Nutrient Cycling in a Eucalyptus obliqua (L'hérit.) Forest. III. Growth, Biomass, and Net Primary Production

1979 ◽  
Vol 27 (4) ◽  
pp. 439 ◽  
Author(s):  
PM Attiwill

The biomass of Eucalyptus obliqua forest in south-eastern Australia was estimated over a 22-year period by using allometric relationships in which tree diameter was the independent variable. Biomass increased from 24 kg m-2 at a stand age of 44 years to 37 kg m-2 at 66 years. Maximum net primary production (NPP) was 1.4 kg m-2 year-1. Biomass accumulation ratios (biomass/NPP) follow a trajectory with age which fits closely R. H. Whittaker's work in temperate forests of the United States. It is proposed that the growth of forests is regulated within three definable and sequential stages: (i) growth of the photosynthetic display and of the metabolic transport system, (ii)development of heartwood as a support structure system, and (iii) maintenance of the ecosystem through the production of litter. Essential to this view is the recognition of heartwood formation as a growth-regulating process rather than as the end-result of an ageing process.

1990 ◽  
Vol 20 (10) ◽  
pp. 1602-1610 ◽  
Author(s):  
P. A. Harcombe ◽  
Mark E. Harmon ◽  
Sarah E. Greene

Using periodic remeasurements of tagged trees in nine 0.4-ha sample plots in a Piceasitchensis (Bong.) Carr. – Tsugaheterophylla (Raf.) Sarg. forest at Cascade Hand Experimental Forest, Oregon, we calculated that biomass of bolewood increased from 570 Mg•ha−1 at age 85 years to 760 Mg•ha−1 at age 138 years. Net primary production of bolewood declined from 11 to about 6 Mg•ha−1•year−1, and mortality loss increased from 2 to about 6 Mg•ha−1•year−1. Values for 37-year-old plots in the same area were 210–360 Mg•ha−1•year−1 bole biomass, 7–20 Mg•ha−1•year−1 bolewood production, and 0–2 Mg•ha−1•year−1 mortality loss. Indications are that bolewood production and biomass were lower in the older plots when they were 37 years old. In the older plots, biomass did not increase between ages 120 and 138. Of the photosynthate potentially available for bolewood production, some replaces biomass lost via mortality and some is allocated to maintenance (respiration plus allocation to fine roots). We estimate that one-quarter to one-half of the production is lost by mortality, and that mortality loss may thus be an important factor limiting forest biomass accumulation.


2019 ◽  
Vol 39 (8) ◽  
pp. 1473-1483 ◽  
Author(s):  
A Collalti ◽  
I C Prentice

Abstract Gross primary production (GPP) is partitioned to autotrophic respiration (Ra) and net primary production (NPP), the latter being used to build plant tissues and synthesize non-structural and secondary compounds. Waring et al. (1998; Net primary production of forests: a constant fraction of gross primary production? Tree Physiol 18:129–134) suggested that a NPP:GPP ratio of 0.47 ± 0.04 (SD) is universal across biomes, tree species and stand ages. Representing NPP in models as a fixed fraction of GPP, they argued, would be both simpler and more accurate than trying to simulate Ra mechanistically. This paper reviews progress in understanding the NPP:GPP ratio in forests during the 20 years since the Waring et al. paper. Research has confirmed the existence of pervasive acclimation mechanisms that tend to stabilize the NPP:GPP ratio and indicates that Ra should not be modelled independently of GPP. Nonetheless, studies indicate that the value of this ratio is influenced by environmental factors, stand age and management. The average NPP:GPP ratio in over 200 studies, representing different biomes, species and forest stand ages, was found to be 0.46, consistent with the central value that Waring et al. proposed but with a much larger standard deviation (±0.12) and a total range (0.22–0.79) that is too large to be disregarded.


2002 ◽  
Vol 32 (1) ◽  
pp. 161-169 ◽  
Author(s):  
Zhong Li ◽  
Michael J Apps ◽  
E Banfield ◽  
Werner A Kurz

The Carbon Budget Model of the Canadian Forest Sector (CBM-CFS2) is a forest inventory-based ecosystem simulation model. It has been used previously for both retrospective and projective analyses of the carbon pools and fluxes of the Canadian forest ecosystems at the national, regional, and stand level. The objective of this study was to determine and evaluate forest net primary production (NPP) in the three Prairie Provinces in west-central Canada, as estimated by the model. The model simulated an averaged aboveground NPP (NPPA) of 172 g C·m–2·year–1 for the regional forests, varying from 72 to 293 g C·m–2·year–1, depending on ecoclimatic province, forest type, age, and site productivity. Comparisons of NPPA estimates for the boreal forest (165–179 g C·m–2·year–1) with results from direct measurements, modeling, and empirical calculations show that the CBM-CFS2 produced reasonable estimates of NPPA. The model incorporates different types of disturbances such as wildfire, harvesting, and insects and is able to evaluate NPP changes with stand age. However, belowground NPP may be overestimated, especially for young and unproductive stands. This can be explained by the current parameter estimates for the fine-root component of belowground biomass and for fine-root turnover rates.


2021 ◽  
Author(s):  
Yunke Peng ◽  
Colin Prentice ◽  
Keith Bloomfield ◽  
Matteo Campioli ◽  
Zhiwen Guo ◽  
...  

<p>Plants not only acquire carbon to sustain biomass production, autotrophic respiration, and the production of non-structural compounds, but also require nitrogen to support carboxylation and growth. However, available observations have not fully been integrated and used for modelling growth, carbon allocation to different compartments, and how different compartments’ nitrogen-to-carbon ratio vary across large climatic and soil gradients. This leaves substantial uncertainty in estimates of the global distribution of growth and nitrogen uptake by plants.</p><p> </p><p>Here, we used the P-model, a first principles-derived and remote sensing-driven model for terrestrial gross primary production (GPP) to simulate the global distribution of GPP. Using comprehensive datasets with locally measured covariates for climatic and edaphic conditions and vegetation structure, we modelled the fractional allocation of GPP to biomass production (BP), aboveground net primary production (ANPP), and leaf NPP based on linear mixed-effects regression models. We defined BP as the sum of NPP in leaves, wood and roots. It thus does not include additional components such as exudates and labile carbon to mycorrhizae. Leaf nitrogen-to-carbon was modelled based on the maximum rate of carboxylation at 25 degrees Celsius (V<sub>cmax25</sub>) and leaf mass per area (LMA). We then used global gridded data for the covariates that entered as predictors in site-level empirical models to simulate global C and N allocated to each component. We finally validated our global simulation results with an extended set of globally distributed GPP, BP and nitrogen-to-carbon ratio observations.</p><p> </p><p>GPP was well predicted (R<sup>2</sup> = 0.61). In forests, ratios of BP/GPP and ANPP/GPP decreased with soil C/N and stand-age but increased with humidity and with the fraction of absorbed photosynthetically active radiation (fAPAR). The ratio of leaf NPP to ANPP, increased with light availability and growth temperature, but decreased with vapor pressure deficit. Leaf nitrogen-to-carbon ratio was positively related to the ratio of V<sub>cmax25</sub> to LMA. Leaf nitrogen resorption efficiency (NRE) was increased in drier and colder environments. Through our data validation at the end, we have shown a prediction for NPP (R<sup>2</sup> = 0.26), ANPP (R<sup>2</sup> = 0.28), leaf NPP (R<sup>2</sup> = 0.39), NRE (R<sup>2</sup> = 0.30), leaf N/C (R<sup>2</sup> = 0.26) and leaf N flux (R<sup>2</sup> = 0.35).</p><p> </p><p>Simulated global total GPP is 125 Pg C yr<sup>-1</sup>. Based on these statistical models, global mean carbon-use-efficiency (BP/GPP) was estimated to be 40%. The ratio of ANPP/BP was 72%, and ANPP was further split with 46% to leaf NPP and 54% to wood NPP. Simulated global total nitrogen acquisition (total of uptake from the soil and symbiotic N fixation) was 860 Tg N yr<sup>-1</sup>. Growth in the leaf, wood and root compartment accounted for 39%, 23% and 38% of global N acquisition, respectively. We suggest that plant adaptations result in higher ANPP, leaf NPP and finally leaf N flux under warmer, wetter, more abundant light and N-rich soil conditions, which aims to support higher rate of photosynthesis with greater nitrogen investment in the leaf.</p>


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
A. Collalti ◽  
A. Ibrom ◽  
A. Stockmarr ◽  
A. Cescatti ◽  
R. Alkama ◽  
...  

Abstract Forest production efficiency (FPE) metric describes how efficiently the assimilated carbon is partitioned into plants organs (biomass production, BP) or—more generally—for the production of organic matter (net primary production, NPP). We present a global analysis of the relationship of FPE to stand-age and climate, based on a large compilation of data on gross primary production and either BP or NPP. FPE is important for both forest production and atmospheric carbon dioxide uptake. We find that FPE increases with absolute latitude, precipitation and (all else equal) with temperature. Earlier findings—FPE declining with age—are also supported by this analysis. However, the temperature effect is opposite to what would be expected based on the short-term physiological response of respiration rates to temperature, implying a top-down regulation of carbon loss, perhaps reflecting the higher carbon costs of nutrient acquisition in colder climates. Current ecosystem models do not reproduce this phenomenon. They consistently predict lower FPE in warmer climates, and are therefore likely to overestimate carbon losses in a warming climate.


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