Hubbry Logo
Magicicada cassiniMagicicada cassiniMain
Open search
Magicicada cassini
Community hub
Magicicada cassini
logo
8 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Magicicada cassini
Magicicada cassini
Magicicada cassini
View on Wikipedia
from Wikipedia
Main article: Cassini periodical cicadas

Magicicada cassini
Female ovipositing
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hemiptera
Suborder: Auchenorrhyncha
Family: Cicadidae
Genus: Magicicada
Species:
M. cassini
Binomial name
Magicicada cassini
(Fisher, 1852)
Synonyms

Cicada cassinii Fisher, 1852[2]

Magicicada cassini (originally spelled cassinii [a]), known as the 17-year cicada, Cassin's periodical cicada or the dwarf periodical cicada,[6] is a species of periodical cicada. It is endemic to North America. It has a 17-year life cycle but is otherwise indistinguishable from the 13-year periodical cicada Magicicada tredecassini. The two species are usually discussed together as "cassini periodical cicadas" or "cassini-type periodical cicadas." Unlike other periodical cicadas, cassini-type males may synchronize their courting behavior so that tens of thousands of males sing and fly in unison.[7][8] The species was first reported to the Academy of Natural Sciences of Philadelphia by Margaretta Morris in 1846.[9] In 1852, the species was formally described by J. C. Fisher and given the specific name cassini in honour of John Cassin, an American ornithologist, whose own report was included by Fisher in his publication.

Description

[edit]

The adult M. cassini is very similar in appearance to other periodical cicadas. It is between 24 and 27 mm (0.94 and 1.06 in) long, measured from the front of the head to the tip of the wings folded over the abdomen. The head is black, the eyes are large and red, the pronotum is black apart from a narrow orange band at the edge of the sternites, and the abdomen is black. The legs are orange and the wings are translucent, with orange veins and dusky markings near the tips.[8]

Distribution and habitat

[edit]

Magicicada cassini is endemic to North America, its range extending across the northern belt of the United States and the southern part of Canada.[8]

Life cycle

[edit]
Mating call Brood XIII sub-brood, 2020

These cicadas are true bugs and after having emerged from underground, the adults feed on sap sucked from trees and shrubs. Males amass in great numbers and sing in unison to attract females. The call lasts for two to four seconds and is a series of ticks followed by a drawn-out buzz which rises and falls in pitch. At the end of a chorus, males move to a new perch before starting the song again. After mating, the females insert their ovipositors into shoots and lay their eggs. These hatch about two months later and the first instar nymphs drop to the ground where they move underground and suck xylem sap from small rootlets. This sap is very low in nutritive value and the nymphs grow very slowly. They will moult five times, moving on to larger roots deep in the soil as they grow over a period of seventeen years. Finally, they all tunnel up through the soil and emerge into the open air, before climbing up the vegetation and shedding their skins for a final time to become adults. Although each population has a seventeen-year life cycle and emerges in synchrony, past environmental events have occasionally disrupted this pattern and there are several different broods in existence in various parts of the insect's range which emerge in different calendar years.[8][10] In fact, their life cycle can range from thirteen to twenty-one years.[11]

The different broods have been numbered, and the most recent emergence of Brood X occurred in Delaware, Georgia, Illinois, Indiana, Kentucky, Maryland, Michigan, North Carolina, New Jersey, New York, Ohio, Pennsylvania, Tennessee, Virginia, Washington, D.C., and West Virginia in May and June 2021.[10][6] Many broods have a sub-brood that emerge a few years before the regular brood. The Brood XIII sub-brood in the Chicago area emerged 4 years early in 2020.

Damage

[edit]

In outbreak years, the cicadas do significant damage to the trees on which they lay eggs, especially saplings. The female cuts a slit in a twig in which to insert her eggs and this often causes the shoot to droop and defoliate. In larger twigs it may allow entry of disease organisms. The burden of feeding of the nymphs is also considerable. However, it has been shown that there is little long-term harm to mature trees.[12]

Alleged reward for blue eyed cicadas

[edit]

A popular reoccurring urban legend purports to say that rare blue (or white) eyed cicadas will fetch rewards of up to one million dollars. According to the legend, biological laboratories, particularly at Vanderbilt University,[13] will pay a reward to any who catch such a specimen. And while it is true that blue eyed cicadas are extremely rare, occurring in only about one in every million insects, no laboratories currently offer any such reward.[14] However, Roy Troutman, an American entomologist and cicada researcher,[15] did in fact offer rewards for living blue eyed cicadas for cicada research in 2008. He is no longer offering rewards.[16]

Notes

[edit]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Magicicada cassini

View on Grokipedia
from Grokipedia
Magicicada cassini, commonly known as Cassini's 17-year , is a of in the Magicicada endemic to eastern , renowned for its synchronized 17-year life cycle that involves prolonged subterranean development as a followed by brief, massive emergences for . This , first described by James Coggswell Fisher in 1851 and named in honor of ornithologist John Cassin, is one of three 17-year periodical cicadas, alongside M. septendecim and M. septendecula, and plays a significant role in forest ecosystems through its periodic resource pulses and strategies. Physically, M. cassini adults are smaller than those of M. septendecim, typically measuring about 2.5–3 cm in length, with a predominantly , striking red eyes, and orange-tinged wing veins at the base. Unlike some congeners, it lacks orange coloration anterior to the wing insertion point behind the eye and has an entirely black ventrally, though faint yellow-orange marks may appear on some western populations; females are slightly larger than males and possess a robust for egg-laying. These features aid in distinguishing it during emergences, which occur in , primarily in May and June, when soil temperatures reach approximately 18°C (64°F). The life cycle of M. cassini exemplifies extreme periodicity, with nymphs spending 17 years underground, feeding on sap from using specialized mouthparts, before emerging en masse as adults that live only 4–6 weeks. Upon , adults climb trees, molt to reveal their winged forms, and engage in chorusing behaviors to attract mates; females then oviposit 600 eggs in small slits made in pencil-thin twigs of trees, often causing branch tip dieback known as "flagging." This strategy synchronizes broods—distinct populations emerging in specific years and regions—such as Broods II, X, XIII, and XIV (which emerged in 2025), minimizing predation through sheer numbers. Distributed across the eastern and , from New York to and south to , M. cassini occupies forested habitats and is present in 10 of the 12 recognized 17-year broods, with emergences varying by brood cycle (e.g., in 2021 covered parts of 15 states). Its chorusing features a distinctive calling —a rapid series of 12–40 ticks (16–25 per second) crescendoing into a 2–4 second shrill buzz—produced by males to form synchronized aggregations, enhancing success and creating auditory landscapes that can reach 90–100 decibels. Ecologically, M. cassini emergences provide a massive, pulsed resource to predators, decomposers, and soil biota, with billions of individuals per brood contributing nutrient-rich that boosts soil nitrogen and stimulates microbial activity, while their oviposition influences tree demography and succession. This —where abundance overwhelms consumers—allows most to reproduce successfully, underscoring the species' evolutionary to periodic histories.

Taxonomy and systematics

Naming and discovery

The first formal report of Magicicada cassini as a distinct periodical cicada came from Margaretta Hare Morris in 1846, who presented her observations of differing larvae and adults near to the Academy of Natural Sciences, noting variations from the known Cicada septendecim. Her findings highlighted a smaller-bodied form with unique behaviors, unearthed during excavations in local orchards, marking an early recognition of among . In 1852, physician and naturalist James C. Fisher formally described the species as Cassinii in the Proceedings of the Academy of Natural Sciences of , naming it in honor of ornithologist John Cassin, who had documented its emergence in 1851 near —the first observed since 1834—and confirmed its separation from C. septendecim based on morphology and vocalizations. Fisher's description emphasized its smaller size (male body length approximately 23 mm), darker coloration, and a buzzing call resembling a grasshopper's, while early 19th-century records, including Cassin's, established its strict 17-year cycle as a key trait distinguishing it from annual . The species was reclassified into the new genus Magicicada by entomologist William T. Davis in 1925, who proposed the name to capture the "magic" of the ' synchronized, long-cycle emergences and to separate them taxonomically from other North American cicadas based on life history and morphology. The original specific epithet "Cassinii" was subsequently emended to "cassini" under (ICZN) rules on prevailing usage, as justified in a 2022 taxonomic review that analyzed historical literature and confirmed "cassini" as the standard form since the mid-20th century to align with original intent and common practice.

Phylogenetic relationships

Magicicada cassini is classified within the Cassini species group of the genus Magicicada, alongside the 13-year periodical M. tredecassini, based on shared acoustic signaling patterns, morphological similarities, and mitochondrial DNA phylogenies that delineate three major lineages in the genus: Decim, Cassini, and Decula. This grouping reflects parallel evolutionary histories across the lineages, where each contains both 13-year and 17-year forms, with M. cassini representing the 17-year member of the Cassini group. Genetic analyses indicate that the between 13-year and 17-year life cycles within the Cassini group occurred relatively recently, approximately 121,000 years ago, contrasting with deeper splits in the Decim group around 197,000 years ago. Whole-mitogenome sequencing reveals minimal genomic sequence between these cycle variants within groups, suggesting that the 17-year synchronization evolved multiple times from 13-year ancestors, potentially driven by predator avoidance, with ongoing limiting differentiation. The overall phylogeographic structure of Magicicada shows three genetic subdivisions per group, shaped by Pleistocene glacial cycles, though the Cassini group's is estimated at about 320,000 years ago for its main clades. The co-evolved bacterial Hodgkinia cicadicola, critical for supplementing nutrients from , has undergone significant degradation in Magicicada , including M. cassini, with metagenomic studies documenting idiosyncratic lineage splitting into multiple interdependent genomes.31311-8) This fragmentation, which has proceeded along divergent paths across , began around 1.5–4 million years ago and involves no transcriptional compensation for imbalanced gene dosages, underscoring the role of relaxed selection in within long-lived hosts like . Such genomic instability highlights the ancient co-speciation between Magicicada and their symbionts, predating the recent life-cycle divergences. A 2022 metagenomic survey using 16S rRNA sequencing of gut microbiomes from 17-year Magicicada broods, including M. cassini, revealed highly similar bacterial compositions across species in the Cassini, Decim, and Decula groups, dominated by Sulcia muelleri and Hodgkinia cicadicola. These shared communities, conserved between nymphal and adult stages, support essential functions like for xylem feeding, indicating that microbial has been retained despite phylogenetic separations within the genus. No subspecies are recognized for M. cassini, which maintains a distinct phylogenetic position within the Cassini group while showing close genetic affinities to other 17-year congeners like M. septendecim in the Decim group, as evidenced by low inter-group divergence in shared genomic regions and co-emergence patterns. Distinctions from M. septendecim are reinforced by unique chorus song structures that serve as species-specific mating signals, reflecting underlying genetic isolation.

Morphology and physiology

External morphology

Magicicada cassini adults are robust insects measuring 24-27 mm in body length, with a wingspan reaching up to 70 mm. The head is black, featuring large red compound eyes positioned widely apart and three ocelli arranged in a triangular formation on the vertex. The thorax consists of a black pronotum marked by a narrow orange posterior band along its rear edge, while the legs exhibit orange striping. The is generally entirely , though some individuals in western or midwestern populations may exhibit faint yellow-orange marks on the ventral surface, and males possess genital claspers at the posterior end. The wings are translucent, supported by prominent orange veins, with blackish tips on the forewings and orange bases on the hind wings. Sexual dimorphism is evident, with males generally smaller than females and bearing external tymbals on the sides of the first abdominal segment for sound production, whereas females have a more robust, pointed terminating in a strong . The red eyes serve as a key diagnostic trait distinguishing M. cassini within the Decim species group.

Physiological adaptations

Magicicada cassini nymphs and adults are adapted to xylem feeding, extracting water and limited nutrients from plant root fluids using specialized piercing-sucking mouthparts that penetrate vessels. This diet is nutrient-poor, particularly in , necessitating reliance on gut endosymbionts for supplementation. analyses reveal that Sulcia and Hodgkinia bacteria dominate the gut community in both nymphs and adults, provisioning essential through symbiotic that compensates for the xylem's deficiencies. These endosymbionts are vertically transmitted and maintain stable populations across the 17-year life cycle, enabling survival on this sparse resource. The species' exceptional longevity underground stems from a low metabolic rate, which conserves energy during the prolonged nymphal phase spent feeding on root xylem fluids. This reduced metabolism, potentially involving enzymes optimized for slow activity, allows nymphs to endure 17 years in soil with minimal nutritional input, avoiding the need for high-energy foraging. Additionally, developmental plasticity influences cycle timing; laboratory studies demonstrate that molting rates vary with temperature, permitting life-cycle lengths from 13 to 21 years under controlled conditions, though field synchrony enforces the 17-year norm. Sound production in M. cassini relies on males' tymbal organs, paired structures on the abdomen that buckle and rebound to generate vibrations through rapid muscle contractions. These organs produce chorus calls with dominant frequencies around 4-6 kHz, forming high-pitched buzzes that synchronize in aggregations to attract females. Females respond to these calls with substrate-borne wing flicks, signaling receptivity without vocalization. Rare genetic mutations in M. cassini occasionally result in blue-eyed individuals, occurring at a frequency of approximately 1 in 1 million. This phenotype arises from anomalies disrupting ommochrome pigment synthesis, which normally imparts the characteristic red eye color; the absence of these pigments reveals underlying blue structural coloration, but the mutation confers no adaptive advantage.

Distribution and habitat

Geographic range

Magicicada cassini is endemic to eastern , with no established populations outside this continent. Its distribution is confined to the eastern and , where arid barriers in the western regions prevent westward expansion. The core geographic range of M. cassini extends from the southern southward to northern Georgia and westward to eastern and , encompassing the Atlantic Coast from New York to the . This range includes southern portions of in and numerous northern U.S. states, such as , , , , and New York. Within this area, populations are associated primarily with 17-year periodical , reflecting the ' life cycle . M. cassini is a key component of , one of the largest 17-year broods by geographic extent, which emerged in 2021 across 15 states including , , , and others from Georgia to New York. It also features prominently in , which emerged in 2024 in the Midwest, spanning , , , , and . These brood-specific patterns result in patchy distributions tied to historical synchrony among populations. The species' range originated from post-glacial colonization following the retreat of the Laurentide Ice Sheet approximately 12,000–14,000 years ago, allowing expansion into newly available deciduous forest habitats across the eastern deciduous forest . Recent studies indicate that while populations remain stable overall, from and has led to increasingly patchy distributions, with some local extirpations but resilience in connected woodland areas.

Habitat preferences

Magicicada cassini nymphs require well-drained, sandy-loam soils for burrowing during their prolonged subterranean phase, typically found in and riparian forests rather than strictly upland areas, with preferences for soils that are neutral to slightly acidic to support root access and development. Compacted or flooded urban soils are avoided, as they impede nymphal movement and survival, leading to reduced densities in such environments. This species associates closely with deciduous woodlands dominated by hardwood trees such as oaks (Quercus spp.), maples (Acer spp.), and hickories (Carya spp.), where the 17-year underground phase relies on xylem fluids from tree roots. Recent studies indicate a strong preference for larger trees exceeding 35 cm in (DBH) for nymph emergence, with higher emergence densities under Quercus alba and Carya species, while oviposition favors smaller Quercus trees under 35 cm DBH in canopy gaps with greater light exposure. In temperate climatic zones of eastern , cold winters facilitate the diapause required for synchronized development, ensuring nymphs remain dormant until cues align. from diminishes suitable woodland patches by increasing and altering microclimates, though populations persist in remnant woodlots and fencerows, albeit with shifted timing compared to rural forests.

Life cycle

Nymphal development

The nymphal stage of Magicicada cassini constitutes the vast majority of its 17-year life cycle, with nymphs remaining underground for approximately 16–17 years after hatching from eggs laid in tree branches. Upon hatching 6–10 weeks after oviposition, first-instar nymphs drop to the soil surface, burrow downward, and begin feeding on root xylem, initiating a prolonged period of subterranean development. This stage is divided into five instars, with molting occurring irregularly—typically annually in early instars but potentially biennially in later ones, depending on the availability of suitable roots and environmental conditions that influence growth rates. Nymphs sustain themselves by sucking xylem sap from the shallow roots of deciduous trees and shrubs, generally at depths of 0–30 cm, using their piercing-sucking mouthparts to extract the nutrient-poor fluid. To facilitate feeding, they construct small mud chimneys or turrets around their burrows, which help maintain access to roots and regulate moisture in the soil tunnel system; these structures can reach 2–8 cm in height and are often observed in areas with high nymph density. Growth during this phase is exceedingly slow, averaging 1–2 mm per year, reflecting the low nutritional value of xylem and the energy demands of burrowing and overwintering. Developmental timing is governed by mechanisms responsive to temperature and photoperiod cues, which synchronize nymphal growth with annual host plant cycles and ensure mass after 17 years; these cues allow for developmental plasticity, resulting in rare off-cycle emergences termed "stragglers" that appear in non-brood years, often four years early or late. Survival through the nymphal stage is challenging, with high mortality attributed to pathogens such as fungi and nematodes, as well as flooding events that can drown burrows during heavy . Studies following the 2021 , including analyses in 2025, have highlighted density-dependent effects on nymph growth and survival, where higher densities correlate with increased competition for and elevated .

Emergence patterns

Magicicada cassini follows a strict 17-year periodicity, emerging synchronously in defined broods across its range. For instance, , one of the largest, last emerged in 2004 and 2021, with the next anticipated in 2038. While M. cassini itself adheres to the 17-year cycle, a closely related species, Magicicada tredecassini, exhibits a 13-year cycle in southern populations, representing a variant periodicity in those regions. The mass emergence is primarily triggered by soil reaching approximately 64°F (18°C) at a depth of 8 inches (20 cm). This environmental cue synchronizes the exit from the soil, typically occurring after a warm in . Fine-tuning of the exact night may involve additional factors, though soil remains the dominant signal. Emergences span 2-4 weeks from May to , depending on and local conditions. A 2025 study analyzing phenology across 1987, 2004, and 2021 found consistent first emergences for M. cassini on day 141 (May 21) in both 1987 and 2021, with average emergence around day 153 (early ) in 2021, though showing greater variance and increased protandry (males emerging 1.72 days before females) in recent events, potentially linked to warming trends. In core areas, densities can exceed 1 million individuals per acre, creating overwhelming numbers that facilitate as a defense mechanism. Straggler emergences, where individuals appear 1 or 4 years off-cycle, remain rare and do not significantly disrupt the brood synchrony.

Adult stage

The adult stage of Magicicada cassini begins immediately after nymphal and eclosion, lasting approximately 2–5 weeks. During this period, adults focus on , with rapid occurring post-mating; females typically die shortly after oviposition, while males succumb soon after. This brief aboveground phase contrasts sharply with the extended subterranean nymphal development, emphasizing the evolutionary prioritization of synchronized mass for . Locomotion in adult M. cassini is characterized by clumsy, short-distance flights, with individuals rarely dispersing more than 50 m in a single bout across open areas or forest edges, though cumulative travel can extend farther through repeated flights. Males commonly perch on tree branches to aggregate for chorusing, facilitating mate attraction, while females exhibit more ground-based crawling to locate oviposition sites in twigs. Adults continue limited feeding on fluids from tree twigs during this stage. Daily rhythms of M. cassini adults are predominantly diurnal, with peak activity—including flight and chorusing—occurring during daylight hours and settling into nocturnal rest at night. Studies from the 2021 Brood X emergence have documented mammal activity responses to cicada density, with some species increasing foraging in high-density areas. Mortality rates among adult M. cassini are exceptionally high, driven primarily by exhaustion from reproductive efforts, predation by birds and other vertebrates, and opportunistic fungal infections. The shed from emerging nymphs persist at soil surfaces, distinctly marking sites of prior emergences and aiding in population monitoring.

Ecology and behavior

Feeding and diet

Magicicada cassini nymphs spend the majority of their 17-year life cycle underground, feeding exclusively on sap extracted from the roots of trees, including oaks (Quercus spp.) and maples (Acer spp.). This nutrient-poor diet, primarily composed of water and dilute minerals, is supplemented by bacterial endosymbionts such as Sulcia muelleri and Hodgkinia cicadicola, which synthesize essential and vitamins to support development. Field studies indicate a strong preference for Quercus species, with nymph densities and oviposition scars significantly higher on these trees compared to Acer, reflecting targeted root feeding on preferred hosts. Notably, there is no evidence of herbivory on leaves or other plant tissues during the nymphal stage. Upon emergence, adult M. cassini shift to feeding on xylem sap from twigs and branches of trees and shrubs, using their piercing mouthparts to access the fluid. Feeding is limited, typically initiating 1–2 days post-emergence and serving mainly to replace water lost during molting and activity, as the short adult lifespan (2–6 weeks) prioritizes reproduction over extensive nutrition. The high water content of this diet helps sustain hydration amid intense chorusing and mating behaviors, though the low solute levels pose challenges for long-term energy demands. Adults exhibit polyphagy, drawing from multiple tree genera like Quercus and Acer, but avoid foliar tissues entirely. The reliance on xylem across life stages underscores adaptations to a low-nutrient niche, with the gut microbiome playing a key role in extracting maximal value from this resource.

Predation and defenses

Magicicada cassini faces predation from a diverse array of animals during its brief adult emergence, with birds serving as the primary predators. Avian species such as starlings (Sturnus vulgaris), common grackles (Quiscalus quiscula), yellow-billed cuckoos (Coccyzus americanus), and red-winged blackbirds (Agelaius phoeniceus) actively consume adult cicadas, often leading to increased foraging activity in emergence areas. Mammals, including squirrels (Sciurus spp.) and raccoons (Procyon lotor), also exploit the abundance, with recent studies documenting heightened mammalian activity and satiation behaviors in high-density cicada patches during 17-year emergences. Reptiles, such as snakes and lizards, opportunistically feed on both nymphs and adults when available. Additionally, the fungal pathogen Massospora cicadina infects emerging adults, hijacking their behavior to facilitate spore transmission while effectively sterilizing and eventually killing the hosts. The primary defense of M. cassini against these predators is , achieved through synchronized mass emergences where billions of individuals overwhelm the capacity of predators to consume them all, ensuring sufficient survival for reproduction. This strategy relies on the cicadas' conspicuous appearance and lack of individual evasion tactics, such as flight or hiding, making the sheer numerical density crucial for population persistence. Adult M. cassini exhibit no specialized chemical or physical defenses beyond this collective approach, though their brief above-ground lifespan limits exposure time. The massive die-off following creates a significant ecological impact, as carcasses deliver a pulse rich in and to soils, enhancing microbial activity and growth in the subsequent year. This temporary resource boom supports detritivores and higher trophic levels, temporarily bolstering food webs by providing high-quality protein to decomposers and . Studies from the 2024 confirmed these enrichment effects in midwestern s. In urban environments, reduces M. cassini population densities, impairing the strategy and increasing vulnerability to predation from remaining predators, which can lead to local population declines.

Reproduction and mating

Courtship behaviors

Males of Magicicada cassini engage in chorusing behaviors to attract females, forming leks where groups of 20-100 individuals synchronize their calls on tree branches in sunlit areas. These choruses produce aggregated songs characterized by a series of rapid ticks followed by a shrill buzz, with phrases lasting 1.5-3 seconds separated by 1-2 second gaps, repeated in cycles that can build to peaks of intensity over several seconds. The of the calling song ranges from 1-3 kHz, enabling long-range attraction while minimizing overlap with other sympatric . Tymbals on the males' abdomen facilitate these sounds through rapid muscle contractions. Females do not produce calling songs but respond to male choruses with wing flicks, generating brief, broad-frequency clicks that serve as acoustic and visual signals to guide males toward them. These responses are timed in a species-specific manner, occurring shortly after a male's phrase to initiate duetting and close-range . During , males transition to specialized calls: Courtship I (shortened calling phrases), Courtship II (continuous buzzing with possible upslurs), and Courtship III (4-6 buzzes per second), which help secure . Wing flicks are detectable both auditorily and visually, with males orienting via both cues in dense aggregations. Species isolation during courtship relies on acoustic differences in song structure and timing, with M. cassini exhibiting a faster tick rate in its calling phrases compared to the slower, more whirring song of the sympatric M. septendecim. Visual cues, such as the absence of a reddish stripe behind the eyes in M. cassini (versus present in M. septendecim), further aid recognition in mixed-brood emergences where multiple species overlap. Lek dynamics involve tree-based choruses where males compete acoustically and visually, with observations from the 2021 Brood X emergence indicating high densities in chorusing sites, enhancing mate location efficiency.

Oviposition and offspring survival

Following mating, female Magicicada cassini engage in oviposition by using their specialized to create V-shaped slits in the bark of pencil-thin twigs, typically 3-7 mm in diameter. Each slit, or eggnest, receives 20-30 eggs, with females often depositing eggs in multiple nests along a single twig. This behavior occurs primarily in and edge habitats, where females show a preference for certain , including oaks (Quercus spp.), (Fraxinus spp.), and (Ulmus spp.). Oaks, in particular, are a common host, comprising a substantial portion of oviposition sites in mixed forests. A single female typically lays 200-600 eggs over her adult lifespan of 3-5 weeks, distributing them across 10-30 twigs to maximize offspring dispersal and reduce risk concentration. Eggs develop for 6-10 weeks during midsummer, after which first-instar nymphs hatch synchronously and drop to the , burrowing into the within minutes to begin feeding on root . This rapid descent is crucial, as the tiny nymphs (about 2 long) lack mobility and are vulnerable to predation or on the surface. Egg survival is low due to several abiotic and biotic factors. Twig desiccation or breakage from excessive oviposition damage causes many to wither before , while host trees can mount induced defenses, such as exuding gum into nests in responsive species like black cherry (), which reduces success. Parasitoid attack on eggs is minimal, as the embedded position in bark provides protection, though fungal infections occasionally contribute. Once hatched, nymph establishment success depends heavily on conditions; dry, compacted leads to high post-hatching mortality in early instars, but rain-softened earth facilitates burrowing and initial attachment. The reproductive strategy ensures brood fidelity to the 17-year cycle, as eggs laid during emergences develop directly into nymphs programmed for synchronized over 17 years, without deviation across generations. This temporal lock-in reinforces the species' periodicity, linking oviposition success to long-term stability in woodlands. Observations from the 2024 emergence, which included M. cassini populations, highlighted ongoing oviposition in fragmented forests, with no major deviations in mating behaviors reported as of 2025.

Human interactions

Agricultural and ecological impacts

Magicicada cassini females cause damage primarily through oviposition, where they use their to make V-shaped in small twigs and branches (typically 3-11 mm in diameter) to deposit eggs, leading to twig dieback known as flagging. This damage is most severe in young trees and saplings, where multiple can weaken branches, resulting in 10-12% canopy flagging on average across native and exotic woody . In orchards, such oviposition can lead to localized branch loss, with heavy attacks potentially affecting up to 20% of branches in vulnerable fruit trees like apples and cherries. Nymphal root-feeding by M. cassini has minor effects on mature trees but can stress saplings by reducing and uptake over their 17-year development cycle. Ecologically, M. cassini emergences provide benefits through the of adult carcasses, which enrich soils with ; post-emergence sites show elevated levels, with inputs estimated at up to 7 kg N/ha in forested areas. This pulse temporarily boosts plant growth and supports detritivores, contributing to without long-term disruption. Additionally, the mass availability of cicadas as prey enhances populations during emergence years, with 63% of monitored showing abundance increases averaging 10.1%, leading to higher in insectivorous birds. Agriculturally, M. cassini impacts are rare in field crops due to their preference for woody plants, but young orchards face risks from oviposition scarring. Mitigation focuses on physical barriers like netting over saplings (1/4-inch mesh) rather than chemical controls, as the adult phase lasts only 4-6 weeks and pesticides are unnecessary and ecologically harmful. During the 2021 emergence, which included M. cassini in the Midwest, localized damage occurred in orchards with visible branch dieback, but affected trees recovered within 1-2 years with no mortality observed.

Cultural significance and research

Magicicada cassini, known as Cassini's periodical cicada, holds a place in North American folklore as a harbinger of summer, with its mass emergences signaling the arrival of warm weather and evoking tales of natural cycles and renewal. In various cultural narratives, periodical cicadas like M. cassini symbolize rebirth and immortality, drawing from broader insect lore that portrays them as carefree symbols of seasonal transformation. The 2021 emergence of Brood X, which prominently featured M. cassini, garnered extensive media attention across outlets like CNN, highlighting the event as a rare "once-in-a-lifetime" spectacle involving billions of insects across 14 states and the District of Columbia. A notable aspect of human fascination with M. cassini involves rare color variants, particularly blue-eyed individuals resulting from a genetic that alters eye pigmentation from the typical to . In 2008, entomologist Roy Troutman offered a $1,000 reward for live blue-eyed specimens to support , but the offer went unclaimed due to their extreme rarity, estimated at one in a million. As of 2025, no active rewards for such variants have been announced, though sightings continue to captivate enthusiasts during emergences. Research on M. cassini has advanced , particularly through studies on life-cycle plasticity; for instance, a 2011 investigation by Marshall et al. demonstrated how environmental factors influence cycle length in closely related , informing models of M. cassini's 17-year periodicity. More recent work includes 2022 metagenomic analyses using 16S rRNA sequencing to explore gut microbiomes and endosymbionts in 17-year , revealing diverse bacterial communities that support nutrient acquisition during long subterranean phases. The species' prime-numbered cycle has also inspired mathematical models of predator avoidance and . Although not currently threatened, M. cassini has no formal global conservation status rank (GNR) from NatureServe, yet populations are monitored for potential desynchronization due to effects on soil temperatures and emergence timing. Early emergences observed in 2017 have raised concerns about warming trends disrupting brood cohesion. initiatives, such as the Cicada Safari app developed by , engage the public in tracking distributions and variants, contributing over 120,000 downloads as of and vital data during events like .

References

  1. https://cicadas.uconn.edu/species/m_cassini/
  2. https://insects.ummz.lsa.umich.edu/fauna/
  3. https://cicadas.uconn.edu/
  4. https://people.clas.ufl.edu/rdholt/files/119.pdf
  5. https://cicadas.uconn.edu/broods/brood_14/
  6. https://orthsoc.org/sina/c700lam58.pdf
  7. https://pmc.ncbi.nlm.nih.gov/articles/PMC9786866/
  8. https://www.scientificamerican.com/article/the-woman-who-solved-a-cicada-mystery-but-got-no-recognition/
  9. https://www.biodiversitylibrary.org/page/5512055
  10. https://biodiversitylibrary.org/part/179066
  11. https://www.biotaxa.org/Zootaxa/article/view/zootaxa.5125.2.8
  12. https://www.pnas.org/doi/10.1073/pnas.1304228110
  13. https://academic.oup.com/mbe/article/36/6/1187/5372347
  14. https://pmc.ncbi.nlm.nih.gov/articles/PMC6123741/
  15. https://www.nature.com/articles/s42003-018-0025-7
  16. https://pmc.ncbi.nlm.nih.gov/articles/PMC8879801/
  17. https://www.pnas.org/doi/10.1073/pnas.1712321115
  18. https://www.nature.com/articles/s41598-022-20527-7
  19. https://pubmed.ncbi.nlm.nih.gov/36217008/
  20. https://www.pnas.org/doi/10.1073/pnas.1220060110
  21. https://pmc.ncbi.nlm.nih.gov/articles/PMC3637745/
  22. https://bugguide.net/node/view/6970
  23. http://insects.ummz.lsa.umich.edu/fauna/Michigan_Cicadas/Periodical/MISCPUB_121.pdf
  24. https://extension.psu.edu/periodical-cicada/
  25. https://pubmed.ncbi.nlm.nih.gov/25975714/
  26. https://www.sciencedirect.com/science/article/abs/pii/S0022191010003045
  27. https://pmc.ncbi.nlm.nih.gov/articles/PMC9550851/
  28. https://academic.oup.com/jinsectscience/article/23/5/13/7289611
  29. https://resjournals.onlinelibrary.wiley.com/doi/10.1111/phen.12283
  30. https://pubmed.ncbi.nlm.nih.gov/17816488/
  31. https://pubs.aip.org/asa/jasa/article/49/1A_Supplement/93/719038/Acoustic-Behavior-of-Three-Sympatric-Species-of-17
  32. https://link.springer.com/article/10.1007/BF00611184
  33. https://www.fieldmuseum.org/about/press/one-in-a-million-blue-eyed-cicada-joins-the-field-museums-research-collections
  34. https://bugoftheweek.com/?offset=1620651600039
  35. https://www.gbif.org/species/165462078
  36. https://www.mdpi.com/1424-2818/5/2/166
  37. https://cicadas.uconn.edu/broods/brood_10/
  38. https://cicadas.uconn.edu/broods/brood_13/
  39. https://esajournals.onlinelibrary.wiley.com/doi/full/10.1002/ecs2.70377
  40. https://nsojournals.onlinelibrary.wiley.com/doi/full/10.1002/wlb3.01496
  41. https://www.jstor.org/stable/2937032
  42. https://www.jstor.org/stable/2421058
  43. https://zoologicalletters.biomedcentral.com/articles/10.1186/s40851-015-0022-3
  44. https://www.annualreviews.org/doi/pdf/10.1146/annurev.en.40.010195.001413
  45. https://link.springer.com/article/10.1007/s11676-023-01617-2
  46. https://pmc.ncbi.nlm.nih.gov/articles/PMC1794023/
  47. https://esj-journals.onlinelibrary.wiley.com/doi/10.1111/1440-1703.12354
  48. https://pmc.ncbi.nlm.nih.gov/articles/PMC5838052/
  49. https://ohioline.osu.edu/factsheet/ENT-58
  50. https://ohioline.osu.edu/sites/ohioline/files/imce/Entomology/ENT-0058-Periodical-Cicadas-2025-0813-TV.pdf
  51. https://extension.umd.edu/resource/cicadas-maryland
  52. https://www.jstor.org/stable/2424544
  53. https://www.researchgate.net/publication/227784739_How_17-year_cicadas_keep_track_of_time
  54. https://www.researchgate.net/publication/23476777_Long-Term_Habitat_Selection_and_Chronic_Root_Herbivory_Explaining_the_Relationship_between_Periodical_Cicada_Density_and_Tree_Growth
  55. https://ucanr.edu/blog/bug-squad/article/cicadas-world-awaits-emergence-brood-x
  56. https://cicadas.uconn.edu/stragglers/
  57. https://www.pubs.ext.vt.edu/444/444-276/444-276.html
  58. https://hort.extension.wisc.edu/articles/periodical-cicadas/
  59. https://animaldiversity.org/accounts/Magicicada_septendecim/
  60. https://link.springer.com/article/10.1007/BF00347604
  61. https://extension.psu.edu/periodical-cicada
  62. https://pmc.ncbi.nlm.nih.gov/articles/PMC10583540/
  63. https://naturalhistory.si.edu/education/teaching-resources/life-science/periodical-cicadas
  64. https://academic.oup.com/jmammal/article/105/5/1190/7700995
  65. https://www.researchgate.net/publication/382624935_THE_PERIODICAL_CICADAS
  66. https://entomoresin.com/1pdf/cicada_evolution.pdf
  67. https://extension.umd.edu/resource/periodical-17-year-brood-x-cicadas
  68. https://pmc.ncbi.nlm.nih.gov/articles/PMC5780379/
  69. https://hydrodictyon.eeb.uconn.edu/projects/cicada/resources/reprints/Williams%2526Simon_1995.pdf
  70. https://www.nature.com/articles/s41598-024-75247-x
  71. http://insects.ummz.lsa.umich.edu/fauna/
  72. https://www.science.org/doi/10.1126/science.adi7426
  73. https://pmc.ncbi.nlm.nih.gov/articles/PMC12532616/
  74. https://news.cornell.edu/stories/2004/05/urbanization-devastating-17-year-cicadas
  75. https://cicadas.uconn.edu/behavior/
  76. https://journals.biologists.com/jeb/article/209/20/4115/16407/Tuning-the-drum-the-mechanical-basis-for-frequency
  77. https://www.nytimes.com/2024/05/17/us/cicadas-sounds-dual-emergence.html
  78. https://www.washingtonpost.com/climate-environment/2021/03/09/cicadas-broodx-environment/
  79. https://insects.ummz.lsa.umich.edu/fauna/Michigan_Cicadas/Periodical/Index.html
  80. https://link.springer.com/article/10.1007/BF00378841
  81. https://esajournals.onlinelibrary.wiley.com/doi/10.1890/13-1518.1
  82. https://www.entsoc.org/news-events/cicada-emergence-2024
  83. https://www.umass.edu/agriculture-food-environment/landscape/fact-sheets/periodical-cicada
  84. https://auf.isa-arbor.com/content/24/5/248
  85. https://extension.psu.edu/tree-fruit-insect-pest-periodical-cicada
  86. https://esajournals.onlinelibrary.wiley.com/doi/10.1002/ecs2.2779
  87. https://esajournals.onlinelibrary.wiley.com/doi/abs/10.1890/04-1175
  88. https://agcrops.osu.edu/newsletter/corn-newsletter/12-2021/are-periodical-cicadas-threat-field-crops
  89. https://extension.illinois.edu/blogs/commercial-fruit-and-vegetable-growers/2024-04-29-management-recommendations-periodical
  90. https://local21news.com/news/local/brood-x-cicadas-left-their-mark-on-local-orchards
  91. https://clay.tulane.edu/wp-content/uploads/sites/341/2021/05/Clay-et-al-Cicadas-CJFR.pdf
  92. https://folklife.si.edu/magazine/cicada-folklore
  93. https://www.cnn.com/2021/05/23/world/cicadas-2021-emergence-scn
  94. http://entomologytoday.org/2021/08/12/2021-brood-x-periodical-cicada-emergence-recap/
  95. https://www.cincinnati.com/story/news/2021/06/07/blue-eyed-cicadas/7582826002/
  96. https://www.cicadamania.com/cicadas/did-someone-offer-a-reward-for-white-or-blue-eyed-cicadas/
  97. https://www.researchgate.net/publication/322897657_Developmental_Plasticity_of_Life-Cycle_Length_in_Thirteen-Year_Periodical_Cicadas_Hemiptera_Cicadidae
  98. https://pubmed.ncbi.nlm.nih.gov/31251652/
  99. https://explorer.natureserve.org/Taxon/ELEMENT_GLOBAL.2.1000314/Magicicada_cassini
  100. https://widerimage.reuters.com/story/getting-up-close-with-cicadas-to-find-climate-change-clues
  101. https://www.msj.edu/news/2021/05/cicada-safari-app-reaches-120000-downloads.html
  102. https://cicadasafari.org/
Add your contribution
Related Hubs
User Avatar
No comments yet.