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Table 2 Abbreviations, descriptions and formulas of available variables for individual-tree diameter growth models

From: Simulating the diameter growth responses of Larix gmelini Rupr. and Betula platyphylla Suk. to biotic and abiotic factors in secondary forests in Northeast China

Attribute

Variable (unit)

Description

Formula

Symbols or explanation

Tree size

\({DBH}_{1}\)(\(\mathrm{cm}\))

Initial tree diameter in the period

\({d}_{1i}\)

\({d}_{2i}\) is the ith final tree diameter in the period, \({d}_{1i}\) is the ith initial tree diameter in the period, and \(\mathrm{ln}\) is the natural logarithm.

\({DBH}_{2}\)(\(\mathrm{cm}\))

Final tree diameter in the period

\({d}_{2i}\)

\({DBH}_{N}\)(\(\mathrm{cm}\))

Reciprocal of initial tree diameter

\(1/{\mathrm{d}}_{1i}\)

\({DBH}_{L}\)(cm)

Initial tree logarithmic diameter

\(\mathrm{ln}({\mathrm{d}}_{1i})\)

Stand attributes

\({D}_{g}\)(\(\mathrm{cm}\))

Quadratic mean diameter

\(\sqrt{(\sum {d}_{1i}^{2})/{n}_{j}}\)

\({d}_{1il}\) is the ith initial tree diameter of larch in the period, \({d}_{1ib}\) is the ith initial tree diameter of birch in the period, \({n}_{j}\) is the number of measured trees, \({n}_{jl}\) is the number of measured trees of larch, \({n}_{jb}\) is the number of measured trees of birch, \({h}_{1i}\) is the initial height of tree \(i\) in the period, \({n}_{k}\) is the number of measured trees in plot \(k\) (3–5 trees selected for measurement according to mean diameter), \(\overline{D }\) is the arithmetic mean diameter of trees, and \(S\) is the plot area.

\({D}_{gl}\)(\(\mathrm{cm}\))

Quadratic mean diameter of larch

\(\sqrt{(\sum {d}_{1il}^{2})/{n}_{jl}}\)

\({D}_{gb}\)(\(\mathrm{cm}\))

Quadratic mean diameter of birch

\(\sqrt{(\sum {d}_{1ib}^{2})/{n}_{jb}}\)

\({H}_{p}\)(\(\mathrm{m}\))

Average height of the dominant species

\(\sum {h}_{1i}/{n}_{k}\)

\({A}_{ge}\)

Age of forest stand

-

\(G\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Total species stand basal area

\(\frac{10000}{S}\left({\sum }_{i=1}^{{n}_{j}}\frac{\pi }{4}{d}_{1i}^{2}\right)\)

\(\mathrm{Ln}G\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Logarithm of \(G\)

\(\mathrm{ln}(G)\)

\({\mathrm{G}}_{l}\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Larch species stand basal area

\(\frac{10000}{S}\left({\sum }_{i=1}^{{n}_{j}}\frac{\pi }{4}{d}_{l1i}^{2}\right)\)

\({\mathrm{G}}_{b}\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Birch species stand basal area

\(\frac{10000}{S}\left({\sum }_{i=1}^{{n}_{j}}\frac{\pi }{4}{d}_{b1i}^{2}\right)\)

\(N\)(trees/ha)

Number of trees per hectare

\(\frac{10000}{S}{n}_{j}\)

\({N}_{l}\)(trees/ha)

Number of trees of larch per hectare

\(\frac{10000}{S}{n}_{jl}\)

\({N}_{b}\)(trees/ha)

Number of trees of birch per hectare

\(\frac{10000}{S}{n}_{jb}\)

Competition effects

\(BAL\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Basal area of larger trees for all species

\(\frac{10000}{S}\left({\sum }_{i=1}^{n}\frac{\pi }{4}{D}_{1q}^{2}\right)\)

\({D}_{1q}\) is the initial diameter of a tree that is larger than the target tree in the period, \({D}_{{1q}_{1}}\) is the initial diameter of a tree that is larger than the intraspecific target tree in the period, \({D}_{{1q}_{2}}\) is the initial diameter of a tree that is larger than the interspecific target tree in the period, and \(n\) is the number of trees.

\({BAL}_{1}\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Intraspecific basal area of larger trees

\(\frac{10000}{S}\left({\sum }_{i=1}^{n}\frac{\pi }{4}{D}_{1{q}_{1}}^{2}\right)\)

\({BAL}_{2}\)(\({\mathrm{m}}^{2}/\mathrm{ha}\))

Interspecific basal area of larger trees

\(\frac{10000}{S}\left({\sum }_{i=1}^{n}\frac{\pi }{4}{D}_{1{q}_{2}}^{2}\right)\)

\(BALD\)

Ratio of \(BAL\) and \({d}_{1}\)

\(BAL/\mathrm{ln}({d}_{1}+1)\)

\({BALD}_{1}\)

Ratio of \({BAL}_{1}\) and \({d}_{1}\)

\({BAL}_{1}/\mathrm{ln}({d}_{1}+1)\)

\({BALD}_{2}\)

Ratio of \({BAL}_{2}\) and \({d}_{1}\)

\({BAL}_{2}/\mathrm{ln}({d}_{1}+1)\)

Diversity index

\(SWI\)

Shannon–Wiener index

\(-{\sum }_{k=1}^{m}\frac{{n}_{1jk}}{{n}_{1j}}\mathrm{ln}\left(\frac{{n}_{1jk}}{{n}_{1j}}\right)\)

\(m\) is the number of species, \({n}_{1jk}\) is the initial number of trees for species \(k\) in plot \(j\) in the period, and \({n}_{1j}\) is the total initial number of trees within plot \(j\) in the period.

\(SPI\)

Simpson’s index

\({\sum }_{k=1}^{m}\frac{{n}_{1jk}({n}_{1jk}-1)}{{n}_{1j}({n}_{1j}-1)}\)

\(TAI\)

Total species abundance

\({\sum }_{k=1}^{m}\frac{{n}_{1jk}}{{n}_{1j}}\)

\({\mathrm{G}}_{LR}\)

Larch basal area proportion (%)

\(\frac{{G}_{l}}{G}\)

\({\mathrm{G}}_{BR}\)

Birch basal area proportion (%)

\(\frac{{G}_{b}}{G}\)

Topographic conditions

\(ALT (\mathrm{m})\)

Elevation

-

 

\(ASP (^\circ )\)

Slope aspect

-

\(SL (^\circ )\)

Slope gradient

-

\({ALTL}_{CA}\)

Logarithmic elevation times cosine of aspect

\(\mathrm{ln}\left(ALT\right)*\mathrm{cos}(ASP)\)

\({ALTL}_{TS}\)

Logarithmic elevation times tangent of slope

\(\mathrm{ln}\left(ALT\right)*\mathrm{tan}(SL)\)