Early effect of elevated nitrogen input on above-ground net primary production of a lower montane rain forest, Panama

2009 ◽  
Vol 25 (6) ◽  
pp. 637-647 ◽  
Author(s):  
Markus Adamek ◽  
Marife D. Corre ◽  
Dirk Hölscher

Abstract:To evaluate N limitation on above-ground net primary production in a tropical lower montane rain forest, an N fertilization experiment was conducted for 2 y. The study site is located at 1200–1300 m asl in the Fortuna forest reserve in western Panama and has a mature, mixed-species stand growing on an Andisol soil. Control and N-fertilized (125 kg urea-N ha−1 y−1) treatments were represented by four replicate plots (each 40 × 40 m, separated by at least 40 m). Stem diameter growth was analysed by diameter at breast height classes and also for the three most abundant species. The three species did not respond to N addition. The response of stem growth and above-ground woody biomass production to N fertilization varied among dbh classes. Stem growth of trees of 10–30 cm dbh increased only in the first year of N addition while trees of 30–50 cm dbh responded in the second year of N addition, which may be due to differences in light conditions between years. Trees >50 cm dbh did not respond during 2 years of N addition. As a result, the overall stem growth and above-ground woody biomass production were not affected by N fertilization. Annual total fine litterfall increased in the first year of N fertilization, while annual leaf litterfall increased in both years of N addition. Above-ground net primary production, of which total fine litterfall constituted 68%, also increased only in the first year of N addition. The magnitude and timing of response of stem diameter growth and litterfall suggest that these aspects of above-ground productivity are not uniformly limited by N availability.

2010 ◽  
Vol 27 (1) ◽  
pp. 73-81 ◽  
Author(s):  
Markus Adamek ◽  
Marife D. Corre ◽  
Dirk Hölscher

Abstract:Nitrogen (N) availability is a major control on fine-root growth and distribution with depth in forest soils. We investigated fine-root dynamics in response to N addition in a montane rain forest with N-limited above-ground production. Control and N-fertilized (125 kg urea-N ha−1 y−1) treatments were laid out in a paired-plot design with four replicates (each 40 × 40 m). During 1.5 y of treatment, fine root-biomass, necromass and production were assessed by sequential coring at three soil depths (organic layer, 0–10 cm and 10–20 cm mineral soil), whereas fine-root redistribution with depth was assessed by ingrowth cores. Total fine-root biomass, necromass and production in the controls were 458 ± 21 g m−2, 101 ± 9 g m−2 and 324 ± 33 g m−2 y−1, respectively. No significant difference at any depth was detected under N fertilization. Fine-root biomass in the organic layer decreased over time under N addition. At 10–20 cm in the mineral soil, fine-root biomass in ingrowth cores increased significantly after 1.5 y of N fertilization compared with the control. The increased available N may have induced the change in fine-root distribution to explore the deeper mineral soil for other nutrients which may cause additional limitation to above-ground production once N limitation is alleviated.


2014 ◽  
Vol 11 (23) ◽  
pp. 6855-6869 ◽  
Author(s):  
S. Rambal ◽  
M. Lempereur ◽  
J. M. Limousin ◽  
N. K. Martin-StPaul ◽  
J. M. Ourcival ◽  
...  

Abstract. The partitioning of photosynthates toward biomass compartments plays a crucial role in the carbon (C) sink function of forests. Few studies have examined how carbon is allocated toward plant compartments in drought-prone forests. We analyzed the fate of gross primary production (GPP) in relation to yearly water deficit in an old evergreen Mediterranean Quercus ilex coppice severely affected by water limitations. Carbon fluxes between the ecosystem and the atmosphere were measured with an eddy covariance flux tower running continuously since 2001. Discrete measurements of litterfall, stem growth and fAPAR allowed us to derive annual productions of leaves, wood, flowers and acorns, and an isometric relationship between stem and belowground biomass has been used to estimate perennial belowground growth. By combining eddy covariance fluxes with annual net primary productions (NPP), we managed to close a C budget and derive values of autotrophic, heterotrophic respirations and carbon-use efficiency (CUE; the ratio between NPP and GPP). Average values of yearly net ecosystem production (NEP), GPP and Reco were 282, 1259 and 977 g C m−2. The corresponding aboveground net primary production (ANPP) components were 142.5, 26.4 and 69.6 g C m−2 for leaves, reproductive effort (flowers and fruits) and stems, respectively. NEP, GPP and Reco were affected by annual water deficit. Partitioning to the different plant compartments was also impacted by drought, with a hierarchy of responses going from the most affected – the stem growth – to the least affected – the leaf production. The average CUE was 0.40, which is well in the range for Mediterranean-type forest ecosystems. CUE tended to decrease less drastically in response to drought than GPP and NPP did, probably due to drought acclimation of autotrophic respiration. Overall, our results provide a baseline for modeling the inter-annual variations of carbon fluxes and allocation in this widespread Mediterranean ecosystem, and they highlight the value of maintaining continuous experimental measurements over the long term.


2020 ◽  
Author(s):  
Raphael Manu ◽  
Marife D. Corre ◽  
Edzo Veldkamp ◽  
Oliver van Straaten

<p>Nutrient availability in tropical forest ecosystems plays a critical role in sustaining forest growth and productivity. Observational evidence for nutrient limitations on net primary productivity (NPP) in the tropics is rare yet crucial for predicting the impacts of human-induced changes on tropical forests, particularly for underrepresented tropical regions in Africa. In an ecosystem-scale nutrient manipulation experiment, we assessed the response of different components of above-ground net primary production (ANPP) to nutrient addition of nitrogen (N), phosphorus (P), potassium (K) and all possible combinations (NP, NK, PK, and NPK) at rates of 125 kg N ha<sup>-1</sup>yr<sup>-1</sup>, 50 kg P ha<sup>-1</sup> yr<sup>-1</sup> and 50 kg K ha<sup>-1</sup>yr<sup>-1</sup>.</p><p>We established 32 (8 treatments × 4 replicates) experimental plots of 40 × 40 m<sup>2</sup> each and measured stem growth of over 15,000 trees with diameter at breast height (dbh) ≥ 1 cm as well as litter production and above-ground woody biomass production (AWBP), of a lower-montane tropical forest (1100 m a.s.l.) in northwestern Uganda.</p><p>After 18 months of nutrient addition, we found that different aspects of ANPP, including litter production and AWBP are controlled by multiple soil nutrients. Specifically, we measured higher total fine-litter production in the N (13.6 ± 1.4 Mg ha<sup>-1 </sup>yr<sup>-1</sup>) and K (13.3 ± 1.8 Mg ha<sup>-1 </sup>yr<sup>-1</sup>) addition plots than the control (11.1 ± 0.6 Mg ha<sup>-1 </sup>yr<sup>-1</sup>) plots. Both reproductive litter (flowers and fruits; 10% of total fine-litter fall) and leaf litter (62% of total fine-litter fall) significantly increased with K addition. In general, fine-litter production in our plots is higher than what has been reported so far for lower-montane tropical forests. Increased AWBP is associated with N addition plots. The response of trees to nutrient addition however, varied with tree sizes. Trees with dbh between 10 – 30 cm increased significantly in AWBP under PK addition. There was no effect of nutrient addition associated with either smaller (1 – 10 cm dbh) or larger trees (dbh > 30 cm). The medium-sized trees which may have experienced resource competition but have now transitioned into the canopy layer (exposed to sunlight) are able to use additional nutrient for active growth. In contrast, bigger trees may allocate extra nutrient for reproduction and leaf-vitality, while smaller trees remain shaded, co-limited by sunlight and therefore unable to utilize increased available nutrients for stem diameter growth. ANPP increased by 39% with N addition and marginally by 23% with K additions relative to the control. In conclusion, our experiment provides evidence of N and potentially K limitation of ANPP in this lower-montane tropical forest, and highlights that, in a highly diverse ecosystem different components of ANPP may be regulated by multiple nutrients. </p>


2011 ◽  
Vol 91 (4) ◽  
pp. 689-696 ◽  
Author(s):  
A. Pantel ◽  
J. T. Romo ◽  
Y. Bai

Pantel, A., Romo, J. T. and Bai, Y. 2011. Above-ground net primary production of plains rough fescue [ Festuca hallii (Vasey) Piper] after a single defoliation on five landform elements. Can. J. Plant Sci. 91: 689–696. Above-ground net primary production (ANPP) was determined for plains rough fescue [Festuca hallii (Vasey) Piper] following a single defoliation to 7.5 cm stubble height on five landform elements in the Northern Mixed Prairie. The landform elements included north aspect-concave slopes, north aspect-convex slopes, south aspect-concave slopes, south aspect-convex slopes, and level uplands. Above-ground net primary production was determined for 2 yr after defoliating plants in May through November. Above-ground net primary production after defoliation was not dependent on landform elements in the first (P=0.23) and second years (P=0.22) after defoliation. In the first year after June through September defoliation, ANPP was reduced 29 to 41% (P <0.01), whereas May, October, or November defoliation had no significant effect on ANPP. Above-ground net primary production did not vary significantly (P=0.61) among months of defoliation in the second year after defoliation. Less ANPP in the first year after June through September defoliation indicates the need for ≥1 yr of deferred use to allow plants to regain their production potential. Unaffected ANPP after May, October, or November defoliation suggests plains rough fescue can be grazed annually. Recuperation of ANPP after defoliation depends on the month of the year in which plains rough fescue is defoliated, but not on landform elements in the Northern Mixed Prairie.


Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2617
Author(s):  
Alicja Szatanik-Kloc ◽  
Justyna Szerement ◽  
Agnieszka Adamczuk ◽  
Grzegorz Józefaciuk

Thousands of tons of zeolitic materials are used yearly as soil conditioners and components of slow-release fertilizers. A positive influence of application of zeolites on plant growth has been frequently observed. Because zeolites have extremely large cation exchange capacity, surface area, porosity and water holding capacity, a paradigm has aroused that increasing plant growth is caused by a long-lasting improvement of soil physicochemical properties by zeolites. In the first year of our field experiment performed on a poor soil with zeolite rates from 1 to 8 t/ha and N fertilization, an increase in spring wheat yield was observed. Any effect on soil cation exchange capacity (CEC), surface area (S), pH-dependent surface charge (Qv), mesoporosity, water holding capacity and plant available water (PAW) was noted. This positive effect of zeolite on plants could be due to extra nutrients supplied by the mineral (primarily potassium—1 ton of the studied zeolite contained around 15 kg of exchangeable potassium). In the second year of the experiment (NPK treatment on previously zeolitized soil), the zeolite presence did not impact plant yield. No long-term effect of the zeolite on plants was observed in the third year after soil zeolitization, when, as in the first year, only N fertilization was applied. That there were no significant changes in the above-mentioned physicochemical properties of the field soil after the addition of zeolite was most likely due to high dilution of the mineral in the soil (8 t/ha zeolite is only ~0.35% of the soil mass in the root zone). To determine how much zeolite is needed to improve soil physicochemical properties, much higher zeolite rates than those applied in the field were studied in the laboratory. The latter studies showed that CEC and S increased proportionally to the zeolite percentage in the soil. The Qv of the zeolite was lower than that of the soil, so a decrease in soil variable charge was observed due to zeolite addition. Surprisingly, a slight increase in PAW, even at the largest zeolite dose (from 9.5% for the control soil to 13% for a mixture of 40 g zeolite and 100 g soil), was observed. It resulted from small alterations of the soil macrostructure: although the input of small zeolite pores was seen in pore size distributions, the larger pores responsible for the storage of PAW were almost not affected by the zeolite addition.


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