Ran Liu

Dr. Ran Liu


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2019 in Colloids and Surfaces B: Biointerfaces
Verified
Journal Article
Closed access
YFYabo Fu
Yabo Fu
HHHaowei He
Haowei He
RLRan Liu
Ran Liu
LZLei Zhu
Lei Zhu
YXYining Xia
Yining Xia
JQJing Qiu
Jing Qiu

1 October 2021 in Biosystems Engineering
Verified
Journal Article
Closed access
RLRan Liu
Ran Liu
JLJian Liu
Jian Liu
HLHuiying Liu
Huiying Liu
XYXinting Yang
Xinting Yang
JBJosé Fernando Bienvenido Bárcena
José Fernando Bienvenido Bárcena
Ming LiMing Li
Ming Li

20 November 2025 in Information Processing in Agriculture
Verified
Journal Article
Open access
Kaige LiuKaige Liu
Kaige Liu
TJTao Ji
Tao Ji
MLMing Li
Ming Li
XYXinting Yang
Xinting Yang
JSJunli Sun
Junli Sun
RLRan Liu
Ran Liu

8 August 2025 in Biosystems Engineering
Verified
Journal Article
Closed access
CZChunhao Zhang
Chunhao Zhang
RLRan Liu
Ran Liu
JYJungang Yang
Jungang Yang
Francisco Rodriguez-DiazFrancisco Rodriguez-Diaz
Francisco Rodriguez-Diaz
MLMing Li
Ming Li

1 May 2025 in Plant Disease
Verified
Journal Article
Closed access
TJTao Ji
Tao Ji
Tito CaffiTito Caffi
Tito Caffi
GFGiorgia Fedele
Giorgia Fedele
RLRan Liu
Ran Liu
Vittorio RossiVittorio Rossi
Vittorio Rossi
Walnut blight, caused by Xanthomonas arboricola pv. juglandis (Xaj), occurs worldwide in almost all areas where the Persian walnut (Juglans regia) is grown, causing significant reductions in nut yield via defoliation and fruit drop. The disease control relies on the calendar-based, repeated use of chemical bactericides, negatively impacting economic and environmental sustainability and potentially inducing Xaj resistance to chemicals. This study developed and validated a mechanistic model incorporating the main stages of the pathogen’s life cycle and the influence of weather under orchard conditions to improve the scheduling of disease control interventions. The model can simulate (i) the mobilization of primary inoculum; (ii) the infection caused by bacteria; and (iii) the lesion formation and production of secondary inoculum. We evaluated the model against 21 independent walnut blight epidemics in Italy (9 epidemics on leaves in five orchards) and the United States (12 epidemics on fruit in six orchards). Overall, the model provided accurate predictions for both the occurrence and nonoccurrence of infection, with a precision and F1-score of 0.866 and 0.844, respectively. The model could accurately predict disease progression across the season, with a concordance correlation coefficient between observed and predicted disease severities of 0.951, a root mean square error of 0.069, and a coefficient of residual mass of 0.024. After further validation, the model can serve as a decision-making tool for the risk-based timing of chemical sprays in walnut blight management.

18 August 2026 in Agronomy
Verified
Journal Article
Open access
PDF file
YSYunyan Shi
Yunyan Shi
MYmengdan yang
mengdan yang
JZJingchao Zhou
Jingchao Zhou
QLQuanhong Liu
Quanhong Liu
HHHuijuan Hou
Huijuan Hou
TJTao Ji
Tao Ji
Greenhouse microclimates exhibit substantial spatial heterogeneity. Conventional evaluations based on average measurements cannot adequately describe the environmental conditions experienced by crops. This study developed a spatial frequency analysis method to quantify long-term temperature and relative humidity heterogeneity. This method was coupled with cucumber yield and downy mildew models to evaluate the biological consequences of environmental variability. Environmental conditions in four representative greenhouse structures were monitored using distributed sensor networks under different weather conditions. The proposed method successfully identified persistent environmental hotspots. The spatial distribution of environmental heterogeneity differed among greenhouse structures, whereas solar radiation primarily controlled its intensity. Long-season monitoring data indicate that the maximum spatial variations in temperature and relative humidity within the brick-wall solar greenhouse, the assembled greenhouse, the glass greenhouse, and the plastic multi-span greenhouse reach up to 10 °C and 46%, 8.5 °C and 46%, 12 °C and 50%, and 7 °C and 32%, respectively. The assembled solar greenhouse and plastic greenhouse exhibited higher environmental uniformity, while the brick-wall solar greenhouse and glass multi-span greenhouse showed pronounced spatial gradients. Environmental heterogeneity resulted in significant within-greenhouse differences in simulated cucumber yield, with the smallest variation occurring in the assembled solar greenhouse (5.3%) and the largest in the glass multi-span greenhouse (39.2%). Disease simulations further revealed clear spatial aggregation of cucumber downy mildew risk, with the southern region of the solar greenhouse exhibiting 17–67% higher cumulative infection risk than other positions. This study establishes an integrated framework linking greenhouse environmental heterogeneity with crop productivity and disease risk, providing a practical basis for spatially differentiated precision greenhouse management and greenhouse structural optimization.