Salt Life: Salinity Drives Ectomycorrhizal Community Structure in the Endangered Pine Rocklands.

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Elena Karlsen-Ayala, Michelle A Jusino, Matthew E Smith, Romina Gazis
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引用次数: 0

Abstract

Pinus densa, an endemic and keystone tree in Florida's endangered pine rocklands ecosystem, faces increasing threats from sea level rise and salt intrusion. Ectomycorrhizal (ECM) fungi are critical for pine recruitment and survival, yet their diversity and response to salinity in this ecosystem have been unstudied. We used metabarcoding to survey the naturally occurring ECM fungi on the roots of mature Pinus densa at eight field sites with varying elevations, soil salinities, habitat patch sizes and distances from the ocean, followed by a manipulative greenhouse experiment to assess potential impacts of rising salinity, with four salinity levels on P. densa seedlings in soils that spanned a salinity gradient to evaluate survival and shifts in ECM communities. Results show that salinity stress threatens both P. densa and its ECM symbionts, with ECM fungal richness positively correlated with elevation and negatively correlated with salinity. Habitat patch size, distance from the ocean and soil pH showed no significant effect on richness, and pH was less predictive of community structure. In seedlings, higher salinity was associated with greater mortality and shifts in ECM community composition favouring Rhizopogon species and Pezizales taxa. These findings underscore the susceptibility of ECM fungi to increased salinity, which may disrupt mutualisms critical for coastal resilience. Understanding how salinity affects mutualistic fungi can inform predictions on the vulnerability of other coastal ecosystems to climate change and sea level rise.

盐的生命:盐度驱动濒危松岩地外生菌根群落结构。
密松(Pinus densa)是佛罗里达州濒临灭绝的松岩生态系统中的一种特有的基石树,它面临着海平面上升和盐入侵日益严重的威胁。外生菌根真菌(ECM)对松树的招募和生存至关重要,但其多样性及其对该生态系统盐度的响应尚未得到研究。在不同海拔、土壤盐度、生境斑块大小和离海洋距离的8个试验点,我们利用元编码技术调查了成熟密松根系上天然存在的ECM真菌,随后进行了温室实验,评估了盐度上升对密松幼苗的潜在影响,并在不同盐度梯度的土壤中设置了4种盐度水平,以评估ECM群落的生存和变化。结果表明,盐度胁迫对密螺旋藻及其ECM共生体均有威胁,ECM真菌丰富度与海拔高度呈正相关,与盐度呈负相关。生境斑块大小、离海洋距离和土壤pH值对群落丰富度无显著影响,pH值对群落结构的预测能力较弱。在幼苗中,较高的盐度与较高的死亡率和ECM群落组成的变化有关,这些变化有利于根抽根和Pezizales分类群。这些发现强调了ECM真菌对盐度增加的敏感性,这可能会破坏对沿海恢复力至关重要的共生关系。了解盐度如何影响共生真菌可以为预测其他沿海生态系统对气候变化和海平面上升的脆弱性提供信息。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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