Bee Bytes: Centris pallida

female Centris pallida
Female Centris pallida


Deserts. Common. Diggers.


Map made with Discoverlife


Name: ‘The Pallid Bee’ or ‘The Digger Bee’ (no official common name)

Family: Apidae (with: carpenter, honey, bumble bees)

States: Arizona, California, New Mexico, Nevada

male C. pallida digging; CC by SA 3.0 link through photo

Centris pallida are known for their vibrant, yellow-green eyes and pale fuzz as they buzz around desert palo verde – females are also known for the lovable ‘chaps’ on their rear legs which help them gather pollen.

C. pallida are some of the best bees at maintaining a stable body temperature; they are often found within 2 degrees Celsius of lethal overheating!

C. pallida females dig long tunnels to lay a single egg in a wax-lined cell, 8-10 cm under the dirt. These cells are provisioned with a soupy, orange-colored bread made of pollen and nectar. After sealing the cell, the mother fills in the whole tunnel with dirt and starts over for her next egg. Females often aggregate in the same area, collectively laying hundred of eggs in a relatively small area.

In early spring, the next generation of adults emerge and aggregate by the thousands to mate. Males emerge first, and begin searching the ground for females. Large males can smell females underground as they start to dig themselves out of their cells and will fight with one another to help dig her out and mate with her. Small males can’t afford to brawl so they employ a sneakier strategy! Hovering on the outside of the aggregation, they wait for escaped females to mate with instead.

Sources and Further Reading:

A friendly webpage written by C. pallida expert, John Alcock that summarizes his papers listed below.

Alcock J, Jones E, Buchmann S (1976). The Nesting Behavior of Three Species of Centris Bees (Hymenoptera: Anthrophoridae). Journal of the Kansas Entomological Society, 49: 469-474.

Alcock J, Jones E, Buchmann S (1976). Location before emergence of the female bee, Centris pallida, by its male (Hymenoptera: Anthrophoridae). Journal of Zoology, 179: 189-99.

Alcock J, Buchmann S (1985). The significance of post-insemination display by male Centris pallida (Hymenoptera: Anthophoridae). Z. Tierpsychol., 68: 231-43.

Alcock J (1976). The social organization of male populations of Centris pallida (Hymenoptera, Anthophoridae). Psyche, 83: 121-31.

Alcock J, Jones C, Buchmann S (1977). Male mating strategies in the bee Centris pallida Fox (Anthophoridae: Hymenoptera). The American Naturalist, 111: 145-55.

Chappell M (1984). Temperature regulation and energetics of the solitary bee Centris pallida during Foraging and intermale mate competition. Physiological Zoology, 57: 215-25.

Gilliam M, Buchmann S, Lorenz B (1984). Microbial flora of the larval provisions of the solitary bees, Centris pallida and Anthophora sp. Apidologie, 15: 1-10.

Roberts S, Harrison J, Hadley N (1998). Mechanisms of thermal balance in flying Centris pallida (Hymenoptera: Anthophoridae). Journal of Experimental Biology, 201: 2321-31.

Roberts S (2005). Effects of flight behavior on body temperature and kinematics during inter-mate male competition in the solitary desert bee Centris pallida. Physiological Entomology, 30: 151-7.

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The Second Quarter: Checking In

Me with my trusty wasp brain! Brain section within this photo credit to the O'Donnell lab and Drexel University.
Me with my trusty wasp brain! Brain section within this photo credit to the O’Donnell lab and Drexel University.

Wow have the past few months flown by – year two of your PhD is no joke! First, I’d like to recognize all the big things I achieved in this last quarter (in no particular order):

  1. Went to ESA EB and presented on wasp brains
  2. Organized a field season to Arizona
  3. Presented a poster and helped my undergraduates make two posters for a conference
  4. Applied for four grants
  5. Finished the termite retina project
  6. Had my first committee meeting #CandidacyBossBattlePart1
  7. Embedded and sliced all the bee/spider brains #BrainDraincomplete
  8. Earned my graduate minor in Undergraduate STEM Education
  9. Was on a podcast! My very first #SuperwomeninScience
  10. Hosted Biotweeps – and had a ton of fun
  11. Brought two new undergraduates into the lab, trained them on the first project, and developed materials for a new mentorship training program that I am implementing

There is a lot to be proud of on this list.

What things didn’t I get to? Well, the blog took a huge backseat (my last Bee Byte is two months ago!) and I did not finish the Pest Mess (one of my big goals in my last goal-setting post) – mostly because all my ants died, before giving them the pesticide… oops.

So what are my goals for quarter two – April through June?

  1. Candidacy Boss Battle, Part 2: Sometime between April and June it’s time for my full-on committee meeting and any revisions to my proposal that may come from this. Bring on the #nerves.
  2. The Pallid Bee: A successful first field season out in Arizona would be a big boon to my thesis. Luckily, I have a great crowd supporting me at University of Arizona – and back home.
  3. Pest Mess (attempt 2?): Shall we try again? Hopefully, in May I’ll have some time to grab fresh Tetramorium and give these last few experiments one more whirl.
  4. Carpenter Contemplation: If Pest Mess doesn’t happen you can bet it will be because of the Carpenter bee project I have sitting in my back pocket, which will require some trips up to NY in May.

Hopefully, I’ll have some time to update this space with exciting news about grants, my field season, and other upcoming trips – as well as more Bee Bytes – ASAP. I’ll be celebrating my plane ride to Arizona with a Bee Byte on my thesis species, Centris pallida, so stay tuned for that – coming April 4!

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Bee Bytes: Do All Bees Sting?

BeeByteLogoMany people are afraid of bees (and wasps) because of their stingers – but not all of our buzzing buddies actually sting. Which bees aren’t so sharp?

Gasteruptiid Wasp by zosterops (CC BY-NC 2.0; link through photo)
‘Gasteruptiid Wasp’ by zosterops (CC BY-NC 2.0; link through photo); the long, thin line at the end is the ovipositor.

1. Male bees (of any species) – A stinger is a modified version of the egg-laying part of a female bee’s body, called the ovipositor. Since males were never meant to lay eggs, they never evolved a stinger.

Despite not being able to sting, many male bees will buzz loudly and curl the end of their abdomen towards anything that grabs them. This mimics a female’s stinging position and the behavior is scary enough that even experienced bee handlers will often reflexively let go!

2. Stingless bees – The meloponines, or stingless honey bees, are a group of approximately 500 species that live in tropical and subtropical zones. Stingless is a bit inaccurate – female bees have stingers, but they are so tiny they cannot pierce human skin.

The 's' points to the incredibly tiny stinger of a meliponine bee. The lips on either side with the hairs are the ends of the abdomen. Michener [2000]
The ‘s’ points to the incredibly tiny stinger of a meliponine bee. The lips on either side with the hairs are the ends of the abdomen. Michener [2000]

Fairy bees (Perdita), and other mining bees (Andrenidae; ~3000 species), lack the part of the stinger that pumps venom, rendering them effectively stingless. Not to be outdone, the Dioxyini, a group of cuckoo bees that lay their eggs in the nests of other bees, have the most reduced stingers of all!

3. Most bees, most of the time – While male bees and bees with reduced stingers may be incapable of stinging you, bees only use their stinger if they are in danger. If you see bees (or wasps), leave the fear behind – move slow and watch your step, and you’ll leave sting-free.

Source for further reading: Michener CD. 2000. The bees of the world. Baltimore: John Hopkins University Press.

*This post modified and condensed from one written for Buzz, Hoot, Roar in 2017- check out their short, informational posts on all kinds of natural life here.


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The First Quarter: New Years Goals

'Happy New Year! Bonne Annee Mes Amis!' by DaPuglet (CC BY-SA 2.0; link through photo).
‘Happy New Year! Bonne Annee Mes Amis!’ by DaPuglet (CC BY-SA 2.0; link through photo).

Happy New Year! May all of our 2018s be better than our 2017s.

I recently talked about goal-setting on Twitter, and how hard its been to follow through on many of my goals in my PhD program due to the ever-changing nature of the degree. The challenges and stresses are highly variable throughout the year, and I’ve come to the realization that annual goals – at least this coming year – probably won’t make much sense for me. Instead, I’ve decided to try out quarterly goals, with one big and two medium size professional goals to work on and evaluate every three months. For my first quarter (Jan 1 – March 31):


  1. Candidacy Boss Battle, Part 1: Plan my first field season and have my first committee meeting
  2. Brain Drain: Get through a round of bee and spider brain embedding
  3. Pest Mess: Run the last few ant trials to get started on that paper (this may extend into May/June)

Now, ‘Candidacy Boss Battle’ probably doesn’t seem like that big of a goal, but I want to give the process, and the emotional toll it’s likely to take on me, the respect it deserves. Here’s what I think that will likely entail:

  1. Reading about 1 paper a day
  2. Scheduling, organizing, attending the committee meeting
  3. Reminding myself to breathe for the 2 weeks prior to the committee meeting
  4. Making significant revisions to the proposal itself
  5. Organizing a field season in an area where I don’t know the facilities or tools
  6. Coming up with a back up idea for if I don’t find the aggregations
  7. Creating a presentation

So, given all the above, I feel like it’s a pretty big goal. Brain Drain is a pretty small goal in comparison, but would give me a cool graphic for my presentations and would keep pushing the spider brain project along as my undergraduates keep chipping away at the backlog. Pest Mess is more ambitious – mostly because it takes a long time to do the work (multiple weeks, uninterrupted), less that it is a lot of work to do. In any case, each of these would keep the lab humming along at a nice pace and my career progressing similarly.

I’ve also been thinking about personal goals for 2018 – 2017 was somewhat unhappy for me and I want to make 2018 better. I think some of this will be hard for me, and realistically won’t happen this year, because changing how you think and what you value is hard. But here are some of the things I’m going to at least try to be more aware of in 2018:

  1. Saying ‘no’ more often.  – I’ve spent a lot of time prioritizing making others happy, helping others, over helping myself. This is, in moderation, a character trait of which I am proud. It has led me to meet amazing people and have incredible, unique experiences. But I also become so busy and stressed that it strains my relationships with those I love, and my relationship with myself. It has given me incapacitating anxiety and led to depression. I need to learn to say ‘yes’ to me, and ‘no’ to others, more often.
  2. Valuing my mental and physical health. – We live in a world where pushing your body and mind beyond what is healthy is romanticized as an incredible devotion to your work. However this devotion hurts, when you take away the Instagram filters. This year, it is time to put my mental and physical health on the priority list – to stop joking about or in any way devaluing the importance of taking care of me.
  3. Bitter or Better. – “When something happens that you cannot control, you can choose to become bitter – or become better. Choose better.” – to paraphrase Sister Karlien from high school. This is something I used to be good at that I’m afraid the past two years have caused me to fall back from. I’ve got a lot of bitterness to let go of, to remember the positive feelings that make me happy. There’s a lot to be grateful for in my life, and even as times are complicated and tough, I need to remember ‘better’ is the way to go.
  4. Accepting my humanity. – Struggling with perfectionism, impostor syndrome, intense fears of failure, and self-imposed unrealistic expectations has only made the graduate school environment even more difficult. This year, I hope to accept my humanity – the process of failure as human, the importance of mistakes, letting go my harsh self-criticisms, seeing others that I admire in a more realistic light.

I hope that your 2018 is off to a good start – and that you use the beginning of the year to reflect on who you wish to become. I am hoping to find some time in future posts to discuss how, after you make a goal, to follow through using different types of step-organizing strategies that work for PhDs and life!

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Bee Bytes: Do Bees Actually Drink Sweat?

BeeByteLogo This past summer, you and I probably shared a similar bee experience: outside on a hot day, little metallic bees stuck to your bare arm, lapping up sweat from your skin.

These bees, called sweat bees, are from the Halictidae family and are very common. Between the US and Canada, there are approximately 520 known species of these shiny, and often colorful (like this Agapostemon texanus), insects. But why do they drink sweat?

Halictus ligatus, public domain photo by Insects Unlocked and Alexis Roberts
Halictus ligatus, public domain photo by Insects Unlocked and Alexis Roberts

Salt is necessary for egg production in insects (a female butterfly can lose more than 50% of the salt she’s born with in just one egg complement) and human sweat is absolutely loaded with it. Many insects have a hard time meeting their salt requirements, since nectar and pollen are not high in salts. This leads insects to drink our sweat, or even tears (a behavior exhibited by some bees from the Apidae family, though they may be after proteins too). Bees, moths, and butterflies will alight on the eyes of crocodiles and drink from mud puddles, feces, and urine to meet their salt needs.

In butterflies, this ‘puddling’ behavior (named for the plethora of butterflies found at mud puddles) is mostly seen in males, who transfer huge amounts of salt to females in their sperm. However female bees are commonly found drinking human sweat (which is why you may have experienced an unpleasant pinch when you try to brush one off your skin). This behavior is not believed to be harmful, so next time you see a sweat bee tell her: ‘Drink up!’

Augochloropsis metallica, public domain photo by Insects Unlocked and Lexi Roberts
female Augochloropsis metallica, public domain photo by Insects Unlocked and Lexi Roberts

Sources and Further Reading:

Adler P, Pearson D (1982). Why do male butterflies visit mud puddles? Canadian Journal of Zoology, 60: 322-5.

Banziger H, Boongird S, Sukumalanand P, Banziger S (2009). Bees (Hymenoptera: Apidae) That Drink Human TearsJournal of the Kansas Entomological Society, 82: 135-50.

Barrows, E (1974). Aggregation Behavior and Response to Sodium Chloride in Females of a Solitary Bee, Augochlora pura (Hymenoptera: Halictidae). The Florida Entomologist, 57: 189-93.

Dangles O, Casas J (2012). The bee and the turtle: a fable from Yasuni National ParkFrontiers in Ecology and the Environment, 10466-7.

Pivnick K, McNeil J (1987). Puddling in butterflies: sodium affects reproductive success in Thymelicus lineola. Physiological Entomology, 12: 461-72.

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Bee Bytes: Agapostemon texanus

Male Agapostemon texanus
Male Agapostemon texanus


Generalist. Widespread. Solitary.


Map made via Discoverlife
Map made via Discoverlife



Name: ‘The Green Sweat Bee’ (there are several)

Family: Halicitinae (with: other sweat bees, alkali bees)

States: Most likely all except Hawaii and Alaska


Agapostemon texanus belongs to one of North America’s most striking genera – all Agapostemon males and females have beautiful, metallic blue/green coloration. Males and females of Agapostemon species look very different (a phenomena called sexual dimorphism). Male abdomens are yellow-and-black/brown striped while female abdomens are consistently metallic and blue-green.

Abdomen of female Agapostemon texanus (public domain image, Lexi Roberts as part of ‘Insects Unlocked’)
Abdomen of female Agapostemon texanus (public domain image, Lexi Roberts as part of ‘Insects Unlocked’)

Of all the AgapostemonA. texanus is the most widespread, appearing from Costa Rica to Southern Canada. In the US, it is most common west of the Mississippi River. A. texanus has two generations a year, with mostly males active in the early fall and mostly females hibernating through the winter and active in spring and early summer (this split is due to a unique system called haplodiploidy).

Female A. texanus are strictly solitary, though females of closely-related species (like A. radiatus) have been found to make all their nests together in one area (called an aggregation) or potentially even use singular nests communally (A. nastus).

Agapostemon texanus (public domain image, Alejandro Santillana as part of ‘Insects Unlocked’)
male Agapostemon texanus (public domain image, Alejandro Santillana as part of ‘Insects Unlocked’)

A. texanus nest in the soil, creating long tunnels by digging. Females search for dark spots under pebbles or leaves to construct the entrance to the nests, making nests hard to spot by parasites. Females leave their nest open during the day as they forage on a variety of flowers (A. texanus are generalists) before closing the nest entrance in the late afternoon/early evening by pushing soil up from inside the main tunnel to close the door for the night. High security area!

Nests tunnels have been found up to 150 cms deep (nearly five feet!).

Sources and Further Reading (first is freely available and has a great drawing of an A. texanus nest!):

Roberts, R (1973). Bees of Northwestern America: Agapostemon (Hymenoptera: Halictidae). Technical Bulletin of the Agricultural Experiment Station at Oregon State University, 125: 1-23.

Eickwort, G (1981). Aspects of the Nesting Biology of Five Nearctic Species of Agapostemon (Hymenoptera: Halictidae). Journal of the Kansas Entomological Society, 54: 337-51.

Porter, C (1983). Ecological Notes on Lower Rio Grande Valley Augochloropsis and Agapostemon (Hymenoptera: Halictidae). The Florida Entomologist, 66: 344-53.

Waddington, K (1979). Flight patterns of Three Species of Sweat Bees (Halictidae) Foraging at Convolvulus arvensis. Journal of the Kansas Entomological Society, 52: 751-8.

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Bee Bytes: Are All Bees Social?

BeeByteLogoThink quick: Bee!

For most of us, a highly social hive of buzzing honey bees come to mind. But this is actually only a tiny sliver of the social structural pie. Here are some (but not all) other types of organization:

Solitary: Most bees are solitary, where a single female makes her nest alone. Solitary bees lay their eggs in small cells on top of a bed of food – the egg later hatches and feeds itself. Adults typically emerge from their cells around the same time, forage, lay their eggs, and then die while larvae/pupae wait underground for the next appropriate ’emergence’ season. This means adult generations do not overlap.

Gregarious nesters: These bees often appear social, as many solitary females will nest individually, but nearby one another, in ‘aggregations’.

Communal nesters: This is when multiple solitary females all share one nest, but lay their own eggs in individual cells within that nest.

Facultatively social: These species can be solitary or social, depending on environmental cues. In one species, Ceratina australensis, two sisters will sometimes form a colony together instead of nesting alone, with one foraging and reproducing and the other acting solely as a guard.

Primitively eusocial: Here, there are reproducing ‘queens’ and nonreproducing (but not sterile) ‘workers’. Queens and workers generally look similar, and workers can sometimes replace queens.

Photo credit: Meghan Barrett Apis mellifera, the Honey Bee
Photo credit: Meghan Barrett
Apis mellifera, the Honey Bee

Advanced eusocial: The honey bee colony: reproducing queens, nonreproducing, functionally sterile workers. Workers and queens do not look similar. The workers care for the queen’s young, and there are overlapping generations of adults.

Additional sources:

Wikipedia has a great chart (bottom of page) showing the differences between terms used to describe sociality, including: Eusocial, Semisocial, Subsocial,and Quasisocial.

This paper discusses some theory on the evolution of eusociality.

This paper addresses how advanced eusociality may have arisen through other types of sociality.

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Grant Writing: Are You Listening?

Photo by Fredrik Rubensson entitled ‘diary writing’ (Creative Commons Attribution-ShareAlike 2.0 Generic), link through photo

Grant writing is a new thing for me, so you should take all my advice with a grain of salt – but this is one piece I think might be worth considering. Grant writing isn’t really a big, scary exercise in writing and self-promotion (well, I mean, it is that too) but more importantly it’s an exercise in listening.

But who are we listening to? To answer this, we must think about who are we in conversation with as we write our grants. There can be several answers to this question – and several audiences for you to consider.

  1. The Grant Reviewers – Imagine you have to sit down and look over hundreds of applications from, mostly, similarly qualified candidates. What would make some stand out? It isn’t likely to be that one extra paper you published – it’s more likely to be that your application was enjoyable and easy to read. When the pages fly by and your story is interesting, you’ll leave the reviewers with a far more positive impression of you, and your science. So spend lots of time perfecting the readability of your writing – the reviewers will thank you.
  2. The Grant-granting Agency – I work as an assistant poetry editor for a literary magazine – in some ways we are a ‘granting agency’ in that we grant author’s work publication in our journal. Nothing is more irritating than reading work that doesn’t fit the stated goals of our magazine! Granting agencies likely feel the same way – if your work doesn’t fit the criteria, or address the points in the application instructions clearly, it doesn’t matter how amazing you are, you simply haven’t demonstrated you deserve this grant. Pay close attention to the wording used in the application for who they are looking to give this money to – and then use that same language to describe yourself and your work, so it’s easy to spot how you fit the bill.
  3. Your Critics – Another creative writing tidbit is the idea of workshops; you bring in a piece of writing and distribute it to your peers, who read it and comment on it – telling you what worked and what didn’t. You usually end up with 15 copies of your work that all say slightly different things… but have some common underlying thread. Apply the same principles to your grant – send it to lots of people, those with and without experience in your field or with you/your projects, etc. The suggestions they send back will vary and you absolutely should not take every suggestion, but look for the underlying themes. Are certain sections unclear? Do you need to reorganize so your question is broader and has more impact on your field? Is the tone bogging the piece down? Listen to what your critics are saying underneath their suggestions to get to some of the real issues with the piece.
  4. Your Cheerleader – Grant writing, maybe because it’s new or maybe because I have some serious impostor syndrome, is some hard stuff. I have to catch myself from making all kinds of qualifying, humbling statements like ‘this was a pretty big paper’ (since grant writing is all about acknowledging your accomplishments). So make sure you have a cheerleader – preferably somebody in your field but not your adviser who can tell you that you are GRRRRRREAT. It could be your mom, but would you really believe her? Find that one professional who can make you feel like others in your field recognize how awesome you are – and then read their email while listening to that ‘New Avengers’ song from ‘Avengers: Age of Ultron’. I promise, you’ll feel ten feet tall after and swagger like you’re Iron Man.
  5. Yourself – If you can’t represent yourself in the grant application, you don’t deserve to get it – whoever you represented does. No matter everyone else’s suggestions, edits, comments, and concerns, make sure before you submit that the grant still sounds like you. No one knows your smarts, skills, achievements, creativity, humor, etc like you do – so always read that last draft with yourself in mind.

Listening is hard and takes practice – pulling out the ‘underlying concerns’ in a critic’s piece or identifying what to do to make your narrative read more easily can be difficult. Not receiving a grant isn’t actually always about you and your qualifications – there are so many nuanced reasons, especially when there’s so little money to give out and such competitive pools of applicants (that you’re a part of!). Put your best application forward, then back away from the result – and be prepared to try again.

Each day, a new day.

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Biopoetics: Input Segregation

Photo entitled 'Ant communication' by Dzipi (CC BY-SA 2.0; link through photo)
Photo entitled ‘Ant communication’ by Dzipi (CC BY-SA 2.0; link through photo)

A huge thank you to, first, Palaver Magazine for publishing this piece here on page 79, and then for Poetry in Data for also publishing this piece here (you can listen to the poem here). I must also acknowledge Dr. Wulfila Gronenberg, as this is a found poem sourced from his 1999 paper: Modality-Specific Segregation of Input to Ant Mushroom Bodies. All of the words in this poem were found in the various sections of Dr. Gronenberg’s paper and – as is the case with all found poetry – it is the essence of the source that provides the true poetic inspiration.

This paper is the foundation for my work in ant neuroanatomy (paper forthcoming, stay tuned!). There is a section of the ant brain called the mushroom bodies, which is known to be involved in learning and memory (among other complex behaviors). There are two regions (the lip and collar) which receive input from different peripheral processing lobes: the optic lobe (which processes visual information and inputs to the collar) and the antennal lobe (which processes chemo-sensory information and inputs to the lip). This study by Gronenberg compared the size and structure of the mushroom bodies across several species of ants, wasps, and different genders of ants (which have vastly different behaviors over their lives).

Based on the differences in mushroom body size between the species, Gronenberg was able to tie individual variation to species-specific behaviors and living conditions. One example would be variation in the role of vision in the ants’ lives. Ant species with reduced eyes had reduced optic lobes and mushroom body ‘collar’ regions (a region we know to be associated with the input of visual information). If you don’t have large eyes, you likely aren’t processing much visual information – so you won’t need large brain regions to deal with vision.

The collar regions of males were found, across many species, to be much larger than that of female workers; male ants fly through the air to find females and mate, giving vision a critical role in their behaviors as compared to grounded, sometimes subterranean female workers of the same species.

Gronenberg showed there was a common design among Hymenopteran (ants, bees, and wasps) mushroom bodies, as well – making this one of the earliest studies to look into mushroom bodies outside of honey bees and Drosophila flies.

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Bee Bytes: Can you #WildID a Bee?

BeeByteLogoOn Twitter, nature-lovers will send scientists photos of an animal asking for a #WildID – or species identification. But can you #WildID a bee?

The answer: sometimes yes (but usually no).


Often bees of the same genera will look very similar (for example these two different species of male Agapostemon):

Agapostemon splendens (public domain image, Lexi Roberts as part of 'Insects Unlocked')
Agapostemon splendens (public domain image, Lexi Roberts as part of ‘Insects Unlocked’)
Agapostemon angelicus (public domain image, Lexi Roberts as part of 'Insects Unlocked')
Agapostemon angelicus (public domain image, Lexi Roberts as part of Insects Unlocked’)








And sometimes, two bees of the same species will look very different (like the abdominal coloration of these two female Augochloropsis metallica):

Augochloropsis metallica (public domain image, Lexi Roberts as part of 'Insects Unlocked')
Augochloropsis metallica (public domain image, Lexi Roberts as part of ‘Insects Unlocked’)
Augochloropsis metallica (public domain image, Lexi Roberts as part of 'Insects Unlocked')
Augochloropsis metallica (public domain image, Lexi Roberts as part of ‘Insects Unlocked’)








This makes telling a bee’s species from a photo very difficult; sometimes the features an entomologist must look at to ID a species are hidden under hairs, or even involve dissecting the bee.

However, sometimes a photo with location data can tell us everything we need to know to #WildID – some species have very distinctive features (especially when we know where the photo was taken, and thus what species are in that range). For example the triangle of black on the thorax of Bombus franklini (featured here), combined with information about the bee’s range, can be used to ID B. franklini with relative certainty. Sometimes even the time or flower a bee was spotted on can help #IDthatBee – if it is an early dawn forager, or a pollen-specialist that only visits a specific species.

Don’t be afraid to #WildID your next bee photo – even if the experts can’t get the species, often the next best thing (genera) can be ascertained with a glance. Check out Bees in Your Backyard to try your hand at IDing to genera, yourself!

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