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INAUGURAL LECTURE SERIES 287 ti URBANIZATION, FRESHWATER I BIODIVERSITY CONSERVATION AND THE CRITICAL ROLE OF AQUATIC INSECTS SYLVESTER SUNDAY OGBOGU, FESN Professor of Zoology F ' J - Q QBAFRNI AWOLOWO UNlVERSlN PRESS, ILE-IFE, NIGERIA.

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INAUGURAL LECTURE SERIES 287

ti URBANIZATION, FRESHWATER

I

BIODIVERSITY CONSERVATION AND THE CRITICAL ROLE OF AQUATIC

INSECTS

SYLVESTER SUNDAY OGBOGU, FESN Professor of Zoology

F'J - Q QBAFRNI AWOLOWO UNlVERSlN PRESS, ILE-IFE, NIGERIA.

SYLVESTER SUXDAY OGBOGU, FESN Professor of Zoology

h omow, FEsi\l 'Zoology

URBAN1 ZATION, FRESHWATER BIODIVERSITY CONSERVATION AND THE

CRITICAL ROLE OF AQUATIC INSECTS

An Inaugural Lecture Delivered at Oduduwa Hall, Obafemi Awolowo University, Ile-I fe, Nigeria

On Tuesday, 24th May, 20 16

SYLVESTER SUNDAY OGBOGU, FESN Professor of Zoology

Inaugural Lecture Series 287

Obafemi Awolowo University Press Limited Ile-Ife, Nigeria

OGBOGU, FESN Zoology

URBANIZATION, FRESHWATER BIODIVERSITY CONSERVATION AND THE

CRITICAL ROLE OF AQUATIC INSECTS

An Inaugural Lecture Delivered at Oduduwa Hall, Obafemi Awolowo University, Jle-Ife, Nigeria

On Tuesday, 24th May, 20 16

SYLVESTER SUNDAY OGBOGU, FESN Professor of Zoology

Inaugural Lecture Series 287

Obafemi Awolowo University Press Limited Ile-Ife, Nigeria

O Obafemi Awolowo University Press Limited, (201 6)

ISSN 0 189-7848

Pri~lted by 'Obafemi Awolowo University Press Limited,

Ile-Ife, Nigeria.

1. PREAMBLE

tsity Press Limited, (201 6 )

1n bl? versity Press Limited, iigeria.

The Vice Chancellor Sir, Principal Officers of the University, Mcmbers of the University Council, Provosts, Deans, Directors, colleagues, students, distinguished ladies and gentlemen, It is with deep sense of humility and gratitude to God that I stand before you today to deliver the 287"' Inaugural Lecture of Obafemi Awolowo University, Ile-Ife and the 1 1"' from the Department of Zoology.

Pcrn~it me to give a concise account of what led to my decision to study Zoology in the University of Ibadan and the choice of the Aquatic or Freshwater Entomology as a sub-discipline in Zoology. As a young boy in the primary school, I was curious about the diversity of organisms and spent most of my time chasing, collecting and playing with grasshoppers, birds and other animals, which was thought then as serendipity to my age mates. This enthusiasm for the study of life fuelled my determination to study all kinds of animals during my tertiary education. It was my dream to work on animals, although the societal influence of aspiring to be a medical doctor was also a desire.

When I was admitted into the University of Ibadan to read Zoology, it was clear to me that the divine hand of God was at work in my choice of career as an academic, because majority of my lecturers encouraged me to proceed for postgraduate studies.

On returning to the University of Ibadan for my postgraduate studies, I had no problems in the choice of a sub-discipline. I recollect with nostalgia that when late Professor Samuel Afolabi Toye addressed my M.Sc. Entomology class, on the need for someone to embark on the study of insect diversity in aquatic ecosystelns as a postgraduate research project, I had no hesitation in signifying my interest. Professor A. Titi Hassan was on hand as the most qualified to supervise my M.Sc dissertation, having worked extensively on the ecology of dragonflies. Professor Hassan willingly accepted me and gave me a research topic on the feeding mechanisnis and habits in a species of dragonfly. My

M.Sc. dissertation exposed me to many phenomena in aquatic ecosystems and elicited enormous curiosity in me.

On completion of the M.Sc. programme in 1987, I did not hesitate to continue, having qualified to embark on a doctoral degree programme. My research foray observed and determined the factors that influenced the diversity and abundance of Mayflies (Ephemeroptera) in tropical man-made reservoirs. Since then, I have approached all my research work with a primary goal - to find out what is there in any aquatic ecosystem and how it survives. In this inaugural lecture, titled "Urbanization, Freshwater Conservation and the Critical Role of Aquatic Insects", I shall discuss the negative impact of urbanization on the integrity of freshwater ecosystems. Using my knowledge of aquatic insect diversity and community structure in the ecosystems, I shall proffer measures aimed at mitigating the impact.

2. INTRODUCTION 2.1 Urbanization The rate at which the world is undergoing urban growth is quite alarming. More than half of the world's population is resident in towns and cities. It has been predicted that by year 2030, this number will further increase given the current global problem of migrations across cities, countries and continents. The attendant rapid urbanization brings huge socioeconomic and environmental transformations especially in Africa and Asia. Although urbanization is expected to bring in a new era of well-being, efficient and sustainable resource utilization and economic growth, it often ushers in social divide, with high level of poverty in the lives of a sizeable proportion of populations in slums and informal settlements coexisting with wealthy communities.

The effects of urbanization are not limited to its direct impact on the lives of people. It also affects organisms and other living systems in the environment. One common effect is the impoverishment of freshwater (reservoir, stream and river) biota as a result of generated waste dumping and inflow of run-off from

,o many phenomena in aquatic curiosity in me.

tnmme in 1987, I did not hesitate i embark on a doctoral degree I observed and determined the ~ l t y and abundance of Mayflies 7-made reservoirs. Since then, I ; work with a primary goal - to

I aquatic ecosystem and how it I. t~tled "Urbanization, Freshwater l ~ l e of Aquatic Insects", I shall urbanization on the integrity of

knowledge of aquatic insect lure in the ecosystems, I shall l~ng the impact.

rindergoing urban growth is quite world's population is resident in

predicted that by year 2030, this \en the current global problem of ies and continents. The attendant ~ocioeconomic and environmental

I Africa and Asia. Although ng in a new era of well-being,

.: utilization and economic growth, with high level of poverty in the

'nopulat~ons in slums and informal thy communities.

!lot limited to its direct impact on -fects organisms and other living

One common effect is the ,esenloir, stream and river) biota as nping and inflow of run-off from

watersheds into the aquatic ecosystems in urban areas.(Fig. 1). The impairment, popularly termed "urban stream syndromev (Booth et (11. 2016) is evidenced by degraded physico-chemical conditions, alteration of con~munity structure, reduction in diversity and/or outright extermination of aquatic insects and other plant and animal communities in the ecosystems.

What Is a Watershed?

P uaterslied IS the area of lalid that drams to a particular polnt along a stream

< - A ~ , : ~ - p+'-y - P

k

"

- - - blmh h - - m. 4

Figurel. An illustration of a watershed (springfieldohio.gov)

2.2 Freshwater Biodiversity Conservation Conservation is the sustainable use of resources which integrates protection with exploitation. Bearing in mind that preservation is a subset of conservation, meaning to keep something without altering or changing it, freshwater conservation can therefore be explained as all management practices that are directed at maintaining the biological integrity (good health) of freshwater ecosystenls. It seeks to protect, preserve and restore the health and biological integrity of freshwater ecosystems and its biodiversity, including the diversity of species. This may involve practices that ensure that renewable resources in then1 are not over-utilized. Freshwater conservation also involves monitoring and shaping the use of watersheds \slhich freshwater ecosystems drain. By so doing, impairment is prevented, reduced and controlled.

To articulate fresliwater conservation strategics, tlie International bnion of the Consen,ation for Natur-c and Natural Resources (IIJCN) in 1995 provided tlie franieuork (Article 13.1 of the In~cmational Covenant on Environment and Development) for the preservation of the health of natural ecosystems. The article states that "parties shall pursue sustainable de~,elopment policies aimed at the eradication of poverty, the general improvement of economic, social and cultural conditions, the conservation of biological diversity, and maintenance of essential ecological processes and life-support systems". It charged stakeholders in affected systems to take appropriate measures to conserve and whcre necessary and possible, restore natural systems which support lifc on Earth in all its diversity, including biological diversity, and to maintain and restore the ecological functions of these systems as an essential basis for sustainable development, including inter alia,

(a) Forests as climate regulators and as natural means to control erosion and floods;

(b) Freshwater wetlands and floodplains as recharge areas for ground waters, floodwater and buffers, filters and oxidizing areas for contaminants.

To give attention to the recommendation 'b' above, freshwater Biologists in general and Aquatic Entomologists in particular have been interested in tlie nature of aquatic insect and other macroinvertebrate conimunities in both impacted and non- impacted freshwater ecosystems (Clements 1994, Sykora et al., 1997, Meyer 1997, Maret et nl., 2003, Kreutzweiser 2008, Somers et rrl . , 20 13, Vandcr Laan, et al., 2003 and Arce et al., 2014). They have also provided information aimed at designing freshwater conservation strategies using the knowledge gained from aquatic insect ecology (e.g. Saunders et at., 2002, Strayer, 2006 and Suski and Cook 2007).

2.3 Aquatic Insects Many members of the arthropod group of animals (invertebrate a ~ i i ~ ~ i a l s with jointed appendages) including insects, live in all kinds of water bodies. These insects (aquatic insects) are known to

\.ation strategies, the International r Knturc and Natural Resources

frame\\ ork (Article 13.1 of the ronnicnt and Development) for the t i n 1 ecosystems. The article states inable cle\.elopment policies aimed v . the gcneral improvement of , conditions, the conservation of intcnance of essential ecological iems". It charged stakeholders in opriate measures to conserve and c, restore natural systems which its diversity, including biological restore the ecological functions of ?usis for sustainable development,

resulators and as natural means to floods; s and floodplains as recharge areas flooda,ater and buffers, filters and

:ontaminants. irnmendation 'b' above, freshwater 1:ic Entomologists in particular have lire of aquatic insect and other its in both inlpacted and non- r:s (Clements 1994, Sykora et nl., ;., 2003, Kreutzweiser 2008, Somers i . , ZOO3 and Arce et a/., 2014). They ion aimed at designing freshwater :he knowledge gained from aquatic

- .

02, Strayer, 2006 and Suski

spend their entire livcs or at least water-borne at some point in their lifc cycles in water bodies. One of the ~iiost amazing characteristics of aquatic insects is the diversity of habitats in which they can be found. There is no aquatic habitat that is too sniall, too large, too cold, too hot, too muddy, with oxygen too low, with currents loo fast, or even with too much pollution for sonie kind of aquatic insects to live there. The only exception is perhaps the marine environments (oceans and bays). However, a few of them live on coral reefs, in tidal pools of marine environments, and in estuaries, where there is a mixture of fresh inland water and salty ocean water.

Many aquatic insects are often not seen unless one curiously explores water bodies. Popular among aquatic insects are the niosquitoes which are considered harmful because they are vectors of pathogens that infect man and his animals. A lot more are quite useful in a way. They include the mayflies (Order: Ephenieroptera), dragonflies and damselflies (Odonata), stoneflies (Plecoptera) true bugs (Hemiptera), fishflies, dobsonflies and alderflies (Megaloptera), caddisflies (Trichoptera), aquatic Caterpillars (Lepidoptera), water beetles (Coleoptera), and true flies (Diptera) (Figs 2).

pod group of animals (invertebrate ;yes) including insects, live in all nsects (aquatic insects) are known to

Figure 2. An array of aquatic insects.

2.4 Aquatic insects and water quality assessments

Enonnous information exists in literature 011 studies which show that aquatic invertebrates (insects in particular) serve as indicators of water quality. The interest in aquatic insects stems from the fact that they are affected by physico-chemical and biological conditions of water bodies. The juvenile stages can not escape pollution, hence they sliow the effects of short- and long-tenn pollution events and the aggregate impacts. In addition to being a critical part o f aquatic food web, many species are intolerant to pollution and accentuate habitat loss not captured by traditional water quality assessments. Aq~~a t i c insects are easy to sample and identify. Apart fro111 direct use of water samples to detemline the concentration of varioi~s metals, dissolved oxygen, organic matter and hydrogen ion, biologists are able to assist the water chemists by using aquatic insects as indicators of water quality. Because some aq~~a t i c insccts are more sensitive to pollution than others, i t is easy to hypo~lies~ze a pollution event if a water body is inhabited by insects that are pollution-tolerant and devoid of pollution-

Lluality assessments I

1 literat~lre on studies which show 1; i n particular) serve as indicators iqt~atic insects stems from the fact

hli!,sico-cliemical and biological blc j~r\.enile stages can not escape i. effccts of short- and long-term 1 ! le impacts. In addition to being a ~ h . many species are intolerant to lit loss not captured by lraditional , ?~ ic insects are easy to sample and

c?f \\.ater samples to determine the i. clissol\.ed oxygen, organic matter -2 ahle to assist the water chemists tlicators of water quality. Because jensiti1.e to pollution than others. i t

event if a water body is inhabited [olerant and devoid of pollution-

sensitive ones (Fig. 3). This is the principle.behind biological water quality assessments. They tell us clearly if water bodies are impaired (or sick) due to pollution or habitat loss.

I Group One Tar#

! . .

%l~?nln c 'rnt~~~.nln

. j . . . .- - Uvnmi" : ;

lhthunflir.

a m ~ r r t k

croup rue Tax. som.wh.1 pmlumn or htr lo*nmorganlsrsaut qullrn -r Index ralw can 1.L - h o u n d k ~ o o d

Figures 3. Pollution sensitive and tolerant macroinvertebrates.

Aquatic insects also provide some freshwater ecosystem services. Through their functional feeding attributes (Fig. 4), they play important roles in energy flow and nutrient dynamics in the aquatic food web. They are involved in a number of important ecosystem processes including leaf-Iitter breakdown especially in urban watersheds.

Filtering Gatherin'g Collectors I 1 ' Collect~rs

%

-- - .2

gredators ---- 2redators 4 (Engulfers) ; '(Piercers)

$Seaveneers Piercer , , \

Herbivores - .w?2,fld a-2 Omnivores

Figure 4. Functional feeding groups in aquatic rnacroinvertebrates.

For example the shredders, gathering and filtering collectors are key players in generating fine particulate organic matter (FPOM) from coarse particulate organic matter (CPOM) and dissolved organic matter (DOM), particularly through their waste products. FPOM is an important high quality food material for other invertebrates and microbes because it is higher in nutrient content than the conditioned leaves (Fig. 5). Therefore, for a conservation biologist who is interested in freshwater ecosystems, the knowledge of composition and distribution, 'adaptations, niches, food habits, food webs and life cycles of aquatic insects, as well as water quality of water bodies is imperative.

1 Gathering Collectors

I" Shredders &. - Predators

(Piercers)

5 7 - Scavengers $I-( and Ca i Omnivores

groups in aquatic !S.

ring and filtering collectors are ~iculate organic matter (FPOM) matter (CPOM) and dissolved Iy through their waste products. uality food material for other ~e it is higher in nutrient content 5 ) . Therefore, for a conservation 1 freshwater ecosystems, the listribution, adaptations, niches, :les of aquatic insects, as well as perative.

Figure 5. Processes in the convertion of DOiM and CPObI to FPOM (Allan 1995).

3. MY CONTRIBUTION TO KNOWLEDGE

3.1 The need to develop and sustain freshwater conservation programmes in Nigeria The Vice-Chancellor Sir, during the early stage of my career as a lecturer carrying out research in Aquatic Entomology, I realized the need, just like any other environmentalist, for Nigeria to have a framework for the conservation of the ecological integrity of its numerous freshwater ecosystems. I launched my research career with studies on the ecology of a very important pollution sensitive group of aquatic insects, the mayflies (Fig. 6), using reference site approach. I compared the water quality and seasonal abundance of mayflies of a relatively pristine lake in the International Institute of Tropical Agriculture (IITA) with that of impacted stream-reservoir system (Awba Dam) in the University of Ibadan (Ogbogu, 199 1).

Nymph Types Crawler Clinger Swimming Burrowing

Nymph Anatomy

-. ";\-/

f 4, : , ',:>$:5(---=1

. , ; <\ :;k+Y2

\'?&*3.*:p2

c<.-k> G? p:! -4" -- jl> ,?i$ .$, <.,I-. J-"

< 1 ::I <..*' s . , :' 2 ,:

/ I "S $0, \

Forewing Pad Thorax -, I Hind "(iiq, Pad

Isonychia

Gills Dorsal Stripe

Tarsus - Posterolateral Spines

-Ta i Is 1

I I * I Foreleg Middle Leg Hind Leg Illustrationby Doug Hall

Figure 6. Mayfly nymphs (larvae) (www.delawareriverguide.net)

The mayfly communities found in both water bodies belonged to three families and were made up of eight species (Table 1). The record of the Cloeon species in that study expanded their distribution map in Nigeria and beyond.

l P =s wimming Burrowing

Isonychia k!.$!$;. Dorsal Strips !-

kc. ---.t-' , sterolateral Spines

..,..--- 1 i

. -Tails \ \ I

e!J 11lustr;ltion by Doug Hall

j in both water bodies belonged to uo of eight species (Table 1). The :S in that study expanded their beyond.

Table 1 : List of Afrotropical Ephemeroptera found in IITA Lake and Oba ~trearnl~eservoir system (Ogbogu 1991). Family and Species IITA Lake Oba StreadFteservoir Baetidae Cloeori nreolot~tm Navas + + Cloeon cylintlr.oc~rl~m~ + Kimrnins* Cloeon ganlhioe Gillies ** + . + C perkinsi Barnard + + - C. smaeleni Lestage Ophelnintostoma kimminsi + Waltz & McCafferty***

- Polymitarcyidae Pordlkn ad~rsto Navas + Caenidae Cner~is s.1. sp. + + '+' and '-' indicate occurrence and absence of the species respectively in the sampling sites. *Now known as Procloeon cylindrocuhrm. **Lava1 stage still confused with C. perkinsi. ***Now known as Ophelmntostomn cnmerounense.

Mr. Vice-Chancellor Sir, it is worthy of note that the record of Caenis sp. in that study was an addition to the six known species in Africa as at 1991. Moreover, the polyrnitarcyid Povilla adusta was recorded for the first time in Nigeria (Fig 7).

Figure 7. Larva of Povilla adusta Navas (Corbet 1957).

There was significant correlation between some inorganic ions in the water and the abundance of Cloeon larvae in areas impacted by treated sewage in IITA Lake. My first publication in a scientific journal was based on a curious observation in which phoretic association occurred between a Caenis sp. larva and the bryozoan Pllrn~llrella sp. statoblast (Ogbogu, 1993) (Fig. 8).

,-

is. .A, -9%

Figure 8: Abdominal region of Caenis s.1. sp. with arrow showing Plumatella sp. attached to the gill cover (Ogbogu 1993).

The statoblast is a dormant stage which normally drifts on water surface but on germination adheres to any handy object. Its association with the mayfly larva was considered accidental but it may aid in dispersal as in the cases between mayflies and other invertebrates (Disney 197 1, Gillies and Elouard 1990). In another study, we (my supervisor and I) concluded that sewage outfall was responsible for the wide fluctuations in pH, total alkalinity, free carbon dioxide, dissolved oxygen, and reduction in the abundance of the mayflies, Cloeon and Cclenis in Awba stream-reservoir system in the University of Ibadan (Ogbogu and Hassan 1996a). Having noted the influence of water quality parameters on the abundance of Cloeon perkinsi larvae, I subsequently sought to determine the effect of individual ions on the most abundant and ubiquitous species of Cloeon, C. perkinsi in the laboratory. From a 48hr laboratory static bioassay, it was observed that phosphate ion was more harmful to the insect larvae while the LCso was 13.5mgIL for nitrate. The conclusion from that

. .-i 0 . 5 3 ~ ~

Coc11i.s 5.1. sp. with arrow showing rl to the gill cover (Ogbogu 1993).

\vli~ch normally drifts on water heres to any handy object. Its I nas considered accidental but it :ases between mayflies and other es and Elouard 1990). lsor and I ) concluded that sewage : \ \ ~ d s fluctuations in pH, total I~sqolved oxygen, and reduction in s. Clocorl and Cnerlrs in Awba nijersity of Ibadan (Ogbogu and tlie influence of water quality

b of Cloeorl perkrrlsi larvae, I 1s the effect of individual ions on 15 species of Cloeorl, C. perkirzsi in abnratnry static bioassay, it was ; more harmful to the insect larvae lr n~trate. The conclusion from that

study (Ogbogu, 2003) was that among many species of mayflies, Cloeor~ was a good candidate for water quality assessment in the water bodies.

An earlier study with the same objective had established the optimum ranges of water temperature and dissolved oxygen concentration for the survival of the Cloeon perkinsi larva in the laboratory. The 24hour LCso for oxygen was found to be 4.35 * 0.141mgl" (Fig 9a), while temperature ranged from 20 to 2S°C with lower and upper LTSoS being 7S°C and 35°C respectively (Fig 9b), (Ogbogu and Hassan 1996b). I also concluded in another study (Ogbogu 1999), that the mayfly Povalla adustn was warm- adapted, after establishing that the temperature for maximum hatching success of its eggs was around 33.20°C.

I 100,-

I an-

- I . , ; a*; ' !

Figure 9a: Orygen tolerance in Cloeo/t perkittsi larvae (Ogbogu and Hassan 1996b).

Figure 9b: Temperature tolerance in Cloeort perkirrsi (Ogbogu and Hassan 1996b).

The Vice-Chancellor Sir, the quest for baseline data on which strategies for conservation of freshwater ecosystems in Nigeria could be based led to further studies on reservoirs. Attention was focused on Opa Reservoir with a study spanning two years. The study revealed that just like the IITA lake in Ibadan, Opa Reservoir in Ile-Ife was dominated by two mayfly genera, Cloeon and Cuenis, and that water current velocity and submerged aquatic plants determined their distribution and abundance (Fig 10) (Ogbogu 200 1 a).

in Cloeorl perkirtsi (Ogbogu and

:st for baseline data on which shwater ecosystems in Nigeria ies on reservoirs. Attention was study spanning two years. The 'A lake in Ibadan, Opa Reservoir 10 mayfly genera, Cloeon and relocity and submerged aquatic tion and abundance (Fig 10)

Figure 10. Monthly mean number of Cloeorr and Caerlis (Ephemeroptera) larvae and monthly fluctuation in water current velocity at Station 3 in Opa stream- reservoir system (Ogbogu 2001a).

My other studies on the reservoir paid attention to the stream below the reservoir where I observed the vital role the aquatic ' .

moss, Fontinalis species (Bryophyta) played in the phenology (annual larval recruitment and adult emergence) of hydropsychid caddisflies (Ogbogu 2000,20Olb, Ogbogu and Akinya 2001).

To characterize the water bodies in Ile-Ife, I started with a study in an adjoining stream which is part of the Opa River tributary network. The stream receives treated sewage effluents from the

twin sewage oxidation ponds in Obafemi Awolowo University, Ile- Ife. From the observed low diversity and populations of pollution sensitive aquatic organisms, it was inferred that the forest stream -

ecosystem was impaired. Significant difference was observed in the number of individual macroinvertebrates and community. structure between two stations located upstream and downstream of the sewage ponds' point source discharge. The preponderance of the pollution-tolerant chironomid larvae indicated a stressed stream ecosystem resulting from the ponds' effluent discharge (Tab. 2), (Ogbogu and Olajide 2002).

Table 2. Composition, distribution and abundance of macroinvertebrates in two stations in a forest stream in Obafemi A~volowo University in May to November 1998. Station 1 above, and Station 2 below effluent discharge (Ogbogu and Olajide 2002). Tanon Station I Aug Scpt Scpt Oct Oct Sov Total

I 0 I 2 0 2 0 0 5 Coleoptera

I1 1 3 3 0 4 3 2 1 6 I 3 I I 0 0 0 0 5

Crustacea (Crabs) I I 0 0 0 5 0 1 0 6 I 0 0 1 0 0 0 0 1

Ostracoda (Cjpris sp.) I I n 1 0 n n n n n 1 n Diptera I 0 0 0 0 0 0 5 5 (C'hironomidae) II 16 82 45 9 90 77 111 430 Diptera I 0 0 0 0 0 0 0 0 (Mosquito larvae) II 0 0 0 0 2 5 I 0 17

. . - . - - . .

Odonata: Zygoptera I 1 17 9 8 8 23 12 78 I I 1 19 45 32 22 51 20 190

r, ,7 ,7 r, ,, 0 I u u u u u

Odonata: Anisoptera I

II 5 0 0 5 0 21 5 16

Total nun nber o f taxa

nber of Total nun I 18 27 13 9 11 23 17 118 ~ n d ~ v ~ d u a ~ s I I 37 116 97 5 1 123 168 148 740 Tutal 55 143 110 60 134 191 165 858

3.2 Aquatic insect faunistics Mr. Vice-Chancellor Sir, a shift in my research focus was enunciated following my comn~unication with late Professor Mich. T. Gillies. He advised that since Nigeria's aquatic insect fauna

~afemi Awolowo University, Ile- ;ity and populations of pollutioli .s inferred that the forest stream :ant difference was observed in ,oinvertebrates and community. zated upstream and downstream discharge. The preponderance of anlae indicated a stressed stream ids' effluent discharge (Tab. 2),

ibution and abundance of s in a forest stream in Obafemi ember 1998. Station 1 above, and Ogbogu and Olajide 2002). 4twi \cpt Oct Oct \o\ Total I I 29 I4 25 06

ift in my research focus was lication with late Professor Mich. e Nigeria's aquatic insect fauna

were largely unknown, it w o ~ ~ l d be logical to embark on faunistics st~idies in Nigeria's freshwater bodies. By so doing errors in the identities of species under study would be avoided. Besides, a framework for characterization of aquatic insect fauna and comn~unity structure in water bodies could be developed to enable and enhance conservation strategies for them in future.

I had earlier reported the occurrence of the heptageniid mayfly genus Cot?zpsorzeuria (Eaton) for the first time in Nigeria, thereby providing additional information on its distribution range in Africa (Ogbogu and Jagun 1999). This was followed by several reports describing many genera and species that were hitherto unknown as part of Nigeria's aquatic insect fauna. The first outcome from the new research foray was a description of the macronematine Acthnloptera &spar Brauer (Ogbogu 2005) (Fig. l l ) , whose morphological features suggested a form distinct from those earlier described for the same species elsewhere in the West African subregion.

Figure 11. Adult a macronematine species of Trichoptera. Photo: Isaac Ehikhamele.

In the larva, the anterior margin of the frontoclypeus was excavated and the foretrochantin had more setae at the distal area than in other species (Fig. 12). This disparity was attributed to possible link between polymorphism and adaptation to habitat and climatic conditions in the species.

Figure 12. Dorsal views of Frontoclypeus and left foreleg of Aethaloptera dispar (Ogbogu 2005).

Descriptions of more species of caddisflies highlighting differences in morphological features from known species were equally carried out. For Anisocentropus species McLachlan (Ogbogu 2006a), the larvae described appeared similar but could be separated from A. usambarensis and other species by the presence of spines on the lateral margin of the pronotum. In addition, the ventral apotome of the head has an anteromedian depression and flat at the anterolateral comers (Fig. 13). A subsequent description of a male adult bred out of larva confirmed this species as A. usambarensis (Ogbogu 2009).

Figure 13. Atrisocentropus sp. larva: Left lateral margin of pronoturn (left), and ventral side of head showing anterior ventral apotorne (right) (Ogbogu 2006a).

ntoclypeus and left foreleg of pbogu 2005).

of caddisflies highlighting ures from known species were tcentroplts species McLachlan ibed appeared similar but could 8nsis and other species by the a1 margin of the pronoturn. In ' the head has an anteromedian :rolateral comers (Fig. 13). A adult bred out of larva confirmed )gbogu 2009).

Examining the larva and adult male of the most common and abundant hydropsychid caddisfly observed in a previous study (Ogbogu 2001b), I identified the species as Cheunlatopsyche digitntn Mosely (Ogbogu, 2006b), although it did not perfectly fit into the key to the adult C. digitnta in Satzner (1984). Unlike in Statzner's (1 984) C. digitara, the distance between the anterior and posterior lateral setal area is shorter than the distance between the anterior and posterior margin of anterior lateral setal area in the head. In the larva, the incision by the left side of anterior margin of frontoclypeus is deeper than the one in the right. The posterior arm of foretronchantin does not have as much setae as that figured for C. digitnta in Statzner (1984) (Fig. 14). My conclusion on these findings highlighted the relationships among several species of CI~ezrr?~ntops~~che which made it difficult in separating the species, but was hinged on previous reports on its microhabitats and distribution pattern. It associates with moss (Bryophyta) as observed by Hynes (1975) and Ogbogu (2001b) in intermittent streams where its abundance is usually high and responds to increase and decrease in stream discharge.

. larva: Left lateral margin of ~ n d ventral side of head showing lotome (right) (Ogbogu 2006a).

Figure 14. Cl~eunratops~~clte digitata (Mosely, 1935): Dorsal view of head showing setal areas in adult male (left), and midleg of larva showing the anterior and posterior arms of the foretrochantin (rght) (Ogbogu 2006b).

It is generally believcd that A/klcr-oslen~ltr~l illienu/?~ Ulrner occurs more in the transition zone between the northern 'dry7 savannah and solneti~nes in southern lowland forest regions, where water current velocity and length of dry period in streams were identified as factors influencing its distribution. But based on the locality of the material collected and examined (Fig. 15), it was concluded that the species can also be found in tropical rainforest region, which is wetter than the adjacent savannah region towards the north (Ogbogu and Adu, 2006). This led us to conclude that M. rrlieriunz is highly plastic and distributed beyond what was known from previous studies. As such it may be as widely distributed as its congener, Ad. cupense Walker, as noted in Scott ( 1983).

Figure 15. Macrostenlunl alieirum larva. Ventral view of head showing stridulatory ridges (left), and dorsal view of right foreleg (right).

My analysis of reports on the Afrotropical species of the leptocerid caddisfly genus Oecetis MeLachlan yielded an apparent lack of knowledge of the fauna in the region. To address this, I studied the mature larva of an unnamed species of the genus from the stream below Opa Reservoir, Ile-Ife, and successfully separated it from other Afrotropical species (Ogbogu 2008). The distinction was based on the pattern of arrangement of 14 muscle scars on the frontoclypeal apotome and the dorsoventrally compressed larval case with large rock fragments (ballast stones) that. are laterally attached (Fig. 16). The species shales the case type with the North American species, 0 . noctlrrrzn Ross, which belongs to the Oecetis

iCnlltnl t r l r o l l r ~ l l Ulmer occurs n the northern 'dry' savannah :I forcst rcglons, whcrc water : r~nd In streams were identified I. But based on the locality of :d (Fig. 15). it \\'as cotlcluded 1 in tropical rainforest region, sa\ annah region towards the

111s led us to conclude that M. buted beyond \+.hat was known na! bc as widely distributed as , rioted in Scott ( 1 983).

I larva. Ventral view of head ridges (left), and dorsal view of

,tropical species of the leptocerid lan yielded an apparent lack of ion. To address this, I studied the ies of the genus from the stream d successfully separated it from 3911 2008). The distinction was nent of 14 muscle scars on the lorsoventrally compressed larval [bsllast stones) that are laterally .ales the case type with the North oss. xvhich belongs to the Oecctis

(Oecetis) fir/-vrr group. To determine the actual identity of this :pecies, I recommended more collection and rearing of larvae for larva-adult association.

Figure 16. Oecefis sp. (larva): 1 . Head (dorsal view) showing muscle scars; 2. Larval case (dorsal view) showing laterally attached rock fragments (Ogbogu 2008).

As observed in Oecetis, the identities of African species of the leptocerid Triaertodes McLachlan are lacking. Efforts at tackling this problem were directed at the description of only the adults of some West African species (Anderson and Holzenthal 2001,2002). This made the knowledge of the species of the genus in the subregion far-fetched, given the poor knowledge of the larvae. My . contribution to the knowledge of this genus in West Africa is a description of the larva of an unnamed species (Figure 17a and b) collected from a forested and well-shaded perennial stream in Obafemi Awolowo University, Ile-Ife, where it closely associates with organic debris (Ogbogu and Okeze 2008).

Figure 17a. Triaenodes sp. larval case, (Ogbogu and Okeze 2008).

Figure 17b. Triaeriodes sp. (larva). 1. Head and pronotum, dorsal view. 2. Head, ventral view. 3. Foreleg with foretrochantin (arrowed), leteral view. 4. Abdominal segments VIII - X and anal prolegs, dorsal view, 5A, Hind leg and 5B middle leg tibia and tarsus, lateral view (Ogbogu and Okeze 2008).

Mr. Vice-Chancellor Sir, the search for taxonomic data on the aquatic insects of southwestern Nigeria also led to my description of a new species of mayfly from Opa River catchment basin named

;e, (Ogbogu and Okeze 2008).

1. Head and pronoturn, dorsal hntral view. 3. Foreleg with wed), leteral view. 4. Abdominal ~d anal prolegs, dorsal view, SA, Idle leg tibia and tarsus, lateral ieze 2008).

Afronunrs opt! sp. n., (Ephemeroptera: Heptageniidae) (Ogbogu and Oyewole 2007). Following the revision of the heptageniid mayfly genus Conrpsonetrria (Webb et al. 2006), the identity of the unknown species earlier described in Ogbogu and Jagun (1999) was confirmed as C. rljaletisis (Ogbogu 2007). In a similar study, the perliid stonefly Neoperla sp. (Needham) was reported for the first time in Nigeria (Ogbogu 2006~).

.. \ 3.3 Urbanization and freshwater biodiversity

Having identified some members of the aquatic insect fauna, the L next was to see how some of them responded to human disturbance

and environmental heterogeneity. I chose caddisflies, one of the EPT (Ephemeroptera, Trichoptera and Plecoptera) taxa, whose members are quite sensitive to aquatic pollution. As a starting point, my postgraduate student and I carried out a detailed study on life history and density of C. digitata larvae below Opa Reservoir spillway and found that as suggested in previous studies, the highest larval density occurred in October during the bloom of the moss Fortfinalis sp. (Bryophyta) (Figs. 18). We also observed that larvae appeared first in July during maximum stream flow velocity and disappeared as a result of adult emergence in January during reduced velocity. Using a morphometric character (head capsule width), we observed five larval instars for C. digitata in the spillway (Fig. 19). We were able to infer the insect's dependence on the moss for its peculiar univoltine life cycle below the reservoir (Ogbogu and Adu 201 1). This adjustment in life cycle and production is an adaptation to an unstable habitat occasioned by changes in flow regime and water discharge below the reservoir. Habitat alteration adversely affects aquatic insect populations, hence changes in the food web and general ecology of freshwater systems.

ch for taxonomic data on the ;cia also led to my description a River catchment basin named

Jul Aug Sep! Oct Nov Dec Jan Feb Mar Apr May June

Time (Month) Figure 18. Density of Clreunzatopsyclie digitata larvae below Opa

Reservoir spillway (Ogbogu and Adu 201 1).

A? ":% <.. <. .: ,- LO ; ,.. ,,-. , ,:. ,;? .: '>U :.L $ ..- -< ,~ > '. <, :> ', :, > > ,>. 2"- 3 < 2" -": 3 ,<* $ ,,* ,:* \' -3 Size (mm)

I I I 111 1 \' V

Figure 19. Size frequency distribution of the head capsule widths of Cheunratopsyche digitata larvae below Opa Reservoir spillway. I - V = larval instars (Ogbogu and Adu 201 1).

I

Jan =t?b Mar Apr Alay June

! (Month)

P S J J C I I ~ digitata larvae below Opa gbogu and Adu 201 1).

Taking the investigation on caddisflies beyond the freshwater ecosystems in the university, we investigated some streams in Ile- Ife metropolis along with those in Obafemi Awolwo University premises to determine how human activities impacted on the distribution and abundance of caddisflies (Amusan and Ogbogu 2013). Six species in six genera and three families were encountered. Of these, C. digitnta was most abundant (Fig. 20) and widely distributed in the water bodies sampled (Tab. 3).

, .. T.. -

7 . i.. -

: C , .I , < . : ' . Cr:

c:kir{::. r ~ e c i c j

Figure 20. Distribution of the caddisfly species in the sampling stations in Ile-Ife (relative to the total number of sampling stations). C.d, Clieumatopsyche digitata; P.s, Polyniorphariisus sinrilis; P.m, Pseudorreureclipsis nrlangensis; A.d, Aethaloptera dispar; D.c, Dipseudopsis confornris; C.n, Ceraclea rtjalaerrsis. (Amusan and Ogbogu 2013)

111 I \" V tion of the head capsule widths of ?ta larvae below Opa Reservoir instars (Ogbogu and Adu 201 1).

Table 3. Occurrence of caddisfly species in sampling stations (streams) located in Ile-Ife metropolis. '+' indicates the occurrence of the species in the sampling stations; '-' indicates the absence of the species in the sampling stations -- (Amusan and 0-gu 2013).

Cadclisfly species Stream location C. P. P. A. D. C.

!!giraru si~rrilis 111a11ge11is i s co~fur~rris rljale~rsis

Opa + + + + Road I + + + + + Obudu + + Parks & gardens + + + Reforestation + Ncw G a r a ~ e + + + + + + Mayfair + + Olonadc + + % Occurrcncc 1 00 50 17.5 50 25 75 -

There was evidence of high level of human activities as some water bodies (e.g. Obudu, Mayfair and Olorodo streams) had very low populations of caddisflies (Tab. 4).

Table 4. Number of individuals of species of caddisflies collected from sampling stations (streams) located in Ile-Ife

(Amusan and Ogbogu 2013). Caddisfly species

Stream location C: P. P. A . D. C Total

digilorn s i 1 1 s n1ln17ge1rsis dispnr corr/or~~lis I ~ ~ I I C I I . ~ ~ ~ O P ~ 46 9 0 I9 23 5 102 bad 1 119 24 0 42 5 1 9 245 Obudu 76 0 0 15 0 0 91

Parks / gardctis 17 7 0 11 0 0 35 Reforestation 2 5 0 0 0 0 0 25 New Garage 7 1 30 6 50 39 17 213 Mayfa~r 17 0 0 9 0 0 2 6 Olonadc 13 0 0 0 4 0 17 Total 384 70 6 146 117 31 754

Contrary to our expectation, some water bodies in the university appeared highly impacted (e.g, the stream in Reforestation area) with low populations of caddisflies as well. At this point it is necessary to draw attention to an example of obvious cases of inipact of urbanization on water bodies. Large quantities of non-

J ~ ~ ~ ~ J ' species in sampling sfations llc-lfe IIIetropoli~. '+' indicates (he

pecies in the sampling stations; i.c

of the species in the sampling Oobogu 2013). \'3- .

r'addisflv species -- - -- - i1 A. D. r.

i s disp~r r o l l f ~ l ; . ~ l , j ~ / ~ l l J , s

+ +

"el of human activities as some ir and Olorodo streams) had very ib. 4).

of species of caddisflies collected (streams) located in Ile-Ife

Oobogu 2013). -3.

? j \ f ~ \ ~ c c i e s :I. D. C Total

!i-pnr con/or~~~is ,~;~I/~,Is; .T I (1 23 5

1 2 5 1 102

. - 9 245

water bodies in the university : Stream in Reforestation area) :s 8s well. At this point it is "ample of obvious cases of

)dies. Large quantities of non-

degradable waste materials are deposited into drainages and stream channels in Ile-Ife, much of which find their way into Opa Reservoir as shown in (Fig. 21). We all know that these pollutants will cause serious pollution if nleasures are not taken to reduce their inflow into the reservoir. Apart from the immediate impact on water quality, the aquatic insect fauna will be completely wiped out. This menace has to be addressed urgently.

Figure 21. Non-degradable waste materials in the channel of the stream supplying Opa Reservoir. Photo: S. S. Ogbogu

3.4 Projecting dragonflies as a focal group in freshwater biodiversity conservation

The Vice-Chancellor Sir, my research interest in aquatic insect faunistics, their distribution and abundance as means of highlighting the effects of urbanization on water quality is further demonstrated by my investigations on dragonflies. Juvenile and adult dragonflies are sensitive to environmental degradation including water quality impairment and forest habitat fragmentation. As human activities continued to impact adversely on freshwater ecosystems, now worsened by the hydrological impact of climate change, it becomes imperative to improve on the robustness of the tools to assess the impacts. However, access to relevant knowledge in designing the tools remains poor because until recently, water quality assessments using aquatic insects largely revolved round EPT taxa metrics. Recent advances made it possible to project Odonata as a focal group in freshwater conservation. In the year 2005, I was invited to participate in a

training workshop organized by the Species Survival Commission of the International Union for the Conservation of Nature (IUCN- SSC) in partnership with Wetlands International in Dakar Senegal (Fig 22). The workshop targeted freshwater biodiversity assessnient for western Africa, using the IUCN criteria in deteniiining the conservation status of organisms. This was followed u p with another workshop to evaluate the freshwater biodiversity assessnient project for western Africa in Accra, Ghana in 2006 (Fig 23).

Figure 22. Participants of the training workshop, Dakar, Senegal. Photo: C. Pollock.

b!, the Species Survival Commission the Conservation of Nature (IUCN-

:lands International in Dakar Senegal

, . l:rgfied freshwater biodiversity

fit" using the lUCN criteria in n status of organisms. This was orhhop to evaluate the freshwater t for western Africa in Accra, Ghana

rralnlng worlishop, Dakar, Senegal.

1 r . Participants of the freshwater biodiversity assessment in western Africa overlooking Lake Volta from Ghana's Akosornbo Dam. Photo: K.-D.B. Dijkstra.

In the 2006 workshop, 1 participated in reviewing the assessments of a number of species including CIzlorocypha glalrca (Selys 1879), C. mclix Longfield 1959 and Helineschnn ser~rhe Pinhey 1962 (Dijkstra 201 0a,b; Claunitzer & Dijkstra 20 10). The outcome of the workshops includes my publications on the status of Odonata in the whole of West and other parts of Africa (Dijkstra et a/ . , 2009, 201 1). The lessons learnt at the workshops also spurred me to revisit the study of dragonflies of Nigeria with my doctoral degree student. Surveys were carried out in tandem in two contrasting habitats, Obafemi Awolowo University Ile-Ife in Osun State and Apomu Forest Reserve in Ondo State. The short-term goal of the studies was to generate taxonomic, ecological and distribution range data on odonate fauna. The long-term goal was to further advance the use of dragonflies in habitat assessment. hence freshwater biodiversity conservation in the Afrotropical region, with improved data on which Dragonfly Biotic Index (BDI) for Nigeria and neighbouring countries will be based in f~~ture.

Mr. Vice-Chancellor Sir. our data on dragonflies of Obaferni Awolowo University revealed 53 species in seven families. Of

these, rliree libelluline and two aeslinid species were recorded as new to Nigeria (Tab. 5) (Fig. 24), (Adu and Ogbogu 201 1).

Table 5. Checklist of Odonata species from Obafemi Awolowo Universitv, _ __ Ile-Ife, (Adu and 0-u 2011).

TAXON *Assessment category

Libellulidae Nesciotherllis pujoli Pinhey, 1971 LC Orthetrrrnz sternn~ale Selys, 1869 LC Pantalc? Jlcrvescens (Fabri tius, 1 798 LC Aeshnidae Heliaeschrrn long$eldae Gambles, 1967 LC H. setlibe Pinhey 1962 DD * From IUCN Red list of Threatened Species. LC = Least Concern, DD = Data Deficient.

Figure 24. Odanata species of Obafemi Awolowo University, Ile- Ife, Nigeria which are new to the country list. a) Nesciotlrentis pujoli (LC), b) Ortlietrun~ stentntale (LC), c) Heliaescliria for~gfiefdae (LC), and d ) H. senrbe OD). All photos are of preserved specimens, (Adu and Ogbogu, 201 1).

t r o aeshnid species were recorded as 24). (Adu and Ogbogu 201 1).

at8 species from Obafemi Awolowo Adu -_.- and Ogbogu 201 1).

"Assessment category

DD ~tened Species. LC = Least

Our study in Apomu forest recorded 103 odonate species in 44 genera and eight families in which the Libellul;dae were the most abundant (Fig. 25), (Adu and Ogbogu 2013). Of these 18 species are new records in Nigeria (Table 6).

Coenagrio Aes hnidae Gomphida

Calopteryg idae 3 %

Protoncuri dat Platy

10% dl dae 6 K

Figure 25. Percentage composition of families of Odonata in Aponmu Forest, May 2008 -2010, (Adu and Ogbogu,

Obafemi Awolowo University, Ile- are new to the country list. a) LC). b) Ortlt etrunt stentnzole (LC), M a e (LC), and d) H. setttk (DD). preserved specimens, (Adu and

Table 6: Checklist of new records of Odonata in Nigeria-(Adu and Ogbogu, 2013)

Suborder1 *Assessment Species Family category

Anisoptera Libellulidae Atoconeura eudo,uia (Kirby, 1908)

Microinncromia rr~iracirlosa (Longfield, 1947) Tetruthemisfr-aseri Legrand 1977 Trither~~is hatwigi Pinhey 1 96 1 Zjgonoides fuellehorzii (Griinberg ( 1 902)

Zygoptera Chlorocyphidae Cltlorocypha radix Longfield, 1959

C. pj~rifoniosa Fraser 1947 Coenagrionidae Aciagriorl heterostrica Fraser 1955

Afiicullagn~a vugir~ale Sjostedt, 19 17 Ceriagrion wheNar~i Longfied 1952 Psezrriagrion hernadi Terzani 200 1 P. hicoer~rlar~s Martin 1907 P. torridurn Selys 1876 Teir~ohasis aNliaudi (Martin, 1 896)

Plathycnemidae Mesocrier~ris saralisa Dijkstra 2008 Plag~cnernis r~yar~sar~a Forster 1 9 1 6

Protoneuridae Elutto~teuru lliba Legrand 1985 E. pasq~rir~ii consige;o 1978 \-I '

*From IUCN Red list of Threatened Species. DD = Data Deficient, LC = Least Concern, NA = Not Applicable, VU = Vulnerable.

It is worthy of note' that although most of the new records are 'assessed as either Data Deficient, Least Concern or Not Applicable, using IUCN criteria, three are Vulnerable in the threatened category (Fig. 26).

f Odonata in Nigeria. (Adu

3pectes "Assessment category

fdo.~io (Kirby, 1 908) LC iil nrircrc~dosa 4 7 ) N A :~ .~er i Legrand 1977 DD :igi Pinhey 1961 LC 'Ilt~honii (Griinberg

LC

?Olir Longfield, 1959 'raser 1947 sus~,-iccc Fraser 1 955 rgi~~crle Sjostedt, 19 17 llatli Longfied 1952 r.trcrcli Terzani 200 1 dartin 1907 1s 1876 ! ~ ~ d i (Martin, 1896) rrlislr Dijkstra 2008 ?7sutla Forster 1 9 1 6 r Legrand 198.5

- - si_ceio 1978 \:I. ned Species. DD = Data Deficient, P.pplicable, VU = Vulnerable.

~lgh most of the new records are ficient, Least Concern or Not .ia, three are Vulnerable in the

Figure 26. Vulnerable odonate species in Apomu Forest Reserve. Tei~iobasis alluadi (VU) (Top left), Photo: J. Renoult; Pserrdagrioll bicoerlrlaris (VU) (Top right), Photo: A Cordero Rivera; and Elattolierrra pasquirzii (VU) (Bottom) Photo: K-D. B. Dijkstra, (Dijkstra et al. 201 1).

Urgent and serious attention needs to be paid to deforestation which is a major threat to the populations of the dragonflies. Given the rapid pace of urbanization in Nigeria as a developing country, these species may soon be critically endangered. This is likely to happen if efforts are not made to conserve our freshwater ecosystems and secure the survival of the species. Conserving Odonata and the freshwater biodiversity they represent implies the maintenance of the structural integrity of both larval and adult habitats - i.e. water bodies and their surrounding riparian landscapes.

The Vice-Chancellor Sir, at this juncture let me join all stakeholders in Obafemi Awolowo University in hailing her as Africa's most beautiful campus. But there are 'silent stakeholders', the dragonflies, whose contributions to the beauty of the campus are never acknowledged. Apart from the beautiful coloration they

exhibit, they provide considerable freshwater ecosystem services. Their juvenile stages (nymphs) are major players in aquatic food web. They prey on a variety of organisms ranging from infusoria to fish fry. Their waste products also contribute to nutrient cycling in aquatic ecosystems. We need to conserve their micro- and macrohabitats (Freshwater ecosystems on campus) to guarantee their survival and enjoy these services. I hereby suggest that as many forested areas are opened up for infrastructural development on campus, we should be mindful of the adverse effects it has on our water bodies through erosion, siltation and sediment transport in streams as well as unnatural flow regimes. These will drastically reduce the populations of the aquatic insects and their role in the conservation of the integrity of water bodies compromised and eventually eliminated. To avoid this catastrophic situation, forest removal should be minimized, because many dragonfly species are stenotopic. They have very narrow tolerance to environmental disturbance and require shade in the adult stage.

4.0 CONCLUSION AND RECOMMENDATIONS The Vice-Chancellor Sir, Nigeria can boast of accomplished and eminent scholars in the field of insect science (Entomology) but the dearth of entomologists with interest in aquatic insects is largely evident in Nigerian Universities and research institutes. It is the realization of this that spurred and sustained my interest in Aquatic Entomology research. I consider myself privileged to be one of the few who by the virtue of their training, are aware of the importance of freshwater biodiversity conservation in environmental health and nation building. I have been working hard to deepen this awareness through the teaching of Entomology in general and research in Aquatic Entomology in particular.

Research outputs on the use of aquatic insects as indictors of water quality has led concerned individuals and groups to call for conservation actions to mitigate anthropogenic disturbance in Nigeria's freshwaters. However, the calls may remain fairly effective or ineffective due to the fact that aquatic biodiversity of most of the country's freshwater ecosystems have not been

ible freshwater ecosystem services. ) are major players in aquatic food orginisms ranging from infusoria to

contribute to nutrient cycling in d to conserve their micro- and systems on campus) to guarantee services. I hereby suggest that as UP for infrastructural development

ful of the adverse effects it has on In. siltation and sediment transpon low regimes. These will drastically quatic insects and their role in the f water bodies compromised and

this catastrophic situation, forest :cause many dragonfly species are ITOW tolerance to environmental the adult stage.

ECOMMENDATIONS 1 Can boast of accomplished and insect science (Entomology) but

Ih interest in aquatic insects is mities and research institutes. It is ed and sustained my interest in consider myself privileged to be 9: their training, are aware of the biodiversity conservation in building. I have been working

q h the teaching of Entomology Entomology in particular.

atif insects as indictors of water duals and groups to call for anthropogenic disturbance in the calls may remain fairly

fact that aquatic biodiversity of r ecosystems have not been

characterized. That is, data are lacking or deficient on the faunistics of Nigeria's freshwater biodiversity. The role of insects in water quality assessments, accentuated by the importance of species identities as presented in this lecture sets the stage for effective freshwater conservation measures in Nigeria.

As a starting point, I hereby call for an inventory of Nigeria's freshwater bodies arranged in groups in terms of type, size, water quality and general ecosystem characteristics. The information should be used to test conservation strategies, develop, implement and regularly update long-term water quality protection programmes. Such programmes should be rooted in proper understanding of local attributes of any given freshwater ecosystem and its watershed to ensure its protection and recovery if impaired. Governments can determine and delineate some freshwater bodies as Freshwater Protected Areas (FPAs) for development of conservation management techniques for use by freshwater scientists, conservationists and managers. Educational materials can be provided to support the public on water quality to ensure awareness and empowerment of freshwater ecosystem stewardship. Above all, governments and private sector can drive the development and evaluation of conservation strategies through massive funding of research and capacity building in freshwater biology.

The Vice-Chancellor Sir, perhaps the easiest and most cost- effective ways of reducing the effects of urbanization on freshwater ecosystems are actions taken at individual and group levels. The use of biodegradable cleaning products to reduce contamination of water bodies cannot be overemphasized. Tree- planting in and around homes can hold soils together and help reduce runoffs. Limited pesticide use reduces the quantity of such contaminants carried into freshwater ecosystems by runoff. Donations to support community projects and volunteering for stream-cleanup help protect freshwater ecosystems for people and nature. Finally, non-governmental organizations (NGOs) with

freshwater conservation mandate can partner with governments and academia to shape and implement their programmes.

5.0. ACKNOWLEDGEMENT Mr. Vice-Chancellor Sir, this lecture will not be complete without appreciating my master's and doctoral degree supervisors, Prof. A. Titi Hassan and late Prof. Samuel Afolabi Toye. They saw the zeal in me and resolved to dedicate their time to midwife the making of a Nigerian Aquatic Entomologist. I will forever be grateful to these erudite scholars and exquisite mentors.

I wish to express my gratitude to Obafemi Awolowo University for providing the platform to realize my dream as an academic in pursuit of knowledge in Aquatic Entomology. The University offered me an appointment as Assistant Lecturer in the Department of Zoology where I rose to become a Professor. I am gratefill to my colleagues in the Department for their love, cooperation and support as well as to all my postgraduate students. I thank the Vice-Chancellor Professor Idowu Bamitale Omole and all the principal officers of this University for providing me the enabling environment to pursue my academic career.

I appreciate the support from Emeritus Professors A. E. Akingbohungbe and R. A. Balogun, Professors J. I. Ighalo, J. I. Nwachukwu, A. 0 . Isichei and J. I. Muoghalu. These high ranking scholars have mentored me through the years in my academic endeavours and family life. I thank Dr. A. 0 . Akintomide, Professors E. A. Agbakwuru and A. A. Salako, and members of Umunna for being there for me and my family. I appreciate the prayers of members of Mount Zion Small Christian Community Apostolate, and the entire Parishioners of Our Lady of Perpetual Light Chapel, pastored by our indefatigable Reverend Father Ayo Abe.

It is my pleasure to acknowledge the tremendous assistance received from late Prof. Mich T. Gillies. He provided the reference materials with which I started as a budding researcher. My

date can partner with governments piemcnr their programmes.

lecture will not be complete without doctoral degree supervisors, Prof A. iuel Afolabi Toye. They saw the zeal their time to midwife the making of ist. I n.ill forever be grateful to these nentors.

to Obafemi Awolowo University for lire my dream as an academic in latic Entomology. The University histant Lecturer in the Department :ome a Professor. I am grateful to cnt for their love, cooperation and postgraduate students. I thank the l\tru Bamitale Omole and all the ~ i t y for providing me the enabling :mic career.

)m Emeritus Professors A. E. 'gun, Professors J. I. Ighalo, J. I. . I. Muoghalu. These high ranking r o u ~ h the years in my academic

thank Dr. A. 0 . Akintomide, d A. 4 . Salako, and members of and my family. I appreciate the

!ion Small Christian Community lionen of Our Lady of Perpetual defatigable Reverend Father Ayo

!dqe the tremendous assistance jiliies. He provided the reference as a budding researcher. My

gratitude also goes to my collaborators abroad who thougl~t it wise to be interested in nly research focus. I am indebted to Emeritus Professor John C. Morse of Clemson University, South Carolina, USA: Professors Ralph. W. Holzenthal of University of Minnesota, St. Pauls, MN, USA and Karl Kjer of University of California, Davies, USA, for providing the travel grant with which I visited their laboratories to study insect identification using morphological and molecular data. I ihank Dr. Oliver Flint Jr. of Smithsonian Institution, USA and Professor Ferdy. C. de Moor of Rhodes University, South Africa for their advice on the study of African caddisflies. To Dr. K-D.B. Dijkstra of Naturalis, Netherlands, I am grateful for his keen interest in my research work on Nigeria's dragonflies and damselflies.

I am highly indebted to my parents. Chief Clement E. Ogbogu (Chinemelu) and Mrs. Rebecca E. Ogbogu (Aru ka akwa) for their unconditional love and parental care for my family through the years. I am grateful to my siblings who have been very supportive in all my endeavours. Some of them have sacrificed their comfort in a number of occasions to ensure that I succeeded as a scholar. I appreciate all my in-laws in general, my Mother-in-law and late Father-in-law in particular, who gave me their daughter as a wife with immense support, and hoped to witness this memora6le occasion. Finally, I express my profound and unreserved gratitude to my nuclear family. I am short of the right words to appreciate the encouragement and care my wife, Dr. Christians Osaikhiuwu Ogbogu (my Exquisite Jewel) and children have always given me. With prayers, they have demonstrated a high level of understanding and patience, particularly when I spend most of my time in the office and laboratory. I thank the Almighty God for them. I return all the glory to God for no man on earth should give glory to himself.

Mr. Vice-Chancellor Sir, ladies and gentlemen, I thank you all for your attention. God bless you all.

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damselflies (Insecta: Odonata) in Obafemi Awolowo University, Ile-Ife, Southwestern Nigeria. Agrion 15(1): 24- 31.

Adu, B.W. and Ogbogu, S.S. (2013) Diversity and community structure of dragonflies and damselflies (Insecta: Odonata) in Apomu forest, southwestern, Nigeria. International Journtil of Agriculttrre and Forest y 3(6): 23 1-239.

Allan, J. D. (1995) Stream Ecology, Structure and Function of Running Waters London, Chapman and Hall.

Amusan, B.O. and Ogbogu, S.S. (2013) Observations on the abundance and distribution of adult caddisflies (Insecta: Trichoptera) in streams and rivers of Ile-Ife, southwestern Nigeria. Internntionnl Journal of Tropical Insect Science 33(3): 163- 169.

Anderson, T. and Holzenthal, R.W. (2001) West african Triaenodes McLachlan (Trichoptera: Leptoceridae). 1. Introduction and subgenus Triaenodella Mosely. Tijdschrg voor Entontologie 144, 225-246.

Anderson, T. and Holzenthal, R.W. (2002) West african Triaenodes McLachlan (Trichoptera: Leptoceridae). 2. Subgenus Triaenodes sensu stricto. Tijdschrift voor Enton~ologie 145: 61-88.

Arce, E., Archaimbault, V. Mondy, C.P. and Usseghio-Polatera, P. (2014) Recovery dynamics in invertebrate communities following water-quality improvement: taxonomy vs trait- based assessment. Freshwater Science 33(4): 1060- 1073.

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