Response of Growth Dynamics of Two Spring Geophytes to Light Regime in a Lime-Beech Forest

Blomaee accumulation, leaf longevity and growth rate of two spring forest geophytes, Scllla blfolla L. and Arum maculatum L. were estimated separately for three size groups within each population of these species. Despite the differences in leaf longevity, both species showed a similar pattern of blomass accumulation In relation to their phenologles and reproductive demands. Eco-physlological acclimation to changing light environment was assumed through photosynthetic parameters and dynamics of leaf area Index In the predominant size group of each species. A light response curve was measured under natural light for each species through the continuum of Its phenology to quantify the photosynthetic photon flux density at light saturation, light-saturated photosynthetic rate, light compensation point, and dark respiration. Light-saturated assimilation per leaf area basis, dark respiration rate and light compensation points were significantly higher in S. blfolla relative to A. maculatum. However, the acclimation of photosynthesis that would respond to light changes in environment was not found in S. bifolla. In contrast, In A. maculatum a marked shift In the light dependence of photosynthesis through the season was noticed, which resulted In a strong photosynthetic acclimation to the low-light conditions. Accompanied by significant leaf area Index, this efficient low-light photosynthesis enabled greater leaf longevity, and consequently longer accumulative period to A. maculatum. From the different parameters that we determined （both photosynthetic acclimation and growth strategy） it would appear that these species belong to two distinct subgroups： S. blfolla to the early and A. maculatum to the late vernals.

Understorey species distinguish late successional and ancient forests after decades of minimum human intervention: A case study from Slovenia

The main species composition drivers in temperate deciduous forests are environmental conditions, a stand?s age and the site history, e.g., the succession stage and past land use, as well as disturbance regime and current management. We compared plant species diversity and composition in late successional and ancient forests, cooccurring on the same small river island applying species accumulation curves and nonmetric multidimensional scaling, respectively. Given the island?s geomorphological characteristics, we expected these to be very similar before human intervention in the past. The forests experienced differing disturbance regimes in the past, while over the last 30 years, human intervention has been the same and reduced to a minimum. The ancient forest in this study had two major characteristics defining it as old, mature forest: continuity of presence for more than 200years and specific composition. The late successional forest experienced major disturbance in the 20th century and was allowed natural regeneration by bordering on the ancient forest, representing a potential species pool,and by decades of minimum human intervention. Our results showed that, even though there was no difference in species richness, we could still detect differences between the forests, particularly in the abundance and species composition of the understorey, among which geophytes had the most indicative importance. To make our results useful on a broader scale, we composed from the literature a species list of plants indicative for ancient forest and tested its application. These results are important for distinguishing between old and mature secondary stands and particularly for identifying old forest stands, which should be conserved and, in the case of fragmented landscapes, included in a network connecting forest fragments.

Phylogenetic endemism of the orchids of Megamexico reveals complementary areas for conservation

Orchid diversity provides a unique opportunity to further our understanding of biotic and abiotic factors linked to patterns of richness,endemism,and phylogenetic endemism in many regions.However,orchid diversity is consistently threatened by illegal trade and habitat transformation.Here,we identified areas critical for orchid conservation in the biogeographic province of Megamexico.For this purpose,we evaluated orchid endemism,phylogenetic diversity,and phylogenetic endemism within Megamexico and characterized orchid life forms.Our results indicate that the majority of the regions with the highest estimates of endemism and phylogenetic endemism are in southern Mexico and northern Central America,mostly located on the Pacific side of Megamexico.Among the most important orchid lineages,several belong to epiphytic lineages such as Pleurothallidinae,Laeliinae and Oncidiinae.We also found that species from diverse and distantly related lineages converge in montane forests where suitable substrates for epiphytes abound.Furthermore,the southernmost areas of phylogenetic diversity and endemism of Megamexico are in unprotected areas.Thus,we conclude that the most critical areas for orchid conservation in Megamexico are located in southern Mexico and northern Central America.We recommend that these areas should be given priority by the Mexican system of natural protected areas as complementary conservation areas.

Nutrient Accumulation in Amaryllis

Amaryllis plants (Hippeastrum hybrid, in the family Amaryllidaceae) are cultivated in Brazil mainly for bulb export. Studies about the nutrient accumulation dynamics by the species are yet incipient when considering Brazilian cultivation conditions. The objective was to determine the nutrient accumulation in amaryllis “Orange Souvereign” cultivated in the field. The experimental design was entirely randomized with four replications and 14 collection periods (at 30, 60, 90, 120, 150, 180, 210, 240, 270, 300, 330, 360, 390, and 420 days after planting). Sampled plants were divided into leaves, bulb, and roots, which were used for determination of nutrient accumulation by leaves (aerial part) and bulb + roots (underground part). Nutrient accumulation of N, P, K, Ca, Mg, S, B, Cu, Fe, Mn, and Zn was calculated for each collection period, and then represented by curves of macro and micronutrient accumulation, as well as accumulation percentages for each plant part. For most macro and micronutrients, the interval of maximum accumulation fell from 301 to 420 days after planting, matching with the cycle final stage of plants cultivated in the field. Accumulated macronutrients by amaryllis plants along the cultivation cycle was, in g·plant-1: 1.57 N;0.19 P;2.58 K;0.64 Ca;0.20 Mg;and 0.29 S, following the descending order: K > N > Ca > S > Mg > P. Accumulated micronutrients, in mg·plant-1, was: 2.18 B;1.17 Cu;22.33 Fe;2.19 Mn;and 4.09 Zn, following the descending order: Fe > Zn > Mn > B > Cu.