Morris, L.A; Miller, R.E. 1994. Evidence for Long · CHAPTER ...1 Tenn Productivity Change as Provided by Field Trials. In: Dyck, W.J.; Cole, D. W.;· Comerford, N.B., comps., eds. Impacts ofForest Harvesting on Long- Tenn Site Productivity. London; · Chapman and Hall: 41-:30. P R 0 VID ED BY FIELD TRIALS EVIDENCE FOR LONG-TERM PRODUCTIVITY CHANGE AS PROVIDED BY FIELD TRIALS L.A. -tORRIS Warne!! School of Fores t Rc!sources. University of Georgia Athens. GA 30602. R".E. :.rrLLER USA · USDA Forl!st Savic(!, PJcific :\onh west Rc! e:rch S tJtion 3625 93A\'e, SW. Oly m pia . WA 93512. uSA INTROOCCTION In lhe p::.st two dl!c ades , considerJble e mphasis has been plac ed on d e ve lopi ng computer models th at can be used to predict effects of m agement pract ices on long - te rm forest productivity ( l, 2. 3. 4 ]. Although the v::tlue of s uc h models as exploratory rese:rch tool c; is widely recognized, ac ceptan ce of their predic te d : changes in fo res t growth is limited. All models incorporate current understanding of forest grow ch . and produce results that are on ly as reliable as th is understand­ ing. B ecause our understanding of factors affec ting forest growth is incomplete, results from carefully c ontrolled field trials, rather than mode! s . provide the more convinc ing evidence of productivity change. In this chapter, we review the best avail able field e v idenc e for change s in long· tenn site produc tiv ity associated wir.h harvest and regenerati on activities. This idence i ncl udes comparisons of growth in successive rotations ev­ an the same plots, results from matched plots. and analy ses of con trol led treatment e xperimen ts. We begin by discussin g assumptions required in analyses of1ong- term field trials and by offering minimum criteria that should be met before acce pti ng results fr9m field :'· . ·.··· j•, 42 £ ,idetice[or fong-temt produc::\•iry changes trinfs as re!inbie evidence for productivity change. We then evaluate evidence for productivity ch:mge Jssocinted with the to!lowing manngement activities: use o monocultures or restricted species. harvest utiiiz:nion and nuuienc re:novJJ, slnsr disposal. and ame!iomtive tre=.trnenc.s inc!uding nutriems and t illage _ ASSU 1PTTONS IN LONG-TER ·( FIELD TRIAL RESEARCH Producth·ity Components There is ;1o generlll y agreed upon usJg•.! for the tc:nns forest pr od uc ii vit y ilnd :;i 1c oroduc:ivitv. While some aut hors tre:H these as inte:-c!1Jn - e:blc tcm1s. othc:. . J.uthors dr::.w disiincrions. F'or?sr proclucth•iry is the more gt.!nt!:-:1 tc!rm t.videly use::i by foresters. boc:nisi5. ecologists, and wildlife scie:1tists. atHJ i fc refers tc growth and maincc::1ance of Jll or Jny pan of the Jssembl:ge of pl:nts Jnd animJI char. exist !n forestS Jt scJies th<lt rJnge from micrcplots co er11ire ecosystems. [r cantr::tst. sire productivity gene:::lly has a more limited scJic :md us::tge. [tis us.:!c by soii scientists and foresters when referring to the growth or c::pacity of a sit-: to grow trees at the scale of individu:1! forest stands. Tr::tdicionally, productivity is .:!:<p ressed as a function of b iotic factors (spccic.s. genotype) and abiotic factors (soil cond itions , slo91!. precipitation). For the pur­ ose of evaluating long-tenn site productivity, these factors divided \nco four components: lane pocemial, c!im:ue, .lfc more convenientl:­ soil capacity, Jnd catJ.­ s tro phe thac differ in deg r ee co which they are .controlled or assumed constll1t ir: long te rm studies (Table 3.1 ) As defined in Chapter 2, "sire quality'' i s decerrninec - . by climate and soil properties (i.e., ca pacity) and is the major focus of long-tern: site productivity studies. The first component. plane potentia!, indudes major factors manipufnced by forest management: tree species. genotype, stoc!dng, and quality and q uanti ty o{ competing vegetation. Although t.his com ponen t : . . productivity as has a majo r influence on forest me:J.Sured by timber or fiber yield, its influence relates more tc utilization and allocation of site resources to t.he desired prod u c es change in resources. th:1n co Iong-terrr. Plane poce:ttia! is not necessariiy related to tong-term site pr odu ctivity For instance, a dec:ease in the c::oacitv of a site to oroduce biomass . . ' . Assumprions in long-rerm field rrial research 43 TAnLEJ.l Factors affecting stand productivity, by groups subject to different le vels of con!Iol in long-term studies. Factors associated with soil capacity arc of prime importance ior C\'Jfuating long-term changes in site productivity associ:ucd with har\'cst Jlld associated practices. GROUP VARIABLES Plant Potential Species. genotype, stocl:ing, plant competition E..\PERIMENTAL CONTROL age. 1inimi7.c differences among ··rotations'' and trc:ltmcnts unless part of c:�pcrimcmat treatmems Climate Soil ClpaC:ty Temperature. precipitation, Diifcrcnccs rcmo\'cd by co-variance humidity, growing season length. lnalyscs for succc$sivc rotations: atmospheric tr:!Mfcrs and lssumcd not to interact with experimental pollution. sunlight trc:;;tmcms in lield studies Soil dcrth. rooting \'Olumc :111d rc trictions, org nic m:ttter E. pc:imcmal manipulation and mc::;,sun:mcnt content. water-holding c:lpucity, nutrient $torngc. nutrh:nt mincr:�fiz tion. nd avail;,biiity Catastroph�.: llurrit::lllt! dam:!gc. \'Oicanic :lcti\'ity. c:mcmc cJrly/l tc ircl!7.t! or drought. insect or i..li$c se epidemics nlll .moci:ucd with tre:umcnts c:m be masked by eliminating species that compete with crop trees. A major effort in productivity research is to control plant factors so that measurements of tree height, stand volume, or stand basal area will provide a reliable index of site productivity and change. The second component includes climatic influences. For most field trials of tong-term site productivity, climate is largely ignored in analyses because: the tong 1) over tenn, climate is assumed to average out (i.e., years of good and poor :]}:7:;. fied by management activities at a specific site. Although evidence for global !I�i�::. .. climate chnnge is increasing, comparisons among management treaunents within i�%; ·a.ro.tation remain valid, providing treaunenrs do not interact with these broad-scale §.Iii{ cli'inatic conditi ons. In contrast, changing climatic conditions severely limit our growth contribute to observed growth); and 2) climate is not controlled or modi­ awi . ·r§f.+. ability to assess site productivity changes among successive rotations. l i. .,s . The third omponent, soil capacity, includes those factors that detennine .the ability of soil to provide support, water, and nutrients required by trees. This · m:.z.. . . !". capacity is maintained through the activities .of a broad range of soil biota that •. ·'.t .::::_:., : · E ·idence jar lang-rerm producrivicy changes 44 conuibuce co deve!opment of soil suucrure., d omposition of organic matter, and nutrient minera.lization :md cr.:msfonmuion. This component is tile main thrust of most long-tenn site produc tivity rese:J.rch. In theory, effects of management p rac tic es on soil can be assessed inde penden dy of tree growth measurements. fr: p ractice. however, such plant-independent evafu::uian of soil cJpaci ty is difficul: and provides only circumsmntiaf evidenc e of productivity chnnge. No c urrent ly available soil ex md biologicJ.l c !ion or bioassay can reliably index the com plex so i l ch emi s try activity that lffect m ine ralization and availabilily of nutrients. co ndition s for root growth. For these reasons. soil cJpncity in forestry :tnc mus: ulti m me!y be evaluated by me:1suremenc of tree growth. The nn:1l c ompo nent. c:lt.ilstr ophe, plays an essential role in de ermining the structure and p roducti v ity of forest stJnds. Same t.:Jtastrophic events like hurric:mes and volc:mic l!ruptions are beyond our control and cJ.n destroy tie!c tri al s. S uc!1 disJsters seldom affect fidd-uial results becJuse the tri::ll is disc:.rde(: when such events occu r. Other cJ.tastrophes. like insect and diseJse cpid e mic . be rela ted m :1 :· ca. or ind uced by, forest practices hence these should not be ignored o: d ismissed as random infl uences without investigation. Acceptable F c!d-Trial EYidence for Productivity Change Worldwide, numerous studies have been estab li shed to evaluate changes in site productivity resulting from forest management ac tivities . Although such studie: i have provided useful insight about seedling establishment. stand growth, nutrier. II ; . ·(' ! I I :; :I i .:I, .. . •t ,. it . il :1 :i ·it ,, l! ·: .: n :i ; ·• :: I'I ;II !j ;l ( :1 1.n : !l II· :i ac cumulation and cycling, and the role of insects and d ise:lS e , they have gener:1il; failed to provid e an answer to t.he central question: How do specific m.anagemen activities affect long-cenn site productiviry? To be acceptable evidence fa: a change in long-term site productivity, three conditions must be met. Erst d ifferences in tree growth must be attribu tab le to d ifferences in site condition r.tt.her chan to d ifferences in resource allocation among target and non-targe species or to differences in plan t potentiaL Seco nd, growth results must be available far a suffic ient duration of time so !.hat the influence of ephemera. differences in initial site conditions has dim in i sh ed and so that the capacity of th:: site to support tree growth is stressed. Fin all y, adequate e perimen tal control mus e ist. We shall address each condition in more detaiL t\ssumprions in long-1erm field :rial research Sdecring Growr!t Measures: The degree to which a 45 site c:m supply physical support., water, and nutrients to trees, and the xte:1t to which tree roots can grow through the soil to utilize these resources, dete:mines the capacity of a si te for tree growth. Theoretically, site productivity can be evaluated by any measure that accurately reflecrs changes in these conditions. The merits of using net prim:uy productivity (NPP), the tot:J.I carbon fixed in org anic matter min u s respiration losses, as a measure of site productivity change has been discussed (5). This measure cle:lf!y has value in ecological studies; however. from a practical st.:J.ndpoinr. measurement of NPP is unwork:lble in long-tetm studies of forest management. Complete characteriz:J.tion of net primary productivity is difficult J.nu subject to large measurement etTor, partic'Jlarly where changes in species composition are involved. Hence, most l ong · \enn studies in forestry rely on growth of the target tree species for Jssessing changes in site productivity. Site index (or height growth) has been the mosr c:;mmonly used measure because height is readilv measured and relative!v less sensitive to stand conditions than - " . . other parameters. Stand b a sal arealnd bole ,·ciume growth or biomass lccumu­ lation provide more cornprehensi\·e measures of st.1Ild growth , but these can only be reliably interpreted where growth differenc s are not Strongly con founded by differences in stand conditions. Defining U111g-Term Response: A second major consideration for evaluating results from field trials of long-term productivity involves the definition of "long­ term." Many management practices have short-term impacts on stand or site conditions that are ephemeral and poorly related to long-term site productivity. .. .... . Control of herbac.eous competition, for example. often promotes rapid tree growth ;_:; : in· young stands but has little influence on growth following crown closure ��< . :-!.,. (except, of cour e. in the case of nitrogen-fixing plants). When competition ·.fr:; control does not result in su bsequent accelerated erosion or nutrient loss, it largely : . ·affects tree growth through changes in resource allocation to trees, rather than :_· . s1;J. through a change in total site resources or productive c apacity such shifts in · .[ f.:· resource allocation will appear 1. :, . as an eariy inc:-ease in tree growth followed by a return to annual growth patterns that do not differ from growth patterns of untreated stands It [6]. The original increase is maintained after crown closure, but 46 £ ·iderrce jor fong-remr produc:iviry changes b a c T I ,} ro1a1ion e-.l ' ,l.ge---'"" FIGuRE 3.1 m:ma Possibie pn.uems of domin mc:nc tre:1U11c:nt: mt ;ree hr::!ghc growth follo\ving (J) initial i n c :-:::1sc in reso u rc (! .:iloc:rion wir.houc ::itc . ch an ge ; (b) i nc:-eas e in long-tenn fJroductivir.y; Jnd (c) :r:nsient i ncre:se followed by long-tenn dc:cre:se in sire ? roduc t i vi ty fUI1her growth improvements are no t evidenr. Hence response does not indicate a change in long-term site (ar'ier (61). this pattern of grow productivity (Figure 3.1 (a The growth oa r te m after he rb ac e ous comcetition con tro l e:xemolifies but or ·' . w of thre characteristic patterns of gro w th response to m:magement. Figures 3.1 C wd (c) illustrate two olhertre atment-induced patterns in st:lnd produ c tivity Figu:. 3 .l(b) ill us trates a difference in site productivity that is maintained; Figure 3.1 (c illustrates a trans i en t change in productivity. Tne di s tinc ti on between Figure 3 1 ( . and Figure 3.1(b) is important. The growth pattern ­ of F!gure 3.1(b) indicJtes chang e in site productivity that will most likely continue into fucure rotation Although the growth pattern of Figure la does not necessmly rule out ¢e possi bility that a positive change in lo ng- term site produc tivi ty may ye oc cu r, ic is mac pro bable that the sail C:l!?acity is not fundamentally different Ulan the controL Th growth pa.rtern in Figure 3.l(c) also re9resents a change in sire produc tivity th;:. wiU likely c on tinue into future rotations. In this case. the pattern i n di c:nes decre:1se in t'raductivity. Assumptions in long-term fie!d trial research 47 Until the pattem of growth change is evident, one has little basis for predicting l11e consequences of management activities on long-term productivity. For slow­ growing stands, a reliable pattern may require 20 or m o re ye:u-s. For faster growing stands or short-rotation plantations, 10 ye:u-s may be adequate co observe these changes and to predict their long-term consequences. ExperimentaL Comrol: According co Mead er a/. (7], experimental designs for long-term stu ies require the fol l owing (see chapter 9 for further discussion on experimental design): I. at least four replications in r :m dom ized or randomized complete block designs: 2. suitable pre-treaunent site and crop inform ation on individual experimental plots; 3. minimum measurement plot ue:ts of 4GO mZ contD.ining at le:J.st 12 remaining trees at the e:1d'or' the experiment: 4. buffer ucas of at le:J..St 10-m width surrounding each measurement plot th a t receive experimental t.re:lUnents. Few studies have been estD.blished which meet these ·experiment.'ll requirementS and none have been cJ.ITied long enough to provide unequivocal results. Thus. our current conclusions about long-tenn site productivity change are based on im­ perfect results and must be continually re-examined as ne'.v information becomes available. Only when results from numerous imperfect s t udies, and our under­ standing of forest growth processes lead to the same conclusions, can we ensure robust conclusions. Research on possible declines in productivity resulting from removing species /i: · · f om a stand or replacing mixed-species stands with plantations of one tree species has been based largely upon results from plots matched with respect to manage..4 - :.;-;,:·-::.. . f;S*;;· ment history and soil conditions or from randomly paired plots. In matched plots, treatment effects and initial site differences are easily confounded by unrecog­ ; :.. .. ·nized but site factors or experimental bias. Such confounding is reduced · · ·· paired-plots where treatments are randomly assigned to experimental units. . ·.�·;::Research on harvest u tiliza ti on is more amenable to controlled experimenta­ on: Comparisons among harvest u tiliza tion options within a rotation can be : sil y designed as valid replicated experiments (see Ch ap t er 9). Unfortunately, t l' : ;tf: ,. ll in f. · .,.... · . important £\•idence jar long-rerm producriviry changes 48 much of che repiic:ued av:1ilable information on harvest utiliZJ.tion comes from non- studies on large. operationally harves ted areas. This is cieariy f ir: response co nutrient mineralization and water quality concerns raised by e:u-i; .Brook watersheds (3]. rese:u-ch on the Hub bard Resul ts from such large-sc:J.Ic studies are frequen liy confounded by differences in tree growth du e to regenera­ tition. Jnd site vari atio n. tion succ::ss. plnnt com Studies of sice chan ge after slash dispos<Il or lrne!ioracive rre:mnents usuaii: have che strongest ex perimen tal replicated and. in designs. Muny of these experiments ue wer _f some. differences in s tocking , plant com peti tion , or i nsec d am age have be:!n minimized (9]. Reg dlc:ss of study purp-ose. minimum requirements for an acceptable desig:­ inc l ude : t) hav i ng lppra priate control plots ag:inst which tre:J.ted plots c:m be evnlu:ued: Jnd 2) being minimized or me n that JJl factors other than tre:unent huve c:na i :sured in order co bee: Jccount for their con tribu t i o n co observe d_ifferences in growth. SPECIES CHANGE AND SINGLE SPECIES ROTATIONS Plants and soils interu.ct. Extension of roots through soil, uptake and return c various nutrients, concribution of or ganic o n temperature and matter, and t he influence. of vegetatic: moisture dis uibution profoundly Jffect soils. Converse!:­ chemical and physicJ.l charilcteristics of the soil affect plant growth and specie distribution. Conc::m about the specifically che than effects of species change on [ong-tenn site productivit:­ effect of conifer establishment, emerged from Europe mor 70 ye s ago. Between the late 1800's and e:u-iy 1900's, conifer plantation were established on marginal crop and forest lands throughout Europe. Limite . i i ·.; . ! experience in plantation establishment, coupled with the degraded condition the lands, resulted in regeneration failures and poor grow th . f3y 1953, c it wa_ generally assumed that site productivity was degraded by conversion·of pasture fannlnnd, or hardwood forests to conifers (10}. Evidence far site productivity was we:1.l.c, such declines however, because it was largely developed frar ' * Species change and single species rotation 49 observations of stands growing on different sites with different histories. These e:l.r!y reports were fol l owed by reports of productivity decline in second-rotation p lantings of Pinus radiara in Australia (11, 121 and New Zealand (13], and Pinus parula in Swaziland [141. None of these studies of species c onversio n meet :til of the previously dis­ cussed criteri a for infening long-tenn site productivity change. If only studies that have adequate growth records and plots matched for similar management history and site conditions are considered (Table 3.2), we c:Il1not conclude that c onver­ sion to conifer plantations leads to long-tetm productivity decline. Growth of second- and third-generation conifer plantations 'is as likely to increase as to d e c ::-e ase . relative to that of the first generation. For instance, Ev:ms (1 51 described resuits t"rom secand-rot:Hion Pinus parula in S waziland where growth on 129 plots ne rotation age (l J-15 ye :l.rs ) was compared with growth of the first rot.ltion on the same plots (Table 3.3). Overall, the second rota tio n averaged slightly less volume production than the firs.c; a subst.Jntial productivity decline was largely contined to one forest block. fn the other four biocks, productivity in the second rot:ltian equalled productivity in the first rotation. This study is particularly nate­ worthy in that e:l.rlier evaluations of the sa.rne plocs by this author suggested a general p r oduct ivity decline had oc curred [t4J. ft illustrates the benefics of extended observations - and the problems of short-tenn data. Squire eta/. [16] evaluated productiv ity of second-rotation radiat.a. pine in Australia using carefully matched plots and stem analysis to compare growth in the current rotation with that in previous rotations. These authors found that on both low- and high-quality · sites, growth through age 5 was greater during the second rotation. As in most such 7:·:.:.. !. studies . the reasons for the improved growth were speculative. but appeared to be H: J} \· ',.due to improved planting and establishment procedures. ,;]> gled from associated questions about harvest utilization, slash disposal, and soil Issues of species change and second-rotation decline are not easily dis entan­ :1 : tillage to be discussed later in this chapter. Tnis dilemma is illustrated by two · ::.;:\.: · t1.r5- L> recent studies that combine results from designed field trials with retrospective {tr, ' 1:: j; {:·:· . r:.:-t::r..-·:.: ompa.risons of previous r otation growth on the same site Cellie (1 7, 18]. · et al. (17] assessed factors affecting heigh t growth of' second-rotation P1nus radzata plantations in South Australia in the same area. as the afore- -;..:. -----· ..:._ .:...___:.;.;::.:...:.:...---·;· .;_-- -. · ..... -·. --·. . . :..;;. = :.::.::..'. ... -·-. :..:... .:-:....- .:::-· :.:. : ::·.: ·... . ------·--- --- --··· ·· ----·-·· . . . ... . ... .. - ... ··----· .. "' •t( v-. 0 TAIILE J.l Summary of selectell invcstit;alious uf secoull-flll<lliuu •h:diue in cuuifo:r pl:wlilliuu Locatlou Australia Specie J'ilws (Vicwrla) rculitllll l!xpcrlmenl<ll Date Last l hllhll:livil)• lt.: uiiS (ill CUIIIJI;Ifi •lll Oc isn U.:suu• EvaLn Variables liht ruti&tiuu) Millchcllplots, 1975 j IICCeHivc Age (yr) hl l)l)lllillillll lfCI.: hcit:lll, S.:Cllilll hll:&ll\111 lhUill lliUII Sl<llld volume hclt;hl: ·1 ld IU jl<ldl Slit::.. fll!illiOU li·l'1i. Cuuuucn1S !ioun:c (IClJ 1111 ·1 :!l1 Ill 1·-1-t% till lllllll.l si1es; vuhw1c :;.I(){J'ii. be!lt:f Ill SeCUIIli Hllillillll Swa;dland Pimu lv(atchcd plot 196-1 10-14 pawla Australia New 'Zcalallll Pinus Mean tree height ami volulllC, SIOIIII.l volume Volume oi ccomJ mt<uion aver< sctl 7% lower. raugctl fhllll - ::HI'A• I o J(i Successive llasal OI!Cil 1- 1(1 'ii. il iiCCOSS (fl!lfO:ij)CCii VC) IJUollili<:S <111<1 Slilllll COIUI!tiliiiS l'ilii/I Matched plots 12-21 ll.:isht, basl!l Mea. S t0111ll VOIUIIIC C:lllbC lli Dccliu.:s in sct:OJHI-r.ll:llion jlhldliCII \"II }' OCCUffCtl Villlilht)'. hill l llll l CUIIIIIHIH ou d.t,:e pll ilhln ; :;..:.:uml- (II) Mos1 u�:�:iiucs cxhihilt:<.l t;rowth 11 cmh oi I ;II)UI e I a. flllolliUII !;IIIWlh !;I!IIClOIIIy l•.:ut:r than lir t-rutaliuu t:ruwlh in luwo.:r slope pusiliOIIS. If applic; hlc 114, lj) winter dhluliht :iliC maaalou 1965 111 MMI:cd 1lcduu: in silc class mdiaw rmlitil(l Scconl.l rotation retluctiou aurilluh:tl (I)J 51 Species change,and single species rotation TA3LE3.3 Comparisons o( rotation-aged Pinus patu/a height and in Swaziland (source: \'Oiume for tim and second rmations (151). 14- ye:IJ' rotation Forest Block First Plots 13-yeu rotation S<!Cond no. A ·--Height (m} 10 18.7 It !7.4 c !7.3 10 17.8 18.7 3 12 . 18.0 17.3 II B DaE no. ··- 9 .; 301 316 306 297 3 301 l3 II 287 286 D&E 12 10 ·- 16..:. 16.5 ' 17.2 18.0" l7A l6A'" 193 275 :9.! 271" no 11 lor p [11] and Bednall (12]. ::.64 26S = rc. pccth·cfy. mentioned stud i es by Keeves ---- 16.4 -Volume (mJ ha'1)- 9 indiC:itc signitic:lnt differences between first and st:ccnd rotations Second Height ( m} 18.5 · 239·- 20 c ·· !6.8 ..... -Volume (mJ !la'1)- A First Plms , 31 1 0 and .01. Th ese investig:Hors estab l i sh e d P. radiara plan ta tions after harvesting matc h ed first- and sec ond r o t a · - tion stands. They compared factOrial combinations of site-prep;u:J.tion treatments and nutrient additions. Weed competition on all plots was minimized by herbi­ cides. At a ge 7. heigh t of th e current rotation exceeded heig ht of the previ o u s rotation at the same age. Although the op timal treatments on bo th first- and second-rotation sites resulted in similar grow th , the treatments that produced this optimal growth differed between fi rs t- and second-rotation sites. Specifically, heigh t gro w th was increased on second-rotation, but not on first-rotation sites, by 1.... .. · , · \l' atments that induded nitrogen additions. These results suggest that removal of · . n i trogen in two rotations reduced site productivity on these sites . )·.; Allen et ai. [18] reported results from a replicated study established after t of part of a Pinus taed.a plantation. Growth of the previous plantation �::r:• } ts es tablished after either harvest of merch .;.·., .- - determined by stem analysis and compared with current rotation growth on , an tab le pine stems (pine stem-only) or. omplete above-ground harvest of pines and competing hardwoods followed , . by e;ther chop-bum or shear-pile and d isk-harrowi ng. Each of these four e a t : . J.l:l nts were split into two subplots where competition was either minimized , !hi.ough repeated herbicide a pplic ati ons or allowed to grow without herbicides. Evidence for fong-rerm productivity changes 52 Like Cdlier c.r ai. (17], these investi gat ors found that height growth thro ug h 3 ye:lis of r.he current (second) roution was greacer than 8- ye:li height growth of r.he first rotation for all tre:u.ments evaiuated. Although growth among the four harvest and site pre;:nrration tre:mnents di ffer ed. competition control had the great­ st in fluence on short-term g rowth . Harvest utilization had no detectable effect on 8-ye:li he i g ht growth. In plots \V here competition was minim ized by repeated h erbic ide lpp iic =.ti on , pine g ro wth was only slightly gre:uer in the more disturbed 5he:l!-pile ·:1nd hmowed site-prepared J.re:J.S than in ch op-b um areas. fn plots \vhere nat ur :l l competition was not controlled, differences between site prepar:l­ ti on tre:uments were larger because site p re parati on provided some control of veget:J.tion. D espi te evidence to the contr::.ry, some au th o rs cl a im lS f:1ct that multiple t"orest rotations with coni fers decre.::se site productivity. For instance, Shepparc [19] writes: "A decline in productivity bet\veen suc:: :ss i ve crops of sprue\! ir. Euro pe w:1s reported ar ound the tum of the ce n tury and similar reports have come: '· 1: for.vard since from a number of pinces for other species in other circumstances Therefore, we must acknowledge that there is ... a danger in growing tree crops ir m on ocu lture." We c onci ude that current evidence does not indicate such declines occur or if they do occur, are probably not related simply to estllbli shment of conife species. In contrast to these results, evidence fro m field trials c!e:l!l y shows th:: addition of nitrogen-fixing tree species to stands on N-deficient sites incre:l.Ses sit· productivity. Hence, removing such beneficial species c o uld reduce long-teffi productivity. In western Washin g ton , USA, fo ur plots (0.08 ha each) in a 48-ye:u--olc Pseud.otsuga. menziesii plantation were matched topographically beside four plol in a strip of the same plantation interplanted with Alnus rubra (20]. In i ti a l tre: density at planting averaged 1,700 Douglas-fir and 3,100 red alder per hectare. B: ge 48, th e four plots in the pure stand averaged 970 Douglas-fir and th ose in th· mixed stand averaged 660 Doug las- fir and 730 alder. The largest 100 Douglas-f per hectare averaged 20% U1ller in the mixed stand and were larger in diamete despite the greater stand density. Douglas-fir volume averaged 217 m3ha·1 in t.h 1 Species change and single species rotation 53 mixed stand versus 203 mJh;r1 in the pure. The additional alder volume in the mixed stand averaged 175 m3ha·1• The growth-enhancing benefits ofN2-fixing :llder at this site are not surprising bec:J.U s e 30 years after interplanting,.soil in nitrogen (1,000 kg ha·1 the mixed stand averaged 33% m ore (21 ]). Moreover, 15-year response in a N-fenilizalion uial in a nearby portion of the same Do ugl as fi r plantation averaged 88% (116 m3ha·1 : - aft er a s ngle application of 314 kg N ha 1 ; [22]). The l arge extended response to i , N fertilizer at t11is location is unusual and attributed to imoroved nuuition and to . seco nd ary effects of increased growth on sund structure. On more naturally­ productive sites. however, growth-promoting benefits of J.lder in mixed stands are less appa.re:H, perhaps ex p l a ined by greater lJTiounts of soil nitrogen at naturally produ ctive sites and the earl y competitive ad\·;;.ntJge of this species [23]. Growth-enhancing effects of a tropic:i N ftix in g tree spec:es. Albiz.ia fa/cataria (L) Fosb., in an equal-aged mixture '>Vith E:lcalyptus salig11a Sm were quantified in Hawaii [24]. At 43 months, E:tc::lypws trees in the m i xe d pl an t i ng s that contained 34% or mo re Albiz.ia were equal to or lil.rger than those in pure sunds receiving four fertilizer a ppl i ca tions :::ch equivalent to 40 kg N, lS kg P, . and 33 kg K per hectare (24]. fn contras t to these results on the west coast of H awai i Isl.and, Albiz.ia grew poorly and provided no growth enhancement in a companion test in a much drier location of the isl and [88]. On N-deficient sites, both N2-fixing species and nitrogen fertilizers are potential means to enhance tree growth, hence site productivity. Use of N2 fixing - : :: plants, however is.more complicated than use of fenilizers for several reasons: , ��· 1) the N,-fixing plants mu st survive and thrive tn sufficient numbers and duration; : .f 2YSo·me N.,-fixing tree species may result in J.ssociated trees being overtopped or a ged this problem can be avoided with early spacing control; and 3) as ...... - . _t : t . :t.:--.::= ,... .. . . . · ?}. J?marized by Binkley ••:'XI ....;:• - [23], larger quanti ties of nitra te and organic N are leached ]} 9,m' pure red alder stands or alder mixtures than from pure Douglas-fir. This ::.-:.:;;:. .. .S mcrease teach i ng losses of nutrien t cations and lower soil pH. In summary, 1 1,. _. • • ; • • ... . ' t mC.cd {ui use >·- ·+' • t · . .• . . . ofN.,-fixing species to enhance stand and site productivity requires . - , efu l.planni- ng and ex cution. r,'l::. Sf:-=::5i.";. ·,· ;::. \ .· ,5!_: .... · 54 E: ·idence [or fong-lernt producriviry changes HARVEST UTILIZATIO N AND NUTRIENT REw!OVAL Nu tri tional Basis fo r Harvesting Impacts Co ncerns abo ut species-induced reduc tio ns in site productivity ue no c succorte by exi sting evidence. yet c o ncerns term productivity s h ou ld tass of essen ti al pbnt about the influence of forest harvest on lam not be summarily dismissed. Direct remov a.i and indire·. nutrientS will oc cu r in forests ma.na.ged for wood and fib, p rod uc tio n . Without nu trient rep lacement by n:uur:1i sources or by praducti vity could fertiliz:lli o : d ec l i ne . Current q uest io ns bout impa.cts of harYest utiiizatic on site productivity center on the rd:nive babnc:: between nutri<:!nt in p u ts ar ex peru. and the c:1 p :1ci ty of so i l co supply nutrientS to a growi ng forest. Exc ellent li terature revie.,vs o n nutrient disui b ut io n and cvdi n g i n m :J. i j - .. forest biomes are J.vaiiable. General reviews of nuuien t cycl i n g in the borea.i ['2.:. tempcr:lte [26j, and tro p ic:1! (271 forest biomes were pub lished in the proc ed iti of the F!fth North Am t! ric :J. n specific forest (!COSystcms Forese Soils Con ference. Liter:ture re vi ews abc J.re also available; (or example. about the dis:.ributi and cyc l i n g of n utri en ts i n d ecid uo u s forests o f B elgium (28 1 .md i n trop ic:1i r: • forestS of Cen U<ll America (29 ) . Disuib ution of nutrients in re p resentative · forest st=J.nds temperate, and tropical forest b iom e s are ? resen ted in within the bore: Ta b l e 3 .4. Within t!:. b io me, variability among stand types is large and tends to mask d i fferences totai n uuient co ntent among che biomes. C!e:1riy, however. com paratively t ar quantities of N, ?, K, and in · Ca. and :vfg u e stored in th e vege t:J.tio n of tropical fore the forest floor of bore:J.i fo res tS . D e pletio n of n u uien ts under various h arves ting regim es has been d ocu m e r. or can be calcu la te d using dam fro m ecosyste!n studies in most commerci important forest types. Most nuuient dep l etion is associated with direct biorr: removal; loss of nuuients through accelerate.d erosion, leac hin g or g aseo us : , is relatively small. Comprehensive revie ws p l antatio n s (37], med i um- a ge forests of re moval rates in short-rotat [38], and [ong-rocation. systems [3 91 ,... completed for a sym posium on the impacts of intensive harve s tin g on fc n uuient cyclin g. General su mm ari es [40, 4 1 ] and summaries far specific reg or forest ecosystems (42. 43 , 44] are also available. The genera! consensus of c ' ' ·, . . Cover Type Picea mariana Picea -Abies Pinus bwtksiana Pi11 us ba11k.ria11a M ixed Quercus Fagus spp. Pitws clliouiiP. palu.rtris ... : • b ' . . TA U LE JA Nutrient content and distcihUlion in major forest biomes. - - - --- For e s t lhxlr ------- V eg e tation -------. p K Ca Mg N I' 1 67 42 1 2 1 ·1 52 15 277 413 27 387 17 1 346 84 1 59 85 146 36 19 52 1-165 213 1 00 43 ·n OitEAL 328 3 2 1 02 1 052 253 (28) . 82 (34 ) ' 2ti 2698 19 81 406 :n 1 3 "/ 2::!()<) 3o7o 234 74 1 20· 1 510 1 ·1 8 <1·1 256 II 326 67 217 3·12 - 1 15 2(1 5 1 ·1 3·1 .j () TltOI'I( :AI . -1 3 7 •kpth). 6460 249 1 ).1 51 Ovcrstory vegetation only, soil 1kpth to 35 em (appmx. mol in 26800 132900 254 365 II 13 3 18 (30] • (30] (31I < (32) 4 920 -1 2 1 7 ·1 •1702 9!!708 1 127 2605 1113 53lB9 2!!9 766 6(:>- 1 0 33 I SO 1 1 ·1 0 22 1 5 4 · 1 80 43 702 <15911 16802 9383 1 65354 500 5 81 1 .5 2 1 03 24 1 468 H 868 187 ND 296 Mg 33 245 5 ·1 · 1 1 5-t Ca 1 16 32 39 IH 29<1 ·00 1'!.. 1 14 o i OO 495 ·1 592 13 )) S ource K 559 3729 5 5 5·1 285 406 - - - - - -- Mineral :soil -------- -----· Mu K Ca N I' - - - - - ­- - - - - - - - - - - - - - - - - - - - - - - - - - - - - ­ k g/ha - - ----- - - - - - - - - - - - - -- - - - - - - - - - - - - - -- 5 2 ·1 3 I 'J 25·1 37 TEMPI.::t t ATE 15 1 ·1 I II 20 51 29 Ccltis-triplochilun 1. 5 3 0 Cawlllillem-ceiba ;· · N Pscudot.mga IIICIIZ.icsii . . .JF}r\1 . 650 508 2576 1!!51.!2 (33 ) I ( 3 5 !" 3969 2!130 ( 36 1 ' 12 J l uit cations •k•cnuiucd by l l t =/t iCIO. •l i ucstiuu. Overs10ry vegetation only. soil depth 10 26 em (approx. rooting tkpth). soil cation:> dctcnuincd h}· I I F/ I I C:IO. digc.stion. Soil depth to 1 00 em, soil cations determ ined by I IF/I ICIO. digestion. Soil t l p th lo 1 00 em, soil P d tennincd by Dray No. I, :mil cations by N l l.(>Ac cxii Ktiuu. < ' ' h Forcst lloor indud s leaf Iiller onl y , soil to to 7 0 em, 40 em depth, total;; by unspcdli u digcstiun. P, and cations extraeted. using i i 1 SO.II ICIO/I IN0 digcstilln. 1 Soil depth 10 base or D h horiwn (approx. 80 em), soil P and cations detwnincd by I I 1SO /I ICI eJtuaction. Soil depth 1 Soil tlcplh 10 60 em, P by I I P/11 1SO. di gestion, cations by N I I.O Ac extractiun. Forest ll oor includes "Iiller" and " trash", soil depth to 30 em. soil I' by Tnmg. cations hy cx trilction in N I I.O Ac. Soil depth 10 30 em, soil P and cations by 1 1 150/ I I CIO/I IN( \ d i ge.stilln. \J\ &•idence for tong-£erm productivity changes 56 reviewers is that conventional stem-onLy harvests littie impact an cree nutrition probably S) occur (and in in future ro t:ltions. A of mid- a ge stands will h osph cri c inpu ts of N an sufficient quantities to appro xi m a tely balance har removals. and soi l reserves of K. C.a. md Mg arc generally c o ns idere d suffic: the absence of atmospheric or weatherin g inp· is based an esti m ated mineral reserves of shai: for numerous rot:ltions. even in A repon so ils as the contr.li)' (321 to determined by we:J.k extraction techn iqu es . B y comparison. large nu tri e nt removals occur i n m o re intensive above-gro : harvests o f short-ro tation forestry. fn a n c:l!'iy review, Kimmins (40] estimated : .1 change from convemion<Il. me!·chamablc stem-only harvest to complete abc gro und tree h:l.I'Vest o fva.rious northern con ifer ty s (hemlock-cedar, pine, spn.. spmce - fi r, hemlod::-nr) and cottonwood. would incrc se removals of N 36-233%, P by 5..!-367%. K by 1 4-236% an d CJ. by 15- 1 79%. \Veils er a/. es tim <Ited th::tt removals of P, K. CJ, Jnd �v{g would do u b l e for ! 6-ye:ll'- old ? : raeda srands [n the somhe::tstem U.S inste:ld of a .• us i n g a c o m p l e te above -gro u nd har­ merchant.1ble·ste:n harvest. E·:en gre: uer removals would oc un der intensive management sch em es such proposed a thinnings i n as 9ro p o sed by Koch (46 j . K h arves ti n g scheme far P. ra.eda which a wo ul d i ncol1'0rate muit: 35-ye:JI rot:uion. A t the end of the ro t.:J.tion, cro p trees would be : vested with their taproot and crown intact. Utilizing Koch 's estimo.tes of projec . b iomass remova l s. and anilable d a t a on n u trient c o nc en trJ ti o n of P. taeda tis: we calculated total nutrient removills under such a system (Table 3 .5). The 2: 1 4, 16. and 4 kgfha, respectively, of N, P, K. Ca. and Mg that would be remc on an ann u al basis are abo u t 35% gre:lter than removals in two 1 6-year iO tati ·: 1 l . with complete abo ve · ground ha.ryest (45j. Results from these earlier analyses h be en confirmed in a more recen t review (4 1 ]. It se ems dear th at increased biorr. locations will cre :J.te ln im b alan c . utilization and/or shorter rota tio n s at sam e :[ : . ' nutrient inpu t-ex pan that co u Ld !e:J.d to groductivity.dec!ines. hi .; . . ·! Di ct Evidence of Productivity D ecline with Increased Although nutrien t-balanc e B iqmass Remava. analyses p ro vide indirect e'lidence for projec: deciines in [on g - \enn site productivity in managed forests, direct evidence of s d ecli n es is rare. Most c ases where decre:l.Sed site p rod ucti vity has been associ ::. Ha!>'esl utilizatioJI and nutrient removal 57 wilh i ncreased utilization of the pre vi ous stand occur on low-quality sites in coo l - climates (Table 3.6) w here the consequences o f N removals are greatest. Lun d kv i s t (47] , after re view in g results of m atc hed plo t experiments of whole-tree harvest­ ing in Pinus sylvestris and Picea abies, co nc l ud ed that, for most sites, growlh of su b sequ en t stands was greatest w hen harvest slash was l eft in place rather th an removed. In general, di fferences in height growth lffi o n g utilization regimes were gre:J.test dwing the fi rst 10 years after p lan tin g : mean tree height in plots planted aiter harvest wilh slash left in p lace ranged from 30% to 40% gre:Her than he i g h t in plots w h e re slash was re mo ved . This early height-grow th advantage, however, . d im i n i s hed there:J.fter. B y age l 6 o n the best qu a l i ty sites, a 3 % reduc ti o n i n height g ro w th w a s associa ted with lo\ver biomass removals, re ve rs i n g the earl ier tre n d o f i m pro ve d growth. Com pto n and Cole (4 8 1 repo rte d sim i l ar resu l ts fo r Do u g l a s fi r grow th after co m p l e te above·ground .biomass remo vo.l that inc l uded forest floor removal , com plete · u·ee harvest (stem , branc hes J.nd fo l i a g e) . or stem-o n ly iemo vnl . On a low-quality and a medium-qua l i ty site, l O-year hei g h t g ro w th w as lowest w he re biomas s removal was greatest. On both si tes. a p p l i c a ti o n of N fert il i ze r removed or reduced growth di iferenc es . It should be no ted that su bordinate vege tion was not controlled i n the studies evaluated by either Lu ndkvist or Cole; tlms. differences i n ve ge ta tio n among treatm e n ts cou ld contribute to the observed tree grow th patterns . Hence, the effect of harvest treatments on soil properties and tree g row lh c o u l d n o t be se p ar a te d fro m the effects of c o m pe ti n g vege tatio n . Re m ai n i n g field trials provide weak evidence for productivity declines after . .: .: : . increas ed harvest util ization. For the longest tenn s tudy of its kind in the USA, . . } ;;:· :.:··. Williams et af. : [49] described res ul ts of h arves t utilization i n P. banksiana m '7:: · Minnesota. Two h arvest-u til izatio n levels were in ves tig a ted : com p le te tree ·; :. %. :... . ·,(flbo ve-ground remo v al of stem, branch, and foliage) or tree length (removal of . .: erchantable portions of the s tem ) . The treatmen ts were applied at two study si tes ·- ·· · · · ;; ··.\.· - ith·. similar so il s but. were not replicated within a si te . At one site, 14 yeais , J I?.llowin g p lan ti n g , average tree height w as 1 1% less on the complete-tree . IW . arves ted plo t than on the tree-length harves ted p lot Con versel y, on the second ..-u: ··. iJ :. .s.it . at the same age, height was 21% greater i n the complete- tree harvested pl o t on the tree-length harvested pl o t. In the p re vio us ly descri bed s tu dy by A l le n ­ . : . ... -· • -;on -,•• • ,l0an - iiiFt·:· ·:" r..·.rs·:... - : .. E. ·idence for long-rerrn producrivicy changes 58 et aL ( 1 81, 1verage 3-ye:u- height gro w th of P. raeda following stem -only h arves versus complete above-ground harvest of pi ne md h ardwoods did not differ. Thi occurred despite large differences in bi o m ass md nu trient remova.is between the two harvest tre:lUnems [50]. Furthennore, despi te differences in gro w th linen site preparation and h erb ici de rre:tUnenrs with i n e:1ch h arves t intensity, there w a. no evidence of interactio n between gro wth response to h::u...:est and th es.! c.re:u . ments. ft m u st be n o te d tha t these l a t te r results are for young stands chat do nc encire!y fui fi l o u r previo usly stated requirements for 1c::e;Jtab lc ne!d evidenc.!. Thz nse m ay yer. t"o l lo w the patte:-:1 of F:gure 3 . 1 (c) c:1n no t b · possibiiity th:u rcs dism issed. · SLAS H D £SPOSAL Slush D isposal Im p acts As is h arv es t uci i i z:1ti o n . s l as h d i s po sil l is also i m port.ilnt in c •::1l uating ;n nag ..; ment im !J:lC:.S on long-term produc ivi ty. Mechanized removli of slash i nca iic o r windrows hJs che gre :ltest potentia! for ne;ptive s i ce i m p:1c:s bec:lUse i t c:. disp lace large quan ti ties of o rgnn i c m ntter, s o i l and associ:Hed nu u i e n ts e n m uc , of the s ite [50, 54. 55, 5 6 ] . In Pinus el/iorii · United S tates. Morris et a/. (56] repo rted that P. · palusrris fo res tS am o u n ts i n the southe:· of N. P. and K displac i n to wi ndrows duri n g p i l i n g w i t h a b lad e exceeded remo vals from s tem h arvestS merchantab. bv s i x fo l d The d i s o l a.c ed nutrients reoresenced m o re than 0% '.. - . .. . the total soil nu tri en t content to a 1 -m deeth. S imilar resul tS h ave been reoone . . for New Zealand (54] and the P i e dm o n t o f the sou thern U.S. (50] , md, h enc e. c.: . probably be genemii zed to m any si tes p re p ared for plmting by these me:: h anic: te:: hn iques (Tab le 3 .7). B urning is ano th er common means for slash disposal . N i tro ge n toss fro . these fi res can be as l arge as d is p l ac em e n t during w i n drow i n g In . bore:!l fares w here debri s and fo res t door accumulations are large, more than 500 kg ;:ilha c:.. be lost during s l as h b u rn i n g [6 1. 62]. Lo sses from o ther forest ty.pes. o we ; e r • . a.: typically lower and m a y be s i mil ar to N removal d uri n g merchanc.acie ste. h arves t (631 . S las h burning is likely to c::lUse funher reductions of N s•ored ve getati o n and soil com po ne n tS. TA B L E 3.5 · Es1ima1ed nu lricm removals in a 35 -ycar ro1a1ion of inlcn ivdr m;ul;tgcd loblolly pine (Pi1111J Ull:£1(1). l l arvcslcd Componcu1 o as s• bi m --- N N u lricnl COIICCnlfa t i on• --- p K - 'Ycj - kg/ha - Ca 1\lg N utricnl removal N p K Ca kg/ha Ms Corritlor thi1111i11g (age •I) 2·1,000 Whole lfcc . 1 65 .0:20 . } ()() . 1 20 .O'JO llltcrmetliatc tll illllillg.r Do1ewood, bark, and taproot Tops, branches, ami foliage D olcwood, bark, and taproot Tops, branches, and fol iage Source: Koch as 5 26 29 .092 .0 1 2 .07 1 20 121 1 54 39 .05 1 .2·1·1 . :!-HI .u:n 1 57 .-155 .0)·1 217 2-1 1 16 1 1 ·1 26 . I IJ 27,300 . 176 . 0- 1 7 . Hit\ 1 52,900 .092 .0 1 2 .07 1 32,900 ..1 5 5 .05 1 . 2 · 1· 1 .OW 4 1i 39 16 .023 1 •1 1 I) I ll 46 (.l')() 1 0<) 1 38 35 .2-10 .05-1 1 50 n 1!0 79 18 753 92 -191! 553 1 •1 1 . · (46). a weighted avcr;tgc usi11g lhc data o r \Vcll:i ami Juq;cn cn 1·1 5 ) ; t;tpmot ctuKcu tr;ttions were asstuued to b e equal t o bolewoou conce nlrat ions. 7 47,700 Tot;ll rcu1ovcd Comp u l cd 40 1 70,700 Fitwl ll an•cst La1cral roots .(130 \Yl .�:h�:::::���t; .rl�d�:;;�.�;:.:. .. -··: . . '!'��!:!!i 'W'¥8-'t'Y"11Mf51tll"'8"� !!?.O:'! · ·. :.: _·:: :·; ·. .: : .--. ·:· :.·:=-=�-��.:i:::=:::: :. :; ;:-.::� ;. ; : ::: -- ·. . . . .. : .. _ ;· -- · - .. -.--.,:·-.·r-- ·-- ,.· -::•:u··-- · ···· ·· · -. , , ........... --- . - J TA II I . E 3.6 0 lnll ucucc of harvc l utili:r.;uion (bioma:ili relllll\'ill) on pmducli dt)' of :.uh eiJIII.:nt :.tanu:i. Location Species Experimental l);uc De it:n• H ejlUII.. 1 9 1!1 USA - Pim1s l l arvcs1 was Nonh lat:t/(1 main plot uf Carolina A c at la.sl Pwducli \'it )' eVii J . ( yf) Variaht..::; 6 $plit - plut In ltCll (3 reps) · lte:iult" I h:i lll, tliamctcr, N1l diifcn:nces i n vuhuw: imlcx; :.uhsc•1u.:nt pine t:mwth tulill accumuliut:d a:.:iLI-..: i i•ll:d with h:u n::-1 hiuma:;:; (ahuve u&ihliHiun Cun uu e u&:; Source Fur plms with ;md without ( 1 8) Difference:; in rcgenefiltion ( 9} ..:ump•.:titiuu cunuul cmund) USA - Pirws Non -replicated 1 969, M i nnesota ba11ksia11a within s i te, 1 97 1 1 4, 1 7 2 :>iiCS I IL:i!;ht. u i•uuet.:r. Result:; were rcvef:'c•l llll 111111 :iiOIII.J h;l:\ill two :;itcs; fullowiug area cumph:te-tree vs. stem- - I I % llll Pseudo- 1 979 CRO on 2 sites (no reps) Washington uug11 confound 1\::iult:i only hilf\'t::-1. piut: height: 1111 USA - ucce:>s ami :iOil Jistucllauec H mcttziesii liiiC :.itc. ·1 I 'J'ii.• :.e..:un.l :.ite Tu&ill heigh&, Must ..:um p lc& e h iu l l l il:\!i hei hl g ro w th renHl\'ill re:\ultcll in 1 '/ '"n• lkt:l\:iL'iC llll Ill\\' ')Uillil)' N · fenil iwtiun elimiluued (52, 53 ) lleatmen& aliffeceuces !'il.:s. 1)'il> increase 1111 hi�:h ' l ualit)' s ite Sweden Summary of Picctl IIUIIlerous HCD t bit:s PiiWS var. 2 1 -25 l lcl&;lll gfllwth. ( icuwth l.::i:i in Mtulie:; \'UIUUie wlu:re hiumas:. reuul\'ill cxpcrimcalls gn::ue:it; ,liffet ence:; between lh:iiUIICIII:i syll•t:stris :>llli1 lle 1 Oil hijlh 'J IIitli&)' ;;ile:> illlll diminish with wnd iljle • CRO .. completely mnuomi:tcd; RCD . , , ' ! , • •. , "' randomized ..:omplclc h l ocl: , .. 7) Slash disposaL 6 i. Apart fro m th e i r effects on nutrient budgets, slash d i s posal and s i te prepara­ tion have numerou s direct and i nd irec t infl uences on soil ph ysical md chemical pro penies. Use of heavy equ i p m e n t can le:1d to soil co m pa c ti o n and d isturbance which h ave been associated with reduced growth in some stud ies (e. g . , (64, 65, 66, 67]). Com paction will be discussed as a separate to p i c i n a s u b se qu en t section. G ro wth Fo l l o wi n g lvfech anical Slash D isposal Vinu a l l y J.l l a v a i la b l e data from c:u-efu l l y desi gned fie l d experiments show that s u rv i v al and e:u-ly growth of plan ted seed lings is greatest o n sites where biomass removals '.•,: ere greatest and w here organic and mineral so i l h o ri zons were most se•:ere ! y distu rbed d u ri n g mechanical slash di sposal (Ta b le 3 .7). f n th e short-term , m ec h a n i c ::1l s l ash d i spo s :1 l o ften en hances plan t.J. tion g ro w th because o f: l ) grea te r ava i l ab i l i ty of n u trients, p art ic u l arl y N; 2) greatly red uced p ! J n t com petition; and on some si tes, 3) am e l i o ra t i o n o f soil compaction duri ng assoc i :J. te d t i l l ::� g e o pe r::�­ tio n s . \'even.he!ess, tree res po nse to these treaunen ts i n o l de r controlled ex peri­ men ts i n d i c :lte s a s h i ft t9ward reduced g row th as the fore s t matures (pattern of Fi gure 3 . 1 ( c)). S uc h res u l ts :u-e c o nsi stent w i th retros pec t i v e site preparation rese:u-ch that s h o w s g rowth reductions assoc i ated w i th n u uien c re m o v a l and so i l d ist urba nce d o n o t appear un ti l after crown-closure. Fo r i nstance, after co m parin g a seri es o f s tands d i ffering in yeais s i nce s i te preparati o n in the Piedmont of south­ eastern USA, B u rger and Klue nd er (68] conc l uded tha t growth o f s tands aged 5 ye:u-s o r less was i m proved by site preparation that included p i l i n g or severe soil . disturbance; in older stands, however, decieased tree heig h t and· stand volume �i�'· :.: . were associated with these treatmen ts. Evaluation of the oldes t of the available . results presented in Tab l e 3.7 seems to confinn this relationsh i p. For i ns tanc e, in · · :.:: . th e Piedmont o f the southeast United S tates, early gro w th of Pinus taeda was ::grea r f :bY.: . ·, on sites prepared by shear-pile and disk harro wing than o n sites prepared h "ppin g fo llo wed by a light burn, even w hen differences in vegetation ':'.-:-:: ... . %,-.c·o mpetition w ere m i n i m ized b y repeated herbicide applications ( 1 8] . Examination . to f.. a.I! nu al he i g h t gro wth curves (Figure 3.2) for this study indicates th at most . of "' ·t· '· i : th hei.g h t growth advantage on shear-pile and h arro wed plots occurred before :!' !:. : · t. ;}g. 6 and su gges ts that heigh t growth o n cho p and burn plots may be greater ·:.• - ·· .... .. . . ter age 6 . A re trospective study on a sim i l ar Piedmont s i te -:'!':':. - < (69) found that I¥9DreFftWP»HI'A'W'Wili1W1i''¥!SRPGa;uJpxrllm»• n·'w,-.,;;· , rc,"ir . . .. : · . :..- : · _:._ . :.... ; -=; ·. : :. ·: .· . ;&;; ' • . • .. ·-· · · -- ··-- · - ·· · -­ --• ··-·---..••• -- ··-· - - - -. - · ·· · · --- ----------·--·--------- ·--·---·--·· · · .. --::- - - - -···· ----- ·'··- --··...-·-·· ·--- · · - - ---· ----------------- - ---- - -- · - · - · · · · ·· - .-. - - . ... ..._ • ••,. . . . .. . . ,. • .•• • • • · .. .. . • •• • .. . .. \ ·-.·: - · l . .... - ·. .. .. . . · ­ - · ; - ­ --­ . . . ... . . . . . . . . ... . . .. .-· . ___... ";.:: .. . ·-·---.-- ·-- . . .... · ·- . ._ .. --·-­ . . • . . ... - J . .. .. . -·------ ·'- · · • . - - ·------ ··- - · L-:'(' TA B LE 3.7 l u llueuce of :>lash llispos;•l anll soil lli:>llu haw:e on Operation:; Sp•:cies tlc .s P. wet/a W i mlrowiut: and burn i ng Date Ex pcrim.:n tal Lo cat i o n cvaluell USA. North Caro li n a in i t . i t:n .subplot:; 1910 in muin plot A uc "' l 'futllll.:t i d l )' 1{..::-uh:. Comuu:ut:i Soun.:.; J)omiuant 1n:e l'inc limwth lifeillest No IJetectahh: hdt:ht aml tut;ll in plut:. p1 .:pafcd hy ( I ll } iiCCUIIIUbliUII llf :.ll.:af- pilcJLiisl;iu iullucucc of hilllllil:.:i h:;a:.t iu du•t•lhuw plms. last eva I. V;u iahle:i ()'f) !I COIIl l lilfillt: 110\f\'e t ut i lh.atiou fuwlh uf :.uh:.<=• l ut:ut )tands_ (3 te llS) hiuUiii.S hilfVCSl - util il.alion UCIIII:i (e \'er:>cd; flfllliU.:th·ity t:feia tef in CUIH!Ill Wlatillll W i nd cu wi n t: . Ji. ttCn {-1 reps) Australia, llc d d iug uulilaltl Windmwing, P. New humint: rmlicaw Zealand V i ctoria 1 ')71 H. 5 lvkau tr..:.: hci !ih l ( ia uwth incn:asctl h)' ;u1d di;uu.:t.:r. h<=•ldint:. Ll.:.:u:;a:>e.t Ia)' :. ;u <l ,·ulum.: CllD (3 reps) I !J 7 K :\.5 M.:au h <:c hdt:ht, (5 7 ) wiudhlWIII Nu :.it:nilkaut d i ff.:r.:uce (5H} diam.:t.:r iuHI :.t.:-1 11 iu ;u.:;L\ with hcavy wccd \'tlluaue I CUIIIJk:liliuu. W.:it;lll: -11%, lliam..:tcr: - 7 '1.· uc inter wiaHIIIlwc•l ;uc;a:a when only iii"Cil:. wi1h luw ..:wupclitillll l"lli iiJlill <:il Win•lmwiug ( m o t rake), . . I'- WC£111 li A. outh C;amlina hc; h l in g , P- ncn (2 rcps . 3 1% - 1 9 7:\ :.i t.:s) 5 h·l.:au u ..:.: hd t; l l l Scalpint:b. 1'. t i l l a •• • · lwnLill t\. ' :. !l\t:.>m·,..,·,;;.�\.¥ '1:v<vit. :&, ¥l'£t.".!•.;""'"""0.\'r'i. 0;, s plil pltll U S A. Fl ori da (kor,da �.l.¢"-.���� ,.,_""""'t*-''<'\_'�' · ">W>""l ,.,".,_'!",••J""z ·"-. (1 , a "i''- ., • f<=Jl:i. 5 sites) - --' -"·· · . 1!.15!1 11 Mean u.:e hdt;ht and dhh. Ulel ..:h;ullilhk ,... . ·. ( 59) h)' Will filtiut: k• t ili-uuion :.las h •lisposal, dliouii I h : ight iuc(..:;,:.cd hy f.:nil i:u:r ;u u l hcdtlinu. d.:ca.:a.setl U u.-u int: fulluwiut; hy tlbk !ipaciut: ;uad .soil harmwiuu iucc�:a:;.:d t:cowth; effects nbo hu.-u inu full,lwc;l h)' :.calpiut: e v;a tuat..: d • . . . ......."' ,.-t•. .."- ". --;.,1_.. .... • .,._._ . (001 · ·- ·····--- -'- ·-·-· !!t>· ·: · Op.:r ;tions · Species Location cvalucd Experimental design Date inil. Hesuhs Comments Soun:c No c.:hange in a\'crage hlllg ·tCi lll (lrtllh!c.:ti \' it)' D um in g (7 1 ) tfC.:CS ;; ·1 . 1 as:.od;llcd w 1 1h slash hanlwoo<.l species; no vegetation contml; oc planting W i mlmwi n g followed by GIOwtll cesJlOHSC (9 0 ) w;,s s i te depc nd ell l , Age a t Pmd uc.:t i d t )' l as t eval. Variable:; (yr) D uming lvl i x cd conifers W i ml mwin g , V-blade, dbk P. w cda Matched plots (non-n:plicateu) at 44 locations 1 9·16)1 U S A, CRD ( 1 2 n:ps)' 1 98 1 P. weda bumiu :. 01111t S muheastern USA, Split-plot (4 reps) :.l;lle:. (uuulefllll:i Imming P. mdima N.:w S I, !>taud vuhum:. C.:lll tlhh h u mi ng 6 G eorg i a and I>- len i l i ;-..a l i on Win d mw i n g , ·10 Smith Carolina harrowing Win d ro wi u c . beddi n g , USA, Washington and On:gon 1 97!-i1 9S I a Mean tc.:.: hd gh t dbk h armw i n staud \"Oiuanc autl lx::.t tiCiiiJilelll l tl t a l the site:. tiHough age 3 b iu m a :.s 011 5()% Of hut eaii)' 1:mwth advam;•gcs diminished hy age 6 1\-J can u ce height. V ari ab le res po ns e 111 s l ash dbpo:.al, sustained response :>laud \"Oillllle a:. ocia1ed w i th 1 i l la1:e ;uut l oc.:a t i u n s ) . CIU) (3 re p s) li was the ami di;uuct.:r, fc1 1 i l i t.atiuu 1971i lU Zealand J\killl lfce hcighl. Nu :>ignilicant difference i n diameiCf illlll areas w ilh heavy weed \'il hUIII.: 11!111 favoccd Dou g las-li c & Cill!h Of 7 treaunents ccsulletl in greatest cwwth 011 ill I site least S i te preparation ( I S) a n d fenili:t;uiou •l i t fcrctl a•uouu i lc.\, H:.:. ul!.:. l:l llii(X:II l.l y Cillegury (58 ) c.:mupclitiou. W e i g ht : - H %, diameter - 7% ur imerw he n only hlw cump•.:litiou w iudruwed ilfCil!\ ••rea:> w ilh c.:umparcll complclely raudomizeu. I n ten t io na l removal of surface Iiller ;u tl minc•< l soi I . ' 1 2 sites, no ceplieation w i t hi n s i t e . • RCO. = randomized comple1e block, CRD = '-.>.> Evidence for lon g -rerm productivity standin g vo lume at age 3 1 of P. raeda planted o n a changes site thnt had been w in d ro w e d was 267 mJ/ha. compared co 345 m.lfha. o n an adjac:!nt si le that had been burned p ri or co pla.ming. Ar. index age 25. height of dominant and co-dominant P. raedc planted in imerwindrow li'e:J.s of tile windrowed sice was 3 .3 m less than height o r trees near windrows or planted o n the djacent burned s i te (a 1 4% reducti o n ) . S terr analyses of t"e lled trees i nd i c:J. led heights of trees plan ted in burned-only anc windrowed s i tes \Vere s i m ilar until about :1ge 7. After age 7. h e i g h t g ro w th wa: less in w i nd rowed Jie:J.s than in the burned-o n l y m!:J.s. One re:1son for the :!:lily g ro w th advant=:ge o ften associ:ued w i th w i n d ro wi n is im proved c o m 9'! ti t i o n contro l . [n the previous l y desc ribe d study b y Al len e r a. ( 1 8 1 . only on chop-and-burn p l o ts w here competition di fferences w e re m i n im i ze:.. by herbicide applic:J.tion did hei g h t gro w th equal o r exc eed gro wth on wi n d ro we plots after age 6. O n non-herbicided 9 lo ts . height gro wth rem ained gre:J.cer : I r I· •.vindrowed plot'i through :1ge 8. ?ualkl resul ts h ave b<:en re;:orted b y D yck <It c: (58], (Tabie 3 . S). Ac l o c a ti o n s when:! h<::lvy wed com petition existed. trees in no r w i nd row e d or burned Jie:s grew ac similar races •h rou gh age 9 . A t [oc:tions whc weed co m peti d on was low. l ul 1,4 . l.l - t.O <:l a.a a a.s !:: 0 - g row th w:J.s I owa i n wi ndro wed piots. ' Chop/no )'aetb,C:id• •C•nd a.• Age (years) · FIGURE 3.2: Annual h e i gh t growth of dominant trees durin g the previom: rotation and nrst 8 years o f c urre n t rotation following four site prepaiation-w· contro l treacmenrs in the North Caro lina P iedm on t (after [1 8)). 65 Slash disposal TAB LE J.S Gcowtll o( 8.5·ycar-old Pinus radiOJa in windrowed :tnd burned plotS \'Crsus in non-prepared plotS. · an wi tll di ffe ren t levels (open, partial, heavy) oi competing vc:gc!;ltion (source: (58]). Hcighl· Diameter'" Stc:m Volume• (m ) (em) (m lfU'ce) 3 .3 ' 3.6'0 3.0 1 4 .6' 1 3 . 3"' .C66' .05i' 9.6' l 5.i' 1 3.9° 1 2.5' .032' .OSP JWJ' Windrowed and burned: Open Partial Hc.a,·y Non·preparetl: . O pen . Pmial 9 .::.• S.i" Hc:J''Y Dissim i l:!r u pcr.;cripts \l·ieSl. a= 0 l ). We o nc l u d e fiOm c p -•.J J, ·ithin a column indic:He signific::nt tliffcrcnccs among trC.1lmCntS Jvai l J b l e Reid trials and rctrospct:tive rcsc:uch th:lt !o n g <c!111 9roducti v i ty is freq uen t l y deleteriously affected b y :1s .,,.indro w i n g but . m chnn e - ic:ll s l ash re m o v al such not b y chopping or other opcr:Hions that !ea\'c the majori ty or" slash in p l ace. Prod u c ti vi ty C h a n ge Fol l o wi ng Sl ash B u rn i n g Most s t u d ies have after harvest versus ences i n n o t fo u n d consiste n t d i fferences i n th ose that were noc burned [/0, growth on areas burned 7 1 J . Mo re o ver e:uly differ­ , tre e growth be twee n b u rned and nonb urned plots are fre q ue n tl y n o t measurements (70). subsLmtiared by l ater A s with results from most mechanical slash removal studies, results from slash bu rn i n g studies are normally confounded : f. · ?Y differences in· vegetation regrowth and seedling escablishment. Slash burning . - · educe to cal "soil nutrients while incre:J.sing their availability. Slash burning Jf iso i ncreases vegetation competition in some pl ac es yet decreases it in others. It ��1i·:.; is difficult to isolate these effec r.s wi tho u t a veget.3.tion-controi treatment. This i s iJ!.: "" ':, . :;, L tru e of older s tud ies s uch as the Morris plor.s eval uated by Mille r and B i g!ey : ji·,: . . . & ,• • I t •' • tl.;f,·- . . . [72) (j7 I]. These matched plots were established 1 946 through 1 95 1 to measure sl :i. burn i g effects ti re hazard and natural regeneration. The plot-pairs we re in · · ;;: ·- . .. n on &i:. r.ep licated at any of :. me plot '-:-: · pairs as h no t locations in western Washington and O regon, USA. regenerated n atu rall y ; other pairs were planted. B urning had . the 44 66 Ew'dence for fong-rernt productivity chang es several effectS o n s u b sequent stands. B y reducing numbers o f adv anc e regenern.­ don. nre shifted SP<!C!es composition away from shade-tolerant conifers. Slash burning nhanc::d regeneration o f P. mem;iesii, primarily be::::tuse more mi nera i soi l was exposed for seeding. When si te index of - :nem:iesii or vol ume pro duc ­ tion of all spec ies were used evidence to genl!ralize a lS measures of site 9roductivity, there was no productivity dedine. S iashbumi ng apparently decre::1sed sund productivity J.t some loc:I.tions. buc incre:::sed it lt others. This rese:u-ch is of ;Jartic:..I! ar i n terest be::::tuse it re tJrescn ts the tong'!st :.nd most widely disuib u ted data. b:J.se o f i ts kind. N verthe!ess. the resu its .::e J.Inbiguous because o f the severn.i confounding fn.ctors and des i g n problems .: scribed above. SO I L P HYSI CAL C O N D rTI O N S ...l.. pm t"rom dfecr.s o n n utrien t budgl!ts. harvesti n g nd other fo res t m annge:n t! n t a c ti vi t i es c:m h:J.ve direct a.nd indirect effects en s o i i factors lffecting si re p ro d uc ­ ti vi ty. In p a.rticu l :u-. use o f .heavy equi pm ent to iemove togs ca n te:.d co so i l compaction 7 particularly o n the l 0-25% of the :;ite in skid trails. md co red uc ed tree growth in some loc atio n s (6 . 65, 661 . but not :.i l occurs, reco very c:tn occur quickly lS [73 ] . Where soil co m pac ti o n reponed by Thorud and Ftissd (74] following harv estin g i n Mi n nesota. or can require more than 50 years as reported by Perry (7 5 ] in North Carolina. and Grece:tn and S:.nds [76] in A us trali a . The risk to lo n g- te rm sice p ro ductiv ity de9e n ds upon the s eed of recovery. R isks are l o w w here c o m pac tio n is lim iced to the surface so i i md/or the J.Ineiiorating effects of freezing and thawing, we tti n g and dryi n g, fauna. ac:ivicy, and root growth are large. DeetJ compaction, pnrticul ari y when assoc i ated with degradation of so i l structure (puddl ing) in warm clim ates with low shrink-sweil so ils, [XJSes a si gnific :mt lon g-term risk. A ·lELIORATIVE TREAT:V[ENTS Reviews of res earc h o n !on g-\erm site productivity tend to focus on h arves t anc associated management activities considered to h:ve go ten tially ne gati ve im pacts Ameliorative rrearmerrts h arve s t- Several 67 and regeneration-associated practices. however, have the po tential to improve productivity throughout the rotation and. perhaps. through multiple rota tions. P Fertilization a t Pla n ting Phosphorus fertilization m ay be the best example of a management practice long-tenn site productivity (Figure 3 . l (b)). On P -deficient that [ mproves ferti l i z a t i on at p l a n t in g has i m pro ved g rowth throu g h out i nto a second rot ati o n . For inst:mce, G en tle ec a si tes, full rotation [77] and a!. (781 re po rt P. radiara growth res po nse to fert i l iza t i o n with two forms of . p hosp h o ru s at age 1 6 in both the n rst rotation and second rotation (Table 3.9). During the first rotation. hei g h t and vo l ume accu m u lat i o n c u r,es c h a ng e in site prod u c ti vity su ggests this trend diverged throughout the rotation ind i c a t ive ( figure 3 . l (b)). Information presented in Tab le 3 . 9 has c on t in ued in the second rotation. \Vh i l e P ferti l ization can provide long-term growth responses, this i s not always t h e c ase (e. g . , [79]). As B allard [89] points out. the g ene ral res po n s e to the l arge amounts o f applied P (50- l is due o r" a removals i n forest harvest (5-70 kg/ha) and t he sustai ned persi s tence of kglha) i n comparison to avai lab i l i ty provided b y thi s amoun t of phosphorus. TAU LE J.9 Re$ponsc of Pinus radiata to a single applic:1tion of phosphorus, in the rol:!tion fertilizer was applied . and in Lhe second rowtion following fertilization (Source: (78]). Stem volwne•* (mliha) (m) ; t��·:-----i)il; Initial RotaJiort ; ;.;;...;:.:: ' No fertilization · - , Dominant tree height;. . . ; ,;;. '= · ;.:.) ... . l-\:y'".. - · .· • Rock phosphate Super phosphate · . 0 · 1:;>!; Se cond Rotation :; '"'f¥·:.:;·:.-:-• :· · No fertilization · .. ' .. ·f9 - .,· · '·'"' Rock ph osphate 13 .7' :.::r;-- n:\-.. : . . Super phosoha!e • ------- 1Jl:; ; ,;,Wilhin a rounion, dissimilar superscriptS indicate s i g nific:lJlt differences (a=.05). To a 10 em (i.b.) diameter 1 1' :'-; . - :;... . - . ... ·. 68 . E'lidence jar long-(l!nn productivity changes 'i ., Liming (C.1 additions) fn co ntrast to w idespre:1d use of lime in agriculture. addition of CJ. and/or Mg t< forestS is re!acive!y rare. Although so me forestS in G erm :m y were limed as eari as 1 360. liming of forestS hns never been widespread. Wied emann ( [80] - p. 27 c;. ci tes several examples of growth incre:1ses of 20 to 25% during two or mar decades after qu ick l ime (ClO) or limestone (CaCO) was add ed to es mb l i s h e : stands of po le - si zed trees with he vy accu muJ ::u i o n o f fo rest Roar (raw humus B aule and Fricker ( [8 1 1 - p 56) concluded: "In the fores t l i m i ng therefore in rna: . cas es is conducted less with the o bject o f providing the trees w i th a. su pp l y c c =:.Jc i u m but pre ·<!minently of improving the physic:::. ! . chem ic:::.! and b iol o g i c : pro perties of the so i l . [t is actual l y possib le to m=:.ke ac id sci is or th o se wi ch a I a · . c a lci u m content capab le of c:uTyi n g bra.::d -leaved trees by limi n g co a su fficie: de p th . rn the l:lSt two decades. i n terest in l i m i ng h=:.s been stim u l at ed b y rec o g r. " tio n of the th rea t to long-term site pro du c v i ty posed by ac:d precipi ta ti o n . Andersson and Lundkvist [821 rec : n tl y summarized results from ! i m i r exoeriments ca m o le t.ed since 1 9 1 2 in S weden, Fin l and . and Germ anv. The . . . au thors concluded that long-tenn incre::1ses in site pro d uc tivity are generai asso c i ated with l i m in g; however. response to l i m i n g often fo llows a pane: similar to, but the reverse o f, he p attern il lustr:lted in Figure 3 . 1 (c). In mo st c ase growth r: ue of l im ed trees fi rst decre:J.sed in com parison to the un l i med c o n e: an d o n l y after abo u t 4 0 years. th en in c re:l.Sed i n c o m pariso n t o the u n l im . co n trol. The authors specu l ated that this growth pattern m ay occur because l ir additions stimulated microbial activity th at immobilized N nonnally av ail a b le :· tree uptake. They also suggested . that mi cronutrient deficiencies may have be induced by. exc essive li"m ing and that positive growth responses o nly occurr after natural acidific:1tion c ompens ated far lime-induced deficiencies. Regardlc of the cause. chlorosis J.nd growth retard atio n can be a sho rt- term consequence lime add itio n on m an y forest sites. ' ; .. . n: f· · 1: ( ;· · ij I I Comparable long-tenn results are not generally availab le outside Eurac Although lim i ng has often been included in programs desi g ned to evaluate for fertiliz:J.tion. few programs have carried liming trials for extended periods of ti. becaus e i ni tial results were not encouraging. For i n stanc e, CJ. add i tions w included as part of the original ferti l izatio n trials i n slash pi n e i n the southeasc:: Conclusions 69 U.S. but were not included in subsequent rese:rrch becnuse Ca additions failed to increase tree growth [83]. Tillage Oilier ameliorative . practices !.hat may have long-tenn benefits are bedding, disk harro wing, or rip p ing which can improve physic:1l conditions restricting root growth. While th e short-tenn benefits of such trea.unents are cle:rr, long-tenn benefits are not. Many responses to tre::lunent see:n to fall into responses illustrated in Figure 3. l (a). Trees planted after these tre:1unents achieve an e:1riy growth advantage which c an be maintained throughout the rot::Ition, bu t !.he advantage or response does not increase; thus, this is not a tong-term change in site productiv­ ity. Such growth responses have been reported for P. el/iouii a n d P. caeda in the C n i ted States following bedding (6], bedding and disk harrowing [84, 35. 861, and following bedding and subsoiling for P. radiaw i n ew Ze:1land [37]. The p:1ttern of response to such tilla.ge tre:lunents may re!:lte to !.he re:1sons for the observed initial response. Responses may be teJ7� porary where benefits of tillage are largely due to: I ) decreased vegetative competi tion; 2) accelerated occupation of rooting volume without an increase in absolute rooting volume; 3) short-term i ncreases in N mineralization; and 4) beneficial changes in thermal . .. regimes or water infiltration and distribution. Responses appear to be long-term : . where amelioration of soi l physical conditions which restricted total rooting . :,.. .�� :; volume were largely responsible for initially poor growth. Thus, bedding of sandy }i· · sites does not ap pear to have long-tenn benefits because much of the in itial ::- ·· ; , benefit is associ'ated with ephemeral increases in nitrogen mineralization and . o petition con trol. Responses to bedding may be long-tenn, however, on fine­ soils where bed confi guratio n is maintained throughout the rotation and drainage improved. .:; CONCLUSIONS of factors affecting forest growth is incomplete; therefore, from carefully controlled field trials. rather !.h an models, provide more ·.understanding 70 £ ·idence jar long- ;enn praducriviry changes convincing evidence of raduc:.ivi ty changes c:ms e d by harvestin g practices. To be acc pmble evidence of change in lo n g te rm site 9raductivity, three cond itio n s - must be met. Firsr. differences i n tree growth m u s t be a ttrib u tab l e to differences in site conditions. rather than to differences in res o urce a1loc:J.tion among targe and non-target species or to d i fferenc es in plan t species or genotype. Second. growth results m ust be available for a sufficient time so that the [nfiuence o f eohemeral d i fferenc es i n ini ti:ll s i te conditions has d i m i n i sh ed m d s a that c:mac ' . ity of the site to su ppo rt tree g ro w th is stressed. Fi nal l y, adeq u ate experi mc:n tai cancra ! must ex ist S h i fts i n reso urc e al loc:.tian will :1\:Jpe:lr as an earl y i nc rease ir. . tree growth. Th i s i nc :-e:1se i s maintained after cro w n c l o s ure but further gro w tl . i m pro vemen ts are nat e vide n t . Hence this pa t te rn of growth res po nse do e s n o in d i c a te l change in lang-\eml si te productivi ty. F':!w studies m e t ad quate ex pe rimental re q u i re m e nts and none have b ee n c:.rri cd long enough to providt [eng-term res u l t s iI . Regn.rdless of study purpose. m i n i m u m requ i rements fc ac c ep tanc e are: l ) app ro p ria te conu·ol plots ag::.i n st v h ich treauncm di fference: I ' I .. II· · .· ; . c:m b e evaluated: and 2) filcmrs oth e r than tre:J.unents have b n m i n i m i ze d c me:IS ured co account for their influence o n observed di fferences in growth. Issues o f spec i e s chan ge an d second-rotation d ec l i n e l!"e not e a s i l y disen t.an gled from . as so ci a ted q ues ti o n s on harvest util ization, slash disposo.l . and so: tillage. D e s p i t e l ac k of evide n ce to sup o rt the concept that n p l ac i n g m ixc vegetation with conifers decreases sile productivity, same au thors continue : accept speci es - in d uc ed declines in productivity as f.:rc t. We con c l ud e chat curre:­ evidence does na t indic:ue such declines occur o r, if they do occur, are pro b ab i not rel ated sim ply t o establishment of conifers and their conti nued managemer. In contrast. evidence from field trials cle:lfly s hows th a t addition of nitroge:­ tixin g tree species to stands an N-deficient sites i n c :-e :l.S e s site productivity. Henc removing such beneficial species co ul d reduce lang-term productivity. Concerns about forest harvest o n [a n g tenn productivi ty s ho u l d no t be surr. - marily dismissed. Direct remav<Ii and indirec t loss of es sen ti al plan t nutrients wi occur i n forests managed for wood and fiber p roduc tio n Without replilc em en c c . natural saurc s or by fertilization, p roductivity co u l d decLine. Although n trie:­ balance analyses pro vi d e indirect evidence far projectin g declines in long-te::­ sice productivity in m anaged forests. direct evidence of tree growth rarely sho\ · Urerarure cited . suc h d e cl i nes Most field trials pro vi d e we:J.k 71 vidence for prod uctivity dec l i ne s that m ay be required to induce productivi ty decline. Apan after i ncreased harvest uti l i zation because of poor study d esi g n and beca u se a n u m b e r of rotations from their effects on nutrient bud gets, slash disposal and site preparation h ave n um e ro us direct and i n d irec t inn ue nces on soil ph ys i c a l and chemic al p rope rti e s Virtu al l y I av ai l :.1 b le r data from ca e fu l l y d esig n e d . field ex peri me n ts show that survival and early growth of plamed seed l i n gs is gre:uest o n si tes w here biomas s remo vals were greatest and where organic Jnd m i neral so i l hori zons were most se ve re l y d isturbed during mechanic::ll slash d is pos a l . One reason fo r th e e:trl y gro w th ad vantage o ften associated w i t h wi n d row i n g i s i m p rove d c o m peti t io n contro l . \Ve - c oncLu de from J va i l a b le field trials Jnd retrospective rese:trc h th:u lo n g te rm produ c t i vity i s frequen t l y d e let e rio u sl y affected by mechan ic:J.I s l as h removal . fn contrJst. most stud ies ha,·e no t fo und consistent d i ffere n c es i n growth on Jiea s b umed after h :trve.st ' \ c rs us those that were not b urned . As w i th re s u l t s fro m m o s t mec h an ic a l s l as h removJ I , e ffe cts on so i l pro perties are norm :1i l y confounded by d i ffere n ces i n \'cgetative regrowth and s edl i n g esta b l i s h m ent. . . Native soil prod ucti v i ty can be i mpro ved O n P-delicient s i t es ferti l i zation a t p l an ti n g can i m prove growth throug ho u t a fu l l ro ta tion a n d i n to a sec on d ro tatio n . - Other am e l i o ra t i ve practices th :lt ca n h ave lo ng te rm b e n e fi ts l!'e bedd i n g , d i sk h arro w i n g , or ri p p i n g w h ich can im p ro ve phy sical conditions re stri c ti n :. _- . growth. While the shott-term bene fi ts of such trea tmen t s to tre e growth are c!e:1r, v. o n g- te rm benefi ts are less evide n t £\ . .The cumulative {¥£. rem ain an t d . . effec ts of repe:Hed harvests and stand ;"".:.0"4 :; root g u nq u ._Data. i fi ' regeneration practices a E ffectively d e si gn ed arid implemented fie ld trials over a r_¥1ge of soi l and climatic conditions are needed to pro vide re l i ab le qu ntific atio n : ' ·... .. from such trials are ne ed ed to provid e independent v al i d at ion of c omputer -;... :-'!'t ,' · ' and our understanding of factors affec tin g tree and stand perform ance · . : :::.: · · ·. ·'' ., r-.... .P astor Si. ... - . ·· tilffl. .. # ... LITERATURE CITED Post. W. 1. . , J. a nd Devel? pment of a l inked fo es t productivi y- soil , p rocess m odel. Oak Rrd e Nauonal Laboratol)', Enviro nmental S c ren ces ·: · · Divisio n Pu b l ic a tio n No. p. · .; - -:�:-..··· . g 2455, 1 985, 1 62 • £ ·idence for lang-terrn produc:ivicy changes , ., _ Kimmins. J.P. Co mmuni ty orgnniza.tion : methods of study and p redic ti o n of the productivity and yie!d of forest ecosys tems . Canadian. Journal c Botany. 1 983. 66, 2654-2672. Reed. D.D Ho !m s. M.J Jones E.A Liechty, H.O and Mroz. G.D. ,:l ecologic:ll growth mo dei for four northern hardwood species in upp< Michigan. fn: Process Modeling oj Forese Growth Responses £nt•ironmemal Stress. (Eds.) R.K. Dixon. R.S. Meidahl . G.A. Ruark, ar W.G. Warre n. Timber Press . Ponlnnd. 1 990. pp. 288-293 . .• 4. .• .• .• Wdnstein. D .A. and B do in . R. E·,alu:uing e ffects of pollutants o n incegrnc, ere:: process.::s : l m odel of c:ubon. water, a.nd nuuient baln.nces. fn: Proce :\4o deling of Forest Ctowrll Responses ro E:tviromnenwl Stress. (Eds. ) R . . D ixon. R.S. fc!dnhl. G.A. Ru:1rk. lnd W.G. Warre n. Ti mber Press. Ponlnr. USA. ! 990. pp. 3 1 3-323 . 5. . 6. ..' 7. \Visiol. K . J.nd Hl!ske!h, J.D. ( Eds.). P!am Cmwrft Modeling for F?esow Jfamzgemem. CRC Press . B oc: R:ton. FL USA. l 987 . Hughes. J.H., C.:rnpbe! l. R.C.. Duzln. H . W . • m d Dudley. C.S. S i ce int. adjusunents for intensive forest managemen t treatments at Nonh C.1rol i Weyerhn.euser Forest Rese:I.rch Tech ni c :l Report 042· l -+04n9124, l 979 . Mead. D .J .. Whyte, A.G.D., Woo l lens. R.C.. and B ee ts , P.N. Desi gning l o : tenn ex peri men ts t o study harves ting im pacts. In: Long·lerm Field TriaL Assess Em·iromnental fmpacrs of Harvesting. Proceedings . IEA/13 E T6. Workshop, Feb . 1 990, Fiorida, USA. (Eds.) W.J. Dyck and C.A. Mees. l' Zealand Forest .Rese:I.rch Institute B ulletin 1 6 1 . 1 99 1 . pp. 1 07 · 1 24 . 8. Likens. G.E B ormnnn. F.H Johnson, N .M Fisher. D.W and Pierce, := Effects of forest cu tting and herbicide treaunent on n u trie n t budge in Hubbard B rook watershed-ecosystem. 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Duvi gneaud, P. and Oen:leyer OcS met S . B iologicJ! c yc l i n g of m i nerals i r te:nperate deciduous forests. In : A n alys is of Temperare Forest Ecosystem: (Ed.) D .E. Reichle. Springer- Verlng, New York. 1 970. pp. 1 99-225 . 29 . Gal ley, F.B McGin nis. J.T C l e men ts , R.G Ch i l d G.L. and Ouever. L · MineraL Cycl in g in a TropicaL Moisr Faresr Ecosysiem. Un iversity o. . Geo rgi a Press, ALhens, 1 97 5, 243 p. 30. Weeunan. G.F. and Webber, B. The influence of wood harvesting o n nutrient status of two spruce stands; Ca11adian Journal of Foresr Research 1 972, 2. 35 1 -369 . 3L 32. .• .• .• , th· . . Foster, N.W. and Morrison. LK. D istribution and cycling of nutrients in natural Pinus bartbiana ecosystem. Ecology, 1 976, 5i, 1 1 0- 1 20. Green. D.C. and G1igal, D .F. Nutrient accumulations in jack pine sr.ands o deep and sh a l low soils over bed roc k Foresr Science. 1 9 80, 26, 25-33 3 . . 33. O vi n g ton J.D . 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