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From mid June to mid July, you can witness the lavender at full bloom meaning rows of purple as far as you can see, rolling over hills and into the sunset.

People flock from all corners of the world to experience the magic of Provence during the summer months with lavender being just one of the many drawcards. You’ll find fresh food markets in medieval villages, the crystal clear seas of the Mediterranean and about a 99% chance of sunny skies!

If your sole desire is to see the beauty of the lavender fields then, I’ve got you covered with this guide to Valensole, the best area in my opinion to photograph the fields. In order to get a great photograph you’ll need a car to zip around because there are a lot of fields, some more maintained than others. It’s also very warm in June and July so you don’t want to be stuck at a bus stop and walking miles to get to each field. There is a lot of information about where is best to see the lavender, photography wise though, you need to think about what type of shot you want.

Are you after a pure blue sky, small cottage or single tree? Or do you prefer a warmer light with sunset glowing above? You’ll need to take this into account otherwise you’ll be spending a lot of time waiting around for the light to be just right instead of covering a bunch of locations and getting more amazing photos.

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Around Provence you will find a collection of areas with lavender fields, from the base of Mount Ventoux, the magnificent Abbaye de Senanque or the regions around Apt, Forcalquier, Mezel and Nyons.

My favourite so far is the Plateau de Valensole. Rich in fields to choose between with a great selection of locations to shoot during the daylight and at sunset facing west.

Below is a map sharing the exact location of my favourite fields…

Best light for lavender photos: Between 6:30-10pm

In summer the sun sets around 9:20pm in Valensole so if you’re after that glowing sparkle of sunshine, it’s best to find your perfect spot before 9pm. I would even suggest getting there at 8:30pm because the sun can do some beautiful things prior to dipping below the horizon so why not be there to capture it? Maybe I’m just that annoying person who always has to be everywhere way too early!

Before sunset you’ll have beautiful blue sky to work with in the fields facing east so around 6-8pm is ideal. Any earlier and during summer you will find a light haze in the distance caused by the heat so it’s best to avoid the middle of the day.

Now for the locations…

Coordinates 43.89145N, 6.0668E

Location #1 D8 Valensole – Puimossion

Best For Distant Landscapes ( Visa Payment Cheap Online Golden Goose Black Glittery Superstar Sneaker Many Kinds Of Sale Online Free Shipping Inexpensive Cheap 2018 sCvNkAx
) : Travelling along the road called D8 from Valensole toward Puimoisson you’ll find a little hotel called Gite le Petit Tele, just before though is a great spot for photographs. Lavender fields sprawl east into the distance toward a row of trees that works as a great linear perspective.

Shah A , Connolly M , Clasper L , McIntyre C , Harvala H , Hale A , Whitaker P , Simmonds P , Peckham D . 2013. Frequency and pathogenicity of rhinovirus associated pulmonary exacerbations in patients with cystic fibrosis EUROPEAN RESPIRATORY JOURNAL , 42

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Human rhinoviruses (HRVs) frequently cause mild upper respiratory tract infections and more severe disease manifestations such as bronchiolitis and asthma exacerbations. HRV is classified into three species within the genus Enterovirus of the family Picornaviridae. HRV species A and B contain 75 and 25 serotypes identified by cross-neutralization assays, although the use of such assays for routine HRV typing is hampered by the large number of serotypes, replacement of virus isolation by molecular methods in HRV diagnosis and the poor or absent replication of HRV species C in cell culture. To address these problems, we propose an alternative, genotypic classification of HRV-based genetic relatedness analogous to that used for enteroviruses. Nucleotide distances between 384 complete VP1 sequences of currently assigned HRV (sero)types identified divergence thresholds of 13, 12 and 13 % for species A, B and C, respectively, that divided inter- and intra-type comparisons. These were paralleled by 10, 9.5 and 10 % thresholds in the larger dataset of >3800 VP4 region sequences. Assignments based on VP1 sequences led to minor revisions of existing type designations (such as the reclassification of serotype pairs, e.g. A8/A95 and A29/A44, as single serotypes) and the designation of new HRV types A101-106, B101-103 and C34-C51. A protocol for assignment and numbering of new HRV types using VP1 sequences and the restriction of VP4 sequence comparisons to type identification and provisional type assignments is proposed. Genotypic assignment and identification of HRV types will be of considerable value in the future investigation of type-associated differences in disease outcomes, transmission and epidemiology.

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Citation information in Europe Pubmed Central

BACKGROUND:  Infection with hepatitis C virus (HCV) is a burgeoning worldwide public health problem, with 170 million infected individuals and an estimated 20 million deaths in the coming decades. While 6 main genotypes generally distinguish the global geographic diversity of HCV, a multitude of closely related subtypes within these genotypes are poorly defined and may influence clinical outcome and treatment options. Unfortunately, the paucity of genetic data from many of these subtypes makes time-consuming primer walking the limiting step for sequencing understudied subtypes. METHODS:  Here we combined long-range polymerase chain reaction amplification with pyrosequencing for a rapid approach to generate the complete viral coding region of 31 samples representing poorly defined HCV subtypes. RESULTS:  Phylogenetic classification based on full genome sequences validated previously identified HCV subtypes, identified a recombinant sequence, and identified a new distinct subtype of genotype 4. Unlike conventional sequencing methods, use of deep sequencing also facilitated characterization of minor drug resistance variants within these uncommon or, in some cases, previously uncharacterized HCV subtypes. CONCLUSIONS:  These data aid in the classification of uncommon HCV subtypes while also providing a high-resolution view of viral diversity within infected patients, which may be relevant to the development of therapeutic regimens to minimize drug resistance.

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