This file was created by scanning the printed publication. Errors identified by the software have been corrected; however, some errors may remain. Effect of Managenlent on. NII.t)~ien.t DYllamics in SOllth.,vesterJ} Pin)70n JII.Jlipt~J· 'V()odlands L. F. DeBano and J. M. Klopatek 1 ----,-------------------------------- Abstract--Pinyon and juniper tre.~s cycle nutrients producing a moo. saic nutrient distribution that is vulnerable to range improvement, ~Jrazing, and fuelwood harvestin~J activities. Prescribed fire rE!leases small amounts of availabh~ nutrl.~nts, but also volatilizes lar~Je quantities. Th.~se impacts on nutrient cycling may affect long te!nn procluctivlty of pinyon juniper woocllands. Pinyon juniper woodlands occupy 62 to 79 million acres in the weste·rn United States (Arnold et a1. 1964) and about 15 million acres in Arizona and New :Mexico (Springfield 1976). These woodlands, which occur in the transition zone between semiarid vegetation (chaparral, desert shrub or grasslands) and coniferous forests, are characterized by a mosaic of pinyon and juniper tree.s; interspace areas are occupi.ed by sparse to dense herbaceous and shrubby vegetation. Pinyonjuniper stands are found on a wide variety of parent materials; soils vary in texture from stony, cobb ley, and gravelly sandy loams to clay loams and clay, and vary in depth from shallow to deep (Aldon and Brown 1971, Pieper 1977, Springfield 1976). In pinyon juniper woodlands a soil nutrient mosaic pattern develops where carbon, nitrogen (N), and available phosphorus (P) are concentrated in the upper soil layers under the tree canopy. This pattern reflects the accumulation of litter by different plant species (Barth 1980, Charley and West 1975, Everett et a1. 1986, Lyons and Gifford 1980, Klopatek 1987). Tree growth rates vary widely between sites in close proximity to one another. Since pinyon juni.per woodlands occur in different climatic regimes, and on a wide variety of soil types, these variable growth rates sug,gest nutrient limitations may exist similar to those found in other forest ecosystems. Although N is usually considered the most limiting nutrient in forest ecosystems (Maars et al. 1983), it appears P and potassium (K) may also be limiting (Barrow 1980, Bunderson et a1. 1985). Past management has emphasized tree removal for range forage improvement, but recently inte,rest has increased in harvesting pinyon and juniper trees for fuelwood. Prescribed fire has been used extensively during both range improvement and slash disposal after fuelwood harvesting. Intensi.ve tree removal and prescribed fire, coupled with continued use for grazing, is expected to alter naturally occurring nutrient cycling processes in these woodlands and thereby affect long term interrelationships among site productivity, succession, and tree growth (Miller at al.. 1981, Young and Evans 1981). This paper presents information on distribution of nutrients and their cycling i.n pi.nyon juniper woodlands, and assesses the effect of different management strategies. Nutrient Cycling and Distribution Pinyon and juniper trees cycle nutrients both horizontally (Tiedemann 1987) and vertically (DeBano et a1. 1987). Tre.e roots penetrate into interspace soils between tree canopi.es where they absorb nutrients and incorporate them into tree biomass. A large portion of the nutrients captured from interspaces are deposited on the soil surface under trees during leaf fall, where they are released in an available form by decomposition, thereby enriching the upper soil laye.rs. Trees also translocate nutrients vertically to the soil surface from deeper in the soil profile by a similar process. The quantity of nutrients cycled by trees varies considerably from one locality to another, depending upon land use, climate, soil, and tree density and size. Published information on nutrient patterns in pinyon juniper woodlands clearly portrays strong vertical and horiz.ontal distribution patterns developing from the above described nutrient cyd.ing regime. The most important vertical com partments are: above ground biomass, litter, and soil nutrients. Nutrients are also distributed and exchanged horiz.ontally between trees and inte.rspaces, resulting in larger amounts of 1De Bano is PrinCipal Soil Scientist. Rcd(y Mountain Fcrest and Range Experiment Station, Forestry Scienc!~s Laboratory, Arizona State University Campus, Tempe, AZ 85287. Station headquartE~m is in Fort Collins, in cooperation with Colorado State University. Klopatek is Associate Professor, Department of Botany and Microbiology, Arizona State University, Tempe, AZ 85287. 157 nutrients being present in the living biomass and litter trees compared to interspaces. The quantities of nutrients store,d in soils unde.r tree canopies has been reported by some authors to be. greater than in interspaces (Everett et aJ.. 1987, Tiede·· mann 1987), while in other cases no sign.ificant differences could be detected (DeBano et aJ.. 1987). Information presented in the literature on N, P, and K were used to develop a model portraying vertical nutrient distribution patterns under trees and in associated interspaces for a typical. pinyon juniper ecosystem (table 1). Data on N presented in table 1 for a pi.nyonjuniper ecosystem was taken from Tiedemann (1987). Distributions of P and K were tak~n from DeBano et a1. (1987), where. soils data for the 0 3.8 cm depth was extrapolated linearly to 60 cm. Important features of the vertical. di.stribution pattern are: (1) a small percentage of the, total nutrient pool resides in plant biomass and litter, and (2) the three nutrients differed in the proportion of a nutrient stored in living biomass and liUer. For example, under tree canopies higher proportions of N are present in litter and above ground biomass compaIed to P and K. About 98 percent of total P in the tree ecosystem is contai.ned in soil, compared to 93 percent for K, and 82 percent for N. Horizontally, N, P, and K are concentrated in a mosaic pattern corresponding to litter and canopy distribution. Although total. N, P, and K in the soil may or may not differ significantly beneath tree canopies and interspaces, more total N, P, and K accumulates in live tree boles, stems, and leaves and in litter under tree canopies than in interspace vegetation (DeBano et a1. 1987). Nutrient Availability Available and total nutrients are delicately balanced because only a small percent of the total nutrient pool is in a readily available form. Vertical and horiz.ontal distribution patterns of available and total nutrients are similar. Horizontal patterns of nitrate N and ammonia N are influenced by tree canopy distribution, with higher concentrations of ammonia N being found in the surface soil under tree canopies compared to interspaces (DeBano et a1.1987). In contrast, nitrate N may or may not differ between trees and interspace areas (DeBano et a1. 1987, Klopatek 1987, Thran and Everett 1987). Management Implications Information on nutrient dynamics can be used for assess·· ing the effect of different management strategies on the nutrient status and productivity of pinyon juniper woodlands. Important strategies include: grazing, fuehvood harvesting, and using prescribed fire either for type conversion or slash disposal following fuelwood harvesting. Tiedemann (1987) estimated N losses over a 100 year peri.od would be 340 kg/ha by grazing and 856 kgjha if chaiJling and burning were used for cover conversion. In contrast, fuelwood harvesting over the same 100 year rotation would remove only about 133 kglha of 158 Table 1.--Arnounts of nitrogen, I)hosphorus, and potasslurn (kg/ha) In above-ground blornass and the eO-cm soli depth under trees and associated InterSI)aCeS In 1)lnyon-)unll)er WOOdlands, and percent In each ecosystem COml)artrnent. Ecosystem cornpartment N1 p2 K2 Trees Foliage Twigs Wood Litter Soil (0-60 ern) Total 108 184 133 1,000 6,615 8,040 (1 ) (2) (2) (12) (82) 20 11 5 44 3,963 4,043 « 1) « 1) « 1) (1 ) (98) 147 5!5 21 65 3,584 3,872 (4) (1 ) « 1) (2) (93) InterSI)aCeS Foliage Soil 4 « 1) 0.2 « 1) 4,527 (>99) 3,963 (>99) 0.2 « 1) 3,584 (>99) 1Data from Tiedemann 1987. 20ata from DeBano et al. 1987. 3percent of total nutrient pool made up by a particular ecosystem compartment. N in the woody material. However, if prescribed fire was used for slash disposal following harvesting, an additional 277 kg/ ha of N would be volatilize,d from twigs and leaves (if 95 percent of the N is volati1iz.ed) i.n addition to variable amounts of the 1000 kglha of N contained in the litter. If large amounts of litter were consumed by fire during slash disposal ope.rations, then an additiona.1400 500 kg/ha of N could be lost. It is not known how grazing would affect P and K pools. Fuelwood harvesting would remove only a small percentage of the P (5 kg/ha) and K (21 kg/ha) nutrient pools during a 100 year rotation. Substantial P would also be lost if the leaves a.nd twigs were burned following fue.lwood harvesting. Nonparticulate losses up to 50% of the total P (16 kg/ha) could occur if these fine materials we.re totally consume.d during burning (Raison et al. 1985). A variable amount of the P contained in the litter could also be lost, depending on the intensity of the fiIe. Similar percentages of K may also be lost because it volatilizes at the same temperature as P (Raison et a1. 1985). The effect of different management activities on available nutrients is not as well understood as on total nutrient pools, although there is some information available on the effect of fire on nutrient availability. Studies in pinyon juniper and other ecosystems show fire acts as a rapid mineralizing agent, and releases ammonia N which is later converted to nitra.te N when conditions are favorable for nitrification (Klopatek 1987). The release of highly available forms of N by fire portrays the impression that burning increa.ses soil fertility on a site. However, total N i.s reduced, and increases in ammonia and nitrate N are short lived because these nutrients are rapidly immobilized biologically. Inorganic P also is released by burning, but it too is quickly i.mmobilized chemically (DeBano and Klopate.k, In press) and may no longer be readily availa.ble for plants. Harvesting also increases the concentration of nitrate N in soil surface layers (DeBano et al. 1987). Nitrate N presumably increases because harvesting reduces inhibition of nitrification, eliminates trees which assimilate any nitrate N being formed, or changes the microclimate. Both s(;il moisture and temperature can be increased by harvesting (Everett and Sharrow 1985) which in turn may affect microbial relationships. Bunderson, E. D.; Weber, D.J.; Davis,J.N.1985.Soilmineral composition and nutrient uptake in Juniperus osteosperma in 17 Utah sites. Soil Sc.ienc.e. 139: 148. Charley, J. L.; 'Vest, N. E. 1975. Plant-induced soil chemical patterns in some shrub-dominated semi-desert ecosystems jn Utah. Journal of Ecology. 63: 945-963. DeBano, L. F.; Klopatek, J.M. (In press.) Phosphorus dynamics of pinyon-juniper soils following simulated burning. Soil Science Society of Ameri.c.a Journal. DeBano, L. F.; Pe.rry, H.M.; Overby, S. 1987. Effe.cts of fuelwood harvesting and slash burning on biomass and nutrient relation.c;hips in a pinyon juniper stand. I'n: Proceedings--pinyon juniper conference; 1986 January 1316; Reno, NV.; R. L. Everett (compiler); Gen. Tech. Rep. INT -215. Ogden, UT: U. S. Department of Agriculture, Forest Service, Intermountain Research Station. 382-386. Summary and Conclusions Pinyon and juniper trees enrich the surface soil beneath their canopies by cycling plant nutdents, both vertically from the subsoil and hodzontally from adjacent interspaces. This produces a spatial distribution. of nutrients roughly corresponding to existing tree canopy cover. Both Nand P undergo extensive horizontal and vertical translocation. Important features of this vertical distribution pattern are: (1) a small percentage of the total nutdent pool resides in plant biomass and litter, and (2) N, P, and K differ in the proportion of a nutrient stored in Hving bioma~ and litter. The location of active nutrient pools beneath tree canopies makes them vulnerable to different management practices such as range improveme.nt and fuelwood harvesting. Prescribed fire is used in both range improvement and slash disposal after fuelwood harvesting. Range improvement practices designed to perma·· nently convert pinyon juniper stands to grassl.ands may have a major impact on the storage and cycling of both above and below ground nutrients, particularly if chaining and burning are used as part of the treatment. Fuelwood harvesting not only removes nutrie.nts directly from the site, but also affects mineralization and the release of available nutrients remaining on the site. Prescribed fire acts as a rapid mine,ralizing agent, making part of the nutdent pool more readily available but at the same time volatilizing substantial amounts of nutrients from the litter and above ground biomass. These losses and changes in nutrient pools may affect the productivity of pinyon juniper woodlands. EvereU, R. L.; Sharrow, S. 1985. Soil water and temperature in harvested and on harvested pinyon-juniper stands. Res. Pap. INT-342. Ogden, UT: U.S. De.partment of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station. EvereU, R. L.; Sharrow, S.; Thran, D. 1986. Soil nutrient distribution under and adjacent to singleleaf pinyon crowns. Soil Science Society of America Journal. 50: 788792. Klopatek, J. M.1987. Nitrogen mineralization and nitrification in mineral soils of pinyon-juniper ecosystems. Soil Science Society of America Jotunal. 51: 453-457. Lyons, S.l\1.; Gifford, G. F. 1980. Impact of incremental surface soil depths on plant production, transpiration ratios, and nitrogen mineralization rates. Journal of Range J\ianagement. 33: 189-196. Maars, R. H.; Roberts, R. D.; Skeffington, R. A.; Bradshaw, A. D. 1983. Nitrogen in the development of ecosystems. In: J. A. Lee et a.1., ed. Nitrogen as an ecologica.l factor. Oxford, England: Blackwell Science Publishing. 131-137. Miller, H. G .1981. Forest fertilization: some guiding concepts. Journal of Forestry. 54: 152-167. Pieper, R. D. 1977: The southwestern pinyon-juniper ecosystem.I'n: Ecology, uses and management of pinyonjuniper woodlands. Gen. Tech. Rep. RJ\I-39. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky l\lountain Forest and Range Expe.riment Station. 3-10. Raison, ILr.; Khanna, P. K.; "'ooels, P. V.1985. Mechanisms of element transfer to the a.tmosphere during vegetation fires. Canadian Journal of Forestry. 15: 132-140. Literature Cited Aldon, E. F.; Brown, J. G., 111.1971. Geologic soil groupings for the pinyon-juniper type on National Forests in New J\lexico. Res. Note Rl\I-197. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky- Mountai.n Forest and Range Experime.nt Station. 4 p. Arnold, J. F.; Jameson, D. A.; Reid, E. H. 1964. The pinyon·· juniper type of Arizona: Effects of grazing, fire, and tree control. Prod. Res. Rep. 84. U.S. Department of Agriculture, Forest Service. 28 p. Barrow, N. J. 1980. Differences among some North American soils in the rate of reaction with phosphate. Journal of Environmental Ouality. 9: 644-648. Barth, R. C. 1980. Influence of pinyon pine trees on soil chemical and physical properties. Soil Science Society of America Journal. 44: 112··114. H."'. Springfield, 1976. Characteristics and management of pinyon-juniper ranges: the status of our knowledge. Res. Pap. Rl\l-160. Fort Col.l.ins, CO: U.S. Department of A~gricu1ture, Forest Service, Rocky 110untain Forest and Range Experiment Station. 32 p. Thran, D. F.; Everett, R. L. 1987. Nutrients in surface soils following tree harvest of singleleaf pinyon. Soil Science Society of America Journal. 51: 462-464. 159 Tiedemann, A. R. 1987. Nutrient accumulations in pinyonjuniper ecosystems--managing for future site productivity. In: Proceedjngs--·pinyon-juni.per conference; 1986 January 13-16; Reno, NV.; R. L. Everett (compiler); Gen. Tech. Rep. INT-215. Ogden, UT: U. S. Department of Agriculture., Forest Service, Intermountain Research Station. 352-359. Young, J. A.; Evans, R. A.1981. Something ofvalue--Energy from wood on rangelands. Rangelands. 3: 10-12. 160