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Since the set of MANs is empty, then for every leaf of the tree the sequence of nodes determined by following arrows is well defined.
When MRT was determined for every leaf cohort (Table 7), early cohorts always had a longer MRT in the open stand in all leaf variables except leaf N.
For every leaf label w such that (w, S ∩ y ) ∈ E T y. prunerList and (w, S ∩ z ) ∈ E T z. prunerList exist, E T yz.
Thus: for every leaf ℓ ∈ { ℒ S c ∖ ℒ X c }, T x ℓ exists, thus, for every pair of leaves { x1, x2} in X c, [ x1, x2, ℓ] is an agreement triplet.
for every { a, b } ∈ { ℒ S c ∖ ℒ T xy } and for every leaf ℓ in T x y, there exists an AST on leaf set ℒ E c ∪ { x, a, b }, thus, [ ℓ, a, b] is an agreement triplet.
for every pair of leaves { a, b } ∈ { ℒ S c ∖ ℒ X c }, there exists an AST on leaf set ℒ E c ∪ { x, a, b }, thus, for every leaf ℓ in X c, [ ℓ, a, b] is an agreement triplet.
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Behavioral studies have shown that M. microtis hunts by flying up and down the vegetation thereby checking every leaf for potential prey [30].
All determination work was conducted at room temperature 3 h after the plants were adapted to the dark condition, and repeat for every 5 7 (each leaf of the seeding repeats once).
For every root and leaf samples, we analyzed four different spots.
Physiological trait abbreviations are: PLHT for plant height, STEM for stem diameter, LNO for leaf number, LDW for leaf dry weight, RDW for root dry weight.
In a randomized block design, we counted necrotic zones every 200 μm for 10 leaf pieces.
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