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Aldabra Giant Tortoise Geochelone gigantea Description: Reaching up to 4 ft and over 700 lbs in size. Their shells range between light to dark brown with a visible neck plate that is not often found in other species of giant tortoises. Their necks are long and leathery to help adapt them to heat. Range: Seychelles (Aldabra Island) Habitat: Atoll islands-mangrove swamps, grasslands, and coastal dunes Diet: Largely herbivores, but may occasionally eat carrion or eggs if vegetable matter is not available. Weight: Males- 560 lbs; Females- 350 lbs Body Length: Second largest species of tortoise. Females can get up to 3 feet long, Males can be 4 feet long. Lifespan: Up to 100+ years Status: Vulnerable Predators: Giant Crab, Rats, Dogs, and Cats all prey on young tortoises, as well as compete for food. Threats: Habitat loss due to development, the introduction of nonnative predators (dogs, cats, rats) and livestock that compete for food (goats), and climate change, which leads to heightened sea levels and severe droughts. Relatives: They are a part of the Aldabrachelys genus, which is the taxonomic home of three giant tortoise species, two extinct species, and the extant Aldabra species. Breeding: Breeding season is from February to May. In courting, the male batters his shell against a female a dozen or more times and makes a deep, trumpeting call. The female buries 9 to 25 tennis-ball-sized eggs which incubate from 110 to 250 days. Reach sexual maturity between 20 to 30 years. Quick Facts: The GSC is home to two male Aldabra tortoises, Traveler and Jack. They may look a little different but that is because they have different shell morphotypes. This means that these two types of shells are adapted to a specific habitat. Aldabra tortoises with domed shells like Traveler are found in humid, cooler, and higher elevation habitats while saddlebacks like Jack are found in drier areas at a lower elevation. There are 3 extant subspecies of the Aldabra Tortoise: Aldabra giant tortoise (ours), Arnold’s giant tortoise, and the Seychelles giant tortoise. Daudin’s giant tortoise was the fourth subspecies but has been declared extinct. There are estimated to be over 150,000-200,000 individuals scattered about the Seychelles islands. It is believed that the oldest living giant tortoise is Jonathon, a 190-year-old Seychelle Giant Tortoise who was hatched around 1832 and resides on the Island of St. Helena in the British Overseas Territory. These tortoises can drink water through their nose, an adaptation that is useful in a mangrove environment. Despite their weight, these tortoises are able to stay afloat in water thanks to hollow honeycomb structures within their shell. In December of 2004, an Aldabra that had been washed away from the Seychelles made the 460-mile journey to the East African Shoreline (Tanzania). Aldabra tortoises are a keystone species that shape their habitat through seed dispersal. The closest relatives of the Aldabra tortoise are the tortoises of Madagascar. Scientists at the Galapagos Conservancy speculate that the ancestors of giant tortoises accidentally reached isolated islands by riding on rafts of plant matter. Conservation: Different species of giant tortoises were once found on a variety of equatorial islands. Unfortunately, over-collection for food by humans and the introduction of invasive species such as rats (which raid nests) and goats (which compete for food) drove all but 10 subspecies of Galapagos tortoises and 3 subspecies of Aldabra tortoises to extinction. It is important that these island ecosystems are carefully preserved as many are home to animals found nowhere else on Earth. Furthermore, Aldabra tortoises are helping to restore island ecosystems by being introduced to islands that have lost their native giant tortoise species. GSC Residents: Name: Traveler Date of Birth: ~December 2000 to December 2001 Sex: Male Origin: Donated from private owner October 13, 2005 Favorite Foods: Strawberries, tomatoes, bananas, watermelon Favorite Enrichment: shell scrubs Trained Behaviors: Target, scale, blood draw From the Keeper: He has a dome shell. This keeps Traveler from having the ability to reach up high like Jack can. Name: Jack Date of Birth: ~December 1989 to December 1990 Sex: Male Origin: Donated from private owner August 17, 2005 Favorite Foods: Tomatoes, strawberries, bananas, watermelon Favorite Enrichment: Shell scrubs Trained Behaviors: Target, scale, blood draw, station, color discrimination From the Keeper: He has a saddleback shell, which allows him to reach up farther for leaves and food. They can feel through the shells which are made up of keratin and bone. He is often mistaken for a rock or a statue for how still he stands at times. Facts about GSC Residents: Daily Schedule Fed main diet 3x a week, Monday, Wednesday, and Saturday. Fed browse every day. More active during the warmer weather. Will sleep, and browse throughout the day. Training Behaviors​ Due to the tortoises' immense size, we utilize several training behaviors to minimize stress on the animals and keepers. Our tortoises are target-trained, allowing us to direct them where we need them to go. Similarly, we are working with the tortoises on the Scale behavior, so that they will voluntarily walk up onto our scale for weighing. They are also working on foot/neck/poke behaviors. The foot behavior allows us to pick up their feet to see if they have any problems. The neck/poke behavior is for when we start drawing blood from their neck for health and wellness checks. Health History Sometimes get runny eyes due to dust, so we spray the ground with the hose to reduce dust. Favorite Story Jack is very sociable and loves to be scratched and rubbed. When we walk away, he will follow us wanting more
Updated 30d ago
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BASIC STRUCTURE AND PROMINENT FUNCTIONS OF VERTEBRATE INTEGUMENT INTRODUCTION The integument or the outer cover of the body is commonly referred to as the skin. Together with its derivatives it makes up the integumentary system. It is continuous with the mucous membrane lining the mouth, eyelids, nostrils, rectum and the openings of the urino-genital ducts. The skin functions primarily to cover and protect the tissues lying beneath it. In other words, it forms the external protective covering of an animal. Forms interface between organism and external environment. Part that the predator sees first, and which offers the first line of defense. Abundantly supplied with sensory nerve endings, which are affected by environmental stimuli and play an important role in communication. General metabolism of the body, temperature regulation and water loss. Character of the skin and its derivatives shows variation in different regions of the body, in different individuals, in the same individual as age advances and in different groups of vertebrates. The type of environment whether aquatic or terrestrial is of importance in connection with these variations. The evolution of vertebrate integument is correlated with the transition of vertebrates from an aquatic to a terrestrial environment. Nevertheless, basic similarities exist in the integument of all vertebrates. INTEGUMENT PROPER In Annelids, Arthropods, integument consists of single layer of cells, the EPIDERMIS, together with an outer non-cellular CUTICLE, secreted by the cells. Annelids have a body covered with an external thin collagenous cuticle (never shed or molted). In Arthropods, the chitinous and rigid cuticle makes up the exoskeleton. Periodic shedding of this cuticle is termed Ecdysis. THE VERTEBRATE SKIN DIFFERS FROM INVERTEBRATE SKIN TWO LAYERS – Outer epidermis derived from ectoderm Inner dermis or corium of mesodermal origin. The relative amount of the two layers varies with the environment. EPIDERMIS – the epidermis is made of stratified epithelium (several layers of columnar epithelium cells). These cells are held together tightly by minute intercellular bridges found on the surface of cells. The innermost layer is stratum Malpighii or stratum germinativum placed over a thin basement membrane. These cells divide constantly to produce new cells. Move upwards, tend to become flattened, protoplasm becomes horny (keratinisation). In fishes and amphibians, this keratinised layer forms a cuticle, but in amniotes, it forms stratum corneum, of hard, horny, flat, cornified cells made largely of keratin, which is tough, waterproof and insoluble protein. It affords protection against mechanical injuries, fungal and bacterial attacks and prevents desiccation. In many Tetrapoda, this layer is shed periodically in pieces or all at once. No stratum corneum in cyclostomes and fishes (since they are fully aquatic) here the epidermis has mucous glands, secreting mucus to keep the skin slimy and protects it from bacteria. The epidermis has no blood vessels and is nourished by capillaries in the dermis. The epidermis rests on a thin basement membrane which separates it from the dermis Dermis has an outer loose layer and inner dense layer Made up of dense connective tissue having cells, muscles, blood vessels, lymph vessels, collagen and elastic fibres, and nerves. Amphibians and reptiles -collagen fibres at right angles in three planes Birds and mammals, they have an irregular arrangement. Substances pass by diffusion from the dermis to the epidermis. Skin contains pigment, if present in epidermis, it occurs as a diffuse substance or as granules. If in dermis, then in the form of granules in special branching cells called chromatophores. The pigment can either collect as a central ball making the skin lighter or spread out into all the branches making the skin darker, thus, chromatophores bring about colour variations. Chromatophores are of many kinds, Melanophores that contain brown to black pigment Lipophores or xanthophores which contain yellow red fatty pigments Iridocytes or guanophores contain crystals of guanine which reflect light. Under dermis, the skin has subcutaneous loose areolar tissue which separates the skin from the underlying muscles, it may contain fat and muscles, especially in mammals. Integument of Anamnia shows a decrease in thickness and also a decrease in the degree of ossification. These are of advantage in allowing greater mobility and in amphibians, they permit respiration by the skin. But in Amniota, the skin becomes progressively thicker to prevent loss of water and to retain body heat. STRUCTURE OF INTEGUMENT IN CYCLOSTOMATA Epidermis is multi-layered (stratified) but has no keratin. It has three types of unicellular gland cells: mucus glands (secrete mucus), club cells (scab-forming cells) and granular cells (unknown function). Below epidermis is the cutis formed of collagen and elastin fibres. Star- shaped pigment cells are also present in the cutis. STRUCTURE OF INTEGUMENT IN PISCES The epidermis has several layers of simple and thin cells, but there is no dead stratum corneum. The outermost cells are nucleated and living. The stratum Malpighii replenishes the outer layers of cells which have some keratin. Unicellular goblet or mucous gland cells are found in the epidermis, as in all aquatic animals. The mucous makes the skin slimy reducing friction between the body surface and water, protects the skin from bacteria and fungi and assists in the control of osmosis. Multicellular epidermal glands like poison glands and light producing organs may also be found. The epidermis rests on a delicate basement membrane. The dermis contains connective tissue, smooth muscles, blood vessels, nerves, lymph vessels and collagen fibres. The connective tissue fibres are generally not arranged at right angles but run parallel to the surface. Scales are embedded in the dermis and projected above the epidermal surface. The colours of fishes are due to chromatophores and iridocytes. STRUCTURE OF INTEGUMENT IN AMPHIBIA: The epidermis has several layers of cells, six to eight cells in thickness and is divisible into three layers: stratum corneum, stratum germinativum and a basal portion in contact with the basement membrane. The outermost layer is a stratum corneum, made of flattened, highly keratinised cells. Such a dead layer appears first in amphibians and is best formed in those which spend a considerable time on land. The stratum corneum is an adaptation to terrestrial life (protects body and prevents excessive loss of moisture). In ecdysis, stratum corneum is cast off in fragments or as a whole in some. (moulting / desquamation i.e., removal of unicellular sheet of stratum corneum). The dermis is relatively thin in amphibians, it is made of two layers - upper loose stratum spongiosum and a lower dense and compact stratum compactum. Connective tissue fibres run both vertically and horizontally. Blood vessels, lymph spaces, glands and nerves are abundant in the stratum spongiosum. There are two kinds of glands, multicellular mucous glands and poison glands in the dermis, but they are derivatives of the epidermis. Mucous gland produces mucus (slimy protective covering, helps in respiration). Amphibian skin is an important organ of respiration. Poison glands produce a mild but unpleasant poison which is protective. In the upper part of the dermis are chromatophores. (melanophores and lipophores) Ability of the skin for changing colour to blend with the environment is well developed. INTEGUMENT IN REPTILIA. The integument is thick and dry, it prevents any loss of water, it has almost no glands. The only glands present are scent glands for sexual activity. The epidermis has a well-developed stratum corneum well adapted to terrestrial life. The horny scales of reptiles are derived from this layer. Ecdysis is necessary to remove dead outer layers, hence scales are shed periodically in fragments or cast in a single slough as in snakes and some lizards Scales often form spines or crests. Below the epidermal scales are dermal bony plates or osteoderms in tortoises, crocodiles and some lizards (Heloderma). The dermis is thick and has an upper layer and a lower layer, upper layer has abundance of chromatophores in snakes and lizards. Lower layer has bundles of connective tissue in which collagen fibres lie at right angles. Leather of high commercial value can be prepared from the skin of many reptiles like lizards, snakes and crocodiles. Many lizards and snakes have elaborate colour patterns, they may be for concealment or as warning colours. There is marked colour change in certain lizards such as chameleon, the colour may change with the environment for concealment or it may change in courtship or threat. The ability of chameleons and some other animals to change colour is known as metachrosis. (metachromatism) In Calotes, chromatophores are controlled by the posterior lobe of pituitary whereas in chameleons they are controlled by the Autonomic Nervous System. INTEGUMENT IN BIRDS Thin, loose, dry and devoid of glands. There is only a uropygial gland at the base of the tail, its oil is used for preening (to clean and tidy its feathers with its beak) and waterproofing the feathers (aquatic birds) Epidermis is delicate except on shanks and feet where it is thick and forms epidermal scales. The rest of the body has a protective covering of epidermal feathers. The keratin producing powers of the epidermis are devoted to producing feathers and scales. The dermis is thin and has interlacing connective tissue fibres, abundant muscle fibres for moving feathers, blood vessels and nerves. The dermis has an upper and lower compact layer, between which is a vascular layer, the dermis also contains fat cells. The skin has no chromatophores. Pigment is found only in feathers and scales. Colour patterns in birds are vivid (concealment, recognition and sexual stimulation) Colours are produced partly by pigments and partly by reflection and refraction from the surface of the feathers. INTEGUMENT IN MAMMALS Skin is elastic and waterproof, much thicker than in other animals, especially the dermis is very thick and is used in making leather. Epidermis is thickest in mammals. Outer stratum corneum containing keratin, cells not dead as believed before. Below this is stratum lucidum (barrier layer), chemical called eleidin Below this stratum granulosum, darkly staining granules of keratohyalin Below this is stratum spinosum whose cells are held together by spiny intercellular bridges. Lastly stratum germinativum which rests on a basement membrane Dermis is best developed in mammals. Upper layer is papillary layer made up of elastic and collagen fibres with capillaries in-between, thrown into folds called dermal papillae, especially in areas of friction Greater lower part of dermis is reticular layer, having elastic and collagen fibres. In both layers there are blood vessels, nerves smooth muscles, certain glands tactile corpuscles and connective tissue fibres in all directions. Below dermis the subcutaneous tissue contains a layer of fat cells forming adipose tissue In the lowest layer of epidermis there are pigment granules, no pigment bearing chromatophores in mammaIs (in man, branching dendritic cells or melanoblasts) FUNCTIONS OF THE INTEGUMENT ▪ PROTECTION ▪ TEMPERATURE CONTROL ▪ FOOD STORAGE ▪ SECRETION ▪ EXCRETION ▪ SENSATION ▪ RESPIRATION ▪ LOCOMOTION ▪ DERMAL ENDOSKELETON ▪ SEXUAL SELECTION 1. Protection: The integument forms a covering of the body and is protective. It protects the body against entry of foreign bodies and against mechanical injuries. It protects the tissues against excessive loss of moisture, this is very important because both aquatic and terrestrial animals are dependent upon water in their bodies for various metabolic activities. The integument forms protective derivatives, such as scales, bony plates, layer of fat, feathers and hair which reduce the effect of injurious contacts. In some animals the skin shows protective colouration which makes the animals resemble their environment, thus, making them almost invisible to their enemies. Poison glands of toads, slippery skin of aquatic animals and an armour of spines of some mammals are protective devices of the integument. The skin forms a covering which prevents the passage of water and solutes in one of the following ways: (a) By formation of cuticle in Protochordata and embryos of fishes and amphibians, (b) By secreting a coat of mucus in fishes and aquatic amphibians, and (c) By formation of keratin layers in the epidermis of tetrapoda. Keratin is formed from the cytoplasm of degenerating cells of the epidermis which finally form a layer of horny stratum corneum. 2. Temperature Control: Heat is produced constantly by oxidation of food stuffs in tissues. This heat is distributed evenly by the circulating blood. The body heat is lost constantly with expired breath, with faeces and urine, and from the surface of the skin. The integument regulates heat and maintains a constant temperature in endothermal animals. In birds the heat is regulated by adjustment of feathers which retain a warm blanket of air, when feathers are held close to the body, they remove warm air and body cooled, when feathers are fluffed out, they keep the warm air enclosed. In mammals, constant evaporation of sweat regulates the body heat. In cold weather contraction of skin’s blood capillaries reduces the loss of body heat. In some animals, fat in the skin prevents loss of heat because it is a non-conductor of heat. 3. Food Storage: The skin stores fat in its layers as reserve food material which is used for nourishment in times of need. In whales and seals the fat of the skin forms a thick layer, called blubber which is not only reserve food but also maintains the body temperature. 4. Secretion: The skin acts as an organ of secretion. Glands of the skin are secretory. In aquatic forms there are secretory mucous glands whose secretions keep the skin moist and slippery. In mammals, sebaceous glands secrete oil which lubricates the skin and hairs. Mammary glands produce milk for nourishment of the young. In birds uropygial glands secrete oil for preening the feathers. Odours of scent glands attract the opposite sex. Lacrymal glands’ secretion wash the conjunctiva of eyeball in mammals. Ear wax (cerumen) secreted by the glands of auditory meatus greases the eardrums and avoids insects to enter the canal. 5. Excretion: The integument acts as an organ of excretion. Shedding of the corneal layer during ecdysis removes some waste substances. In mammals metabolic waste (salts, urea and water) is removed from the blood by means of sweat. Chloride secreting cells are found in gills of marine fishes. 6. Sensation: The skin is an important sense organ because it has various kinds of tactile cells and corpuscles which are sensory to touch, temperature changes, heat, cold, pressure and pain. 7. Respiration: In amphibians, the moist skin acts as an organ of respiration, in frogs the respiratory function of the skin is greater than that of the lungs. 8. Locomotion: Derivatives of the integument bring about locomotion in some animals, such as the fins of fishes aid in locomotion in water, the web of skin in the feet of frogs and aquatic birds aid in swimming, feathers of the wings and tail of birds are used for flying, and extensions of the integument forming “wings” of flying lizards, extinct pterodactyls, flying squirrels and bats. 9. Dermal Endoskeleton: The skin contributes to the endoskeleton. It forms the dermal bones of vertebrates and also forms parts of the teeth. Endoskeleton of head protects the brain and sense organs. In the body it protects the soft, tender viscera. 10. Sexual Selection: The skin acts as an organ of sexual selection. It provides the feathers of birds which often have brilliant colours which are for sexual attraction. Some integumentary glands of mammals produce odours far attracting the opposite sex. Antlers of male deer distinguish it from female. Besides the above functions, mammalian skin synthesizes the vitamin D with the help of Sebum of sebaceous glands. Brood pouches beneath skin in some fishes and amphibians protect unhatched eggs. Nasal glands of tetrapods, keep the nostrils free of dirt and water. Skin also has the power of absorption of oils, ointments, etc
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Organismal close-up: Introduction to the Honeybee. Origins. Honeybees are eusocial. This means that they have the highest level of sociality in animals. When it comes to the structure of the bee: there is the queen who lays eggs and then the worker bees ( lifetime fitness:0, they dont reproduce) Sociality issue: why are they doing what theyre doing? If they dont reproduce Same mother not the same father Eusocial definition: defined by cooperative brood care (including care of offspring from other individuals), overlapping generations within a colony of adults, and a division of labor into reproductive and non-reproductive groups. They evolved from wasp-like ancestors ( predetory/carvineous hymenopteras) ( sting to paralize) in the Cretaceous period, about 145-65 million years ago. Also, during this period, flowering plants became dominant in the world’s flora. Therefore, bees and flowers have been coevolving for over 100 million years. Most wasps are solitary Some are social wasps/bees Wasps parallel bees Ants: hypersocial From their wasp-like ancestors, bees inherited their narrow waist, a stinger, and the ability to build nests. The narrow waist permits the abdomen to be pointed in many directions for stinging and laying eggs. Not their abdomen Thorax= first segment of the abdomen Use the narrow poriton of the “abdomen” to be more mobile To sting To lay eggs The stinger, used in wasps to kill or paralyze prey, is used by bees to defend the colony from robbers. However, wasps are predators, whereas bees feed almost exclusively on nectar and pollen gathered from flowers. Flowers provide the complete diet for the bee colony. Evolution of social structure. Most bees and wasps are solitary species in that individual females lay eggs in either burrows or wood crevices. They provision each egg with pollen and nectar (bees) or prey (wasps). Usually each egg with its food is placed in its own “cell”, which is walled off from the adjoining cell. In these solitary species, the bee/wasp mother never meets her children (she leaves them after provisioning the nest). No colony, all individual bees doing their own thing ( solitary species) Early social species. A few burrowing species are social, where the mother waits for the daughters to be born, and then these daughters help the mother forage and dig or form extra cells for her to lay eggs in. These working daughters are the beginning of the “worker caste”. Social→ female will hang out with the mother after being hatched and then work together to do thing like build nests and find food More advanced species, like bumblebees and yellow-jacket wasps: Here the workers are far more numerous (hundreds in bumblebees and thousands in yellow-jackets). The workers are smaller than the mother “queen” (queen caste), and often have different color patterns. Behavior has been partitioned too. Workers forage, build the nest, and defend it. The queen never leaves the nest and only lays eggs. Annual vs. perennial. In the previous examples, the colony is annual, that is, the foundress queen creates workers (and males), and the colony grows until the end of the growing season, when all bees die except new queens that have been inseminated. ( everyone dies except the new queen burried in the soil→ foundress quen) These new foundress queens will overwinter in a burrow or crevice, and in the spring, start feeding and building a new colony. The colony lasts only ONE YEAR If you see a bee fling around in december= that is a queen bee Only in honeybees (Genus Apis) is the colony perennial, potentially living forever. ( 1 colony= 50/80, 000 bees) Two adaptations have permitted this: Honey storage away from the brood combs (developing offspring). Allows honeybees to survive periods of harsh environmental conditions, like winter and droughts. Supplies the energy to heat the colony during winter. Honeybees use the honey to shiver, which creates heat. During drought, nectar flow (flower availability) may stop (called a “dearth”), but the stored honey can be used until nectar flow resumes. What if it gets warm and then cold all of the sudden→ die HONEY→ colony species fully rely on this to get through harsh environmental conditions Colony formation by swarming. In the late spring, large honeybee colonies reproduce by swarming, which splits the colony. Split into 2 in april The other half leaves and gets their own queen The new colony has a mated queen and a lot of workers and is “ready to go”. This is a big advantage over solitary or more primitive social species that must start each spring with a single foundress queen. Bees use honey to get through winter Bee species. Honeybees are members of the genus Apis. This genus is native to Europe, Asia, and Africa (not the Americas). The number of Apis species is debatable, the number varying from 4 to 15 depending on the taxonomic treatment. There are basically 4 distinct honeybee groups: Dwarf Honeybee: Apis florea & other. Only ¼ inch long. Native from Iran through SE Asia. The comb of the nest is small and only contains a few ounces of honey. Open nest The comb is a single small plate. The nest is usually concealed under leaves or in a cave. People do cut these nests down to harvest the honey, but little honey harvest is achieved. Couple ounces of honey Giant Honeybee: A. dorsata. Large bees about 0.7 inches long. Geographical distribution similar to Dwarf Honeybee. In Nepal, Tibet, and India. The comb of the nest is a large exposed plate which is strong and can contain up to 50 lbs of honey. The nest is not in the dark and must be fully illuminated; they usually hang down from tree branches, placed about 80 ft in the air. Ununsual because nests are in the open and not hidden These bees are aggressive if the nest is raided, and will pursue the raider for up to 300 feet. The copious honey is greatly prized by local peoples. Eastern Honeybee: A. cerana & others. Slightly smaller than the Western Honeybee. Wide distribution covering most of Asia. Over this wide range, several races have evolved, for instance an Indian and Burmese race, a Japanese race, etc. Sometimes these are considered species, other times as subspecies. The nest consists of several combs hanging in parallel plates, each plate being separated by a consistent distance (the “bee space”). Found in dark hollow trees and caves. Bee space= very specific value Comb separated by bee space= they will be int hat space only If too far or too close= bees will purpusefully put it back Everyone tries to understand this concept to grow honey easer ( reasons or beekeepers) In less tropical regions, they store a decent amount of honey. Western Honeybee: A. mellifera. The most widely distributed bee on Earth. It has been under human domestication for so long that its origins are unclear. It appears to be native to Africa, and from there it spread into Europe (perhaps 10,000 years ago), and later with colonial expansion into North America and Australia. The nest is like the Eastern Honeybee, with parallel plates and a dark interior. This nesting behavior adapts well to the artificial nests made by humans. With such a wide range, many races have evolved, often recognized as subspecies. Italian Honeybee, Apis mellifera ligustica: Yellow- and orange-banded abdomen. Originally from Italy and Sicily, now the most widely distributed race in the world. There are better choices for cold regions. They are gentle, disease-resistant, and good foragers. Carniolan Honeybee, A. m. carnica: Dusky brown with more muted orange bands. Originally from Austria and the Balkan region. Has been transported worldwide, like the Italian. Second most popular race after the Italian. Often used in cooler northern areas since they fly in cooler weather than Italians. Gentle, disease-resistant, good nest defenders, and make lots of honey. German Black or Dark European Honeybee, A. m. mellifera: A cold-weather resistant race, from western Europe including Britain, and north and west of the Alps. African Honeybee, A. m. scutellata: Native to southern and central Africa. Looks a lot like the Italian. High honey yields, great disease-resistance, and highly defensive. Accidentally released in Brazil in 1957. After release, hybridized with more gentle European races, giving rise to “Africanized bees”. Cape Honeybee, A. m. capensis: From the Cape Peninsula in South Africa. Unlike other honeybees, female workers are able to lay fertile eggs. In areas where the African and Cape races co-occur, the Cape queens can enter the African colonies, undetected, and lay eggs which lead to laying workers, which eventually destroy the colony. The only bees that can have worker bees lay eggs Egyptian Honeybee, A. m. lamarcki: Small and dark with yellow abdominal bands. Native to the Nile valley region. Defensive behavior and low honey production. This was probably the race used by ancient Egyptians. Today it doesnt make as much honey The Buckfast bee: A hybrid bee developed by Brother Adam at Buckfast Abbey in Devon, England, in 1919. The stimulus to create this new bee came from the massive bee losses caused by the Isle of Wight disease, which occurred between 1906 and 1919 on the Isle of Wight in southern England. Brother Adam at Buckfast Abbey noticed that hybrids between Italian and German Black honeybee survived the disease, and so he began an extensive breeding program to create the Buckfast bee, which is a hybrid involving honeybee strains from Italy, England, France, Turkey, Greece, and two African strains. SUMMARY: hybirds of bees (=buckfast bee) did not die due to the disease → highly disease resistant Buckfast bees have many desirable characteristics and are widely available. Castes. Long abdomen on queen= for big ovaries for the kids Bigger shiefd for protection MASSIVE eyes for drone / furry tail A Western honeybee colony or hive is composed of thousands of individual bees. At the height of summer, a hive may contain up to 50,000 bees. Most of these individuals are workers, which are sterile females. A few hundred individuals are drones, which are fertile males. The hive normally has only one queen, who is female and fertile. These bee castes are easy to distinguish with the naked eye. Each caste has its own roles within the colony. Sex & genetics. Of the three castes, only the queen normally lays eggs. The queen becomes fertilized by mating with several drones on her nuptial flight. The queen stores sperm in a special organ (the spermatheca). What determines sex in the offspring? Unlike humans, bees have no sex chromosomes. Haplodiploidy. (diploid= female, haploid=male) It was previously thought that sex was determined by the number of chromosomes in the organism. In haplodiploidy, queens and workers are diploid with 32 chromosomes, and drones are haploid with 16. When laying eggs, the queen makes the decision to either fertilize or not fertilize the egg. A fertilized egg is diploid and makes either a worker or another queen, whereas an unfertilized egg is haploid and will form a male drone. During inbreeding studies carried out by investigators, diploid drones were created, which brought into question the idea that chromosome number alone determines sex. Sex determination locus (SDL). This genetic locus (a physical position on a chromosome) was hypothesized to exist over 70 years ago. At this locus, a diploid bee can have two genes (alleles) present, whereas a haploid bee can only have one gene present. In a diploid bee, if both genes are the same (called a homozygous genotype), the bee is male (diploid drone). If the genes are different (called a heterozygous genotype), the bee is female. In a haploid bee, only one gene is present (called a hemizygous genotype), which results in a male (drone). Complementary Sex Determiner (csd) gene. In 2003, the actual gene for sex determination was discovered. It is called the Complementary Sex Determiner (csd) gene, which has at least 15 variants (alleles). The product of the csd gene (protein) is required for the bee to become female. This protein binds to the mRNA made from a feminizer gene called fem, causing it to function a certain way, leading to a female. If it does not bind, the function of fem will differ, leading to a male. The product of the csd gene will only be able to bind to fem if both alleles at the SDL are different (heterozygous). Workers, basic structure. The worker is the “routine” bee, which is between ½ - ¾ inch in length, with an almost cylindrical body. Workers, like other castes, can see well, have the ability to detect sound, and have antennae that sense the physical and chemical environment. Chemicals called pheromones are picked up by the antennae, and these chemicals are used to control many activities within the hive. Mouthparts. Worker mouth parts consist of mandibles and a proboscis. The two mandibles oppose each other like scissors, and they are used to bite, chew, and hold objects. The proboscis is a tubular apparatus used for sucking up nectar, and to regurgitate the nectar back in the hive. Pollen collection. One major activity of workers is collection of pollen, which is accomplished by the many feathery hairs on the body. When visiting a flower to drink nectar, pollen adheres to the hairs, and the bee brushes the pollen onto the hind legs using legs bearing special stiff hairs resembling a comb (the pollen brush). When the hind legs are rubbed together, pollen is forced into a specially modified joint on the legs, which then presses the pollen mass into a hard cake. This pollen cake is held in place by a fringe of hairs called the corbicula or pollen basket. These pollen masses are easily seen on workers entering the hive after visiting flowers and are the color of the pollen they have collected. Stinger. As is widely known, workers bear a stinger at the tip of the abdomen. It is used to defend the hive. It is modified from the egg-laying ovipositor; therefore, males don’t have a stinger. The stinger is barbed, and when she attempts to withdraw it after stinging a human, it gets stuck and pulls out some of her abdominal organs, the venom sac and a muscular pumping mechanism. The worker will soon die. The stinger will remain in the skin and will continue pumping venom. It will also release alarm pheromones into the air which alarms other bees to pursue the victim. Wax glands. On the undersurface of the bee’s abdomen are located 8 wax glands. In these glands, special cells secrete beeswax, which forms a blob at first, and then forms into a flat scale or chip shape. These chips are about 1/8-inch-long and can often be seen protruding out from below the abdomen. The beeswax is used to build the comb. The bee scratches off the wax from the glands with its legs, and passes it to its mandibles. Beeswax is mixed with saliva and chewed to make it malleable and the perfect consistency for use. Beeswax is an energetically demanding material to produce. How much honey is needed to make a pound of wax is not agreed on, with estimates varying widely. A reasonable value is about 20 lbs of honey to make 1 lb of beeswax. Workers, early development. An egg laid by the queen hatches in 3 or 4 days. The young larva is visited by adult worker bees, called nurse bees. The larva receives over 140 small meals over a span of five days, at which time the larva is fully grown. This is about nine days after the egg was laid. Larval diet. During the first 3 days of the larva’s life, nurse bees feed the larva a protein-rich secretion from their mandibular and hypopharyngeal glands. This substance is called either “brood food” or “royal jelly”. Its protein content comes from the pollen consumed by the nurse bees. After the 3rd day, nurse bees dilute the brood food with honey and pollen, and the total amount of food fed to the larva is reduced. (For comparison, if the larva is destined to become a queen, nurse bees continue feeding the larva brood food in unlimited quantities. The brood food is never diluted with honey and pollen nor is it reduced in amount.) Larva grown, sealed in. Once the larva is fully grown (about nine days after the egg was laid), the nurse bees seal the cell with wax, which is tan in color and somewhat porous. It takes the nurse bees over 100 visits and 6 hours of effort to seal the cell. Inside the sealed cell, the larva transforms into a pupa, and then undergoes metamorphosis into an adult. Emergence. Generally, a worker bee emerges from her pupal cell 21 days after the egg was laid. For comparison, a drone takes 24 days and a queen 16 days. These development times are similar in the Eastern honeybee, possibly because both species regulate the hive temperature to about 95 deg F. A newly emerged worker bee spends a few hours grooming herself until she is dry. Early life as an adult in the hive. Getting fed. For the next few days, she will stay in the nest and “ask” other workers for food. She sticks her tongue out at the passing workers, and they will respond by opening their mandibles, dropping their tongue a bit, and then regurgitating a droplet of sugary liquid from which the new bee drinks (a process called trophallaxis). After about 3 days, the new bees begin to feed on honey reserves in the honey-storage cells, and on protein-rich pollen located in certain pollen-storage cells. Work duties. During days 4 and 5, the bee may start feeding the developing brood. At first, she can only feed older larvae, which don’t require pure brood food, as she can only regurgitate honey and pollen. By day 6, her hypopharyngeal glands start making brood food, so she can then feed the younger larvae. She uses the protein-rich pollen that she has eaten to make the brood food. From days 10 to 12, her brood food glands are exhausted, so she stops feeding the larvae. Her wax glands start making wax, so she begins making and repairing comb. Workers, adult development. Figure. Consecutive flights of five individual bees. (a, b, c) Consecutive orientation flights of three bees. (d, e) Complete orientation phase before the first foraging flights (FO) of two bees. Venture out, orientation. Also, from days 10 to 12, she will leave the hive for the first time. On her first trip outside, she will defecate for the first time. Orientation. At first, she hovers near the hive to learn the environment around the hive. These are called orientation flights. Circling pattern, with ever-wider circles. Later, she will fly further away. Meeting foragers, making honey. For the next week or two she will stay mostly in the hive, meeting the incoming forager bees. These foragers come into the hive with a full honey stomach and pollen load, and when she meets them, they will regurgitate the liquid and pass it to her (she drinks it). She will take it deep within the hive and regurgitate it, then swallow it, and repeat. As she does this, she partially digests the sucrose in the nectar into fructose and glucose (using the enzyme invertase). This manipulation of the liquid also dries it down to 17-18% moisture, which is extremely concentrated. The final product is honey, which is then deposited into honey-storage cells. Drying of the honey is also aided by the other workers that continually fan their wings to create a draft. She also places the pollen load from the foragers into the pollen-storage cells. Workers, housekeeping, graduation to foraging. Also, during the first weeks in the hive, she will do general housecleaning, like removing debris and dead bees. Observing older foragers. By week 3 or 4, she becomes a forager, and starts off by closely observing the returning older foragers. She especially observes the scout foragers that found new sources of pollen and nectar. These scouts perform communication “dances” that tell the other foragers where the food is located. It takes the new forager time to learn the language of the dancing. Once she figures it out, she will join the foraging force. Foraging duties. When foraging, she is focused primarily on collecting nectar and pollen. But she also will drink water and collect propolis, which is a sticky sap exuded by trees. Propolis is used in the hive to seal gaps and holes and to improve the strength of combs. Guard bees. A small number of bees will become guards, which stand near the hive entrance with their front legs held off the surface, making them look like they are going to pounce. They guard the entrance against non-hive bees and honey robbers. Retirement (death). During summer, she works so hard that she dies within 5 or 6 weeks from emergence. If she emerged in the fall, her activities are far more restricted, and she could live for 5 or 6 months. Workers, communication. Foragers can communicate the presence, direction, nutritional value, and distance to food sources by “dancing” on the comb surface and regurgitating the food. Food is close by. If the food source is within a few hundred feet of the hive, the forager will do the “round dance”, where she moves in circles, alternating between clockwise and counterclockwise directions. The other workers pay close attention to the dance. The forager is covered with scents from the food source, and the other bees will leave the hive in search of matching odors. Food is far away. If the food is further away, the “waggle dance” or “figure-eight” dance is performed. Here there are two circles, one clockwise and the other counterclockwise, with a straight line connecting them. The straight line portion contains several clues: The angle of the line relative to the vertical axis of the comb represents the angle of the sun relative to the food source. The length of the line represents the distance. The intensity of waggling back and forth suggests the quality of the source, with greater waggling corresponding to greater quality. Since the hive is totally dark inside, the observing workers cannot see the dance but instead sense it by vibrations and probably by other means. Workers will press their abdomen to the comb and vibrate signals back to the dancer, and she will regurgitate some of the food for the workers to sample. When traveling to the food source, the foragers can detect the sun’s position in the sky even on overcast days. Queen, basic structure. The queen is longer and narrower than the worker. She is up to ¾ inch in length. Her head and eyes are smaller in comparison to the workers, because she does not forage outside the hive. She has a very short tongue because she never sips nectar from flowers, but is fed directly by her “attendants” (a group of worker bees, also called a “retinue”). Her mandibles are also different, and associated with them are large mandibular glands, which secrete the “queen mandibular pheromone” (QMP) or “queen substance”. (Workers also have these glands, but they don’t secrete QMP.) Her abdomen is long because it contains many eggs. Her legs are not adapted for pollen combing and holding. She has no wax glands. She has a stinger, however it is not barbed like the worker stinger. It is only used for one purpose: killing rival queens. Queen, pheromone. QMP is a complex mixture of chemicals, with only about 24 of them being well known. The queen is constantly attended by her “attendant” workers, which monitor, lick, groom, feed, and exchange body fluids with her. As a result, the attendants pick up the pheromone. The attendants then spread the pheromone to other workers. Within the hive in general, each bee is frequently exchanging fluids and food with other bees, so the pheromone gets spread among all bees in the hive. The presence of QMP is how workers in the hive know that the queen is present. If the queen secretes normal levels of QMP and the hive is not overly crowded, each worker in the hive feels “queenright”, that is, a normally functioning queen is present. If levels of QMP in the hive drop because the queen is not producing enough, the workers will begin preparations to make a new queen. This is termed supersedure. Also, if the number of workers in the hive gets too large, the QMP will get diluted so much that each worker no longer feels “queenright”. This may lead to swarming behavior. To prevent swarming, each worker needs a daily QMP dose of about 0.001 mg. QMP is how the queen exerts her control over the hive. It: Suppresses ovary development in the workers. Therefore, normally workers cannot lay eggs. More about laying workers: If QMP levels drop too much or the queen dies or is removed, ovaries in the workers will develop and they will begin laying eggs. This leads to only drone offspring (because workers are not inseminated and cannot fertilize the eggs), which quickly leads to the death of the hive (unless corrective action is taken by the beekeeper). It is believed that in every colony a few workers are regularly laying eggs, but the prevalence of this is very, very low. See information on the Cape Honeybee (later lecture), where laying workers and clonal offspring can be common. Prevents workers from making new queens. Stimulates foraging and brood rearing. Attracts attendant workers. Helps keep the swarm together when the queen leaves the hive during swarming. Serves as a mating attractant for drones during her nuptial flight. Maintains the general “morale” of the hive. Lack of QMP makes the bees nervous and agitated. Queen, reproduction. Normally, the queen is the only bee in a hive that lays eggs. Eggs are laid singly at the bottom of a cell in the comb. During summer, a healthy queen can lay 1,500 eggs per day, which is more than her body weight. In one year, a queen can produce 200,000 workers. Queen, development. Queen development is very similar to worker development, with a few exceptions. As stated previously, during the first three days of the larva’s life, it is fed brood food. After that, nurse bees continue feeding queen larvae the brood food in unlimited amounts until the larva is fully grown (nine days after the egg was laid). The cell in which the queen develops is very large and peanut-shaped. It is called a “queen cell”. Workers construct this large cell in preparation for making a queen. So much brood food is fed to the larva that the cell fills with it, appearing as a milky white fluid. The queen emerges from the cell 16 days after the egg was laid. Queen life span. On average, queens live from one to three years. But queens can: “Wear out” and produce insufficient QMP. Have their QMP diluted by the hive getting too crowded. Can die or be removed from the hive. All of these fates will stimulate the workers to create new queens (if they have eggs or young larvae to work with). If a queen makes insufficient QMP or the hive is too crowded, workers will gradually make queen cells. If a queen dies or is removed, workers detect her absence within hours and start making queen cells. Queen death in new hive. A new colony with an unmated or poorly mated queen (and therefore no eggs, larvae, or brood) is vulnerable to failing. Such a colony might result from a swarm or from installing a new package of bees into a hive box. The queen embarks on mating flights and hopefully gets successfully mated and returns to the hive. But what if she is killed on her flight (by a bird, dragonfly, etc.)? The colony is doomed because the workers lack the eggs or young larvae from which to make new queens. Workers will eventually start laying eggs, leading to all drone offspring and death of the colony. (A beekeeper who notices this within about two weeks could simply install a new queen that has already been mated.) Queen cells. Queen cells are large, peanut-shaped cells found on the comb face, comb edges, and comb bottoms. There are three types: Emergency. When a queen is killed (or removed by a beekeeper), the workers create these cells from pre-existing cells containing eggs or young larvae. They remodel the cell to fit a developing queen. Such cells may be smaller than the other two kinds of queen cells. Swarm. Under crowding (or other) conditions, workers will gradually create swarm cells, usually many in number, and generally hanging off the bottom of the comb. Swarm cells in the hive tend to be of varying ages. Supersedure. The workers detect that something is wrong with the queen, and they work to replace her by making supersedure cells. A hive usually has two of these cells placed on the face of the comb, but the number and position can vary. The supersedure cells tend to be of the same age. Queen replacement. For the workers to create a new queen, the hive MUST have eggs, or larvae that are no older than three days. If they are older, they will have been fed diluted brood food and be on their way to forming workers. If the original queen is failing or gone, and there are no eggs or three-day or younger larvae, the hive is doomed. All current larvae are on the path to becoming workers, and no queens can be made. Without a queen, no eggs are laid, therefore no brood are made, and within about six weeks all workers (and the hive) will be dead. Queen, birth/regicide/insemination. Virgin queen emerges. When the adult queen chews her way out of the queen cell, she is now a “virgin” queen. Usually, before a virgin queen emerges, the old queen in the hive will leave with some of the workers, forming a swarm. Therefore, the new virgin queen should not encounter a mated queen in the hive. Regicide. Generally there are several other queen cells in the hive. Once the first queen emerges, she is groomed and dried by her attendants. She then seeks out all other queen cells in the hive, tears open the cells with her mandibles, and stings the other queens, queen larvae, and queen pupae to death. Workers can block it. Sometimes, workers will prevent the first-hatched queen from killing the other queens. Workers line up and block her. In this case, the workers want several queens to emerge, and for each to leave with their own swarm. See section on swarming. Nuptial flight. The virgin queen then exits the hive on her “nuptial flight”. She seeks out groups of drones that have gathered at tree tops or other elevated locations (“drone congregation areas”, covered later). The queen and drones locate each other visually and chemically; drones release attractant pheromones, and the queen releases QMP. Once the drones detect the queen, they follow her and attempt to mate for about 30 minutes, and they may fly several miles during this time. Insemination. Drones approach the queen from below, and grasp her abdomen with their legs. The drone inserts his endophallus (a penetrating organ of his genitalia) into the queen’s sting cavity. He then releases his grip and allows his body to flip backward. This body flexing compresses his abdominal organs, which causes an ejaculation of sperm into the queen. The endophallus then snaps off of his body (with an audible “snap”), and he falls to the ground and dies. After mating, the endophallus protrudes from the queen’s abdomen and is termed the “mating sign”, a clear indication that she is no longer a virgin. This mating sign is thought to serve as a sort of plug preventing the sperm from leaking out of the queen. Additional drones can then mate; the mating sign is structured so that a subsequent drone’s endophallus can easily dig out the mating sign and some of the previous drone’s sperm. Once the queen returns to the hive, workers will remove the mating sign. After mating, the queen will begin laying eggs in three or four days. Drones, basic structure. Drones are male. They are larger than workers, about ¾ inch long. They are also much heavier and robust, and hairier. The eyes of a drone are huge and cover most of the head, meeting at the top of the head. Like the queen, the drone does not forage, build the nest, rear brood, or defend the hive. As such he lacks a long tongue, pollen basket, wax glands, and stinger. The purpose of a drone is to locate and mate with a virgin queen. Drones, development. In general, there are no drones in the hive during early spring. Worker bees decide when it is time to make drones, and will construct special drone cells that are larger than normal worker cells. These drone cells are often built at the edge of the comb, and are easy to see because the wax cap protrudes out from the comb surface like the tip of a bullet. When the queen detects these larger cells, she lays a single unfertilized egg in them, resulting in a drone. By mid-summer, there can be hundreds of drones in the hive. Similarities and differences to worker development. Timing of the larval development is similar to the worker, and it is fed the same diet as a worker. The main difference is that it takes 24 days from the egg for an adult drone to emerge from the cell. (For comparison, the worker takes 21 days.) Drones, activity. Drones live within the hive for their first couple of weeks of life, and then start making afternoon flights from the hive. They fly very fast, and join up with drones from other hives to form a “drone comet”, which flies through the neighborhood, visiting certain sites frequently. Drones release “drone pheromone” which attracts other flying drones, which promotes drone congregation. These sites are called “drone congregation areas”, and are often the tops of certain trees or a certain edge of a certain forest. Year after year, drones congregate at these same areas. It is thought that these areas are conducive to mating success. Drones only live a short time, and no intergenerational learning is possible, so how they know to visit these places every year is not understood. As previously stated, the drones give off attractant pheromones to attract the queen. Likewise, the queen’s QMP attracts the drones. Drones, life span. Drones cannot feed themselves, so are totally at the mercy of the workers. If he never gets the chance to mate, the workers commit fratricide. By late fall, when the hive is preparing for winter, workers push the drones out of the hive to starve. Drones are not useless in the hive; they assist in hive temperature regulation. Drones are one way that a colony can send its genes out into the world. Colony reproduction. Swarming is the natural means by which new honeybee colonies are created. It usually occurs in early spring, just before or during the main “nectar flow” (availability of pollen and nectar in the environment). This timing allows the new colony to have ample time and resources to build a new comb and rear brood. When the density of bees in the colony reaches about 36 bees per cubic inch, preparations for swarming begin. As previously stated, dilution of QMP is likely the reason. There are probably other reasons too. Process of swarming. Preparations. Queen cups and cells, egg laid. Preparations begin several days before the actual swarm occurs. The workers start with the construction of queen cups, which are large, wide cell bases usually constructed at the edge of the comb. These cups are then lengthened to form the queen cells (swarm cells), which are spacious. The cells are vertically oriented, and usually near the bottom of the comb. They appear as inch-long, dimpled, peanut-shaped swellings to the beekeeper. The queen lays fertilized eggs in these queen cells. When they hatch, the workers feed the larvae copious brood food in unlimited amounts for about 8 days, at which time the cells are capped with wax. Once the queen cells are capped, the hive is on the pathway to swarming and preventing it is very difficult. Scout bees. A few days prior to swarming, scout bees examine the environment for suitable new nesting sites. These scouts are experienced foragers that know the local area well. Conditioning the old queen for flight. During the swarming, the old queen must fly. Remember that the last time the queen flew was during her nuptial flights. The old queen is bloated with eggs and too heavy to fly, so the workers put her on a “diet” to thin her down so that she can fly again. Workers feed her little and chase her around for exercise. The old queen will greatly slow down her egg laying during this conditioning phase. Changes to worker behavior. Workers engorge themselves with honey. (Why? They will need that energy to build honeycomb at the new colony location.) Foraging activity stops temporarily. Swarming begins and ends. When the swarm begins, the old queen and 10,000 to 20,000 workers leave and fly as a mass, led by the scout bees. The speed of the swarm varies from about ½ - 6 mph, and its shape usually starts off spherical and eventually becomes egg-shaped as it moves. Back in the original colony, the new queens have not yet emerged. Commonly, the swarm will find a resting place on its way to the new nest site. Such a resting swarm is a large and noticeable object (it is during this resting phase that a beekeeper can capture the swarm). A swarm hanging temporarily on a tree branch (for example), is a large mass of workers (with full bellies) surrounding the old queen. Swarms are known to be gentle, since a full honey stomach prevents bees from stinging. If the swarm sits long enough to use up its food it can become aggressive. (The “bee beard” worn by beekeepers is a swarm.) Scouts will urge the swarm onward to the nesting site, and to guide them there, they release Nasonov pheromone from their Nasonov gland at the tip of their abdomen. The swarm is attracted to this pheromone. (Nasonov pheromone is also used at the entrance of the hive to help foragers find the entrance, and it is placed on flowers to guide other foragers to the flowers. A bee releasing the pheromone will raise its abdomen in the air and expose the gland, and then fan its wings vigorously.) Upon arrival at the new site, workers begin construction of the new comb. Recall that workers can make a lot of wax because they engorged themselves on honey before leaving the old hive (equal to about 40% of their body weight). (Like a 170 lb. man eating 68 lbs. of honey.) In a few days, the comb is usable and the queen begins laying eggs to establish the new colony. Occasionally, a swarm will not find a new site and will build an open-air colony. Back in the original colony. The original colony is termed the parent colony. Swarm cells begin to hatch, regicide or not. The first queen to emerge is a virgin queen, and is therefore skinny and is not too different in size from the workers. She seeks out and destroys the other virgin queens that are developing. The virgin queen will then take her orientation flights, then her nuptial flights, get mated to usually about a dozen or so drones (in a drone congregation area), and then return to the colony and begin to lay eggs. Prevention of regicide. Sometimes, workers prevent the virgin queen from killing the other virgin queens. In this case it is believed that the workers sense poor conditions for swarm success (that is, likely low success in setting up a new colony), so they allow multiple swarms to issue from the parent hive to increase the chances that a new colony will establish. These are usually called afterswarms. The first hatched virgin queen will leave with a small afterswarm, and then the next hatched virgin queen may leave with yet another afterswarm, etc. At some point a final virgin queen resides in the parent hive. Each afterswarm issued by the parent hive is small and they get smaller and smaller as the workers in the parent hive are used up.
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3 DAVID HUME - Careful analysis of the notion of self. "A wise man proportions his belief to the evidence."- DAVID HUME said JOHN LOCKE - Human mind at birth is a blank paper or tabula rasa. "What worries you, masters you."-JOHN LOCKE said SELF- it is the person who knows his/her feelings, emotions, memory and experiences. SELF SCHEMA- are mental concept by which one organizes one's world. The self-schema that makes self-concept will assist one to organize and recall one's experiences NO MAN IS AN ISLAND- this phrase expresses the idea that human beings do badly when isolated from others. We need to be part of the community in order to thrive. Society is part of human life. It has a great impact and contribution of who we are. Its influences can effect our behaviors and attitudes. SOCIALIZATION- Describes the process by which people learn the attitudes, values, and behaviors that are appropriate and expected by their culture and community. - Typically occurs through the observation of and interaction with the people we are surrounded. THEY ALL HAVE SOMETHING TO TEACH US ABOUT HOW WE SHOULD ACT WITHIN OUR COMMUNITY. - Also shapes our self image, or how we view ourselves. CHARLES HORTON COOLEY LOOKING GLASSS SELF THEORY- Our view of ourselves comes not only from our direct contemplation of our personal qualities, but also from our perceptions about how we are being perceived by others. CRITICAL ASPECT OF THIS THEORY: We are not actually being influenced by the opinions of others, but instead, we are being influences by what we imagine the opinions of other people to be. ACCORDING TO THIS THEORY, WE MIGHT DEVELOP OUR SELF IDENTITIES BASED ON BOTH CORRECT AND INCORRECT PERCEPTIONS OF HOW OTHERS SEE US. WE CAN ALSO BE INFLUENCED BY FUTURE INTERACTIONS. 2 IMPORTANT DIMENSIONS OF THIS EVALUATION: SELF-ESTEEM- is the belief that one is good and valuable to others. (boastful and timid) 1.PROCESS OF INTERACTION- a person observes others behavior for pieces of information how they are appraising him. 2PERSONAL EFFICACY - another aspect of evaluation. Based on this principle, a person believes that he can rise above obstacles or challenges and eventually achieves his goal.
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