Life history and larval density of Cheumatopsyche digitata Mosely (Trichoptera: Hydropsychidae) in Opa Reservoir spillway, Ile-Ife, southwestern Nigeria

Zoosymposia ◽  
2011 ◽  
Vol 5 (1) ◽  
pp. 401-407
Author(s):  
SYLVESTER OGBOGU ◽  
WILLIAMS ADU

The life history and density of Cheumatopsyche digitata Mosely (Trichoptera: Hydropsychidae) were examined below Opa Reservoir in Ile-Ife, southwestern Nigeria. This caddisfly is the only species that occurs immediately below the impoundment auxiliary spillway where it closely associates with an aquatic bryophyte, Fontinalis sp. We collected larvae every month between July 2004 and June 2005 as long as larvae were available in the study site. The instar growth ratio was fairly constant and ranged from 1.198 to 1.402 (mean ± standard error = 1.285 ± 0.073) but mean head capsule width increased with larval development. The frequency distribution of head capsule width of larvae clustered into 5 size classes, suggesting 5 larval instars for C. digitata in the study site. Density of larvae ranged from 1,100 to 11,150 inds.m-2 (mean ± SE = 6739  inds.m-2 ± 3904.70), the highest densities occurring in October 2004 during the bloom of Fontinalis. The first larval instar appeared in July 2004. Adult emergence occurred mainly in December 2004 through January 2005 at the onset of reservoir draw-down and death of Fontinalis. These patterns indicate that C. digitata tended to show a univoltine life cycle in the study site.

Author(s):  
Alec R. Lackmann ◽  
Malcolm G. Butler

Except for one unconfirmed case, chironomid larvae have been reported to pass through four larval instars between egg and pupal stages. We have observed a fifth larval instar to be a standard life-cycle feature of the podonomine Trichotanypus alaskensis Brundin 1966 in tundra ponds on the Arctic Coastal Plain near Barrow, Alaska. T. alaskensis has a one-year life cycle in these arctic ponds. Adults emerge in June ~2-3 weeks after pond thaw, then mate and oviposit; most newly-hatched larvae reach instar IV by October when pond sediments freeze. Overwintering larvae complete instar IV within a few days of thaw, then molt again to a fifth larval instar. Imaginal discs, normally seen only during instar IV in Chironomidae, develop across both instars IV & V prior to pupation and adult emergence. While monitoring larval development post-thaw in 2014, we noticed freshly-molted T. alaskensis larval exuviae a week or more prior to any pupation by that species. In 2015-16 we reared overwintering instar IV larvae from single pond sources, individually with daily monitoring, through molts to instar V, pupa, and adult. Some overwintering instar II and III larvae were reared as well, but were few in number. During 2016 we also reared T. alaskensis progeny (from eggs) through instar II, thus documenting head capsule size ranges for all five instars in a single pond’s population. Without individual rearings, the fifth larval instar was not readily apparent for two reasons: 1) The molt itself occurs immediately after thaw and is so synchronous it is difficult to discern in daily field samples. 2) The head capsule size increment between instars IV-V is much lower than the ratio predicted by the Brooks-Dyar Rule. Up through instar IV, the Brooks-Dyar ratio for T. alaskensis ranged 1.30-1.61, but during the IV-V molt head capsule dimensions (sexes pooled) increased by a ratio of 1.09 – comparable to the magnitude of sexual dimorphism in head capsule size within each of the final two larval instars. Individual rearings coupled with 2014-2016 field surveys in nine other ponds suggest that five larval instars is an obligatory trait of this species at this location. As this is the first confirmed case of five larval instars in a chironomid, the phylogenetic uniqueness of this trait needs further investigation.


Holzforschung ◽  
2002 ◽  
Vol 56 (4) ◽  
pp. 335-359 ◽  
Author(s):  
P. Oevering ◽  
A.J. Pitman

Summary Pselactus spadix attack of marine timbers was characterised by circular emergence holes 1.48±0.05 mm in diameter and adult tunnels (1.49±0.34 mm) breaking through the wood surface. Larval tunnels measured 0.407–1.892 mm in diameter, initiated from adult tunnels and increased in diameter away from the adult tunnel terminating in frass free pupal chambers (1.6±0.3 mm × 3.5±0.7 mm). Observations of larval tunnel locations indicated oviposition occurred inside the adult tunnels. P. spadix life history was investigated in Scots pine (Pinus sylvestris) heartwood at 22±2 °C and 99±1% r.h. Mean adult longevity was 11.5±6.5 months, with mean post-mating longevity for males (11.7±2.9 months) significantly longer than for females (6.3±1.1 months). Adults of at least 2–3 months old were found mating in galleries, which, with observations of the larval tunnel pattern, indicated P. spadix can complete its life cycle without emerging from wood. Five larval instars were identified by measurement of 1722 head capsule widths and application of Dyar's law. Mean development time from 2nd instar to adult emergence was 70.5±6.9 weeks and pupation took 14.6±5.8 days. Development from 2nd instar to reproductive adult took between 17–20 months, with life cycle approximating 24 months at 22±2 °C and 99±1%


1987 ◽  
Vol 65 (1) ◽  
pp. 156-163 ◽  
Author(s):  
Olga Kukal ◽  
Peter G. Kevan

The life history of Gynaephora groenlandica was studied in the high arctic at Alexandra Fiord, Ellesmere Island. Life history events (larval development, pupation, adult emergence, mating, oviposition, hatching, and moulting to the second larval instar) occurred only in the 3–4 weeks before mid-July. Larvae fed mainly on Salix arctica. They stopped feeding by the end of June, hid, and spun hibernacula. Nineteen percent of third- and fourth-instar larvae were parasitized by the wasp Hyposoter pectinatus (Ichenumonidae); 52% of fifth- and sixth-instar larvae and pupae were parasitized by the fly Exorista sp. (Tachinidae). We estimated that G. groenlandica has a life cycle lasting 14 years. Parasitism caused 56% of overall mortality, whereas cumulative winter mortality was calculated as 13% of a cohort passing through a 14-year life cycle. Peak of activity of adult parasitoids coincided with inactivity of Gynaephora larvae during July. Selective pressure of parasitism may restrict development of G. groenlandica to a short period before adult parasitoids are most active. The importance of parasitoids in the life history of G. groenlandica suggests that parasitism is as significant as climate in population regulation of insects living in the high arctic.


2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
James Adebayo Ojo ◽  
Adebayo Amos Omoloye

The maize weevil,Sitophilus zeamaisMotschulsky (Coleoptera: Curculionidae), is one of the most destructive pests of stored cereals. Knowledge of the life history and biology is important to the development of an integrated pest management program. Investigation was carried out on developmental biology ofS. zeamaison four main cereal crops, maize, rice, sorghum, and millet, under laboratory conditions. Egg incubation, oviposition periods, and larval instar development were not different significantly among the food hosts. Number of eggs laid varied significantly among the cereal grains; mean fecundity was highest on maize (67.2±3.16) and lowest on millet (53.8±0.17). Number of immature (larva and pupa) and adult stages varied significantly among the cereal grains. There exist four larval instars with a varied mean head capsule width, with a mean total instar larval developmental period of 23.1, 22.2, 22.2, and 21.6 d on maize, rice, sorghum, and millet, respectively. There was linear relationship and significant correlation between the stages of larval development and head capsule width. The mean developmental period from egg to adult varied, being highest on maize (34.7 d) and lowest on sorghum (33.5 d).


1969 ◽  
Vol 59 (1) ◽  
pp. 51-62
Author(s):  
Rafael Inglés Casanova ◽  
Silverio Medina Gaud

The life cycle of the sphingid moth, Manduca sexta (L.), the tobacco hornworm, was investigated in Puerto Rico. Descriptions of the stages, including measurements of the egg (length and width), larva (length and head capsule width), pupa (length), and the duration of each of the stages are given. The estimated leaf consumption by each larval instar, a list of known host plants, and the natural enemies known to occur in Puerto Rico are included.


1965 ◽  
Vol 97 (9) ◽  
pp. 962-969
Author(s):  
Louis F. Wilson

AbstractThe pine gall weevil has a 3-year life cycle on red pine (Pinus resinosa Ait.) in Michigan. Adults oviposit from June to August, depositing 1 to 10 eggs in a niche chewed in the bark of a branch internode. Larvae first emerge in August, feed as a group toward the cambium, and then radiate out along the xylem. Head capsule measurements from 1585 larvae indicate that there are three larval instars. Gall development begins in June of the second year, shortly after the larvae begin the second instar. The third instar commences in June of the third year. Pupation occurs in May of the fourth season; adult emergence follows in June. Overwintering occurs in the egg stage or in the three larval instars. Adults do not overwinter, and apparently three distinct broods occur in Michigan.


2021 ◽  
Vol 117 (1) ◽  
pp. 1
Author(s):  
Gousul NISA ◽  
Abdul A. BUHROO

<p>A study on biology, morphometrics and geometrical progression of <em>Thysanoplusia orichalcea</em> was conducted on <em>Solanum tuberosum</em>under laboratory conditions. Different stages viz., egg, larva, pupa and adult of <em>T. orichalcea</em> were observed for their duration and morphometric measurements. The pest depicted five larval instars and moultedfour times during the entire period. The average pre oviposition and oviposition period was observed to be 3.80 and 2.80 days respectively.Further, fecundity ranges between 381.0-400.0 with an average of 388.0 eggs. The mean incubation period was found to be 4.2 days. The average larval, pre pupal and pupal period was completed in 23.1, 1.4 and 9.5 days respectively. While mean adult longevity on <em>S. tuberosum</em> was 7.45 days. The total life cycle was completed in 41.0-51.0 days with an average of 45.65 days. Moreover, mean head capsule width of first, second, third, fourth and fifth larval instar was found to be 0.33, 0.54, 0.88, 1.46 and 2.24 mm respectivelywith Dyar’s ratio/ growth ratio of 1.63 mm. The expected head capsule width of first, second, third, fourth and fifth larval instar wasobserved as 0.33, 0.53, 0.86, 1.40 and 2.28 mm respectively.</p>


2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
James Adebayo Ojo ◽  
Adebayo Amos Omoloye

The tamarind weevil, Sitophilus linearis Herbst (Coleoptera: Curculionidae), is an important pest of tamarind and other Caesalpinioideae. Investigating its life history is important in the implementation of management strategy. Its life history was monitored daily to understand its developmental biology on tamarind seed following standard procedures under laboratory conditions of 24–30°C temperature, 60–70% relative humidity, and 12L : 12D photoperiod. The egg incubation period lasted 3.17 ± 0.07 days. A mated female of S. linearis laid an average of 165 ± 5.78 eggs during an oviposition period of 86.8 ± 2.47 days. There were four larval instars, with a total larval developmental period of 16 days. The pupal period lasted 8 days, and adult lived 108.5 ± 3.61 days. The overall growth ratio for the four instars was 1.33. There was a regular relationship and significant correlation (r=0.94) between the stages of larval development and head capsule width.


1976 ◽  
Vol 54 (2) ◽  
pp. 266-284 ◽  
Author(s):  
G. Pritchard

Collections of all stages of the crane fly, Tipula sacra have been made over a period of years from a series of abandoned beaver ponds in the Kananaskis Valley, Alberta. The growth of larvae was followed by head-capsule measurements and weights. Eggs hatch within a month; first-instar larvae grow rapidly and enter the second instar after a few weeks. The second instar may last for 3 months and the third instar usually lasts for 6 months, including the first winter. Most larvae spend almost a full year in the fourth instar and overwinter for a second time. However, there was much variation in growth rate within the population. Adult emergence curves were consistent in form in 4 years. Each spanned a period of just over 2 months, although individual adults lived for only a few days. These curves snowed two peaks, the second of which contained 15–20% of the year's emergents. These two groups may represent different cohorts that have grown at different rates, suggesting that the life history may be semivoltine or univoltine. The sex ratio changes from about 1:1 in the third instar to 2:1 in favor of males in the late fourth instar, pupa, and adult.


1998 ◽  
Vol 76 (7) ◽  
pp. 1371-1381 ◽  
Author(s):  
W Dean Morewood ◽  
Richard A Ring

Many studies have explored the adaptations of arctic and alpine Gynaephora species (Lepidoptera: Lymantriidae) to their environment, and base-line life-history information is important for the interpretation of such studies. Data and observations on G. groenlandica (Wocke) collected in recent years at Alexandra Fiord, Ellesmere Island, Canada, contradict some of the life-history information previously published for this species from the same site. Detailed analysis of larval head capsule widths and consideration of growth ratios indicate that there are seven rather than six larval instars and that the pattern of development does not deviate significantly from that defined by the Brooks-Dyar rule. Field-rearing of larvae indicates that first-instar larvae overwinter, while field- and laboratory-rearing both indicate that larvae moult once per year, every year. These data and observations greatly shorten and simplify the life history from that previously published and suggest a life cycle of 7 rather than 14 years. This revised life cycle is not presented as an absolute, in recognition of the potential for individual variation, but rather as typical of the developmental pattern of most of the population. As such, it should provide a useful base line for further studies, especially those addressing the influence of predicted climate change in the Arctic.


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