Zoology Terms Starting With B
Zoology Glossary: B
Bilateral Symmetry
/ by-LAT-er-ul SIM-eh-tree / · Latin bilateralis (two-sided) + Greek symmetria
Bilateral Symmetry is a body plan in which a single plane divides the body into left and right halves that are mirror images of each other.
Bilateral symmetry is the dominant body plan among active, motile animals and evolved in association with directed movement and cephalization, the concentration of sensory organs and nervous tissue at the leading end of the body. The bilaterian grade includes the vast majority of animal phyla, from flatworms to vertebrates, all sharing a common ancestor estimated to have lived roughly 600 to 700 million years ago during the Ediacaran period. This body plan supports streamlined forms suited to forward locomotion and allows paired sensory structures to compare signals from two sides, improving directional detection.
Developmental costs are higher than for radial symmetry, requiring more precisely coordinated gene expression along the anterior-posterior and dorsal-ventral axes.
Some animals that appear bilaterally symmetrical as adults begin life with radial symmetry. Sea urchins and sea stars are radially symmetrical adults that develop from bilaterally symmetrical larvae, placing them within the bilaterian clade despite their adult form.
Bilateral animals are perfectly identical on left and right sides. Internal organs such as the heart, liver, and stomach are consistently asymmetric, and even external features like claw size in fiddler crabs differ markedly between sides.
A tiger shark (Galeocerdo cuvier) displays bilateral symmetry, with paired pectoral fins, paired eyes, and a musculature arranged symmetrically around a head-to-tail axis. Internally, the liver is asymmetric, with the right lobe accounting for up to 20% of the shark's total body weight and serving as a buoyancy organ.
Binomial Nomenclature
/ by-NOH-mee-ul noh-men-KLAY-cher / · Latin binomius, two names; nomenclatura, calling by name
Binomial Nomenclature is the standardized scientific naming system in which every species receives a unique two-part name consisting of a capitalized genus name followed by a lowercase specific epithet.
Carl Linnaeus formalized this system in the tenth edition of Systema Naturae in 1758, the date now recognized as the starting point for zoological nomenclature. The genus name is always capitalized and the specific epithet is always lowercase; both are italicized in print or underlined in handwriting. When a species name is repeated in the same document after its first full appearance, the genus may be abbreviated to its initial letter, as in H.
sapiens for Homo sapiens. The International Code of Zoological Nomenclature governs priority rules, ensuring that the earliest validly published name takes precedence when multiple names exist for the same species.
Linnaeus assigned names to more than 4,400 animal species in the 1758 edition of Systema Naturae, many of which remain valid today, including Homo sapiens and the European hedgehog, Erinaceus europaeus.
Common names are sufficient for scientific communication. The same organism can carry dozens of different common names across languages and regions, while a binomial name is recognized by researchers worldwide regardless of their native language.
The domestic cat is named Felis catus, with Felis identifying the genus and catus identifying the species within that genus. This name distinguishes the domestic cat from its close relative the wildcat, Felis silvestris, even though the two can interbreed where their ranges overlap.
Bioacoustics
/ by-oh-ah-KOO-stiks / · Greek bios, life; akoein, to hear; -ics, study
Bioacoustics is the scientific study of sound production, transmission, and reception in living organisms, encompassing how animals generate sounds, how those sounds travel through air or water, and how animals use acoustic signals to communicate, navigate, find food, and avoid predators.
Researchers use hydrophones, directional microphones, and accelerometers to capture animal sounds in the field, then apply digital signal processing to identify species and classify behaviors from the recordings. Passive acoustic monitoring can track nocturnal, cryptic, or wide-ranging animals that are difficult to observe directly, and long-term deployments have recorded seasonal shifts in bat activity, frog breeding choruses, and whale migration routes. Roger Payne and Scott McVay’s 1971 analysis of humpback whale (Megaptera novaeangliae) vocalizations demonstrated that these sequences have a hierarchical, song-like structure that changes progressively across breeding seasons.
Forests, coral reefs, and rivers each produce distinctive acoustic signatures whose species richness and temporal patterns reflect the ecological condition of the habitat.
Sperm whales (Physeter macrocephalus) produce clicks that reach approximately 230 decibels, making them among the loudest sounds generated by any animal. These clicks are used for echolocation at depths exceeding 1,000 meters, where no sunlight penetrates.
Bioacoustics covers only bird songs. The field encompasses whale calls, bat echolocation, insect stridulation, frog advertisement calls, fish drumming, and the effects of human-generated noise on all of these signals.
Researchers monitoring the critically endangered Yangtze finless porpoise (Neophocaena asiaeorientalis ssp. asiaeorientalis) deploy hydrophone arrays along the Yangtze River to detect echolocation clicks. Population estimates derived from acoustic detections in a 2020 survey suggested fewer than 1,000 individuals remained in the wild.
Bipedalism
/ by-PEE-duh-liz-um / · Latin bi (two) + pedalis (of the foot) + -ism
Bipedalism is a form of locomotion in which an animal moves on two legs, supported by skeletal and muscular adaptations that maintain balance and propulsion without the use of forelimbs for weight-bearing.
Habitual bipedalism in hominins required substantial skeletal remodeling from a quadrupedal ancestor, including a bowl-shaped pelvis that supports abdominal organs and anchors the gluteal muscles used in stabilizing each stride. The femur angles inward from hip to knee, placing the foot beneath the body’s center of mass and reducing lateral sway. Fossil evidence from Laetoli, Tanzania, dated to approximately 3.6 million years ago, preserves footprints attributed to Australopithecus afarensis that show a heel-to-toe gait consistent with obligate bipedalism.
This locomotor shift freed the forelimbs for manipulation but narrowed the birth canal relative to neonatal head size, producing the unusually helpless state of human newborns compared with other primates.
Theropod dinosaurs, the lineage that includes Tyrannosaurus rex, were obligate bipeds, and birds are their direct descendants. Bipedalism in the theropod lineage therefore predates hominin bipedalism by more than 200 million years.
Bipedalism means walking upright exactly as modern humans do. Hopping kangaroos and running ostriches are also bipedal, using two-legged locomotion with postures and gaits entirely different from the human striding walk.
Ostriches (Struthio camelus) are obligate bipeds capable of sustaining running speeds of around 45 kilometers per hour and reaching brief bursts near 70 kilometers per hour, making them the fastest living bipedal animals. Their vestigial wings contribute 0 forward thrust but are spread during courtship displays and used for balance during sharp turns. The long tendons of the leg store and release elastic energy with each stride.
Blastocyst
/ BLAS-toh-sist / · Greek blastos (bud, sprout) + kystis (bladder, sac)
Blastocyst is a hollow, fluid-filled structure formed during early mammalian embryonic development, consisting of an outer trophoblast layer and an inner cell mass enclosed within a fluid-filled cavity called the blastocoel.
The blastocyst forms from the morula through cavitation, a process in which fluid pumped by the outer cells accumulates internally and separates the trophoblast from the inner cell mass. Trophoblast cells secrete human chorionic gonadotropin, which prevents regression of the corpus luteum and sustains progesterone production, maintaining the uterine lining until the placenta can take over hormonal support. This hormonal signal is the basis of pregnancy tests, which detect human chorionic gonadotropin in urine as early as ten days after fertilization.
Inner cell mass cells are pluripotent, meaning each can give rise to any of the roughly 200 cell types found in the adult body, and these cells are the source material for embryonic stem cell research.
In some mammals, including European roe deer (Capreolus capreolus), the blastocyst can remain dormant in the uterus for several months through a process called embryonic diapause before implanting and resuming development, timing birth to coincide with favorable spring conditions.
A blastocyst is a miniature fully formed animal. At the blastocyst stage, the embryo consists of only about 70 to 100 cells organized into two distinct lineages, with no differentiated tissues or organs present.
In humans, the blastocyst reaches the uterus approximately five to six days after fertilization and contains roughly 70 to 100 cells at the time of implantation. Trophoblast invasion begins around day 6 or 7, establishing the physical and hormonal connection between embryo and mother that will sustain the pregnancy. The inner cell mass then gives rise to the embryo proper while outer trophoblast cells contribute to the placenta.
Reproductive System Fun Facts →Brood Parasite
/ BROOD PAR-uh-syte / · Middle English brood + Greek para (beside) + sitos (food)
Brood Parasite is an organism that exploits the parental investment of another species by depositing its eggs or young in that species' nest, causing the host to raise the parasite's offspring.
Avian brood parasitism has evolved independently at least seven times and is obligate in roughly 1% of bird species, including cuckoos, cowbirds, honeyguides, and some ducks. The common cuckoo (Cuculus canorus) lays an egg that closely mimics the host’s eggs in color and pattern, and the cuckoo chick that hatches ejects all host eggs and nestmates within its first few days of life. A co-evolutionary arms race drives this system, with hosts evolving egg recognition and rejection behavior and parasites evolving increasingly precise egg mimicry in response.
Some host species, such as the superb fairy-wren (Malurus cyaneus), teach their eggs a unique call that chicks must repeat after hatching, allowing parents to identify and abandon parasite chicks that cannot produce the correct signal.
The brown-headed cowbird (Molothrus ater) parasitizes more than 220 host species across North America, the broadest host range recorded for any brood parasite. A single female cowbird can lay up to 40 eggs in a single breeding season, distributing them across many host nests.
Brood parasitism is the same as nest stealing. Brood parasites do not take over a nest; they deposit eggs and leave, relying entirely on the host's own parental behavior to incubate and feed the parasite's offspring.
The common cuckoo lays its eggs in the nests of reed warblers (Acrocephalus scirpaceus) and other small passerines, with each female specializing on a single host species. A newly hatched cuckoo chick weighs only a few grams at hatching but grows to outweigh its foster parents within about two weeks, demanding more food than the host pair would normally deliver to an entire brood.
