In this paper, we present the morphology, taxonomy, anatomy, and palynology of Papaver somniferum. A detailed morphological description and illustrations of the species are provided, along with information about the identification, distribution, cultivation areas, habitats, pollinators, specimens examined, growing periods, phenology, etymology, vernacular name, and uses. The species can be characterized as a glabrous and glaucous herb with unlobed or pinnately lobed leaves, and an amplexicaul base; variations in color and morphological characteristics of petals; and white filaments, occasionally purple with a white basal part, broadened at the apical part. Two rings of discontinuous and widely spaced collateral vascular bundles are recognized in the transverse section of the stems. The shape of epidermal cells on the adaxial surface is polygonal, while that on the abaxial surface is polygonal or irregular. The anticlinal cell walls of the epidermal cells on the adaxial surface are straight or slightly curved, while those on the abaxial surface are straight, slightly curved, sinuate, or strongly sinuate. The stomata are anomocytic and are confined to the lower epidermis. The stomatal density is 54–199/mm² (with a mean of 89.29 ± 24.97). The mesophyll is not distinctly differentiated into palisade and spongy regions. Laticifers are found in the phloem areas of the stems and leaves. The pollen grains can be spheroidal or prolate spheroidal in shape, sometimes oblate spheroidal [polar axis (P) diameter/equatorial axis (E) diameter ratio = 0.99–1.12 (with a mean of 1.03 ± 0.03)]. The pollen aperture is tricolpate and the exine sculpturing is microechinate.

In this paper, we present the morphology, taxonomy, anatomy, and palynology of Arundo donax. A detailed morphological description and illustrations of the species are provided, along with information about the identification, distribution, the specimens examined, habitat and ecology, the International Union for Conservation of Nature (IUCN) conservation assessment, phenology, etymology, vernacular name, and uses. The species can be distinguished by its large, tall rhizomatous perennial reed; cauline leaves; an open, large, plumose panicle inflorescence; subequal glumes as long as the spikelets; glabrous rachilla; all bisexual florets; and a lemma with a straight awn and with long white hairs outside below the middle part. In this study, two names were lectotypified: Arundo bifaria and A. bengalensis, which are synonyms of A. donax. The culm internodes in the transverse section have numerous vascular bundles scattered in the ground tissue, and the parenchyma cells have significantly lignified cell walls. Vascular bundles are composed of phloem and xylem and are enclosed in a continuous sclerenchymatous bundle sheath. The chloroplasts in the transverse section of the leaf blades are found only in the mesophyll cells but are absent in the bundle sheath cells, which indicates that it is a C3 grass. The leaves have stomata on both surfaces and are confined to the intercostal zones. The stomata are typically paracytic, with two lateral subsidiary cells placed parallel to the guard cells. The stomatal density is higher on the abaxial surface [450–839/mm² (606.83 ± 72.71)] relative to the adaxial surface [286–587/mm² (441.27 ± 50.72)]. The pollen grains are spheroidal or subspheroidal [polar axis length/equatorial axis length ratio (P/E ratio) = 0.89–1.16 (1.02 ± 0.07)] with a single pore surrounded by a faint annulus, and the exine sculpturing is granular.

Rattans of the genus Korthalsia are ecologically and economically important non-timber forest resources in Southeast Asia, yet their conservation is limited by knowledge of species-specific distribution patterns and environmental constraints. We modeled the potential distributions of four Korthalsia species (K. flagellaris, K. laciniosa, K. rigida, and K. scortechinii) using species distribution models (SDMs). Models were fitted in R using the sdm package, and ensemble maps were generated by combining predictions from Random Forest (RF), Generalized Linear Models (GLMs), Generalized Additive Models (GAM), and GLMnet. The top predictors influencing habitat distribution included soil physical structure, atmospheric moisture demand, and canopy light availability. The dominance of these factors reflects three distinct and non-interchangeable environmental axes that regulate belowground moisture dynamics, atmospheric constraints on gas exchange, and the energetic requirements for recruitment. All four species ensemble models significantly outperformed the null model, and spatial block cross-validation (k = 5, 200 km blocks) indicated a marginal drop in area under the curve (AUC) values, confirming a predictive signal under geographically independent evaluation. Ensemble suitability maps identified Peninsular Malaysia, Borneo, and Sumatra as centers of predicted habitat. Core habitat was estimated to be less than 0.6% of total suitable area for all species, ranging from 980 km² (K. scortechinii) to 19,256 km² (K. rigida), with anthropogenic modification exceeding 50% in the core habitat in K. flagellaris and K. rigida. These results provide the first species-specific baseline for these Korthalsia across Southeast Asia, supporting more targeted conservation and restoration planning under varying habitat constraints.