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Averaged interval shot (12 exposures). This sample is not really sharp, but still nice. With Pentax K-1 you don't need ND filters.
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This photo has been graciously provided to be used in the GRID-Arendal resources library by: GRID-Arendal/Studio Atlantis
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
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View my items for sale, or convo me for a custom item:
I custom draft patterns for fit and style, and can base your design on a photograph, sketch, or combine multiple inspiration ideas into one great garment!
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Some frequently asked questions:
Yes, I do international shipping orders
yes, I source/find/purchase/provide the materials for your garment, unless you have some that you would like used
Yes, I make items in ALL sizes. Every single one. I can custom design something no matter what your height/weight/bra-size etc. I even have experience working with non-average figures including loss of appendages (arms, legs, etc.) and accommodating a severe disability/unusual shape.
Yes, i respond to everyone. I will always reply! (if you don't hear from me, i either didn't get the message, or am on a freak internet break)
Yes, I can do rush orders, please convo as soon as you can about planning
Yes, i can do payment plans for larger projects, convo me
Yes, I am a real person in California USA, I am not an assembly line/sweatshop/slavedriver. Me and my family work on every item start to finish.
Yes, I love Project Runway, but no, i don't want to be on it!
Yes, I love the odd/strange/weird projects, but I also love the impeccably simple bridal gown as well.
No, I do not have a minimum. Small projects are welcome.
Yes, I help with the total package. I can help you find the accessories you need to complete the look, and all the underpinnings and other garments you may need to get the right shape for the garment. I like to make sure you are happy with the end result as much as I am.
If you have a question not on here, please feel free to convo me at the above sites.
Thanks for viewing!
Mom Box - Smoke Free Home -
Fashion Bug Size 6M Average Blue Melrose Jeans,
Levis Boot Cut Size 6L Light Blue Jeans
Paris Blues Size 7 Blue Jeans
Faded Glory Stretch Bootcut Classic Size Average 6 Black Jeans
Foster Jeans Co. Seize 6 Navy Blue Jeans
My Funny Valentine Brown Long Sleeve Shirt (XXL- runs small - moved to box 2)
apt 9 Size Small floral long sleeve shirt - cream
apt 9 Size small floral long sleeve shirt - grey
energe world wear Size M long sleeve shirt - green
Worthington Size Small long sleeve sweater green
wave, but very good memory. Those two girls in the middle frame slept on Susan Gilmore beach and were walking home at around 5.30 in the morning. It was shit cold for me in my car with lots of clothes, i can only imagine what it would have been like in a miniskirt. They were very keen to tell me it was their formal in the night ahead. Despite the previous description these girls where in fact quite glamorous.
It's not usual I pick up a cold, my yearly average is just over 1 (I did once go 3 years without a cold!)
However, being exposed to a work colleagues cold has proven too much and today has developed into a full blown cold, chances of which, I'll be right as rain by the time Monday comes along
See My entire photostream at:
www.flickr.com/photos/spookykittencouture
View my items for sale, or convo me for a custom item:
I custom draft patterns for fit and style, and can base your design on a photograph, sketch, or combine multiple inspiration ideas into one great garment!
Please feel free to contact me at either site above, I usually respond within 24 hours.
Some frequently asked questions:
Yes, I do international shipping orders
yes, I source/find/purchase/provide the materials for your garment, unless you have some that you would like used
Yes, I make items in ALL sizes. Every single one. I can custom design something no matter what your height/weight/bra-size etc. I even have experience working with non-average figures including loss of appendages (arms, legs, etc.) and accommodating a severe disability/unusual shape.
Yes, i respond to everyone. I will always reply! (if you don't hear from me, i either didn't get the message, or am on a freak internet break)
Yes, I can do rush orders, please convo as soon as you can about planning
Yes, i can do payment plans for larger projects, convo me
Yes, I am a real person in California USA, I am not an assembly line/sweatshop/slavedriver. Me and my family work on every item start to finish.
Yes, I love Project Runway, but no, i don't want to be on it!
Yes, I love the odd/strange/weird projects, but I also love the impeccably simple bridal gown as well.
No, I do not have a minimum. Small projects are welcome.
Yes, I help with the total package. I can help you find the accessories you need to complete the look, and all the underpinnings and other garments you may need to get the right shape for the garment. I like to make sure you are happy with the end result as much as I am.
If you have a question not on here, please feel free to convo me at the above sites.
Thanks for viewing!
. . . more than 200.000 chapatis are made on an average day!
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GURU KA LANGAR
Guru Ka Langar The tradition of serving langar Initiated by Guru Nanak Dev Ji and then established by the 3rd Guru Sri Guru Amar Dass Ji at Goindwal.
Even the Mughal King Akbar came and sat among the ordinary people to share langar.
The institution of Guru ka Langar has served the community in many ways. It has ensured the participation of women and children in a task of service for mankind. Women play an important role in the preparation of meals, and the children help in serving food to the pangat. Langar also teaches the etiquette of sitting and eating in a community situation, which has played a great part in upholding the virtue of sameness of all human beings; providing a welcome, secure and protected sanctuary.
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Everyone is welcome to share the Langar; no one is turned away. Each week a family or several families volunteer to provide and prepare the Langar. This is very generous, as there may be several hundred people to feed, and caterers are not allowed. All the preparation, the cooking and the washing-up is done by volunteers and or by voluntary helpers (Sewadars).
In the Golden Temple Community Kitchen at an average 75,000 devotees or tourists take langar in the Community Kitchen daily; but the number becomes almost double on special occasions. On average 5.000 kg Wheat Flour, 1.250 kg Cereals, 500 kg Rice, 5000 Ltr Milk, 500 kg Sugar, 250 kg Pure Ghee is used a day. Nearly 100 LPG Gas Cylinders are used to prepare the meals. 100’s of employees and devotees render their services to the kitchen.
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IMPORTANCE OF LANGAR TO SIKHISM
Bhai Desa Singh in his Rehitnama says, "A Sikh who is 'well to do' must look to the needs of his poor neighbours. Whenever he meets a traveller or a pilgrim from a foreign country, he must serve him devotedly.
Maharaja Ranjit Singh made grants of jagirs to gurdwaras for the maintenance of langars. Similar endowments were created by other Sikh rulers as well. Today, practically every gurdwara has a langar supported by the community in general. In smaller gurdwaras cooked food received from different households may comprise the langar. In any case, no pilgrim or visitor will miss food at meal time in a gurdwara. Sharing a common meal sitting in a pangat is for a Sikh is an act of piety. So is his participation in cooking or serving food in the langar and in cleaning the used dishes. The Sikh ideal of charity is essentially social in conception. A Sikh is under a religious obligation to contribute one-tenth of his earnings (daswand) for the welfare of the community. He must also contribute the service of his hands whenever he can, service rendered in a langar being the most meritorious.
GOLDEN TEMPLE AMRITSAR
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
Currently, Erin stands out as the graduate with the highest academic average at DW Poppy Secondary School. Her remarkable 97.58 percent average comes in AP English, AP Psychology, Calculus 12, Biology 12, History 12, Band 12 and Choir 12. But, this is only a small example of why Erin is an inspiration to us all.
Erin is a leader in the DWP Music Program and an active member of Student Government and Graduation Council. Erin also volunteers her time as an Assistant at the Aldergrove Figure Skating Club.
Erin hopes to become a Physician in her future years.
See www.faceresearch.org/ for more details. See xn--80ax0d.blogspot.com/2009/09/blog-post_06.html for more comments.
The Eurasian eagle-owl (Bubo bubo) is a species of eagle-owl that resides in much of Eurasia. It is also called the Uhu and it is occasionally abbreviated to just the eagle-owl in Europe. It is one of the largest species of owl, and females can grow to a total length of 75 cm (30 in), with a wingspan of 188 cm (6 ft 2 in), with males being slightly smaller. This bird has distinctive ear tufts, with upper parts that are mottled with darker blackish colouring and tawny. The wings and tail are barred. The underparts are a variably hued buff, streaked with darker colouring. The facial disc is not very defined and the orange eyes are distinctive.
Eurasian eagle-owls are found in many habitats, but are mostly birds of mountainous regions or other rocky areas, often those near varied woodland edge and shrubby areas with openings or wetlands to hunt a majority of their prey. Additionally, they inhabit coniferous forests, steppes, and other areas at varied elevations that are typically relatively remote. Eurasian eagle-owls are occasionally found amongst farmland and in park-like settings within European cities, even rarely within busier urban areas. The eagle-owl is mostly a nocturnal predator, hunting for a range of different prey species. Predominantly, their diet is composed of small mammals such as rodents and rabbits, but they also prey on larger mammals and birds of varying sizes. Other secondary prey can include reptiles, amphibians, fish, large insects and other assorted invertebrates. The species typically breeds on cliff ledges, in gullies, among rocks, or in other concealed locations. The nest is a scrape containing a clutch of 2–4 eggs typically, which are laid at intervals and hatch at different times. The female incubates the eggs and broods the young, and the male provides food for her, and when they hatch, for the nestlings, as well. Continuing parental care for the young is provided by both adults for about five months. At least 12 subspecies of the Eurasian eagle-owl are described.
In addition to being one of the largest living species of owl, the Eurasian eagle-owl is also one of the most widely distributed.[9] With a total range in Europe and Asia of about 51.4 million km2 (19.8 million sq mi) and a total population estimated to be between 100,000 and 500,000 individuals, the IUCN lists the bird's conservation status as being of least concern, although the trend is listed as decreasing. The vast majority of eagle-owls live in Continental Europe, Scandinavia, Russia (which is almost certainly where the peak numbers and diversity of race occurs), and Central Asia. Additional minor populations exist in Anatolia, the northern Middle East, the montane upper part of South Asia, China, Korea and in Japan; in addition, an estimated 12 to 40 pairs are thought to reside in the United Kingdom as of 2016 (where they are arguably non-native), a number which may be on the rise, and have successfully bred in the UK since at least 1996. Tame eagle-owls have occasionally been used in pest control because of their size to deter large birds such as gulls from nesting.
Description
The Eurasian eagle-owl is among the larger birds of prey, smaller than the golden eagle (Aquila chrysaetos), but larger than the snowy owl (Bubo scandiacus), despite some overlap in size with both of those species. It is sometimes referred to as the world's largest owl, although Blakiston's fish owl (B. blakistoni) is slightly heavier on average and the much lighter weight great grey owl (Strix nebulosa) is slightly longer on average. Heimo Mikkola reported the largest specimens of eagle-owl as having the same upper body mass, 4.6 kg (10 lb), as the largest Blakiston’s fish owl and attained a length around 3 cm (1.2 in) longer. In terms of average weight and wing size, the Blakiston’s is the slightly larger species seemingly, even averaging a bit larger in these aspects than the biggest eagle-owl races from Russia. Also, although 9 cm (3.5 in) shorter than the largest of the latter species, the Eurasian eagle-owl can weigh well more than twice as much as the largest great grey owl. The Eurasian eagle-owl typically has a wingspan of 131–188 cm (4 ft 4 in – 6 ft 2 in), with the largest specimens possibly attaining 2 m (6 ft 7 in). The total length of the species can vary from 56 to 75 cm (22 to 30 in). Females can weigh from 1.75 to 4.6 kg (3.9 to 10.1 lb), and males can weigh from 1.2 to 3.2 kg (2.6 to 7.1 lb). In comparison, the barn owl (Tyto alba), the world's most widely distributed owl species, weighs about 0.5 kg (1.1 lb) and the great horned owl (B. virginianus), which fills the eagle-owl's ecological niche in North America, weighs around 1.4 kg (3.1 lb).
Eurasian eagle-owl in captivity
Besides the female being larger, little external sexual dimorphism is seen in the Eurasian eagle-owl, although the ear tufts of males reportedly tend to be more upright than those of females. When an eagle-owl is seen on its own in the field, distinguishing the individual’s sex is generally not possible. Gender determination by size is possible by in-hand measurements. In some populations, the female typically may be slightly darker than the male. The plumage coloration across at least 13 accepted subspecies can be highly variable. The upper parts may be brown-black to tawny-buff to pale creamy gray, typically showing dense freckling on the forehead and crown, stripes on the nape, sides, and back of the neck, and dark splotches on the pale ground colour of the back, mantle, and scapulars. A narrow buff band, freckled with brown or buff, often runs up from the base of the bill, above the inner part of the eye, and along the inner edge of the black-brown ear tufts. The rump and upper tail-coverts are delicately patterned with dark vermiculations and fine, wavy barring, the extent of which varies with subspecies. The underwing coverts and undertail coverts are similar, but tend to be more strongly barred in brownish-black.
The primaries and secondaries are brown with broad, dark brown bars and dark brown tips, and grey or buff irregular lines. A complete moult takes place each year between July and December. The facial disc is tawny-buff, speckled with black-brown, so densely on the outer edge of the disc as to form a "frame" around the face. The chin and throat are white with a brownish central streak. The feathers of the upper breast generally have brownish-black centres and reddish-brown edges except for the central ones, which have white edges. The chin and throat may appear white continuing down the center of the upper breast. The lower breast and belly feathers are creamy-brown to tawny buff to off-white with a variable amount of fine dark wavy barring, on a tawny-buff ground colour. The legs and feet (which are feathered almost to the talons) are likewise marked on a buff ground colour but more faintly. The tail is tawny-buff, mottled dark grey-brown with about six black-brown bars. The bill and feet are black. The iris is most often orange but is fairly variable. In some European birds, the iris is a bright reddish, blood-orange colour but then in subspecies found in arid, desert-like habitats, the iris can range into an orange-yellow colour (most closely related species generally have yellowish irises, excluding the Indian eagle-owl).
Standard measurements and physiology
Among standard measurements for the Eurasian eagle-owl, the wing chord measures 378 to 518 mm (14.9 to 20.4 in), the tail measures 229–310 mm (9.0–12.2 in) long, the tarsus measures 64.5–112 mm (2.54–4.41 in), and the total length of the bill is 38.9–59 mm (1.53–2.32 in). The wings are reportedly the smallest in proportion to the body weight of any European owl, when measured by the weight per area of wing size, was found to be 0.72 g/cm2. Thus, they have quite high wing loading. The great horned owl has even smaller wings (0.8 g/cm2) relative to its body size. The golden eagle has slightly lower wing loading proportionately (0.65 g/cm2), so the aerial abilities of the two species (beyond the eagle’s spectacular ability to stoop) may not be as disparate as expected. Some other owls, such as barn owls, short-eared owls (Asio flammeus), and even the related snowy owls have lower wing loading relative to their size, so are presumably able to fly faster, with more agility, and for more extended periods than the Eurasian eagle-owl. In the relatively small race B. b. hispanus, the middle claw, the largest talon, (as opposed to rear hallux-claw, which is the largest in accipitrids) was found to measure from 21.6 to 40.1 mm (0.85 to 1.58 in) in length. A 3.82 kg (8.4 lb) female examined in Britain (origins unspecified) had a middle claw measuring 57.9 mm (2.28 in), on par in length with a large female golden eagle hallux-claw. Generally, owls do not have talons as proportionately large as those of accipitrids, but have stronger, more robust feet relative to their size. Accipitrids use their talons to inflict organ damage and blood loss, whereas typical owls use their feet to constrict their prey to death, the talons serving only to hold the prey in place or provide incidental damage. The talons of the Eurasian eagle-owl are very large and not often exceeded in size by diurnal raptors. Unlike the great horned owls, the overall foot size and strength of the Eurasian eagle-owl is not known to have been tested, but the considerably smaller horned owl has one of the strongest grips ever measured in a bird.
The feathers of the ear tufts in Spanish birds (when not damaged) were found to measure from 63.3 to 86.6 mm (2.49 to 3.41 in).[26] The ear openings (covered in feathers as in all birds) are relatively uncomplicated for an owl, but are also large, being larger on the right than on the left as in most owls, and proportionately larger than those of the great horned owl. In the female, the ear opening averages 31.7 mm (1.25 in) on the right and 27.4 mm (1.08 in) on the left, and in males, averages 26.8 mm (1.06 in) on the right and 24.4 mm (0.96 in) on the left. The depth of the facial disc and the size and complexity of the ear opening are directly correlated to the importance of sound in an owl’s hunting behaviour. Examples of owls with more complicated ear structures and deeper facial disc are barn owls, long-eared owls (Asio otus), and boreal owls (Aegolius funereus). Given the uncomplicated structure of their ear openings and relatively shallow, undefined facial discs, hunting by ear is secondary to hunting by sight in eagle-owls; this seems to be true for Bubo in general. More sound-based hunters such as the aforementioned species likely focus their hunting activity in more complete darkness. Also, owls with white throat patches such as the Eurasian eagle-owl are more likely to be active in low-light conditions in the hours before and after sunrise and sunset rather than the darkest times in the middle of the night. The boreal and barn owls, to extend these examples, lack obvious visual cues such as white throat patches (puffed up in displaying eagle-owls), again indicative of primary activity being in darker periods.
Distinguishing from other species
The great size, bulky, barrel-shaped build, erect ear tufts, and orange eyes render this as a distinctive species. Other than general morphology, the above features differ markedly from those of two of the next largest subarctic owl species in Europe and western Asia, which are the great grey owl and the greyish to chocolate-brown Ural owl (Strix uralensis), both of which have no ear tufts and have a distinctly rounded head, rather than the blocky shape of the eagle-owl’s head. The snowy owl is obviously distinctive from most eagle-owls, but during winter the palest Eurasian eagle-owl race (B. b. sibiricus) can appear off-white. Nevertheless, the latter is still distinctively an ear-tufted Eurasian eagle-owl and lacks the pure white background colour and variable blackish spotting of the slightly smaller species (which has relatively tiny, vestigial ear tufts that have only been observed to have flared on rare occasions).
Unique camouflage pattern
The long-eared owl has a somewhat similar plumage to the eagle-owl, but is considerably smaller (an average female eagle-owl may be twice as long and 10 times heavier than an average long-eared owl). Long-eared owls in Eurasia have vertical striping like that of the Eurasian eagle-owl, while long-eared owls in North America show a more horizontal striping like that of great horned owls. Whether these are examples of mimicry either way is unclear but it is known that both Bubo owls are serious predators of long-eared owls. The same discrepancy in underside streaking has also been noted in the Eurasian and American representations of the grey owl. A few other related species overlap minimally in range in Asia, mainly in East Asia and the southern reaches of the Eurasian eagle-owl’s range. Three fish owls appear to overlap in range, the brown (Ketupa zeylonensis) in at least northern Pakistan, probably Kashmir, and discontinuously in southern Turkey, the tawny (K. flavipes) through much of eastern China, and Blakiston's fish owl in the Russian Far East, northeastern China, and Hokkaido. Fish owls are distinctively different looking, possessing more scraggy ear tufts that hang to the side rather than sit erect on top of the head, and generally have more uniform, brownish plumages without the contrasting darker streaking of an eagle-owl. The brown fish owl has no feathering on the tarsus or feet, and the tawny has feathering only on the upper portion of the tarsi, but the Blakiston’s is nearly as extensively feathered on the tarsi and feet as the eagle-owl. Tawny and brown fish owls are both slightly smaller than co-occurring Eurasian eagle-owls, and Blakiston’s fish owls are similar or slightly larger than co-occurring large northern eagle-owls. Fish owls, being tied to the edges of fresh water, where they hunt mainly fish and crabs, also have slightly differing, and more narrow, habitat preferences.
In the lower Himalayas of northern Pakistan and Jammu and Kashmir, along with the brown fish owl, the Eurasian eagle-owl at the limit of its distribution may co-exist with at least two to three other eagle-owls. One of these, the dusky eagle-owl (B. coromandus) is smaller, with more uniform tan-brownish plumage, untidy uniform light streaking rather than the Eurasian’s dark streaking below and an even less well-defined facial disc. The dusky is usually found in slightly more enclosed woodland areas than Eurasian eagle-owls. Another is possibly the spot-bellied eagle-owl (B. nipalensis), which is strikingly different looking, with stark brown plumage, rather than the warm hues typical of the Eurasian, bold spotting on a whitish background on the belly, and somewhat askew ear tufts that are bold white with light brown crossbars on the front. Both species may occur in some parts of the Himalayan foothills, but they are not currently verified to occur in the same area, in part because of the spot-bellied’s preference for dense, primary forest. Most similar, with basically the same habitat preferences and the only one verified to co-occur with the Eurasian eagle-owls of the race B. b. turcomanus in Kashmir is the Indian eagle-owl (B. bengalensis). The Indian species is smaller, with a bolder, blackish facial disc border, more rounded and relatively smaller wings, and partially unfeathered toes. Far to the west, the pharaoh eagle-owl (B. ascalaphus) also seemingly overlaps in range with the Eurasian, at least in Jordan. Although also relatively similar to the Eurasian eagle-owl, the pharaoh eagle-owl is distinguished by its smaller size, paler, more washed-out plumage, and the diminished size of its ear tufts.
Moulting
The Eurasian eagle-owls’ feathers are lightweight and robust, but nevertheless need to be replaced periodically as they become worn. In the Eurasian eagle-owl, this happens in stages, and the first moult starts the year after hatching with some body feathers and wing coverts being replaced. The next year, the three central secondaries on each wing and three middle tail feathers are shed and regrow, and the following year, two or three primaries and their coverts are lost. In the final year of this postjuvenile moult, the remaining primaries are moulted and all the juvenile feathers will have been replaced. Another moult takes place during years 6-12 of the bird's life. This happens between June and October after the conclusion of the breeding season, and again it is a staged process with six to nine main flight feathers being replaced each year. Such a moulting pattern lasting several years is repeated throughout the bird's life.
Taxonomy
The Eurasian eagle-owl was formally described by the Swedish naturalist Carl Linnaeus in 1758 in the tenth edition of his Systema Naturae under the binomial name Strix bulbo. Although Linnaeus specified the "habitat" as "Europa" the type locality is restricted to Sweden. The Eurasian eagle-owl is now placed in the genus Bubo that was introduced by André Duméril in 1805.
The genus Bubo with 20 extant species includes most of the larger owl species in the world today. Based on an extensive fossil record and a central distribution of extant species on that continent, Bubo appears to have evolved into existence in Africa, although early radiations seem to branch from southern Asia, as well. Two genera belonging to the scops owls complex, the giant scops owls (Otus gurneyi) found in Asia and the Ptilopsis or the white-faced scops owl found in Africa, although firmly ensconced in the scops owl group, appear to share some characteristics with the eagle-owls. The Strix genus is also related to Bubo, and is considered a "sister complex", with Pulsatrix possibly being intermediate between the two. The Eurasian eagle-owl appears to represent an expansion of the genus Bubo into the Eurasian continent. A few of the other species of Bubo seem to have been derived from the Eurasian eagle-owl, making it a "paraspecies", or they at least share a relatively recent common ancestor.
The pharaoh eagle-owl, distributed in the Arabian Peninsula and sections of the Sahara Desert through North Africa where rocky outcrops are found, was until recently considered a subspecies of the Eurasian eagle-owl. The pharaoh eagle-owl apparently differs about 3.8% in mitochondrial DNA from the Eurasian eagle-owl, well past the minimum genetic difference to differentiate species of 1.5%. Smaller and paler than Eurasian eagle-owls, the pharaoh eagle-owl can also be considered a distinct species largely due to its higher-pitched and more descending call, and the observation that Eurasian eagle-owls formerly found in Morocco (B. b. hispanus) apparently did not breed with the co-existing pharaoh eagle-owls. On the contrary, the race still found together with the pharaoh eagle-owl in the wild (B. b. interpositus) in the central Middle East has been found to interbreed in the wild with the pharaoh eagle-owl, although genetical materials have indicated B. b. interpositus may itself be a distinct species from the Eurasian eagle-owl, as it differs from the nominate subspecies of the Eurasian eagle-owl by 2.8% in mitochondrial DNA. For three Asian Eurasian eagle-owl subspecies (B. b. ussuriensis, B. b. kiautschensis and B. b. hemachlana, respectively), it was found that they met the criterion for subspecies well, with a high haplotype diversity and in spite of a relatively recent common ancestor and low genetic diversity. The Indian eagle-owl (B. bengalensis) was also considered a subspecies of the Eurasian eagle-owl until recently, but its smaller size, distinct voice (more clipped and high-pitched than the Eurasian), and the fact that it is largely allopatric in distribution (filling out the Indian subcontinent) with other Eurasian eagle-owl races has led to it being considered a distinct species. The mitochondrial DNA of the Indian species also appears considerably distinct from the Eurasian species. The Cape eagle-owl (B. capensis) appears to represent a return of this genetic line back into the African continent, where it leads a lifestyle similar to Eurasian eagle-owls, albeit far to the south. Another offshoot of the northern Bubo group is the snowy owl. It appears to have separated from other Bubo species at least 4 million years ago.
The fourth and most famous derivation of the evolutionary line that includes the Eurasian eagle-owl is the great horned owl, which appears to have been the result of primitive eagle-owls spreading into North America. According to some authorities, the great horned owls and Eurasian eagle-owls are barely distinct as species, with a similar level of divergence in their plumages as the Eurasian and North American representations of the great grey owl or the long-eared owl. More outward physical differences exist between the great horned owl and the Eurasian eagle-owl than in those two examples, including a great size difference favoring the Eurasian species, the great horned owl’s horizontal rather than vertical underside barring, yellow rather than orange eyes, and a much stronger black bracket to the facial disc, not to mention a number of differences in their reproductive behaviour and distinctive voices. Furthermore, genetic research has revealed that the snowy owl is more closely related to the great horned owl than are Eurasian eagle-owls. The most closely related species beyond the pharaoh, Indian, and Cape eagle-owls to the Eurasian eagle-owl is the smaller, less powerful and African spotted eagle-owl (B. africanus), which was likely to have divided from the line before they radiated away from Africa. Somehow, genetic materials indicate the spotted eagle-owl appears to share a more recent ancestor with the Indian eagle-owl than with the Eurasian eagle-owl or even the sympatric Cape eagle-owl. Eurasian eagle-owls in captivity have produced apparently healthy hybrids with both the Indian eagle-owl and the great horned owl. The pharaoh, Indian, and Cape eagle-owls and the great horned owl are all broadly similar in size to each other, but all are considerably smaller than the Eurasian eagle-owl, which averages at least 15–30% larger in linear dimensions and 30–50% larger in body mass than these other related species, possibly as the eagle-owls adapted to warmer climates and smaller prey. Fossils from southern France have indicated that during the Middle Pleistocene, Eurasian eagle-owls (this paleosubspecies is given the name B. b. davidi) were larger than they are today, even larger were those found in Azerbaijan and in the Caucasus (either B. b. bignadensis or B. bignadensis), which were deemed to date to the Late Pleistocene. About 12 subspecies are recognized today.
Habitat
Eagle-owls are distributed somewhat sparsely, but can potentially inhabit a wide range of habitats, with a partiality for irregular topography. They have been found in habitats as diverse as northern coniferous forests to the edge of vast deserts. Essentially, Eurasian eagle-owls have been found living in almost every climatic and environmental condition on the Eurasian continent, excluding the greatest extremities, i.e. they are absent from humid rainforest in Southeast Asia, and the high Arctic tundra, both of which they are more or less replaced by other species of Bubo owls. They are often found in the largest numbers in areas where cliffs and ravines are surrounded by a scattering of trees and bushes. Grassland areas such as alpine meadows or desert-like steppe can also host them so long as they have the cover and protection of rocky areas. The preference of eagle-owls for places with irregular topography has been reported in most known studies. The obvious benefit of such nesting locations is that both nests and daytime roosts located in rocky areas and/or steep slopes would be less accessible to predators, including man. Also, they may be attracted to the vicinity of riparian or wetlands areas, because the soft soil of wet areas is conducive to burrowing by the small, terrestrial mammals normally preferred in the diet, such as voles and rabbits.
Due to their preference for rocky areas, the species is often found in mountainous areas, and can be found up to elevations of 2,100 m (6,900 ft) in the Alps, 4,500 m (14,800 ft) in the Himalayas, and 4,700 m (15,400 ft) in the adjacent Tibetan Plateau. They can also be found living at sea level and may nest amongst rocky sea cliffs. Despite their success in areas such as subarctic zones and mountains that are frigid for much of the year, warmer conditions seem to result in more successful breeding attempts per studies in the Eifel region of Germany. In a study from Spain, areas primarily consisting of woodlands (52% of study area being forested) were preferred with pine trees predominating the oaks in habitats used, as opposed to truly mixed pine-oak woodland. Pine and other coniferous stands are often preferred in great horned owls, as well, due to the constant density, which make overlooking the large birds more likely. In mountainous forest, they are not generally found in enclosed wooded areas, as is the tawny owl (Strix alucco), instead usually near forest edge. Only 2.7% of the habitat included in the territorial ranges for eagle-owls per the habitat study in Spain consisted of cultivated or agricultural land. Compared to golden eagles, though, they can visit cultivated land more regularly in hunting forays due to their nocturnal habits, which allow them to largely evade human activity. Other accounts make clear that farmland is only frequented where its less intensively farmed, holds more extensive treed and bushy areas, and often has limited to no irrigation; farmland areas with fallow or abandoned fields are more likely to hold more prey, so are prone to less frequent human disturbance. In the Italian Alps, almost no pristine habitat remained, and eagle-owls nested locally in the vicinity of towns, villages, and ski resorts.
Although found in the largest numbers in areas sparsely populated by humans, farmland is sometimes inhabited, and they even have been observed living in park-like or other quiet settings within European cities. Since 2005, at least five pairs have nested in Helsinki. This is due in part to feral European rabbits (Oryctolagus cuniculus) having recently populated the Helsinki area, originally from pet rabbits released to the wild. The number is expected to increase due to the growth of the European rabbit population in Helsinki. European hares (Lepus europaeus), the often preferred prey species by biomass of the eagle-owls in their natural habitat, live only in rural areas of Finland, not in the city centre. In June 2007, an eagle-owl nicknamed 'Bubi' landed in the crowded Helsinki Olympic Stadium during the European Football Championship qualification match between Finland and Belgium. The match was interrupted for six minutes. After tiring of the match, following Jonathan Johansson's opening goal for Finland, the bird left the scene. Finland's national football team have had the nickname Huuhkajat (Finnish for "Eurasian eagle-owls") ever since. The owl was named "Helsinki Citizen of the Year" in December 2007. In 2020, a brood of three eagle-owl chicks was raised by their mother on a large, well-foliaged planter on an apartment window in the city centre of Geel, Belgium.
Distribution
The Eurasian eagle-owl is one of the most widely distributed of all owl species, although it is far less wide-ranging than the barn owl, the short-eared owl (Asio flammeus) and long-eared owl and lacks the circumpolar range of boreal species such as great grey owl, boreal owl and northern hawk owl (Surnia ulula). This eagle-owl reaches its westernmost range in the Iberian Peninsula, both almost throughout Spain and more spottily in Portugal. From there, the Eurasian eagle-owl ranges widely in the south of France from Toulouse to Monaco and as far north into the central part of the country as in Allier. Farther north, they are found sporadically and discontinuously in Luxembourg, southern and western Belgium and scarcely into the Netherlands. It is infrequently found in southern and central United Kingdom. In Germany, the eagle-owl can be found in large but highly discontinuous areas, mostly in the south and central areas but is almost entirely absent in areas such as Brandenburg. Across from its south German range, this species range is nearly continuous into the Czech Republic, Slovakia, northern and eastern Hungary and very spottily into Poland. In the fairly montane countries of Switzerland and Austria, the eagle-owl can be found fairly broadly. In Italy, the Eurasian eagle-owl is found where the habitat is favorable in much of the northern, western and central portions down to as far south Melito di Porto Salvo. From Italy, this species sweeps quite broadly along the Mediterranean coast in Southeastern Europe from Slovenia mostly continuously to most of Greece and Bulgaria. In eastern Europe, the Eurasian eagle-owl is found essentially throughout from central Romania to Estonia. The species also occupies a majority of Finland and Scandinavia, where most broadly found in Norway, somewhat more spottily in Sweden and in Denmark it is found widely in Jutland (absent from the islands).
The Eurasian eagle-owl's range in Russia is truly massive, with the species apparently nearly unbound by habitat, with their distribution only excluding them from the true Arctic zone, i.e. their range stops around the tree line. If not the most densely populated species, they almost certainly stand as Russia's most widely distributed owl species. From Russia, they are found throughout Central Asia, residing continuously in each nation from Kazakhstan down to Afghanistan. In Asia Minor, they are found broadly in Georgia, Azerbaijan and somewhat so in western and southern Turkey but is quite sporadic in distribution overall in Turkey. A spotty range also exists in the Middle East in Syria, Iraq, Lebanon, Israel, Jordan and western Iran, the species being found broadly only in north and western Iran. In South Asia, the Eurasian eagle-owl is found mostly often in northern Pakistan, northern Nepal and Bhutan and more marginally into far northern India. This species resides throughout Mongolia, almost the entirety of China (mainly absent only from southern Yunnan and southern Guangxi). From China and eastern Russia, the Eurasian eagle-owl is found throughout Korea, Sakhalin, the Kuril Islands and rarely into Japan in northern Hokkaido. Besides the Kurils, the farthest eastern part of the range for this species is in Magadan in the Russian Far East.
Behaviour
The Eurasian eagle-owl is largely nocturnal in activity, as are most owl species, with its activity focused in the first few hours after sunset and the last few hours before sunrise. In the northern stretches of its range, partial diurnal behaviour has been recorded, including active hunting in broad daylight during the late afternoon. In such areas, full nightfall is essentially non-existent at the peak of summer, so eagle-owls must presumably hunt and actively brood at the nest during daylight. The Eurasian eagle-owl has a number of vocalizations that are used at different times. It will usually select obvious topographic features such as rocky pinnacles, stark ridges and mountain peaks to use as regular song posts. These are dotted along the outer edges of the eagle-owl's territory and they are visited often but only for a few minutes at a time.
Vocal activity is almost entirely confined to the colder months from late fall through winter, with vocal activity in October through December mainly having territorial purposes and from January to February being primarily oriented towards courtship and mating purposes. Vocalizations in a Spanish study begin no sooner than 29 minutes after sunset and end no later than 55 minutes before sunrise. The territorial song, which can be heard at great distance, is a deep resonant ooh-hu with emphasis on the first syllable for the male, and a more high-pitched and slightly more drawn-out uh-hu for the female. It is not uncommon for a pair to perform an antiphonal duet. The widely used name in Germany as well as some other sections of Europe for this species is uhu due to its song. At 250–350 Hz, the Eurasian eagle-owls territorial song or call is deeper, farther-carrying and is often considering "more impressive" than the territorial songs of the great horned owl or even that of the slightly larger Blakiston's fish owl, although the horned owl’s call averages slightly longer in duration and the Blakiston's call is typically deeper.[7] Other calls include a rather faint, laughter-like OO-OO-oo and a harsh kveck-kveck. Intruding eagle-owls and other potential dangers may be met with a "terrifying", extremely loud hooo. Raucous barks not unlike those of ural owls or long-eared owls have been recorded but are deeper and more powerful than those species’ barks. Annoyance at close quarters is expressed by bill-clicking and cat-like spitting, and a defensive posture involves lowering the head, ruffling the back feathers, fanning the tail and spreading the wings.
The Eurasian eagle-owl rarely assumes the so-called "tall-thin position", which is when an owl adopts an upright stance with plumage closely compressed and may stand tightly beside a tree trunk. Among others, the long-eared owl is among the most often reported to sit with this pose. The great horned owl has been more regularly recorded using the tall-thin, if not as consistently as some Strix and Asio owls, and it is commonly thought to aid camouflage if encountering a threatening or novel animal or sound. The Eurasian eagle-owl is a broad-winged species and engages in a strong, direct flight, usually consisting of shallow wing beats and long, surprisingly fast glides. It has, unusually for an owl, also been known to soar on updrafts on rare occasions. The latter method of flight has led them to be mistaken for Buteos, which are smaller and quite differently proportioned. Usually when seen flying during the day, it is due to being disturbed or displaced from its roost by humans or mobbing animals, such as crows. Eurasian eagle-owls are highly sedentary, normally maintaining a single territory throughout their adult lives.
Eurasian eagle-owl are considered a completely non-migratory bird, as are all members of the Bubo genus excluding the snowy owl. Even those near the northern limits of their range, where winters are harsh and likely to bear little in food, the eagle-owl does not leave its native range. In 2020, a study presented evidence of a short distance distribution by adult eagle-owls in the fall subsequent to breeding, with 5 adults found to move over 20 km (12 mi) away from their nests. There are additionally claimed cases from Russia of Eurasian eagle-owls moving south for the winter, as the icebound, infamously harsh climate there may be too severe even for these hardy birds and their prey. Similarly, Eurasian eagle-owls living in the Tibetan highlands and Himalayas may in some anecdotal cases vacate their normal territories when winter hits and move south. In both of those examples, these are old, unverified reports and there is no evidence whatsoever of consistent, annual migration by Eurasian eagle-owls and the birds may eke out a living on their normal territories even in the sparsest times.
Dietary biology
Eurasian eagle-owls are strictly territorial and will defend their territories from interloping eagle-owls year around, but territorial calling appears to peak around October to early January. Territory size is similar or occasionally slightly greater than great horned owl: averaging 15 to 80 km2 (5.8 to 30.9 sq mi). Territories are established by the male eagle-owl, who selected the highest points in the territory from which to sing. The high prominence of singing perches allows their song to be heard at greater distances and lessens the need for potentially dangerous physical confrontations in the areas where territories may meet. Nearly as important in territorial behaviour as vocalization is the white throat patch. When taxidermied specimens with flared white throats were placed around the perimeter of eagle-owl territories, male eagle-owls reacted quite strongly and often attacked the stuffed owl, reacting more mildly to a stuffed eagle-owl with a non-flared white throat. Females were less likely to be aggressive to mounted specimens and did not seem to vary in their response whether exposed to the specimens with or without the puffed up white patch. In January and February, the primary function for vocalization becomes for the purpose of courtship. More often than not, eagle-owls will pair for life but usually engage in courtship rituals annually, most likely to re-affirm pair bonds. When calling for the purposes of courtship, males tend to bow and hoot loudly but do so in a less contorted manner than the male great horned owl. Courtship in the Eurasian eagle-owl may involve bouts of "duetting", with the male sitting upright and the female bowing as she calls. There may be mutual bowing, billing and fondling before the female flies to a perch where coitus occurs, usually taking place several times over the course of a few minutes.
Nests
The male selects breeding sites and advertises their potential to the female by flying to them and kneading out a small depression (if soil is present) and making staccato notes and clucking noises. Several potential sites may be presented, with the female selecting one. In Baden-Wurttenberg, Germany, the amount of male nest site visits were found to increase in time spent over the pre-laying breeding season from a mean of 29 minutes to 3 hours with frequent incubation like sitting by the male. Like all owls, Eurasian eagle-owls do not build nests or add material but nest on the surface or material already present. Eurasian eagle-owls normally nest on rocks or boulders, most often utilizing cliff ledges and steep slopes, as well as crevices, gullies, holes or caves. Rocky areas that also prove concealing woodlots as well as, for hunting purposes, that border river valleys and grassy scrubland may be especially attractive. If only low rubble is present, they will nest on the ground between rocks. Often, in more densely forested areas, they've been recorded nesting on the ground, often among roots of trees, under large bushes and under fallen tree trunks. Steep slopes with dense vegetation are preferred if nesting on the ground, although some ground nests are surprisingly exposed or in flat spots such as in open spots of the taiga, steppe, ledges of river banks and between wide tree trunks. All Eurasian eagle-owl nests in the largely forested Altai Krai region of Russia were found to be on the ground, usually at the base of pines. This species does not often use other bird’s nests as does the great horned owl, which often prefers nests built by other animals over any other nesting site. The Eurasian eagle-owl has been recorded in singular cases using nests built by common buzzards (Buteo buteo), golden eagle, greater spotted (Clanga clanga) and white-tailed eagles (Haliaeetus albicilla), common ravens (Corvus corax) and black storks (Ciconia nigra). Among the eagle-owls of the fairly heavily wooded wildlands of Belarus, they more commonly utilize nests built by other birds than most eagle-owls, i.e. stork or accipitrid nests, but a majority of nests are still located on the ground. This is contrary to the indication that ground nests are selected only if rocky areas or other bird nests are unavailable, as many will utilize ground nests even where large bird nests seem to be accessible. Tree holes being used for nesting sites are even more rarely recorded than nests constructed by other birds. While it may be assumed that the eagle-owl is too large to utilize tree hollows, when other large species like the great grey owl have never been recorded nesting in one, the even more robust Blakiston's fish owl nests exclusively in cavernous hollows. The Eurasian eagle-owl often uses the same nest site year after year.
Parental behaviour
In Engadin, Switzerland, the male eagle-owl alone hunts until the young are 4 to 5 weeks old and the female spends all her time brooding at the nest. After this point, the female gradually resumes hunting from both herself and the young and thus provides a greater range of food for the young. While it may seem contrary to the species’ highly territorial nature, there is one verified cases of polygamy in Germany, with a male apparently mating with two females, and cooperative brooding in Spain, with a third adult of undetermined sex helping a breeding pair care for the chicks. The response of Eurasian eagle-owls to humans approaching at the nest is quite variable. The species is often rather less aggressive than some other owls, including related species like the spot-bellied eagle-, great horned and snowy owls, many of the northern Strix species, and even some rather smaller owl species, which often fearlessly attack any person found to be nearing their nests. Occasionally, if a person climbs to an active nest, the adult female eagle-owl will do a distraction display, in which they feign an injury. This is an uncommon behavior in most owls and is most often associated with small birds trying to falsely draw the attention of potential predators away from their offspring. More commonly, the adults withdraw to a safe distance, as their nests are usually well-camouflaged. Occasionally if cornered both adults and nestlings will do an elaborate threat display, also rare in owls in general, in which the eagle-owls raise their wings into a semi-circle and puff up their feathers, followed by a snapping of their bills. Apparently, eagle-owls of uncertain and probably exotic origin in Britain are likely to react aggressively to humans approaching the nest. Also, aggressive encounters involving eagle-owls around their nest, despite being historically uncommon, apparently have increased in recent decades in Scandinavia. The discrepancy of aggressiveness at the nest between the Eurasian eagle-owl and its Nearctic counterpart may be correlated to variation in the extent of nest predation that the species endured during the evolutionary process.
Eggs and offspring development
The eggs are normally laid at intervals of three days and are incubated only by the female. Laying generally begins in late winter but may be later in the year in colder habitats. During the incubation period, the female is brought food at the nest by her mate. A single clutch of white eggs is laid; each egg can measure from 56 to 73 mm (2.2 to 2.9 in) long by 44.2 to 53 mm (1.74 to 2.09 in) in width, and will usually weigh about 75 to 80 g (2.6 to 2.8 oz). In Central Europe, eggs average 59.8 mm × 49.5 mm (2.35 in × 1.95 in), and in Siberia, eggs average 59.4 mm × 50.1 mm (2.34 in × 1.97 in). Their eggs are only slightly larger than those of snowy owls and the nominate subspecies of great horned owl, while similar in size to those of spot-bellied eagle-owls and Blakiston's fish owls. The Eurasian eagle-owl’s eggs are noticeably larger than those of Indian eagle-owl and pharaoh eagle-owls. Usually clutch size is one or two, rarely three or four, and exceptionally to six. The average number of eggs laid varies with latitude in Europe. Clutch size ranges from 2.02 to 2.14 in Spain and the massifs of France, and 1.82 to 1.89 in central Europe and the eastern Alps; in Sweden and Finland, the mean clutch size is 1.56 and 1.87, respectively. While variation based on climate is not unusual for different wide-ranging palearctic species, the higher clutch size of western Mediterranean eagle-owls is also probably driven by the presence of lagomorphs in the diet, which provide high nutritional value than most other regular prey. The average clutch size, attributed as 2.7, was the lowest of any European owl per one study. One species was attributed with an even lower clutch size in North America, the great grey owl with a mean of 2.6, but the mean clutch size was much higher for the same species in Europe, at 4.05.
In Spain, incubation is from mid-January to mid-March, hatching and early nestling period is from late March to early April, fledging and postfledging dependence can range from mid-April to August, and territorial/courtship is anytime hereafter; i.e. the period between the beginning of juvenile dispersal to egg laying; from September to early January. The same general date parameters were followed in southern France. In the Italian Alps, the mean egg-laying date was similarly February 27, but the young were more likely to be dependent later, as all fledglings were still being cared for by the end of August, and some even lingered under parental care until October. In northern climes, the breeding season shifts somewhat later by as much as a month so that egg laying may be as late as late March or early April. Nonetheless, the Eurasian eagle-owl is one of the earliest nesting bird species in Europe or northern, temperate Asia.
The first egg hatches after 31 to 36 days of incubation. The eggs hatch successively; although the average interval between egg-laying is 3 days, the young tend to hatch no more than a day or two apart. Like all owls that nest in the open, the downy young are often a mottled grey with some white and buff, which provides camouflage. They open their eyes at 4 days of age. The chicks grow rapidly, being able to consume small prey whole after roughly 3 weeks. In Andalusia, the most noticeable development of the young before they leave the nest was the increase of body size, which was the highest growth rate of any studied owl and faster than either snowy or great horned owls. Body mass increased fourteen times over from 5 days old to 60 days old in this study. The male continues to bring prey, leaving it on or around the nest, and the female feeds the nestlings, tearing up the food into suitably sized pieces. The female resumes hunting after about 3 weeks, which increases the food supply to the chicks. Many nesting attempts produce two fledglings, indicating that siblicide is not as common as in other birds of prey, especially a few species of eagles. In Spain, males are thought to be the first egg laid to reduce the likelihood of sibling aggression due to the size difference, thus the younger female hatchling is less likely to be killed since it is similar in size to its older sibling.
Apparently, the point at which the chicks venture out of the nest is driven by the location of the nest. In elevated nest sites, chicks usually wander out of the nest at 5 to as late as 7 weeks of age, but have been recorded leaving the nest if the nest is on the ground as early as 22 to 25 days old. The chicks can walk well at 5 weeks of age and by 7 weeks are taking short flights. Hunting and flying skills are not tested prior to the young eagle-owls leaving the nest. Young Eurasian eagle-owls leave the nest by 5–6 weeks of age and typically can be flying weakly (a few metres) by about 7–8 weeks of age. Normally, they are cared for at least another month. By the end of the month, the young eagle-owls are quite assured fliers. A few cases have been confirmed of adult eagle-owls in Spain feeding and caring for postfledgling juvenile eagle-owls that were not their own.
Like many large owls, Eurasian eagle-owls leave the nest while still in a functionally flightless state and with large amounts of second down still present, but will fly shortly thereafter.
A study from southern France found the mean number of fledglings per nest was 1.67. In central Europe, the mean number of fledglings per nest was between 1.8 and 1.9. The mean fledgling rate in the Italian Alps was 1.89, thus being similar. In the Italian Alps, heavier rainfall during breeding decreased fledgling success because it inhibited the ability of the parents to hunt and potentially exposed nestlings to hypothermia. In the reintroduced population of eagle-owls in Eifel, Germany, occupied territories produced an average of 1.17 fledglings, but not all occupying pairs attempted to breed, with about 23% of those attempting to breed being unsuccessful. In slightly earlier studies, possibly due to higher persecution rates, the mean number of young leaving the nest was often lower, such as 1.77 in Bavaria, Germany, 1.1 in lower Austria, and 0.6 in southern Sweden. An experimental supplemental feeding program to young eagle-owls on two small Norwegian islands were found to increase mean numbers of fledglings from a mean of about 1.2 to 1.7 despite evidence that increased human activity near the nest decreased owlet survivability. While sibling owls are close in the stage between leaving the nest and fully fledged, about 20 days after leaving the nest, the family unit seems to dissolve and the young disperse quickly and directly. All told, the dependence of young eagle-owls on their parents lasts for 20 to 24 weeks. Independence in central Europe is from September to November. The young leave their parents' care normally on their own, but are also sometimes chased away by their parents. The young Eurasian eagle-owls reach sexual maturity by the following year, but do not normally breed until they can establish a territory at around 2–3 years old. Until they are able to establish their own territories, young eagle-owls spend their lives as nomadic "floaters", and while they also call, select inconspicuous perch sites unlike breeding birds. Male floaters are especially wary about intrusion into an established territory to avoid potential conspecific aggression.
Status
he Eurasian eagle-owl has a very wide range across much of Europe and Asia, estimated to be about 32,000,000 km2 (12,000,000 sq mi). In Europe, the population is estimated at 19,000 to 38,000 breeding pairs, and in the whole world around 250,000 to 2,500,000 individual birds. The population trend is thought to be decreasing because of human activities, but with such a large range and large total population, the International Union for Conservation of Nature has rated the bird as being of least concern. Although roughly equal in adaptability and wideness of distribution, the great horned owl, with a total estimated population up to 5.3 million individuals, apparently has a total population that is roughly twice that of the Eurasian eagle-owl. Numerous factors, including a shorter history of systematic persecution, lesser sensitivity to human disturbance while nesting, somewhat greater ability to adapt to marginal habitats and widespread urbanization, and slightly smaller territories may play into the horned owls greater numbers in modern times. Eurasian eagle-owls are listed in Appendix II of the Convention on International Trade in Endangered Species (CITES) meaning international trade (including in parts and derivatives) is regulated.
Longevity
The Eurasian eagle-owl surely is one of the longest-living owls on average. The eagle-owl can live for up to 20 years in the wild. At one time, the oldest ringed eagle-owl was considered a 19-year-old specimen. Some studies posited that in protected areas, lifespans ranging up to 15–20 years may not be uncommon. A record-breaking specimen banded in the wild was subsequently found to survive to be 27 years and 9 months old. Like many other bird species in captivity, they can live much longer without having to endure difficult natural conditions, and have possibly survived up to 68 years in zoo collections. Healthy adults normally have no natural predators, thus are considered apex predators. The leading causes of death for this species are man-made; electrocution, traffic accidents, and shooting frequently claim the lives of eagle-owls.
Anthropogenic mortality
Electrocution was the greatest cause of mortality in 68% of 25 published studies, and accounted, on average, for 38.2% of the reported eagle-owl deaths. This was particularly true in the Italian Alps, where the number of dangerous, uninsulated pylons near nests was extremely high, but is highly problematic almost throughout the species’ European distribution. In one telemetry study, 55% of 27 dispersing young were electrocuted within 1 year of their release from captivity, while electrocution rates of wild-born young are even higher. Mortality in the Swiss Rhine Valley was variable, in radio-tagged, released individuals, most died as a result of starvation (48%) rather than human-based causes, but 93% of the wild, untagged individuals found dead were due to human activities, 46% due to electrocution, and 43% due to collision with vehicles or trains. Insulation of pylons is thought to result in a stabilisation of the local population due to floaters taking up residence in unoccupied territories that formerly held deceased eagle-owls. Eurasian eagle-owls from Finland were found mainly to die due to electrocution (39%) and collisions with vehicles (22%). Wind turbine collisions can also be a serious cause of mortality locally.
Eagle-owls have been singled out historically as a threat to game species, thus to the economic well-being of landowners, game-keepers, and even governmental agencies, and as such, have been singled out for widespread persecution. Local extinctions of Eurasian eagle-owls have been primarily due to persecution. Examples of this include northern Germany in 1830, the Netherlands sometimes in the late 19th century, Luxembourg in 1903, Belgium in 1943, and central and western Germany in the 1960s. In trying to determine causes of death for 1476 eagle-owls from Spain, most were unknown and undetermined types of trauma. The largest group that could be determined, 411 birds, was due to collisions, more than half of which were from electrocution, while 313 were due to persecution, and merely 85 were directly attributable to natural causes. Clearly, while pylon safety is perhaps the most serious factor to be addressed in Spain, persecution continues to be a massive problem for Spanish eagle-owls. Of seven European nations where modern Eurasian eagle-owl mortality is well-studied, continual persecution is by far the largest problem in Spain, although also continues to be serious (often comprising at least half of studied mortality) in France. From France and Spain, nearly equal numbers of eagle-owls are poisoned (for which raptors might not be the main target), or shot intentionally.
Conservation and reintroductions
While the eagle-owl remains reasonably numerous in some parts of its habitat where nature is still relatively little disturbed by human activity, such as the sparsely populated regions of Russia and Scandinavia, concern has been expressed about the future of the Eurasian eagle-owl in Western and Central Europe. There, very few areas are not heavily modified by human civilisation, thus exposing the birds to the risk of collisions with deadly man-made objects (e.g. pylons) and a depletion of native prey numbers due to ongoing habitat degradation and urbanisation.
In Spain, long-term governmental protection of the Eurasian eagle-owl seems to have no positive effect on reducing the persecution of eagle-owls. Therefore, Spanish conservationists have recommended to boost education and stewardship programs to protect eagle-owls from direct killing by local residents. Unanimously, biologists studying eagle-owl mortality and conservation factors have recommended to proceed with the proper insulation of electric wires and pylons in areas where the species is present. As this measure is labour-intensive and therefore rather expensive, few efforts have actually been made to insulate pylons in areas with few fiscal resources devoted to conservation such as rural Spain. In Sweden, a mitigation project was launched to insulate transformers that are frequently damaged by eagle-owl electrocution.
Large reintroduction programs were instituted in Germany after the eagle-owl was deemed extinct in the country as a breeding species by the 1960s, as a result of a long period of heavy persecution. The largest reintroduction there occurred from the 1970s to the 1990s in the Eifel region, near the border with Belgium and Luxembourg. The success of this measure, consisting in more than a thousand eagle-owls being reintroduced at an average cost of US$1,500 per bird, is a subject of controversy. Those eagle-owls reintroduced in the Eifel region appear to be able to breed successfully, and enjoy nesting success comparable with wild eagle-owls from elsewhere in Europe. Mortality levels in the Eifel region, though, appear to remain quite high due to anthropogenic factors. Also, concerns exist about a lack of genetic diversity of the species in this part of Germany. Apparently, the German reintroductions have allowed eagle-owls to repopulate neighbouring parts of Europe, as the breeding populations now occurring in the Low Countries (the Netherlands, Belgium, and Luxembourg) are believed to be the result of influx from regions further to the east. Smaller reintroductions have been done elsewhere, and the current breeding population in Sweden is believed to be primarily the result of a series of reintroductions. Conversely to numerous threats and declines incurred by Eurasian eagle-owls, areas where human-dependent, non-native prey species such as brown rats (Rattus norvegicus) and rock pigeons (Columba livia) have flourished, have given the eagle-owls a primary food source and allowed them occupy regions where they were once marginalized or absent.
Occurrence in Great Britain
The Eurasian eagle-owl at one time occurred naturally in Great Britain. Some, including the RSPB, have claimed that it had disappeared about 10,000–9,000 years ago, after the last ice age, but fossil remains found in Meare Lake Village indicate the eagle-owl occurring as recently as roughly 2,000 years ago in the fossil record. The lack of presence of the Eurasian eagle-owl in British folklore or writings in recent millennium may indicate the lack of occurrence by this species there. The flooding of the land bridge between Britain and continental Europe may have been responsible for their extirpation as they only disperse over limited distances, although early human persecution presumably played a role as well. Some reportages of eagle-owls in Britain have been revealed to actually be great horned owls or Indian eagle-owls, the latter a particularly popular owl in falconry circuits.[110] Some breeding pairs do still occur in Britain, though the exact number of pairs and individuals is not definitely known. The World Owl Trust stated that they believe some eagle-owls occurring in North England and Scotland are naturally occurring, making the flight of roughly 350 to 400 km (220 to 250 mi) from the west coast of Norway to Shetland and the east coast of Scotland, as well as possibly from the coasts of the Netherlands and Belgium to the south. Although not migratory, eagle-owls can disperse some notable distances in young birds seeking a territory.
Prior studies of eagle-owl distribution have indicated a strong reluctance to cross large bodies of water in the species. Many authorities state that the Eurasian eagle-owls occurring in Britain are individuals that have escaped from captivity. While, until the 19th century, wealthy collectors may have released unwanted eagle-owls, despite press to the contrary, no evidence of any organization or individual intentionally releasing eagle-owls recently with the intent to establish a breeding population has been found. Many feel that the eagle-owl would be classified as an "alien" species. Due to its predatory abilities, many, especially those in the press, have expressed alarm of their effect on "native" species. From 1994 to 2007, 73 escaped eagle-owls were not registered as returned, while 50 escapees were recaptured. Several recorded breeding attempts have been studied, and most were unsuccessful, due in large part to incidental disturbance by humans and some due to direct persecution, with eggs having been smashed.
Effect on conservation-dependent species
As highly opportunistic predators, Eurasian eagle-owls hunt almost any appropriately sized prey they encounter. Most often, they take whatever prey is locally common and can take a large number of species considered harmful to human financial interests, such as rats, mice, and pigeons. Eurasian eagle-owls do take rare or endangered species, as well. Among the species considered at least vulnerable (up to critically endangered as in the mink and eel, both heavily overexploited by humans) to extinction known to be hunted by Eurasian eagle-owls are Russian desman (Desmana moschata) Pyrenean desman (Galemys pyrenaicus), barbastelle (Barbastella barbastellus), European ground squirrel (Spermophilus citellus), southwestern water vole (Arvicola sapidus), European mink (Mustela lutreola), marbled polecat (Vormela peregusna), lesser white-fronted goose (Anser erythrops), Egyptian vulture (Neophron percnopterus), greater spotted eagle (Clanga clanga), eastern imperial eagle (Aquila heliaca), saker falcon (Falco cherrug), houbara bustard (Chlamydotis undulata), great bustard (Otis tarda), spur-thighed tortoise (Testudo graeca), Atlantic cod (Gadus morhua), European eel (Anguilla anguilla) and lumpfish (Cyclopterus lumpus).
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Potentilla carniolica Kern., syn.: Potentilla micrantha Ramon ssp. carniolica (Kern) Gams
Carnolian Cinqufoil, DE: Krainer Fingerkraut
Slo.: kranjski petoprstnik
Dat.: June 4. 2015
Code: Bot_883/2015_DSC7071
All Lat.: 46.36035 Long.: 13.70272
Habitat: grassland, former pasture, mowed once per year, flat terrain, shallow, calcareous ground, half shade, exposed to direct rain, average precipitations ~ 3.000 mm/year, average temperature 7 - 9 deg C, elevation 600 m (2.000 feet), alpine phytogeographical region.
Substratum: soil.
Place: Lower Trenta valley between villages Soča and Trenta, lower part of Na melu place near Trenta 2b cottage, East Julian Alps, Posočje, Slovenia EC
Comment: Potentilla carniolica is, contrary to its species name (carnolica - Carniola is a historical name of a part of present Slovenia territory), actually a plant growing mainly in Dinaric mountains of Balkan Peninsula. It was first found at the northern edge of its distribution area and hence inadequately named. It enters the Alps only on its extreme northern part of distribution area and exclusively on the territory of Slovenia, where it is a quite rare species. In Slovenian Alps only a few stands in the Kamnik Alps has been known up to now. This find is its first known occurrence in the Julian Alps and at the same time its most northwest occurrence known.
Potentilla carniolica is probably often overlooked. It has similar appearance as other much more common white blooming Potentilla-s (Potentilla micrantha, Potentilla sterilis, Potentilla caulescens) and superficially even as genus Fragaria members, namely very common wild strawberry (Fragaria vesca) and eventually green strawberry (Fragaria viridis). However, plants with similar white flowers, which have leaves compound from three leaflets, have no stolons, don't have red inner side of sepals, which do not develop berries and which are covered in addition to long simple hairs also with short glandular hairs are surely Potentilla carniolica.
Ref.:
(1) Personal communication. Determination confirmed by Dr. Igor Dakskobler, Natural History Institute 'Jovan Hadži', Slovenian Academy of Science and Art.
(2) A. Martinči et all., Mala Flora Slovenije (Flora of Slovenia - Key) (in Slovenian), Tehnična Založba Slovenije (2007) (in Slovene), p 256.
(3) D. Aeschimann, K. Lauber, D.M. Moser, J.P. Theurillat, Flora Alpina, Vol. 2., Haupt (2004), p 782.
(4) R. Domac, Flora Hrvatske (Flora of Croatia) (in Croatian), Školska Knjiga, Zagreb (1994), p 172.
(5) N. Jogan (ed.), Gradivo za Atlas flore Slovenije (Materials for the Atlas of Flora of Slovenia), CKSF (2001), p 297.
Meerkats are born with hair but not full coats and with their eyes closed. They will live in the wild up to 10 years. However, in captivity they can live to be 15 years of age. Although they are relatively healthy animals, they are unfortunately prone to bovine tuberculosis and have been known to get rabies. When they are adults at about one year of age they will weigh around 2 pounds (750 - 820 grams) and stand an average of 12 inches high (30 centimeters). When they are on all four of their feet their height is only 6 inches (15 centimeters). Like all mongooses, they are agile hunters; however, they differ considerably from most of their other relatives. Unlike the typical mongoose of which there are around 35 types, Meerkats live in communities and depend on one another for survival. There are three other types of sociable mongooses, the Banded, the Kousi Mansi and the Dwarf mongooses. They also live in groups, but are not usually found in the Kalahari desert. While most mongooses are nocturnal, Meerkats hunt during the day. They live at night in burrows, which are complex tunnel systems consisting of mounds, access holes, and tunnels which lead to numerous sleeping chambers. A Meerkat community is called a mob or gang, and can number up to 40. There is always a dominate alpha male and dominate alpha female in each gang. The Meerkats larger mongoose relatives typically live alone or in pairs. These intelligent animals are extremely communicative and posses a large vocabulary. They flourish in their environment and are not endangered.
Meerkats live in southern part of Africa which is dominated by the Kalahari desert - The Kalahari spreads over the countries of South Africa, Namibia, Angola, Botswana, and Zimbabwe. The Kalahari desert has little rainfall and an arid climate with open plains. It spreads across the Southern part of Africa covering over one million square miles and is 10 times the size of Great Britain. The land is covered by a porous or soft sand that in many places is bright orange in color. The temperature in the summer months of October to April can reach 115 (f) or around 40 (c) which can give a sand temperature of 158 (f) or 70(c). In this harsh environment the difference between being in the sun and shade can be up to 86 (f) or 30 (c). The winter months from May to September are very different from the summer, you will see highs around 70 (f) or 22 (c) during the short days and lows at night down to 14 (f) or -10 (c). Winter is the dry season.
The average rainfall is 12 inches (300 millimeters) which comes between January and April. This is towards the end of the summer. There is little surface water but there is quite a bit of moisture below the sand. Generally, the broad plains of the Kalahari are covered with a thin coat of different types of grass and thorn scrub. When it rains during the summer, which is rare, the desert transforms into a lush carpet of plants, grasses, and flowers.
The Kalahari consists of both soft and compacted sands, ranging in color from bright orange to white. Meerkats like the soft sand when digging for food as it lessons the energy requirements in this harsh environment. However, they prefer compact sand to build their burrows which would collapse in softer sands. There could be any number of reasons Meerkats flourish in this environment, though all relate to competition for food and predators. One could speculate that the Meerkat may be a weaker type of mongoose that would find competing for food with other mongooses a tremendous hardship or that their coats would stand out making them easy prey for others. What is known is that Meerkats have specially adapted to the Kalahari, which is described later. The Yellow and the Slender mongooses also live in the Kalahari but generally live in harmony with the Meerkats. This is primarily because they each have a different diet and are not in competition for food. Unfortunately the Yellow mongoose will sometimes eat a Meerkat pup (baby), so meerkats will keep their distance from Yellows when there are pups around. Many other animals have also adapted over time in order to survive in this harsh environment, making the Kalahari a remarkable and interesting place. Even within this barren and harsh environment, animals and plant life flourish.
Animals in the Kalahari have a 40% lower metabolic rate then their counterparts in other parts of the world. This adaptation allows animals to survive with less food and water. Of course,the Kalahari's intense heat puts animals at risk of overheating, making the ability to efficiently regulate body temperature a necessity. Body size is key, the smaller the animal the faster the loss and gain of body heat. The "mouse-to-elephant curve" measures this relationship. The general idea is as follows, a gerbil has a 50 times higher metabolic rate than a elephant (per gram of bodyweight); therefore, the amount of energy from food that the gerbil needs to maintain its body temperature is greater than the elephants, making the need for food gathering almost constant. The Meerkat looses 5% of its body weight over night making the search for food very important every day. Can you imagine losing 5% of your body weight over night ? They can also get their fluid requirements from what they eat, so water sources while not a neccessity are helpful.
by: Lester Levy Jr
Meerkats.net
Meerkat characteristics - Meerkats at adulthood will grow to a standing height of 12 inches (30 centimeters) and weigh around 2 lbs. (750-820 grams). A pregnant female will weigh around 2.8 lb. (1.1 kilos). Their legs are short and their bodies are long and thin. Their tails are also long and thin with a dark tip. The reason for the dark tip is to identify other gang members while foraging for food. Meerkats forage for food with their tails in an upright position enabling them to easily identify their fellow gang members. Meerkats reach sexual maturity at 10 months and adulthood at 11 months. Both males and females share similar physical traits such as short hair and gray or tan markings. The markings on their backs are unique and no two are the same. They have dark brown or black bands around their eyes. Their ears are tipped with black or dark brown. They have dark bands on their sides and back. Their faces and throat are predominately a shade of white. There are four digits on each foot with very sharp non-retractile claws which are curved. They use their claws to dig their burrows. Meerkats also have the unique ability to close their ears, this is to keep dirt out while they burrow, which they do quite often.
Meerkats fur ranges in color from silver to orange to brown. Much of this depends on the subspecies as well as the sand color in which they live.Even in close proximity in the Kalahari you will find Meerkats with tanish fur in the dried out riverbeds and orange fur in the dunes above. Their coats have a great ability to act as both an insulation to keep heat in and an exhaust system to prevent them from overheating in the harsh climate. In the winter they will spread their hair out so to create a heat insulation effect much like a wet suit. Their stomach acts as a sort of solar panel during the winter months. Under a thin layer of stomach hair is a patch of dark skin which collects heat from the winter sun in order to provide warmth on cool days.
Meerkats vision is outstanding. They have a dark band around their eyes, which reduces any glare from the sun. As a result, Meerkats have the ability to see a predatory bird as they look directly into the sun. A Meerkat removes sand from its eyes by blinking. Between the eye and eye lid there is a white membrane called the nictitating membrane. This membrane acts as a windshield wiper and removes sand from their eyes with every blink. However, their ability to see things close up is not as good. Furthermore, they seem to have a problem with depth perception, not being able to focus within 20 feet (6 meters) of themselves. Often they will bob their head up and down trying to get the perspective right. As a result of this nearsightedness, they will often miss food directly in front of them. They often depend on their sense of smell to find food.
babies eating scorpion
meerkat.org
Meerkat cuisine .- Agile Meerkats always forage for their food in groups but catch and eat their food alone as their diet usually consist of small portions. As they search for their food they spread apart from one another on the desert floor. This distance between foraging Meerkats averages from 6 feet (2 meters) to 45 feet (15 meters), but can extend to 150 feet (50meters). The distance often depends on the availability of food. Generally Meerkats stay at their burrow one or two nights, so there line of foraging is usually from one burrow system to the next. During the winter when there is no grass and food is sparse they have been seen being as far as 150 feet (50 meters) apart. In the late summer when desert grass may reach three feet high and food is abundant they will forage about 6 feet (2 meters) apart. Meerkats frequently communicate with each other while they are looking for food in order to warn of possible dangers in the area or hear a distress call if one gets lost. Usually there is a Meerkat acting as a sentry watching for danger as the others look for food. This is usually the one that is the best fed at the time, there is no evidence that either sex has a predominance for sentry duty. If trouble arises, an alarm is sounded by the sentry and the gang will band together in a mob ( a mob is when Meerkats band together to fight) to assess what the danger is, and take appropriate defense actions. Meerkats will sometimes collect food for their pups and babysitters back at the den. The young pups as they learn to search for food will follow the adults to help supplement their diet. Current studies show that the pup that gives the loudest begging call gets the most food from the adults.
Most of the Meerkats food is found underground and their specially adapted bodies are perfect for this. Their front claws are curved and act as shovels. They often have to dig their own body weight in dirt just to get a small insect. Foraging for a Meerkat means digging here and there and occasionally finding a tasty morsel on the surface then moving forward with the gang on the endless search for food. A typical Meerkats diet consists of worms, crickets, grasshoppers, small rodents, lizards, small snakes, birds, eggs, fruit, and ant larvae (which they especially love). Insects are a particularly good source of nutrition for the Meerkats because they reproduce rapidly and supply an almost constant food source. I have even had the rare chance to see a Meerkat find a Kalahari truffle which is rare and very expensive in stores. He seemed to enjoy it immensely. Meerkats also love to eat poisonous scorpions which are plentiful. They do this by quickly biting off their stingers and then consuming the rest. Meerkats appear to be resistant to many deadly venom's which greatly increases the variety of their diet. A Meerkat will often drag any poisonous prey such as a scorpion or millipede across the sand before eating it. They do this to remove the chemical defenses of their soon to be meal. They will make use of a water source if one is nearby but Meerkats have developed the ability to get all their liquid requirements from their diet. In the summer, the Meerkats must work harder to get their food because the insects have burrowed deeper in the sand in order to be closer to moisture. The rain brings the insects back to the surface, which means feast to the Meerkat.
The Meerkat home - As mentioned previously, the Meerkats live in underground burrows which consist of entrance holes, tunnels, and sleeping chambers. There may be up to 70 different entrances to the burrow system which may also serve as an exit if the Meerkat is inside the burrow system. They are territorial and maintain an area of about one to three square miles. Their territorial expansion depends on the size of the gang, as well as, the abundance of food and water in the area. Meerkats mark their territory with the use of their anal gland or saliva from their cheek. This marking is done by the alpha male of the gang. They will protect their boundaries ferociously against other gangs. They have from 6 to 15 dens in their territory and will move dens every day or two. The breeding burrow ,which is where the offspring are born, is an exception to the frequent moves. Meerkats will stay at a breeding burrow for about three weeks. It is at this time that the young are able leave the burrow and start to learn to forage for food with the adults. In addition to this, the parasite loads become heavy in the burrow and fill with ticks, fleas and other undesirables after three weeks. Breeding burrows differ from other burrows in that they will have higher mounds of sand around the entrance holes. This is a result of the continual renovation of the tunnels and sleeping chambers necessary for the longer stays. The mounds of dirt around the entrances can reach up to three feet high. When breeding is successful Meerkats often return to the same breeding burrows to have there young. As the Meerkats rotate burrows, the insect population of each abandoned burrow has the opportunity to multiply. Furthermore, the burrow system itself needs to regenerate while the feces left behind becomes food for other animals and the parasite load decreases. When dens are not being used, snakes and ground squirrels often find them to be convenient residences. Mixed everywhere in the Meerkat territory are bolt holes. A bolt hole is a small system of entrances and tunnels between burrows. These bolt holes give Meerkats a place to take cover if danger arises if they are out foraging.
The strategic reasoning behind such an elaborate construction of multiple entrances, is to provide many alternative exits if a dangerous intruder should invade their home. Likewise they have multiple entrances in the burrow if the danger is from the outside. They sleep in groups, cuddled up or on top of each other for warmth as they are particularly sensitive to the cold. In the summer they tend to space out when they sleep. Their sleeping chambers are usually 6 to 8 feet under ground. This keeps the temperature in the sleeping chamber at a more constant level, cooler in the summer and warmer in the winter. There are several sleeping chambers in the den but they will only use one at a time, in the breeding burrows there will be more sleeping chambers. They will move sleeping chamber because of build up of contaminates. What may seem odd to you is, Meerkats will urinate in their dens. This could be for several reasons first it may aid in a marking system to one another. Second Meerkats don't survive well alone so to go outside at night to go to the bathroom is not a prudent thing. In captivity though Meerkats can be trained to go to the bathroom in a litter box. There are certain beetles that share their den that they don't eat. These insects will eat their deification. Above the tunnel system, there is usually a dirt mound resulting from all of their excavation. This higher vantage point serves as a lookout point for the small Meerkats. From this outpost of sorts, they can survey the terrain for predators. This done in the the morning before they leave the burrow for foraging and in the evening before they go to bed.
Other animals, such as squirrels or the yellow mongoose, sometimes share the Meerkats burrow. Because these animals do not compete with the Meerkats for food, they are allowed to share the den. When pup are born they will keep the yellow mongoose away because they will eat a Meerkat pup. Predators, such as cobras, are not welcome houseguests. Meerkats will purposely harass a cobra in the open so to discourage it from entering the den.
Meerkats sometimes move their territories when food becomes to sparse or when another gang of Meerkats forces them from their previous den. Often territories overlap one another and a stronger Meerkat gang will overtake a weaker gangs burrow system. This forces the weaker gang to take the loss and try to expand in another direction, or wait tell they are stronger and retake the lost burrow system.
Family standing on home
meerkat.org
babies feeding
meerkat.org
Mating and reproduction - Meerkats try, but do not usually mate for life. Mating in the gang is suppose to be reserved for the alpha male and alpha female, but things happen to change this. First the alpha male might die or be overthrown by another male from inside their gang or another gang. Or the alpha female might mate with a male from a wondering male from another gang while out foraging for food, the alpha male never knowing. What they won't do is mate with another direct family member. When the dominate female is ready to breed she will chase away all the other beta families that can bear children, this will be females at 10 months and older. The temporary outcast will follow the gang until the alpha female has had her pups (babies) and regains her strength. This is done because she wants only her offspring in the gang and another beta female might try and displace her during her weakened time of giving birth. The trailing females often get impregnated from males from other gangs they encounter. Often they will abort these births. If the do give birth they will attempt to sneak them in with the pups of the alpha female. The alpha female will if she notices kill and eat the beta females babies. The beta female have about a 20% chance of getting the young snack in with the alphas females pups. A interesting note, if the alpha female pup die, no other meerkat will eat them. A few days after the birth of the alphas pups, the once outlasted females will rejoin the gang and help with the giving milk to the new pups if they are able. It was once observed that a beta female killed the alpha females pups just after birth and replace them with her pups a few days later, the alpha female not knowing the difference. They can breed every two months but tend to successfully breed two to three times a year depending on food availability. There was one gang observed breeding four times in a year. The gestational period is 70 days resulting in a litter of usually five to six. The pregnant female will increase her body weigh approximately 40% gestation (see - Meerkats are a type of mongoose). The babies, called pups, are born with sparse fur and eyes closed. For the first two weeks they stay in the sleeping chamber and drink their mothers or milk producing females. The third week they will venture outside and stay around the burrow system with a babysitter. . During this period when the alpha female is not feeding the young, babysitters will watch the pups while the alpha female goes out to feed, fortifying her supply of milk and her strength. She will do less sentry duty at this time and never babysitting. From week 4 to week 6 the pups will forage with their elders getting nourishment from both milk and insects. At 6 weeks to 16 weeks they will find their own food as well as be supplemented by the elders, and no longer getting milk. Studies show that the pups that make the loudest begging calls get fed the most from the elders. After sixteen weeks they are on there own to find there food Each pup will be taken on by a adult Meerkat which will act as a mentor, who will take the responsibility to teach the pup necessary skills for foraging for food as well as responding to danger. Male Meerkats tend to mentor male pups and female Meerkats tend to mentor the female pups. Many of skills Meerkats have are taught by the mentors rather then being instinctual.
Meerkats reach sexual maturity at 10 months, and reach adulthood at 11 months. After 10 months a Meerkat may venture out of the gang looking for breeding opportunities. They may also leave to form new gangs or join other gangs. They also may stay with their original gang for up to three years before venturing out. They also may leave in groups of two or three. It takes a brave Meerkat to leave the gang because the road out if filled with many dangers for the sole are small group.
Typical day of a Meerkat - Meerkats are extremely social animals. Observing Meerkats is a wonderful experience. They love grooming one another, wrestling and playing with one other. They have avid curiosities and can make a toy of almost anything. Even with all this play, Meerkats do not ignore the need for security. One Meerkat always seems to be a sentry and stands guard to keep the gang safe.
There typical day consist of, they wake up early in the morning as the first rays of sun stretch across the Kalahari. The first to come out of the burrow is usually the last one in from the preceding night. This Meerkat surveys the area to make sure the coast is clear after that the others start to rise one by one from several entrances. They start by soaking up the sun to warm up there bodies from the nights sleep by facing the sun and using their stomachs as solar panels.. One may observe some digging around the entrances, this seems to be more like exercise to warm their bodies up. Then the young start to scurry around play and grooming one another, as the elders spend time grooming sunning. Once hunger starts to set in, the search for food is on. The alpha male sets the direction for the day and decide weather or not to move towards another burrow system.. Scurrying hear and there and digging here and there, but always one is on sentry. As the day goes on and the heat sets in they will stop for a rest. These rest periods are longer during the summers but so are the days. As the day cools they are off again in the afternoon in search of food. Just before sunset they will arrive at the den for the night. At this time they will commence on repairs of the den as well as well deserved grooming and giving one another affection which is really marking one another with the anal gland or cheek saliva. As the sun falls, they descend one by one into the burrow for sleep all huddled together. Lastly, they don't like the rain and will stay in their burrow and not forage for food until the rain stops.
Interestingly enough Meerkats seem to identify one another my smell rather than sight. That is why the are constantly marking one another. For instance if a Meerkat gets separated for some time and try to rejoin the gang, the gang will think it is a intruder and get in a mobbing defense stance ( mobbing is when they huddle together so to look bigger and present aggressive behavior) until they smell what they think is the unknown Meerkat. Once the sent is recognized everything is fine.
Two babies playing - by -Alain Degre
A sentry in a tree
by:Alain Degre
Meerkats social structure - To survive, Meerkats must live in groups for protection, as the desert presents many challenges. Each Meerkat has an important, role to perform. It was first thought Meerkats had well defined roles in their gang from being a sentry to baby sitting to foraging for food for the young. Recent studies have disprove this and actually show that hormonal changes in Meerkats influence their behavior. Also the conditions around the burrow system effect their responsibilities. When food and water is abundant more time is spent being sentries, renovating the burrow systems, relaxing and caring for the young. Some things are instinctual while others are taught to the pups by the elders. For example raising young is a learned behavior for Meerkats. If a pup is separated at birth and kept as a pet, and the pup gets pregnant. She will not know how to raise her young or teach them how to forage for food. Meerkat roles vary:
alpha male - Dominate male of the gang, has breeding rights to the alpha female. The dominate male is not necessarily decided by the largest male in the gang.
alpha female - Dominate female of the gang, all betas are subservient to her. Only one that is suppose to breed in the gang.
beta male - Subservient males will leave the gang by 3 years in search of better breeding opportunities. They are 10 months or older
beta female - Subservient females will support the alpha Meerkats. They will be driven temporally from the gang by the alpha female when she is ready to get pregnant. They will leave the gang by 3 years in search of better breeding opportunities. At 10 months or older they are at sexual maturity.
pups - Meerkat babies, 10 months or younger.
babysitter - Stays with the pups while the gang is out foraging for food. Different gang members take the responsibility different days, this is not domiated by males of females. Generally though the least hungry Meerkat will do the babysitting. The alpha female never baby-sits. This duty is for Meerkats 6 months or older.
sentry - Watches over the gang to spot danger. It is either done standing on the ground or climbing a tree or bush. Known to climb up to 30 feet in a tree to do sentry duty. This duty is not dominated by males or female. There is a sentry on watch both at the burrow system as well as when the gang is foraging for food. During times of less available food less sentry duty is done when searching for food.
excavating - Necessary to renovate burrow systems. Often Meerkats will get one behind another and work together to move sand out of the burrow system. Like how firemen would hand buckets of water to one another to put out a fire in the old days.
mentoring - A elder Meerkat will take on the responsibility of teach a pup the do's and do don'ts of being a Meerkat. This includes how to raise young, how to forage for food, and what dangers lurk about.
grooming - Meerkats like to groom one another, and in fact have a natural reflex to groom when the area where there back and tail meet is stimulated. They will remove ticks and fleas from one anther and actually eat them, though these parasites are not a normal part of the diet
play fighting - Often done by the young in the morning and to a lesser degree in the evening. Adults will also play fight. This teaches the young to fight as well puts a dominance order to the gang.
Beta males and famales often leave the gang by three years to live with different gangs or join together to form different gangs in order to increase their chances to breed. Meerkats that embark on this journey alone or in groups of two or three face great danger, as Meerkats are most vulnerable when they few in number. Sometimes Meerkats will ally themselves with one another and takeover another gang, and getting rid of the competitive alpha male and perhaps the alpha female.
The size and makeup of the meerkat community determines what duties each will have. There is usually a dominate male and female in the community although there also seems to be a second in command. I have seen a case where the alpha female was killed and the alpha male did not seem to know what to do. He had not taken on another alpha female because that would mean a female from the outside. It was felt he would at some point leave the gang in search of throwing out another alpha male from a rival gang. The alpha male is responsible for marking the territory, some of the foraging trips turn into more of scouting trips so the alpha male can mark the outer boundaries of the territory. These tend to be days of more movement and less foraging for food.
Fights happen between rival Meerkat gangs. It generally happens for two reasons. One is territory conflict. When one gang encroaches on another gangs territory. Once the two gangs come in contact with one another they group up together and fluff their fur out and jump up and down to make themselves appear bigger, also making allot of noise. This is called mobbing. Each gang is assessing the others strength. Sometimes they separating and go opposite directions other times a ferocious fight breaks out. Meerkats will kill rival gang members if they can. Also during a fight 2 or 3 Meerkats may jump on a rival biting and scratching him. It will look like a big pile of dust. During or directly after attacks, the dominant male will take a few minutes to asses the situation and decide weather there was a victory or his gang members have fled, in this case he will retreat himself. The other case happens when roaming Meerkats either solo or in small groups are looking for better breeding possibilities try to join other gangs. Mobbing occurs and they may be or may not be successful at joining the gang..
#How did the Meerkat evolve
How did the Meerkat evolve - According to Sean Doolan, they evolved from the southern tip of Africa or the Cape of Good Hope,where a type of extinct Meerkat, called the Suricata Suricatta major, has been found . The extinct Meerkat was similar to the banded mongoose. The current theory is that the Meerkat evolved from the banded mongoose. As the weather climate changed in the region, so did the Meerkats ability to survive in drier conditions.
Why the meerkat stands - Meerkats walk and run on all four, there head is only six inches above ground in this state. When they stand, their total height is 12 inches, providing them with a much better vantage point to see danger. In order to attain an even better vantage point, they will also climb trees and bushes. Their vision is good but depth perception does not appear to be as strong. They bob their head up and down to get distance measurement when objects or close. this gives them different focal points.When facing a threat, they will stand, arch their bodies and erect their tails in an attempt to appear bigger.
What threatens Meerkats? - The threats to a meerkat come from sky, land and weather. In the sky, the Martial Eagle, with a wing span of six feet, can easily prey on adults, while other smaller birds of prey prefer to snatch the young. When the winged predator is seen the alarm goes out and all sprint for nearby bolt holes. If they are not near any bolt holes the will lie on the ground and depend on camouflage They also may take cover in thorny bushes where the birds dare not venture. On the ground, the jackal and other wild cats are the Meerkats primary foe; however, when banded together, Meerkats have the ability to chase away a jackal. Badgers can also be a threat, as their burrowing can penetrate the Meerkats den making them more vulnerable prey. As mentioned previously, the cobra sometimes threatens meerkat young. Meerkats will mob a cobra relentlessly if it tries to enter their burrow. They are agile enough to avoid a snakes strike. They even have the ability to kill a cobra. If they come across one while our foraging they will temporarily mob it and once the situation is under control move on. A puff header snake will also eat Meerkat pups. I have read about a sighting in which a group of Banded mongooses actually climbed a tree to rescue one of their family members from a eagle. Both the Banded mongoose and the meerkat have similar social habits.
Meerkats are also threatened by other competitive gangs as mentioned above. The sentry's alarm will sound if another gang of Meerkats is encroaching upon marked territory. The fights are fierce but sometimes fatal as submission is the goal. The winners, usually the larger of the groups, take or keep the burrow system in question. One interesting note after the fight and Meerkats try and rejoin there gang small fight break out because they have difficulty recognizing each other by sight. The Meerkat rejoining their gang may smell like the rival gang. After the conflict, the winners will hug and congratulate each other with human-like gestures, this is rely remarking each other.. Often non-dominant Meerkats defect from the losing group to the winner's side.
The summer rains also threaten the Meerkats. When rain approaches, the sentry sends the alarm off. As there are often newborns during this time, they must make sure the are on high ground so to avoid a flooding of the burrow system. The alpha female will transport the young one by one to the higher ground burrow. At night they may get stuck in a flooding burrow system.
The most famous of all Meerkats - There are two famous Meerkats that should be mentioned One is Timone, who was featured in the Lion King. Timone, the cartoon character, is based on the real-life Meerkat Timone who which is domesticated resides outside of Palm Springs, California at the only private refuge for Meerkats in existence. For more information, visit www.meerkats.com. You can actually go and visit Timone and hand feed other Meerkats there. I did and it was a terrific experience.
The second is Ziziphus of the Lazuli gang. She is a wild Meerkat and lives in the Kalahari and has been the subject of numerous documentaries and films. One of her more prominent projects is Walking With Meerkats which is a National Geographic documtory filmed in 2000.
Meerkat communication - Meerkats constantly communicate with one another in three different ways: scent, sound, and body language. There have over 20 different sounds that have been recorded which have different meanings. These calls can be broken down into six different groups: lost calls, alarm calls, leading the group calls, pup feeding calls, guarding calls, and foraging calls. For example, while out looking for food, they are are constantly communicating in what sounds like a kind of growling. It helps them to keep track of one another's location since they forage up to 15 feet (5 meters) apart. When the young are learning how to forage, they are very loud and can be heard up to a hundred yards away. If they become separated from the adults, the volume of their cries increases so that an adult will come to get them. They have numerous sounds that are used when grooming and playing
When on guard duty, there is an entirely different assortment of sounds employed. These sounds are constant and communicate to everyone else what is happening during the watch. When everything is fine, the sentry emits mellow tones. When a predator is spotted at a distance, a beeping sound is given, almost like a yellow alert. If the predator gets closer, the sound differentiates depending on the type of predator. The martial eagle tends to get the most frantic alarm even from great distance. Meerkats allow some predators to get very close before they sound the red alert (up to 100 feet from the den).
One last interesting point, sound can be broken up into one, two, three, and even four syllable calls.
How the seasons effect Meerkats -
In the Savanna desert, temperatures can vary greatly. Remember, Meerkats live on southern hemisphere as opposed to the United States and Europe which are on the northern hemisphere. South of the equator and the seasons are opposite of those in the northern hemisphere. The Kalahari summer is considered the wet season, . The summer months October to April temperature can reach 115 (f) or around 40 (c) which can give a sand temperature of 158 (f) or 70(c). In this harsh environment the difference between being in the sun and shade can be up to 86 (f) or 30 (c). The winter months from May to September are very different from the summer, you will see highs around 70 (f) or 22 (c) during the short days and lows at night down below freezing to 14 (f) or -10 (c). Winter is the dry season. Because of these dramatic temperature changes, their feeding habits change accordingly
In the wet season or summer, Meerkats get up early in order to avoid looking for food in the heat. As the day gets warmer, they look for food in shaded areas. At mid-day they return to their den or find a nice, shaded spot for a mid-day nap. If they nap outside, they will lie on their belly with legs stretched out and often throw cooler sand on their back. They will pant during the summer this aids in reducing their body temperature. The yellow mongoose shares this behavior. They wake for a late afternoon feeding which ends at sunset. This season is a virtual feast for Meerkats, as the rain brings out an abundance of food and vegetation especially towards the end of summer from January to April. Grasses on the dunes can reach heights of over three feet tall! Meerkats will eat to their hearts content and their little bellies stick out.
In the dry season or winter, they wait until it warms up a little (9 a.m.) to go and look for food. No mid-day naps at this time. They stay out all day and get back around 4:30 p.m. Meerkats then remain in their den to avoid the rapid and severe temperature change night brings. Food is not as abundant during this time and foraging for food is more difficult. They have to do allot more digging and cover more territory to find adequate nutrition. They will also eat ants, ant eggs, millipedes, and small beetles which are less appealing to them than their summer favorites of lizards, insect larvae, and scorpions.
Meerkats like most other living creatures change their behavior patterns as conditions change. As one reads about the charertistics of any animal you must know whether the animal was observed in captivity or in the wild. Unfortunately most of what has been written about Meerkats has been in captivity, because of the remote habitat where they live makes it hard reach. Therefor it is interesting to understand how their behavior changes when confined to zoos.
The gang will find many differences in captivity. For example food will be abundant and the normal procurement of food such as digging is not necessary. Also space is significantly limited. So the Meerkats will not migrate from burrow to burrow, but stay in one burrow system. They also are not able to forage for food keeping them within meters of there burrow system for their whole lives. Predators are non existent in captivity so there alert systems are dulled. In captivity one will find Meerkats living longer and bigger. Meerkats do fine in captivity, in fact for the Meerkat which spends most of its time looking for food in the wild, this is probably a vacation. In captivity Meerkats are known to mate up to twice a year while in the wild they only mate once a year. Their cuisine is quite different to. In captivity the keepers may feed mice, worms and other sorted insects locally available. A Scorpion, a Meerkat delight would never be seen. Meerkats that don't get along with the gang will be separated and put in another habitat.
Would Meerkats make good pets? - The answer to this question is no, not really. In the United States, you need special permits to keep these animals. The government mandates strict specification for Meerkats enclosures as well as their climate. Meerkats will think your family is their gang and the are the alpha. When you have guest to your home they will get aggressive towards them. A host of other animals would make more appropriate pets! I have run into many people in southern part of Africa that keep Meerkats as pets and say they can be friendly. They are terrific pets though if you have a scorpion infestation problem.
Party.0 is an alcohol-free alternative to weekend drinking parties. Started by UW Oshkosh students, they are averaging 150 people per party.
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
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I really badly messed this shot up. I left my viewfinder uncovered and the camera auto metered to 0.5s instead of more like 3s (the sun was behind me). The result was 15 badly underexposed frames. Adobe Camera Raw wanted to add 3EV to get the levels up to "normal". Doing so added MASSIVE amounts of noise. Luckilly the image averaging technique is brilliant for recovering from this sort of thing.
So this got processed rather than binned.
This is a 71s Image Averaged shot of 15 frames.
Average division of incubation duties between male and female bald eagles in the Chesapeake Bay. Females do the lion’s share of the incubation mostly because they take the night shift. Composite data from seven eagle nests monitored with video cameras.
DAY 1 of the FINALE to the 2021 Motorsport Season and the end of the Season Brings us once again Back to Brands Hatch for a weekend Dedicated to the Enduro KA Series with Many Ford KA'S Ready to do Battle on the Track along with other Support Races such as Champion of Brands MSVT Track Day Trophy and MSV Super Cup Championship to name Just a Few.
With a Full Day of Motorsport on the Circuit Each Driver was Getting their Car Ready and making sure they had a Really Hardy Breakfast Before Getting into their Cars to Begin their Respective Qualifying Sessions for the Day.
Lets Get to it and See what The Last Event of the Motorsport Season Brings and who has Taken the First Pole of the Weekend.
Champion Of Brands-(Qualifying)
First Up onto the Circuit was The Champion of Brands and these Cars are Formula Ford Based and can be Very Quick in a Straight Line and through the Corner. With Cars such as the Van Diemen JL13 and the Ray GR16 Thease Cars and Drivers know how to Really Push Hard and Get Superb Results.
Lets Find Out who Took Pole and By How Much
In First Place Taking the First Pole Position of the Weekend was (Morgan Quinn) in his Formula Ford 1600 Kent with a Best Lap Time of 50.561 and a Top Speed of 86.00mph. Brilliant Work there Morgan Fantastic Lap to Start the Weekend of with a Bang.
In Second Place was (Lucas Romanek) in his Van Diemen JL13 with a Best Lap Time of 50.594 and a Top Speed of 85.95mph. Amazing Drive there Lucas Fantastic Work and a Very Good Spot on the Front Row for Race 1.
In Third Place was (Johnny Cochran) in his Formula Ford LA10 with a Best Lap Time of 51.250 and a Top Speed of 84.85mph. Great Drive there Johnny Fantastic Car Control and a Brilliant Lap to Complete The Top Three.
A Really Great First Qualifying Session of the Day with the Likes of Morgan Lucas and Johnny all taking the Top Three Spots in Qualifying but will anyone Else in the Field be able to Beat them off the Line into the First Corner at Paddock Hill Bend?
Lets Find Out
Champion Of Brands-(Race 1 Results)
After a Thrilling Qualifying Session which saw the likes of Morgan Quinn take Pole Position from Second Place Lucas Romanek with Johnny Cochran in Third Position in a Very Close Battle at the Top, it was Now Time to see which of thease Top Three Drivers could Defend their Positions thought the Race and who would be Brave Enough to make a Challenge for the Podium.
In First Place Taking the Victory was (Lucas Romanek) in his Van Diemen JL13 with a Best Lap Time of 50.711 and an Average Speed of 84.44mph. Congratulations Lucas a Really Well Deserved Win Under Immense Pressure Thought The Entire Race from Morgan Quinn. Brilliant Drive.
In Second Place was (Morgan Quinn) in his FF 1600 Kent with a Best Lap Time of 50.564 and an Average Speed of 84.42mph. Super Job out there Morgan Only 0.131 Seconds Behind Lucas and Some Really Good Defending and Battling From both of You Thought the Race. Fantastic Drive and Well Deserved.
In Third Place was (Benjamin Cochran) in his Formula Ford LA10 with a Best Lap Time of 51.095 and an Average Speed of 83.99mph. Great Work there Benjamin Keeping Hold of that P3 Position and Doing some Incredible work to Keep that Car on the Tarmac in Conditions that were Already Quite Dark.
A Really Thrilling Race to Open up the Weekend with the Likes of Lucas, Morgan and Benjamin all Taking Superb Victories in Race 1 as Well As Proving Thrilling Battles at The Top End of the Field.
Really Well Done to (Morgan Quinn) who also Took the Fastest Lap of the Race an Incredible (50.564) Second Lap Around The Famous Indy Circuit. Amazing Driving from Morgan.
A Big Congratulations to All of the other Drivers who also Took Part Your Passion and Dedication is Immense.
With One Last Race to Go will the likes of Lucas Romanek be able to Make it 2 out of 2 Wins for Champion of Brands or will the likes of both Benjamin and Morgan try to take that Last Victory Away from Him?
Lets Find Out
Champion Of Brands-(Race 2 Results FINAL)
In First Place taking the Last Victory for Champion of Brands Is (Lucas Romanek) in his Van Diemen JL13 with a Best Lap Time of 50.825 and an Average Speed of 83.45mph. Congratulations Once Again Lucas Two out of Two Wins and no Doubt a Very Happy Team and Family Awaiting You Before and After the Podium Fantastic Driving All Weekend.
In Second Place was (Morgan Quinn) in his FF 1600 Kent with a Best Lap Time of 50.754 and an Average Speed of 82.99mph. Very Well Driven there Morgan Great to See Such an Intense Battle Between you and Lucas for Victory in Conditions that were Almost Impossible to see anything in. Incredible Dedication and Drive.
In Third Place was (Benjamin Cochran) in his Formula Ford LA10 with a Best Lap Time of 51.862 and an Average Speed of 81.70mph. Nice Work there Benjamin Fantastic Driving in both Qualifying and The Two Races with a Brilliant P3 Finnish to Round off The Weekend for Champion of Brands.
What a Fantastic Day it has been for Champion of Brands seeing some Incredible Racing Action and a huge amount of Competitiveness from the Likes of Lucas Morgan and Benjamin who All Drove Fantastically and Put on One Hell of a Good Show.
A Huge Congratulations to both Lucas and Morgan as Well Who were in a Class of their Own at The Front of the Field Racing in Deteriorating Lighting Conditions with no Front Headlights on their Formula Fords to Light their Way around The Indy Circuit they Both Drove Insanely Well.
MSV Super Cup-(Qualifying)
Next Up onto the Circuit for the Day was the MSV Super Cup Championship and with a Wide Range and Variety of Racing Cars on Display it will be Very Interesting to see how many different Battles will Develop thought Both Qualifying and The Race.
From BMW E36's to Seat Super Copa's and even a Peugeot 205 GTI This Series has a Huge Amount of Variety Racing Within it.
Lets Take a Look at Qualifying and See Who Came Where
In First Place taking Pole Position was (Darren Goes) in his Seat Cup Racer with a Best Lap Time of 52.257 and a Top Speed of 82.21mph. Great Work there Darren Really Pushing the Car Hard and Having to Extract Everything from both Car and Driver to take P1. Super Job.
In Second Place was the Pairing of (A Bradley and D Bradley) in their BMW E36 with a Best Lap Time of 52.621 and a Top Speed of 82.64mph. Really Well Driven Gentlemen Very Close to Darren looking Forward to a Competitive First Race Between you All.
In Third Place was (Gary Hufford) in his BMW E46 M3 with a Best Lap Time of 52.723 and a Top Speed of 82.48mph. Nice Work there Gary Keeping that Fast and Capable BMW on the Track Looked to be no Easy Task but what a Fantastic Position to Start the First Race in.
Another Really Close Qualifying Session Between the likes of Darren Goes and the Pairing of A Brandley and D Bradley at the Top with Third Place Gary Hufford Following Closely Behind them.
With Their Only Race of the Day Coming Up Next will Daren Be able to Fend off the Charging Pair of A Bradley and D Bradley to take Home Victory or Will the Likes of Gary Hufford Surprise them All and Take the Victory for Himself?
Let's Find Out!
MSV Super Cup-(Race 1 Results FINAL)
In First Place Taking Victory was (Darren Goes) in his Seat Cup Racer with a Best Lap Time of 52.891 and an Average Speed of 77.05mph. Congratulations Darren A Well Deserved Victory Under Immense Pressure the Entire Time and No Doubt a Very Proud and Happy Family Waiting for Him Back in the Paddock.
In Second Place was the Pairing of (Brytchta/Smith) in their Seat Super Copa with a Best Lap Time of 52.594 and an Average Speed of 77.04mph. Great Drive from Both of You and Keeping Right on the Heels of Darren All The Time as well as Putting up a Huge Fight for First Place. Superb Drive and a Well Deserved P2 Finnish.
In Third Place was the Pairing of (A Bradley and D Bradley) in their BMW E36 with a Best Lap Time of 52.680 and an Average Speed of 76.93mph. Great Work to the Both of You Putting Pressure on Second Place Brytchta and Smith.
What an Intense Finnish to the Super Cup Championship with the Likes of Darren Goes Brytchta/Smith and A Bradley and D Bradley All Taking Superb Podium Finishes and no Doubt Going Back Home to a Very Happy and Proud Family of Great People.
Congratulations to All of the Other Drivers who were Also Out there Giving it their All You Guys are What Brings to Sprit of Every Racing Series to Life. Keep Working Hard and I'm Sure your Time Will Come.
MSVT Trackday Championship-(Qualifying)
Next Up was the Track Day Championship and with Another Massive Grid of 32 Cars from All Different Makes such as BMW Volkswagen Renault Ford and Caterham it was Going to be a Dynamic Qualifying Session with Many Different Cars and Drivers All Battling for Positions thought the Qualifying Session.
Lets Find Out who Came Out on Top and Who will be Starting on the Front Row for what Promises to be a Very Exciting and Close Race Later on.
In First Place taking the Victory and The Fastest Lap was (Scott Parkin) in his VW Golf TDI with a Best Lap Time of 54.419 and a Top Speed of 79.90mph. Congratulations Scott a Brilliant Pole Lap and Fantastic Car Control thought Every Corner.
In Second Place was (Chris Payne) in his Caterham Supersport with a Best Lap Time of 54.540 and an Average Speed of 79.73mph. Awesome Drive there from Chris Keeping up at The Front with Scott and Trading Fastest Laps thought the Qualifying Session. I Think both of them are going to put on a Brilliant Display of Racing Later.
In Third Place was The Pairing of (Keen and Roberts) in their Honda Civic Type R with a Best Lap Time of 55.231 and a Top Speed of 78.73mph. Amazing Drive from Thease Two Both Pushing Hard and Securing a Brilliant P3 Position for The Race. Great Job.
What a Qualifying Session with the Likes of Scott Parkin and Chris Payne Both Looking to be Very Competitive and Ready to Take Each other Head On Come the Race. But Will the Pairing of Keen and Roberts Come in and Also do Battle with Them?
Lets Find Out!
MSVT Trackday Championship-(Race 1 Results FINAL)
In First Place taking the Victory was (Scott Parkin) in his VW Golf TDI with a Best Lap Time of 54.706 and an Average Speed of 70.47mph. Congratulations Scott what a Performance and a Really Dominant Display of Driving to take Home a Wonderful Victory.
In Second Place was (Chris Payne) in his Caterham Supersport with a Best Lap Time of 54.397 and an Average Speed of 70.35mph. Amazing Drive there Chris Really Working Hard to Keep that 2nd Position while Also Fighting Hard to take 1st away from Scott at the front during some Laps.
In Third Place was (John Lyne) in his BMW E36 328i with a Best Lap Time of 55.309 and an Average Speed of 68.87mph. Congratulations John P3 with a Very Clean and Perfectly Controlled Drive thought, Its so Great to See a New Face on the Podium and Taking Victory. His Family and Close Friends Will be Very Proud of Him Indeed.
Another Incredible Race Today with the Likes of Scott Chris and John All Taking Home Superb Victories and no Doubt some Fantastic Memories from the Days Events too.
A Big Congratulations to both the Pairing of Keen and Roberts too who also put in a Monstrous Qualifying Lap to Land P3 on the Gird. Finishing the Race in 8th is not too Bad but I'm sure they have a lot of Work to-do Back at the Workshop and Will Come Back Next Year with an even more Competitive Honda Ready to Go.
Finally Congratulations to the Many other Drivers who also Took Part in this Race You All Put in a Tone of Hard Work and Dedication and I'm Sure that Over Time We Will See Some of You also on the Podium Just like John Lyne Today.
MSVT Trackday Trophy-(Qualifying)
Now it was Time for The Penultimate Qualifying and Race of the Day for the Track Day Trophy. Just like with the Previous Track Day Championship Many of the Same cars that Competed Before Also Entered This Race Giving Some Drivers a Second change to Show their Skills and Talents on the Race Track.
Lets take a Look at Qualifying and See Who will be on Pole This Time.
In First Place Taking Pole Position and The Fastest Lap was The Pairing of (R. Parkin and S. Parkin) in their VW Golf with a Best Lap Time of 53.795 and a Top Speed of 80.83mph. Incredible Work by both of the Parkin Pair as Scott Parkin Previously Won in Super Cup and Now he takes His Second Pole Position of the Day! Brilliant Driving.
In Second Place was (Chris Kirby) in his Caterham 1.6 Super Sport with a Best Lap Time of 53.863 and a Top Speed of 80.73mph. Brilliant Driving there Chris Keeping the Two Parkins on their Toes and Almost Taking Away Pole Position from them by Just 0.068 at The Checkered Flag.
In Third Place was the Pair of (Palk and Pottinger) in their Reno Clio with a Best Lap Time of 54.757 and a Top Speed of 79.41mph. Very Well Done both Palk and Pottinger on a Well Deserved and Defended P3 Finish by Less than a Second to Start on the Second Row for The Race.
A Super Fast and Really Exciting Qualifying Session Once Again with the Pairing of R. Parkin and S. Parkin Taking Pole Position Followed Closely by Chris Kirby in Second Place and Finally The Pairing of Palk and Pottinger in Third Place.
With The Race Just Around the Corner Will it be the Pairing of R Parkin and Scott Parkin Taking Victory Once More or Will a New Challenger Appear to take the Fight right to the Front of the Field?
MSVT Trackday Trophy-(Race 1 Results FINAL)
In First Place Taking the Victory is (R.Parkin and S.Parkin) in their VW Golf with a Best Lap Time of 54.046 and an Average Speed of 74.44mph. What a Dominant Display of Driving from thease Two Drivers in a Class of their Own they Have Managed to Win in Both Trackday Championship and Trackday Trophy. Brilliant Driving Well Deserved.
In Second Place was (John Lyne) in his BMW E36 328 with a Best Lap Time of 55.415 and an Average Speed of 73.09mph. Congratulations Once Again John P2 Finish and a Lot of Smiles and Congratulations from the Family I'm sure when you Return to the Paddock. Great Driving All Weekend.
In Third Place was (Stewart Donavan) in his Toyota Celica with a Best Lap Time of 55.083 and an Average Speed of 73.08mph. Congratulations Stewart P3 and Another New Face on the Podium and a Brilliant Looking Celica too. Fantastic Driving Great Job.
What a Brilliant Race from the Trackday Trophy with the Likes of Scott Parkin and R Parkin Taking the Spoils on P1 Followed Closely by John Lyne in P2 and Finally Stewart Donavan in P3.
A Big Congratulations Once Again to All of the other Drivers who took Part and Fought their way Through the Field to Finnish at The Checkered Flag. Keep Racing and Keep Pushing.
Enduro KA -(Qualifying)
After a Long Days Racing and with Night Falling Fast The Headlights of The Enduro KA'S Began to Illuminate the Indy Circuit.
Every Part of the Track was a Wash with Darkness and The Only Thing Illuminating the Way for Each Driver was The Bright Headlights and LED'S Fitted to Each Car with some Teams and Driver Trying their Luck on the KA'S Standard Headlights to Brighten their Way to Victory.
A Silent Hum Came From the Engines as they Raced Around the Indy Circuit with Each Driver Pushing Hard to Set the Fastest Time Possible.
The Tension in the Air was Electrifying as Drivers Danced their Cars Through Traffic and Had Small Battles with One Another Trying to see what their Opponents Tactics were and How Brave each of Them Dare Go in Terms of Pace.
It Wasn't Long before Each Driver Began to Put their Right Foot Hard Down and Push their
73BHP KA To its Limits Trying Desperately to Grab Hold of Pole Position Ahead of Sundays Intense 8 Hour 500 Minute Race.
After a Really Hectic Day of Both Qualifying and Racing Lets Find Out Who Took The Last Pole of Today and Who Will be Starting on The Front Row for Tomorrow's 8 Hour Endurance Race.
In First Place Taking the Victory and pole Position was Team (IP Racings) (Adam Blair / Scott Parkin / Oliver Wilmot / Mark Witherington) in their Ford KA with a Best Lap Time of 1:02.845 and a Top Speed of 69.19mph. Congratulations IP Racing Fantastic Work and a Super Start to the Endurance Race at The Very Front of The Grid.
In Second Place Following Closely Behind by Just 0.261 Seconds was Team (JTR) Elliot Mason / Nick Tandy / David Mason / James Rhodes in their Ford KA with a Best Lap Time of 1:03.106 and a Top Speed of 68.90mph. Superb Job there JTR Fantastic Effort and Really Good Pace to Gain P2 on the Grid for Tomorrow.
In Third Place was Team (Octane Junkies) (Adam Smith / Martyn Smith / Bazza Ward) in their Ford KA with a Best Lap Time of 1:03.110 and a Top Speed of 68.90mph. Great Work Octane Junkies Pushing Hard and Giving it Everything for P3.
After an Intense Qualifying Session the Likes of
Team IP Racings
(Adam Blair / Scott Parkin / Oliver Wilmot / Mark Witherington) Start the Endurance Race in First Place with
(JTR) Elliot Mason / Nick Tandy / David Mason / James Rhodes in Second Place Followed By
(Octane Junkies) (Adam Smith / Martyn Smith / Bazza Ward) in Third Place with the Top Three Very Closely Matched on Lap Times Thought Qualifying.
With Tomorrows Endurance Race being 8 Hours and The use of Driver Changes after 2 Hours in a Team with Four Drivers as Well as Pit Stops and a Whole Field of 45 Cars and Drivers Will the Likes of Team IP Racing Be able to Hold Out and Take Victory After 8 Gruelling Hours of Hard Racing.
Or Will JTR or Octane Junkies Try and Take that Thunder Away From Them? and Can Anyone Else Have a Go at Taking The Victory?
Only Time Will Tell!
See You All On Sunday.........!
Information On Race Results Found on TSL Timing Solutions
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers
The Finale to the BARC Club Car Championships Weekender at Brands Hatch and after a Very Thrilling set of both Qualifying Sessions and Races which took place on the Saturday it was Time once again for each Driver to strap in and get ready for some high speed Racing Action thought the Sunday.
In Tribute to the Marshall who was Tragically Killed on the Saturday Some Car and Driver Pairings were Racing with Orange Hearts on their Cars as a Tribute to all of Motorsports Family of Marshalls for who without Racing would not be possible. Thank You!
So Lets get started and see what the days events Haver to Offer and who can Push their Machinery to the Limits and beyond for a Victory.
Britcar Endurance Championship - Trophy Category (Race 1 Results FINAL)
The Britcar Endurance Trophy was the First up and it was time to see who could claim that elusive Pole Position and to see if anyone else could challenge the Top Three Drivers Lets see how things turned out.
In First Place was the Pairing Of (Datum Motorsport's Axel Van Nederveen and Adriano Medeiros) in their Ginetta G55A with a Best Lap Time of 52:193 and an Average Speed of 64.75mph. Congratulations Axel and Adriano a Really Fantastic Drive and A Super Victory.
In Second Place was (SVG's Mark Lee) in his Ginetta G56A with a Best Lap Time of 52.086 and an Average Speed of 64.70mph. Amazing Drive Mark Keeping that Ginetta on the Track and Taking Second Place while Nearly Matching the Speed of Axel and Adriano. Well Done.
In Third Place was (Terry Stephens) in his Peugeot 308 with a Best Lap Time of 53.421 and an Average Speed of 64.50mph. Well Fought Terry a Fantastic Finish in Third Place and Staying Ahead by just over 11 seconds to the Pair of Jasver and Bryan in 4th. Amazing Job.
A Really Enjoyable and Exciting First Race of the Sunday with High Speed Action and Incredible Victories on Track. Congratulations Axel Adriano Mark and Terry. Lets see what Race 2 Brings in terms of the Action.
Britcar Endurance Championship - Trophy Category (Race 2 Results FINAL)
Race 2 For Britcar Next and after a Very Fast and Action Packed First Race Will we see a New Face on the Top Step of the Podium? Lets find out.
In First Place was the Pairing of (Woodrow Motorsport's Simon Baker and Kevin Clarke) in their BMW 1 Series with a Best Lap Time of 51.837 and an Average Speed of 78.22mph. Amazing work Simon and Kevin who have Beaten the Pairing Of (Datum Motorsport's Axel Van Nederveen and Adriano Medeiros) to Victory. An Incredible Drive by Both of them Well Done.
In Second Place was (SVG Mark Lee) in his Ginetta G56A with a Best Lap Time of 52.281 and an Average Speed of 76.89mph. Again a Huge Congratulations to Mark Lee for hanging onto that Second Place Despite Fierce Competition during The Race. Amazing Drive.
In Third Place was (Simon Green Motorsport's Pairing of Jasver Sapra and Brian Branson) in their BMW M3 E46 with a Best Lap Time of 52.718 and an Average Speed of 76.88mph. Congratulations Jasver and Brain Brilliant Drive and well Defended to keep that Third Place in Tact.
Two Incredible Races with Two Very Different Outcomes of Race Winners and Runners Up The Britcar Endurance Trophy is Proving to be Very Competitive this Year.
A Huge Congratulations to Simon Kevin Mark Jasver and Brain for some Amazing Racing and Victories and Good Luck to All Other Drivers. Keep working Hard and Pushing for that All Important Victory.
CTCRC Edmundson Electrical Classic / Historic Thunder Saloons (Race 1 Result FINAL)
Next Up was the CTCRC Electrical and Historic Thunder Saloons and After a Thrilling Qualifying Session Yesterday Lets see what Each Driver has got and who can Push to the Limits for that All Important Victory.
In First Place was (Jason West) in his BMW E46 M3 3200 with a Best Lap Time of 51.907 and an Average Speed of 59.84mph. Congratulations Jason for Another Incredible Drive for First Place and a well Deserved Victory Amongst some Stiff Competition.
In Second Place was (Andrew Wilson) in his Holden Monaro 7000 with a Best Lap Time of 52.418 and an Average Speed of 59.96mph. Well Done Andrew Fantastic Driving and a Super Defensive Drive for Second Place.
In Third Place was (Samuel Wilson) in his Aston Martin V8 Vantage with a Best Lap Time of 52.699 and an Average Speed of 59.50mph. Amazing Work Samuel and a Beautiful Example of the Aston Martin V8 Vantage on Display Showing its Raw Power and Racing Pedigree to Finish in Third Place.
A Fantastic Finish to The Historic and Electrical Thunder Saloons Racing at The Weekend. A Huge Congratulations to Our Top Three Finishers Jason Andrew and Samuel. Fantastic Racing from all Three of you and Good Luck to all other Drivers Keep Tuning and Working Hard and I'm sure Victory Will not be too Far Away from you.
CTCRC JEC Saloon & GT Championship & Burton Power BOSS (Race 2 Results FINAL)
Next Up CTCRC Saloon and GT Championships and with some Fierce Competition on Display during not only Qualifying but also Their First Race on the Saturday Which saw Malcom Harding Storm to an Insane Victory who Will be able to Take him on and Potentially Steal his Crown during the Next Race Today? Lets See.
In First Place was (Malcom Harding) in his Ford Escort MK2 Zakspeed 2500 with a Best Lap Time of 53.888 and an Average Speed of 78.49mph. Another Incredible Victory for Malcom that Highly Modified Zakspeed Escort Really Shows off the Power and Performance of a True Champion and a Fantastic Driver. Congratulations Malcom.
In Second Place was (Steven Goldsmith) in his Ford Anglia 105e 260 with a Best Lap Time of 54.335 and an Average Speed of 78.21mph. Another Storming Drive to Achieve Second Place for Steven. Fantastic Driving and Amazing Car Control through Every Corner. Congratulations Steven.
In Third Place was (Tom Robinson) in his Jaguar XJ6 4000 with a Best Lap Time of 55.481 and an Average Speed of 55.481mph. Congratulations Tom Superb Display of Driving Ability behind the Jag and a Well Deserved Third Place for Him.
Another Incredible Weekend of Racing for the CTCRC Saloon and GT Championships with Some New and Some Old Drivers Stepping onto the Podium. Massive Congratulations to Malcolm Steven and Tom for their First Second And Third Place Finishes. Keep Up the Good Work and Never Stop Trying.
CTCRC Laser Tools Pre 93 & Simply Serviced Pre 03 Touring Cars (Race 1 Results FINAL)
Now Its Time for The Laser Tools Pre 93 and Simply Serviced Pre 03 Touring Cars to make their way back onto The Track for what Looked to be a Spectacular Race. A Whole Range of Different Cars to Race Against and Stiff Competition after Qualifying Proves that This Race will be One not to be Missed. Lets See what Unfolded.
In First Place was (Gary Prebble) in his Honda Civic EG 2000 with a Best Lap Time of 54.100mph and an Average Speed of 78.60mph. Well Done Gary a Really Well Deserved First Place Victory and an Amazing Drive to the Flag.
In Second Place was (David Griffith) in his BMW E36 M3 3058 with a Best Lap Time of 54.558 and an Average of 78.42mph. Incredible Drive their David Pushing that BMW For Everything that it Has got to Achieve Second Place.
In Third Place was (Kam Tunio) in his Honda Civic EK9 1595 with a Best Lap Time of 55.347 and an Average Speed of 77.05mph. Well Driven Kam Super Driving on Display and a Well Deserved Third Place Finish.
Another Amazing Race for The Pre 93 and Pre 03 Touring Cars and a Huge Congratulations to Gary David and Kam for their First Second and Third Place Victories. Keep up the Hard Work and Good Luck to everyone Else wherever your Next Races take you.
CTCRC Poultec Classic Race Engines Pre 66 Touring Cars (Race 1 Results)
Now it was Time for the Fan Favourite to Enter onto the Brands Hatch Circuit with the Pre 66 Touring Cars Championship. With Mini's Lotus Cortina's and Ford Falcons. This was One Race that No One Wanted to Miss. After a Very Fast Paced Qualifying Session on the Saturday Which saw (Alan Greenhalgh) take Pole Position who Will be able to Challenge Him During the Race and Snatch Victory Away from Him.
In First Place was (Alan Greenhalgh) in his Ford Falcon with A Best Lap Time of 58.707 and an Average Speed of 72.63mph. Congratulations Alan A Beautiful Example of the Ford Falcon and Certainly a Very Fast One too. Congratulations on Your Victory.
In Second Place was (Robyn Slater) in his Ford Anglia 1550 with a Best Lap Time of 58.992 and an Average Speed of 72.06mph. Very Good Drive their From Robyn to Secure Second Place in The First Race of the Day for the Pre 66 Touring Cars.
In Third Place was (Barry Sime) in his Morris Mini Cooper S 1293 with a Best Lap Time of 59.116 and an Average Speed of 71.95mph. Fantastic Work their Barry Keeping that Little Rocket on The Track looked to be Very Challenging but A Very Well Deserved Third Place.
What A First Race for The Historic Pre 66 Touring Cars showing The Power and Pride Each Driver takes in Both Racing and Preservation on Their Beloved Racing Machines. Congratulations to Alan Robyn and Barry on their First Second and Third Place Finishes. Lets See what New Challenges Await Them in Race 2 The Final Race of The Day for Them.
CTCRC Poultec Classic Race Engines Pre 66 Touring Cars (Race 2 Results FINAL)
The Epic FINALE To The Pre 66 Touring Cars Race was A Race in Wet Conditions Making it even more Challenging for The Top Three Drivers. Who would Win and be able to Retain if not Take on thease Three Giants of Touring Car Racing in thease Conditions. Lets See How Things Concluded.
In First Place was (Barry Sime) in his Morris Mini Cooper S 1293 with a Best Lap Time of 1:11.482 and an Average Speed of 58.62mph. Amazing Work Barry to take Home a Superb Victory and a Brilliant Bit of Wet Weather Driving in The Mini Well Done.
In Second Place was (John Davies) in his Austin Mini Cooper S 1293 with a Best Lap Time of 1:11.416 and an Average Speed of 58.38mph. Amazing Work John Racing A Mini in thease Conditions is Very Tricky and Yet both You and Barry made it look Easy.
In Third Place was (James Ibbotson) in his Hillman Imp Super 998 with a Best Lap Time of 1:11.518 and an Average Speed of 58.12mph. Well Done James Sliding that Imp around in the Wet for a Magnificent Third Place was Well Deserved.
What A Race to End the Day for the Pre 66 Touring Cars and with So many Old and New Winners Lets Hope we Get to see More Races like This One Thought the Rest of the 2021 Season. A Big Congratulations to Barry John and James on their Respective Victories and Keep Trying Everyone Else The Hard Work will Pay off.
CTCRC Shell Oils Pre 83 Touring Cars (Race 1 FINAL)
Up Next The Pre 83 Touring Cars took to the Track for Their Only Race of The Day and from what We Have Seen Already This Race also looks like its going to be a Very Strong Battle for First Second and Third Place. Lets See who Came First and Took that All Important Victory.
In First Place was (Mark Lucock) in his Ford Escort MK1 RS2000 2040 with a Best Lap Time of 57.687 and an Average Speed of 74.53mph. Amazing work there Mark Pushing All the Power the RS2000 Engine Has and Keeping it on Track to Score an Amazing Victory.
In Second Place was (Stephen Primett) in his Ford Escort MK1 2037 with a Best Lap Time of 57.503 and an Average Speed of 74.52mph. Another Brilliant Drive from the Likes of Stephen Keep the Pace with Mark and Making for some Fierce Competition Thought the Race.
In Third Place was (Mike Luck in his BMW E21 320 1998 with a Best Lap Time of 57.236 and an Average Speed of 74.46mph. Super Driving there Mike to take Third Place and a Very Classic Looking BMW Indeed.
What A Race from the Pre 83 Touring Cars showcasing Speed Power and What a Touring Car was Made to do around a Race Track. A Big Congratulations to Mark Stephen and Mike on their First Second and Third Place Finishes. Keep Racing and Keep Having Fun Out There.
Junior Saloon Car Championship (Race 1 Result FINAL)
The Junior Saloon Car Championship was Up Next and Even Though the Age Range of thease Next Drivers Taking to the Circuit Might Shock you at The Fact that Many of them are as Young as 15 Years of age don't be Fooled Because thease Guys Know how to Race Having been brought up from Carting since the age of 4. They are always a Fan Favourite and After Qualifying on the Saturday its Anyone's Game as to Who Wins and Who Losses in Thease Races.
In First Place was (Ruben Hage) in his Citroen Saxo VTR 1600 with a Best Lap Time of 59.967 and an Average Speed of 65.65mph. Congratulations Ruben What A Drive and an Incredible Run for First Place Fending off the Other On Coming Drivers. Truly a Championship Winning Drive.
In Second Place was (Harvey Caton) in his Citroen Saxo VTR 1600 with a Best Lap Time of 59.629 and an Average Speed of 65.64mph. Very Well Driven there Harvey Staying very Close to Ruben in First Place and Keeping Him on His Toes Thought the Entire Race.
In Third Place was (Charlie Hand) in his Citroen Saxo VTR 1600 with a Lap Time of 1:00.006 and an Average Speed of 65.57mph. Solid Third Place there Charlie Keep Up the Momentum and Never Give Up Chasing Your Dreams.
What a Fantastic Race from the Junior Saloon Car Championship with New Winners on the Podium and Some Close Wheel to Wheel Action Thought the Race Thease Guys will be Fantastic To see in Future Racing Series All Over The World. Congratulations to Ruben Harvey and Charlie for First Second and Third Place and Good Luck to All Other Aspiring Young Drivers Following in the Footsteps of Your Greatest Racing Heroes.
Kumho BMW Championship (Race 1 Results)
Finally it was Time for the Last Two Races of the Day the Kumo BMW Championship. Featuring The Makes and Models of Many BMW'S taking to the Circuit for Race 1. After a Busy Day Qualifying on Saturday Lets See what Each Driver Cando in The Frist of Two Races for their Championship.
In First Place was (Niall Bradley) in his BMW E46 M3 with a Best Lap Time of 50.920 and an Average Speed of 83.60mph. Brilliant Driving There Niall Pushing the Power of the BMW Engine to Max and Putting the Pedal to the Metal the Whole Race. A Superb Victory.
In Second Place was (Michael Vitulli) in his BMW E36 M3 3200 with a Best Lap Time of 51.158 and an Average Speed of 83.45mph. Another Incredible Driver Pushing Hard and Taking Second Place. Well Done Michael.
In Third Place was (James Card) in his BMW E46 M3 3200 with a Best Lap Time of 51.154 and an Average Speed of 83.42mph. Very Well Done their James Keep Pushing.
Three Fantastic Drivers in Niall Michael and James all Fighting for that Victory and Showing The Racer Inside each and Everyone of them. Lets see what Their Final Race of the Day Brings Them.
Kumho BMW Championship (Race 2 Results FINAL)
In First Place was (Niall Bradley) in his BMW E46 M3 with a Best Lap Time of 53.581 and an Average Speed of 77.79mph. Another Well Deserved First Place Finish to Round of The Days Racing. Congratulations Niall Go and Celebrate with The Team In Style.
In Second Place was (Darren Morgan Owen) in his BMW E46 M3 3200 with a Best Lap Time of 53.200 and an Average Speed of 77.43mph. Super Drive There Darren for Second Place and a New Winner onto The Podium.
In Third Place was (Brad Sheean) in his BMW E46 M3 3200 with a Best Lap Time of 53.227 and an Average Speed of 77.13mph. Fantastic Drive there Brad and Some Incredible Car Control thought the Entire Race to Finish Third.
And That Concludes Racing for the Kumho BMW Championship with 4 Different Winners Across two Races and A lot of Really Fast Action you could not Have Asked for a better Finish to The End of The Days Racing. Massive Congratulations to Niall Darren and Brad and Good Luck to all Other Competing Drivers who are still Looking for that almighty Victory.
That Concludes Racing for The BARC Club Car Championships Weekend A Big Congratulations to All of the Drivers of Every Team and a Huge Thank You to Marshalls Far and Wide as Without Your Support Events like This and Champion Drivers May Never Get to Achieve Their Dreams.
See You All At The Next One!
The treats arrived a little early for Average Betty this month! Flip to page 67 of the October MacLife Magazine and you'll see Betty in the latest MacGourmet Deluxe advertisement for Mariner Software. It's an honor for Betty to represent MacGourmet Deluxe and appear in such a well-respected publication. Thanks, Mariner Software! Betty loves you!
Greensboro, NC - 2/25/10
A Face to Face "social practice" event, The Soapbox Salon: Lee Walton's Search for the Most Average Bowlers