Jacob's Cheeselets Snacks Sharing Tub, 280g

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Calyx with appendages greater than or equal to 0.25 mm long, the rim rarely undulate, lobed or torn Flowering calyx with rim 0.5 to 1 mm long, the appendages 0.25–11 mm long, free at their bases, not forming a continuous shelf of tissue; Mexico and Central America, 350–3000 m The treelet algorithm is a binary agglomerative hierarchical clustering algorithm. In terms of a hierarchical graph only, the two most correlated nodes are combined at a given step. For an n by p data matrix, there are total p– 1 layers for a graph combined to completion. The binary combination allows for the multi-resolution interpretability of the resulting basis. At each node a principal components analysis is applied to the pair of variables. The node is then represented by the two components, the first component becoming a “sum” variable, and the second the “difference” variable. Since only the sum variable is allowed to combine in higher levels of the graph, the difference variable remains behind as a residual measure of the combination. Each treelet, comprised of one node (sum variable) and its associated difference variables can be represented by a orthonormal basis.

Calyx teeth at anthesis lax or slightly spreading, not widely spreading or reflexed; corolla lobes usually noticeably pubescent abaxially; first sympodial unit poorly developed above ground, the plant body often prostrate; rare species of the Sierra de Nanchititla (state of México) Lycianthes somniculenta (Kunze ex Schltdl.) Bitter var. cladotricha Bitter, Abh. Naturwiss. Verein Bremen 24 [preprint]: 413. 1919. Type: Mexico. Morelos: Cuernavaca, in moist copses, 5000 ft, Jun–Jul 1896, C. Pringle 6399 (lectotype designated by Dean 2004 pg. 395: MEXU [00029023]; isolectotypes: B [not seen, cited by Bitter 1919, probably destroyed], BM [000514912], BR [000000552840], E [E00570140], G [G00343072, G00343073], GH [00021855], GOET [GOET003441, GOET003440], HBG [HBG-511362], JE [JE00004691], K [K000063119], M [M-0166091], MEXU [00029022, 00029023], MO [MO-153222], NDG [NDG45130], NY [00138707], PH [00016314], S [S-G-9982], UC [104211], W [acc. # 1897-4064], WRSL [cited by Bitter 1919, not seen], WU [acc. # 037953], Z [Z-000028495]). Calyx usually nearly glabrous, the calyx appendages less than 2 mm long in flower, less than 3 mm long in fruit; plants glabrous to sparsely pubescent, the trichomes less than 1 mm long; mature berry dark purple (if fruit not present, also try 19b); greater than 1000 m in elevation

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The sympodial units of Lycianthes terminate in inflorescences. The majority of inflorescences are located on the upper sympodia and appear axillary. The peduncle in most Lycianthes is reduced and usually not visible, resulting in an umbellate inflorescence of one to many pedicelled flowers; in a minority of species (e.g. L. amatitlanensis, L. nitida), a short peduncle is present, often covered with the many pedicel scars of fallen flowers. In a minority of the species, the inflorescence is always a solitary flower (e.g. all the herb species of series Meizonodontae, L. stephanocalyx, L. textitlaniana, L. amatitlanensis, L. gorgonea); all the other species can have one to many flowers. However, usually only one to a few flowers at a time are present at a single axil. Shrub to large vine to 10 m tall; trichomes tan, yellow, or red-brown, simple to furcate, 1–4 mm long; calyx often densely pubescent, the appendages in flower 7–17 mm long; mature berry 15–30 mm in diameter Leaf blades glabrous to pubescent, but trichomes not restricted to the axils where the primary veins meet the midvein on the abaxial side; stamens equal or unequal in length

Filaments glabrous; exocarp of berry green; placental area green and juicy; disturbed clearings and agricultural fields of mountains of state of Oaxaca Larger leaf blades 3–13 × 2–5 cm, the abaxial side obscured by a dense tomentum of overlapping, short-stalked, white to tan, stellate or multangulate-stellate trichomes less than 0.25 mm in diameter; calyx 2.5–4.5 mm long in flower, 6–8 mm in diameter in fruit; anthers 3–4 mm long Leaf blades glabrous and shiny on both sides, rarely with a few appressed-ascending trichomes to 0.25 mm long; corolla stellate in outline, adaxially white with yellow-green or purple markings near the base; anthers yellow, the connective usually dark in color Terborgh J, Huanca Nuñez N, Alvarez Loayza P, Cornejo Valverde F. Terborgh J, et al. Ecology. 2017 Nov;98(11):2895-2903. doi: 10.1002/ecy.1991. Epub 2017 Sep 25. Ecology. 2017. PMID: 28833033 BT - Proceedings of the Eleventh International Conference on Artificial Intelligence and StatisticsThe color of the corollas of Lycianthes included here range from white to purple on the adaxial side; the abaxial side may be the same color as the adaxial side, or the lobes may be green. As described elsewhere ( Dean 2004; Dean et al. 2017a, 2019b), many Lycianthes have darker-colored markings on the adaxial side of the corolla. These markings range from purple stripes on the lobes, to a ring of purple color at the base, or green or yellow patches of color on the lobes (Fig. ​ (Fig.4 4). Shrub, sometimes scandent, to 5 (7) m tall; trichomes white, off-white, tan, light yellow, brown or light purple, but never red-brown, simple, to 2.5 mm long; calyx glabrous to densely pubescent, the appendages in flower 0.5–9 mm long; mature berry less than 15 mm in diameter Plant with obvious glandular trichomes (to 1 mm long or more), at least on the pedicels and/or calyx, sometimes also on the leaves and stem In terms of a clustering algorithm, we applaud the authors for having a well defined goal: estimation of the true correlation matrix. Generally cluster analysis, though built from localized structure, does not identify that as its far-reaching goal leaving consistency theory nonexistent. We would like to point out that in terms of clustering, a particular consistency theory for the estimation of the mean and covariance matrix based on Bernstein’s inequality, as well as the sensitivity and reproducibility of the estimate based on bootstrap resampling, was presented in van der Laan and Bryan (2001) and subsequent articles.