ABSTRACT
This corrects the article 10.3791/66737.
ABSTRACT
The alteration of stand age instigates modifications in soil properties and microbial communities. Understanding the impacts of stand age on soil enzyme stoichiometry and microbial nutrient limitations in Camellia oleifera plantation is crucial for nutrient management. Taking C. oleifera plantation across four age groups (<10 a, 15-25 a, 30-50 a, >60 a) in a subtropical red soil region as test objects, we examined the response of soil enzyme stoichiometry and microbial nutrient limitations to change in stand age and analyzed the pathways for such responses. The results showed that, compared to that of stand age <10 a, enzyme C:N in the 15-25 a was increased and enzyme N:P was significantly reduced. Microbial biomass carbon (MBC), microbial biomass nitrogen (MBN), and microbial biomass phosphorus (MBP) exhibited a trend of initially decreasing and then increasing with stand age. MBN and MBN:MBP were significantly higher in the <10 a compared to that in the 30-50 a. MBC:MBN was significantly higher in the 30-50 a and >60 a compared to the <10 a and 15-25 a. Results of redundancy analysis revealed that soil nutrients, microbial biomass and their stoichiometry explained 92.4% of the variations in enzyme stoichiometry. Partial least squares path modeling (PLS-PM) results demonstrated that soil organic carbon (SOC) had a positive effect on microbial C limitation; MBN, MBN:MBP, MBC:MBP, SOC, and total nitrogen had a nega-tive overall effect on microbial P limitation, whereas soil C:N had a positive overall effect on microbial P limitation. There was a significant positive correlation between microbial C and P limitations. With increasing stand age, microbial nutrient limitation shifted from N and P limitation (<10 a) to C and P limitation (15-25 a, 30-50 a, >60 a).
Subject(s)
Camellia , Carbon , Nitrogen , Phosphorus , Soil Microbiology , Soil , Camellia/metabolism , Camellia/growth & development , Camellia/chemistry , Soil/chemistry , Nitrogen/metabolism , Nitrogen/analysis , Carbon/metabolism , Phosphorus/metabolism , Nutrients/metabolism , Nutrients/analysis , Time Factors , China , BiomassABSTRACT
A total of five samples of Chrysomya megacephala samples - three fresh samples, one sample stored in alcohol for 2 years, and one sample stored in dry sealed storage for 2 years protected from light only - were selected to investigate whether a blood DNA extraction kit could extract DNA from necrophilous flies and to determine whether alcohol could prolong the preservation of necrophilous flies' DNA. First, the blood DNA extraction kit was used to extract DNA from their thorax tissues. Then, the DNA purity and concentration were examined using a microplate reader and a fluorometer. Finally, PCR amplification and electrophoresis of the extracted DNA were done with necrophilic fly-specific primers located in the mitochondrial CO I gene sequence. The results showed that the DNA purity of all samples was greater than 2.0. The DNA concentration was observed to be of the following order: fresh samples > alcohol-preserved old samples > untreated, old samples. All samples had specific electrophoretic bands after PCR amplification. In conclusion, a blood DNA extraction kit can be used to extract DNA from necrophilic flies successfully, and the DNA concentration of fresh fly samples is greater than that of old fly samples. The flies can be stored in alcohol for a long time.
Subject(s)
DNA , Polymerase Chain Reaction , Animals , DNA/isolation & purification , DNA/genetics , Polymerase Chain Reaction/methods , Calliphoridae/genetics , Calliphoridae/chemistryABSTRACT
Diatom testing is an essential auxiliary means in forensic practice to determine whether the corpse drowned in water and to infer the drowning location. Diatom testing is also an important research content in the field of the environment and plankton. The diatom molecular biology testing technology, which focuses on diatom DNA as the primary research object, is a new method of diatom testing. Diatom DNA extraction is the basis of diatom molecular testing. At present, the kits commonly used for diatom DNA extraction are expensive, which increases the cost of carrying out related research. Our laboratory improved the general whole blood genomic DNA rapid extraction kit and obtained a satisfactory diatom DNA extraction effect, thus providing an alternative economical and affordable DNA extraction solution based on glass beads for related research. The diatom DNA extracted using this protocol could satisfy many downstream applications, such as PCR and sequencing.
Subject(s)
Diatoms , Drowning , Humans , Diatoms/genetics , DNA/genetics , Plankton , Polymerase Chain Reaction , Water , LungABSTRACT
BACKGROUND: With an increase in recent years in the number of people receiving cosmetic facial injection treatments of hyaluronic acid, the incidence of hyaluronic acid embolism has also increased commensurately. Hyaluronic acid embolism leads to serious complications, including blindness, eye and eyelid movement disorders, skin necrosis, and cerebral embolism. However, there is a lack of robust clinical evidence regarding the benefits of treatment for hyaluronic acid embolism by intraarterial thrombolysis therapy. METHODS: This study included 24 patients with a decrease in visual acuity and other complications induced by facial hyaluronic acid injection. Patients underwent emergency intraarterial thrombolysis therapy by injection of hyaluronidase (500 to 1500 units) alone or hyaluronidase (750 to 1500 units) combined with urokinase (100,000 to 250,000 units), followed in both cases by a general symptomatic treatment and nutritional therapy. RESULTS: Ten (42 percent) of 24 patients ultimately had improvements to visual acuity, even when the clinical application of the thrombolytic treatments had passed the recommended window for optimal treatment. In all cases, patients' facial skin necrosis was restored to nearly normal appearance. In addition, the authors found that hyaluronidase combined with urokinase was a more effective therapy than hyaluronidase alone. CONCLUSIONS: The authors' results indicate that intraarterial thrombolysis therapy is beneficial to patients suffering from blindness induced by hyaluronic acid embolism. The therapy was shown to be worthy of clinical application because it alleviated the impairment to patients' vision and was also beneficial in the recovery from other serious complications, including eye movement disorder, eye edema, headaches, and skin necrosis. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.
Subject(s)
Blindness/drug therapy , Cosmetic Techniques/adverse effects , Dermal Fillers/adverse effects , Embolism/drug therapy , Ophthalmic Artery/pathology , Thrombolytic Therapy/methods , Adult , Angiography, Digital Subtraction , Blindness/etiology , Dermal Fillers/administration & dosage , Drug Therapy, Combination/methods , Embolism/diagnostic imaging , Embolism/etiology , Embolism/pathology , Eye/blood supply , Female , Follow-Up Studies , Humans , Hyaluronic Acid/administration & dosage , Hyaluronic Acid/adverse effects , Hyaluronoglucosaminidase/therapeutic use , Injections, Intra-Arterial , Injections, Subcutaneous/adverse effects , Male , Ophthalmic Artery/diagnostic imaging , Retrospective Studies , Treatment Outcome , Urokinase-Type Plasminogen Activator/therapeutic use , Visual AcuityABSTRACT
Four drip points was monitored for a year in Jiangjun cave, Anshun county of Guizhou province, China. The result shows that drip water responding to rainfall is very quick (0-9 days). Drip water chemical components are directly originated from soil and greatly affected by the soil thickness. The thinner soil is, the less substances water dissolves. Water passes more quickly, which decreases the possibility of dilution happening in drip water, simultaneously, increases the contribution of rock to drip compositions. In some cases, JJD-1 and JJD-4 are affected by dilution, however, different sources of water affect drip water dynamic process, which leads to piston flow for JJD-1, and increase drip ratio and water head pressure for JJD-2 as well while water is of much quantity. All of these processes affect drip compositions in second effect intensity. Element variations of 4 drip waters are mainly controlled by the process of rock dissolution and calcite precipitation while water transports in the route and acts with soil and rock. Consequently, as an important karst environmental factor, soil decides and controls drip compositions of cave drip waters, which means more attentions must be paid to soil in future study.