Roxy
Modern
Thybrid
T.A.L.K.
Top flavors
earthyspicycitrus
Terpenes
CalmingEnergizing
T.A.L.K. effects are mostly calming.
T.A.L.K.
T.A.L.K. is a modern hybrid cannabis strain derived from European hybrid genetics. Designed for domestic cultivation, this variety reaches maturity with a 55-day flowering cycle and is suitable for both indoor and outdoor environments. Growers can expect a high yield from this plant, though its cultivation difficulty is classified as moderate, requiring consistent maintenance to ensure optimal development.
The aromatic profile of T.A.L.K. is defined by its primary terpene, myrcene, which provides the base for the strain’s sensory experience. This is complemented by secondary caryophyllene and tertiary limonene, creating a nuanced chemical profile that reflects its modern genetic composition. These terpenes work in concert to define the specific olfactory and flavor properties characteristic of the strain.
Users of T.A.L.K. typically experience effects characterized as relaxed, happy, and uplifted. This THC-dominant profile makes the strain well-suited for addressing common use cases including the management of stress, pain, and sleep difficulties. The genetic impact of the strain is evidenced by its notable offspring, which include Cookie Slush and Sour Time.
Terpene Profile
Synergies (+) and conflicts (−) are relative to each other within this profile.
myrcene ~60%caryophyllene ~28%limonene ~12%
| Terpene | Share | Character | Likely role |
|---|---|---|---|
| myrcene | ~60% | earthy | relaxing · solo |
| caryophyllene | ~28% | spicy | relaxing · social |
| limonene | ~12% | citrus | social · creative |
Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.
Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.
~28%
spicy
●●○○
Russo 2011: only terpene that is a selective full CB2 agonist (100 nM); Gertsch et al. 2008: acts as dietary cannabinoid; unique anti-inflammatory and gastric cytoprotective properties.
Russo 2011: increases serotonin in prefrontal cortex + dopamine in hippocampus via 5-HT1A; Johns Hopkins 2024: significantly reduced anxiety vs THC alone.
Effects
Reported effects — derived from terpene chemistry and cannabinoid profile.
◎
relaxed
eveningPrimary endpoint of myrcene+linalool sedating combinations; GABA modulation is the dominant mechanistic driver.
◉
happy
anytime△
uplifted
morningLimonene anxiolytic/antidepressant via serotonin elevation in prefrontal cortex (Russo 2011); mood improvement without full euphoria; key for balanced-1-1 profiles.
Genetic Profile
Balanced Hybrid
■ Indica 50%■ Sativa 50%
Equal indica and sativa genetics. Balanced body and mind effects.
THC-Dominant
High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.
Genealogy
Parentage, ancestry, and genetic relatives of T.A.L.K..
Ancestry
Grandparents
Arcadian
myrcene· relaxed· happy
Aurora B
myrcene· relaxed· happy
Indica / Sativa
myrcene· relaxed· happy
▾
Siblings
Share parent europe hybrid
Offspring — 1 strains bred from T.A.L.K.
Composite Traits
Where to buy T.A.L.K.
No verified dispensaries on file — find it on Leafly.
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What would T.A.L.K. × ? produce?
Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.
Build a cross with T.A.L.K. →Similar strains
Same primary terpene with overlapping effects.
Frequently Asked Questions
Is T.A.L.K. indica or sativa?
T.A.L.K. is modeled here as a balanced hybrid (equal indica and sativa genetics).
What terpene is dominant in T.A.L.K.?
Myrcene is shown as the dominant terpene at approximately ~60%. Caryophyllene follows as the secondary terpene.
Is T.A.L.K. good for daytime use?
T.A.L.K. is versatile and works across different times of day depending on dose and individual response.
How accurate is this data?
See the "Data confidence" card in the sidebar. Terpene profiles and effects are chemistry-informed estimates — individual responses depend on phenotype, source, and personal chemistry.