability of acquired characteristics rejected the Darwinian theory of natural selection and competition leading to survival of the fittest. It proposed natural cooperation as opposed to natural selection. The endosymbiotic archaea secrete RNA viroids. The archaeal RNA viroids are converted to DNA viroids by endogenous HERV reverse transcriptase and integrated into the genome by HERV integrase. Archaeal endosymbiosis can occur consequent to global warming, dietary fibre deficiency, stress and exposure to low level EMF which leads to increased colonic archaeal growth and endosymbiosis. The archaea will secrete RNA viroids which can get converted to DNA viroids and get integrated into the genome functioning as jumping genes modulating gene expression. The RNA viroids and their DNA templates getting integrated into the genome consequent to environmental stress leads to genomic flexibility and dynamicity which can be inherited. Exposure to environmental stress can alter the genome changing body function in response to stress and genomic change which is acquired is hereditable. This fits in with the neo-Lamarckian concept of hereditability of acquired characteristics.

The Ayurvedic system deals with symbiotic medicine and symbiotic disease. Ayurveda, the traditional Indian System of Medicine, deals with the theory of the three tridosha states (both physical and psychological): Vata, Pitta and Kapha. The kapha state has been demonstrated as equivalent to right hemispheric dominant hyperdigoxinemic state. This kapha state has got increased colonic and endosymbiotic archaeal growth leading to neanderthalisation of the species. This leads to generation of the Warburg phenotype and increase incidence of civilizational diseases. The kapha state leads to generation of new RNA and DNA viruses as well as bacterial superbugs to which the population in the kapha state is resistant. The pitta state is equivalent to the left hemispheric dominant hypodigoxinemic state. The pitta state has decreased colonic and endosymbiotic archaeal growth leading to homo sapienisation of the species. It is characterised by low body-mass index and protection from civilizational diseases. The vata state has got normal colonic and endosymbiotic archaeal growth and is a neutral transitional species. The basis of Ayurveda, pranayama, yoga, mantras & yagnas is symbiotic medicine.

The history of India can be considered as an eternal conflict between the Neanderthalic Indo-European Aryo-Dravidians and the homo sapien Semitic African migrants to India. The African migrants who travelled along the Makhran coast and settled in India were dominated by the Indo-European Aryo-Dravidian Neanderthalic groups that entered India following the breakage of the Lemurian Antarctic homeland. The Indo-European Aryo-Dravidian elite formed the caste system of Kshatriyas, Brahmins, Vaisysas and Sudras. The Nair community can be considered as a prototypical Indo-European Aryo-Dravidian representative.

Consciousness is a fundamental part of matter. The substrate of everything is of mental character. Mind is the first and most direct thing in our experience and all else is remote experience. The fact that all matter is conscious solves the hard problems of consciousness. Consciousness cannot arise out of unconsciousness. The individuals and social groups were reflections of the protoconsciousness field and linked together. The different castes and races can be described as a dissociative identity disorder of the protoconsciousness field. There was unity among the races and castes in the protoconsciousness field.

The Indo-Europeans and Aryo-Dravidians have a common origin in peninsular India and Antarctica as a part of Lemurian landmass. The exposure to global warming and low level EMF leads to archaeal endosymbiosis and neanderthalisation of the population. This leads to generation of Neoneanderthals or new Aryo-Dravidians or Indo-Europeans. This postulates an out of Asia hypothesis. The Indo-Europeans, Aryans, Dravidians, Mongoloids, Australian aboriginals and Neanderthals are synonymous and they arose in the Lemurian Antarctican continent. This fits in with the out of Asia hypothesis which postulated that Hindustan was the place where human evolution took place. Humans are related to the primates of South and South-East Asia including the Lemurs. The Lemurian continent or Kumari Kandam is the place where the Indo-Europeans, Aryo-Dravidians and Neanderthals originated. It includes Australia, South India, Antarctica and Madagascar. This postulates an Antarctic hyperborean home for the Vedas.