Kernel Bioassay Evaluation of Maize Ear Rot and Genome-Wide Association Analysis for Identifying Genetic Loci Associated with Resistance to Fusarium graminearum Infection.

Gibberella ear rot (GER) caused by Fusarium graminearum (teleomorph Gibberella zeae) is one of the most destructive diseases in maize, which severely reduces yield and contaminates several potential mycotoxins in the grain. However, few efforts had been devoted to dissecting the genetic basis of maize GER resistance. In the present study, a genome-wide association study (GWAS) was conducted in a maize association panel consisting of 303 diverse inbred lines. The phenotypes of GER severity were evaluated using kernel bioassay across multiple time points in the laboratory. Then, three models, including the fixed and random model circulating probability unification model (FarmCPU), general linear model (GLM), and mixed linear model (MLM), were conducted simultaneously in GWAS to identify single-nucleotide polymorphisms (SNPs) significantly associated with GER resistance. A total of four individual significant association SNPs with the phenotypic variation explained (PVE) ranging from 3.51 to 6.42% were obtained. Interestingly, the peak SNP (PUT-163a-71443302-3341) with the greatest PVE value, was co-localized in all models. Subsequently, 12 putative genes were captured from the peak SNP, and several of these genes were directly or indirectly involved in disease resistance. Overall, these findings contribute to understanding the complex plant-pathogen interactions in maize GER resistance. The regions and genes identified herein provide a list of candidate targets for further investigation, in addition to the kernel bioassay that can be used for evaluating and selecting elite germplasm resources with GER resistance in maize.

Ethnobotanical study on edible flowers in Xishuangbanna, China.

BACKGROUND: Edible flowers (EFs) represent valuable sources of both food and medicinal resources, holding the promise to enhance human well-being. Unfortunately, their significance is often overlooked. Ethnobotanical studies on the EFs are lacking in comparison with their botanical and phytochemical research. The practice of consuming flowers as food has a rich culture and long history in China, especially among different linguistic groups in Xishuangbanna, Yunnan. However, economic activities have led to a decline of this tradition. Consequently, preserving the traditional knowledge and culture tied to the EFs in Xishuangbanna becomes both essential and pressing. METHODS: The field ethnobotanical survey was conducted in Xishuangbanna during five visits in April 2021 and May 2023, covering 48 villages and 19 local markets of all three county-level areas and 9 different linguistic groups. By conducting a comprehensive literature review and on-site field surveys, relevant information regarding the EFs of Xishuangbanna was systematically collected and documented. Additionally, the relative frequency of citation (RFC) values were calculated from the survey data. RESULTS: A total of 212 taxa (including species and varieties) of EFs from 58 families and 141 genera were documented in the study area. The edible parts of flowers were classified into 13 categories including peduncle, petal, flower buds, inflorescence as a whole, and etc. They were consumed in 21 ways and as 8 types of food. The inflorescence was the most commonly consumed category, accounting for 85 species (40.1%) of the total categories. They always eat flowers as vegetables (184 species, 86.8%). The preparing form of stir-frying was the preferred food preparation method (138, 65.1%). The Xishuangbanna locals had profound knowledge of which EFs required specific processing to remove their toxicity or bitterness. The dishes can be made from either exclusively from the flowers themselves or by incorporating them alongside other plant parts like stems and leaves. Some EFs with high RFC value, such as Musa acuminata and Bauhinia variegata var. candida, showed significant cultural meanings. These edible flowers occupy specific positions in local traditional culture. CONCLUSION: Traditional knowledge regarding edible flowers holds substantial significance and serves as a representative element of the flower-eating culture in Xishuangbanna. Nevertheless, this knowledge and cultural practice are currently decreasing. Serving as a bridge between tradition and modernity, the flower-eating culture, which derives from local people's practical experience, shows the potential of EFs and can be applied to the conservation of biocultural diversity, healthy food systems, and sustainable development.

Self-Powered Integrated Sensing System with In-Plane Micro-Supercapacitors for Wearable Electronics.

Self-powered integrated sensor with high-sensitivity physiological signals detection is indispensable for next-generation wearable electronic devices. Herein, a Ti3 C2 Tx /CNTs-based self-powered resistive sensor with solar cells and in-plane micro-supercapacitors (MSCs) is successfully realized on a flexible styrene-ethylene/butylene-styrene (SEBS) electrospinning film. The prepared Ti3 C2 Tx /CNTs@SEBS/CNTs nanofiber membranes exhibit high electrical conductivity and mechanical flexibility. The laser-assisted fabricated Ti3 C2 Tx /CNTs based-MSCs demonstrate a high areal energy density of 52.89 and 9.56 µWh cm-2 with a corresponding areal power density of 0.2 and 4 mW cm-2 . Additionally, the MSCs exhibit remarkable capacity retention of 90.62% after 10 000 cycles. Furthermore, the Ti3 C2 Tx /CNTs based-sensor exhibits real-time detection capability for human facial micro-expressions and pulse single under physiological conditions. The repeated bending/release tests indicate the long-time cycle stability of the Ti3 C2 Tx /CNTs based-sensor. Owing to the excellent sensing performance, the sensing array was also fabricated. It is believed that this work develops a route for designing a self-powered sensor system with flexible production, high performance, and human-friendly characteristics for wearable electronics.

Two-Dimensional Magnetic Semiconducting Heterostructures of Single-Layer CrI3-CrI2.

Single-layer heterostructures of magnetic materials are unique platforms for studying spin-related phenomena in two dimensions (2D) and have promising applications in spintronics and magnonics. Here, we report the fabrication of 2D magnetic lateral heterostructures consisting of single-layer chromium triiodide (CrI3) and chromium diiodide (CrI2). By carefully adjusting the abundance of iodine based on molecular beam epitaxy, single-layer CrI3-CrI2 heterostructures were grown on Au(111) surfaces with nearly atomic-level seamless boundaries. Two distinct types of interfaces, i.e., zigzag and armchair interfaces, have been identified by means of scanning tunneling microscopy. Our scanning tunneling spectroscopy study combined with density functional theory calculations indicates the existence of spin-polarized ground states below and above the Fermi energy localized at the boundary. Both the armchair and zigzag interfaces exhibit semiconducting nanowire behaviors with different spatial distributions of density of states. Our work presents a novel low-dimensional magnetic system for studying spin-related physics with reduced dimensions and designing advanced spintronic devices.

Facile Preparation of Dual Functional Wearable Devices Based on Hindered Urea Bond-Integrated Reprocessable Polyurea and AgNWs.

With the advancement of material science and electronic technology, wearable devices have been integrated into daily lives, no longer just a stirring idea in science fiction. In the future, robust multifunctionalized wearable devices with low cost and long-term service life are urgently required. However, preparing multifunctional wearable devices robust enough to resist harsh conditions using a commercially available raw material through a simple process still remains challenging. In this work, reprocessable polyurea (HUBTPU) with a hard segment of hindered urea bonds (HUBs) and a soft segment of polyether is synthesized via a facile one-pot method. The robust dual functional wearable devices were obtained by simply spray-coating silver nanowires (AgNWs) on HUBTPU elastomer substrates. Due to the dynamic combination and decomposition of the HUBs and hydrogen bonds at 130 °C, the robust elastomer demonstrates favorable adhesion to various substrates. Especially, the partially embedded AgNW structure is also achieved by using ethanol as a spray solvent. The adhesion of HUBTPU substrates and embedded structure leads to stronger interfacial adhesion and stability compared to non-adhesive substrates. The as-obtained HUBTPU electrodes are able to be heated to 115 °C by applying a low voltage and sensing the strain deformation caused by human movement, which means that the electrodes are endowed with both electrical heating capability and strain sensing functionality. Therefore, this strategy reveals a potential way to prepare multifunctional wearable devices using other conductive particles and adhesive functional polymer substrates.

Pitaya-Structured Microspheres with Dual Laser Wavelength Responses for Polymer Laser Direct Writing.

A unique pitaya-structured graphene/TiO2@PS microsphere with dual laser wavelength responses is designed and prepared via a facile approach of polymer melt blending. The graphene/TiO2 particles ("pitaya seeds") are homogeneously distributed in the polystyrene ("pitaya pulp") of the microspheres with an average size of 1.5 µm. The graphene in microspheres serves not only as a laser absorber that has responses to both 355 nm UV and 1064 nm NIR lasers but also as a reducing agent of TiO2 during laser direct writing (LDW). As expected, benefiting from the unique pitaya-structured structure, the graphene/TiO2@PS microsphere can remarkably improve the performance of both NIR and UV LDW of polymers. The results of characterizations reveal that the black color caused by NIR LDW is due to the generation of the amorphous carbon and the color change after UV LDW is owing to the formation of black sp/sp2 carbon compounds. Meanwhile, some TiO2 in microspheres is reduced into the black/gray titanium oxides of Ti2+ and Ti3+ after NIR and UV LDW, respectively. The above co-contribution endows the graphene/TiO2@PS microspheres with an outstanding color-changing ability. This pitaya-structured microsphere will have a profound effect on polymers' laser direct writing.

In-Situ Templating Growth of Homeostatic GeP Nano-Bar Corals with Fast Electron-Ion Transportation Pathways for High Performance Li-ion Batteries.

We propose an in situ template method to directionally induce the construction of germanium phosphide nanobar (GeP-nb) corals with an adjustable aspect ratio. The GeP nanobars grown onto conductive matrix with high aspect ratio expose more quickest electron-ion transportation facets for fast reaction dynamics. The customized GeP-nb electrode delivers a self-healable homeostatic behavior by reversibly stabilizing GeP crystalline structure through multi-phase reactions to maintain structural integrity and cycling stability (850 mAh g-1 at 1 A g-1 after 500 cycles). As a result, the GeP-nb presents the highest Li+ diffusion coefficient (6.21×10-11  cm2 s-1 ) among all the Ge-based anode materials studied so far, rendering an excellent rate performance (620 mAh g-1 at 5 A g-1 ) as a lithium-ion battery (LIB) anode.

Ionic Liquid-Assisted 3D Printing of Self-Polarized ß-PVDF for Flexible Piezoelectric Energy Harvesting.

Three-dimensional (3D) printing technologies have unparalleled advantages in constructing piezoelectric devices with three-dimensional structures, which are conducive to improving the efficiency of energy harvesting. Among them, fused deposition modeling (FDM) is the most widely used thanks to its low cost and wide range of molding materials. However, as the best piezoelectric polymer, a high electroactive ß-phase poly(vinylidene fluoride) (PVDF) piezoelectric device cannot be directly obtained by FDM printing because the ß-crystal is unstable at the molten state. Herein, we develop for the first time ionic liquid (IL)-assisted FDM for direct printing of ß-PVDF piezoelectric devices. An IL can induce and maintain ß crystals during melt extrusion and FDM printing, ensuring that the ß-crystal in the printed PVDF device is as high as 98.3%, which is the highest in 3D-printed PVDF as far as we know. Furthermore, the shearing force provided by the FDM facilitates the directional arrangement of the dipoles, resulting in the printed PVDF device having self-polarization characteristics without poling. Finally, the piezoelectric output voltage of the 3D-printed PVDF device is 4.7 times that of the flat PVDF device, and its area current density (17.5 nA cm-2) is more than that of the reported 3D-printed PVDF piezoelectric device in the literature by two orders of magnitude. The one-step 3D printing strategy proposed in this paper can realize the rapid preparation of complex-shaped and lightweight self-polarized ß-PVDF-based piezoelectric devices for energy harvesting.

Imaging Vacancy Defects in Single-Layer Chromium Triiodide.

As a van der Waals magnetic semiconductor, chromium triiodide (CrI3) is widely considered for its high research value and potential applications. Defects in CrI3 are inevitably present and significantly alter the material properties. However, experimental identification of defects of CrI3 at the atomic level is still lacking. Here for the first time, we carried out a scanning tunneling microscopy (STM) study and density functional theory calculations to explore the intrinsic defects in monolayer CrI3 grown by molecular beam epitaxy. The three most common types of intrinsic point defects, i.e., I vacancy (VI), Cr vacancy (VCr), and multiatom CrI3 vacancy (VCrI3) with distinct spatial distributions of the localized defect states, are identified and characterized by high-resolution STM. Moreover, defect concentrations are estimated based on our experiments, which agree with the calculated formation energies. Our findings provide vital knowledge on the types, concentrations, electronic structures, and migration mechanism of the intrinsic point defects in monolayer CrI3 for future defect engineering of this novel 2D magnet.

Top-Down Direct Preparation of Orange-Yellow Dye Similar to Psittacofulvins from Commercial Polymer by Laser Writing.

Laser manufacturing is a promising method for the design and preparation of high value-added materials. When the laser acts on the polymer precursors, some wonderful phenomena will always occur and accompanied by the generation of new substances. Herein, we report a top-down approach for the direct preparation of orange-yellow dye that is similar to psittacofulvins from commercial polymer resins by laser writing. Conjugated double bonds and micro-rough structures are formed simultaneously on laser-irradiated polymer substrate surfaces. The typical polyconjugated structures of psittacofulvin dyes were confirmed by micro-Raman and Raman imaging results. Temperature-dependent Fourier transform infrared and X-ray photoelectron spectroscopy further demonstrated the formation mechanism of laser-induced psittacofulvins dyes based on the chemical composition. Further, optical microscopy, laser confocal microscopy, and scanning electron microscopy were carried out to characterize the physical morphologies of laser-irradiated polymer substrates. A unique advantage of preparing psittacofulvins dye using laser writing is its simple steps, and the dye can be converted directly from the appropriate precursor substrate. Interestingly, the laser-irradiated polymer substrate surface undergoes color change. This laser-induced color patterning is attractive due to the characteristics of high precision, flexibility, and maskless; any patterns can be easily designed and produced on the polymer at desired positions.

Single-layer CrI3 grown by molecular beam epitaxy.

Single- and few-layer chromium triiodide (CrI3), which has been intensively investigated as a promising platform for two-dimensional magnetism, is usually prepared by the mechanical exfoliation. Here, we report direct growth of single-layer CrI3 using molecular beam epitaxy in ultrahigh vacuum. Scanning tunneling microscopy (STM), together with density functional theory (DFT) calculation, revealed that the iodine trimers, each of which consists of three I atoms surrounding a three-fold Cr honeycomb center, are the basic units of the topmost I layer. Different superstructures of single-layer CrI3 with periodicity around 2-4 nm were obtained on Au(1 1 1), while only the 1 × 1 structure was observed on the graphite substrate. At an elevated temperature of 423 K, single-layer CrI3 began to decompose and transformed into single-layer chromium diiodide. Our bias-dependent STM images suggest that the unoccupied and occupied states are spatial-separately distributed, consistent with the results of our DFT calculation. We also discussed the role of charge distribution in the super-exchange interactions among Cr atoms in single-layer CrI3.

New Strategy to Achieve Laser Direct Writing of Polymers: Fabrication of the Color-Changing Microcapsule with a Core-Shell Structure.

This paper proposed an efficient and environmentally friendly strategy to prepare a new color-changing microcapsule with a core-shell structure for laser direct writing of polymers, and only the physical melt blending of polymers was employed. The laser absorber (SnO2) and the easily carbonized polymer (PC) were designed as the "core" and the "shell" of the microcapsule, respectively. The microcapsules were in situ formed during melt blending. Scanning electron microscopy, transmission electron microscopy, and energy-dispersive spectrometry confirmed the successful preparation of SnO2/PC microcapsules with a core-shell structure. Their average diameter was 2.2 µm, and the "shell" thickness was 0.21-0.24 µm. As expected, these SnO2/PC microcapsules endowed polymers with an outstanding performance of near-infrared (NIR) laser direct writing. Raman spectroscopy and X-ray photoelectron spectroscopy indicated that the color change was ascribed to the polymer carbonization because of the instantaneous high temperature caused by the SnO2 absorption of NIR laser energy. Optical microscopy observed a thick carbonization layer of 234 µm. Moreover, Raman depth imaging revealed the carbonization distribution, confirming that the amorphous carbon produced by the carbonization of the PC "shell" is the key factor of SnO2/PC microcapsules to provide polymers an outstanding performance of laser direct writing. This color-changing microcapsule has no selectivity to polymers because of providing a black color source (the carbonization of PC) itself, ensuring the high contrast and precision of patterns or texts after laser direct writing for all general-purpose polymers. We believe that this novel strategy to achieve laser direct writing of polymers will have broad application prospects.

A Lactate/Oxygen Biofuel Cell: The Coupled Lactate Oxidase Anode and PGM-Free Fe-N-C Cathode.

The rapid development of both wearable and implantable biofuel cells has triggered more and more attention on the lactate biofuel cell. The novel lactate/oxygen biofuel cell (L/O-BFC) with the direct electron transfer (DET)-type lactate oxidase (LOx) anode and the platinum group metal (PGM)-free Fe-N-C cathode is designed and constructed in this paper. In such a reasonable design, the surface-controlled direct two-electron electrochemical reaction of the lactate oxidase was determined by cyclic voltammetry (CV) on the carbon nanotube (CNT) modified electrode with favorable high electrochemical active surface area and electronic conductivity. Additionally, the biosensor based on DET-type LOx modified electrode impressively presented linear response to lactate with different concentrations from 0.000 mM to 12.300 mM. In particular, the apparent Michealis-constant (KMapp) calculated as 0.140 mM clearly indicates that LOx on CNT has strong affinity to the substrate lactate. Meanwhile, 4e- transfer oxygen reduction reaction (ORR) was proven to take place on the Fe-N-C catalysts inthe 0.1 M PBS system, indicating the advantage by using the Fe-N-C catalysts at the cathode of L/O-BFC. Last but not least, the L/O-BFC with the direct electron transfer (DET)-type lactate oxidase(LOx) anode and the Fe-N-C cathode produced an superior open circuit potential (OCP) of 0.264 V and a maximum output power density (OPD) of 24.430 µW cm-2 in O2 saturated 95.020 mM lactate solution. The above results will not only bring about significant interest in developing a DET-type biofuel cell, but also offer guiding direction to explore novel catalyst materials for the biofuel cell. This work enriches the research content and may push developments of the implantable and wearable biofuel cell forward.

Laser-Induced Selective Metallization on Polymer Substrates Using Organocopper for Portable Electronics.

Our work proposed a facile strategy for selective fabrication of the precise metalized patterns onto polymer substrates through the laser direct structuring (LDS) technology using organocopper compounds. Copper oxalate (CuC2O4) and copper acetylacetonate [Cu(acac)2] which can be used as laser sensitizers were first introduced into an acrylonitrile-butadiene-styrene (ABS) matrix for preparing LDS materials. After the activation with 1064 nm pulsed near-infrared laser, the Cu0 (metal copper) was generated from CuC2O4 and Cu(acac)2 and then served as catalyst species for the electroless copper plating (ECP). A series of characterizations were conducted to investigate the morphology and analyze the surface chemistry of ABS/CuC2O4 and ABS/Cu(acac)2 composites. Specially, the X-ray photoelectron spectroscopy analysis indicated that 58.3% Cu2+ in ABS/CuC2O4 was reduced to Cu0, while this value was 63.9% for ABS/Cu(acac)2. After 30 min ECP, the conductivities of copper circuit on ABS/CuC2O4 and ABS/Cu(acac)2 composites were 1.22 × 107 and 1.58 × 107 Ω-1·m-1, respectively. Moreover, the decorated patterns and near-field communication circuit were demonstrated by this LDS technology. We believe that this study paves the way for developing organocopper-based LDS materials, which have the potential for industrial applications.

Selective Metallization Induced by Laser Activation: Fabricating Metallized Patterns on Polymer via Metal Oxide Composite.

Recently, metallization on polymer substrates has been given more attention due to its outstanding properties of both plastics and metals. In this study, the metal oxide composite of copper-chromium oxide (CuO·Cr2O3) was incorporated into the polymer matrix to design a good laser direct structuring (LDS) material, and the well-defined copper pattern (thickness =10 µm) was successfully fabricated through selective metallization based on 1064 nm near-infrared pulsed laser activation and electroless copper plating. We also prepared polymer composites incorporated with CuO and Cr2O3; however, these two polymer composites both had very poor capacity of selective metallization, which has no practical value for LDS technology. In our work, the key reasons causing the above results were systematically studied and elucidated using XPS, UV-vis-IR, optical microscopy, SEM, contact angle, ATR FTIR, and so on. The results showed that 54.0% Cu2+ in the polymer composite of CuO·Cr2O3 (the amount =5 wt %) is reduced to Cu0 (elemental copper) after laser activation (irradiation); however, this value is only 26.8% for the polymer composite of CuO (the amount =5 wt %). It was confirmed that to achieve a successful selective metallization after laser activation, not only was the new formed Cu0 (the catalytic seeds) the crucial factor, but the number of generated Cu0 catalytic seeds was also important. These two factors codetermined the final results of the selective metallization. The CuO·Cr2O3 is very suitable for applications of fabricating metallic patterns (e.g., metal decoration, circuit) on the inherent pure black or bright black polymer materials via LDS technology, which has a prospect of large-scale industrial applications.

Fabricating Metallic Circuit Patterns on Polymer Substrates through Laser and Selective Metallization.

Nowadays, with the rapid development of portable electronics, wearable electronics, LEDs, microelectronics, and bioelectronics, the fabrication of metallic circuits onto polymer substrates with strong adhesion property is an ever-increasing challenge. In this study, the high-resolution and well-defined metallic circuits were successfully prepared on the polymer surface via laser direct structuring (LDS) based on copper hydroxyl phosphate [Cu2(OH)PO4], and the key mechanism of the selective metallization was systematically investigated. XPS confirmed that Cu0 (elemental copper) was formed through photochemical reduction reaction of Cu2(OH)PO4, after 1064 nm NIR pulsed laser irradiation. During the electroless plating, because it is the important active catalytic center, this newly formed Cu0 was the key factor to achieve the successful selective metallization. SEM revealed that after the electroless plating, the copper layer actually physically anchored into the polymer substrate, giving an excellent mechanical adhesion property of the obtained metallic patterns. In addition, the micro-Raman surface imaging approved the generation of the amorphous carbon on the polymer composites' surface after NIR laser irradiation, and the chemical reaction region caused by the pulsed laser spot was found at approximately 40 µm. This environmentally friendly and effective strategy for fabricating circuit patterns on the polymer surface has a possible application in the printed circuit plate (PCB) industry.

Local Controllable Laser Patterning of Polymers Induced by Graphene Material.

Graphene has been successfully applied to the field of polymer laser patterning. As an efficient 1064 nm near-infrared (NIR) pulsed laser absorber, only 0.005 wt % (50 ppm) of graphene prepared by mechanical exfoliation endowed polymer materials with very good NIR pulsed laser patterning. Optical microscopy observed that the generated black patterns came from the local discoloration of the polymer surface subjected to the laser irradiation, and the depth of the discolored layer was determined to be within 221-348 µm. The X-ray photoelectron spectroscopy confirmed that the polymer surface discoloration was contributed by the local carbonization of polymers caused by graphene due to its high photothermal conversion capacity. Raman depth imaging successfully detected that the generated carbon in the discolored layer was composed of amorphous carbon and complex sp/sp2-carbon compounds containing C≡C or conjugated C═C/C≡C structures. This study also provides a simple guideline to fabricate laser-patterning polymer materials based on graphene. We believe that graphene has broad application prospects in the field of polymer laser patterning. Importantly, this work opens up a valuable, feasible direction for the practical application of this new carbon material.

A Simple Way to Achieve Legible and Local Controllable Patterning for Polymers Based on a Near-Infrared Pulsed Laser.

This study developed a simple way to achieve legible and local controllable patterning for polymers based on a near-infrared (NIR) pulsed laser. The polycarbonate-coated nano antimony-doped tin oxide (nano ATO) was designed as a core-shell structure that was tailored to be responsive to a 1064 nm NIR laser. The globular morphology of polycarbonate-coated nano ATO with a diameter of around 2-3 µm was observed by scanning electron microscopy and transmission electron microscopy. This core-shell structure combined the excellent photothermal conversion efficiency of nano ATO and the high char (carbon) residue of polycarbonate. The X-ray photoelectron spectroscopy results of a polymer-patterning plate after laser irradiation demonstrated that, through local controlled photochromism, the well-defined legible patterns can be fabricated on the polymer surfaces contribute to the synergistic effect consisting of polycarbonate carbonization and nano ATO photothermal conversion. Furthermore, polymers doped with a minimal content of polycarbonate-coated nano ATO can achieve a remarkable patterning effect. This novel laser-patterning approach will have wide promising applications in the field of polymer NIR pulsed-laser patterning.

[In-depth interviews on late stage schistosomiasis patients about factors related to prevention and treatment in the rural areas].

OBJECTIVE: To explore factors related to current prevention and treatment of Advanced cases on schistosomiasis. METHODS: In-depth interviews were introduced to the qualitative study on 61 Advenced cases of schistosomiasis in Dongting Lake regions. Sampling was accidentally and judgmentally performed. RESULTS: Related factors on prevention and treatment of Advenced cases of schistosomiasis would include: higher degree of social support for patients (61/61), excessive dependence on the past pattern of schistosomiasis control, lack of the idea that one should be responsible for his/her own health, lack of knowledge about prevention and treatment of schistosomiasis (28/61), older age (57.40 +/- 10.80), lower education (4.70 years), less family income, lack of effective medical insurance system and efficient close-to-client system. CONCLUSION: Active participation from patients, medical institutions and society was needed to control Late Stage Schistosomiasis. Health education campaign should be intensified to improve the health awareness for schistosomiasis among residents in the heavy endemic areas. Medical insurance system should be set up in epidemic areas, while public health and cure systems for important diseases should be intensified in rural areas. The ability of public health system to be responsive and the accessibility of residents to health service system should be improved in rural areas as well.