On the public citation graph

Do mycorrhizal network benefits to survival and growth of interior Douglas‐fir seedlings increase with soil moisture stress?

0 signed · 98 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4757-2855-2openalex-snapshot

Plant Physiological Ecology

inferredcites →https://doi.org/10.1007/978-94-010-9013-1openalex-snapshot

Plant Physiological Ecology

inferredcites →https://doi.org/10.1007/bf00204014openalex-snapshot

Nitrogen amendments reduce the growth of extramatrical ectomycorrhizal mycelium

inferredcites →https://doi.org/10.1007/s00442-002-1078-2openalex-snapshot

Direct nocturnal water transfer from oaks to their mycorrhizal symbionts during severe soil drying

inferredcites →https://doi.org/10.1007/s00442-007-0852-6openalex-snapshot

Tree proximity, soil pathways and common mycorrhizal networks: their influence on the utilization of redistributed water by understory seedlings

inferredcites →https://doi.org/10.1007/s00442-008-1136-5openalex-snapshot

Mycorrhizal networks and distance from mature trees alter patterns of competition and facilitation in dry Douglas-fir forests

inferredcites →https://doi.org/10.1007/s004420000385openalex-snapshot

Morphotype community structure of ectomycorrhizas on Douglas fir ( Pseudotsuga menziesii Mirb. Franco) seedlings grown under elevated atmospheric CO 2 and temperature

inferredcites →https://doi.org/10.1007/s00572-006-0083-4openalex-snapshot

Methods to control ectomycorrhizal colonization: effectiveness of chemical and physical barriers

inferredcites →https://doi.org/10.1007/s00572-011-0406-yopenalex-snapshot

Mycorrhizal networks affect ectomycorrhizal fungal community similarity between conspecific trees and seedlings

inferredcites →https://doi.org/10.1016/j.agrformet.2004.10.004openalex-snapshot

Models of climatic normals for genecology and climate change studies in British Columbia

inferredcites →https://doi.org/10.1034/j.1600-0706.2003.12276.xopenalex-snapshot

Is there a trade‐off between the plant's growth response to elevated CO 2 and subsequent litter decomposability?

inferredcites →https://doi.org/10.1038/41557openalex-snapshot

Net transfer of carbon between ectomycorrhizal tree species in the field

inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00273.xopenalex-snapshot

Novel in‐growth core system enables functional studies of grassland mycorrhizal mycelial networks

inferredcites →https://doi.org/10.1046/j.1365-2486.2003.00646.xopenalex-snapshot

Elevated CO2 and temperature alter nitrogen allocation in Douglas‐fir

inferredcites →https://doi.org/10.1046/j.1365-2699.2000.00215.xopenalex-snapshot

Functional roles of remnant plant populations in communities and ecosystems

inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00923.xopenalex-snapshot

Stomatal responses of Douglas‐fir seedlings to elevated carbon dioxide and temperature during the third and fourth years of exposure

inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00834.xopenalex-snapshot

Reciprocal transfer of carbon isotopes between ectomycorrhizal Betula papyrifera and Pseudotsuga menziesii

inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00698.xopenalex-snapshot

Ectomycorrhizal fungal communities in young forest stands regenerating after clearcut logging

inferredcites →https://doi.org/10.1080/17550874.2010.502564openalex-snapshot

Pathways for below-ground carbon transfer between paper birch and Douglas-fir seedlings

inferredcites →https://doi.org/10.1080/713608315openalex-snapshot

Nitrogen Transfer Within and Between Plants Through Common Mycorrhizal Networks (CMNs)

inferredcites →https://doi.org/10.1093/jxb/erm009openalex-snapshot

Common mycorrhizal networks provide a potential pathway for the transfer of hydraulically lifted water between plants

inferredcites →https://doi.org/10.1111/j.0030-1299.2004.13184.xopenalex-snapshot

Responses of temperate woody seedlings to shade and drought: do trade‐offs limit potential niche differentiation?

inferredcites →https://doi.org/10.1111/j.1365-2745.2005.00977.xopenalex-snapshot

Ectomycorrhizal fungal communities at forest edges

inferredcites →https://doi.org/10.1111/j.1365-2745.2009.01624.xopenalex-snapshot

Net carbon transfer between Pseudotsuga menziesii var. glauca seedlings in the field is influenced by soil disturbance

inferredcites →https://doi.org/10.1111/j.1461-0248.2005.00822.xopenalex-snapshot

Spatially disjunct effects of co‐occurring competition and facilitation

inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01036.xopenalex-snapshot

Relationships between needle nitrogen concentration and photosynthetic responses of Douglas‐fir seedlings to elevated CO2 and temperature

inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01047.xopenalex-snapshot

Evaluating ecosystem responses to rising atmospheric CO 2 and global warming in a multi‐factor world

inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01545.xopenalex-snapshot

Ectomycorrhizal networks and seedling establishment during early primary succession

inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02377.xopenalex-snapshot

Hydraulic redistribution of water from Pinus ponderosa trees to seedlings: evidence for an ectomycorrhizal pathway

inferredcites →https://doi.org/10.1139/b04-116openalex-snapshot

Mycorrhizal networks: a review of their extent, function, and importance

inferredcites →https://doi.org/10.1198/jasa.2002.s236openalex-snapshot

Analysis of Messy Data, Vol III: Analysis of Covariance

inferredcites →https://doi.org/10.1890/0012-9615(2002)072[0505:ioetom]2.0.co;2openalex-snapshot

INFLUENCES OF ESTABLISHED TREES ON MYCORRHIZAS, NUTRITION, AND GROWTH OF QUERCUS RUBRA SEEDLINGS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4816693openalex-extracted

Drivers of Natural Colonisation and Regeneration within Planted Woodlands: Towards an Integrated Approach to Increase Resilience

inferred← citeshttps://doi.org/10.1002/9781118314364.ch4openalex-snapshot

Mycorrhizal Networks and Seedling Establishment in Douglas‐Fir Forests

inferred← citeshttps://doi.org/10.1002/ecm.70032openalex-snapshot

Time will tell: The temporal and demographic contexts of plant–soil microbe interactions

inferred← citeshttps://doi.org/10.1002/hyp.14919openalex-snapshot

Soil moisture and temperature dynamics in juvenile and mature forest as a result of tree growth, hydrometeorological forcings, and drought

inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_5openalex-snapshot

Resource Transfer Between Plants Through Ectomycorrhizal Fungal Networks

inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_9openalex-snapshot

Experimentally Testing Effects of Mycorrhizal Networks on Plant-Plant Interactions and Distinguishing Among Mechanisms

inferred← citeshttps://doi.org/10.1007/978-981-13-6480-8_5openalex-snapshot

Exploring the Role of Mycorrhizae as Soil Ecosystem Engineer

inferred← citeshttps://doi.org/10.1007/978-981-16-8770-9_15openalex-snapshot

Ectomycorrhizal Networks and Silviculture in Mediterranean Forests

inferred← citeshttps://doi.org/10.1007/s00572-011-0406-yopenalex-snapshot

Mycorrhizal networks affect ectomycorrhizal fungal community similarity between conspecific trees and seedlings

inferred← citeshttps://doi.org/10.1007/s00572-015-0630-yopenalex-snapshot

Host and habitat filtering in seedling root-associated fungal communities: taxonomic and functional diversity are altered in ‘novel’ soils

inferred← citeshttps://doi.org/10.1007/s00572-018-0841-0openalex-snapshot

Ectomycorrhizal fungal communities in high mountain conifer forests in central Mexico and their potential use in the assisted migration of Abies religiosa

inferred← citeshttps://doi.org/10.1007/s10021-011-9502-2openalex-snapshot

Ectomycorrhizal Networks of Pseudotsuga menziesii var. glauca Trees Facilitate Establishment of Conspecific Seedlings Under Drought

inferred← citeshttps://doi.org/10.1007/s11027-025-10270-5openalex-snapshot

Potential of mycorrhizal fungi in soil C sequestration under climate change scenario: current research and prospects

inferred← citeshttps://doi.org/10.1007/s11258-018-0893-4openalex-snapshot

Effects of changes in soil moisture and precipitation patterns on plant-mediated biotic interactions in terrestrial ecosystems

inferred← citeshttps://doi.org/10.1007/s11258-021-01126-4openalex-snapshot

Friend or foe? The role of biotic agents in drought-induced plant mortality

inferred← citeshttps://doi.org/10.1007/s40502-019-00491-7openalex-snapshot

Interplant communication via hyphal networks

inferred← citeshttps://doi.org/10.1007/s40974-016-0038-3openalex-snapshot

Understanding the ecology of tree-seedling growth in dry tropical environment: a management perspective

inferred← citeshttps://doi.org/10.1016/b978-0-12-804312-7.00011-5openalex-snapshot

Integrating Ectomycorrhizas Into Sustainable Management of Temperate Forests

inferred← citeshttps://doi.org/10.1016/b978-0-12-804312-7.00017-6openalex-snapshot

Soil Water Retention and Availability as Influenced by Mycorrhizal Symbiosis

inferred← citeshttps://doi.org/10.1016/b978-0-12-804312-7.00018-8openalex-snapshot

Mycorrhizal Networks and Forest Resilience to Drought

inferred← citeshttps://doi.org/10.1016/b978-0-444-63865-6.00002-8openalex-snapshot

Soil–Plant–Atmosphere Interactions

inferred← citeshttps://doi.org/10.1016/j.envexpbot.2013.10.018openalex-snapshot

The role of ectomycorrhizas in heavy metal stress tolerance of host plants

inferred← citeshttps://doi.org/10.1016/j.envpol.2020.115711openalex-snapshot

Ecological consequences of space rocket accidents in Kazakhstan between 1999 and 2018

inferred← citeshttps://doi.org/10.1016/j.fbr.2012.01.001openalex-snapshot

Mycorrhizal networks: Mechanisms, ecology and modelling

inferred← citeshttps://doi.org/10.1016/j.foreco.2012.09.025openalex-snapshot

Seedling genetics and life history outweigh mycorrhizal network potential to improve conifer regeneration under drought

inferred← citeshttps://doi.org/10.1016/j.foreco.2018.09.007openalex-snapshot

Tamm Review: Reforestation for resilience in dry western U.S. forests

inferred← citeshttps://doi.org/10.1016/j.foreco.2022.120270openalex-snapshot

Growth and spatial patterns of natural regeneration in Sierra Nevada mixed-conifer forests with a restored fire regime

inferred← citeshttps://doi.org/10.1016/j.foreco.2022.120584openalex-snapshot

Tamm review: Forest understorey and overstorey interactions: So much more than just light interception by trees

inferred← citeshttps://doi.org/10.1016/j.foreco.2024.121981openalex-snapshot

Site conditions shaped the effect of silvicultural management on the biodiversity of ectomycorrhizal fungi in mixed Nothofagus forests

inferred← citeshttps://doi.org/10.1016/j.funeco.2014.01.005openalex-snapshot

Mycorrhizal fungi mediation of terrestrial ecosystem responses to global change: mini-review

inferred← citeshttps://doi.org/10.1016/j.funeco.2015.05.011openalex-snapshot

Ectomycorrhizal fungal communities in Nothofagus nervosa ( Raulí ): A comparison between domesticated and naturally established specimens in a native forest of Patagonia, Argentina

inferred← citeshttps://doi.org/10.1016/j.funeco.2021.101117openalex-snapshot

Host phylogeny is the primary determinant of ectomycorrhizal fungal community composition in the permafrost ecosystem of eastern Siberia at a regional scale

inferred← citeshttps://doi.org/10.1016/j.gecco.2020.e01352openalex-snapshot

Potential role of common mycorrhizal networks in improving plant growth and soil physicochemical properties under varying nitrogen levels in a grassland ecosystem

inferred← citeshttps://doi.org/10.1016/j.ppees.2016.01.004openalex-snapshot

Soil fungi promote nitrogen transfer among plants involved in long-lasting facilitative interactions

inferred← citeshttps://doi.org/10.1016/j.rhisph.2017.09.004openalex-snapshot

Xerotolerance of Penicillium and Phialocephala fungi, dominant taxa of fine lateral roots of woody plants in the intermountain Pacific Northwest, USA

inferred← citeshttps://doi.org/10.1038/s41559-023-01986-1openalex-snapshot

Positive citation bias and overinterpreted results lead to misinformation on common mycorrhizal networks in forests

inferred← citeshttps://doi.org/10.1038/s41598-023-41191-5openalex-snapshot

Benefits of symbiotic ectomycorrhizal fungi to plant water relations depend on plant genotype in pinyon pine

inferred← citeshttps://doi.org/10.1080/17429145.2025.2548579openalex-snapshot

Kin recognition in plants-an ecological perspective: an overview of plant kin recognition under different resources, consequences and future challenges

inferred← citeshttps://doi.org/10.1080/17550874.2017.1283649openalex-snapshot

Testing the importance of a common ectomycorrhizal network for dipterocarp seedling growth and survival in tropical forests of Borneo

inferred← citeshttps://doi.org/10.1093/aobpla/plv050openalex-snapshot

Inter-plant communication through mycorrhizal networks mediates complex adaptive behaviour in plant communities

inferred← citeshttps://doi.org/10.1111/1365-2745.13507openalex-snapshot

Beyond seedlings: Ectomycorrhizal fungal networks and growth of mature Pseudotsuga menziesii

inferred← citeshttps://doi.org/10.1111/1365-2745.13986openalex-snapshot

Spatial turnover of fungi and partner choice shape mycorrhizal networks in epiphytic orchids

inferred← citeshttps://doi.org/10.1111/1462-2920.12741openalex-snapshot

Whose truffle is this? Distribution patterns of ectomycorrhizal fungal diversity in T uber melanosporum brûlés developed in multi‐host M editerranean plant communities

inferred← citeshttps://doi.org/10.1111/nph.13360openalex-snapshot

Local adaptation in migrated interior Douglas‐fir seedlings is mediated by ectomycorrhizas and other soil factors

inferred← citeshttps://doi.org/10.1111/nph.13797openalex-snapshot

Stable isotope probing implicates a species of C ortinarius in carbon transfer through ectomycorrhizal fungal mycelial networks in A rctic tundra

inferred← citeshttps://doi.org/10.1111/nph.14325openalex-snapshot

Transfer of 13C between paired Douglas‐fir seedlings reveals plant kinship effects and uptake of exudates by ectomycorrhizas

inferred← citeshttps://doi.org/10.1111/pce.15508openalex-snapshot

Arbuscular Mycorrhizal Fungi Boost Development of an Invasive Brassicaceae

inferred← citeshttps://doi.org/10.18845/tm.v33i4.4601openalex-snapshot

Internet de las plantas: comunicación a través de la red micorrízica

inferred← citeshttps://doi.org/10.3184/003685017x14968299580423openalex-snapshot

The Whispering World of Plants: ‘The Wood Wide Web’

inferred← citeshttps://doi.org/10.3389/ffgc.2020.620436openalex-snapshot

Partial Retention of Legacy Trees Protect Mycorrhizal Inoculum Potential, Biodiversity, and Soil Resources While Promoting Natural Regeneration of Interior Douglas-Fir

inferred← citeshttps://doi.org/10.3389/ffgc.2022.995487openalex-snapshot

Restoring bigcone Douglas-fir post-fire in drought-stricken Southern California: Assessing the effects of site choice and outplanting strategies

inferred← citeshttps://doi.org/10.3389/ffgc.2024.1512518openalex-snapshot

Opinion: Response to questions about common mycorrhizal networks

inferred← citeshttps://doi.org/10.3389/ffunb.2021.735299openalex-snapshot

Common Mycorrhizae Network: A Review of the Theories and Mechanisms Behind Underground Interactions

inferred← citeshttps://doi.org/10.3389/fmicb.2024.1183024openalex-snapshot

Common mycorrhizal network: the predominant socialist and capitalist responses of possible plant–plant and plant–microbe interactions for sustainable agriculture

inferred← citeshttps://doi.org/10.3389/fpls.2018.00626openalex-snapshot

Alternaria Brassicae Induces Systemic Jasmonate Responses in Arabidopsis Which Travel to Neighboring Plants via a Piriformsopora Indica Hyphal Network and Activate Abscisic Acid Responses

inferred← citeshttps://doi.org/10.3389/fpls.2022.840343openalex-snapshot

A Database on Mycorrhizal Traits of Chinese Medicinal Plants

inferred← citeshttps://doi.org/10.3389/frmbi.2024.1331341openalex-snapshot

Utilizing symbiotic relationships and assisted migration in restoration to cope with multiple stressors, and the legacy of invasive species

inferred← citeshttps://doi.org/10.3390/fire9060234openalex-snapshot

Scars on the Steppe: A Comparative Analysis of Soyuz First Stage and Abort Mode Impacts on Arid Ecosystems in Kazakhstan at 2024

inferred← citeshttps://doi.org/10.3390/ijms241612628openalex-snapshot

Variability of Functional Groups of Rhizosphere Fungi of Norway Spruce (Picea abies (L.) H.Karst.) in the Boreal Range: The Wigry National Park, Poland

inferred← citeshttps://doi.org/10.3390/ijpb14030060openalex-snapshot

Effects of Biochar on Drought Tolerance of Pinus banksiana Seedlings

inferred← citeshttps://doi.org/10.3390/microorganisms7120586openalex-snapshot

Root-Associated Fungal Communities in Two Populations of the Fully Mycoheterotrophic Plant Arachnitis uniflora Phil. (Corsiaceae) in Southern Chile

inferred← citeshttps://doi.org/10.3390/microorganisms8020230openalex-snapshot

Formation of Common Mycorrhizal Networks Significantly Affects Plant Biomass and Soil Properties of the Neighboring Plants under Various Nitrogen Levels

inferred← citeshttps://doi.org/10.64898/2026.05.07.723550openalex-snapshot

Ectomycorrhizal networks propagate carbon deficit and drought stress among trees

inferred← citeshttps://doi.org/10.70675/15f32752za04dz46adz8598z70a702c527faopenalex-snapshot

Symbioses mycorhiziennes des orchidées épiphytes

inferred← citeshttps://doi.org/10.70675/5f5df32bz7eafz4a0bzad93z88b5e81a9bebopenalex-snapshot

Développement racinaire du hêtre (fagus sylvatica) en interaction avec d'autres espèces forestières et en fonction de la disponibilité en eau. Conséquences sur la croissance et le fonctionnement hydrique et carbone.

inferred← citeshttps://doi.org/10.70675/ea2c67fczb9bfz4354zb36czf16fbcc1e257openalex-snapshot

Interactions biotiques et biologie reproductive de la Truffe noire, Tuber melanosporum (Vittad.) : des truffières spontanées aux plantations

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.