Termit - Termite

Termit
Vaqtinchalik diapazon: Erta bo'r - yaqinda
Coptotermes formosanus shiraki USGov k8204-7.jpg
Formosan er osti termitlari (Koptotermalar formosanus)
Askarlar (qizil rangli boshlar)
Ishchilar (och rangdagi boshlar)
Ilmiy tasnif e
Qirollik:Animalia
Filum:Artropoda
Sinf:Hasharot
Kohort:Polineeoptera
Super buyurtma:Dictyoptera
Buyurtma:Blattodea
Qoidabuzarlik:Isoptera
Brullé, 1832
Oilalar

Kratomastotermitidae[1]
Mastotermitidae
Termopsidae[2]
Archotermopsidae
Hodotermitidae
Stolotermitidae
Kalotermitidae
Arxeorinotermitidae
Stylotermitidae
Rinotermitidae
Serritermitidae
Termitidae

Termitlar bor eusocial hasharotlar da tasniflangan taksonomik daraja ning buzg'unchilik Isopterayoki kabi epifamily Termitoidae buyurtma doirasida Blattodea (bilan birga hamamböceği ). Bir vaqtlar termitlar alohida-alohida tasniflangan buyurtma hamamböceği dan, lekin yaqinda filogenetik Tadqiqotlar shuni ko'rsatadiki, ular xuddi tarakanlardan kelib chiqqan opa-singillar guruhi o'rmonga, bu turdagi hamamböceği Kriptokerkus. Avvalgi hisob-kitoblarga ko'ra, kelishmovchiliklar davomida yuz bergan Yura davri yoki Trias. So'nggi hisob-kitoblarga ko'ra, ularning kelib chiqishi bor Kech yura,[3] dagi birinchi fotoalbom yozuvlari bilan Erta bo'r. Taxminan 3,106 turlari hozirda tavsiflanadi, yana bir necha yuztasi qolgan. Garchi bu hasharotlar ko'pincha "oq chumolilar" deb nomlansa ham,[4] ular emas chumolilar va chumolilar bilan chambarchas bog'liq emas.

Chumolilar va boshqalar kabi asalarilar va ari alohida tartibdan Hymenoptera, termitlar odatda steril bo'lgan "ishchilar" va "askarlar" ga bo'linadi. Barcha koloniyalarda "qirollar" deb nomlangan unumdor erkaklar va "qirolichalar" deb nomlangan bir yoki bir nechta unumdor urg'ochilar mavjud. Termitlar asosan oziqlanadi o'lik o'simlik materiallari va tsellyuloza, odatda, yog'och shaklida, barg axlati, tuproq yoki hayvonlarning go'ngi. Termitlar asosiy hisoblanadi tergovchilar, ayniqsa subtropik va tropik mintaqalar bo'lib, ularni yog'och va o'simlik moddalarini qayta ishlash katta ekologik ahamiyatga ega.

Termitlar Yerdagi eng muvaffaqiyatli hasharotlar guruhlari qatoriga kiradi, aksariyat quruqliklarni mustamlaka qiladi Antarktida. Ularning koloniyalari bir necha yuz kishidan tortib bir necha million kishilik ulkan jamiyatlarga qadar o'zgarib turadi. Termit malikalari ma'lum bo'lgan har qanday hasharotlar orasida eng uzoq umr ko'rishadi, ba'zi malika 30-50 yilgacha yashaydi. To'liq metamorfozga uchragan chumolilardan farqli o'laroq, har bir alohida termit an orqali o'tadi to'liq bo'lmagan metamorfoz bu tuxum orqali davom etadi, nimfa va kattalar bosqichlari. Koloniyalar quyidagicha tavsiflanadi superorganizmlar chunki termitlar o'z-o'zini tartibga soluvchi sub'ektning bir qismini tashkil qiladi: koloniyaning o'zi.[5]

Termitlar ba'zi bir inson madaniyati ratsionidagi noziklik hisoblanadi va ko'plab an'anaviy dorilarda qo'llaniladi. Bir necha yuz turdagi binolar, ekinlar yoki plantatsiya o'rmonlariga jiddiy zarar etkazishi mumkin bo'lgan zararkunandalar sifatida iqtisodiy ahamiyatga ega. Kabi ba'zi turlari G'arbiy Hindiston quruq daraxt termiti (Cryptotermes brevis), deb hisoblanadi invaziv turlar.

Etimologiya

Isoptera infraqizil nomi Yunoncha so'zlar iso (teng) va ptera (qanotli), bu old va orqa qanotlarning deyarli teng o'lchamlarini bildiradi.[6] "Termit" quyidagidan kelib chiqadi Lotin va Kech lotin so'z terminlar ("o'tin qurti, oq chumoli"), lotincha ta'sirida o'zgartirilgan terere ("silamoq, kiymoq, yemirmoq") oldingi so'zdan tarmaklar. Termit uyasi a nomi bilan ham tanilgan muddatli yoki termitarium (ko‘plik) termitariya yoki termitariumlar).[7] Ilgari ingliz tilida termitlar "yog'och chumolilar" yoki "oq chumolilar" deb nomlangan.[8] Zamonaviy atama birinchi marta 1781 yilda ishlatilgan.[9]

Taksonomiya va evolyutsiya

The giant northern termite is the most primitive living termite. Its body plan has been described as a cockroach's abdomen stuck to a termite's fore part. Its wings have the same form as roach wings, and like roaches, it lays its eggs in a case.
Gigant shimoliy termitning tashqi ko'rinishi Mastotermes darwiniensis termitlar va hamamböcekler o'rtasidagi yaqin munosabatlar haqida dalolat beradi.

Ilgari termitlar Isoptera tartibida joylashtirilgan edi. 1934 yildayoq ularning yog'ochdan foydalanadigan hamamböceği (tur) bilan chambarchas bog'liqligi haqida takliflar qilingan edi Kriptokerkus, daraxtzor) ularning simbiotik ichaklari o'xshashligiga asoslangan flagellates.[10] 1960 yillarda F. A. McKittrick ba'zi termitlar va shunga o'xshash morfologik xususiyatlarni qayd etganida, ushbu gipotezani tasdiqlovchi qo'shimcha dalillar paydo bo'ldi. Kriptokerkus nimfalar.[11] 2008 yilda DNK tahlili dan 16S rRNK ketma-ketliklar[12] tartibni o'z ichiga olgan evolyutsion daraxt ichida joylashgan termitlarning holatini qo'llab-quvvatladi Blattodea hamamböceği o'z ichiga olgan.[13][14] Hamamböceğin jinsi Kriptokerkus termitlar bilan eng kuchli filogenetik o'xshashlikni baham ko'radi va termitlarga singil guruh hisoblanadi.[15][16] Termitlar va Kriptokerkus o'xshash morfologik va ijtimoiy xususiyatlarni baham ko'ring: masalan, ko'pchilik hamamböceği ijtimoiy xususiyatlarini namoyon qilmaydi, lekin Kriptokerkus o'z yoshlariga g'amxo'rlik qiladi va boshqalarni namoyish etadi ijtimoiy xulq-atvor kabi trofallaks va allogrooming.[17] Termitlar avlodning avlodlari deb o'ylashadi Kriptokerkus.[13][18] Ba'zi tadqiqotchilar termitlarni saqlab qolish uchun ko'proq konservativ choralarni taklif qilishdi Termitoidae, an epifamily hamamböceği buyrug'i doirasida, bu termitlarning oila darajasida va undan pastroq tasnifini saqlaydi.[19] Termitlar uzoq vaqtdan beri hamamböceği va bilan chambarchas bog'liq deb qabul qilingan mantidlar va ular bir xil super buyurtmada tasniflanadi (Dictyoptera ).[20][21]

Eng qadimiy aniq termit fotoalbomlar sana erta Bo'r, ammo Bo'r davridagi termitlarning xilma-xilligi va mikroorganizmlar va bu hasharotlar o'rtasidagi mutalizmni ko'rsatadigan dastlabki fotoalbom yozuvlari hisobga olinsa, ular ilgari yura yoki triasda paydo bo'lgan.[22][23][24] Yura davri kelib chiqishining mumkin bo'lgan dalillari yo'q bo'lib ketgan degan taxmindir Fruitafossor termitlarni iste'mol qilar ekan, uning morfologik jihatdan zamonaviy termit bilan oziqlanadigan sutemizuvchilarga o'xshashligi.[25] Kashf etilgan eng qadimgi termit uyasi Yuqori bo'r yilda G'arbiy Texas, bu erda eng qadimgi najas pelletlari ham topilgan.[26] Termitlar ilgari paydo bo'lgan degan da'volar qarama-qarshiliklarga duch keldi. Masalan, F. M. Vesner Mastotermitidae termitlar yana qaytib kelishi mumkin Kechki Permian, 251 million yil oldin,[27] va qanotlariga yaqin o'xshash fotoalbom qanotlari Mastotermalar eng ibtidoiy tirik termit bo'lgan Mastotermitidae kashf etilgan Permian Kanzasdagi qatlamlar.[28] Bu davrda birinchi termitlar paydo bo'lishi ham mumkin Karbonli.[29] Fotoalbom yog'ochlarning buklangan qanotlari gumburlaydi Piknoblattina, 1a va 2a segmentlari o'rtasida konveks shaklida joylashtirilgan, ko'rinishda bo'lganlarga o'xshaydi Mastotermalar, xuddi shu naqshga ega bo'lgan yagona tirik hasharotlar.[28] Krishna va boshq.Shunga qaramay, shartli ravishda termitlar deb tasniflangan barcha paleozoy va trias hasharotlari aslida termitlarga aloqasi yo'q va Isopteradan chiqarib tashlanishi kerak.[30] Boshqa tadqiqotlar shuni ko'rsatadiki, termitlarning kelib chiqishi ancha yaqinlashib, ajralib chiqqan Kriptokerkus qachondir Erta bo'r.[3]

Ishchining so'l obrazi.

Ibtidoiy ulkan shimoliy termit (Mastotermes darwiniensis) boshqa termitlar bilan taqsimlanmagan ko'plab hamamböceğe o'xshash xususiyatlarni namoyish etadi, masalan, tuxumlarini sallarga tashlash va qanotlarida anal loblar.[31] Isoptera va Cryptocercidae-ni guruhga birlashtirish taklif qilingan "Ksilofagodea ".[32] Ba'zan termitlarni "oq chumolilar" deb atashadi, ammo chumolilarga o'xshashligi ularning ijtimoiyligi bilan bog'liq. konvergent evolyutsiyasi[33][34] 100 million yildan ko'proq oldin kastalar tizimini rivojlantirgan birinchi ijtimoiy hasharotlar termitlar bilan.[35] Termit genomlari odatda boshqa hasharotlarnikiga nisbatan nisbatan katta; birinchi to'liq ketma-ketlikdagi termit genomi, ning Zootermopsis nevadensis, jurnalda chop etilgan Tabiat aloqalari, taxminan 500 Mb dan iborat,[36] keyinchalik ikkita genom nashr etilgan bo'lsa, Makrotermes natalensis va Kriptotermalar sekundusi, 1,3 Gb atrofida ancha katta.[37][34]

Dictyoptera
Blattodea
Blattoidea
Termitoidae / Infraorder Isoptera

Termitidae

Rinotermitidae

Kalotermitidae

Archotermopsidae

Hodotermitidae

Mastotermitidae

Cryptocercoidae

Cryptocercidae (jigarrang kapotli hamamböceği)

Blattidae (Sharqiy, Amerika va boshqa hamamböceği)

Blaberoidea

Blaberidae (Gigant hamamböceği)

Ektobiidae (qism)

Ectobiidae (qism)

Corydioidea

Corydiidae (Qum hamamböceği va boshqalar)

Nocticolidae (G'or hamamböceği va boshqalar)

Alienoptera

Mantodea (Mantiya)

2013 yilga kelib, taxminan 3106 tirik va fotoalbom termit turlari 12 oilada tan olingan, tasniflangan; identifikatsiya qilish uchun odatda reproduktiv va / yoki askar kastlari talab qilinadi. Infraqizil Isoptera subfamilalarni tegishli tasnifida ko'rsatib, quyidagi qoplama va oilaviy guruhlarga bo'linadi:[30]

Bazal termit oilalari

Epifamily Termitoidae
Oila Kratomastotermitidae
Oila Mastotermitidae
   Parvorder Euisoptera
Oila Termopsidae
Oila Archotermopsidae
Oila Hodotermitidae
Oila Stolotermitidae
Oila Kalotermitidae

Neoisoptera

So'zma-so'z "yangi termitlar" ma'nosini anglatuvchi Neoisoptera (evolyutsion ma'noda) yaqinda paydo bo'lgan nanorder odatda "yuqori termitlar" deb ataladigan oilalarni o'z ichiga oladi, ammo ba'zi rasmiylar ushbu atamani faqat eng katta oilaga nisbatan qo'llaydilar Termitidae. Ikkinchisida xarakterli Pseudergate nymphlari yo'q (ko'plab "pastki termitlar" ishchi nymphlari reproduktiv kastlarga aylanish qobiliyatiga ega: qarang quyida ). "Yuqori termitlar" da tsellyuloza hazm qilish jarayoni birgalikda rivojlangan ökaryotik ichak mikrobiota[38] va ko'plab nasllar kabi qo'ziqorinlar bilan simbiyotik aloqalarga ega Termitomitsalar; aksincha, "pastki termitlar" odatda mavjud flagellates va prokaryotlar ularning orqa ichaklarida. Endi bu erda beshta oila mavjud:

Tarqatish va xilma-xillik

Termitlar bundan mustasno, barcha qit'alarda uchraydi Antarktida. Termit turlarining xilma-xilligi past Shimoliy Amerika va Evropa (Evropada ma'lum bo'lgan 10 tur va Shimoliy Amerikada 50 tur), lekin juda yuqori Janubiy Amerika, bu erda 400 dan ortiq tur ma'lum.[39] Hozir tasniflangan 3000 termit turlaridan 1000 tasi topilgan Afrika, bu erda ma'lum mintaqalarda tepaliklar juda ko'p. Shimolda taxminan 1,1 million faol termit höyüğünü topish mumkin Kruger milliy bog'i yolg'iz.[40] Yilda Osiyo, asosan tarqalgan 435 turdagi termitlar mavjud Xitoy. Xitoyda termit turlari yumshoq bilan cheklangan tropik va subtropik Yangtsi daryosining janubidagi yashash joylari.[39] Yilda Avstraliya, termitlarning barcha ekologik guruhlari (dampwood, drywood, yer osti) endemik 360 dan ortiq tasniflangan turlari bilan mamlakatga.[39]

Termitlar yumshoq katikulalari tufayli salqin va sovuq joylarda yashamaydi.[41] Termitlarning uchta ekologik guruhi mavjud: dampwood, drywood va er osti. Dampwood termitlari faqat ignabargli o'rmonlarda, quruq daraxt termitlari esa qattiq yog'ochli o'rmonlarda uchraydi; er osti termitlari juda xilma-xil sohalarda yashaydi.[39] Quruq daraxtlar guruhining bir turi G'arbiy Hindiston quruq daraxt termitidir (Cryptotermes brevis ), bu Avstraliyada invaziv tur.[42]

Qit'a bo'yicha Isopteraning xilma-xilligi:
OsiyoAfrikaShimoliy AmerikaJanubiy AmerikaEvropaAvstraliya
Turlarning taxminiy soni4351,0005040010360

Tavsif

Ishchining boshini yaqindan ko'rish

Termitlar odatda kichik bo'lib, ularning uzunligi 4 dan 15 millimetrgacha (0,16 dan 0,59 gacha).[39] Barcha mavjud termitlarning eng kattasi bu turlarning malikalari Makrotermes bellicosus, uzunligi 10 santimetrdan (4 dyuym) gacha.[43] Yo'qolib ketgan yana bir ulkan termit Gyatermes styriensis, gullab-yashnagan Avstriya davomida Miosen qanotlari 76 millimetr (3,0 dyuym) va tanasining uzunligi 25 millimetr (0,98 dyuym) bo'lgan.[44][eslatma 1]

Ko'pgina ishchilar va askarlar termitlari butunlay ko'rlar, chunki ularning bir juft ko'zlari yo'q. Biroq, ba'zi turlari, masalan Hodotermes mossambicus, bor aralash ko'zlar ular yo'naltirish va quyosh nurini oy nuridan ajratish uchun foydalanadilar.[45] The alates (qanotli erkaklar va urg'ochilar) lateral bilan birga ko'zlari bor ocelli. Yanal ocelli, ammo oilalarda bo'lmagan barcha termitlarda mavjud emas Hodotermitidae, Termopsidae va Archotermopsidae.[46][47] Boshqa hasharotlar singari termitlar ham til shaklida kichik shaklga ega labrum va a klypeus; klypeus postklypeus va anteklipga bo'linadi. Termit antennalari teginish, ta'm, hid (shu jumladan feromonlar), issiqlik va tebranishni sezish kabi bir qator funktsiyalarga ega. Termit antennasining uchta asosiy segmentiga a kiradi skeyp, pedicel (odatda skeypdan qisqaroq) va flagellum (skeyp va pedikeldan tashqari barcha segmentlar).[47] Og'iz qismlarida a maxillae, labium va to'plam pastki jag '. Maksiller va labium bor palpalar bu termitlarga oziq-ovqat va ishlov berishni sezishga yordam beradi.[47]

Barcha hasharotlarga, termitning anatomiyasiga mos keladi ko'krak qafasi uchta segmentdan iborat: the protoraks, mezotoraks va metatoraks.[47] Har bir segmentda juftlik mavjud oyoqlari. Alatlarda qanotlar mezotoraks va metatoraksda joylashgan. Mezotoraks va metatoraks ekzoskelet plitalari yaxshi rivojlangan; protoraks kichikroq plitalarga ega.[48]

Bilan birga qanotni ko'rsatadigan diagramma klypeus va oyoq

Termitlarda o'nta segmentli qorin, ikkita plastinka, va tergitlar va sternitlar.[49] O'ninchi qorin segmentida bir juft kalta bor cerci.[50] O'nta tergit bor, ulardan to'qqiztasi keng, bittasi cho'zilgan.[51] Reproduktiv organlar hamamböceğe o'xshash, ammo soddalashtirilgan. Masalan, intromitent organ erkak aleytalarda mavjud emas va spermatozoidlar harakatsiz yoki aflagellatdir. Ammo, Mastotermitidae termitlarida cheklangan multiflagellat sperma mavjud harakatchanlik.[52] Ayollarda jinsiy a'zolar ham soddalashtirilgan. Mastotermitidae urg'ochilarida boshqa termitlardan farqli o'laroq, an ovipositor, bu xususiyat ayol hamamböceği bilan o'xshashdir.[53]

Termitlarning reproduktiv bo'lmagan kastalari qanotsiz va harakatlanish uchun faqat olti oyoqlariga suyanadi. Alates faqat qisqa vaqt davomida uchishadi, shuning uchun ular oyoqlariga ham ishonadilar.[49] Oyoqlarning ko'rinishi har bir kastada o'xshash, ammo askarlarning oyoqlari kattaroq va og'irroq. Oyoqlarning tuzilishi boshqa hasharotlarga mos keladi: oyoq qismlariga a kiradi koksa, trokanter, suyak suyagi, tibia va tarsus.[49] Shaxsning oyog'idagi tibia suyaklari soni turlicha. Ba'zi bir termit turlari aroliumga ega, ular orasida joylashgan tirnoqlari, bu tekis sirtlarga chiqadigan turlarda mavjud, ammo ko'pchilik termitlarda yo'q.[54]

Chumolilarnikidan farqli o'laroq, orqa qanotlari va old qanotlari teng uzunlikda.[6] Ko'pincha alaytlar kambag'al uchuvchilar; ularning texnikasi o'zlarini havoga uchirish va tasodifiy yo'nalishda uchishdir.[55] Tadqiqotlar shuni ko'rsatadiki, katta termitlarga nisbatan kichikroq termitlar uzoq masofalarga ucha olmaydi. Termit parvoz qilganda uning qanotlari to'g'ri burchak ostida qoladi va termit tinch holatda qanotlari tanaga parallel bo'lib qoladi.[56]

Kast tizimi

Termitlarning kast tizimi
A - Shoh
B - Qirolicha
C - Ikkinchi darajali malika
D. - Uchinchi darajali malika
E - askarlar
F - ishchi

Ishchi termitlar koloniya ichida eng ko'p mehnatni o'z zimmasiga oladi, ular em-xashak, oziq-ovqat mahsulotlarini saqlash, zoti va uyalarini saqlash uchun javobgardir.[57][58] Ishchilarga hazm qilish vazifasi yuklatilgan tsellyuloza oziq-ovqat tarkibida va shuning uchun zararlangan o'rmonda topilishi mumkin bo'lgan kast. Ishchi termitlarning boshqa uydoshlarini ovqatlantirish jarayoni ma'lum trofallaks. Trofallaks - azotli tarkibiy qismlarni konvertatsiya qilish va qayta ishlash uchun samarali ovqatlanish taktikasi.[59] Bu ota-onalarni nasldan tashqari barcha nasllarni boqishdan ozod qiladi, bu esa guruhning ancha kattalashishiga imkon beradi va zarur ichak simbionlari avloddan avlodga o'tishini ta'minlaydi. Ba'zi termit turlari ishlarni alohida kast sifatida ajralib chiqmasdan bajarishda nimfalarga tayanishi mumkin.[58] Ishchilar erkak yoki ayol bo'lishi mumkin va odatda steril, ayniqsa, em-xashak joyidan ajratilgan uyasi bo'lgan termitlarda. Steril ishchilarni ba'zan haqiqiy ishchilar deb atashadi, unumdor bo'lganlar esa, o'rmonda joylashgan Archotermopsidae singari, yolg'onchi ishchilar deb atashadi.[60]

Harbiy kast anatomik va xulq-atvorli ixtisoslarga ega va ularning yagona maqsadi mustamlakani himoya qilishdir.[61] Ko'plab askarlarning katta boshlari yuqori darajada o'zgartirilgan kuchli jag'lari bor, shuning uchun ular o'zlarini boqolmaydilar. Buning o'rniga, balog'atga etmagan bolalar singari, ular ishchilar tomonidan oziqlanadi.[61][62] Fontanellar, Himoya sekretsiyasini chiqaradigan peshonadagi oddiy teshiklar, Rhinotermitidae oilasiga xos xususiyatdir.[63] Ko'plab turlar askarlarning kattaroq va quyuqroq boshi va katta mandibularidan foydalangan holda aniqlanadi.[58][61] Ba'zi termitlar orasida askarlar tor tunnellarini to'sish uchun globusli (frazemotik) boshlaridan foydalanishlari mumkin.[64] Har xil turdagi askarlarga kichik va katta askarlar va nasutlar kiradi, ular shoxga o'xshash nozulning frontal proektsiyasiga ega (nasus).[58] Ushbu noyob askarlar zararli, yopishqoq sekretsiyani purkashga qodir diterpenlar ularning dushmanlariga.[65] Azotni biriktirish nasutli ovqatlanishda muhim rol o'ynaydi.[66] Askarlar odatda sterildirlar, ammo ba'zi Archotermopsidae turlari jinsiy a'zolarga ega bo'lib, askarga o'xshash boshlari bilan neotenik shakllarga ega ekanligi ma'lum.[67]

Voyaga etgan koloniyaning reproduktiv kastasiga qirolicha va qirol deb ataladigan unumdor ayol va erkak kiradi.[68] Koloniya malikasi koloniya uchun tuxum ishlab chiqarish uchun javobgardir. Chumolilarnikidan farqli o'laroq, shoh u bilan umr bo'yi juftlashadi.[69] Ba'zi turlarda malika qorinlari ko'payishi uchun keskin shishiradi hosildorlik, deb nomlanuvchi xususiyat fizogastrizm.[57][68] Turlarga qarab, malika yilning ma'lum bir davrida reproduktiv qanotli alotlarni ishlab chiqarishni boshlaydi va koloniyadan ulkan to'dalar paydo bo'ladi. nikoh parvozi boshlanadi. Ushbu to'dalar turli xil yirtqichlarni jalb qiladi.[68]

Hayot davrasi

A termite nymph looks like a smaller version of an adult but lacks the specialisations that would enable identification of its caste.
Yosh termit nimfasi. Nimfalar birinchi navbatda ishchilarga murojaat qilishadi, ammo boshqalar bundan keyin askar bo'lishlari mumkin alates.
Termit va boshqa termitlarning qanotlarini ichki deraza tokchasida to'kdi. Qanotlarni to'kish reproduktiv suzish bilan bog'liq.[70]

Termitlar ko'pincha. Bilan taqqoslanadi ijtimoiy Gimenopteralar (chumolilar va turli xil asalarilar va arilar), ammo ularning evolyutsion kelib chiqishi turlicha bo'lib, hayot aylanish jarayonida katta farqlarga olib keladi. Eusocial Hymenopterada ishchilar faqat ayollardir. Erkaklar (dronlar) gaploid bo'lib, urug'lanmagan tuxumlardan rivojlanadi, urg'ochilar (ishchilar ham, malika ham) diploid bo'lib, urug'lantirilgan tuxumlardan rivojlanadi. Aksincha, koloniyada ko'pchilikni tashkil etadigan ishchi termitlar diploid ikkala jinsdagi shaxslar va urug'lantirilgan tuxumlardan rivojlanadi. Turlarga qarab, erkak va ayol ishchilar termit koloniyasida turli xil rollarga ega bo'lishi mumkin.[71]

Termitning hayot aylanishi an bilan boshlanadi tuxum, ammo asalarilar yoki chumolilarnikidan farq qiladi, chunki ular rivojlanish jarayoni deb ataladi to'liq bo'lmagan metamorfoz, tuxum, nymph va kattalar bosqichlari bilan.[72] Nymphlar kichik kattalarga o'xshaydi va bir qator o'tib ketadi naychalar ular o'sganda. Ba'zi turlarda tuxum to'rtta mollanish bosqichidan, nimfalar esa uchtadan o'tadi.[73] Dastlab nymphlar ishchilar bilan to'qnash kelishadi, so'ngra ba'zi ishchilar qo'shimcha muolajalardan o'tib, askar yoki ittifoqdoshga aylanishadi; ishchilar faqat alyfa nimfalariga urilish orqali alatesga aylanishadi.[74]

Nimfalarning kattalarga aylanishi bir necha oy davom etishi mumkin; vaqt davri oziq-ovqat mavjudligiga, haroratga va koloniyaning umumiy aholisiga bog'liq. Nimfalar o'zlarini boqishga qodir emasliklari sababli, ishchilar ularni boqishlari kerak, ammo ishchilar koloniyaning ijtimoiy hayotida ham ishtirok etishadi va boshqa vazifalarni bajaradilar: masalan, uya boqish, qurish yoki saqlash yoki malikaga qarash.[58][75] Feromonlar termit koloniyalarida kast tizimini tartibga soladi, bu juda kam sonli termitlardan tashqari unumdor malika bo'lishiga yo'l qo'ymaydi.[76]

Qirolichalar eusocial termit Retikulitermalar speratus qurbon qilmasdan uzoq umr ko'rishga qodir hosildorlik. Ushbu uzoq umr ko'rgan malikalar oksidlovchi zararning sezilarli darajada past darajasiga ega, shu jumladan oksidlovchi DNK shikastlanishi, ishchilarga, askarlarga va nimfalarga qaraganda.[77] Zararning pastki darajalari oshganligi sababli ko'rinadi katalaza, himoya qiluvchi ferment oksidlovchi stress.[77]

Ko'paytirish

Hundreds of winged termite reproductives swarming after a summer rain, filling the field of the photograph.
Yomg'irdan keyin nikoh parvozi paytida Alates girdobida

Termit alaytalari koloniyadan faqat a nikoh parvozi joy oladi. Alate erkak va urg'ochi birlashib, keyin koloniya uchun munosib joy izlash uchun qo'nadilar.[78] Termit qirol va malika bunday joyni topmaguncha juftlashmaydi. Qachonki, ikkalasi uchun ham katta bo'lgan kamerani qazib olishadi, kirish joyini yopib, juftlashishga kirishadilar.[78] Juftlik qilgandan keyin, juftlik hech qachon ko'chaga chiqmaydi va butun umrini uyada o'tkazadi. Nikoh uchish vaqti har bir turda turlicha. Masalan, ba'zi turlardagi alates yozda kun davomida, boshqalari esa qishda paydo bo'ladi.[79] Tushlik parvozi, shuningdek, alates ko'plab chiroqlar bo'lgan joylarni aylanib chiqqandan keyin, qorong'i vaqtda boshlanishi mumkin. Nikoh parvozi boshlanadigan vaqt atrof-muhit sharoitiga, kun vaqtiga, namlikka, shamol tezligiga va yog'ingarchiliklarga bog'liq.[79] Koloniyada termitlar soni ham turlicha bo'lib, odatda yirik turlari 100-1000 kishidan iborat. Biroq, ba'zi bir termit koloniyalar, shu jumladan ko'p sonli shaxslar, millionlab kishini tashkil qilishi mumkin.[44]

Malika koloniyaning dastlabki bosqichlarida faqat 10-20 dona tuxum qo'yadi, ammo koloniya bir necha yoshga to'lganida kuniga 1000 ga yaqin tuxum qo'yadi.[58] Voyaga etganida, asosiy malika tuxum qo'yishga qodir. Ba'zi turlarda etuk malika qorinni juda kengaygan va kuniga 40 ming tuxum tug'ishi mumkin.[80] Ikki etuk tuxumdonda 2000 ga yaqin bo'lishi mumkin tuxumdonlar har biri.[81] Qorin qirolichaning tanasi uzunligini juftlashishdan avval bir necha baravar ko'paytiradi va erkin harakatlanish qobiliyatini pasaytiradi; xizmatchilar yordam berishadi.

Tuxumni parvarish qilish harakati Retikulitermalar speratus bolalar bog'chasidagi ishchilar

Qirol dastlabki juftlashgandan keyin biroz kattalashib boradi va umr bo'yi qirolicha bilan juftlashishda davom etadi (termit malika 30 yoshdan 50 yoshgacha yashashi mumkin); bu chumoli koloniyalaridan juda farq qiladi, unda malika bir marta erkak (lar) bilan juftlashadi va jinsiy hujayralarni umrbod saqlaydi, chunki erkak chumolilar juftlashganidan ko'p o'tmay vafot etadi.[69][75] Agar malika yo'q bo'lsa, termit qiroli feromonlarni ishlab chiqaradi, ular o'rnini bosuvchi termit malikalarini rivojlanishini rag'batlantiradi.[82] Malika va qirol monogam bo'lganligi sababli, sperma raqobati yuzaga kelmaydi.[83]

Alatesga aylanish yo'lida to'liq bo'lmagan metamorfozdan o'tgan termitlar potentsial qo'shimcha reproduktivlar sifatida ishlaydigan ba'zi bir termit turlarida subkasteni hosil qiladi. Ushbu qo'shimcha reproduktivlar faqat qirol yoki malika vafot etgandan keyin yoki asosiy reproduktivlar koloniyadan ajratilganda asosiy reproduktivlarga aylanadi.[74][84] Qo'shimchalar o'lik birlamchi reproduktivni almashtirish qobiliyatiga ega, shuningdek, koloniyada bitta qo'shimcha qo'shimcha bo'lishi mumkin.[58] Ba'zi malikalar jinsiy ko'payishdan ikkinchisiga o'tish qobiliyatiga ega jinssiz ko'payish. Tadqiqotlar shuni ko'rsatadiki, termit malikalar koloniya ishchilarini ishlab chiqarish uchun qirol bilan juftlashganda, malika ularning o'rnini ko'paytiradi (neotenik malikalar) partenogenetik jihatdan.[85][86]

Neotropik termit Embiratermes neotenicus va boshqa bir qancha turlar asosiy qirolni o'z ichiga olgan asosiy qirolichani yoki 200 gacha bo'lgan koloniyalarni ishlab chiqaradi neotenik orqali paydo bo'lgan malikalar partilogenez asosiy qirolicha.[87] Shakli partenogenez ehtimol ish bilan ta'minlanadi heterozigotlik o'tish qismida genom onadan qizga, shunday qilib qochish qarindoshlarning tushkunligi.

Xulq-atvor va ekologiya

Parhez

A dense pile of termite faecal pellets, about 10 centimeters by 20 centimeters by several centimeters in height, which have accumulated on a wooden shelf from termite activity somewhere above the frame of this photograph.
Termit najas pelletlari

Termitlar tergovchilar, har qanday parchalanish darajasida o'lik o'simliklarni iste'mol qilish. Ular ekologik tizimda o'lik yog'och, najas va o'simliklar kabi chiqindilarni qayta ishlash orqali muhim rol o'ynaydi.[88][89][90] Ko'p turlar eyishadi tsellyuloza, tolani parchalaydigan ixtisoslashgan o'rta ichakka ega.[91] Termitlar asosiy manbadir (11%) atmosferadagi metan, eng asosiylardan biri issiqxona gazlari, tsellyuloza parchalanishidan hosil bo'lgan.[92] Termitlar asosan simbiotik protozoa (metamonadalar ) va boshqalar mikroblar kabi flagellate protistlar ichaklarida ular uchun tsellyulozani hazm qilish, bu esa o'zlarining foydalanishlari uchun oxirgi mahsulotlarni o'zlashtirishlariga imkon beradi.[93][94]Termit ichaklarida mavjud bo'lgan mikrobial ekotizim Yer yuzida boshqa joyda bo'lmagan ko'plab turlarni o'z ichiga oladi. Termitlar bu simbiontlarsiz, ularning ichaklarida mavjud bo'lib, ularni boshqa termitlarning madaniyati bilan oziqlantirgandan keyin rivojlantiradi.[95] Gut protozoa, masalan Trikonimfa, o'z navbatida, simbiotikga tayanadi bakteriyalar zarur bo'lgan bir qismini ishlab chiqarish uchun ularning yuzalariga o'rnatilgan ovqat hazm qilish fermentlari. Ko'pgina yuqori termitlar, ayniqsa Termitidae oilasida, o'zlari ishlab chiqarishi mumkin tsellyuloza fermentlar, ammo ular asosan bakteriyalarga ishonadilar. Termitidae flagellates yo'qolgan.[96][97][98] Tadqiqotlar natijasida turlar topildi spiroxetalar atmosferadagi azotni hasharotlar foydalanishi mumkin bo'lgan shaklga o'rnatishga qodir bo'lgan termit ichaklarida yashash.[99] Olimlarning termitli ovqat hazm qilish trakti va mikrobial endosimbiontlarning o'zaro bog'liqligini tushunishi hali ham ibtidoiy; ammo barcha termit turlarida haqiqat shuki, ishchilar koloniyaning boshqa a'zolarini o'simlik moddalarini hazm qilish natijasida hosil bo'lgan moddalar bilan yoki og'iz yoki anus.[59][100] Yaqindan bog'liq bakteriyalar turlaridan kelib chiqadigan bo'lsak, termitlar va hamamböceği deb taxmin qilinadi ichak mikrobiota ulardan kelib chiqadi diktoopteran ajdodlar.[101]

Kabi ba'zi turlari Gnathamitermes tubiformans mavsumiy ovqatlanish odatlariga ega. Masalan, ular imtiyozli ravishda qizilni uch-awn (Aristida longiseta ) yozda, Buffalograss (Buchloe daktiloidlari ) maydan avgustgacha va ko'k grama Bouteloua gracilis bahorda, yozda va kuzda. Koloniyalari G. tubiformans bahorda oziqlanish faolligi yuqori bo'lgan kuzga qaraganda ozroq ovqat iste'mol qiling.[102]

Turli xil o'rmonlar termit hujumiga moyilligi bilan farq qiladi; farqlar namlik, qattiqlik, qatron va lignin miqdori kabi omillarga bog'liq. Bir tadqiqotda quruq daraxt termiti Cryptotermes brevis qat'iyan afzal terak va chinor odatda termit koloniyasi tomonidan rad etilgan boshqa o'rmonlarga o'rmon. Ushbu imtiyozlar qisman shartli yoki o'rganilgan xatti-harakatni ifodalagan bo'lishi mumkin.[103]

Termit amaliyotining ba'zi turlari qo'ziqorin etishtirish. Ular turlarga ixtisoslashgan qo'ziqorinlarning "bog'ini" saqlab turishadi Termitomitsalar, hasharotlarning najasi bilan oziqlanadi. Qo'ziqorinlarni iste'mol qilganda, ularning sporalari yangi najas pelletlarida unib chiqish orqali tsiklni yakunlash uchun termitlarning ichaklari orqali zarar etkazmasdan o'tadi.[104][105] Molekulyar dalillar shuni ko'rsatadiki, oila Makrotermitinlar taxminan 31 million yil oldin qishloq xo'jaligini rivojlantirgan. Afrikaning va Osiyoning yarimaridli savanna ekotizimlaridagi quruq yog'ochning 90 foizidan ko'prog'i ushbu termitlar tomonidan qayta ishlangan deb taxmin qilinadi. Dastlab yomg'ir o'rmonida yashagan qo'ziqorinlarni etishtirish ularga Afrika savannasini va boshqa yangi muhitlarni mustamlaka qilishga imkon berdi va oxir-oqibat Osiyoga tarqaldi.[106]

Termitlar ovqatlanish odatlariga qarab ikki guruhga bo'linadi: pastki termitlar va yuqori termitlar. Pastki termitlar asosan yog'och bilan oziqlanadi. Yog'ochni hazm qilish qiyin bo'lgani uchun, termitlar qo'ziqorin bilan yuqadigan yog'ochni iste'mol qilishni afzal ko'rishadi, chunki uni hazm qilish osonroq va zamburug'lar oqsilga boy. Ayni paytda, yuqori termitlar turli xil materiallarni, shu jumladan najasni, chirindi, o't, barg va ildiz.[107] Pastki termitlardagi ichak tarkibida ko'plab bakteriyalar turlari mavjud protozoa, yuqori termitlarda esa protozoa bo'lmagan bir necha turdagi bakteriyalar mavjud.[108]

Yirtqichlar

Qisqichbaqa o'rgimchak qo'lga olingan alate bilan

Termitlar turli xil iste'mol qilinadi yirtqichlar. Faqat bitta termit turi, Hodotermes mossambicus, oshqozon tarkibida 65 bo'lgan qushlar va 19 sutemizuvchilar.[109] Artropodlar kabi chumolilar,[110][111] sentipedlar, hamamböceği, kriketlar, ninachilar, chayonlar va o'rgimchaklar,[112] sudralib yuruvchilar kabi kaltakesaklar,[113] va amfibiyalar kabi qurbaqalar[114] va qurbaqalar ikkita termit bilan iste'mol qiling o'rgimchaklar oilada Ammoxenidae mutaxassis termit yirtqichlar bo'lish.[115][116][117] Boshqa yirtqichlar kiradi avarvarks, bo'rilar, chumolilar, ko'rshapalaklar, ayiqlar, bilbies, ko'p qushlar, echidnalar, tulkilar, galagos, numbats, sichqonlar va pangolinlar.[115][118][119][120] The bo'ri bu hasharotlarga qarshi sutemizuvchi birinchi navbatda termitlar bilan oziqlanadi; u oziq-ovqat mahsulotlarini ovoz bilan, shuningdek, askarlar chiqaradigan hidni aniqlash orqali topadi; bitta bo'ri uzun, yopishqoq tilidan foydalanib, bir kechada minglab termitlarni iste'mol qilishga qodir.[121][122] Yalqov ayiqlar uydoshlarini iste'mol qilish uchun ochiq tepaliklarni sindirish, esa shimpanze bor ishlab chiqilgan vositalar o'z uyasidan termitlarni "baliq" qilish. Erta ishlatilgan suyak vositalarining naqshini tahlil qiling hominin Paranthropus robustus ushbu vositalardan termit uyalarini qazish uchun foydalanganliklarini taxmin qilmoqda.[123]

Matabele chumoli (Megaponera analis) o'ldiradi a Makrotermes bellicosus reyd paytida termit askar.

Barcha yirtqichlar orasida chumolilar termitlarning eng katta dushmani hisoblanadi.[110][111] Ba'zi chumolilar nasllari termitlarning maxsus yirtqichlari hisoblanadi. Masalan, Megaponera reyderlik faoliyatini amalga oshiradigan, ba'zilari bir necha soat davom etadigan qat'iy termitli (termitofag) tur.[124][125] Paltothyreus tarsatus boshqa bir termit-reyd turidir, har bir alohida tarkibida termitlarni iloji boricha ko'p to'playdi pastki jag ' uyga qaytishdan oldin, kimyoviy yo'llar orqali reyd maydoniga qo'shimcha uy do'stlarini jalb qilish paytida.[110] Malayziya asosiyerotin chumolilari Eurhopalothrix heliscata o'zlarini tor joylarga bosib, termitlarni ovlashning boshqa strategiyasidan foydalanadi, chunki ular chirigan yog'och korpusli termit koloniyalarida ov qilishadi. Ichkariga kirgach, chumolilar o'zlarining o'ljalarini kalta, ammo o'tkir mandibular yordamida tortib olishadi.[110] Tetramorium uelense kichik termitlar bilan oziqlanadigan ixtisoslashgan yirtqichlar turidir. Skaut termitlar mavjud bo'lgan hududga 10-30 nafar ishchini jalb qiladi va ularni stinger bilan immobilizatsiya qilib o'ldiradi.[126] Centromyrmex va Iridomirmex koloniyalar ba'zan uyalar termit uyumlari va shuning uchun termitlar bu chumolilar tomonidan o'lja qilinadi. Hech qanday munosabat uchun (yirtqichlardan tashqari) dalillar ma'lum emas.[127][128] Boshqa chumolilar, shu jumladan Acanthostichus, Kamponot, Krematogaster, Silindromirmeks, Leptogenis, Odontomachus, Oftalmopon, Pachikondila, Ritidoponera, Solenopsis va Vasmaniya, shuningdek, termitlarning o'ljasi.[118][110][129] Bu barcha chumolilar turlaridan farqli o'laroq va juda ko'p o'lja bo'lishiga qaramay, Dorilus chumolilar kamdan-kam hollarda termitlarni iste'mol qiladilar.[130]

Chumolilar reydlar o'tkazadigan yagona umurtqasizlar emas. Ko'pchilik spekoid ari va bir nechta turlari, shu jumladan Polybiya va Angiopolibiya Termitlarning nikoh parvozi paytida termit tepaliklariga hujum qilishlari ma'lum.[131]

Parazitlar, patogenlar va viruslar

Termitlar parazitlar tomonidan asalarilar, arilar va chumolilarga qaraganda kamroq uchraydi, chunki ular odatda ularning tepalarida yaxshi himoyalangan.[132][133] Shunga qaramay, termitlarga turli xil parazitlar yuqadi. Ulardan ba'zilari dipteran pashshalarini o'z ichiga oladi,[134] Pyemotlar oqadilar va ko'p sonli nematod parazitlar. Ko'p nematod parazitlari tartibda Rhabditida;[135] boshqalari turkumga kiradi Mermis, Diplogaster aerivora va Harteria gallinarum.[136] Yaqinda parazitlar hujumi xavfi ostida koloniya yangi joyga ko'chishi mumkin.[137] Kabi qo'ziqorin patogenlari Aspergillus nomius va Metarhizium anisopliae ammo, ular termit koloniyasiga katta tahdiddir, chunki ular mezbonga xos emas va koloniyaning katta qismlarini yuqtirishlari mumkin;[138][139] uzatish odatda to'g'ridan-to'g'ri jismoniy aloqa orqali sodir bo'ladi.[140] M. anisopliae termit immunitet tizimini susaytirishi ma'lum. Yuqtirish A. nomius faqat koloniya katta stressga duch kelganda paydo bo'ladi.

Termitlar viruslar bilan yuqadi, shu jumladan Entomopoksvirinalar va Yadro polihedroz virusi.[141][142]

Joylashtirish va em-xashak

Ishchi va askar kastalarida qanot yo'qligi va shu sababli hech qachon uchmasligi va reproduktivlar qanotlarini qisqa vaqt davomida ishlatganligi sababli, termitlar asosan harakatlanish uchun oyoqlariga suyanadi.[49]

Ovqatlanish xatti-harakatlari termit turiga bog'liq. Masalan, ayrim turlar o'zlari yashaydigan yog'och tuzilmalar bilan oziqlanadi, boshqalari esa uyaga yaqin bo'lgan ovqatni yig'ib oladi.[143] Ko'pgina ishchilar kamdan-kam hollarda ochiq joylarda topiladi va himoyasiz em-xashak yemaydilar; ularni yirtqichlardan himoya qilish uchun choyshab va uchish-qo'nish yo'lagiga tayanadi.[57] Er osti termitlari oziq-ovqat izlash uchun tunnellar va galereyalar qurishadi va oziq-ovqat manbalarini topishga muvaffaq bo'lgan ishchilar ishchilarni jalb qiladigan fagostimulyant feromonni yotqizish orqali qo'shimcha uydoshlarini yollashadi.[144] Em-xashak ishchilari bir-birlari bilan aloqa qilish uchun semiokimyoviy vositalardan foydalanadilar,[145] va uyasidan tashqarida em-xashak qilishni boshlaydigan ishchilar feromonlarni sternal bezlaridan chiqarib yuboradilar.[146] Bir turda, Nasutitermes costalis, em-xashak ekspeditsiyasining uch bosqichi mavjud: birinchi navbatda, askarlar ushbu hududni izlashadi. Oziq-ovqat manbasini topgach, ular boshqa askarlar bilan muloqot qilishadi va ishchilarning ozgina kuchi paydo bo'la boshlaydi. Ikkinchi bosqichda ishchilar ko'p sonli joyda paydo bo'lishadi. Uchinchi bosqich mavjud askarlar sonining kamayishi va ishchilar sonining ko'payishi bilan belgilanadi.[147] Izolyatsiya qilingan termit ishchilari shug'ullanishi mumkin Levi parvozi o'zlarining do'stlarini topish yoki oziq-ovqat uchun ozuqa uchun optimallashtirilgan strategiya sifatida xatti-harakatlar.[148]

Musobaqa

Ikki koloniya o'rtasidagi raqobat doimo natijaga olib keladi agonistik xatti-harakatlar bir-biriga qarab, janjallarga olib keladi. Ushbu janjallar ikkala tomonning o'limiga va ba'zi hollarda hududni egallashiga yoki yo'qotishiga olib kelishi mumkin.[149][150] O'lik termitlarning jasadlari dafn etilgan "qabriston chuqurlari" mavjud bo'lishi mumkin.[151]

Tadqiqotlar shuni ko'rsatadiki, termitlar ozuqa joylarida bir-biriga duch kelganda, ba'zi termitlar boshqa termitlarning kirib kelishining oldini olish uchun ataylab yo'llarni to'sib qo'yishadi.[145][152] Izlanishli tunnellarda topilgan boshqa koloniyalardan o'lik termitlar hududning ajralib chiqishiga va shu bilan yangi tunnellarni qurish zarurligiga olib keladi.[153] Ikki raqib o'rtasidagi ziddiyat har doim ham ro'y beravermaydi. Masalan, ular bir-birlarining o'tish joylarini to'sib qo'yishlari mumkin bo'lsa-da, koloniyalar Makrotermes bellicosus va Makrotermes subhyalinus har doim ham bir-biriga nisbatan tajovuzkor emas.[154] O'z joniga qasd qilish ma'lum bo'lgan Koptotermalar formosanus. Beri C. formosanus koloniyalar jismoniy to'qnashuvlarga duch kelishi mumkin, ba'zi termitlar ozuqa tunnellariga mahkam siqilib o'ladi, tunnelni muvaffaqiyatli to'sib qo'yadi va barcha agonistik harakatlarni tugatadi.[155]

Reproduktiv kasta orasida neotenik malikalar birlamchi reproduktivlar bo'lmaganida dominant malika bo'lish uchun o'zaro raqobatlashishlari mumkin. Malikalar o'rtasidagi bu kurash yakka qirolichadan boshqasini yo'q qilishga olib keladi, u qirol bilan mustamlakani egallaydi.[156]

Chumolilar va termitlar bir-biri bilan uyalash uchun raqobatlashishi mumkin. Xususan, termitlarni o'lja qiladigan chumolilar odatda daraxtlarni uyalash turlariga salbiy ta'sir ko'rsatadi.[157]

Aloqa

O'rda Nasutitermes oziq-ovqat uchun marshrutda, feromonlarni kuzatib borish va qoldirish

Ko'pgina termitlar ko'r-ko'rona, shuning uchun aloqa asosan kimyoviy, mexanik va feromonli signallar orqali sodir bo'ladi.[46][145] Ushbu aloqa usullari turli xil tadbirlarda, jumladan, em-xashak, reproduktivlarning joylashishini aniqlash, uyalar qurish, uydoshlarini tanib olish, nikohda uchish, dushmanlarni topish va ularga qarshi kurashish va uyalarni himoya qilishda qo'llaniladi.[46][145] Aloqa qilishning eng keng tarqalgan usuli - bu antenna.[145] Bir qator feromonlar ma'lum, shu jumladan kontaktli feromonlar (ular ishchilar trofallaksi yoki parvarish bilan shug'ullanganda yuqadi) va signal, iz va jinsiy feromonlar. Frontal bezdan signal beruvchi feromon va boshqa himoya kimyoviy moddalar ajralib chiqadi. Trail feromonlari sternum bezidan ajralib chiqadi va jinsiy feromonlar ikkita bez manbalaridan kelib chiqadi: sternal va tergal bezlari.[46] Termitlar oziq-ovqat qidirish uchun tashqariga chiqqanda, o'simliklar bo'ylab ustunlar qatoriga ozuqa berishadi. Izni ob'ektlar qoplagan najas qatlamlari yoki uchish-qo'nish yo'laklari orqali aniqlash mumkin. Workers leave pheromones on these trails, which are detected by other nestmates through olfactory receptors.[62] Termites can also communicate through mechanical cues, vibrations, and physical contact.[62][145] These signals are frequently used for alarm communication or for evaluating a food source.[145][158]

When termites construct their nests, they use predominantly indirect communication. No single termite would be in charge of any particular construction project. Individual termites react rather than think, but at a group level, they exhibit a sort of collective cognition. Specific structures or other objects such as pellets of soil or pillars cause termites to start building. The termite adds these objects onto existing structures, and such behaviour encourages building behaviour in other workers. The result is a self-organised process whereby the information that directs termite activity results from changes in the environment rather than from direct contact among individuals.[145]

Termites can distinguish nestmates and non-nestmates through chemical communication and gut symbionts: chemicals consisting of hydrocarbons released from the cuticle allow the recognition of alien termite species.[159][160] Each colony has its own distinct odour. This odour is a result of genetic and environmental factors such as the termites' diet and the composition of the bacteria within the termites' intestines.[161]

Mudofaa

To demonstrate termite repair behaviour, a hole was bored into a termite nest. Over a dozen worker termites with pale heads are visible in this close-up photo, most facing the camera as they engage in repair activities from the inside of the hole. About a dozen soldier termites with orange heads are also visible, some facing outwards from the hole, others patrolling the surrounding area.
Termites rush to a damaged area of the nest.

Termites rely on alarm communication to defend a colony.[145] Alarm pheromones can be released when the nest has been breached or is being attacked by enemies or potential pathogens. Termites always avoid nestmates infected with Metarhizium anisopliae spores, through vibrational signals released by infected nestmates.[162] Other methods of defence include intense jerking and secretion of fluids from the frontal gland and defecating faeces containing alarm pheromones.[145][163]

In some species, some soldiers block tunnels to prevent their enemies from entering the nest, and they may deliberately rupture themselves as an act of defence.[164] In cases where the intrusion is coming from a breach that is larger than the soldier's head, soldiers form a falanx -like formation around the breach and bite at intruders.[165] If an invasion carried out by Megaponera analis is successful, an entire colony may be destroyed, although this scenario is rare.[165]

To termites, any breach of their tunnels or nests is a cause for alarm. When termites detect a potential breach, the soldiers usually bang their heads, apparently to attract other soldiers for defence and to recruit additional workers to repair any breach.[62] Additionally, an alarmed termite bumps into other termites which causes them to be alarmed and to leave pheromone trails to the disturbed area, which is also a way to recruit extra workers.[62]

Nasute termite soldiers on rotten wood

The pantropical subfamily Nasutitermitinae has a specialised caste of soldiers, known as nasutes, that have the ability to exude noxious liquids through a horn-like frontal projection that they use for defence.[166] Nasutes have lost their mandibles through the course of evolution and must be fed by workers.[65] Turli xil monoterpene uglevodorod erituvchilar have been identified in the liquids that nasutes secrete.[167] Xuddi shunday, Formosan subterranean termites have been known to secrete naftalin to protect their nests.[168]

Soldiers of the species Globitermes sulphureus commit suicide by autothysis – rupturing a large gland just beneath the surface of their cuticles. The thick, yellow fluid in the gland becomes very sticky on contact with the air, entangling ants or other insects that are trying to invade the nest.[169][170] Another termite, Neocapriterme taracua, also engages in suicidal defence. Workers physically unable to use their mandibles while in a fight form a pouch full of chemicals, then deliberately rupture themselves, releasing toxic chemicals that paralyse and kill their enemies.[171] The soldiers of the neotropik termite family Serritermitidae have a defence strategy which involves front gland autothysis, with the body rupturing between the head and abdomen. When soldiers guarding nest entrances are attacked by intruders, they engage in autothysis, creating a block that denies entry to any attacker.[172]

Workers use several different strategies to deal with their dead, including burying, cannibalism, and avoiding a corpse altogether.[173][174][175] Qochish uchun patogenlar, termites occasionally engage in necrophoresis, in which a nestmate carries away a corpse from the colony to dispose of it elsewhere.[176] Which strategy is used depends on the nature of the corpse a worker is dealing with (i.e. the age of the carcass).[176]

Relationship with other organisms

The Western Underground Orchid lives completely underground. It is unable to photosynthesize, and it is dependent on underground insects such as termites for pollination. The flower head shown is only about 1.5 centimetres across. Dozens of tiny rose-coloured florets are arranged in a tight cluster, surrounded by petals that give the flower the appearance of a pale miniature tulip.
Rhizanthella gardneri is the only orchid known to be pollinated by termites.

Bir turi qo'ziqorin is known to mimic termite eggs, successfully avoiding its natural predators. These small brown balls, known as "termite balls", rarely kill the eggs, and in some cases the workers tend to them.[177] This fungus mimics these eggs by producing a cellulose-digesting enzyme known as glucosidases.[178] A unique mimicking behaviour exists between various species of Trichopsenius beetles and certain termite species within Retikulitermalar. The beetles share the same kutikula uglevodorodlar as the termites and even biosynthesize them. This chemical mimicry allows the beetles to integrate themselves within the termite colonies.[179] The developed qo'shimchalar on the physogastric abdomen of Austrospirachtha mimetes allows the beetle to mimic a termite worker.[180]

Some species of ant are known to capture termites to use as a fresh food source later on, rather than killing them. Masalan, Formica nigra captures termites, and those who try to escape are immediately seized and driven underground.[181] Certain species of ants in the subfamily Ponerinae conduct these raids although other ant species go in alone to steal the eggs or nymphs.[157] Ants such as Megaponera analis attack the outside of mounds and Dorilina ants attack underground.[157][182] Despite this, some termites and ants can coexist peacefully. Some species of termite, including Nasutitermes corniger, form associations with certain ant species to keep away predatory ant species.[183] The earliest known association between Azteka ants and Nasutitermes termites date back to the Oligocene to Miocene period.[184]

An ant raiding party collecting Pseudocanthotermes militaris termites after a successful raid

54 species of ants are known to inhabit Nasutitermes mounds, both occupied and abandoned ones.[185] One reason many ants live in Nasutitermes mounds is due to the termites' frequent occurrence in their geographical range; another is to protect themselves from floods.[185][186] Iridomirmex also inhabits termite mounds although no evidence for any kind of relationship (other than a predatory one) is known.[127] In rare cases, certain species of termites live inside active ant colonies.[187] Some invertebrate organisms such as beetles, caterpillars, flies and millipedes are termitophiles and dwell inside termite colonies (they are unable to survive independently).[62] As a result, certain beetles and flies have evolved with their hosts. They have developed a gland that secrete a substance that attracts the workers by licking them. Mounds may also provide shelter and warmth to birds, lizards, snakes and scorpions.[62]

Termites are known to carry pollen and regularly visit flowers,[188] so are regarded as potential pollinators for a number of flowering plants.[189] One flower in particular, Rhizanthella gardneri, is regularly pollinated by foraging workers, and it is perhaps the only Orxideya flower in the world to be pollinated by termites.[188]

Many plants have developed effective defences against termites. However, seedlings are vulnerable to termite attacks and need additional protection, as their defence mechanisms only develop when they have passed the seedling stage.[190] Defence is typically achieved by secreting antifeedant chemicals into the woody cell walls.[191] This reduces the ability of termites to efficiently digest the tsellyuloza. A commercial product, "Blockaid", has been developed in Australia that uses a range of plant extracts to create a paint-on nontoxic termite barrier binolar uchun.[191] An extract of a species of Australian figwort, Eremofila, has been shown to repel termites;[192] tests have shown that termites are strongly repelled by the toxic material to the extent that they will starve rather than consume the food. When kept close to the extract, they become disoriented and eventually die.[192]

Relationship with the environment

Termite populations can be substantially impacted by environmental changes including those caused by human intervention. A Brazilian study investigated the termite assemblages of three sites of Caatinga under different levels of anthropogenic disturbance in the semi-arid region of northeastern Braziliya were sampled using 65 x 2 m transects.[193] A total of 26 species of termites were present in the three sites, and 196 encounters were recorded in the transects. The termite assemblages were considerably different among sites, with a conspicuous reduction in both diversity and abundance with increased disturbance, related to the reduction of tree density and soil cover, and with the intensity of trampling by cattle and goats. The wood-feeders were the most severely affected feeding group.

Uyalar

Termite workers at work
Photograph of an arboreal termite nest built on a tree trunk high above ground. It has an ovoid shape and appears to be larger than a basketball. It is dark brown in colour, and it is made of carton, a mixture of digested wood and termite faeces that is strong and resistant to rain. Covered tunnels constructed of carton can be seen leading down the shaded side of the tree from the nest to the ground.
An arboreal termite nest in Mexico
Termite nest in a Bankiya, Palm Beach, Sydney.

A termite nest can be considered as being composed of two parts, the inanimate and the animate. The animate is all of the termites living inside the colony, and the inanimate part is the structure itself, which is constructed by the termites.[194] Nests can be broadly separated into three main categories: subterranean (completely below ground), epigeal (protruding above the soil surface), and arboreal (built above ground, but always connected to the ground via shelter tubes ).[195] Epigeal nests (mounds) protrude from the earth with ground contact and are made out of earth and mud.[196] A nest has many functions such as providing a protected living space and providing shelter against predators. Most termites construct underground colonies rather than multifunctional nests and mounds.[197] Primitive termites of today nest in wooden structures such as logs, stumps and the dead parts of trees, as did termites millions of years ago.[195]

To build their nests, termites primarily use faeces, which have many desirable properties as a construction material.[198] Other building materials include partly digested plant material, used in carton nests (arboreal nests built from faecal elements and wood), and soil, used in subterranean nest and mound construction. Not all nests are visible, as many nests in tropical forests are located underground.[197] Species in the subfamily Apicotermitinae are good examples of subterranean nest builders, as they only dwell inside tunnels.[198] Other termites live in wood, and tunnels are constructed as they feed on the wood. Nests and mounds protect the termites' soft bodies against desiccation, light, pathogens and parasites, as well as providing a fortification against predators.[199] Nests made out of carton are particularly weak, and so the inhabitants use counter-attack strategies against invading predators.[200]

Arboreal carton nests of mangrov botqog'i - turar joy Nasutitermes are enriched in lignin and depleted in cellulose and xylans. This change is caused by bacterial decay in the gut of the termites: they use their faeces as a carton building material. Arboreal termites nests can account for as much as 2% of above ground carbon storage in Puerto-Riko mangrove swamps. Bular Nasutitermes nests are mainly composed of partially biodegraded wood material from the stems and branches of mangrove trees, namely, Rizofora mangalasi (red mangrove), Avitsennia germinans (black mangrove) and Laguncularia racemose (white mangrove).[201]

Some species build complex nests called polycalic nests; this habitat is called polycalism. Polycalic species of termites form multiple nests, or calies, connected by subterranean chambers.[118] The termite genera Apicotermes va Trinervitermes are known to have polycalic species.[202] Polycalic nests appear to be less frequent in mound-building species although polycalic arboreal nests have been observed in a few species of Nasutitermes.[202]

Höyükler

Nests are considered mounds if they protrude from the earth's surface.[198] A mound provides termites the same protection as a nest but is stronger.[200] Mounds located in areas with torrential and continuous rainfall are at risk of mound erosion due to their clay-rich construction. Those made from carton can provide protection from the rain, and in fact can withstand high precipitation.[198] Certain areas in mounds are used as strong points in case of a breach. Masalan, Cubitermes colonies build narrow tunnels used as strong points, as the diameter of the tunnels is small enough for soldiers to block.[203] A highly protected chamber, known as the "queens cell", houses the queen and king and is used as a last line of defence.[200]

Turning turlari Makrotermalar arguably build the most complex structures in the insect world, constructing enormous mounds.[198] These mounds are among the largest in the world, reaching a height of 8 to 9 metres (26 to 29 feet), and consist of chimneys, pinnacles and ridges.[62] Another termite species, Amitermes meridionalis, can build nests 3 to 4 metres (9 to 13 feet) high and 2.5 metres (8 feet) wide. The tallest mound ever recorded was 12.8 metres (42 ft) long found in the Democratic Republic of the Congo.[204]

The sculptured mounds sometimes have elaborate and distinctive forms, such as those of the compass termite (Amitermes meridionalis va A. laurensis), which builds tall, wedge-shaped mounds with the long axis oriented approximately north–south, which gives them their common name.[205][206] This orientation has been experimentally shown to assist termoregulyatsiya. The north–south orientation causes the internal temperature of a mound to increase rapidly during the morning while avoiding overheating from the midday sun. The temperature then remains at a plateau for the rest of the day until the evening.[207]

Shelter tubes

Photo taken upwards from ground level of shelter tubes going up the shaded side of a tree. Where the main trunk of the tree divides into separate major branches, the shelter tube also branches. Although the nests are not visible in this photo, the branches of the shelter tube presumably lead up to polycalic sister colonies of the arboreal termites that built these tubes.
Nasutiterminae shelter tubes on a tree trunk provide cover for the trail from nest to forest floor.

Termites construct shelter tubes, also known as earthen tubes or mud tubes, that start from the ground. These shelter tubes can be found on walls and other structures.[208] Constructed by termites during the night, a time of higher humidity, these tubes provide protection to termites from potential predators, especially ants.[209] Shelter tubes also provide high humidity and darkness and allow workers to collect food sources that cannot be accessed in any other way.[208] These passageways are made from soil and faeces and are normally brown in colour. The size of these shelter tubes depends on the number of food sources that are available. They range from less than 1 cm to several cm in width, but may be dozens of metres in length.[209]

Odamlar bilan munosabatlar

Zararkunandalar sifatida

Termite mound as an obstacle on a runway at Xorixalar (Namibiya )
Termite damage on external structure

Owing to their wood-eating habits, many termite species can do significant damage to unprotected buildings and other wooden structures.[210] Termites play an important role as decomposers of wood and vegetative material, and the conflict with humans occurs where structures and landscapes containing structural wood components, cellulose derived structural materials and ornamental vegetation provide termites with a reliable source of food and moisture.[211] Their habit of remaining concealed often results in their presence being undetected until the timbers are severely damaged, with only a thin exterior layer of wood remaining, which protects them from the environment.[212] Of the 3,106 species known, only 183 species cause damage; 83 species cause significant damage to wooden structures.[210] In North America, 18 subterranean species are pests;[213] in Australia, 16 species have an economic impact; in the Indian subcontinent 26 species are considered pests, and in tropical Africa, 24. In Central America and the West Indies, there are 17 pest species.[210] Among the termite genera, Koptotermalar has the highest number of pest species of any genus, with 28 species known to cause damage.[210] Less than 10% of drywood termites are pests, but they infect wooden structures and furniture in tropical, subtropical and other regions. Dampwood termites only attack lumber material exposed to rainfall or soil.[210]

Drywood termites thrive in warm climates, and human activities can enable them to invade homes since they can be transported through contaminated goods, containers and ships.[210] Colonies of termites have been seen thriving in warm buildings located in cold regions.[214] Some termites are considered invasive species. Cryptotermes brevis, the most widely introduced invasive termite species in the world, has been introduced to all the islands in the West Indies and to Australia.[42][210]

Termite damage in wooden house stumps

In addition to causing damage to buildings, termites can also damage food crops.[215] Termites may attack trees whose resistance to damage is low but generally ignore fast-growing plants. Most attacks occur at harvest time; crops and trees are attacked during the dry season.[215]

The damage caused by termites costs the southwestern United States approximately $1.5 billion each year in wood structure damage, but the true cost of damage worldwide cannot be determined.[210][216] Drywood termites are responsible for a large proportion of the damage caused by termites.[217] The goal of termite control is to keep structures and susceptible ornamental plants free from termites.;[218] Structures may be homes or business, or elements such as wooden fence posts and telephone poles. Regular and thorough inspections by a trained professional may be necessary to detect termite activity in the absence of more obvious signs like termite swarmers or alates inside or adjacent to a structure. Termite monitors made of wood or cellulose adjacent to a structure may also provide indication of termite foraging activity where it will be in conflict with humans. Termites can be controlled by application of Bordo aralashmasi or other substances that contain mis kabi xromlangan mis arsenat.[219]

To better control the population of termites, various methods have been developed to track termite movements.[216] One early method involved distributing termite bait laced with immunoglobulin G (IgG) marker proteins from rabbits or chickens. Termites collected from the field could be tested for the rabbit-IgG markers using a rabbit-IgG-specific tahlil qilish. More recently developed, less expensive alternatives include tracking the termites using egg white, cow milk, or soy milk proteins, which can be sprayed on termites in the field. Termites bearing these proteins can be traced using a protein-specific Elishay sinov.[216]

Oziq-ovqat sifatida

Mozambican boys from the Yawo tribe collecting flying termites
These flying alates were collected as they came out of their nests in the ground during the early days of the rainy season.

43 termite species are used as food by humans or are fed to livestock.[220] These insects are particularly important in impoverished countries where malnutrition is common, as the oqsil from termites can help improve the human diet. Termites are consumed in many regions globally, but this practice has only become popular in developed nations in recent years.[220]

Termites are consumed by people in many different cultures around the world. In many parts of Africa, the alates are an important factor in the diets of native populations.[221] Groups have different ways of collecting or cultivating insects; sometimes collecting soldiers from several species. Though harder to acquire, queens are regarded as a delicacy.[222] Termite alates are high in nutrition with adequate levels of yog ' and protein. They are regarded as pleasant in taste, having a nut-like flavour after they are cooked.[221]

Alates are collected when the rainy season begins. During a nuptial flight, they are typically seen around lights to which they are attracted, and so nets are set up on lamps and captured alates are later collected. The wings are removed through a technique that is similar to tanib olish. The best result comes when they are lightly roasted on a hot plate or fried until crisp. Yog ' is not required as their bodies usually contain sufficient amounts of oil. Termites are typically eaten when livestock is lean and tribal crops have not yet developed or produced any food, or if food stocks from a previous growing season are limited.[221]

In addition to Africa, termites are consumed in local or tribal areas in Asia and North and South America. Avstraliyada, Mahalliy avstraliyaliklar are aware that termites are edible but do not consume them even in times of scarcity; there are few explanations as to why.[221][222] Termite mounds are the main sources of soil consumption (geophagy ) in many countries including Keniya, Tanzaniya, Zambiya, Zimbabve va Janubiy Afrika.[223][224][225][226] Researchers have suggested that termites are suitable candidates for human consumption and space agriculture, as they are high in protein and can be used to convert inedible waste to consumable products for humans.[227]

Qishloq xo'jaligida

Scientists have developed a more affordable method of tracing the movement of termites using traceable proteins.[216]

Termites can be major agricultural pests, particularly in East Africa and North Asia, where crop losses can be severe (3–100% in crop loss in Africa).[228] Counterbalancing this is the greatly improved water infiltration where termite tunnels in the soil allow rainwater to soak in deeply, which helps reduce runoff and consequent soil erosion through bioturbatsiya.[229] In South America, cultivated plants such as eucalyptus, upland rice and sugarcane can be severely damaged by termite infestations, with attacks on leaves, roots and woody tissue. Termites can also attack other plants, including cassava, kofe, paxta, fruit trees, maize, peanuts, soybeans and vegetables.[21] Mounds can disrupt farming activities, making it difficult for farmers to operate farming machinery; however, despite farmers' dislike of the mounds, it is often the case that no net loss of production occurs.[21] Termites can be beneficial to agriculture, such as by boosting ekinlarning hosildorligi and enriching the soil. Termites and ants can re-colonise untilled land that contains crop stubble, which colonies use for nourishment when they establish their nests. The presence of nests in fields enables larger amounts of rainwater to soak into the ground and increases the amount of nitrogen in the soil, both essential for the growth of crops.[230]

Ilm-fan va texnologiyada

The termite gut has inspired various research efforts aimed at replacing Yoqilg'i moyi with cleaner, renewable energy sources.[231] Termites are efficient bioreaktorlar, capable of producing two litres of vodorod from a single sheet of paper.[232] Approximately 200 species of microbes live inside the termite hindgut, releasing the hydrogen that was trapped inside wood and plants that they digest.[231][233] Through the action of unidentified enzymes in the termite gut, lignotsellyuloza polimerlar are broken down into sugars and are transformed into hydrogen. The bacteria within the gut turns the sugar and hydrogen into tsellyuloza atsetat, an atsetat Ester of cellulose on which termites rely for energy.[231] Community DNA sequencing of the microbes in the termite hindgut has been employed to provide a better understanding of the metabolik yo'l.[231] Genetic engineering may enable hydrogen to be generated in bioreactors from woody biomass.[231]

Ning rivojlanishi avtonom robotlar capable of constructing intricate structures without human assistance has been inspired by the complex mounds that termites build.[234] These robots work independently and can move by themselves on a tracked grid, capable of climbing and lifting up bricks. Such robots may be useful for future projects on Mars, or for building levees to prevent flooding.[235]

Termites use sophisticated means to control the temperatures of their mounds. As discussed above, the shape and orientation of the mounds of the Australian compass termite stabilises their internal temperatures during the day. As the towers heat up, the solar chimney effect (stek effekti ) creates an updraft of air within the mound.[236] Wind blowing across the tops of the towers enhances the circulation of air through the mounds, which also include side vents in their construction. The solar chimney effect has been in use for centuries in the Yaqin Sharq va Yaqin Sharq for passive cooling, as well as in Europe by the Rimliklarga.[237] It is only relatively recently, however, that climate responsive construction techniques have become incorporated into modern architecture. Especially in Africa, the stack effect has become a popular means to achieve natural ventilation and passive cooling in modern buildings.[236]

Madaniyatda

The pink-hued Eastgate Centre

The Eastgate markazi is a shopping centre and office block in central Xarare, Zimbabwe, whose architect, Mik Pirs, ishlatilgan passiv sovutish inspired by that used by the local termites.[238] It was the first major building exploiting termite-inspired cooling techniques to attract international attention. Other such buildings include the Learning Resource Center at the Sharqiy Afrikaning katolik universiteti va Kengash uyi 2 bino Melburn, Avstraliya.[236]

Few zoos hold termites, due to the difficulty in keeping them captive and to the reluctance of authorities to permit potential pests. One of the few that do, the Bazel hayvonot bog'i yilda Shveytsariya, has two thriving Macrotermes bellicosus populations – resulting in an event very rare in captivity: the mass migrations of young flying termites. This happened in September 2008, when thousands of male termites left their mound each night, died, and covered the floors and water pits of the house holding their exhibit.[239]

African tribes in several countries have termites as totemlar, and for this reason tribe members are forbidden to eat the reproductive alates.[240] Termites are widely used in traditional popular medicine; they are used as treatments for diseases and other conditions such as asthma, bronxit, ovozning balandligi, influenza, sinusit, tonzillit and whooping cough.[220] Nigeriyada, Macrotermes nigeriensis is used for spiritual protection and to treat wounds and sick pregnant women. In Southeast Asia, termites are used in ritual practices. In Malaysia, Singapore and Thailand, termite mounds are commonly worshiped among the populace.[241] Abandoned mounds are viewed as structures created by spirits, believing a local guardian dwells within the mound; bu sifatida tanilgan Keramat and Datok Kong. In urban areas, local residents construct red-painted shrines over mounds that have been abandoned, where they pray for good health, protection and luck.[241]

Shuningdek qarang

Izohlar

  1. ^ It is unknown whether the termite was female or male. If it was a female, the body length would be far greater than 25 millimetres when mature.

Adabiyotlar

  1. ^ Behrensmeyer, A. K.; Turner, A. "Fossilworks, Gateway to the Paleobiology Database".
  2. ^ Engel, M.S .; Grimaldi, D.A.; Krishna, K. (2009). "Termites (Isoptera): their phylogeny, classification, and rise to ecological dominance". Amerika muzeyi Novitates. 2009 (3650): 1–27. doi:10.1206/651.1. hdl:2246/5969. ISSN  0003-0082. S2CID  56166416.
  3. ^ a b Evangelista, Dominic A.; Vipfler, Benjamin; Béthoux, Olivier; Donat, Aleksandr; Fujita, Mari; Kohli, Manpreet K.; Legendre, Frédéric; Liu, Shanlin; Machida, Ryuichiro; Misof, Bernxard; Peters, Ralph S. (2019-01-30). "An integrative phylogenomic approach illuminates the evolutionary history of cockroaches and termites (Blattodea)". Qirollik jamiyati materiallari B: Biologiya fanlari. 286 (1895): 20182076. doi:10.1098/rspb.2018.2076. ISSN  0962-8452. PMC  6364590. PMID  30963947.
  4. ^ "Termite". Merriam-Webster.com.
  5. ^ Bignell, Roisin & Lo 2010, p. 2018-04-02 121 2.
  6. ^ a b Cranshaw, W. (2013). "11". Bugs Rule!: An Introduction to the World of Insects. Princeton, Nyu-Jersi: Princeton University Press. p. 188. ISBN  978-0-691-12495-7.
  7. ^ Lobeck, A. Kohl (1939). Geomorphology; an Introduction to the Study of Landscapes (1-nashr). University of California: McGraw Hill Book Company, Incorporated. 431-432 betlar. ASIN  B002P5O9SC.
  8. ^ Xarper, Duglas. "Termite". Onlayn etimologiya lug'ati.
  9. ^ "Termite". Merriam-Webster Onlayn Lug'ati. Olingan 5 yanvar 2015.
  10. ^ Cleveland, L.R.; Hall, S.K.; Sanders, E.P.; Collier, J. (1934). "The Wood-Feeding Roach Kriptokerkus, its protozoa, and the symbiosis between protozoa and roach". Memoirs of the American Academy of Arts and Sciences. 17 (2): 185–382. doi:10.1093/aesa/28.2.216.
  11. ^ McKittrick, F.A. (1965). "A contribution to the understanding of cockroach-termite affinities". Amerika entomologik jamiyati yilnomalari. 58 (1): 18–22. doi:10.1093/aesa/58.1.18. PMID  5834489.
  12. ^ Ware, J.L.; Litman, J.; Klass, K.-D.; Spearman, L.A. (2008). "Relationships among the major lineages of Dictyoptera: the effect of outgroup selection on dictyopteran tree topology". Tizimli entomologiya. 33 (3): 429–450. doi:10.1111/j.1365-3113.2008.00424.x. S2CID  86777253.
  13. ^ a b Inward, D.; Bekkaloni, G.; Eggleton, P. (2007). "Buyurtmaning o'limi: keng ko'lamli molekulyar filogenetik tadqiqotlar termitlarning eusocial hamamböceği ekanligini tasdiqlaydi". Biologiya xatlari. 3 (3): 331–5. doi:10.1098 / rsbl.2007.0102. PMC  2464702. PMID  17412673.
  14. ^ Eggleton, P.; Bekkaloni, G.; Inward, D. (2007). "Response to Lo va boshq.". Biologiya xatlari. 3 (5): 564–565. doi:10.1098 / rsbl.2007.0367. PMC  2391203.
  15. ^ Ohkuma, M.; Noda, S.; Hongoh, Y.; Nalepa, C.A.; Inoue, T. (2009). "Inheritance and diversification of symbiotic trichonymphid flagellates from a common ancestor of termites and the cockroach Kriptokerkus". Qirollik jamiyati materiallari B: Biologiya fanlari. 276 (1655): 239–245. doi:10.1098/rspb.2008.1094. PMC  2674353. PMID  18812290.
  16. ^ Lo, N.; Tokuda, G.; Watanabe, H.; Rose, H.; Slaytor, M.; Maekawa, K.; Bandi, C.; Noda, H. (June 2000). "Evidence from multiple gene sequences indicates that termites evolved from wood-feeding cockroaches". Hozirgi biologiya. 10 (13): 801–814. doi:10.1016/S0960-9822(00)00561-3. PMID  10898984. S2CID  14059547.
  17. ^ Grimaldi, D.; Engel, M.S. (2005). Hasharotlarning rivojlanishi (1-nashr). Kembrij: Kembrij universiteti matbuoti. p.237. ISBN  978-0-521-82149-0.
  18. ^ Klass, K.D.; Nalepa, C.; Lo, N. (2008). "Wood-feeding cockroaches as models for termite evolution (Insecta: Dictyoptera): Kriptokerkus va boshqalar Parasphaeria boleiriana". Molekulyar filogenetik va evolyutsiyasi. 46 (3): 809–817. doi:10.1016/j.ympev.2007.11.028. PMID  18226554.
  19. ^ Lo, N.; Engel, M.S .; Cameron, S.; Nalepa, C.A.; Tokuda, G.; Grimaldi, D.; Kitade, O..; Krishna, K.; Klass, K.-D.; Maekawa, K.; Miura, T.; Thompson, G.J. (2007). "Comment. Save Isoptera: a comment on Inward va boshq.". Biologiya xatlari. 3 (5): 562–563. doi:10.1098/rsbl.2007.0264. PMC  2391185. PMID  17698448.
  20. ^ Costa, James (2006). The other insect societies. Garvard universiteti matbuoti. 135-136-betlar. ISBN  978-0-674-02163-1.
  21. ^ a b v Capinera, J.L. (2008). Entomologiya entsiklopediyasi (2-nashr). Dordrext: Springer. pp.3033 –3037, 3754. ISBN  978-1-4020-6242-1.
  22. ^ Vrsanky, P.; Aristov, D. (2014). "Termites (Isoptera) from the Jurassic/Cretaceous boundary: Evidence for the longevity of their earliest genera". Evropa Entomologiya jurnali. 111 (1): 137–141. doi:10.14411/eje.2014.014.
  23. ^ Poinar, G.O. (2009). "Description of an early Cretaceous termite (Isoptera: Kalotermitidae) and its associated intestinal protozoa, with comments on their co-evolution". Parazitlar va vektorlar. 2 (1–17): 12. doi:10.1186/1756-3305-2-12. PMC  2669471. PMID  19226475.
  24. ^ Legendre, F.; Nel, A .; Svenson, G.J.; Robillard, T.; Pellens, R.; Grandcolas, P.; Escriva, H. (2015). "Phylogeny of Dictyoptera: Dating the Origin of Cockroaches, Praying Mantises and Termites with Molecular Data and Controlled Fossil Evidence". PLOS ONE. 10 (7): e0130127. Bibcode:2015PLoSO..1030127L. doi:10.1371/journal.pone.0130127. PMC  4511787. PMID  26200914.
  25. ^ Luo, Z.X.; Wible, J.R. (2005). "A Late Jurassic digging mammal and early mammalian diversification". Ilm-fan. 308 (5718): 103–107. Bibcode:2005Sci...308..103L. doi:10.1126/science.1108875. PMID  15802602. S2CID  7031381.
  26. ^ Rohr, D.M.; Boucot, A. J.; Miller, J.; Abbott, M. (1986). "Oldest termite nest from the Upper Cretaceous of west Texas". Geologiya. 14 (1): 87. Bibcode:1986Geo....14...87R. doi:10.1130/0091-7613(1986)14<87:OTNFTU>2.0.CO;2.
  27. ^ Weesner, F.M. (1960). "Evolution and Biology of the Termites". Entomologiyaning yillik sharhi. 5 (1): 153–170. doi:10.1146/annurev.en.05.010160.001101.
  28. ^ a b Tilyard, R.J. (1937). "Kansas Permian insects. Part XX the cockroaches, or order Blattaria". Amerika Ilmiy jurnali. 34 (201): 169–202, 249–276. Bibcode:1937AmJS...34..169T. doi:10.2475/ajs.s5-34.201.169.
  29. ^ Henry, M.S. (2013). Symbiosis: Associations of Invertebrates, Birds, Ruminants, and Other Biota. New York, New York: Elsevier. p. 59. ISBN  978-1-4832-7592-5.
  30. ^ a b Krishna, K.; Grimaldi, D.A.; Krishna, V.; Engel, M.S. (2013). "Treatise on the Isoptera of the world" (PDF). Amerika Tabiat Tarixi Muzeyining Axborotnomasi. 1. 377 (7): 1–200. doi:10.1206/377.1. S2CID  87276148.
  31. ^ Bell, W.J.; Rot, LM .; Nalepa, C.A. (2007). Cockroaches: ecology, behavior, and natural history. Baltimor, MD: Jons Xopkins universiteti matbuoti. p.161. ISBN  978-0-8018-8616-4.
  32. ^ Engel, M. (2011). "Family-group names for termites (Isoptera), redux". Hayvonot bog'i tugmachalari (148): 171–184. doi:10.3897/zookeys.148.1682. PMC  3264418. PMID  22287896.
  33. ^ Thorne, Barbara L (1997). "Evolution of eusociality in termites" (PDF). Ekologiya va sistematikaning yillik sharhi. 28 (5): 27–53. doi:10.1146/annurev.ecolsys.28.1.27. PMC  349550. Arxivlandi asl nusxasi (PDF) 2010-05-30 kunlari.
  34. ^ a b Harrison, Mark C.; Jongepier, Evelien; Robertson, Hugh M.; Arning, Nicolas; Bitard-Feildel, Tristan; Chao, Hsu; Childers, Christopher P.; Dinh, Huyen; Doddapaneni, Harshavardhan; Dugan, Shannon; Gowin, Johannes; Greiner, Carolin; Han, Yi; Hu, Haofu; Hughes, Daniel S. T.; Huylmans, Ann-Kathrin; Kemena, Carsten; Kremer, Lukas P. M.; Lee, Sandra L.; Lopez-Ezquerra, Alberto; Mallet, Ludovic; Monroy-Kuhn, Jose M.; Moser, Annabell; Murali, Shwetha C.; Muzny, Donna M.; Otani, Saria; Piulachs, Maria-Dolors; Poelchau, Monica; Qu, Jiaxin; Schaub, Florentine; Wada-Katsumata, Ayako; Worley, Kim C.; Xie, Qiaolin; Ylla, Guillem; Poulsen, Michael; Gibbs, Richard A.; Schal, Coby; Richards, Stephen; Belles, Xavier; Korb, Judith; Bornberg-Bauer, Erich (2018). "Hemimetabolous genomes reveal molecular basis of termite eusociality". Tabiat ekologiyasi va evolyutsiyasi. 2 (3): 557–566. doi:10.1038/s41559-017-0459-1. PMC  6482461. PMID  29403074.
  35. ^ "Termites had first castes". Tabiat. 530 (7590): 256. 2016. Bibcode:2016Natur.530Q.256.. doi:10.1038/530256a. S2CID  49905391.
  36. ^ Terrapon, Nikolas; Li, Cai; Robertson, Xyu M.; Dji, Lu; Men, Xuehong; But, Uorren; Chen, Chjensheng; Childers, Kristofer P.; Glastad, Karl M.; Goxale, Kaustubx; va boshq. (2014). "Termit genomidagi muqobil ijtimoiy tashkilotning molekulyar izlari". Tabiat aloqalari. 5: 3636. Bibcode:2014 yil NatCo ... 5.3636T. doi:10.1038 / ncomms4636. PMID  24845553.
  37. ^ Poulsen, Maykl; Xu, Xaofu; Li, Cai; Chen, Chjensheng; Xu, Luohao; Otani, Sariya; Nygaard, Sann; Nobre, Taniya; Klaubauf, Silviya; Shindler, Filipp M.; va boshq. (2014). "Qo'ziqorinlarni parvarish qiladigan termitda o'simliklarning parchalanishiga qo'shimcha simbion qo'shimchalar". Milliy fanlar akademiyasi materiallari. 111 (40): 14500–14505. Bibcode:2014PNAS..11114500P. doi:10.1073 / pnas.1319718111. PMC  4209977. PMID  25246537.
  38. ^ Koller, T; Ditrix, S; Sheffrahn, RH; Bruney, A (2012). "Ichak atrofini va bakterial mikrobiyotani yuqori aniqlikda tahlil qilish, o'tin bilan oziqlanadigan yuqori termitlarda ichakning funktsional bo'linishini aniqlaydi (Nasutitermes spp.) ". Amaliy va atrof-muhit mikrobiologiyasi. 78 (13): 4691–4701. doi:10.1128 / aem.00683-12. PMC  3370480. PMID  22544239.
  39. ^ a b v d e "Termit biologiyasi va ekologiyasi". Texnologiya, sanoat va iqtisodiyot bo'limi Kimyoviy mahsulotlar filiali. Birlashgan Millatlar Tashkilotining Atrof-muhit dasturi. Arxivlandi asl nusxasi 2014 yil 10-noyabrda. Olingan 12 yanvar 2015.
  40. ^ Meyer, V.V.; Braack, L.E.O .; Biggs, XC; Ebersohn, C. (1999). "Shimoliy Kruger milliy bog'idagi termit uyumlarining tarqalishi va zichligi Makrotermalar Holmgren (Isoptera: Termitidae) ". Afrika entomologiyasi. 7 (1): 123–130.
  41. ^ Sanderson, M.G. (1996). "Termitlarning biomassasi va ularning metan va karbonat angidrid chiqindilari: global ma'lumotlar bazasi". Global biogeokimyoviy tsikllar. 10 (4): 543–557. Bibcode:1996GBioC..10..543S. doi:10.1029 / 96GB01893.
  42. ^ a b Xizer, N.V. (1971). "Ekzotik quruq daraxt termiti Cryptotermes brevis (Walker) (Isoptera: Kalotermitidae) va Kvinslenddagi endemik avstraliyalik quruq daraxt termitlari ". Avstraliya Entomologiya jurnali. 10 (2): 134–141. doi:10.1111 / j.1440-6055.1971.tb00022.x.
  43. ^ Claybourne, Anna (2013). Chumolilar koloniyasi va boshqa hasharotlar guruhlari. Chikago, Ill.: Geynemann kutubxonasi. p. 38. ISBN  978-1-4329-6487-0.
  44. ^ a b Engel, M.S .; Gross, M. (2008). "Avstriya (Isoptera), Shtiriya so'nggi myosenidan olingan ulkan termit". Naturwissenschaften. 96 (2): 289–295. Bibcode:2009NW ..... 96..289E. doi:10.1007 / s00114-008-0480-y. PMID  19052720. S2CID  21795900.
  45. ^ Heidecker, J.L .; Leuthold, RH (1984). "Terim termitida kollektiv em-xashakni tashkil etish Hodotermes mossambicus (Isoptera) "deb nomlangan. Xulq-atvor ekologiyasi va sotsiobiologiyasi. 14 (3): 195–202. doi:10.1007 / BF00299619. S2CID  22158321.
  46. ^ a b v d Kosta-Leonardo, AM; Haifig, I. (2010). "Isopteradagi feromonlar va ekzokrin bezlar". Vitaminlar va gormonlar. 83: 521–549. doi:10.1016 / S0083-6729 (10) 83021-3. ISBN  9780123815163. PMID  20831960.
  47. ^ a b v d Bignell, Roisin & Lo 2010, p. 7.
  48. ^ Bignell, Roisin & Lo 2010, 7-9 betlar.
  49. ^ a b v d Bignell, Roisin & Lo 2010, p. 11.
  50. ^ Robinson, Vashington (2005). Shahar hasharotlari va araxnidlar: shahar entomologiyasi bo'yicha qo'llanma. Kembrij: Kembrij universiteti matbuoti. p.291. ISBN  978-1-139-44347-0.
  51. ^ Bignell, Roisin & Lo 2010, p. 12.
  52. ^ Riparbelli, M.G; Dallai, R; Merkati, D; Bu, Y; Callaini, G (2009). "Centriole simmetriya: kichik organizmlardan katta ertak". Hujayraning harakatchanligi va sitoskelet. 66 (12): 1100–5. doi:10.1002 / sm.20417. PMID  19746415.
  53. ^ Nalepa, Kaliforniya; Lenz, M. (2000). "Ootheca Mastotermes darwiniensis Froggatt (Isoptera: Mastotermitidae): oothecae hamamböceği bilan homologiya ". Qirollik jamiyati materiallari B: Biologiya fanlari. 267 (1454): 1809–1813. doi:10.1098 / rspb.2000.1214. PMC  1690738. PMID  12233781.
  54. ^ Krosland, MWJ; Su, N.Y.; Scheffrahn, RH (2005). "Termolitlarda Arolia (Isoptera): funktsional ahamiyati va evolyutsion yo'qotilishi". Sociaux hasharotlari. 52 (1): 63–66. doi:10.1007 / s00040-004-0779-4. S2CID  26873138.
  55. ^ Bignell, Roisin & Lo 2010, p. 9.
  56. ^ Bignell, Roisin & Lo 2010, p. 10.
  57. ^ a b v Bignell, Roisin & Lo 2010, p. 13.
  58. ^ a b v d e f g "Termitlar". Avstraliya muzeyi. Olingan 8 yanvar 2015.
  59. ^ a b Machida, M .; Kitade, O .; Miura, T .; Matsumoto, T. (2001). "Yaponiyadagi nam-yog'ochli termitda proktodeal trofallaksis orqali azotni qayta ishlash Hodotermopsis japonica (Isoptera, Termopsidae) ". Sociaux hasharotlari. 48 (1): 52–56. doi:10.1007 / PL00001745. ISSN  1420-9098. S2CID  21310420.
  60. ^ Xigashi, Masaxiko; Yamamura, Norio; Abe, Takuya; Berns, Tomas P. (1991-10-22). "Nima uchun barcha termit turlari steril ishchi kastiga ega emas?". Qirollik jamiyati materiallari B: Biologiya fanlari. 246 (1315): 25–29. doi:10.1098 / rspb.1991.0120. ISSN  0962-8452. PMID  1684665. S2CID  23067349.
  61. ^ a b v Bignell, Roisin & Lo 2010, p. 18.
  62. ^ a b v d e f g h Krishna, K. "Termit". Britannica entsiklopediyasi. Olingan 11 sentyabr 2015.
  63. ^ Busvine, JR (2013). Hasharotlar va gigiena Tibbiy va maishiy ahamiyatga ega hasharotlar zararkunandalari biologiyasi va ularga qarshi kurash (3-nashr). Boston, MA: Springer AQSh. p. 545. ISBN  978-1-4899-3198-6.
  64. ^ Meek, SP (1934). Omborlarni saqlash omborida termit nazorati. Amerika mudofaaga tayyorlik assotsiatsiyasi. p. 159.
  65. ^ a b Prestvich, GD (1982). "Tetratsikllardan makrotsikllarga qadar". Tetraedr. 38 (13): 1911–1919. doi:10.1016/0040-4020(82)80040-9.
  66. ^ Prestvich, G. D. Bentli, B.L .; Duradgor, E.J. (1980). "Neotropik nasut termitlari uchun azot manbalari: fiksatsiya va selektiv em-xashak". Ekologiya. 46 (3): 397–401. Bibcode:1980 yil Oecol..46..397P. doi:10.1007 / BF00346270. ISSN  1432-1939. PMID  28310050. S2CID  6134800.
  67. ^ Torn, B. L.; Breisch, N. L.; Muscedere, M. L. (2003-10-28). "Termizitlarda evotsiallik va harbiy kastning rivojlanishi: turlararo raqobat va tezlashtirilgan merosning ta'siri". Milliy fanlar akademiyasi materiallari. 100 (22): 12808–12813. Bibcode:2003PNAS..10012808T. doi:10.1073 / pnas.2133530100. ISSN  0027-8424. PMC  240700. PMID  14555764.
  68. ^ a b v Xorvud, M.A .; Eldridge, RH (2005). Yangi Janubiy Uelsdagi termitlar 1-qism. Termit biologiyasi (PDF) (Texnik hisobot). O'rmon resurslarini o'rganish. ISSN  0155-7548. 96-38.
  69. ^ a b Keller, L. (1998). "Chumolilar va termitlarda qirolichaning yashash muddati va koloniyasining xususiyatlari". Sociaux hasharotlari. 45 (3): 235–246. doi:10.1007 / s000400050084. S2CID  24541087.
  70. ^ Srinivasan, Amia (2018 yil 10-sentyabr). "Termitlar bizga nimani o'rgatishi mumkin". Nyu-Yorker. Arxivlandi asl nusxasidan 2020 yil 7 martda.
  71. ^ Korb, J. (2008). "Termitlar, gemimetabololi diploid oq chumolilar?". Zoologiyada chegara. 5 (1): 15. doi:10.1186/1742-9994-5-15. PMC  2564920. PMID  18822181.
  72. ^ Devis, P. "Termitni aniqlash". G'arbiy Avstraliya qishloq xo'jaligi departamentidagi entomologiya. Arxivlandi asl nusxasi 2009-06-12.
  73. ^ Neoh, KB .; Li, KY (2011). "Quruq daraxt termitining etuk va boshlang'ich koloniyasining rivojlanish bosqichlari va kast tarkibi, Cryptotermes dudleyi (Isoptera: Kalotermitidae) ". Iqtisodiy entomologiya jurnali. 104 (2): 622–8. doi:10.1603 / ec10346. PMID  21510214. S2CID  23356632.
  74. ^ a b "Mahalliy er osti termitlari". Florida universiteti. Olingan 8 yanvar 2015.
  75. ^ a b Shnayder, M.F. (1999). "Termit hayot tsikli va kast tizimi". Frayburg universiteti. Olingan 8 yanvar 2015.
  76. ^ Simpson, S.J .; Qilich, G.A .; Lo, N. (2011). "Hasharotlarda polifenizm". Hozirgi biologiya. 21 (18): 738–749. doi:10.1016 / j.cub.2011.06.006. PMID  21959164. S2CID  656039.
  77. ^ a b Tasaki E, Kobayashi K, Matsuura K, Iuchi Y (2017). "Uzoq umr ko'rgan termit malikasida samarali antioksidant tizim". PLOS ONE. 12 (1): e0167412. Bibcode:2017PLoSO..1267412T. doi:10.1371 / journal.pone.0167412. PMC  5226355. PMID  28076409.
  78. ^ a b Miller, D.M. (2010 yil 5 mart). "Er osti termit biologiyasi va o'zini tutishi". Virginia Tech (Virjiniya shtati universiteti). Olingan 8 yanvar 2015.
  79. ^ a b Guj, D.X .; Smit, K.A .; Olson, C .; Beyker, P. (2001). "Drywood Termitlar". Qishloq xo'jaligi va hayot fanlari kolleji. Arizona universiteti. Olingan 16 sentyabr 2015.
  80. ^ Kaib M.; Xaker M .; Brandl, R. (2001). "Termitning bir jinsli va ko'pburchak koloniyalarida tuxum qo'yishi Macrotermes michaelseni (Isoptera, Macrotermitidae) ". Sociaux hasharotlari. 48 (3): 231–237. doi:10.1007 / PL00001771. S2CID  35656795.
  81. ^ Gilbert, ijrochi muharrirlar, G.A. Kerkut, L.I. (1985). Hasharotlarning fiziologiyasi, biokimyosi va farmakologiyasi (1-nashr). Oksford: Pergamon Press. p. 167. ISBN  978-0-08-026850-7.
  82. ^ Uayt, T. (2003). Feromonlar va hayvonlarning xulq-atvori: hid va ta'm bilan aloqa (2004 yil tuzatishlar bilan nashr. Nashr). Kembrij: Kembrij universiteti matbuoti. p.119. ISBN  978-0-521-48526-5.
  83. ^ Morrow, E.H. (2004). "Qanday qilib sperma dumini yo'qotdi: aflagellat sperma evolyutsiyasi". Kembrij falsafiy jamiyati biologik sharhlari. 79 (4): 795–814. doi:10.1017 / S1464793104006451. PMID  15682871. S2CID  25878093.
  84. ^ "Qo'shimcha reproduktiv". Gavayi universiteti. Arxivlandi asl nusxasi 2014 yil 30 oktyabrda. Olingan 16 sentyabr 2015.
  85. ^ Yashiro, T .; Matsuura, K. (2014). "Termit malikalari jinsiy aloqadan jinssiz ko'payishga o'tish uchun tuxumlarning sperma eshiklarini yopadilar". Milliy fanlar akademiyasi materiallari. 111 (48): 17212–17217. Bibcode:2014 yil PNAS..11117212Y. doi:10.1073 / pnas.1412481111. PMC  4260566. PMID  25404335.
  86. ^ Matsuura, K .; Vargo, E.L .; Kavatsu, K .; Labadie, P. E.; Nakano, H .; Yashiro, T .; Tsuji, K. (2009). "Termitlarda jinssiz ko'payish orqali malika merosxo'rligi". Ilm-fan. 323 (5922): 1687. Bibcode:2009 yil ... 323.1687M. doi:10.1126 / science.1169702. PMID  19325106. S2CID  21785886.
  87. ^ Fougeyrollas R, Dolejšova K, Sillam-Dussès D, Roy V, Poteaux C, Hanus R, Roisin Y (iyun 2015). "Embiratermes neotenicus yuqori termitida jinssiz malika merosxo'rligi". Proc. Biol. Ilmiy ish. 282 (1809): 20150260. doi:10.1098 / rspb.2015.0260. PMC  4590441. PMID  26019158.
  88. ^ Bignell, Roisin & Lo 2010, 13-14 betlar.
  89. ^ Freymann, B.P .; Buitenverf, R .; Desouza, O .; Olff (2008). "Termopitlarning (Isoptera) tropik ekotizimdagi o'txo'rlar go'ngini qayta ishlashda ahamiyati: sharh". Evropa Entomologiya jurnali. 105 (2): 165–173. doi:10.14411 / eje.2008.025.
  90. ^ de Souza, O.F .; Jigarrang, V.K. (2009). "Amazonka termit jamoalariga yashash joylari parchalanishining ta'siri". Tropik ekologiya jurnali. 10 (2): 197–206. doi:10.1017 / S0266467400007847.
  91. ^ Tokuda, G.; Vatanabe, X.; Matsumoto, T .; Noda, H. (1997). "Yog'ochni iste'mol qiladigan yuqori termitda tsellyuloza hazm qilish, Nasutitermes takasagoensis (Shiraki): sellyulozalarning tarqalishi va endo-beta-1,4-glyukanaza xususiyatlari ". Zoologiya fanlari. 14 (1): 83–93. doi:10.2108 / zsj.14.83. PMID  9200983. S2CID  2877588.
  92. ^ Ritter, Maykl (2006). Jismoniy muhit: jismoniy geografiyaga kirish. Viskonsin universiteti. p. 450. Arxivlangan asl nusxasi 2007 yil 18 mayda.
  93. ^ Ikeda-Otsubo, V.; Brune, A. (2009). "Termit ichaklaridagi flagellates va ularning bakterial endosimbiontslarining kospitsiyasi: Trikonimfa turlari va Nomzod Endomikrobium trichonymphae "deb nomlangan. Molekulyar ekologiya. 18 (2): 332–342. doi:10.1111 / j.1365-294X.2008.04029.x. PMID  19192183. S2CID  28048145.
  94. ^ Slaytor, M. (1992). "Termitlar va hamamböceği ichida tsellyuloza hazm qilish: simbiontlar qanday rol o'ynaydi?". Qiyosiy biokimyo va fiziologiya B. 103 (4): 775–784. doi:10.1016 / 0305-0491 (92) 90194-V.
  95. ^ "Termit ichak va uning simbiyotik mikroblari". iBiologiya. Olingan 2020-05-16.
  96. ^ Vatanabe, H ..; Noda, H.; Tokuda, G.; Lo, N. (1998). "Termit kelib chiqishi tsellyuloza geni". Tabiat. 394 (6691): 330–331. Bibcode:1998 yil natur.394..330W. doi:10.1038/28527. PMID  9690469. S2CID  4384555.
  97. ^ Tokuda, G.; Vatanabe, H. (2007). "Termitlarda yashirin tsellyulozalar: eski gipotezani qayta ko'rib chiqish". Biologiya xatlari. 3 (3): 336–339. doi:10.1098 / rsbl.2007.0073. PMC  2464699. PMID  17374589.
  98. ^ Li, Z.-Q .; Liu, B.-R .; Zeng, V.-H.; Xiao, W.-L .; Li, Q.-J .; Zhong, J.-H. (2013). "Oziqlanish odatlari har xil bo'lgan flagellatsiz termitlar ichaklarida selülaza faolligining xususiyati". Hasharotlarga oid jurnal. 13 (37): 37. doi:10.1673/031.013.3701. PMC  3738099. PMID  23895662.
  99. ^ "Termit ichak va uning simbiyotik mikroblari". iBiologiya. Olingan 2020-05-16.
  100. ^ Geetha Iyer Scroll.in (2017 yil 09-mart) Nega hindular juda yomon ko'rilgan termit tepasiga sig'inishadi "[Askar termitlari] va reproduktiv kastlar o'zlarining ozuqaviy moddalarini ishchilardan og'iz yoki anal trofallaksis orqali oladi.
  101. ^ Ditrix, C .; Koller T .; Brune, A. (2014). "Termit ichak mikrobiotasining hamamböceği kelib chiqishi: bakteriyalar birlashmasi tarkibidagi naqshlar asosiy evolyutsion voqealarni aks ettiradi". Amaliy va atrof-muhit mikrobiologiyasi. 80 (7): 2261–2269. doi:10.1128 / AEM.04206-13. PMC  3993134. PMID  24487532.
  102. ^ Allen, CT .; Foster, D.E .; Ueckert, D.N. (1980). "Cho'l termitining mavsumiy ovqatlanish odatlari, Gnathamitermes tubiformans, G'arbiy Texasda ". Atrof-muhit entomologiyasi. 9 (4): 461–466. doi:10.1093 / ee / 9.4.461.
  103. ^ McMahan, E.A. (1966). "Yog'ochni termit bilan oziqlantirish bo'yicha termitlarni o'rganish" (PDF). Gavayi entomologik jamiyati. 19 (2): 239–250. ISSN  0073-134X.
  104. ^ Aanen, D.K .; Eggleton, P.; Rouland-Lefevre, S.; Guldberg-Froslev, T.; Rozendahl, S .; Boomsma, J.J. (2002). "Qo'ziqorin o'sadigan termitlar evolyutsiyasi va ularning mutualist qo'ziqorin simbiontlari". Milliy fanlar akademiyasi materiallari. 99 (23): 14887–14892. Bibcode:2002 yil PNAS ... 9914887A. doi:10.1073 / pnas.222313099. JSTOR  3073687. PMC  137514. PMID  12386341.
  105. ^ Myuller, U.G .; Jerardo, N. (2002). "Qo'ziqorinlarni etishtirish hasharotlari: ko'p kelib chiqishi va turli xil evolyutsion tarixlari". Milliy fanlar akademiyasi materiallari. 99 (24): 15247–15249. Bibcode:2002 yil PNAS ... 9915247M. doi:10.1073 / pnas.242594799. PMC  137700. PMID  12438688.
  106. ^ Roberts, EM; Todd, CN .; Aanen, D.K .; Nobre, T .; Xilbert-Volf, H.L.; O'Konnor, PM; Tapanila, L .; Mtelela, S.; Stivens, NJ (2016). "Tanzaniya, Rukva Rift havzasidagi in situ qo'ziqorin bog'lari bo'lgan oligotsen termit uyalari hasharotlar qishloq xo'jaligi uchun Afrikadan kelib chiqqan paleogenni qo'llab-quvvatlaydi". PLOS ONE. 11 (6): e0156847. Bibcode:2016PLoSO..1156847R. doi:10.1371 / journal.pone.0156847. PMC  4917219. PMID  27333288.
  107. ^ Radek, R. (1999). "Termitlar bilan bog'liq bo'lgan flagellates, bakteriyalar va zamburug'lar: xilma-xilligi va ovqatlanishdagi funktsiyasi - sharh" (PDF). Ekotropika. 5: 183–196.
  108. ^ Breznak, J.A .; Brune, A. (1993). "Lignosellulozani termitlar tomonidan hazm qilishda mikroorganizmlarning roli". Entomologiyaning yillik sharhi. 39 (1): 453–487. doi:10.1146 / annurev.en.39.010194.002321.
  109. ^ Kok, O.B .; Xevitt, PH. (1990). "Terim termitining qushlar va sutemizuvchilar yirtqichlari Hodotermes mossambicus (Xagen) Janubiy Afrikaning yarim quruq mintaqalarida ». Janubiy Afrika jurnali. 86 (1): 34–37. ISSN  0038-2353.
  110. ^ a b v d e Xölldobler, B .; Uilson, E.O. (1990). Chumolilar. Kembrij, Massachusets: Garvard universiteti matbuotining Belknap matbuoti. pp.559–566. ISBN  978-0-674-04075-5.
  111. ^ a b Kullini, TW; Greys, J.K. (2000). "Er osti termitlarini biologik nazorat qilish istiqbollari (Isoptera: Rhinotermitidae) Koptotermalar formosanus". Entomologik tadqiqotlar byulleteni. 90 (1): 9–21. doi:10.1017 / S0007485300000663. PMID  10948359.
  112. ^ Din, W.R.J .; Milton, S.J. (1995). "Janubiy Afrikaning qurg'oqchil janubidagi Karuudagi eski dalalardagi o'simlik va umurtqasizlar yig'indisi". Afrika ekologiya jurnali. 33 (1): 1–13. doi:10.1111 / j.1365-2028.1995.tb00777.x.
  113. ^ Veyd, VW. (2002). Cho'l tizimlari ekologiyasi. Burlington: Elsevier. p. 216. ISBN  978-0-08-050499-5.
  114. ^ Reygan, D.P.; Waide, RB (1996). Tropik yomg'ir o'rmonining oziq-ovqat tarmog'i. Chikago: Chikago universiteti matbuoti. p.294. ISBN  978-0-226-70599-6.
  115. ^ a b Bardgett, R.D .; Herrick, J.E .; Olti, J .; Jons, TX .; Kuchli, D.R .; van der Putten, W.H. (2013). Tuproq ekologiyasi va ekotizim xizmatlari (1-nashr). Oksford: Oksford universiteti matbuoti. p. 178. ISBN  978-0-19-968816-6.
  116. ^ Bignell, Roisin & Lo 2010, p. 509.
  117. ^ Cho, JC.; Krespi, BJ (1997). Hasharotlar va araxnidlarda ijtimoiy xulq-atvorning rivojlanishi (1-nashr). Kembrij: Kembrij universiteti matbuoti. p.76. ISBN  978-0-521-58977-2.
  118. ^ a b v Abe, Y .; Bignell, D.E .; Higashi, T. (2014). Termitlar: evolyutsiya, ijtimoiylik, simbiozlar, ekologiya. Springer. 124–149 betlar. doi:10.1007/978-94-017-3223-9. ISBN  978-94-017-3223-9. S2CID  30804981.
  119. ^ Uilson, D.S .; Klark, AB (1977). "Terim termitida quruqlikdan yuqori himoya, Hodotermes mossambicus". Janubiy Afrikaning entomologik jamiyati jurnali. 40: 271–282.
  120. ^ Lavelle, P .; Ispaniya, A.V. (2001). Tuproq ekologiyasi (2-nashr). Dordrext: Kluwer Academic. p.316. ISBN  978-0-306-48162-8.
  121. ^ Richardson, P.K.R .; Soqolchi, S.K. (1984). "Hyena oilasi". Makdonaldda D. (tahr.) Sutemizuvchilar entsiklopediyasi. Nyu-York, NY: Fayllarni nashr qilish to'g'risidagi faktlar. pp.158–159. ISBN  978-0-87196-871-5.
  122. ^ Mills, G.; Harvey, M. (2001). Afrika yirtqichlari. Vashington, Kolumbiya: Smithsonian Institution Press. p. 71. ISBN  978-1-56098-096-4.
  123. ^ d'Erriko, F.; Backwell, L. (2009). "Erta gominin suyagi vositalarining ishlashini baholash". Arxeologiya fanlari jurnali. 36 (8): 1764–1773. doi:10.1016 / j.jas.2009.04.005.
  124. ^ Lepage, M.G. (1981). "Étude de la prédation de Megaponera oyoq osti qiladi (F.) sur les population récoltantes de Macrotermitinae dans un ecosystème half-aride (Kajiado-Kenya) ". Sociaux hasharotlari (ispan tilida). 28 (3): 247–262. doi:10.1007 / BF02223627. S2CID  28763771.
  125. ^ Levieux, J. (1966). "Note préliminaire sur les colonnes de chasse de Megaponera faollashadi F. (Hyménoptère Formicidæ) ". Sociaux hasharotlari (frantsuz tilida). 13 (2): 117–126. doi:10.1007 / BF02223567. S2CID  2031222.
  126. ^ Longxurst, S .; Beyker, R .; Xau, P.E. (1979). "Yirtqich chumolilarda kimyoviy kripsis". Experientia. 35 (7): 870–872. doi:10.1007 / BF01955119. S2CID  39854106.
  127. ^ a b Uiler, V.M. (1936). "Ponerin va boshqa chumolilarning termitlarga bo'lgan ekologik munosabatlari". Amerika San'at va Fanlar Akademiyasi materiallari. 71 (3): 159–171. doi:10.2307/20023221. JSTOR  20023221.
  128. ^ Shattak, S.O .; Xeterik, B.E. (2011). "Chumolilar turini qayta ko'rib chiqish Iridomirmex (Hymenoptera: Formicidae) " (PDF). Zootaxa. 2845: 1–74. doi:10.11646 / zootaxa.2743.1.1. ISBN  978-1-86977-676-3. ISSN  1175-5334.
  129. ^ Traniello, J.F.A. (1981). "Termitni yollash strategiyasida dushmanni to'xtatish: askarlar tomonidan uyushtirilgan em-xashak Nasutitermes costalis". Milliy fanlar akademiyasi materiallari. 78 (3): 1976–1979. Bibcode:1981PNAS ... 78.1976T. doi:10.1073 / pnas.78.3.1976. PMC  319259. PMID  16592995.
  130. ^ Shöning, C .; Moffett, MW (2007). "Termit uyasiga bostirib kiradigan haydovchi chumolilar: nega eng katolik yirtqichlar kamdan-kam hollarda bu mo'l-ko'l o'ljani olishadi?" (PDF). Biotropika. 39 (5): 663–667. doi:10.1111 / j.1744-7429.2007.00296.x.
  131. ^ Mill, AE (1983). "Braziliyalik termit alate to'dalari va reproduktiv moddalarning tarqalishida ishlatiladigan ba'zi tuzilmalar (Isoptera: Termitidae) bo'yicha kuzatuvlar". Tabiiy tarix jurnali. 17 (3): 309–320. doi:10.1080/00222938300770231.
  132. ^ Schmid-Gempel 1998 yil, p. 61.
  133. ^ Schmid-Gempel 1998 yil, p. 75.
  134. ^ Uilson, E.O. (1971). Hasharotlar jamiyatlari. 76 (5-nashr). Kembrij, Massachusets: Garvard universiteti matbuotining Belknap matbuoti. p. 398. ISBN  978-0-674-45495-8.
  135. ^ Schmid-Gempel 1998 yil, p. 59.
  136. ^ Schmid-Gempel 1998 yil, 301-302 betlar.
  137. ^ Schmid-Gempel 1998 yil, p. 19.
  138. ^ Vayzer, J .; Xrdi, I. (2009). "Pyemotes - oqadilar termitlarning parazitlari sifatida". Zeitschrift für Angewandte Entomologie. 51 (1–4): 94–97. doi:10.1111 / j.1439-0418.1962.tb04062.x.
  139. ^ Xovven, T .; Efstation, Kaliforniya; Elliott, M.L .; Su, NY (2012). "Er osti termitlarida ikkita qo'ziqorin paraziti o'rtasida resurslar raqobati". Naturwissenschaften vafot etdi. 99 (11): 949–58. Bibcode:2012NW ..... 99..949C. doi:10.1007 / s00114-012-0977-2. PMID  23086391. S2CID  16393629.
  140. ^ Schmid-Gempel 1998 yil, 38, 102-betlar.
  141. ^ Xovven, T .; Mullins, A.J .; Efstation, Kaliforniya; Su, N.-Y. (2013). "Termitdagi virusga o'xshash alomatlar (Isoptera: Kalotermitidae) dala koloniyasida". Florida entomologi. 96 (4): 1612–1614. doi:10.1653/024.096.0450. S2CID  73570814.
  142. ^ Al Fazairi, A.A .; Hassan, FA (2011). "Termitlarni yuqtirish Spodoptera littoralis Yadro polihedroz virusi ". Xalqaro tropik hasharotlar jurnali. 9 (1): 37–39. doi:10.1017 / S1742758400009991. S2CID  84743428.
  143. ^ Traniello, J.F.A.; Leuthold, RH (2000). Termitlarda yem-xashak va ekologiya. Springer Niderlandiya. 141–168 betlar. doi:10.1007/978-94-017-3223-9_7. ISBN  978-94-017-3223-9.
  144. ^ Reynxard, J .; Kaib, M. (2001). "Er osti termitida em-xashak va yollash paytida iz aloqasi Retikulitermes santonensis De Feytaud (Isoptera, Rhinotermitidae) ". Hasharotlarning o'zini tutish jurnali. 14 (2): 157–171. doi:10.1023 / A: 1007881510237. S2CID  40887791.
  145. ^ a b v d e f g h men j Kosta-Leonardo, AM; Haifig, I. (2013). Turli xil xatti-harakatlar paytida termit aloqasi Hayvonlarning biokommunikatsiyasi. Springer Niderlandiya. 161-190 betlar. doi:10.1007/978-94-007-7414-8_10. ISBN  978-94-007-7413-1.
  146. ^ Kosta-Leonardo, A.M. (2006). "Ishchilarda ko'krak bezi morfologiyasi Coptotermes gestroi (Isoptera, Rhinotermitidae) ". Mikron. 37 (6): 551–556. doi:10.1016 / j.micron.2005.12.006. PMID  16458523.
  147. ^ Traniello, J.F .; Busher, C. (1985). "Neotropik termitda em-xashak paytida polietizmni kimyoviy tartibga solish Nasutitermes costalis". Kimyoviy ekologiya jurnali. 11 (3): 319–32. doi:10.1007 / BF01411418. PMID  24309963. S2CID  27799126.
  148. ^ Miramontes, O .; DeSouza, O .; Paiva, L.R .; Marins, A .; Orozko, S .; Aegerter, CM (2014). "Levi parvozlari va termit ishchilarining o'ziga o'xshash kashfiyotchi xatti-harakatlari: modelga mos kelmaslikdan tashqari". PLOS ONE. 9 (10): e111183. arXiv:1410.0930. Bibcode:2014PLoSO ... 9k1183M. doi:10.1371 / journal.pone.0111183. PMC  4213025. PMID  25353958.
  149. ^ Jost, C .; Xayfig, I .; de Kamargo-Ditrix, KR.; Kosta-Leonardo, A.M. (2012). "Termitlarda turlararo raqobat ta'sirini baholash uchun taqqoslanadigan tunnel tarmog'i yondashuvi". Sociaux hasharotlari. 59 (3): 369–379. doi:10.1007 / s00040-012-0229-7. S2CID  14885485.
  150. ^ Polizzi, JM .; Forschler, B.T. (1998). "Ichki va turlararo agonizm Retikulitermalar lazzatlanishlar (Kollar) va R. virginicus (Banklar) va arenaning ta'siri va laboratoriya tahlillarida guruh kattaligi ". Sociaux hasharotlari. 45 (1): 43–49. doi:10.1007 / s000400050067. S2CID  36235510.
  151. ^ Darlington, J.P.E.C. (1982). "Termit uyasi bilan oziqlantirishda ishlatiladigan er osti yo'llari va saqlash quduqlari Macrotermes michaelseni Kajiadoda, Keniya ". Zoologiya jurnali. 198 (2): 237–247. doi:10.1111 / j.1469-7998.1982.tb02073.x.
  152. ^ Kornelius, M.L .; Osbrink, W.L. (2010). "Tuproq turi va namlik mavjudligining Formosan er osti termitining (Isoptera: Rhinotermitidae) em-xashak harakatlariga ta'siri". Iqtisodiy entomologiya jurnali. 103 (3): 799–807. doi:10.1603 / EC09250. PMID  20568626. S2CID  23173060.
  153. ^ Toledo Lima, J .; Kosta-Leonardo, A.M. (2012). "Er osti termitlari (Isoptera: Rhinotermitidae): Turli xil joylashish shakllari bilan ekvivalent oziq-ovqat resurslaridan foydalanish". Hasharotlarga oid fan. 19 (3): 412–418. doi:10.1111 / j.1744-7917.2011.01453.x. S2CID  82046133.
  154. ^ Jmxasli, P.; Leuthold, RH (1999). "Termitlar ichidagi koloniyani tanib olish Makrotermes subhyalinus va Makrotermes bellicosus (Isoptera, Termitidae) ". Sociaux hasharotlari. 46 (2): 164–170. doi:10.1007 / s000400050128. S2CID  23037986.
  155. ^ Messenger, M.T .; Su, NY (2005). "Louis Armstrong Park, Luiziana shtatining Yangi Orlean shahridan Formosan er osti termit (Isoptera: Rhinotermitidae) koloniyalari o'rtasidagi agonistik xatti-harakatlar". Sotsiobiologiya. 45 (2): 331–345.
  156. ^ Korb, J .; Vayl, T .; Hoffmann, K .; Foster, K.R .; Rehli, M. (2009). "Termitlarda reproduktiv bostirish uchun zarur bo'lgan gen". Ilm-fan. 324 (5928): 758. Bibcode:2009Sci ... 324..758K. doi:10.1126 / science.1170660. PMID  19423819. S2CID  31608071.
  157. ^ a b v Metyu, T.T.G .; Rays, R .; DeSouza, O .; Ribeyro, SP (2005). "Chumolilar (Hymenoptera: Formicidae) va daraxt daraxtlari (Isoptera: Termitidae) o'rtasidagi yirtqichlik va aralashuv raqobati" (PDF). Sotsiobiologiya. 46 (2): 409–419.
  158. ^ Evans, T.A .; Inta, R .; Lay, JC.S .; Lenz, M. (2007). "Oziq-ovqat tebranish signallari em-xashaklarni jalb qiladi va quruq daraxt termitidagi oziq-ovqat hajmini aniqlaydi Kriptotermalar sekundusi". Sociaux hasharotlari. 54 (4): 374–382. doi:10.1007 / s00040-007-0958-1. S2CID  40214049.
  159. ^ Kosta-Leonardo, AM; Kasarin, F.E .; Lima, J.T. (2009). "Isopterada kimyoviy aloqa". Neotropik entomologiya. 38 (1): 747–52. doi:10.1590 / S1519-566X2009000100001. PMID  19347093.
  160. ^ Richard, F.-J .; Xant, J.X. (2013). "Ijtimoiy hasharotlarda intrakolonik kimyoviy aloqa" (PDF). Sociaux hasharotlari. 60 (3): 275–291. doi:10.1007 / s00040-013-0306-6. S2CID  8108234.
  161. ^ Dronnet, S .; Lohou, C .; Christides, J.P .; Bagnères, AG (2006). "Kutikulyar uglevodorod tarkibi kiritilgan termit koloniyalari o'rtasidagi genetik munosabatni aks ettiradi Retikulitermes santonensis Feytaud "deb nomlangan. Kimyoviy ekologiya jurnali. 32 (5): 1027–1042. doi:10.1007 / s10886-006-9043-x. PMID  16739021. S2CID  23956394.
  162. ^ Rozengaus, RB .; Traniello, J.F.A.; Chen, T .; Braun, JJ .; Karp, RD (1999). "Ijtimoiy hasharotlarda immunitet". Naturwissenschaften. 86 (12): 588–591. Bibcode:1999NW ..... 86..588R. doi:10.1007 / s001140050679. S2CID  10769345.
  163. ^ Wilson, DS (1977). "Terim termitida yer usti yirtqichlardan himoya qilish, Hodotermes mossambicus (Xagen) "deb nomlangan. Janubiy Afrikaning entomologik jamiyati jurnali. 40: 271–282.
  164. ^ Belbin, R.M. (2013). Tashkilotning kelgusi shakli. Nyu-York: Routledge. p. 27. ISBN  978-1-136-01553-3.
  165. ^ a b Uilson, E.O. (2014). Abadiyat oynasi: biologning Gorongosa milliy bog'i bo'ylab yurishi (Birinchi nashr). Simon va Shuster. 85, 90-betlar. ISBN  978-1-4767-4741-5.
  166. ^ Miura, T .; Matsumoto, T. (2000). "Nasut termitida askar morfogenezi: askar nasusini hosil qiladigan diskka o'xshash tuzilmani kashf etish". Qirollik jamiyati materiallari B: Biologiya fanlari. 267 (1449): 1185–1189. doi:10.1098 / rspb.2000.1127. PMC  1690655. PMID  10902684.
  167. ^ Prestvich, G.D .; Chen, D. (1981). "Askarlarning mudofaa sirlari Trinervitermes bettonianus (Isoptera, Nasutitermitinae): Allopatrik populyatsiyalarning kimyoviy o'zgarishi ". Kimyoviy ekologiya jurnali. 7 (1): 147–157. doi:10.1007 / BF00988642. PMID  24420434. S2CID  27654745.
  168. ^ Chen, J .; Xenderson, G.; Grimm, S C.; Lloyd, S. V.; Laine, R. A. (1998-04-09). "Termitlar uyalarini naftalin bilan fumigatsiya qilishadi". Tabiat. 392 (6676): 558–559. Bibcode:1998 yil Natur.392..558C. doi:10.1038/33305. S2CID  4419882.
  169. ^ Piper, Ross (2007), Favqulodda hayvonlar: qiziquvchan va g'ayrioddiy hayvonlar entsiklopediyasi, Greenwood Press, p. 26, ISBN  978-0-313-33922-6
  170. ^ Bordere, C .; Robert, A .; Van Tuyen, V .; Peppuy, A. (1997). "O'z joniga qasd qilishning mudofaa xatti-harakatlari Globitermes sulphureus Haviland askarlari (Isoptera) ". Sociaux hasharotlari. 44 (3): 289–297. doi:10.1007 / s000400050049. S2CID  19770804.
  171. ^ Sobotnik, J .; Burginon, T .; Xanus, R .; Demianova, Z .; Pytelkova, J .; Mares, M .; Foltinova, P.; Preisler, J .; Kvakka, J .; Krasulova, J .; Roisin, Y. (2012). "Eski termit ishchilarida portlovchi ryukzaklar". Ilm-fan. 337 (6093): 436. Bibcode:2012Sci ... 337..436S. doi:10.1126 / science.1219129. PMID  22837520. S2CID  206540025.
  172. ^ ŠobotnÍk, J.; Burginon, T .; Xanus, R .; Veyda, F.; Roisin, Y. (2010). "Askarlarda mudofaa bezlarining tuzilishi va funktsiyasi Glossotermes oculatus (Isoptera: Serritermitidae) ". Linnean Jamiyatining Biologik jurnali. 99 (4): 839–848. doi:10.1111 / j.1095-8312.2010.01392.x.
  173. ^ Ulyshen, MD; Shelton, T.G. (2011). "Termit jasadga javob berish xatti-harakatlaridagi signal sinergizmining dalillari". Naturwissenschaften. 99 (2): 89–93. Bibcode:2012NW ..... 99 ... 89U. doi:10.1007 / s00114-011-0871-3. PMID  22167071. S2CID  2616753.
  174. ^ Su, NY (2005). "Formosan er osti termitlarining (Isoptera: Rhinotermitidae) o'lja yoki qayta tiklanmaydigan termititsidlarga kengaytirilgan em-xashak maydonlarida ta'siri". Iqtisodiy entomologiya jurnali. 98 (6): 2143–2152. doi:10.1603/0022-0493-98.6.2143. PMID  16539144. S2CID  196618597.
  175. ^ Quyosh, Q .; Xeyns, K.F .; Chjou, X. (2013). "Tug'ma va o'ziga xos jasadlarga pastki termitning differentsial javobgarligi". Ilmiy ma'ruzalar. 3: 1650. Bibcode:2013 yil NatSR ... 3E1650S. doi:10.1038 / srep01650. PMC  3629736. PMID  23598990.
  176. ^ a b Neoh, K.-B .; Yeap, B.-K .; Tsunoda, K .; Yoshimura, T .; Li, CY .; Korb, J. (2012). "Termitlar tana go'shtidan qochadimi? Xulq-atvori javoblari tana go'shti tabiatiga bog'liq". PLOS ONE. 7 (4): e36375. Bibcode:2012PLoSO ... 736375N. doi:10.1371 / journal.pone.0036375. PMC  3338677. PMID  22558452.
  177. ^ Matsuura, K. (2006). "Sklerotiy hosil qiluvchi qo'ziqorin tomonidan termit-tuxum taqlid qilish". Qirollik jamiyati materiallari B: Biologiya fanlari. 273 (1591): 1203–1209. doi:10.1098 / rspb.2005.3434. PMC  1560272. PMID  16720392.
  178. ^ Matsuura, K .; Yashiro, T .; Shimizu, K .; Tatsumi, S .; Tamura, T. (2009). "Kuku zamburug'i tsellyuloza hazm qiladigan ferment b-glyukozidaza ishlab chiqarish orqali termit tuxumlarini taqlid qiladi". Hozirgi biologiya. 19 (1): 30–36. doi:10.1016 / j.cub.2008.11.030. PMID  19110429. S2CID  18604426.
  179. ^ Xovard, R.V .; McDaniel, C.A .; Blomquist, G.J. (1980). "Integral mexanizm sifatida kimyoviy mimika: termitofilning katikulyar uglevodorodlari va uning egasi". Ilm-fan. 210 (4468): 431–433. Bibcode:1980Sci ... 210..431H. doi:10.1126 / science.210.4468.431. PMID  17837424. S2CID  33221252.
  180. ^ Uotson, J.A.L. (1973). "Austrospirachtha mimetes Shimoliy Avstraliyadan yangi termitofil korototsin (Coleoptera: Staphylinidae) ". Avstraliya Entomologiya jurnali. 12 (4): 307–310. doi:10.1111 / j.1440-6055.1973.tb01678.x.
  181. ^ Forbes, H.O. (1878). "Termitlar chumolilar asirligida saqlanmoqda". Tabiat. 19 (471): 4–5. Bibcode:1878Natur..19 .... 4F. doi:10.1038 / 019004b0. S2CID  4125839. (obuna kerak)
  182. ^ Darlington, J. (1985). "Doryline chumolilar va termit uyalarini himoya qilish hujumlari (Hymenoptera; Formicidae; Isoptera; Termitidae)". Sotsiobiologiya. 11: 189–200.
  183. ^ Quinet Y, Tekule N & de Biseau JC (2005). "O'zaro munosabatlarning o'zaro ta'siri Crematogaster brevispinosa rochai Forel (Hymenoptera: Formicidae) va nasutitermesning ikki turi (Isoptera: Termitidae) ". Hasharotlarning o'zini tutish jurnali. 18 (1): 1–17. doi:10.1007 / s10905-005-9343-y. S2CID  33487814.
  184. ^ Koti, D.; Ariya, C .; Garroust, R .; Uils, P .; Legendre, F .; Nel, A .; Korb, J. (2014). "Taphonomiyani KT-tahlil qilish bilan amberdagi birinchi antitermit sinkinizatsiyasi". PLOS ONE. 9 (8): e104410. Bibcode:2014PLoSO ... 9j4410C. doi:10.1371 / journal.pone.0104410. PMC  4139309. PMID  25140873.
  185. ^ a b Santos, P.P.; Vaskoncellos, A .; Jaxini, B .; Delabie, J.H.C. (2010). "Nasutitermes spp daraxt daraxtlari uyalariga bog'langan chumoli faunasi (Hymenoptera, Formicidae): Braziliyaning Bahia janubi-sharqidagi kakao plantatsiyasida (Isoptera, Termitidae)". Revista Brasileira de Entomologia. 54 (3): 450–454. doi:10.1590 / S0085-56262010000300016.
  186. ^ Jaffe, K .; Ramos, C .; Issa, S. (1995). "Umumiy uyalarni taqsimlovchi chumolilar va termitlar o'rtasidagi trofik ta'sirlar". Amerika entomologik jamiyati yilnomalari. 88 (3): 328–333. doi:10.1093 / aesa / 88.3.328.
  187. ^ Trager, JC (1991). "Yong'in chumolilarini qayta ko'rib chiqish, Solenopsis geminata guruh (Hymenoptera: Formicidae: Myrmicinae) ". Nyu-York Entomologik Jamiyati jurnali. 99 (2): 141–198. doi:10.5281 / zenodo.24912. JSTOR  25009890.
  188. ^ a b Cingel, N.A. van der (2001). Orkide changlanishining atlasi: Amerika, Afrika, Osiyo va Avstraliya. Rotterdam: Balkema. p. 224. ISBN  978-90-5410-486-5.
  189. ^ McHatton, R. (2011). "Orkide changlanishi: ajoyib dunyoni o'rganish" (PDF). Amerika orkide jamiyati. p. 344. Olingan 5 sentyabr 2015.
  190. ^ Cowie, R. (2014). Afrikadagi biologga palapartishlikdan sayohat. Raleigh, Shimoliy Karolina: Lulu Press. p. 169. ISBN  978-1-304-66939-1.
  191. ^ a b Tan, K.H. (2009). Ekologik tuproqshunoslik (3-nashr). Boka Raton, Florida: CRC Press. 105-106 betlar. ISBN  978-1-4398-9501-6.
  192. ^ a b Klark, Sara (2005 yil 15-noyabr). "O'simlik ekstrakti termitlarning o'lishini to'xtatadi". ABC. Arxivlandi asl nusxasi 2009 yil 15-iyunda. Olingan 8 fevral 2014.
  193. ^ Vaskonsellos, Aleksandr; Bandeyra, Adelmar G.; Moura, Flaviya Mariya S.; Araujo, Virginiya Farias P.; Gusmão, Mariya Avani B.; Reginaldo, Constantino (2010 yil fevral). "Braziliya shimoli-sharqidagi yarim quruq Kaatingada turli xil bezovtalik rejimlarida uchta yashash joyidagi termit yig'ilishlari". Arid Environments jurnali. Elsevier. 74 (2): 298–302. Bibcode:2010JArEn..74..298V. doi:10.1016 / j.jaridenv.2009.07.007. ISSN  0140-1963.
  194. ^ Bignell, Roisin & Lo 2010, p. 3.
  195. ^ a b Noirot, C .; Darlington, J.P.E.C. (2000). Termit uyalari: me'morchilik, tartibga solish va mudofaa Termitlarda: evolyutsiya, ijtimoiylik, simbiozlar, ekologiya. Springer. 121-139 betlar. doi:10.1007/978-94-017-3223-9_6. ISBN  978-94-017-3223-9.
  196. ^ Bignell, Roisin & Lo 2010, p. 20.
  197. ^ a b Eggleton, P.; Bignell, D.E .; Sands, V.A .; Moddsli, N. A .; Lauton, J. X .; Vud, T.G .; Bignell, NC (1996). "Janubiy Kamerun, Mbalmayo o'rmon qo'riqxonasida turli darajadagi bezovtalik darajasidagi termitlarning xilma-xilligi, mo'lligi va biomassasi". Qirollik jamiyatining falsafiy operatsiyalari B: Biologiya fanlari. 351 (1335): 51–68. Bibcode:1996RSPTB.351 ... 51E. doi:10.1098 / rstb.1996.0004.
  198. ^ a b v d e Bignell, Roisin & Lo 2010, p. 21.
  199. ^ De Visse, S.N .; Freymann, B.P .; Schnyder, H. (2008). "Afrika savanasida termitariyadagi umurtqasizlar o'rtasidagi trofik o'zaro ta'sir: barqaror izotop yondoshuvi". Ekologik entomologiya. 33 (6): 758–764. doi:10.1111 / j.1365-2311.2008.01029.x. S2CID  33877331.
  200. ^ a b v Bignell, Roisin & Lo 2010, p. 22.
  201. ^ Veyn, KX.; Kim, A.W.; Moss-Xeys, V .; Sneyp, CE .; Diaz, M.C .; Xon, N.S .; Engelxart, S.E .; Xorton, B.P. (2013). "Mangrov to'qimalarining daraxtli termitlar bilan parchalanishi (Nasutitermes acajutlae) va ularning mangrov C tsiklidagi roli (Puerto-Riko): Kimyoviy tavsif va organik moddalarning aniqligi -13C, C / N, ishqoriy CuO oksidlanish-GC / MS va qattiq holat yordamida " (PDF). Geokimyo, geofizika, geosistemalar. 14 (8): 3176–3191. Bibcode:2013GGG .... 14.3176V. doi:10.1002 / ggge.20194 yil.
  202. ^ a b Royzin, Y .; Pasteels, J. M. (1986). "Termitlarda ko'payish mexanizmlari: polikalizm va ko'pburchak Nasutitermes polygynus va N. costalis". Sociaux hasharotlari. 33 (2): 149–167. doi:10.1007 / BF02224595. S2CID  41799894.
  203. ^ Perna, A .; Jost, C .; Kutyure, E .; Valverde, S .; Douady, S .; Theraulaz, G. (2008). "Termit uyalaridagi galereya tarmoqlarining tuzilishi Kubitermlar spp. rentgen tomografiyasi bilan aniqlandi ". Naturwissenschaften vafot etdi. 95 (9): 877–884. Bibcode:2008NW ..... 95..877P. doi:10.1007 / s00114-008-0388-6. PMID  18493731. S2CID  15326313.
  204. ^ Glenday, Kreyg (2014). Ginnesning rekordlar kitobi-2014. pp.33. ISBN  978-1-908843-15-9.
  205. ^ Jeklin, P. (1991). "Yo'nalishdagi moslashuvchan o'zgarishga dalillar Amitermalar (Isoptera, Termitinae) Shimoliy Avstraliyadan kelgan höyükler ". Avstraliya Zoologiya jurnali. 39 (5): 569. doi:10.1071 / ZO9910569.
  206. ^ Jeklin, PM; Munro, U. (2002). "Termit tomonidan höyüğün qurilishida magnit signallardan foydalanishga oid dalillar Amitermes meridionalis (Isoptera: Termitinae) ". Avstraliya Zoologiya jurnali. 50 (4): 357. doi:10.1071 / ZO01061.
  207. ^ Grigg, G.C. (1973). "Magnit" termit höyüğünün shakllanishi va yo'nalishining ba'zi oqibatlari " (PDF). Avstraliya Zoologiya jurnali. 21 (2): 231–237. doi:10.1071 / ZO9730231.
  208. ^ a b Hadlington, P. (1996). Avstraliya termitlari va boshqa keng tarqalgan yog'och zararkunandalari (2-nashr). Kensington, NSW, Avstraliya: Yangi Janubiy Uels universiteti matbuoti. 28-30 betlar. ISBN  978-0-86840-399-1.
  209. ^ a b Kan, L .; Easton, B. (2010). II boshpana. Bolinas, Kaliforniya: Boshpana nashrlari. p. 198. ISBN  978-0-936070-49-0.
  210. ^ a b v d e f g h Su, N.Y .; Scheffrahn, RH (2000). Termitlar binolarning zararkunandalari sifatida Termitlarda: evolyutsiya, ijtimoiylik, simbiozlar, ekologiya. Springer Niderlandiya. 437-453 betlar. doi:10.1007/978-94-017-3223-9_20. ISBN  978-94-017-3223-9.
  211. ^ Torn, PhD, Barbara L. (1999). NPMA tadqiqotlari Er osti termitlari to'g'risida. Dann Loring, VA: NPMA. p. 22.
  212. ^ "Termitlar". Viktoriya qurilish boshqarmasi. Viktoriya hukumati. 2014 yil. Olingan 20 sentyabr 2015.
  213. ^ Torn, PhD, Barbara L. (1999). NPMA tadqiqotlari Er osti termitlari to'g'risida. Dann Loring, VA: NPMA. p. 2018-04-02 121 2.
  214. ^ Greys, J.K .; Kutten, G.M .; Sheffrahn, RH; Makekevan, D.K. (1991). "Birinchi hujum Kichkina odam kanadalik bino (Isoptera: Kalotermitidae) ". Sotsiobiologiya. 18: 299–304.
  215. ^ a b Sands, VA (1973). "Termitlar tropik oziq-ovqat ekinlari zararkunandalari sifatida". Tropik zararkunandalarga qarshi kurash. 19 (2): 167–177. doi:10.1080/09670877309412751.
  216. ^ a b v d Flores, A. (2010 yil 17-fevral). "Yangi tahlil termitlarni, boshqa hasharotlarni kuzatishda yordam beradi". Qishloq xo'jaligi tadqiqotlari xizmati. Amerika Qo'shma Shtatlari Qishloq xo'jaligi vazirligi. Olingan 15 yanvar 2015.
  217. ^ Su, N.Y .; Sheffrahn, RH (1990). "Qo'shma Shtatlardagi iqtisodiy jihatdan muhim termitlar va ularning nazorati" (PDF). Sotsiobiologiya. 17: 77-94. Arxivlandi asl nusxasi (PDF) 2011-08-12.
  218. ^ Torn, PhD, Barbara L. (1999). NPMA tadqiqotlari Er osti termitlari to'g'risida. Dann Loring, VA: NPMA. p. 40.
  219. ^ Elliott, Sara (26 may 2009). "Qanday qilib mis termitlarni ushlab turishi mumkin?". HowStuffWorks.
  220. ^ a b v Figueirêdo, R.E.C.R.; Vaskoncellos, A .; Policarpo, I.S .; Alves, R.R.N. (2015). "Ovqatlanadigan va dorivor termitlar: global nuqtai nazar". Etnobiologiya va etnomeditsina jurnali. 11 (1): 29. doi:10.1186 / s13002-015-0016-4. PMC  4427943. PMID  25925503.
  221. ^ a b v d Nyakupfuka, A. (2013). Global lazzatlar: Qadimgi Gavayi ta'limotining qalbingizdagi lavhani tozalash va o'zingizni yuksak darajaga ko'tarish uchun yo'qolgan havolalarni toping.. Bloomington, Indiana: BalboaPress. 40-41 betlar. ISBN  978-1-4525-6791-4.
  222. ^ a b Bodenxaymer, F.S. (1951). Hasharotlar inson oziqi sifatida: Inson ekologiyasining bir bobi. Gollandiya: Springer. 331-350 betlar. ISBN  978-94-017-6159-8.
  223. ^ Geissler, PW. (2011). "Tuproqni iste'mol qilishning ahamiyati: Luo bolalari orasida geofagiyaning ijtimoiy va madaniy jihatlari". Afrika. 70 (4): 653–682. doi:10.3366 / afr.2000.70.4.653.
  224. ^ Knudsen, J.W. (2002). "Akula udongo (yerni iste'mol qilish odati): Kilimanjaro tog'ining yon bag'irlarida Chagga ayollari orasida ijtimoiy va madaniy amaliyot". Afrikalik mahalliy bilim tizimlari jurnali. 1 (1): 19–26. doi:10.4314 / indilinga.v1i1.26322. ISSN  1683-0296. OCLC  145403765.
  225. ^ Nchito, M.; Venzel Geysler, P.; Mubila, L .; Friis, H.; Olsen, A. (2004). "Temir va multimikronutrientli qo'shimchalarning geofagiyaga ta'siri: Lusakadagi Zambiyalik maktab o'quvchilari o'rtasida ikkitadan faktorial tadqiqotlar". Tropik tibbiyot va gigiena qirollik jamiyatining operatsiyalari. 98 (4): 218–227. doi:10.1016 / S0035-9203 (03) 00045-2. PMID  15049460.
  226. ^ Saathoff, E .; Olsen, A .; Kvalsvig, J.D .; Geissler, PW. (2002). "Geofagiya va uning janubiy Afrikaning KvaZulu-Natal shahridan bo'lgan qishloq o'quvchilarida geogelmint infektsiyasi bilan bog'liqligi". Tropik tibbiyot va gigiena qirollik jamiyatining operatsiyalari. 96 (5): 485–490. doi:10.1016 / S0035-9203 (02) 90413-X. PMID  12474473.
  227. ^ Katayama, N .; Ishikava, Y .; Takaoki, M .; Yamashita, M.; Nakayama, S .; Kiguchi, K .; Kok, R .; Vada, X.; Mitsuhashi, J. (2008). "Entomofagiya: kosmik qishloq xo'jaligining kaliti" (PDF). Kosmik tadqiqotlardagi yutuqlar. 41 (5): 701–705. Bibcode:2008AdSpR..41..701S. doi:10.1016 / j.asr.2007.01.027.
  228. ^ Mitchell, JD (2002). "Termitlar Janubiy Afrikadagi ekinlar, o'rmon xo'jaligi, yaylovlar va inshootlarning zararkunandalari sifatida va ularga qarshi kurash". Sotsiobiologiya. 40 (1): 47–69. ISSN  0361-6525.
  229. ^ Löffler, E .; Kubiniok, J. (1996). "Tailand shimoli-sharqi Thorat platosida er shaklining rivojlanishi va bioturbatsiya" (PDF). Siam Jamiyatining Tabiiy Tarix Axborotnomasi. 44: 199–216.
  230. ^ Evans, T.A .; Deyvz, T.Z .; Uord, P.R .; Lo, N. (2011). "Chumolilar va termitlar quruq iqlim sharoitida hosilni ko'paytiradi". Tabiat aloqalari. 2: 262. Bibcode:2011 yil NatCo ... 2..262E. doi:10.1038 / ncomms1257. PMC  3072065. PMID  21448161.
  231. ^ a b v d e "Termite Power". DOE qo'shma genom instituti. Amerika Qo'shma Shtatlari Energetika vazirligi. 14 Avgust 2006. Asl nusxasidan arxivlangan 2006 yil 22 sentyabr. Olingan 11 sentyabr 2015.CS1 maint: yaroqsiz url (havola)
  232. ^ Xirschler, B. (2007 yil 22-noyabr). "Termitlarning ichak reaktsiyasi bioyoqilg'i uchun o'rnatildi". ABC News. Olingan 8 yanvar 2015.
  233. ^ Roach, J. (2006 yil 14 mart). "Termit quvvati: zararkunandalarning jasadi yangi yoqilg'ini yaratishi mumkinmi?". National Geographic News. Olingan 11 sentyabr 2015.
  234. ^ Verfel, J .; Petersen, K .; Nagpal, R. (2014). "Termitdan ilhomlangan robot qurilish guruhida jamoaviy xulq-atvorni loyihalash". Ilm-fan. 343 (6172): 754–758. Bibcode:2014Sci ... 343..754W. doi:10.1126 / science.1245842. PMID  24531967. S2CID  38776920.
  235. ^ Gibney, E. (2014). "Termitdan ilhomlangan robotlar qasrlar qurishmoqda". Tabiat. doi:10.1038 / tabiat.2014.14713. S2CID  112117767.
  236. ^ a b v "Tropikadagi termitlar yashil me'morchiligi". Me'mor. Keniyaning me'moriy assotsiatsiyasi. Olingan 17 oktyabr 2015.
  237. ^ Tan, A .; Vong, N. (2013). "Tropikadagi quyosh bacalarini parametrlarini aniqlash bo'yicha tadqiqotlar". Energiya. 6 (1): 145–163. doi:10.3390 / en6010145.
  238. ^ Tsoroti, S. (2014 yil 15-may). "Bu nima bino? Eastgate Mall". Harare yangiliklari. Olingan 8 yanvar 2015.
  239. ^ "Im Zoo Bazel fliegen Termiten aus-da o'ladi". Neue Zürcher Zeitung (nemis tilida). 2014 yil 8-fevral. Olingan 21 may 2011.
  240. ^ Van-Xuis, H. (2003). "Afrikaning Sahroi janubidagi hasharotlar oziq-ovqat sifatida" (PDF). Hasharotlarga oid fan va uning qo'llanilishi. 23 (3): 163–185. doi:10.1017 / s1742758400023572.
  241. ^ a b Neoh, K.B. (2013). "Termitlar va Janubi-Sharqiy Osiyodagi insoniyat jamiyati" (PDF). Axborot byulleteni. 30 (66): 1–2.

Keltirilgan adabiyot

  • Bignell, D.E .; Royzin, Y .; Lo, N. (2010). Termitlar biologiyasi: zamonaviy sintez (1-nashr). Dordrext: Springer. ISBN  978-90-481-3977-4.
  • Schmid-Gempel, P. (1998). Ijtimoiy hasharotlarda parazitlar. Nyu-Jersi: Prinston universiteti matbuoti. ISBN  978-0-691-05924-2.

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