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The embryology of Lytta viridana Le Conte (Coleoptera:Meloidae). V. The blastoderm, germ layers, and body segments

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jmor.1050530211openalex-snapshot
Comments on the origin of the midgut in insects
inferredcites →https://doi.org/10.1007/bf00596217openalex-snapshot
Struktur und erste Differenzierung im Ei des Mehlk�fers Tenebrio molitor
inferredcites →https://doi.org/10.1111/j.1469-185x.1930.tb00891.xopenalex-snapshot
THE FORMATION OF GERM LAYERS IN INSECTS
inferredcites →https://doi.org/10.1111/j.1469-185x.1960.tb01416.xopenalex-snapshot
CONCERNING HEAD DEVELOPMENT IN THE ARTHROPODS
inferredcites →https://doi.org/10.1242/jcs.s2-71.282.313openalex-snapshot
The Development of the larval and adult mid-gut of Calandra oryzae (Linn.): The Rice Weevil
inferredcites →https://doi.org/10.1242/jcs.s2-78.309.91openalex-snapshot
Observations on the Embryology of Corynodes pusis (Coleoptera, Chrysomelidae)
inferredcites →https://doi.org/10.1242/jcs.s2-80.318.159openalex-snapshot
The Embryonic Development of Calandra oryzae
inferredcites →https://doi.org/10.5281/zenodo.16543727openalex-snapshot
Facts and theories concerning the insect head
inferredcites →https://doi.org/10.5962/bhl.title.5890openalex-snapshot
Animal tissue techniques

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/asp.84.e198736zenodo-depositor-declared
Embryonic development of Tenomerga mucida and Satonius kurosawai – First embryological information on Archostemata and Myxophaga (Coleoptera) does not support their sister group relationship
inferred← citeshttps://doi.org/10.1002/9780470514573.ch6openalex-snapshot
Evolutionary Aspects of Primordial Germ Cell Formation
inferred← citeshttps://doi.org/10.1002/jmor.1051520205openalex-snapshot
Embryogenesis of Xyleborus ferrugineus (Fabr.) (Coleoptera, Scolytidae). I. External morphogenesis of male and female embryos
inferred← citeshttps://doi.org/10.1002/jmor.1051720104openalex-snapshot
Structure and development of the larval visual system in embryos of Lytta viridana leconte (coleoptera, meloidae)
inferred← citeshttps://doi.org/10.1002/jmor.1051810105openalex-snapshot
Mesodermal organogenesis in the embryo of the primitive moth, Neomicropteryx nipponensis Issiki (Lepidoptera, Micropterygidae)
inferred← citeshttps://doi.org/10.1007/978-94-011-6514-3_18openalex-snapshot
Embryology
inferred← citeshttps://doi.org/10.1007/978-94-011-6514-3_4openalex-snapshot
The Head and Cervix
inferred← citeshttps://doi.org/10.1007/bf00879624openalex-snapshot
Mitotic waves and embryonic pattern formation: No correlation inCallosobruchus (Coleoptera)
inferred← citeshttps://doi.org/10.1007/s004270000128openalex-snapshot
Homeotic evidence for the appendicular origin of the labrum in Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/0020-7322(81)90005-2openalex-snapshot
Alimentary canal formation of the scorpion fly, Panorpa pryeri Maclachlan (Mecoptera : Panorpidae)
inferred← citeshttps://doi.org/10.1016/b978-0-08-017069-5.50012-3openalex-snapshot
PTERYGOTE INSECTS
inferred← citeshttps://doi.org/10.1016/b978-0-08-018753-2.50050-2openalex-snapshot
Literature cited
inferred← citeshttps://doi.org/10.1016/j.asd.2003.07.001openalex-snapshot
Embryonic development of the sensory innervation of the clypeo–labral complex: further support for serially homologous appendages in the locust
inferred← citeshttps://doi.org/10.1016/j.asd.2014.10.001openalex-snapshot
The embryonic development of Stylops ovinae (Strepsiptera, Stylopidae) with emphasis on external morphology
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.11.004openalex-snapshot
Extraembryonic development in insects and the acrobatics of blastokinesis
inferred← citeshttps://doi.org/10.1016/s1467-8039(02)00016-6openalex-snapshot
Morphological and molecular data argue for the labrum being non-apical, articulated, and the appendage of the intercalary segment in the locust
inferred← citeshttps://doi.org/10.1016/s1467-8039(03)00042-2openalex-snapshot
Early steps in building the insect brain: neuroblast formation and segmental patterning in the developing brain of different insect species
inferred← citeshttps://doi.org/10.1016/s1467-8039(03)00043-4openalex-snapshot
Spatial and temporal pattern of neuroblasts, proliferation, and Engrailed expression during early brain development in Tenebrio molitor L. (Coleoptera)
inferred← citeshttps://doi.org/10.1080/08912963.2018.1561672openalex-snapshot
Archaeomalthus-(Coleoptera, Archostemata) a ‘ghost adult’ of Micromalthidae from Upper Permian deposits of Siberia?
inferred← citeshttps://doi.org/10.1101/gad.3.3.399openalex-snapshot
Isolation, structure, and expression of labial, a homeotic gene of the Antennapedia Complex involved in Drosophila head development.
inferred← citeshttps://doi.org/10.1139/z96-114openalex-snapshot
Structure and development of larval antennae in embryos of Lytta viridana LeConte (Coleoptera: Meloidae)
inferred← citeshttps://doi.org/10.1242/dev.112.4.899openalex-snapshot
The molecular genetics of head development in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1242/dev.205168openalex-snapshot
The dynamic evolution of panarthropod germ cell specification mechanisms
inferred← citeshttps://doi.org/10.1603/0013-8746(2006)99[592:cdeitd]2.0.co;2openalex-snapshot
Cellularization During Embryogenesis in Thermobia domestica (Zygentoma: Lepismatidae)
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