Authors: Tamar Gutnick, Daniel S Rokhsar, Michael J Kuba...

Underlying all animal behaviors, from the simplest reflexive reactions to the more complex cognitive reasoning and social interaction, are nervous systems uniquely adapted to bodies, environments, and challenges of different animal species. Coleoid cephalopods - octopuses, squid, and cuttlefish - are widely recognized as the most behaviorally complex invertebrates and provide exciting opportunities for studying the neural control of behaviour. These unusual molluscs evolved over 400 million years ago from slow-moving armored forms to active predators of coastal and open ocean ecosystems. In this primer we will discuss how, during cephalopod evolution, the relatively simple ganglion-based molluscan nervous system has been extensively transformed to control the complex bodies and process extensive visual, tactile, and chemical sensory inputs, and summarize some recent findings about their fascinating behaviors.

Topics: Animals; Cephalopoda; Ecosystem; Mollusca; Invertebrates; Octopodiformes; Nervous System; Decapodiformes

PubMed: 37875088
DOI: 10.1016/j.cub.2023.08.094

Authors: Sebastián R Najle, Xavier Grau-Bové, Anamaria Elek...

The assembly of the neuronal and other major cell type programs occurred early in animal evolution. We can reconstruct this process by studying non-bilaterians like placozoans. These small disc-shaped animals not only have nine morphologically described cell types and no neurons but also show coordinated behaviors triggered by peptide-secreting cells. We investigated possible neuronal affinities of these peptidergic cells using phylogenetics, chromatin profiling, and comparative single-cell genomics in four placozoans. We found conserved cell type expression programs across placozoans, including populations of transdifferentiating and cycling cells, suggestive of active cell type homeostasis. We also uncovered fourteen peptidergic cell types expressing neuronal-associated components like the pre-synaptic scaffold that derive from progenitor cells with neurogenesis signatures. In contrast, earlier-branching animals like sponges and ctenophores lacked this conserved expression. Our findings indicate that key neuronal developmental and effector gene modules evolved before the advent of cnidarian/bilaterian neurons in the context of paracrine cell signaling.

Topics: Animals; Biological Evolution; Ctenophora; Gene Expression; Neurons; Phylogeny; Single-Cell Analysis; Invertebrates; Paracrine Communication

PubMed: 37729907
DOI: 10.1016/j.cell.2023.08.027

Authors: Matthew L Nicotra

Most colonial marine invertebrates live as surface encrustations in benthic environments. As they grow, these animals frequently encounter other members of their own species. These encounters typically lead to conflict, in which the colonies aggressively compete for space, or co-existence, in which the colonies peacefully border each other. Sometimes, however, interacting colonies will engage in a form of cooperation in which they fuse together and actively share resources.

Topics: Animals; Cooperative Behavior; Invertebrates

PubMed: 31163159
DOI: 10.1016/j.cub.2019.03.039

Authors: Kenneth J Lohmann

In the beginning there was great confusion about animal migration. Aristotle, noting that the types of birds around him changed with the seasons, concluded that summer redstarts turned into robins at the onset of winter, and that garden warblers became blackcaps [1]. Others thought that birds disappear in winter because they hibernate submerged in mud. In a case of art decidedly not imitating life, a 16th century illustration accompanying the writings of Swedish Archbishop Olaus Magnus showed a fishing net filled with hibernating swallows being pulled from a lake [1]. Gradually, over centuries, these fanciful early explanations gave way to an understanding that migration is a widespread phenomenon and that Earth is alive with itinerant animals traversing continents, seas, and skies (Figure 1).

Topics: Animal Migration; Animals; Invertebrates; Vertebrates

PubMed: 30205070
DOI: 10.1016/j.cub.2018.08.016

Review

Authors: Simon Conway Morris

Topics: Animals; Biological Evolution; Fossils; Invertebrates

PubMed: 15649355
DOI: 10.1016/j.cub.2004.12.008

Review

Authors: Eleanor R Haine

Despite the fact that all vertically transmitted symbionts sequester resources from their hosts and are therefore costly to maintain, there is an extraordinary diversity of them in invertebrates. Some spread through host populations by providing their hosts with fitness benefits or by manipulating host sex ratio, but some do not: their maintenance in host lineages remains an enigma. In this review, I explore the evolutionary ecology of vertically transmitted symbionts and their impact on host resistance, and provide an overview of the evidence for the three-way interactions between these symbionts, natural enemies and invertebrate hosts. A number of recent empirical and theoretical studies suggest that vertically transmitted symbionts may protect their hosts from pathogens. If this 'symbiont-mediated protection' is widespread, it is likely that vertically transmitted symbionts contribute significantly to variation in measures of invertebrate resistance to natural enemies.

Topics: Animals; Ecosystem; Host-Parasite Interactions; Invertebrates; Population Dynamics; Species Specificity; Symbiosis

PubMed: 18055391
DOI: 10.1098/rspb.2007.1211

Review

Authors: Nadia S Sloan, Leigh W Simmons

Female genitalia have been largely neglected in studies of genital evolution, perhaps due to the long-standing belief that they are relatively invariable and therefore taxonomically and evolutionarily uninformative in comparison with male genitalia. Contemporary studies of genital evolution have begun to dispute this view, and to demonstrate that female genitalia can be highly diverse and covary with the genitalia of males. Here, we examine evidence for three mechanisms of genital evolution in females: species isolating 'lock-and-key' evolution, cryptic female choice and sexual conflict. Lock-and-key genital evolution has been thought to be relatively unimportant; however, we present cases that show how species isolation may well play a role in the evolution of female genitalia. Much support for female genital evolution via sexual conflict comes from studies of both invertebrate and vertebrate species; however, the effects of sexual conflict can be difficult to distinguish from models of cryptic female choice that focus on putative benefits of choice for females. We offer potential solutions to alleviate this issue. Finally, we offer directions for future studies in order to expand and refine our knowledge surrounding female genital evolution.

Topics: Animals; Biological Evolution; Female; Genitalia, Female; Invertebrates; Vertebrates

PubMed: 31267594
DOI: 10.1111/jeb.13503

Authors: S N Patek, A P Summers

Invertebrate biomechanics focuses on mechanical analyses of non-vertebrate animals, which at root is no different in aim and technique from vertebrate biomechanics, or for that matter the biomechanics of plants and fungi. But invertebrates are special - they are fabulously diverse in form, habitat, and ecology and manage this without the use of hard, internal skeletons. They are also numerous and, in many cases, tractable in an experimental and field setting. In this Primer, we will probe three axes of invertebrate diversity: worms (Phylum Annelida), spiders (Class Arachnida) and insects (Class Insecta); three habitats: subterranean, terrestrial and airborne; and three integrations with other fields: ecology, engineering and evolution. Our goal is to capture the field of invertebrate biomechanics, which has blossomed from having a primary focus on discoveries at the interface of physics and biology to being inextricably linked with integrative challenges that span biology, physics, mathematics and engineering.

Topics: Animals; Biomechanical Phenomena; Ecology; Ecosystem; Invertebrates; Phylogeny

PubMed: 28535384
DOI: 10.1016/j.cub.2017.04.012

Review

Authors: Ramón Muñoz-Chápuli

Endothelial cells, which are the main agents of the angiogenic process in vertebrates, are lacking in the vessels of invertebrates. These are limited by the basement membranes of epithelial or myoepithelial cells. This fact leads to the questions of how vessels grow in invertebrates and how vertebrate angiogenesis evolved. We herein review the knowledge available about vascular growth in invertebrates. The cases described include the ascidian Botryllus, the annelid Hirudo and the squid Idiosepius. All these processes of vascular growth in invertebrates show substantial differences with the vertebrate angiogenesis, although the signalling system mediated by VEGF and its receptor VEGFR seems to be involved in all cases. However, VEGF signalling is used by many processes of cell directional migration, and it cannot be considered as a hallmark of angiogenesis. We also describe the close similarity between the molecular control of the endothelial angiogenesis and the branching morphogenesis of the tracheal system of insects. In both cases, the process is regulated by hypoxia and activates a leading tip cell which inhibits responsiveness of the adjacent cells through a Delta/Notch signalling pathway. We suggest that endothelial angiogenesis in vertebrates arose through cooption of this hypoxia-sensing mechanism by replacing the FGF/FGFR axis of insects by a VEGF/VEGFR-mediated system, and adding a second layer of control of the endothelial state (quiescent or activated) mediated by angiopoietins and Tie receptors. This evolutionarily new control mechanism of endothelial angiogenesis establishes an endothelial/perivascular cell crosstalking which does not exist in invertebrates.

Topics: Animals; Biological Evolution; Blood Vessels; Drosophila; Endothelial Cells; Invertebrates; Models, Biological; Neovascularization, Physiologic; Receptors, Vascular Endothelial Growth Factor; Signal Transduction; Vascular Endothelial Growth Factor A; Vertebrates

PubMed: 21732276
DOI: 10.1387/ijdb.103212rm

Review

Authors: Feifei Zhu, Dong Li, Keping Chen...

Glycosylation refers to the covalent attachment of sugar residues to a protein or lipid, and the biological importance of this modification has been widely recognized. While glycosylation in mammals is being extensively investigated, lower level animals such as invertebrates have not been adequately interrogated for their glycosylation. The rich diversity of invertebrate species, the increased database of sequenced invertebrate genomes and the time and cost efficiency of raising and experimenting on these species have enabled a handful of the species to become excellent model organisms, which have been successfully used as tools for probing various biologically interesting problems. Investigation on invertebrate glycosylation, especially on model organisms, not only expands the structural and functional knowledgebase, but also can facilitate deeper understanding on the biological functions of glycosylation in higher organisms. Here, we reviewed the research advances in invertebrate glycosylation, including N- and O-glycosylation, glycosphingolipids and glycosaminoglycans. The aspects of glycan biosynthesis, structures and functions are discussed, with a focus on the model organisms Drosophila and Caenorhabditis. Analytical strategies for the glycans and glycoconjugates are also summarized.

Topics: Animals; Caenorhabditis elegans; Drosophila melanogaster; Glycoconjugates; Glycosaminoglycans; Glycosphingolipids; Glycosylation; Invertebrates; Polysaccharides; Species Specificity

PubMed: 30958118
DOI: 10.1098/rsob.180232