“We do not believe any group of men adequate enough or wise
enough to operate without scrutiny or without criticism. We know that
the only way to avoid error is to detect it, that the only way to detect
it is to be free to inquire. We know that in secrecy error undetected
will flourish and subvert”. – J Robert Oppenheimer.
You cannot fail to recall the neurotic
freaking out over last summer’s Siberian heatwave, when a new record
temperature for the Arctic of 38C was set at Verhojansk:
The event was one of last year’s main climate poster children, along
with wildfires. Each year, the climate establishment pick on one or two
unusual weather events, in an attempt to convince us all that the planet
is quickly spinning out of control. To most people, such temperatures
are unheard of in the Arctic, as they naturally assume the region is
frozen all year round.
As I inconveniently pointed out at the time, the new record of 38.0C
was only 0.7C higher than recorded in the same location in 1988.
But that was only one day. Now we have the full data for the year, we
can compare temperatures for the whole of the summer at Verhojansk.
Data from NASA GISS confirms that, while it was unusually warm there
last year, the hottest summer was actually way back in 1917:
Summer temperatures at Verhojansk can clearly swing wildly from year
to year, depending on meteorological conditions. Last summer brought an
extended period of high pressure, delivering sunny weather and a hot
airmass from the south.
Other years can bring cold and wet weather from the Arctic Ocean.
It was “weather”and not “climate change” which was responsible for Siberia’s hot summer.
High temperatures are quite common in the Eurasian Arctic
summer. Temperatures over 34 Celsius have been recorded at Tiksi
(latitude 71 degrees north) on the edge of the Laptev Sea, and over 36
Celsius at Khatanga (similar latitude) at the eastern base of the Taymyr
Peninsula. It is worth noting that the Verkhoyansk record occured on 20
June with 24 hour insolation, and also that Verkhoyansk is noted for
its extremes, both hot and cold enhanced by its situation.
BBC inviting comment in an on line survey https://www.bbc.co.uk/send/u61149175
enjoy…. if you want to pass comment on wall to wall climate and covid scaremongering
In their ‘submission received’ email, they say: “We’ll keep it for up
to 270 days – and if we don’t use it we’ll then delete it and any other
information you sent us.
We really appreciate your help to understand what you think and feel about the BBC.”
It wasn’t even “one day”, it was simply one moment. The
“day” may not have been the hottest – it might have been colder to start
with and then got colder quickly after the high temperature. Using Tmax
as the temperature for a period is simply wrong.
Some may remember the discussions we had on this topic regarding the
situation in the UK, puzzled at the claims of miraculously cleansed air –
which did not seem to be very obvious in the actual monitoring station
data.
Other research has already agreed that PMs did not decrease
significantly, increased even, in the period after traffic almost
disappeared overnight from UK roads.
This new paper also suggests that in London, after the traffic
vanished, ozone increased by 26%, and NO2 decreased by only 10%, with
-2% and -8% respectively due to lockdown.
London has a lot of highly polluting buses and taxis and as I thought
with the Marylebone Road data, the pollution was mostly related to
those and not private cars – they returned at different times/rates, the
pollution only really increased after the bus/taxi movements increased
again. That small -8% in NO2 is likely mostly not due to cars.
It is now obvious that a total ban on private ICE cars in London (and
elsewhere) will not make any significant different to air quality and
private motorists have been unfairly and politically targeted. Air
quality in the UK is already extremely good, with massive improvements
in recent decades, and ICE car emissions standards are extremely high.
History suggests the globe will continue to warm on and off
until the next ice age starts, so expect more cherrypicking of
short-term weather events as evidence of…well, nothing really.
In 1917 the Thames froze in London, reported the Dailey
telegraph. People had problems acquiring coal. There was a rumpus about
45 cwt of the stuff being sent to a museum while others were in fuel
poverty.
My main point there is that time and geography constrained temperature events do not have a global warming interpretation.
For that one must look at the global warming data
These data are over long time spans and the temperature data are for
large geographical regions that are significant portions of the globe.
Most amerindian groups are derived from two ancestral lineages, which formed in Siberia prior to the Last Glacial Maximum, between about 36,000 and 25,000 years ago, East Eurasian and Ancient North Eurasian. They later dispersed throughout the Americas after about 16,000 years ago (an exception are the Na Dene and Eskimo–Aleut speaking groups, which are partially derived from Siberian populations which entered the Americas at a later time).
Analyses of genetics among Amerindian and Siberian populations have been used to argue for early isolation of founding populations on Beringia and for later, more rapid migration from Siberia through Beringia into the New World. The microsatellite diversity and distributions of the Y lineage specific to South America indicates that certain Amerindian populations have been isolated since the initial peopling of the region. The Na-Dené, Inuit and Indigenous Alaskan populations exhibit Haplogroup Q-M242; however, they are distinct from other indigenous Amerindians with various mtDNA and atDNA mutations. This suggests that the peoples who first settled in the northern extremes of North America and Greenland derived from later migrant populations than those who penetrated farther south in the Americas. Linguists and biologists have reached a similar conclusion based on analysis of Amerindian language groups and ABO blood group system distributions.
Autosomal DNA
Genetic diversity and population structure in the American landmass is also measured using autosomal (atDNA) micro-satellite markers genotyped; sampled from North, Central, and South America and analyzed against similar data available from other indigenous populations worldwide. The Amerindian populations show a lower genetic diversity than populations from other continental regions.
Observed is a decreasing genetic diversity as geographic distance from
the Bering Strait occurs, as well as a decreasing genetic similarity to
Siberian populations from Alaska (the genetic entry point).
Also observed is evidence of a higher level of diversity and lower level
of population structure in western South America compared to eastern
South America. There is a relative lack of differentiation between Mesoamerican and Andean
populations, a scenario that implies that coastal routes were easier
for migrating peoples (more genetic contributors) to traverse in
comparison with inland routes.
The over-all pattern that is emerging suggests that the Americas
were colonized by a small number of individuals (effective size of about
70), which grew by many orders of magnitude over 800 – 1000 years.
The data also shows that there have been genetic exchanges between
Asia, the Arctic, and Greenland since the initial peopling of the
Americas.
Moreno-Mayar et al. (2018) have identified a basal Ancestral Native American (ANA) lineage. This lineage formed by admixture of early East Asian and Ancient North Eurasian lineages prior to the Last Glacial Maximum, ca. 36–25 kya. Basal ANA diverged into an "Ancient Beringian"
(AB) lineage at ca. 20 kya. The non-AB lineage further diverged into
"Northern Native American" (NNA) and "Southern Native American" (SNA)
lineages between about 17.5 and 14.6 kya. Most pre-Columbian lineages
are derived from NNA and SNA, except for the American Arctic, where
there is evidence of later (after 10kya) admixture from Paleo-Siberian lineages.
In 2014, the autosomal DNA of a 12,500+-year-old infant from Montana was sequenced.
The DNA was taken from a skeleton referred to as Anzick-1, found in
close association with several Clovis artifacts. Comparisons showed
strong affinities with DNA from Siberian sites, and virtually ruled out
that particular individual had any close affinity with European sources
(the "Solutrean hypothesis").
The DNA also showed strong affinities with all existing Amerindian
populations, which indicated that all of them derive from an ancient
population that lived in or near Siberia, the Upper Palaeolithic Mal'ta population.
According to an autosomal genetic study from 2012,
Native Americans descend from at least three main migrant waves from
East Asia. Most of it is traced back to a single ancestral population,
called 'First Americans'. However, those who speak Inuit languages from the Arctic inherited almost half of their ancestry from a second East Asian migrant wave. And those who speak Na-dene,
on the other hand, inherited a tenth of their ancestry from a third
migrant wave. The initial settling of the Americas was followed by a
rapid expansion southwards, by the coast, with little gene flow later,
especially in South America. One exception to this are the Chibcha speakers, whose ancestry comes from both North and South America.
Linguistic studies have backed up genetic studies, with ancient patterns having been found between the languages spoken in Siberia and those spoken in the Americas.
Two 2015 autosomal DNA genetic studies confirmed the Siberian
origins of the Natives of the Americas. However an ancient signal of
shared ancestry with Australasians (Natives of Australia, Melanesia and
the Andaman Islands) was detected among the Natives of the Amazon region. The migration coming out of Siberia would have happened 23,000 years ago.
A "Central Siberian" origin has been postulated for the paternal
lineage of the source populations of the original migration into the
Americas.
Membership in haplogroups Q and C3b implies indigenous American patrilineal descent.
The micro-satellite
diversity and distribution of a Y lineage specific to South America
suggest that certain Amerindian populations became isolated after the
initial colonization of their regions.
The Na-Dené, Inuit and Indigenous Alaskan populations exhibit haplogroup Q (Y-DNA) mutations, but are distinct from other indigenous Amerindians with various mtDNA and autosomal DNA (atDNA) mutations. This suggests that the earliest migrants into the northern extremes of North America and Greenland derived from later migrant populations.
Haplogroup Q
Q-M242 (mutational name) is the defining (SNP) of Haplogroup Q (Y-DNA) (phylogenetic name). In Eurasia, haplogroup Q is found among indigenous Siberian populations, such as the modern Chukchi and Koryak peoples. In particular, two groups exhibit large concentrations of the Q-M242 mutation, the Ket (93.8%) and the Selkup (66.4%) peoples. The Ket are thought to be the only survivors of ancient wanderers living in Siberia. Their population size is very small; there are fewer than 1,500 Ket in Russia. The Selkup have a slightly larger population size than the Ket, with approximately 4,250 individuals.
Starting the Paleo-Indians period, a migration to the Americas across the Bering Strait (Beringia) by a small population carrying the Q-M242 mutation took place. A member of this initial population underwent a mutation, which defines its descendant population, known by the Q-M3 (SNP) mutation. These descendants migrated all over the Americas.
Haplogroup Q-M3 is defined by the presence of the rs3894 (M3) (SNP).
The Q-M3 mutation is roughly 15,000 years old as that is when the
initial migration of Paleo-Indians into the Americas occurred. Q-M3 is the predominant haplotype in the Americas, at a rate of 83% in South American populations, 50% in the Na-Dené populations, and in North American Eskimo-Aleut populations at about 46%. With minimal back-migration of Q-M3 in Eurasia, the mutation likely evolved in east-Beringia, or more specifically the Seward Peninsula or western Alaskan interior. The Beringia land mass began submerging, cutting off land routes.
Since the discovery of Q-M3, several subclades of M3-bearing populations have been discovered. An example is in South America, where some populations have a high prevalence of (SNP) M19, which defines subclade Q-M19. M19 has been detected in (59%) of Amazonian Ticuna men and in (10%) of Wayuu men. Subclade M19 appears to be unique to South American Indigenous peoples, arising 5,000 to 10,000 years ago.
This suggests that population isolation, and perhaps even the
establishment of tribal groups, began soon after migration into the
South American areas. Other American subclades include Q-L54, Q-Z780, Q-MEH2, Q-SA01, and Q-M346 lineages. In Canada, two other lineages have been found. These are Q-P89.1 and Q-NWT01.
Haplogroup R1
Haplogroup R1 (Y-DNA) is the second most predominant Y haplotype found among indigenous Amerindians after Q (Y-DNA). The distribution of R1 is believed by some to be associated with the re-settlement of Eurasia following the last glacial maximum. One theory that was introduced during European colonization. R1 is very common throughout all of Eurasia except East Asia and Southeast Asia. R1 (M173) is found predominantly in North American groups like the Ojibwe (50-79%), Seminole (50%), Sioux (50%), Cherokee (47%), Dogrib (40%) and Tohono O'odham (Papago) (38%).
A study of Raghavan et al. 2013 found that autosomal evidence
indicates that skeletal remain of a south-central Siberian child
carrying R* y-dna (Mal'ta boy-1)
"is basal to modern-day western Eurasians and genetically closely
related to modern-day Amerindians, with no close affinity to east
Asians. This suggests that populations related to contemporary western
Eurasians had a more north-easterly distribution 24,000 years ago than
commonly thought." Sequencing of another south-central Siberian (Afontova Gora-2)
revealed that "western Eurasian genetic signatures in modern-day
Amerindians derive not only from post-Columbian admixture, as commonly
thought, but also from a mixed ancestry of the First Americans."
It is further theorized if "Mal'ta might be a missing link, a
representative of the Asian population that admixed both into Europeans
and Native Americans."
On FTDNA public tree, out of 626 US indigenous Americans
K-YSC0000186 , all are Q , R1b-M269, R1a-M198, 1 R2-M479 and 2 most
likely not tested further than R1b-M343 .
Haplogroup C-P39
Haplogroup C-M217 is mainly found in indigenous Siberians, Mongolians, and Kazakhs. Haplogroup C-M217 is the most widespread and frequently occurring branch of the greater (Y-DNA) haplogroup C-M130. Haplogroup C-M217 descendant C-P39 is most commonly found in today's Na-Dené speakers, with the highest frequency found among the Athabaskans at 42%, and at lower frequencies in some other Native American groups. This distinct and isolated branch C-P39 includes almost all the Haplogroup C-M217 Y-chromosomes found among all indigenous peoples of the Americas.
Some researchers feel that this may indicate that the Na-Dené migration occurred from the Russian Far East after the initial Paleo-Indian colonization, but prior to modern Inuit, Inupiat and Yupik expansions.
In addition to in Na-Dené peoples, haplogroup C-P39 (C2b1a1a) is also found among other Native Americans such as Algonquian- and Siouan-speaking populations.
C-M217 is found among the Wayuu people of Colombia and Venezuela.
Maternal lineages
The
common occurrence of the mtDNA Haplogroups A, B, C, and D among eastern
Asian and Amerindian populations has long been recognized, along with
the presence of Haplogroup X. As a whole, the greatest frequency of the four Amerindian associated haplogroups occurs in the Altai-Baikal region of southern Siberia.
Some subclades of C and D closer to the Amerindian subclades occur
among Mongolian, Amur, Japanese, Korean, and Ainu populations.
When studying human mitochondrial DNA (mtDNA) haplogroups, the results indicated until recentllyily that Indigenous Amerindian haplogroups, including haplogroup X,
are part of a single founding East Asian population. It also indicates
that the distribution of mtDNA haplogroups and the levels of sequence
divergence among linguistically similar groups were the result of multiple preceding migrations from Bering Straits populations.
All indigenous Amerindian mtDNA can be traced back to five haplogroups, A, B, C, D and X.
More specifically, indigenous Amerindian mtDNA belongs to
sub-haplogroups A2, B2, C1b, C1c, C1d, D1, and X2a (with minor groups
C4c, D2a, and D4h3a).This suggests that 95% of Indigenous Amerindian mtDNA is descended from a
minimal genetic founding female population, comprising sub-haplogroups
A2, B2, C1b, C1c, C1d, and D1. The remaining 5% is composed of the X2a, D2a, C4c, and D4h3a sub-haplogroups.
X is one of the five mtDNA haplogroups found in Indigenous
Amerindian peoples. Unlike the four main American mtDNA haplogroups (A,
B, C and D), X is not at all strongly associated with east Asia.
Haplogroup X genetic sequences diverged about 20,000 to 30,000 years
ago to give two sub-groups, X1 and X2. X2's subclade X2a occurs only at a
frequency of about 3% for the total current indigenous population of
the Americas. However, X2a is a major mtDNA subclade in North America; among the Algonquian peoples, it comprises up to 25% of mtDNA types. It is also present in lower percentages to the west and south of this area — among the Sioux (15%), the Nuu-chah-nulth (11%–13%), the Navajo (7%), and the Yakama (5%). Haplogroup X is more strongly present in the Near East, the Caucasus, and Mediterranean Europe.
The predominant theory for sub-haplogroup X2a's appearance in North
America is migration along with A, B, C, and D mtDNA groups, from a
source in the Altai Mountains of central Asia.
Sequencing of the mitochondrial genome from Paleo-Eskimo
remains (3,500 years old) are distinct from modern Amerindians, falling
within sub-haplogroup D2a1, a group observed among today's Aleutian Islanders, the Aleut and Siberian Yupik populations. This suggests that the colonizers of the far north, and subsequently Greenland, originated from later coastal populations. Then a genetic exchange in the northern extremes introduced by the Thule people (proto-Inuit) approximately 800–1,000 years ago began.
These final Pre-Columbian migrants introduced haplogroups A2a and A2b
to the existing Paleo-Eskimo populations of Canada and Greenland,
culminating in the modern Inuit.
Frequency distribution of the main mtDNA American haplogroups in Native American populations.
A 2013 study in Nature reported that DNA found in the 24,000-year-old remains of a young boy from the archaeological Mal'ta-Buret' culture suggest that up to one-third of indigenous Americans' ancestry can be traced back to western Eurasians, who may have "had a more north-easterly distribution 24,000 years ago than commonly thought"
"We estimate that 14 to 38 percent of Amerindian ancestry may originate
through gene flow from this ancient population," the authors wrote.
Professor Kelly Graf said,
"Our findings are significant at two levels. First, it shows that Upper Paleolithic Siberians came from a cosmopolitan population of early modern humans that spread out of Africa to Europe and Central and South Asia. Second, Paleoindian skeletons like Buhl Woman
with phenotypic traits atypical of modern-day indigenous Americans can
be explained as having a direct historical connection to Upper
Paleolithic Siberia."
A route through Beringia is seen as more likely than the Solutrean hypothesis.
An abstract in a 2012 issue of the "American Journal of Physical
Anthropology" states that "The similarities in ages and geographical
distributions for C4c and the previously analyzed X2a lineage provide
support to the scenario of a dual origin for Paleo-Indians. Taking into
account that C4c is deeply rooted in the Asian portion of the mtDNA
phylogeny and is indubitably of Asian origin, the finding that C4c and
X2a are characterized by parallel genetic histories definitively
dismisses the controversial hypothesis of an Atlantic glacial entry
route into North America."
Another study, also focused on the mtDNA (that which is inherited through only the maternal line),
revealed that the indigenous people of the Americas have their maternal
ancestry traced back to a few founding lineages from East Asia, which
would have arrived via the Bering strait.
According to this study, it is probable that the ancestors of the
Native Americans would have remained for a time in the region of the Bering Strait, after which there would have been a rapid movement of settling of the Americas, taking the founding lineages to South America.
According to a 2016 study, focused on mtDNA lineages, "a small
population entered the Americas via a coastal route around 16.0 ka,
following previous isolation in eastern Beringia for ~2.4 to 9 thousand
years after separation from eastern Siberian populations. Following a
rapid movement throughout the Americas, limited gene flow in South
America resulted in a marked phylogeographic structure of populations,
which persisted through time. All of the ancient mitochondrial lineages
detected in this study were absent from modern data sets, suggesting a
high extinction rate. To investigate this further, we applied a novel
principal components multiple logistic regression test to Bayesian
serial coalescent simulations. The analysis supported a scenario in
which European colonization caused a substantial loss of pre-Columbian
lineages".
Paleoamericans
There is genetic evidence for an early wave of migration to the Americas.
It is uncertain whether this "Paleoamerican" (also "Paleoamerind", not to be confused with the term
Paleo-Indian
used of the early phase of Amerinds proper) migration took place in the
early Holocene, thus only shortly predating the main Amerind peopling
of the Americas, or whether it may have reached the Americas
substantially earlier, before the Last Glacial Maximum.
Genetic evidence for "Paleoamerinds" consists of the presence of apparent admixture of archaic Sundadont lineages to the remote populations in the South American rain forest, and in the genetics and cranial morphology of Patagonians-Fuegians.
Nomatto et al. (2009) proposed migration into Beringia occurred between
40k and 30k cal years BP, with a pre-LGM migration into the Americas
followed by isolation of the northern population following closure of
the ice-free corridor.
A 2016 genetic study of native peoples of the Amazonian region of
Brazil (by Skoglund and Reich) showed evidence of admixture from a
separate lineage of an otherwise unknown ancient people. This ancient
group appears to be related to modern day "Australasian" peoples (i.e. Aboriginal Australians and Melanesians). This "Ghost population" was found in speakers of Tupian languages. They provisionally named this ancient group; "Population Y", after Ypykuéra, "which means ‘ancestor’ in the Tupi language family".
Archaeological evidence for pre-LGM human presence in the Americas was first presented in the 1970s. notably the "Luzia Woman" skull found in Brazil and the Monte Verde site in Chile, both discovered in 1975.
Other notable sites of early human inhabitation found in North America
include Paisley Caves, Oregon and Bluefish Caves, Canada.
In
Latin America in particular, significant racial admixture took place
between the indigenous Amerind population, the European-descended
colonial population, and the Sub-Saharan African populations imported as slaves.
From about 1700, a Latin American terminology developed to refer to the
various combinations of mixed racial descent produced by this.
Many individuals who self-identify as one race exhibit genetic evidence of a multiracial ancestry.
The European conquest of South and Central America, beginning in the
late 15th century, was initially executed by male soldiers and sailors
from the Iberian Peninsula (Spain and Portugal).
Native Americans in the United States are more likely than any other racial group to practice racial exogamy, resulting in an ever-declining proportion of indigenous ancestry among those who claim a Native American identity.
In the United States 2010 census, nearly 3 million people indicated that their race was Native American (including Alaska Native).
This is based on self-identification, and there are no formal defining criteria for this designation.
Especially numerous was the self-identification of Cherokee ethnic origin, a phenomenon dubbed the "Cherokee Syndrome."
The context is the cultivation of an opportunistic ethnic identity related to the perceived prestige associated with Native American ancestry. Native American identity
in the Eastern United States is mostly detached from genetic descent,
and especially embraced by people of predominantly European ancestry.
Some tribes have adopted criteria of racial preservation, usually through a Certificate of Degree of Indian Blood, and practice disenrollment of tribal members unable to provide proof of Native American ancestry. This topic has become a contentious issue in Native American reservation politics.
Ancient Beringians
25 kya Beringia during the LGM 16-14 kya peopling of the Americas just after the LGM
Recent archaeological findings in Alaska have shed light on the
existence of a previously unknown Native American population that has
been academically named "Ancient Beringians." Although it is popularly agreed among archeologists that early settlers had crossed into Alaska from Russia through the Bering Strait land bridge,
the issue of whether or not there was one founding group or several
waves of migration is a controversial and prevalent debate among
academics in the field today. In 2018, the sequenced DNA of a native
girl, whose remains were found at the Sun River archaeological site in
Alaska in 2013, proved not to match the two recognized branches of
Native Americans and instead belonged to the early population of Ancient
Beringians.
This breakthrough is said to be the first direct genomic evidence that
there was potentially only one wave of migration in the Americas that
occurred, with genetic branching and division transpiring after the
fact. The migration wave is estimated to have emerged about 20,000 years
ago.
The Ancient Beringians are said to be a common ancestral group among
contemporary Native American populations today, which differs in results
collected from previous research that suggests that modern populations
are descendants of either Northern and Southern branches.
Experts were also able to use wider genetic evidence to establish that
the split between the Northern and Southern American branches of
civilization from the Ancient Beringians in Alaska only occurred about
17,000 and 14,000 years, further challenging the concept of multiple migration waves occurring during the very first stages of settlement.
Blood groups
Frequency of O group in indigenous populations. Note the predominance of this group in Indigenous Americans.
Prior to the 1952 confirmation of DNA as the hereditary material by Alfred Hershey and Martha Chase, scientists used blood proteins to study human genetic variation. The ABO blood group system is widely credited to have been discovered by the Austrian Karl Landsteiner, who found three different blood types in 1900. Blood groups are inherited from both parents. The ABO blood type is controlled by a single gene (the ABO gene) with three alleles: i, IA, and IB.
Research by Ludwik and Hanka Herschfeld during World War I found that the frequencies of blood groups A, B and O differed greatly from region to region.
The "O" blood type (usually resulting from the absence of both A and B
alleles) is very common around the world, with a rate of 63% in all
human populations.
Type "O" is the primary blood type among the indigenous populations of
the Americas, in-particular within Central and South America
populations, with a frequency of nearly 100%. In indigenous North American populations the frequency of type "A" ranges from 16% to 82%. This suggests again that the initial Amerindians evolved from an isolated population with a minimal number of individuals.
The standard explanation for such a high population of Native Americans with blood type O comes from the idea of Genetic drift,
in which the small nature of Native American populations meant the
almost complete absence of any other blood gene being passed down
through generations.
Other related explanations include the Bottleneck explanation which
states that there were high frequencies of blood type A and B among
Native Americans but severe population decline during the 1500s and
1600s caused by the introduction of disease from Europe resulted in the
massive death toll of those with blood types A and B. Coincidentally, a
large amount of the survivors were type O.
Distribution of ABO blood types in various modern Indigenous Amerindian populations Test results as of 2008
A team led by Ripan Malhi, an anthropologist at the University of Illinois in Urbana, conducted a study where they used a scientific technique known as whole exome sequencing to test immune-related gene variants within Native Americans. Through analyzing ancient and modern native DNA, it was found that HLA-DQA1,
a variant gene that codes for protein in charge of differentiating
between healthy cells from invading viruses and bacteria were present in
nearly 100% of ancient remains but only 36% in modern Native Americans. These finding suggest that European-borne epidemics such as smallpox
altered the disease landscape of the Americas, leaving survivors of
these outbreaks less likely to carry variants like HLA-DQA1. This made
them less able to cope with new diseases. The change in genetic makeup
is measured by scientists to have occurred around 175 years ago, during a
time when the smallpox epidemic was ranging through the Americas.
Meanwhile, over in the US, 1917 was the coldest year on record, as was the Spring of that year.
Forgive me if I’m wrong, but I thought the 38 degree reading was very questionable and unlikely to be confirmed? What have I missed?
Don’t let the BBC know that it wasn’t a record.
‘Normal’ for Jan is -41/-48C, -55/-56C today, lows of -62C forecast in next few days.
Just the weather pendulum!
NTZ on Arctic ‘warming’. Says pretty much what we’ve all pointed out before.
https://notrickszone.com/2021/01/13/arctic-temps-show-little-change-over-past-90-years-in-sync-with-oceanic-surface-temperature-cycles/
High temperatures are quite common in the Eurasian Arctic summer. Temperatures over 34 Celsius have been recorded at Tiksi (latitude 71 degrees north) on the edge of the Laptev Sea, and over 36 Celsius at Khatanga (similar latitude) at the eastern base of the Taymyr Peninsula. It is worth noting that the Verkhoyansk record occured on 20 June with 24 hour insolation, and also that Verkhoyansk is noted for its extremes, both hot and cold enhanced by its situation.
BBC inviting comment in an on line survey
https://www.bbc.co.uk/send/u61149175
enjoy…. if you want to pass comment on wall to wall climate and covid scaremongering
Done!
In their ‘submission received’ email, they say: “We’ll keep it for up to 270 days – and if we don’t use it we’ll then delete it and any other information you sent us.
We really appreciate your help to understand what you think and feel about the BBC.”
I have a feeling they won’t be keeping mine!
I bet they don’t get the chance to change/alter/massage/dicredit that record! But I bet they try.
It wasn’t even “one day”, it was simply one moment. The “day” may not have been the hottest – it might have been colder to start with and then got colder quickly after the high temperature. Using Tmax as the temperature for a period is simply wrong.
O/T Effect of lockdown on air pollution in UK.
Some may remember the discussions we had on this topic regarding the situation in the UK, puzzled at the claims of miraculously cleansed air – which did not seem to be very obvious in the actual monitoring station data.
Other research has already agreed that PMs did not decrease significantly, increased even, in the period after traffic almost disappeared overnight from UK roads.
This new paper also suggests that in London, after the traffic vanished, ozone increased by 26%, and NO2 decreased by only 10%, with -2% and -8% respectively due to lockdown.
https://wattsupwiththat.com/2021/01/13/first-lockdowns-effect-on-air-pollution-was-overstated-our-study-reveals/
London has a lot of highly polluting buses and taxis and as I thought with the Marylebone Road data, the pollution was mostly related to those and not private cars – they returned at different times/rates, the pollution only really increased after the bus/taxi movements increased again. That small -8% in NO2 is likely mostly not due to cars.
It is now obvious that a total ban on private ICE cars in London (and elsewhere) will not make any significant different to air quality and private motorists have been unfairly and politically targeted. Air quality in the UK is already extremely good, with massive improvements in recent decades, and ICE car emissions standards are extremely high.
History suggests the globe will continue to warm on and off until the next ice age starts, so expect more cherrypicking of short-term weather events as evidence of…well, nothing really.
In 1917 the Thames froze in London, reported the Dailey telegraph. People had problems acquiring coal. There was a rumpus about 45 cwt of the stuff being sent to a museum while others were in fuel poverty.
Coal ships used to pull up on the beach near me, after a storm you can find lost coal washed up or uncovered, some chunks are the size of a football.
Here is my work on the Verkhoyansk thing for what it’s worth.
https://tambonthongchai.com/2020/07/19/agw-heat-wave-in-siberia/
My main point there is that time and geography constrained temperature events do not have a global warming interpretation.
For that one must look at the global warming data
These data are over long time spans and the temperature data are for large geographical regions that are significant portions of the globe.
https://tambonthongchai.com/2021/01/11/global-warming-dec2020/