Fine root production, mortality, and turnover in response to simulated nitrogen deposition in the subtropical Abies georgei (Orr) forest.

Increased nitrogen deposition has important effects on below-ground ecological processes. Fine roots are the most active part of the root system in terms of physiological activity and the main organs for nutrient and water uptake by plants. However, there is still a limited understanding of how nitrogen deposition affects the fine root dynamics in subtropical Abies georgei (Orr) forests. Consequently, a three-year field experiment was conducted to quantify the effects of three forms of nitrogen sources ((NH4)2SO4, NaNO3, and NH4NO3) at four levels (0, 5, 15, and 30 kg N·ha-1·yr-1) on the fine root dynamics in Abies georgei forests using a randomized block-group experimental design and minirhizotron technique. The first year of nitrogen addition did not affect the first-class fine roots (FR1, 0 < diameter < 0.5 mm) and second-class fine roots (FR2, 0.5 < diameter < 1.0 mm). The next two years of nitrogen addition significantly increased the production, mortality, and turnover of FR1 and FR2; the three year of nitrogen addition did not affect the dynamics of the third- class fine roots (FR3, 1.0 < diameter < 1.5 mm) and fourth- class fine roots (FR4,1.5 < diameter < 2.0 mm). Nitrogen addition positively affected the dynamics of FR1, FR2, FR3 and FR4 by positively affecting the carbon, nitrogen, and phosphorus contents of fine roots and indirectly affecting the soil pH. Increased carbon allocation to FR1 and FR2 may represent a phosphorus acquisition strategy when nitrogen is not the limiting factor. The nitrogen addition forms and levels affected the fine root dynamics in the following orde: NH4NO3 > (NH4)2SO4 > NaNO3 and high nitrogen > medium nitrogen > low nitrogen. The results suggest that the different-diameter fine root dynamics respond differently to different nitrogen addition forms and levels, and linking the different-diameter fine roots to nitrogen deposition is crucial.

[Nutrient accumulation and cycling in pure and mixed plantations of Azadirachta indica and Acacia auriculiformis in a dry-hot valley, Yunnan Province, southwest China].

To ease the implementation of effective nutrient management for plantations with different vegetation restoration patterns and to assist in the selection of appropriate species and forestation patterns, nutrient (N, P, K, Ca and Mg) accumulation and cycling were investigated and compared in three plantations (10-year-old Azadirachta indica, Acacia auriculiformis and mixed A. indica--A. auriculiformis plantations) in Yuanmou Valley, a dry-hot valley of Yunnan Province, Southwestern China. The result showed that total nutrient accumulations were 333.05, 725.61 and 533.85 kg x hm(-2) in pure plantations of A. indica and A. auriculiformis, and in A. indica--A. auriculiformis mixed plantation, respectively. The nutrient accumulation of various organs was ranked as branches > stems > roots > leaves > bark in the A. indica plantation and branches > stems > leaves > roots > bark both in the A. auriculiformis plantation and in the mixed plantation. Changes in accumulation of various nutrients in the mixed plantation were similar to that in the A. auriculiformis plantation (Ca > N > K > Mg > P), which were different from the A. indica plantation (Ca > K > N > Mg > P). Annual net nutrient accumulation, return and absorption in these plantations ranged from 62.72 to 162.19 kg x hm(-2) x a(-1), 48.82 to 88.86 kg x hm-2 a-1 and 111.54 to 251.05 kg x hm(-2) x a(-1), respectively, which were all the highest in the A. auriculiformis planta- tion, followed by the mixed plantation, and were the lowest in the A. indica plantation. The nutrient utilization coefficient, the cycling coefficient and the recycling period were estimated to be from 0.34 to 0.39, 0.35 to 0.44, and 6.54 to 8.17 a, respectively. The lower nutrient return and circulation rate of N or P in the A. indica plantation showed that this plantation had a poor ability to maintain soil fertility, while the highest nutrient circulation rate of N or P was observed in the A. auriculiformis plantation that displayed the advantage in maintaining soil nutrients and stand productivity. The nutrient return and nutrient absorption in the mixed plantation were 167.2% and 186.2%, of those in the A. indica plantation, and the circulation rate of N, P and K were higher than those in the A. indica plantation, while the recycling period of Ca in mixed plantation was 50% shorter than that in A. auriculiformis plantation. Soil fertility and nutrient supply were improved in the A. indica and A. auriculiformis mixed plantation.

Genetic characterization and fine mapping of a yellow-seeded gene in Dahuang (a Brassica rapa landrace).

The development of yellow-seeded cultivars in Brassica rapa (B. rapa) would improve the quality and quantity of available oil. The identification and mapping of the seed coat color gene may aid in the development of yellow-seeded cultivars and facilitate introgression of the yellow-seeded gene into desirable Brassica napus (B. napus) lines through marker-assisted selection. In the current study, we investigated the inheritance of a yellow-seeded landrace in B. rapa, "Dahuang", originating from the Qinghai-Tibetan plateau. Genetic analysis revealed that the phenotype of the yellow-seeded trait in Dahuang is controlled by one recessive gene, termed Brsc1. Mapping of the Brsc1 gene was subsequently conducted in a BC(1) population comprised 456 individuals, derived from (Dahuang × 09A-126) × Dahuang. From a survey of 256 amplified fragment length polymorphism (AFLP) primer combinations, 10 tightly linked AFLP markers were obtained. The closest AFLP markers flanking Brsc1, Y10 and Y06, were 0.2 and 0.4 cM away, respectively. Subsequently, using simple sequence repeat (SSR) markers in the reference map, the Brsc1 gene was mapped on A09 in B. rapa. Blast analysis revealed that seven AFLP markers showed sequence homology to A09 of B. rapa, wherein six AFLP markers in our map were in the same order as those in A09 of B. rapa. The two closest markers, Y10 and Y06, delimited the Brsc1 gene within a 2.8 Mb interval. Furthermore, Y05 and Y06, the two closest AFLP markers on one side linked to Brsc1, were located in scaffold000059 on A09 of B. rapa, whereas the closet AFLP marker on the opposite side of Brsc1, Y10, was located in scaffold000081 on A09 of B. rapa. Molecular markers developed from these studies may facilitate marker-assisted selection (MAS) of yellow-seeded lines in B. rapa and B. napus and expedite the process of map-based cloning of Brsc1.