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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

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