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  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>The Investigation of the Additive Allometric Models of Biomass</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Vladimir A. Usoltsev</string-name>
          <email>Usoltsev50@mail.ru</email>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Ivan S. Tsepordey</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>Botanical Garden of the Ural Branch of the, Russian Academy of Sciences</institution>
          ,
          <addr-line>620100, Russia, Ekaterinburg</addr-line>
        </aff>
        <aff id="aff1">
          <label>1</label>
          <institution>Ural State Forestry Engineering University</institution>
          ,
          <addr-line>620100, Russia, Ekaterinburg</addr-line>
        </aff>
      </contrib-group>
      <abstract>
        <p>When using the unique in terms of the volumes of databases on the level of a stand of Picea and Abies spp., the trans-Eurasian additive allometric models of biomass for Eurasian forests are developed for the first time, and thereby the combined problem of model additivity and generality is solved. The additive model of forest biomass of Picea and Abies is harmonized in three levels, one of which provides the principle of additivity of biomass components, the second one is associated with the introduction of dummy independent variables localizing model for eco-regions of Eurasia, and the third one makes the biomass structure of spruce and fir compatible by means of binary variable. The model can be developed further according to the third level of harmonization, when instead of the binary variable one can include another block of dummy variables coding the membership of actual biomass data of each eco-region to basic forestforming wood species in Eurasia. This might be a subject for further research.</p>
      </abstract>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>-</title>
      <p>Introduction</p>
      <p>
        In recent years, the scientific branch associated with the estimating the biological productivity of trees and stands is
the most intensely developed in two aspects: (1) in compiling the world's actual data bases on biological productivity at
the levels of forest stands and sample trees with their development through global and transcontinental patterns
[
        <xref ref-type="bibr" rid="ref21 ref25 ref28 ref29 ref4 ref47 ref8">47,29,28,8,25, 21,4</xref>
        ] and (2) in the development of methodological bases of regression modeling with the aim to
improve the accuracy of our estimates and the correctness of the empirical models of biological productivity of forests and
their constituent trees.
      </p>
      <p>
        The development of generic allometric biomass models [
        <xref ref-type="bibr" rid="ref24 ref26 ref30 ref32 ref35 ref48 ref53 ref6 ref7">35,30,7,24,53,6,48,26,32</xref>
        ] is replaced by the phasing out of
them and moving on to the concept of their harmonizing in terms of component composition.
      </p>
      <p>
        Harmonization implies at least two directions: (1) designing of compatible regional models based on dummy
variables [
        <xref ref-type="bibr" rid="ref10 ref15 ref16 ref17 ref18 ref19 ref20 ref22 ref33 ref36 ref38 ref40 ref42 ref43 ref44 ref47 ref49 ref50 ref51 ref52">40,36,38,47,10,22,20,50,49,15,33,19,52,16,18,17,51,42,43,44</xref>
        ] and (2) designing of compatible models based on
the principles of additivity of biomass component composition [
        <xref ref-type="bibr" rid="ref12 ref13 ref14 ref2 ref23 ref3 ref31 ref31 ref42 ref46 ref5 ref9">23,5,3,2,9,31,13,12,14,31,42,46</xref>
        ].
      </p>
      <p>Additive biomass models usually are designed on the tree level, but on the stand level they are presented today with
single studies [1,11,42,46,45) without any attempts of their regionalization. In our study, the first attempt of combined
solution the problem of additivity and universality of biomass allometric models of forest stands on the examples of the
genera of Picea sp. and Abies sp.
nally, for the original components, i.e. firstly for needles and branches and secondly for stem wood and stem bark,
according to their structure taken into account:
lnPi = ai +bi (lnA)+ci (lnA)2+ di (lnH)+ei (lnD)+fi (lnN)+giYk + ΣhijXj,
(1)
where Pi is biomass of i-th component, t per ha; А is stand age, yrs; Н is the mean height of a stand, m; D is the mean
diameter at breast height, сm; N is tree density, thousand trees per ha; a-h are regression coefficients; i is designation of
biomass component: total (t), aboveground (a), roots (r), crown (c), stems above bark (s), needles (f), branches (b), stem
wood (w) and stem bark (bk); Yk is binary variable: for spruce k = 1, for fir k = 0; j are the codes of dummy variables
for ecoregions designation, from 0 to 7. After the anti-log transformation the model (1) has the form</p>
      <p>Pi = ai AbiAci(lnA)Hdi DeiNfiegiYkeΣhijXj (2)</p>
      <p>Approximation of the model (1) on actual biomass data gives the regression coefficients and indices of adequacy. All
regression coefficients of numerical variables are significant at the level of probability P0.95, and the equations are
adequate to original data.</p>
      <p>
        At the second stage of the study, the structure of the additive model and its calculating algorithm proposed by
Chinese researchers [
        <xref ref-type="bibr" rid="ref12 ref34">34,12</xref>
        ] are modified in accordance with the specifics of our study, and the result obtained in the form
of additive and regionally distributed model of triple harmonization is shown in the Table 1. The model is valid in the
range of actual data of stand age, mean height, mean diameter and tree density and is characterized by the triple
harmonization: one of which provides the principle of additivity of biomass components, the second one is related to the
introduction of dummy variables that localizing model for eco-region of Eurasia and the third one conforms (harmonizes)
the biomass structure of spruce and fir through the binary variable.
      </p>
      <p>At the third stage of the study the adequacy comparison between the additive model (Table 1) and the initial
(original) equations (1). As an additive model and initial equations (1) are tabulated on actual biomass-forming indices and
the calculated biomass values were compared with the actual ones using the formulas:</p>
      <p>where Yi - actual value; Ŷi - calculated value according to the model; Ῡ - mean actual value of the all (N) plots; p = 5
– number of variables; N – total plot number, involving into calculating R2 and RMSE.</p>
      <p>The results of comparison of the adequacy of two modeling methods are summarized in the Table 2, indicating
higher adequacy of additive model compared to the original (non-additive) equations.</p>
      <p>,
(3)
* Designations see equation (1).</p>
      <p>
        The additive model designed (Table 1) includes four numeric independent variables. When its tabulating, the
problem occurs, which is that we can give (know) of four independent variables (A, D, H, N) only stand age, and the
remaining three variables can be entered into the table in the form of calculated values, obtained by using the system of
auxiliary recursive equations [
        <xref ref-type="bibr" rid="ref46">46</xref>
        ]. Such equations are designed using the original database and are shown in the Table 3.
      </p>
      <p>The results of sequential tabulation of equations 3 and 1 are the rather cumbersome table, the volume of which
exceeds the format of a journal article. Therefore, a comparative analysis of the biomass structures of spruce and fir stands
of different ecoregions we limit with the age 60 years (Table 4). According to the Table 4, the highest biomass values
correspond to the regions with minimal index of continentality, adjacent to the Atlantic and Pacific coasts, and the
lowest values to the regions of Siberia, with its maximum index of continentality.
WME A. alba 21,5 23,8 0,980 47,9 20,9 27,1 52,6 206,9 186,9 20,0
ЕРR A. sibirica 15,9 16,8 1,375 27,2 11,8 15,4 28,4 114,4 103,3 11,1
Ural A. sibirica 14,1 15,6 1,091 27,8 14,3 13,5 22,9 77,6 68,5 9,1
Cau A. nordmanniana 21,7 30,9 1,131 49,4 16,7 32,6 17,4 188,4 169,8 18,6
MES A. sibirica 13,9 15,8 1,154 18,9 8,3 10,6 16,3 60,3 52,2 8,1
FE A. nephrolepis 14,2 16,8 2,537 35,9 12,8 23,1 27,9 119,6 102,9 16,7
Japan AA.. svaeicthcahliiin,eAn.sfiisr,ma 11,6 16,3 2,398 242,5 191,8 43,9 18,6 25,2 50,7 147,9 128,6 19,3
China Cunninghamia lanceolata 11,7 18,6 0,859 300,7 246,9 63,2 25,7 37,5 53,9 183,6 162,5 21,2
* Denotes of the ecoregions: WME – Western and Middle Europe; ЕРR – European part of Russia; Ural – Ural region; Cau – Caucasus; MES – Middle and Eastern Siberia;
FE – Far Eastern province (Primorye).</p>
      <p>Negative correlation of calculated indices of spruce and fir biomass with continentality index by [48,4,27) is
characterized by a correlation coefficient -0.92 to total phytomass and -0.89 for aboveground ones on the
probability level above P95.</p>
      <p>Conclusion</p>
      <p>Thus, for the first time, when using the unique in terms of volume database on the examples of the genera
Picea sp. and Abies sp. the comparative analysis of biomass structure of forest stands on the territory of Eurasia is
fulfilled in a new light, the result of which is the additive allometric model, harmonized on three levels, one of
which provides the principle of additivity of biomass components, the second one relates to the involving dummy
variables, localizing the model along to ecoregions of Eurasia, and the third one harmonizes the structure of a
transcontinental model of spruce and fir stands by involving the binary variable into biomass model. It is shown
that the model demonstrates differences between spruce and fir stand biomass not only for its absolute values for
stem, needles, branches and roots (as is typical for trivial independent models that includes only dummy
variables), but also for their ratios, i.e. the differences in the biomass structure.</p>
    </sec>
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