Fine-Root Biomass Distribution and Production Along a Barrier Island Chronosequence

1996 ◽  
Vol 135 (2) ◽  
pp. 205 ◽  
Author(s):  
Mark J. Stevenson ◽  
Frank P. Day
2018 ◽  
Vol 38 (11) ◽  
Author(s):  
吕渡 LÜ Du ◽  
杨亚辉 YANG Yahui ◽  
赵文慧 ZHAO Wenhui ◽  
雷斯越 LEI Siyue ◽  
张晓萍 ZHANG Xiaoping

2005 ◽  
Vol 35 (7) ◽  
pp. 1617-1625 ◽  
Author(s):  
A Claus ◽  
E George

Fine-root (<2 mm) biomass and biomass distribution were determined in different age-classes of three European forest chronosequences dominated by Fagus sylvatica L., Picea abies (L.) Karst., and Quercus cerris L., respectively. Root samples were taken with the auger method. There was a clear effect of stand age on standing fine-root biomass, with the highest fine-root biomass in adult but not mature stands. The vertical fine-root biomass distribution showed, at all sites, high densities of roots in the top soil layers and with depth a gradual decrease of fine-root biomass density. The difference in total fine-root biomass between the different age-classes appeared to be due to differences in the top soil layers. Fine-root biomass in the lower soil layers was less variable along the life cycle of the forests. Only in very young stands, specific root length of fine roots was higher than in the other age-classes. The present data together with other published values suggest that fine-root biomass in tree stands develops in three phases: rapid increase after a clear-cut harvest up to a maximum of fine-root biomass; a decrease during maturation of the stand; and a steady-state in mature stands.


2013 ◽  
Vol 36 (7) ◽  
pp. 645-654 ◽  
Author(s):  
Yun-Ke LIU ◽  
Chuan FAN ◽  
Xian-Wei LI ◽  
Yin-Hua LING ◽  
Yi-Gui ZHOU ◽  
...  

2021 ◽  
Vol 130 ◽  
pp. 108031
Author(s):  
Wen Li ◽  
Yifei Shi ◽  
Dandan Zhu ◽  
Wenqian Wang ◽  
Haowei Liu ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Tina Unuk Nahberger ◽  
Gian Maria Niccolò Benucci ◽  
Hojka Kraigher ◽  
Tine Grebenc

AbstractSpecies of the genus Tuber have gained a lot of attention in recent decades due to their aromatic hypogenous fruitbodies, which can bring high prices on the market. The tendency in truffle production is to infect oak, hazel, beech, etc. in greenhouse conditions. We aimed to show whether silver fir (Abies alba Mill.) can be an appropriate host partner for commercial mycorrhization with truffles, and how earthworms in the inoculation substrate would affect the mycorrhization dynamics. Silver fir seedlings inoculated with Tuber. aestivum were analyzed for root system parameters and mycorrhization, how earthworms affect the bare root system, and if mycorrhization parameters change when earthworms are added to the inoculation substrate. Seedlings were analyzed 6 and 12 months after spore inoculation. Mycorrhization with or without earthworms revealed contrasting effects on fine root biomass and morphology of silver fir seedlings. Only a few of the assessed fine root parameters showed statistically significant response, namely higher fine root biomass and fine root tip density in inoculated seedlings without earthworms 6 months after inoculation, lower fine root tip density when earthworms were added, the specific root tip density increased in inoculated seedlings without earthworms 12 months after inoculation, and general negative effect of earthworm on branching density. Silver fir was confirmed as a suitable host partner for commercial mycorrhization with truffles, with 6% and 35% mycorrhization 6 months after inoculation and between 36% and 55% mycorrhization 12 months after inoculation. The effect of earthworms on mycorrhization of silver fir with Tuber aestivum was positive only after 6 months of mycorrhization, while this effect disappeared and turned insignificantly negative after 12 months due to the secondary effect of grazing on ectomycorrhizal root tips.


Forests ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 823
Author(s):  
Anna Zielonka ◽  
Marek Drewnik ◽  
Łukasz Musielok ◽  
Marcin K. Dyderski ◽  
Dariusz Struzik ◽  
...  

Forest ecosystems significantly contribute to the global organic carbon (OC) pool, exhibiting high spatial heterogeneity in this respect. Some of the components of the OC pool in a forest (woody aboveground biomass (wAGB), coarse root biomass (CRB)) can be relatively easily estimated using readily available data from land observation and forest inventories, while some of the components of the OC pool are very difficult to determine (fine root biomass (FRB) and soil organic matter (SOM) stock). The main objectives of our study were to: (1) estimate the SOM stock; (2) estimate FRB; and (3) assess the relationship between both biotic (wAGB, forest age, foliage, stand density) and abiotic factors (climatic conditions, relief, soil properties) and SOM stocks and FRB in temperate forests in the Western Carpathians consisting of European beech, Norway spruce, and silver fir (32 forest inventory plots in total). We uncovered the highest wAGB in beech forests and highest SOM stocks under beech forest. FRB was the highest under fir forest. We noted a considerable impact of stand density on SOM stocks, particularly in beech and spruce forests. FRB content was mostly impacted by stand density only in beech forests without any discernible effects on other forest characteristics. We discovered significant impacts of relief-dependent factors and SOM stocks at all the studied sites. Our biomass and carbon models informed by more detailed environmental data led to reduce the uncertainty in over- and underestimation in Cambisols under beech, spruce, and fir forests for mountain temperate forest carbon pools.


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