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Rawson's Retreat Penfolds 2012
South Eastern Australia Zone
Australia
Riesling
Cena: 78
Alk: 12,00%
Kolor: b
Nr 14721
www
Legenda (ocena):
8 - wybitnie, prawdziwe arcydzieło
7 - bardzo dobre, wino z dużą klasą
6 - dobre, interesujące
5 - całkiem niezłe, przyzwoite
4 - słabe
Brak gwiazdki
3 - omijać z daleka, wino z wyraźnymi wadami

Inne od Penfolds:
Autumn Koonunga Hill 2010 Sout..

Rawson's Retreat 2009 South Ea..

Rawson's Retreat 2007 South Ea..

Koonunga Hill 2006 South Easter..

Bin 28 Kalimna 2006 South Aust..

Koonunga Hill 2005 South Austra..

Winemaker's Selection 2005 Sout..

RWT 2005 Barossa Shiraz

Bin 389 2004 South Australia Ca..

Bin 138 2004 South Eastern Aust..

Bin 28 Kalimna 2003 South Easte..

Bin 128 2002 Coonawarra Shiraz
Grange 2001 South Australia Sh..

Koonunga Hill 2001 South Eastern..

Rawson Retreat 2001 South Austra..
Koonunga Hill 2001 South Eastern..
Bin 128 1999 Coonawarra Shiraz
Bin 707 1998 South Australia Ca..

Bin 707 1996 South Australia Ca..

Grange 1995 South Australia Shi..

star (2013-09-25) Ocena: 6
Znowu mi się to wino podoba. Nic z zamorskiej obfitości i słodyczy. Chude, wycyzelowane, sprężyste i mineralne. Jakby z Niemiec, a może raczej Austrii. Fajne posmaki, mało owocowe, gdzieś pewno z siarką się może skojarzyć, ale szlachetnie, mało dozową, w sam raz, dającą właśnie to mineralne namaszczenie. Bardzo smaczne, lekko musujące jak gdyby, choć bez przesady. Stare roczniki fajne - 2007 i 2009, teraz przeskok i znowu jest dobrze, a nawet bardzo dobrze. Oby tak dalej! Cena resto przez kieliszki pomnożona - więc przydrogo. @Nowa Łódź/PWW/FWS

star (2013-09-26)
O aromatach nafcianych Rieslinga mowa na (pralinka) Wine-Pages.com.

In addition to the intensifying and complexing of terpenoid aromas, bottle-ageing induces Riesling's famous petrol (kerosene, gasoline or paraffin) aroma. Anyone who has ever siphoned-off petrol will know that its head-splitting vapour has nothing in common with the classic petrolly aroma of a mature Riesling. It does not literally smell or taste of petrol. Yet for those who know and enjoy the zesty-honeyed richness of a great Riesling, petrolly is one of the most precisely defined, exquisitely evocative words in the wine tasting vocabulary. Some critics might come up with a veritable fruit-salad of descriptors, only some of which may be recognised by equally experienced tasters, but there is not one iota of doubt in the mind of anyone who has ever experienced the classic petrolly aroma of a mature Riesling that it is an instantly recognisable term, and one that is used without pretension. But what causes it, and is it possible to have too much of this good thing?
Riesling's so-called petrol aroma has been identified as trimethyldihydronaphthalene or, to be precise, 1,1,6-trimethyl-1,2-dihydronaphthalene (Simpson, 1978). TDN is a C13 norisoprenoid, which some class as a terpene, but others do not. It is a moot point; a semantic argument upon which chemists continue to differ. TDN is rarely found in grapes or, indeed, young wine, although its precursors are, and they are primarily carotenoids (may chemists state definitely beta-carotene, others probably alpha-carotene, while some think quite possibly both). Beta and alpha carotenes (and lutein a by-product of alpha carotene metabolism) are all antioxidants. These precursors exist in all grape varieties, thus TDN can be found in almost every wine, although the ratio of lutein to carotene is usually low, thus the TDN potential for most wines will be well under the perception threshold level of 20ppb. However, the ratio of beta carotene to lutein is higher in Riesling than for any other grape variety. If ,as most scientists believe, beta carotene is the primary precursor for TDN, this may explain why, after lengthy bottle-maturation, the wines from this variety can accumulate as much as 200ppb TDN, ten-times the perception level. This is why mature Riesling is famed for its so-called petrolly aroma.
TDN can also be produced by the hydrolysis of two megastigma-3,6,9-triols linked to a sugar molecule (Strauss et al, 1986) and it has been theorised that the hydrolysis of a sugar molecule called 2,6,10,10-tetramethyl-1-oxaspiro[4,5]dec-6-ene-2,8-diol can create TDN (Winterhalter, 1991; Silva Ferreira & Guedes de Pinho, 2004)

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