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Tree growth-survival relationships link two demographic processes that individually dictate the composition, structure and functioning of forest ecosystems. While these relationships vary intra-specifically, it remains unclear how this reflects environmental variation and disturbance. We examined the influence of a 700-m elevation gradient and an = 6.7 earthquake on intra-specific variability in growth-survival relationships. We expected that survival models that incorporated recent growth would be better supported than those only using other factors known to influence tree survival. We used a permanent plot network that representatively sampled a monodominant forest in New Zealand's Southern Alps in 1974 and that was remeasured seven times through to 2009. The relationships were assessed using pre-earthquake growth and survival, pre-earthquake growth and post-earthquake survival (0-5 years post-earthquake), and post-earthquake growth and survival (5+ years post-earthquake). Survival was related to growth of 4504 trees on 216 plots using Bayesian modelling. We hypothesised there would be a positive, logistic relationship between growth and survival. Pre-earthquake, we found a positive, logarithmic growth-survival relationship at all elevations. At higher elevations, trees grew more slowly but had higher survival than trees at lower elevations, supporting our hypothesised demographic trade-off with elevation. The earthquake altered growth-survival relationships from those found pre-earthquake and 0-5 years post-earthquake survival held little relationship with growth. A strong, logarithmic growth-survival relationship developed 5+ years post-earthquake because of enhanced survival of fast-growing trees yet low survival of slow-growing trees. . Our findings demonstrate a trend in growth-survival relationships along an elevation gradient. If we assume a gradual climate warming is the equivalent of a forest stand shifting to a lower elevation, then data from our pre-earthquake period suggest that tree growth-survival relationships at any elevation could adjust to faster growth and lower survival. We also show how these novel growth-survival relationships could be altered by periodic disturbance.
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http://dx.doi.org/10.1002/ece3.70467 | DOI Listing |
Drug Deliv Transl Res
September 2025
Department of Infectious Diseases and Hepatology, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Erqi District, Zhengzhou City, Henan Province, 450000, China.
This study aimed to utilize the mRNA-lipid nanoparticle (mRNA-LNP) platform to achieve in situ hepatic expression of an interferon-α (IFN-α)/anti-glypican-3 (anti-GPC3) fusion protein (GPA01), enhancing IFN-α targeting and antitumor activity to provide a precision therapy strategy for GPC3-positive hepatocellular carcinoma (HCC). mRNA encoding a GPC-3/IFN-α bispecific fusion protein was designed and synthesized, encapsulated in lipid nanoparticles, and transfected into HCC cell lines (HepG2) for in vitro characterization of protein expression, binding activity, and gene induction. Orthotopic HCC models (HepG2-luc) and subcutaneous tumor model (Hepa 1-6/hGPC3-hi) were established in mice to evaluate tumor growth, survival, and immune cell infiltration following treatment with mRNA-LNP or control agents.
View Article and Find Full Text PDFFoods
August 2025
School of Food Science and Engineering, South China University of Technology, Wushan Road 381, Guangzhou 510640, China.
is a key periodontal pathogen whose cysteine proteases, gingipains (Rgp and KGP), are essential for nutrient acquisition and virulence. Targeting gingipains may attenuate bacterial pathogenicity and prevent related systemic diseases. This paper aimed to review advances in food-derived natural products that inhibit or gingipains, with emphasis on mechanisms, potency, and translational potential.
View Article and Find Full Text PDFArch Pharm (Weinheim)
August 2025
Department of Pharmaceutical Chemistry, ISF College of Pharmacy, Moga, Punjab, India.
3-Phosphoglycerate dehydrogenase (PHGDH) is a key enzyme in the serine biosynthesis pathway, supporting cancer cell growth, survival, and proliferation. Its overexpression is frequently observed in aggressive cancers such as breast cancer, melanoma, and glioma, where it drives tumor growth, metastasis, and resistance to oxidative stress. Targeting PHGDH with small-molecule inhibitors has emerged as a promising therapeutic strategy.
View Article and Find Full Text PDFFront Immunol
August 2025
Clinical Medical College, Yangzhou University, Yangzhou, China.
Moonlighting enzymes perform multiple distinct functions under different conditions without relying on gene fusion, splicing, or polymerization. Many classical metabolic enzymes, beyond their involvement in pathways like glycolysis and glutamine metabolism, also function as transcription factors, RNA-binding proteins, or signaling molecules. These dual roles are crucial in processes such as cancer metabolic reprogramming, immune evasion, and drug resistance.
View Article and Find Full Text PDFSci Total Environ
August 2025
Marine Ecology Laboratory, Department of Life Sciences, Presidency University, 86/1, College Street, Kolkata 700073, India. Electronic address:
The incessant release of anthropogenic CO in the atmosphere has accentuated ocean warming (OW) and elevated the partial pressure of dissolved CO₂, culminating in a foreseeable decline in oceanic pH. Thus, the present study endeavors to elucidate the concomitant impacts of OW and ocean acidification (OA) on the eco-physiological responses of Etroplus suratensis over a 30-day mesocosm experiment. Physiological parametres, encompassing ingestion, absorption, respiration, and excretion rates, were measured to gauge the scope for growth (SfG).
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