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Knowledge about the biogeographic affinities of the world’s tropical forests helps to better understand regional differences in forest structure, diversity, composition, and dynamics. Such understanding will enable anticipation of region-specific responses to global environmental change. Modern phylogenies, in combination with broad coverage of species inventory data, now allow for global biogeographic analyses that take species evolutionary distance into account. Here we present a classification of the world’s tropical forests based on their phylogenetic similarity. We identify five principal floristic regions and their floristic relationships: (i) Indo-Pacific, (ii) Subtropical, (iii) African, (iv) American, and (v) Dry forests. Our results do not support the traditional neo- versus paleotropical forest division but instead separate the combined American and African forests from their Indo-Pacific counterparts. We also find indications for the existence of a global dry forest region, with representatives in America, Africa, Madagascar, and India. Additionally, a northern-hemisphere Subtropical forest region was identified with representatives in Asia and America, providing support for a link between Asian and American northern-hemisphere forests.
Twenty-one species of Mysidae were sampled by three ANDEEP expeditions to the Southern Ocean with epibenthic sledges dragged over the deep-sea floor in the realm of 58–71° S and 00–65° W, depth 774–5190 m. Previously known ranges are significantly extended southward for four species and to greater depth in the same four species plus two other species. Supplementary descriptions are given for Amblyops tattersalli and Dactylamblyops murrayi, and a first description of a (subadult) male for Thalassomysis tattersalli. The definitions of the genera Amphiakrops gen. nov., Chelamblyops gen. nov., Desmocornea gen. nov. and Schizurakrops gen. nov. are mainly based on the structure of the eyes as well as of the antennal peduncle, chelate second thoracic endopod and telson. These structures are also important for the descriptions of Amblyops arianii sp. nov., A. bipapillatus sp. nov., Amblyopsoides fenestragothica sp. nov., A. lepidophthalma sp. nov., Amphiakrops brandtae gen. et sp. nov., Dactylamblyops benthophilus sp. nov., Desmocornea subchelata gen. et sp. nov., Paramblyops petrescui sp. nov., Schizurakrops meesi gen. et sp. nov., Scolamblyops muehlenhardtae sp. nov., Stellamblyops doryphorus sp. nov. and Mysidella antarctica sp. nov. Six previously described taxa are recombined as Amblyopsoides laticauda comb. nov., Amphiakrops bidigitatus comb. nov., A. japonicus comb. nov., Chelamblyops globorostris comb. nov., Meierythrops tattersalli comb. nov. and M. triangulatus comb. nov. One species is revised back to the initial combination as Dactylamblyops japonicus. All except one (Mysidella antarctica sp. nov.) newly described (12), newly recombined (6) or back-combined (1) species belong to the Erythropinae. Keys to the resulting 61 genera and 263 species of Erythropinae and 18 species of Mysidellinae are given at the world-wide scale. Ocular papillae with a terminal pore (sensory pore organ) are recorded in nine ANDEEP species. The organ of Bellonci is identified on the reduced eyes in 16 species, among which D. subchelata gen. et sp. nov. has many ommatidia arranged in a self-contained ribbon which shows a banded rhabdom only in non-adults. Reduction of visual elements together with shrinking of ocular papillae during ontogenetic development suggest that non-adults of D. subchelata and T. tattersalli stay in the photic zone for feeding and growth and then descend only once during their lifetime to the abyss for reproduction.
Three species of Lophogastrida and eight Mysida are documented for samples from 5161–5497 m bottom depth in the Angola Basin. Previously known latitudinal ranges are extended southward for five species, and bathymetric ranges extended beyond 5000 m for six species. Upon revision of the subfamily Petalophthalminae (Mysidae), four species previously attributed to the genus Petalophthalmus are integrated into Ipirophthalmus gen. nov. as I. liui gen. et comb. nov., I. caribbeanus gen. et comb. nov., I. oculatus gen. et comb. nov., and I. macrops gen. et comb. nov., mainly based on the structure of eyes and presence of setae on the telson. Petalophthalmus cristatus sp. nov. is described based on its reduced cornea and the structure of eyestalks, rostrum, mandibles, and telson. The structure of mouthparts, foregut and maxillipeds suggests an omnivorous mode of life. The diagnosis of the tribe Calyptommini (Mysidae: Erythropinae) is widened to cover the 3-segmented, uniramous fourth male pleopod and the non-incised eyeplate with horn-like rudiments of eyestalks in Abyssomysis cornuta gen. et sp. nov. The structure of mandibles, foregut, and second maxilliped suggest detritus feeding in this species. Keys to the Calyptommini and Petalophthalminae are given.
Revised definitions are given for the genus Mysidium Dana, 1852, and its eight previously known species, based on material from Curaçao, Bonaire and SE-Brazil, along with the evaluation of published data. Type material of Diamysis columbiae Zimmer, 1915, M. cubanense Băcescu & Ortiz, 1984 and M. rubroculatum Băcescu & Ortiz, 1984 is examined. A lectotype is designated for D. columbiae Zimmer, 1915, a senior synonym of Mysidium columbiae (Zimmer, 1915). Two new species are described, M. triangulare Wittmann sp. nov. from Curaçao and M. antillarum Wittmann sp. nov. from Curaçao and Bonaire. Known ranges are extended by first records of M. cubanense from Curaçao and Bonaire and of M. integrum W.M. Tattersall, 1951 from SE Brazil. Three morphologically different groups are established at the subgeneric level: (1) the nominotypical subgenus Mysidium Dana, 1852 with M. gracile (Dana, 1852), M. integrum, M. cubanense, M. rubroculatum and M. triangulare sp. nov. from the West Atlantic plus M. rickettsi Harrison & Bowman, 1987 from the East Pacific; (2) Occimysidium Wittmann subgen. nov. represented only by M. pumae Ortiz, Hendrickx & Winfield, 2017 from the Pacific coast of Mexico; and finally (3) Orientomysidium Wittmann subgen. nov. comprising M. columbiae and M. antillarum sp. nov. from the West Atlantic. The poorly known M. iliffei Băcescu, 1991 is not assigned to any subgenus. A key to the resulting three subgenera and ten nominal species of the genus Mysidium is given.
Four new species of the subgenus Heteromysis (Olivemysis) were detected in material from (sub)-tropical aquaria in six public aquarium institutions around the globe. Modifications of pleopods by spines represent the strongest structural complex used for differentiation within this subgenus: male pleopods 1–4 modified in H. smithsoniana sp. nov., male pleopods 2–4 plus female pleopod 2 in H. hornimani sp. nov. and H. waikikensis sp. nov. Additional important diagnostic characters are provided by the antennulae, uropods, and telson. The male of H. sixi sp. nov. represents a very rare case within the genus Heteromysis by having only pleopod 2 modified by flagellate spines. The definition of the subgenus Olivemysis is modified in order to include H. sixi sp. nov. A summary of pleopod modifications in the genus Heteromysis and a key to the species of the subgenus Olivemysis are given. The here described new taxa more than double the number of Heteromysis species known from aquaria yet unknown in nature from three to seven.