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The sebastine rosefishes (Helicolenus), found in both the northern Atlantic and Pacific oceans, have morphological affinities with the subfamily Scorpaeninae.
The attribution to crayfishes is based on their association and morphological affinities with the crayfish fossil burrows L. baqueroensis from the same geologic units.
While Paleoamericans show strong morphological affinities with Australo-Melanesians, Amerindians are clearly associated with East Asians.
However, Johnson [ 29] found morphological affinities with other groups (non haemulids), such as the rugosity on the frontal bone surface similar to a few apogonids, bramids, and serranids as well as to Acanthocepola Lobotes Pseudopentaceros and Sphyraenops, and the shape of the spine-like crest that projects beyond the posterior margin of the cranium that is well-developed in preflexion larvae.
Previous suggestions have included Sudan or the Arabian Peninsula, based on morphological affinities with Arabian species [ 55] and even further afield in the Canary Islands, Cape Verde Islands, Madeira or Spain [ 3], which could be explained by naturalised populations, introduced via ancient trade routes, being mistaken for indigenous elements of the flora.
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Although the microscopic males are provided with chaetae on the posterior portion of the body, the females have no opisthosome, which makes the morphological affinity with annelids more difficult to recognize.
Platykotta akaina, with a possibly squat-lobster-like body form, dates back to the Late Triassic (~201.6-228 MYandand has strong morphological affinity with the superfamilies Chirostyloidea and Galatheoidea.
The last hypothesis seemed the most likely, because her closest morphological affinities were with the insect world.
Magnesium ions have been introduced to increase the physicochemical, structural, and morphological affinities of the composite with natural bone (Serre et al. [1998]).
The Harpacteinae fossil genus Dasumiana Wunderlich, 2004 from Eocene Baltic amber [ 111] shows close morphological affinities in the male bulb with the present day genus Holissus (Arnedo, pers. obs).
In our results, S. arbutifolia and S. cardiophylla are consistently placed as sister species, which is consistent with former studies [ 9, 15, 20] and their morphological affinities (both possess pendulous catkins, have connate stamens with bracts at their base, and have deciduous stigmas after flowering), and supports the grouping of both species in subgenus Pleuradenia Kimura.
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