Assessing fine-root biomass and production in a Scots pine stand – comparison of soil core and root ingrowth core methods

Soil core and root ingrowth core methods for assessing fine-root (< 2 mm) biomass and production were compared in a 38-year-old Scots pine (Pinus sylvestris L) stand in eastern Finland. 140 soil cores and 114 ingrowth cores were taken from two mineral soil layers (0–10 cm and 10–30 cm) during 1985–1988. Seasonal changes in root biomass (including both Scots pine and understorey roots) and necromass were used for calculating fine-root production. The Scots pine fine-root biomass averaged annually 143 g/m² and 217 g/m² in the upper mineral soil layer, and 118 g/m² and 66 g/m² in the lower layer of soil cores and ingrowth cores, respectively. The fine-root necromass averaged annually 601 g/m² and 311 g/m² in the upper mineral soil layer, and 196 g/m² and 159 g/m² in the lower layer of soil cores and ingrowth cores, respectively. The annual fine-root production in a Scots pine stand in the 30 cm thick mineral soil layer, varied between 370–1630 g/m² in soil cores and between 210 – 490 g/m² in ingrowth cores during three years. The annual production calculated for Scots pine fine roots, varied between 330–950 g/m² in soil cores and between 110 – 610 g/m² in ingrowth cores. The horizontal and vertical variation in fine-root biomass was smaller in soil cores than in ingrowth cores. Roots in soil cores were in the natural dynamic state, while the roots in the ingrowth cores were still expanding both horizontally and vertically. The annual production of fine-root biomass in the Scots pine stand was less in root ingrowth cores than in soil cores. During the third year, the fine-root biomass production of Scots pine, when calculated by the ingrowth core method, was similar to that calculated by the soil core method. Both techniques have sources of error. In this research the sampling interval in the soil core method was 6–8 weeks, and thus root growth and death between sampling dates could not be accurately estimated. In the ingrowth core method, fine roots were still growing into the mesh bags. In Finnish conditions, after more than three growing seasons, roots in the ingrowth cores can be compared with those in the surrounding soil. The soil core method can be used for studying both the annual and seasonal biomass variations. For estimation of production, sampling should be done at short intervals. The ingrowth core method is more suitable for estimating the potential of annual fine-root production between different site types.     

UNDERGROUND SYSTEMS OF GAMBEL OAK (QUERCUS GAMBELII) IN CENTRAL UTAH

Excavation to a depth of 1 m of a 3 × 4 m portion of a clone of Quercos gambelii revealed the presence of a massive underground system of lignotubers, interconnecting rhizomes and roots. Lignotubers comprised the greatest proportion (72%) of the total below ground biomass (81 t/ha). Lignotubers are distinctive in appearance: they are an enlarged stemlike structure with numerous clusters of adventitious buds on the surface. Anatomically, they are comparable to the above ground stems with growth rings. Lignotubers are lobed and distorted, giving the appearance of a burl. Rhizomes are round to I-beam in shape with a star-shaped pith, distinct annual rings, bud traces, and branch gaps. There were also clusters of adventitious buds on rhizomes, although not as dense as those on the lignotubers. Roots are oval in cross section with discernible growth rings, no pith, and no bud traces.     

Rooting strategy of naturally regenerated beech in Silver birch and Scots pine woodlands

This study investigated the belowground development and strategy of late-successional European beech (Fagus sylvatica L.) in ageing natural Scots pine (Pinus sylvestris L.) and Silver birch (Betula pendula Roth.) woodlands in a French volcanic mid-elevation area. For this purpose root biomass, root profile and fine-root architecture of competitor trees were examined in 53 mixed pine–beech and 42 birch–beech woodlands along a stand maturation gradient, using the root auger technique (0–75-cm). The total beech fine-root biomass highly correlated with aerial dimensions such as stem height and girth, whereas it moderately correlated with its age, thus indicating the effects of competition. Basic stand biometric data such as stand density and basal area had no significant effect on beech root biomass. Conversely, competition indices taking into account the vertical dimensions of competitor trees were efficient, probably due to redundancy with beech height. At similar age and height, beeches under birch had a greater belowground development than beeches under pine. Each species exhibited specific rooting pattern and plasticity of fine-root architecture along the gradients of stand maturation and competition. Beech had a heart-shaped rooting habit in both mixings, which strongly increased along stand maturation. Its fine-root system adopted a foraging strategy to respond to increasing stand competition. The Scots pine fine-root system was plate-like and showed a low morphological plasticity, thus presumably a conservative strategy. Silver birch exhibited a high biomass and a foraging capacity in the topsoil but a loose root system in the subsoil. The coexistence of pine and beech roots in the upper soil presumably leads to a high belowground competition. Beech root system becomes predominant throughout the soil profile and it adopts an efficient foraging strategy, but at the expense of its belowground development. Conversely, the niche partitioning strategy between beech and birch may explain why beech develops strongly belowground in spite of the fact that birch has a dense rooting and a competitive fine-root architecture. As a consequence, beech mid-term regeneration and development may be facilitated under birch as compared with pine.     

Fine-root morphological and growth traits in a Turkey-oak stand in relation to seasonal changes in soil moisture in the Southern Apennines, Italy

We investigated the effects of seasonal changes in soil moisture on the morphological and growth traits of fine roots (<2?mm in diameter) in a mature Turkey-oak stand (Quercus cerris L.) in the Southern Apennines of Italy. Root samples (diameter:?<0.5, 0.5?C1.0, 1.0?C1.5, and 1.5?C2.0?mm) were collected with the Auger method. Mean annual fine-root mass and length on site was 443?g?m^?2 (oak fine roots 321?g?m^?2; other species 122?g?m^?2) and 3.18?km?m^?2 (oak fine roots 1.14?km?m^?2; other species 2.04?km?m^?2), respectively. Mean specific root length was 8.3?m?g^?1. All fine-root traits displayed a complex pattern that was significantly related to season. In the four diameter classes, both fine-root biomass and length peaked in summer when soil water content was the lowest and air temperature the highest of the season. Moreover, both fine-root biomass and length were inversely related with soil moisture (p?<?0.001). The finest roots (<0.5?mm in diameter) constituted an important fraction of total fine-root length (79?%), but only 21?% of biomass. Only in this root class, consequent to change in mean diameter, specific root length peaked when soil water content was lowest showing an inverse relationship (p?<?0.001). Furthermore, fine-root production and turnover decreased with increasing root diameter. These results suggest that changes in root length per unit mass, and pulses in root growth to exploit transient periods of low soil water content may enable trees to increase nutrient and water uptake under seasonal drought conditions.     

Carbon Allocation into Different Fine-Root Classes of Young Abies alba Trees Is Affected More by Phenology than by Simulated Browsing

Abies alba (European silver fir) was used to investigate possible effects of simulated browsing on C allocation belowground by ¹³CO₂ pulse-labelling at spring, summer or autumn, and by harvesting the trees at the same time point of the labelling or at a later season for biomass and for ¹³C-allocation into the fine-root system. Before budburst in spring, the leader shoots and 50% of all lateral shoots of half of the investigated 5-year old Abies alba saplings were clipped to simulate browsing. At harvest, different fine-root classes were separated, and starch as an important storage compartment was analysed for concentrations. The phenology had a strong effect on the allocation of the ¹³C-label from shoots to roots. In spring, shoots did not supply the fine-roots with high amounts of the ¹³C-label, because the fine-roots contained less than 1% of the applied ¹³C. In summer and autumn, however, shoots allocated relatively high amounts of the ¹³C-label to the fine roots. The incorporation of the ¹³C-label as structural C or as starch into the roots is strongly dependent on the root type and the root diameter. In newly formed fine roots, 3–5% of the applied ¹³C was incorporated, whereas 1–3% in the ≤0.5 mm root class and 1–1.5% in the >0.5–1.0 mm root class were recorded. Highest ¹³C-enrichment in the starch was recorded in the newly formed fine roots in autumn. The clipping treatment had a significant positive effect on the amount of allocated ¹³C-label to the fine roots after the spring labelling, with high relative ¹³C-contents observed in the ≤0.5 mm and the >0.5–1.0 mm fine-root classes of clipped trees. No effects of the clipping were observed after summer and autumn labelling in the ¹³C-allocation patterns. Overall, our data imply that the season of C assimilation and, thus, the phenology of trees is the main determinant of the C allocation from shoots to roots and is clearly more important than browsing.     

Temporal changes in spatial pattern of fine-root mass and nutrient concentrations in Indian bamboo savanna

Abstract. Temporal variations in the spatial distribution of fine-root mass and nutrient concentrations were studied in recently harvested and mature bamboo savanna sites in the dry tropical Vindhyan region in India. The soil block method and root-free-soil cages were used to investigate fine-root dynamics. The mean annual fine-root biomass was 596 and 690 g/m² in harvested and mature sites, respectively. The fine-root net production calculated by different methods ranged from 486 to 749 g m^-2 yr^-1 in the harvested site and 485 to 875 g m^-2 yr¹ in the mature site. All fine-root mass fractions decreased with increase in distance from the base of bamboo clumps, and the herb root mass showed the reverse trend. Bamboo fine roots were better developed in the 10 - 20 cm soil depth and those of herbs in the upper 10 cm. The ingrowth of fine roots in root-free-soil cages showed maximum biomass accumulation during the rainy season (64.2 - 69.9 g m^-2 mo^-1) and minimum in the summer (4.5 - 7.5 g m^-2 mo^-1). The fine-root nutrient concentrations were strongly related to their diameter. The fine-root nutrient concentrations varied considerably in different seasons. The highest nutrient concentrations in all categories were recorded in summer followed by winter and rainy seasons. Nutrient concentrations in live roots were always greater than those found in dead roots in different diameter classes. We suggest the occurrence of nutrient retranslocation from senescent roots to surviving roots in bamboo savanna. Fine roots in the bamboo savanna increased as a function of N-mineralization and nitrification rates. This tendency further increased after the harvest of bamboo, suggesting the crucial role of fine roots in the bamboo savanna after the harvesting of bamboo culms.     

Relative importance of Na+, Cl−, and abscisic acid in NaCl induced inhibition of root growth of rice seedlings

The relative importance of endogenous abscisic acid (ABA), as well as Na⁺ and Cl^– in NaCl-induced responses related to growth in roots of rice seedlings were investigated. The increase in ammonium, proline and H₂O₂ levels, and cell wall peroxidase (POD) activity has been shown to be related to NaCl-inhibited root growth of rice seedlings. Increasing concentrations of NaCl from 50 to 150 mM progressively decreased root growth and increased both Na⁺ and Cl^–. Treatment with NaCl in the presence of 4,4-diisothiocyano-2,2-disulfonic acid (DIDS, a nonpermeating amino-reactive disulfonic acid known to inhibit the uptake of Cl^–) had less Cl^– level in roots than that in the absence of DIDS, but did not affect the levels of Na⁺, and responses related to growth in roots. Treatment with 50 mM Na-gluconate (the anion of which is not permeable to membrane) had similar Na⁺ level in roots as that with 100 mM NaCl. It was found that treatment with 50 mM Na-gluconate effected growth reduction and growth-related responses in roots in the same way as 100 mM NaCl. All these results suggest that Cl^– is not required for NaCl-induced responses in root of rice seedlings. Endogenous ABA level showed no increase in roots of rice seedlings exposed to 150 mM NaCl. It is unlikely that ABA is associated with NaCl-inhibited root growth of rice seedlings.     

Fine-root mass, growth and nitrogen content for six tropical tree species

Although fine roots might account for 50% of the annual net primary productivity in moist tropical forests, there are relatively few studies of fine-root dynamics in this biome. We examined fine-root distributions, mass, growth and tissue N and C concentrations for six tree species established in 16-year-old plantations in the Caribbean lowlands of Costa Rica in a randomized-block design (n = 4). The study included five native species (Hyeronima alchorneoides, Pentaclethra macroloba, Virola koschnyi, Vochysia ferruginea and Vochysia guatemalensis) and one exotic (Pinus patula). Under all species >60% of the total fine-root mass to 1 m deep was located in the uppermost 15 cm of the soil. Fine-root live biomass and necromass (i.e., the mass of dead fine-roots) varied significantly among species but only within the uppermost 15 cm, with biomass values ranging from 182 g m⁻² in Pinus to 433 g m⁻² in Hyeronima plots, and necromass ranging from 48 g m⁻² in Pinus to 183 g m⁻² in Virola plots. Root growth, measured using ingrowth cores, differed significantly among species, ranging from 304 g m⁻² year⁻¹ in Pinus to 1,308 g m⁻² year⁻¹ in Hyeronima. These growth rates were one to five times those reported for moist temperate areas. Turnover rates of fine-root biomass ranged from 1.6 to 3.0 year⁻¹ in Virola and Hyeronima plots, respectively. Fine-root biomass was significantly and positively correlated with fine-root growth (r = 0.79, P < 0.0001), but did not correlate with fine-root turnover (r = 0.10, P = 0.20), suggesting that fine-root accumulation is a function of growth rate rather than mortality. Fine-root longevity was not correlated (r = 0.20, P = 0.34) and growth was negatively correlated with root N concentration across species (r = −0.78, P < 0.0001), contrary to reported trends for leaves, perhaps because N was relatively abundant at this site.     

Growth dynamics of superficial roots in Portuguese plantations ofEucalyptus globulus Labill. studied with a mesh bag technique

Summary The variation in growth of the fine roots of blue gum (Eucalyptus globulus labill. ssp.globulus) in the 0–40 cm soil layer was studied from March 1982 to March 1983 at Quinta do Furaduoro, Óbidos, Portugal. A mesh bag method was used; bags of nylon net were inserted into a clay soil and a sandy soil and filled with root-free soil. They were resampled after 2, 4, 6 and 12 months in both places and, in a separate series in the sandy soil every second month throughout the year.The ingrowth of roots was high during the winter months but there was also a surprisingly high ingrowth during the spring-early summer period. There was also some root growth during the driest part of the yearviz. July–September.The amount of fine roots reached a maximum of about 260 g dw m^–2 after about 6 months in the sandy soil, whereas it took at least 12 months to reach the somewhat higher level of 450 g dw m^–2 in the clay soil. At that level the decomposition of dead roots was expected to equal the formation of new roots. Dead roots appeared after only 2 months. There was a higher proportion of dead roots in the clay soil than in the sandy soil, 35% as compared with 20% on an average, which indicates a slower decomposition or a higher mortality at equal decomposition rates in the clay than and in the sandy soil. The present data gives an indication of a minimum fine root production in mature Eucalyptus stands of at least 600 g dw m^–2 yr^–1.     

江河源区高山嵩草(Kobresia pygmaea)草甸植物和土壤碳、氮储量对覆被变化的响应

以青海省果洛州藏族自治州甘德县青珍乡高山嵩草Kobresia pygmaea草甸轻度退化草地和重度退化草地为研究对象,通过植物地上部分主要功能群(禾草类、杂类草、莎草类)、植物根系和土壤碳、氮浓度及储量动态研究,结果表明:高寒小嵩草草甸轻度退化草地地上部分主要功能群碳、氮浓度和C ∶ N比值明显高于重度退化草地的浓度.同一草地类型主要功能群比较,碳、氮浓度依次为杂类草>禾草类>莎草类;植物地上部分的碳、氮浓度明显高于地下根系的碳、氮浓度.重度退化草地植物根系碳、氮浓度高于轻度退化草地植物根系碳、氮浓度.重度退化草地土壤总有机碳浓度显著低于轻度退化草地土壤总有机碳浓度,随着土层的加深碳、氮浓度有减少的趋势.江河源区高山嵩草草甸的土壤有机碳、氮储量最大,植物根系碳、氮储量居中,植物地上部分碳、氮储量最小.重度退化草地总有机碳储量(13554.3 g/m2)较轻度退化草地储量(14669.2 g/m2)下降7.60%.其中,0～40cm土壤层碳储量下降4.10%,植物根系碳储量下降59.97%,植物地上部分碳储量下降15.39%;重度退化草地总氮储量(3780.6 g/m2)较轻度退化草地储量(3352.7 g/m2)高12.76%,其中,0～40cm土壤中总氮储量高13.07%,植物根系全氮储量下降55.09%,植物地上部分全氮下降16.00%.由于草地退化损失有机碳11149 kg/hm2,而全氮增加4278 kg/hm2.     

Relationship between morphological and physiological responses to waterlogging and salinity in Sporobolus virginicus (L.) Kunth

The effects of waterlogging and salinity on morphological and physiological responses in the marsh grass Sporobolus virginicus (L.) Kunth were investigated in a 4×2 factorial experiment. Plants were subjected to four salinity levels (0, 100, 200 and 400 mol m^–3 NaCl) and two soil inundation conditions (drained and flooded) for 42 days. Flooding at 0 mol m^–3 NaCl caused initiation of adventitious surface roots, increased internal acration and plant height, induced alcohol dehydrogenase activity (ADH), and decreased belowground biomass and the number of culms per plant. Salinity increase from 0 to 400 mol m^–3 NaCl under drained conditions increased leaf and root proline concentrations and decreased photosynthesis, aboveground biomass, number of culms per plant and number of internodes per culm. Concurrent waterlogging and salinity induced ADH activity and adventitious surface roots but decreased plant height and aboveground biomass. Internal air space increased with waterlogging from 0 to 100 mol m^–3 NaCl but further increases in salinity to 400 mol m^–3 reduced air space. Combined waterlogging and salinity stresses, however, had no effect on photosynthesis or on the concentrations of proline in leaves or roots. These results are discussed in relation to the widespread colonization by S. virginicus of a wide range of coastal environments varying in soil salinity and in the frequency and intensity of waterlogging.     

Annual and seasonal changes in fine root biomass of a Quercus ilex L. forest

The biomass, production and mortality of fine roots (roots with diameter <2.5 mm) were studied in a typical Mediterranean holm oak (Quercus ilex L.) forest in NE Spain using the minirhizotron methodology. A total of 1212 roots were monitored between June of 1994 and March of 1997. Mean annual fine root biomass in the holm oak forest of Prades was 71±8 g m^–2 yr^–1. Mean annual production for the period analysed was 260+11 g m^–2 yr^–1. Mortality was similar to production, with a mean value of 253±3 g m^–2 yr^–1. Seasonal fine root biomass presented a cyclic behaviour, with higher values in autumn and winter and lower in spring and summer. Production was highest in winter, and mortality in spring. In summer, production and mortality values were the lowest for the year. Production values in autumn and spring were very similar. The vertical distribution of fine root biomass decreased with increasing depth except for the top 10–20 cm, where values were lower than immediately below. Production and mortality values were similar between 10 and 50 cm depth. In the 0–10 cm and the 50–60 cm depth intervals, both production and mortality were lower.     

The impact of zooplankton status on the management of Lake Kinneret (Israel)

Monthly averages of standing stock wet biomass of zooplankton in Lake Kinneret (Israel) varied between 11 and 76 g m^–2 during 1969–1981, with the exception of two months. Averaged contributions of different groups were: Cladocera 58%, Copepoda 35% and Rotifera 7%. Total standing crop wet biomass is highest during January–June, averages varied between 35 and 50 g m^–2, and decreases during summer–fall (23–36 g m^–2). The winter biomass of Cladocera fluctuated between 22 and 35 g m^–2 and dropped to a range of 9–23 g m^–2 in summer, whereas copepod biomass varied very little around an average of 18 g (ww) m^–2 with the exception of low values from April to June. The stock biomass of Rotifera is relatively high during winter floods season (December-March) whilst in summer it is very low.Young stages of fish in Lake Kinneret feed mostly on zooplankton and zoobenthic forms. The most abundant fish in the Kinneret ecosystem, Mirogrex terraesanctae terraesanctae, also feed on zooplankton at the adult stage throughout the year, and herbivorous fish consume zooplankton during the summer when lake plankton resources are limited.The summer ecosystem of Lake Kinneret is characterised as a steady state type, in which the impact of the zooplankton-chain is of great importance. Increase of predation pressure on zooplankton by fish can disequilibrate the balanced trophic relations existing between nannoplankton production and zooplankton grazing capacity. Such a situation can lead to organics accumulation as nannoplankton blooms, resulting in water quality deterioration. Management options aimed at preventing collapse of zooplankton populations are discussed.     

Root biomass changes after drainage and fertilization of a low-shrub pine bog

The stump and root systems of Scots pine (Pinus sylvestris) and field-layer vegetation were sampled before (1984) and three growing seasons after drainage and fertilization (1987) of a low-shrub pine bog. Average below-ground biomass of the field layer was 548 gDW m^–2 in 1984, with no significant treatment effects during experimentation. The stump-plus-root biomass of the pine stands was 1464 gDW m^–2 in the virgin state, and had increased to 1854 gDW m^–2 three years after the NPK-fertilizer treatment. The distribution over fractions also changed with this treatment. The fraction of fine roots ( < 1 mm) in stump-root biomass increased from 4% (56 gDW m^–2) to 11% (196 gDW m^–2), while the other compartments changed less. Total pine root length was 729 mm^–2 in 1984. Root length increased by 94% to 1380 mm^–2 on NPK-fertilized plots. Most of the fine pine roots were in the surface layer (0–10 cm), 79% in 1984 and 88% in 1987, and few pine roots were deeper than 20 cm. Maximum root length of fine pine roots ( < 1 mm) was estimated to be 2710 mm^–2 at about 800 gDW m^–2 (NPK treatment), and the corresponding maximum for small pine roots (=1–10 mm) was 227 mm^–2 at 809 gDW m^–2. Drainage stimulated net growth of fine roots, but this treatment also caused higher mortality rates of small roots. The fine roots responded to fertilization with higher net growth rate, and secondary growth of the large roots ( > 10 mm) was improved. The observed changes in root biomass and structure are explained as strategic adaptations to altered hydrological and nutritional circumstances in the root zone after drainage and fertilization.     

CO2 and N-fertilization effects on fine-root length, production, and mortality: a 4-year ponderosa pine study

We conducted a 4-year study of juvenile Pinus ponderosa fine root (≤2 mm) responses to atmospheric CO₂ and N-fertilization. Seedlings were grown in open-top chambers at three CO₂ levels (ambient, ambient+175 μmol/mol, ambient+350 μmol/mol) and three N-fertilization levels (0, 10, 20 g m⁻² year⁻¹). Length and width of individual roots were measured from minirhizotron video images bimonthly over 4 years starting when the seedlings were 1.5 years old. Neither CO₂ nor N-fertilization treatments affected the seasonal patterns of root production or mortality. Yearly values of fine-root length standing crop (m m⁻²), production (m m⁻² year⁻¹), and mortality (m m⁻² year⁻¹) were consistently higher in elevated CO₂ treatments throughout the study, except for mortality in the first year; however, the only statistically significant CO₂ effects were in the fine-root length standing crop (m m⁻²) in the second and third years, and production and mortality (m m⁻² year⁻¹) in the third year. Higher mortality (m m⁻² year⁻¹) in elevated CO₂ was due to greater standing crop rather than shorter life span, as fine roots lived longer in elevated CO₂. No significant N effects were noted for annual cumulative production, cumulative mortality, or mean standing crop. N availability did not significantly affect responses of fine-root standing crop, production, or mortality to elevated CO₂. Multi-year studies at all life stages of trees are important to characterize belowground responses to factors such as atmospheric CO₂ and N-fertilization. This study showed the potential for juvenile ponderosa pine to increase fine-root C pools and C fluxes through root mortality in response to elevated CO₂.     

Effects of fire,mowing and nitrogen addition on root characteristics in tall-grass prairie

Abstract. Root harvests and root windows were used to study the influence of fire, mowing and nitrogen additions on root lengths, biomass, and nitrogen content in tall-grass prairie. Four years of nitrogen additions (10 g m² yr^?1) increased below-ground mass by 15 % and nitrogen concentration in that mass by 77 %. In general, live roots and rhizomes exhibited greater increases in nitrogen concentrations than detrital roots and rhizomes. After four years of treatment, live roots and rhizomes immobilized an additional 1.5 to 5 g/m² of nitrogen, depending upon specific treatment, while dead roots and rhizomes immobilized an additional 3 to 3.5 g/m². Average root growth parameters, as measured with root windows, were positively correlated with above-ground peak foliage biomass; however, the only significant correlation was between average new root growth and above-ground peak foliage biomass (r = 0.73, p ≤ 0.04). Root growth and decay, as measured by annual mean values for eight root windows over a four year interval, were insensitive to climatic and treatment effects.     

Estimating seasonal and annual carbon inputs,and root decomposition rates in a temperate pasture following field 14C pulse-labelling

Using a ¹⁴C pulse-labelling technique, we studied the seasonal changes in assimilation and partitioning of photoassimilated C in the plant–root–soil components of a temperate pasture. Pasture and soil samples were taken after 4-h, and 35-day chase periods, to examine these seasonal ¹⁴C fluxes. Total C and ¹⁴C were determined in the shoot, root and soil system. The amounts of C translocated annually to roots and soil were also estimated from the seasonal ¹⁴C distribution and pasture growth. The in situ field decomposition of newly formed roots during different seasons, also using ¹⁴C-labelling, was studied for one year in undisturbed rhizosphere soil. The ¹⁴C-labelled roots were sampled five times and decomposition rates were calculated assuming first-order decomposition.Annual pasture production at the site was 16 020 kg DM ha^–1, and pasture growth varied with season being highest (75–79 kg ha^–1 d^–1) in spring and lowest (18–20 kg ha^–1 d^–1) in winter. The above- and below-ground partitioning of ¹⁴C also varied with the season. The respiratory ¹⁴C–CO₂ losses, calculated as the difference between the total amounts of ¹⁴C recovered in the soil-plant system at 4 h and 35 days, were high (66–70%) during the summer, autumn and winter season, and low (37–39%) during the spring and late-spring season. Pasture plants partitioned more C below-ground during spring compared with summer, autumn and winter seasons. Overall, at this high fertility dairy pasture site, 18 220 kg C/ha was respired, 6490 kg remained above-ground in the shoot, and 6820 kg was translocated to roots and 1320 kg to soil. Root decomposition rate constant (k) differed widely with the season and were the highest for the autumn roots. The half-life was highest (111 days) for autumn roots and lowest (64 days) for spring roots. About one-third of the root label measured in the spring season disappeared in the first 5 weeks after the initial 35 Day of allocation period. The late spring, summer, late summer and winter roots had intermediate half-lives (88–94 days). These results indicate that seasonal changes in root growth and decomposition should be accounted for to give a better quantification of root turnover.     

The population ecology of gammarus tigrinus (sexton) in the reed beds of the Tjeukemeer

The population ecology of Gammarus tigrinus (Sexton) was studied in the Tjeukemeer during 1969 and 1970. G. tigrinus reaches very high densities — up to 24,000/m² in parts of the study area. In 1970, the summer densities were 2–21/2 times greater than in 1969. Individuals do not grow to such large sizes in the summer as at other times of the year. Females begin to carry eggs in March or April and reproduction ceases in November. Large females have larger broods than smaller animals and the average size of the brood varies with the time of year. The egg incubation period and growth rate are dependent upon temperature. At summer temperatures females became sexually mature after about four weeks and the egg incubation period is about io days. The entire population is turned over about three times during the year. A combination of rapid growth rate, early onset of sexual maturity and high fecundity are probably responsible for the rapid spread of G. tigrinus throughout much of the Netherlands.     

Light and tree size influence belowground development in yellow birch and sugar maple

The effects of light and tree size on the root architecture and mycorrhiza of yellow birch (Betula alleghaniensis Britton) and sugar maple (Acer saccharum Marsh) growing in the understory of deciduous forests in southern Québec, Canada were studied. At the study site, small (<50 m²), medium (101–200 m²) and large (201–500 m²) canopy gaps were investigated. From within these gaps, 17 yellow birch and 23 sugar maple saplings from 40 to 600 cm in height were sampled. In both species, root biomass and morphological traits were strongly correlated with tree size, but only weakly with light availability. Increased root biomass was primarily allocated to coarse roots and secondarily to fine roots. Yellow birch roots were longer, had a larger area, more endings and branches and grew more rapidly than sugar maple roots. Mycorrhizal colonization increased with available light and declined with tree age in sugar maple and was positively associated with tree size in yellow birch. The study demonstrates that tree size is a very important determinant of how belowground systems acclimate to understory conditions.     

Nitrate deposition in northern hardwood forests and the nitrogen metabolism of Acer saccharum marsh

It is generally assumed that plant assimilation constitutes the major sink for anthropogenic Nitrate NO ₃ ^– deposited in temperate forests because plant growth is usually limited by nitrogen (N) availability. Nevertheless, plants are known to vary widely in their capacity for NO ₃ ^– uptake and assimilation, and few studies have directly measured these parameters for overstory trees. Using a combination of field and greenhouse experiments, we studied the N nutrition of Acer saccharum Marsh. in four northern hardwood forests receiving experimental NO ₃ ^– additions equivalent to 30 kg N ha^–1 year^–1. We measured leaf and fine-root nitrate reductase activity (NRA) of overstory trees using an in vivo assay and used ¹⁵N to determine the kinetic parameters of NO ₃ ^– uptake by excised fine roots. In two greenhouse experiments, we measured leaf and root NRA in A. saccharum seedlings fertilized with 0–3.5 g NO ₃ ^– –N m^–2 and determined the kinetic parameters of NO ₃ ^– and NH ₄ ⁺ uptake in excised roots of seedlings. In both overstory trees and seedlings, rates of leaf and fine root NRA were substantially lower than previously reported rates for most woody plants and showed no response to NO ₃ ^– fertilization (range = non-detectable to 33 nmol NO ₂ ^– g^–1 h^–1). Maximal rates of NO ₃ ^– uptake in overstory trees also were low, ranging from 0.2 to 1.0 mol g^–1 h^–1. In seedlings, the mean V _max for NO ₃ ^– uptake in fine roots (1 mol g^–1 h^–1) was approximately 30 times lower than the V _max for NH ₄ ⁺ uptake (33 mol g^–1 h^–1). Our results suggest that A. saccharum satisfies its N demand through rapid NH ₄ ⁺ uptake and may have a limited capacity to serve as a direct sink for atmospheric additions of NO ₃ ^– .