PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest
PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest
PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest
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vation that species such as Brewer spruc e<br />
(Picea breweriana), Port-Orford-cedar<br />
(Chamaecyparis lawsoniana), vine maple<br />
(Ater circinatum), and rhododendron<br />
(Rhododendron macrophyllum) are restricte d<br />
to areas with low potential transpiration . Th e<br />
most valuable index, however, was the rati o<br />
of actual to potential transpiration (T/PT)<br />
Which integrates for water, the demand, th e<br />
supply, and the control b the plant . Where<br />
sot moisture was never inadequate and th e<br />
evaporative stress remained low, the ratio wa s<br />
1 .0. Where water became limiting and hig h<br />
evaporative stress was common, ratios of 0 . 3<br />
were calculated . Under these conditions, both<br />
forest composition and growth were dramatically<br />
affected .<br />
Measurement and Interpretation of Soi l<br />
Fertility and Plant Nutritio n<br />
Soil profiles from each stand were reconstructed<br />
to a depth of 60 cm and taken into<br />
controlled environment chambers where seedlings<br />
of Douglas-fir and Shasta red fir were<br />
grown for a period of 5 months (Waring an d<br />
Youngberg 1972) . The dry weight yields at<br />
the end of the experiment were used as a bio -<br />
assay of soil fertility, representing the supply<br />
of nutrients available to conifers . Foliar analyses<br />
were made on reference trees, first durin g<br />
the time of maximum demand when ne w<br />
foliage was being produced and again after al l<br />
shoot and diameter growth had ceased in th e<br />
fall. In the first period, 1-year-old foliage wa s<br />
assessed because it represents a major sourc e<br />
of mobile nitrogen, phosphorus, and potassium.<br />
Three categories of nutrient availability<br />
can be identified : (1) where no nutritional<br />
stress occurs during the year ; (2) where nutrition<br />
is adequate only when shoot and<br />
diameter growth has ceased ; and (3) where<br />
nutrition is inadequate year around (Warin g<br />
and Youngberg 1972) . These three categorie s<br />
may be further refined and are of consider -<br />
able value in reaching decisions concernin g<br />
fertilization. The composition of vegetatio n<br />
is, however, insensitive to this classification of<br />
nutrient availability .<br />
Only on soils where an imbalance of nutrients<br />
or toxic amounts of certain heavy metals<br />
were present did special plant communitie s<br />
develop. In this paper, therefore, we hav e<br />
assigned plants to one of three categories of<br />
tolerance to infertile soils developed from<br />
ultrabasic parent materials : In class 1 ar e<br />
those which are tolerant ; class 2 is made up of<br />
those species that are intolerant ; and in class 3<br />
are those plants both tolerant and competitively<br />
restricted to ultrabasic soils .<br />
Vegetation as an Index to Environmen t<br />
Can we use plants to define their environment,<br />
or more precisely, the environment expressed<br />
through reference plants? To test thi s<br />
idea, we selected 47 species from more than<br />
600 in the local flora and recorded thei r<br />
distributional limits in relation to various<br />
environmental plant indices (table 2) . For<br />
some plants we knew only the approximat e<br />
ranges and occasionally we had insufficien t<br />
data to set particular index limits .<br />
In forest ecosystems where plant composition<br />
is known, the range of environmenta l<br />
indices may be predicted from information i n<br />
table 2 . In table 3, the plant response indice s<br />
were thus predicted for the 25 stand s<br />
described in table 1 . Therefore for the blac k<br />
oak forest, stand 3, where Rhus diversiloba ,<br />
Arbutus menziesii, Lonicera hispidula, and<br />
Quercus chrysolepis grew, one can assess fro m<br />
table 2 that the Temperature Growth Inde x<br />
lies between 98 and 96, the Plant Moistur e<br />
Stress Index at 25 .4, and the ratio of transpiration<br />
to potential transpiration as 0 .29 .<br />
Plants that were exclusively adapted t o<br />
ultrabasic soils, such as Jeffrey pine, isolated<br />
those ecosystems (stands 4, 5, and 25) . Those<br />
forests with oak (stands 3, 8, and 21 )<br />
exhibited the greatest water stress, th e<br />
warmest environments, and the greatest control<br />
of transpiration . At the other extreme ,<br />
mountain hemlock forests (stands 6, 18, 15 ,<br />
and 24) had the coolest environments and<br />
lowest potential transpiration .<br />
In figure 5, the midpoint of the predicted<br />
Temperature Growth Index from table 3 is<br />
plotted against the Temperature Growt h<br />
Index calculated from temperature records .<br />
The regression has an r2 of 0 .93, and is highl y<br />
86